Front. Endocrinol. Frontiers in Endocrinology Front. Endocrinol. 1664-2392 Frontiers Media S.A. 10.3389/fendo.2021.740174 Endocrinology Systematic Review Nesfatin-1 Receptor: Distribution, Signaling and Increasing Evidence for a G Protein-Coupled Receptor – A Systematic Review Rupp Sophia Kristina 1 Wölk Ellen 2 Stengel Andreas 1 2 * 1 Department of Psychosomatic Medicine and Psychotherapy, University Hospital Tübingen, Tübingen, Germany 2 Charité Center for Internal Medicine and Dermatology, Department for Psychosomatic Medicine, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, Berlin, Germany

Edited by: Liliane Schoofs, KU Leuven, Belgium

Reviewed by: Tommaso Angelone, University of Calabria, Italy; Hendrik Lehnert, University of Salzburg, Austria

*Correspondence: Andreas Stengel, andreas.stengel@med.uni-tuebingen.de

This article was submitted to Neuroendocrine Science, a section of the journal Frontiers in Endocrinology

 10 09 2021 2021 12 740174 12 07 2021 26 08 2021 Copyright © 2021 Rupp, Wölk and Stengel 2021 Rupp, Wölk and Stengel

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

 Background

Nesfatin-1 is an 82-amino acid polypeptide, cleaved from the 396-amino acid precursor protein nucleobindin-2 (NUCB2) and discovered in 2006 in the rat hypothalamus. In contrast to the growing body of evidence for the pleiotropic effects of the peptide, the receptor mediating these effects and the exact signaling cascades remain still unknown.

 Methods

This systematic review was conducted using a search in the Embase, PubMed, and Web of Science databases. The keywords “nesfatin-1” combined with “receptor”, “signaling”, “distribution”, “pathway”, g- protein coupled receptor”, and “binding” were used to identify all relevant articles reporting about potential nesfatin-1 signaling and the assumed mediation via a Gi protein-coupled receptor.

 Results

Finally, 1,147 articles were found, of which 1,077 were excluded in several steps of screening, 70 articles were included in this systematic review. Inclusion criteria were studies investigating nesfatin-1’s putative receptor or signaling cascade, observational preclinical and clinical studies, experimental studies, registry-based studies, cohort studies, population-based studies, and studies in English language. After screening for eligibility, the studies were assigned to the following subtopics and discussed regarding intracellular signaling of nesfatin-1 including the potential receptor mediating these effects and downstream signaling of the peptide.

 Conclusion

The present review sheds light on the various effects of nesfatin-1 by influencing several intracellular signaling pathways and downstream cascades, including the peptide’s influence on various hormones and their receptors. These data point towards mediation via a Gi protein-coupled receptor. Nonetheless, the identification of the nesfatin-1 receptor will enable us to better investigate the exact mediating mechanisms underlying the different effects of the peptide along with the development of agonists and antagonists.

 gut-brain axis food intake NUCB2 nucleobindin-2 stress nesfatin-1 Deutsche Forschungsgemeinschaft10.13039/501100001659 1 Introduction

Since the discovery of nesfatin-1 in 2006 in the rat hypothalamus (1), there has been a vast amount of research to further explore the pleiotropic physiological functions of this peptide. Nesfatin-1 is an 82-amino acid polypeptide generated via post-translational processing of hypothalamic nucleobindin-2 (NUCB2), a protein of 396 amino acids, whose sequence is highly conserved from fish to mammals (2) pointing towards its physiological relevance. The peptide is predominantly localized in food intake-regulatory nuclei e.g., the arcuate nucleus (Arc), the paraventricular nucleus (PVN) and the nucleus of the solitary tract (3, 4). Accordingly, the peptide became first known for its anorexigenic effects; however, subsequent studies unraveled its many other properties, such as cardiovascular effects, lipid metabolism, reproduction functions, and emotion- related functions (5–7). Subsequently, the peptides’ central part, nesfatin-130-59, which has been identified as the active core of the peptide, was reported to reduce food intake after intracerebroventricular (icv) injection in mice (8, 9) and in rats (10).

However, multiple studies have indicated that nesfatin-1 is also secreted by peripheral tissues such as adipose tissue, gastric mucosa, pancreatic endocrine beta cells and testes and its expression level was found to be 20 times higher in endocrine cells of the oxyntic gastric mucosa than in the brain (11–13).

Numerous studies have reported multifunctional effects of nesfatin-1: peripheral nesfatin-1 affects glucose homeostasis (14) and shows anti-apoptotic and anti-inflammatory effects (15). In addition, peripherally administered nesfatin-1 induces vasoconstriction and elevates blood pressure (16), and moreover decreases antral and duodenal motility (17) and reduces gastric emptying (18). Taken together, the role of nesfatin-1 goes far beyond its initially observed function as a negative modulator of food intake.

In contrast to the growing body of evidence of the pleiotropic peptide’s effects, the receptor mediating these effects is still largely unknown. Although several studies suggest that the peptide activates extracellular and intracellular regulatory pathways involving multiple putative binding sites (19), a specific nesfatin-1 receptor has not yet been identified. Therefore, the present paper was designed to systematically review the findings about nesfatin-1 signaling, especially by focusing on its potential receptor. This systematic review will discuss the state of knowledge on nesfatin-1 signaling, the putative mediation via a Gi protein-coupled receptor and highlight respective direct and indirect evidence. Lastly, gaps in knowledge will be highlighted to encourage further research hopefully leading to the identification of the nesfatin-1 receptor.

 2 Methods

We followed the preferred reporting items for systematic reviews and meta-analyses (PRISMA) (20) to report the results of this review.

2.1 Search Strategy

This article is a systematic review; articles related to the topic, were searched, collected, and screened. Articles released from the earliest day of publication to the day the search was performed were included. The search was conducted on November 22nd in 2020. We searched Embase, PubMed and Web of Science using the following keywords: “nesfatin-1” combined with “receptor”, “signaling”, “distribution”, “pathway”, G-protein coupled receptor”, and “binding” ( Table 1 ). All studies that contained material applicable to the topic were considered. We investigated the reference lists of the included studies to find other potential articles for inclusion. Local experts in the field were consulted for additional studies. Retrieved manuscripts were extracted using a standardized collection tool. Gray literature was not considered due to lack of essential information usually affecting this type of research. There was no date (all studies until November 2020) or species restriction in the search, but the search was limited to texts in English.

The search strategy of this review.

Search Engines and Databases

Embase

PubMed

Web of Science
Search date up to 2020, November, 22
Search terms Strategy: #1 and #2, #1 AND #3, #1 AND #4, #1 AND #5, #1 AND #6, #1 AND #7

#1 “Nesfatin-1”

#2 “Receptor”

#3 “Signaling”

#4 “Distribution”

#5 “Pathway”

#6 “G-protein coupled receptor”

#7 “Binding”
2.2 Inclusion and Exclusion Criteria

The inclusion criteria were as follows: (1) observational preclinical and clinical studies, experimental studies, registry-based studies, cohort studies, population-based studies; (2) Studies that were written in English (3) Studies investigating nesfatin-1 putative receptor or signaling cascade.

The exclusion criteria were as follows: (1) Review articles, surveys, case reports, comments, letters, conference abstracts or posters, and economic evaluation; (2) Studies for which abstracts or full-text articles were not available; (3) Studies that were not available in English; (4) Studies with absence of outcome data.

 2.3 Study Selection and Data Extraction

One reviewer screened all titles and abstracts retrieved from the electronic searches to identify potentially eligible articles. Full texts of the potentially eligible articles were retrieved. Two reviewers (S.R. and E.W.) screened all full text articles and potentially eligible or unclear full-text articles, determined whether they were eligible or not eligible and recorded the reason for exclusion. Any disagreements between both reviewers were resolved through discussion.

The quality of the studies included in this review was assessed with respect to risk of bias within individual and across studies by thoroughly evaluating the study designs, selection of population/species, methodological procedures applied as well as presentation of the results. Following a full-text review of the eligible studies, one reviewer (E.W.) extracted the relevant data. From each included study the following information was extracted: first author of the publication, year of publication, title, population/species, size of the respective population/species, study type, research question/purpose, and key findings ( Table 2 ).

Main findings of articles (in alphabetical order) included and discussed in this systematic review.

First author Year Species n Study type Main findings Risk of bias
Angelone T (21) 2013 Wistar rats 6 rats/group – in total n = 24 Experimental intervention study By using a nesfatin-1 antibody, the presence of nesfatin-1 was identified in the rat heart. Exogenous nesfatin-1 directly showed negative inotropic and lusitropic effects without affecting coronary motility. These effects were mediated by involving pGC-NPR-A, the cGMP/PKG pathway, and ERK1/2.
Ayada C (22) 2015 Male Wistar rats 7 rats/group – in total n = 28 Experimental intervention study Nesfatin-1 induced heart failure during clinical treatments by increasing expression of the cardiac L-type Ca2+ channel. Selection bias
Aydin B (23) 2018 Male Sprague-Dawley rats 7 rats/group – in total n = 70 Experimental intervention study Nesfatin-1 elevated mean arterial pressure and modulates heart rate in rats via the central cholinergic system. Selection bias
Barutcigil A (24) 2018 Male Wistar rats Not indicated Experimental intervention study Nesfatin-1 dose-dependently induced a relaxation on the endothelium-intact thoracic aorta of rats and produced positive inotropic and chronotropic effects on atria. These effects might be beta-1 receptor independent, while involving the NO-cGMP cascade. Selection bias
Brailoiu GC (25) 2013 Male and female Sprague-Dawley rats (in vitro), male Sprague-Dawley rats (in vivo), Nucleus ambiguous neurons 6 rats/group (in vitro), 5 rats/group (in vivo) Experimental intervention study Nesfatin-1 increased cytosolic Ca2+ levels via a Gi/o-coupled mechanism in cardiac vagal neurons of nucleus ambiguous by involving P/Q type voltage-activated Ca2+ channels. Moreover, nesfatin-1 led to a dose-dependent depolarization of cardiac vagal neurons via a Gi/o-coupled mechanism. Selection bias
Brailoiu GC (26) 2007 Hypothalamic neurons, male and female Sprague-Dawley rats 170 neurons, different group sizes, number of rats not indicated Experimental intervention study In rats nesfatin-1 was present in hypothalamic and brainstem neurons and stimulated Ca2+ influx via GPCR.
Buzcu H (27) 2019 Female Sprague-Dawley rats 8 rats/group – in total n = 56 Experimental intervention study In acute pancreatitis nesfatin-1 showed an antioxidant and anti-inflammatory effect via the melanocortin signaling pathway. Selection bias
Chen X (28) 2015 Male C57BL/6 mice, male Wistar rats 6 rats/group – in total n = 12,10 mice/group – in total n = 30 Experimental intervention study Nesfatin-1 reduced dark-phase food intake in mice by inhibiting excitability of dopaminergic neurons in the VTA and reducing dopamine release in the nucleus acumbens. Selection bias
Chen Z (29) 2018 Human neuroblastoma SH-SY5Y cells 4 cells/group – in total n = 24 Experimental intervention study In human neuroblastoma SH-SY5Y cells nesfatin-1 led to an over-expression of synapsin I and phosphorylated ERK1/2 mediated via CRF1.
Dong J (30) 2013 Male Kumming SPF mice Not indicated Experimental intervention study Nesfatin-1 normalized free fatty acids and was thus able to improve lipid disorder via activation of AMPK-ACC pathway in T2DM mice. Selection bias
Dore R (31) 2017 Male Wistar rats, male, C57BL/6N wild type mice Different group sizes (5-10/group), 6 groups in total Experimental intervention study Nesfatin-1 treatment increased dry heat loss, iBAT and tail temperature through activation of the melanocortin system. Selection bias
Erfani S (32) 2018 Male Wistar rats 7 rats/group – in total n = 28 Experimental intervention study Nesfatin-1 had neuroprotective effects in neuronal cells and neuroinflammatory processes caused by brain ischemia by decreasing activation of caspase-3. Selection bias
Fan XT (33) 2018 Male C57BL/6J mice (GHSR+/+) and (GHSR-/-) 6-8 GHSR+/+ mice/group – in total n = 38, 3-5 GHSR-/-mice/group – in total n = 17 Experimental intervention study Nesfatin-1 required GHSR for mediating its effects on food intake and glucose metabolism. Selection bias
Feijóo-Bandín S (34) 2013 humans, male Sprague-Dawley rats, HL-1 cardiac muscle cells of mice 178 men, 90 women, 44 rats, number of muscle cells not indicated, different group sizes Experimental intervention study Cardiomyocytes can synthesize and release nesfatin-1 and the peptide stimulated glucose uptake by HL-1 cells and cardiomyocytes and translocation of GLUT4 to the periphery of these cells. Selection bias
Feng H (35) 2017 Male Wistar rats 144 rats, group sizes not indicated Experimental intervention study Nesfatin-1-expressing neurons in the hippocampus project to the VMH and there, nesfatin-1 modulated GD-responsive neurons and thus had an impact on the control of gastrointestinal functions. Selection bias
Gao S (36) 2016 Sprague-Dawley rats Not indicated Experimental intervention study Nesfatin-1 altered firing rates of GD-responsive VMH neurons, thereby inhibiting food intake, gastric acid production, gastric motility, and gastric emptying.
Ge JF (37) 2015 Male Sprague-Dawley rats 10 rats/group – in total n = 40 Experimental intervention study Nesfatin-1 mediated anxiety-like behavior in rats without altering memory. Selection bias
Guo FF (38) 2015 Male Wistar rats Not indicated Experimental intervention study Nesfatin-1 acted as an inhibitory neurotransmitter to regulate gastric motility via the LHA-PVN pathway. Selection bias
Heidarza-deh H (39) 2018 Male meat-type chicken 44 chicken/group – in total n = 304 Experimental intervention study In neonatal chicks nesfatin-1 used CRF1/CRF2 as well as H1-R and H3-R to mediate its anorexigenic effect. Selection bias
Ishida E (40) 2012 mouse neuroblastoma cell line NB41A3, male C57/BL6 (B6) mice Not indicated Observational study Nesfatin-1 bound to cell surface of NB41A3 cells and mouse hypothalamus indicating the presence of a specific nesfatin-1 receptor. Moreover, nesfatin-1 induced phosphorylation of CREB via binding to a Gi/o protein-coupled receptor and by utilizing Ca2+ influx and/or MAPK signaling cascade. Selection bias
Iwasaki Y (41) 2009 Male ICR mice Not indicated Experimental intervention study Peripheral nesfatin-1 stimulated Ca2+ influx through voltage-gated N-type channels, thereby directly activating afferent vagal neurons. Selection bias
Jia FY (42) 2013 Male Sprague-Dawley rats 9 rats/group – in total n = 36 Experimental intervention study Nesfatin-1 was involved in CRF/CRF1 signaling pathways in the brain, contributing to visceral hypersensitivity in rats. Selection bias
Jiang L (43) 2020 human neuroblastoma SH-SY5Y cells, Sprague-Dawley rats 5 human samples, 15 rats/group – in total n = 45 Experimental intervention study Treatment with nesfatin-1 obviated cartilage degeneration in rats which plays a major role in the development of osteoarthritis.
Kan JY (44) 2016 humans, male inbred mice (BALB/cByJNarl) 119 healthy donors, 160 colon cancer patients – in total n = 279 subjects, number of mice not indicated Experimental intervention study Nesfatin-1/NUCB2 increased invasion, migration and mesenchymal phenotype in colon cancer via LKB1/AMPK/TORC1/ZEB1 signaling pathways and may be a prospective marker for prediction of metastasis. Selection bias
Kerbel B (45) 2012 goldfish Carassius auratus n = 36 Experimental intervention study There is a possible relationship between nesfatin-1 and ghrelin, CCK and orexin A in goldfish to regulate food intake.
Levata L (46) 2019 Male C57BL/6J mice Not indicated Experimental intervention study Nesfatin-1 increased peripheral sympathetic outflow, resulting in iBAT thermogenesis and body weight loss. Selection bias
Li C (47) 2014 Wistar rats Not indicated Experimental intervention study In the substantia nigra nesfatin-1 post-synaptically hyperpolarized dopaminergic neurons, thus leading to a direct inhibition of these neurons.
Li T (48) 2021 human HTR-8/trophoblasts Not indicated Experimental intervention study Overexpression of nesfatin-1 increased human trophoblast proliferation, migration, invasion, and epithelial-mesenchymal transition and simultaneously suppressed oxidative stress.
Li ZL (49) 2013 Male Wistar rats n = 348 in different experiments Experimental intervention study Nesfatin-1 modulated gastrointestinal motility by affecting ghrelin-responsive GD neurons in the arcuate nucleus in rats. Selection bias
Li Z (14) 2013 Male C57BL/6J mice, HFD- induced obese mice, Sprague-Dawley rats Approximately n = 44 mice, number of rats not indicated Experimental intervention study Peripheral nesfatin-1 administration altered glucose metabolism in mice via increasing insulin secretion and insulin sensitivity by altering AKT phosphorylation and GLUT 4 membrane translocation in the adipose tissue, liver and skeletal muscle.
Lu QB (50) 2018 Wistar-Kyoto rats, spontaneous hypertensive rats (SHR), human VSMCs, rat VSMCs 6 Wistar-Kyoto rats/group – in total n = 84, 6 SHR/group – in total n = 68 Experimental intervention study Nesfatin-1 promoted VSMC differentiation and proliferation, leading to hypertension and vascular remodeling.
Maejima Y (51) 2017 Male C57BL/6J mice, HEK239 cells 16 mice/group – in total n = 35 Experimental intervention study Nesfatin-1/NUCB2 expression was found in pancreatic beta-cells in mice. Here, nesfatin-1 was found to inhibit Kv-channels in a direct manner. Selection bias
Maejima Y (52) 2009 Male Wistar rats, Zucker-lean rats, Zucker-fatty rats Not indicated Experimental intervention study Nesfatin-1 induced anorexia in a leptin-independent, but melanocortin-dependent manner via oxytocin neurons in the PVN.
Mazza R (53) 2015 goldfish Carassius auratus 4 goldfish/group – in total n = 44 Experimental intervention study Exposure of the isolated and perfused working heart to nesfatin-1 resulted in positive inotropism.
Mori Y (54) 2019 Male C57BL/6J mice, transgene nucleobindin-2 mice, human VECs and VSMCs n = 25 C57BL/6J mice, n = 13 transgene mice, different group sizes Experimental intervention study Nesfatin-1 administration dose-dependently suppressed peripheral artery remodeling in vascular endothelial cells and decreased neointimal hyperplasia. Selection bias
Nair N (55) 2016 Male and female zebrafish (Danio rerio 8 zebrafish/group – in total n = 64 Experimental intervention study NUCB2/nesfatin-1 may be localized in cardiomyocytes in zebrafish and administration of nesfatin-1 led to inhibition of end diastolic and end systolic volumes, decreasing heart rate and cardiac output.
Nakata M (56) 2011 Male ICR mice Not indicated Experimental intervention study Nesfatin-1 dose-dependently stimulated both insulin secretion in islets and intracellular Ca2+ levels in beta-cells under elevated plasma glucose concentration. Selection bias
Oh I (1) 2006 Zucker obese rats, male Wistar rats n = 4-10 rats/group, exact number of rats not indicated Experimental intervention study Nesfatin-1-induced satiety was associated with leptin-independent melanocortin signaling in the hypothalamus. Selection bias
Osaki A (57) 2014 Male ICR mice 3 mice/group – in total n = 18 Experimental intervention study Nesfatin-1 plays a physiological role in regulating blood pressure in mice by altering vascular contractility. Selection bias
Ozcan M (58) 2016 Wistar rats Not indicated Experimental intervention study Nesfatin-1 interacted with a GPCR and used a PKC-dependent mechanism to induce calcium influx in neonatal rat dorsal root ganglion neurons.
Ozturk CC (59) 2015 Male Sprague-Dawley rats n = 48 rats, group sizes not indicated Experimental intervention study The anti-inflammatory effects of nesfatin-1 in colitis were mediated via oxytocin and ghrelin receptors. Selection bias
Price CJ (60) 2008 Male Sprague-Dawley rats Number of rats not indicated, 85 neurons Experimental intervention study In the PVN nesfatin-1 regulated the membrane potential of different subtypes of neurons. Selection bias
Price CJ (61) 2008 Male Sprague-Dawley rats Number of rats not indicated, 102 neurons Experimental intervention study Nesfatin-1 exposure led to hyperpolarization in NPY-expressing neurons in the arcuate nucleus. These effects might be mediated via KATP channels. Selection bias
Prinz P (62) 2016 Male Sprague-Dawley rats n = 6 rats Observational study Bound nesfatin-1 radiolabel was detected in various peripheral organs and several brain nuclei.
Ramanja-neya M (63) 2015 Female Wistar rats, human H295R adrenal cortex cells, mouse Y1 tumor cells Not indicated Experimental intervention study Nesfatin-1 administration suppressed adrenocortical cell growth while increasing apoptosis. Selection bias
Ranjan A (64) 2019 Male Parks strain mice n = 21 mice Experimental intervention study Nesfatin-1 in mouse testes led to an increase in testosterone production, which was accompanied by higher expression of steroidogenic enzymes and insulin receptor protein.
Ranjan A (65) 2019 Male Parks strain mice n = 27 mice Experimental intervention study Nesfatin-1 played a role in spermatogenesis and steroidogenesis of prepubertal mice by direct action on the testis in association with the progression to puberty.
Ranjan A (66) 2020 Male Parks strain mice 10-20 mice/group – in total n = 50 Experimental intervention study Nesfatin-1 played a crucial role in ameliorating the testicular functions of T2DM mice by altering the circulating lipid profile.
Shen XL (67) 2017 Male C57BL/6J mice, MES23.5 cells 6 mice/group – in total n = 30 Experimental intervention study Nesfatin-1 showed a neuroprotective effect in dopaminergic neurons by protecting against MPP+/MPTP-induced neurotoxicity. These effects might be mediated via activation of the C-Raf-ERK1/2 signaling cascade. Selection bias
Shimizu H (9) 2009 Male ICR mice, db/db mice Not indicated Experimental intervention study The middle segment of nesfatin-1 caused anorexia via a leptin-independent mechanism.
Stengel A (18) 2009 Male Sprague-Dawley rats Not indicated Experimental intervention study Nesfatin-1 in rats led to a delayed inhibition of food intake in the dark phase, involving CRF2 receptor-dependent pathways. Selection bias
Tan J (68) 2016 HGSMC cells 20,000 cells/group – in total n = 60,000 Experimental intervention study Nesfatin-1 inhibited HGSMC viability and adhesion.
Tanida M (69) 2015 Male Wistar rats, Zucker fatty rats, HFD rats 7 Wistar rats/group – in total n = 28, 5-6 Zucker fatty rats/group – in total n = 20-22, 5-6 HFD rats/group – in total n = 20-22 Experimental intervention study Hypothalamic ERK signaling underlain the sympathoexcitatory effect of nesfatin-1 on energy intake and lipid metabolism.
Tanida M (70) 2011 Male Wistar rats 4-10 rats/group – in total n = 28 Experimental intervention study Nesfatin-1 modulated central sympathetic outflow, thereby stimulating renal sympathetic outflow and increasing blood pressure. Selection bias
Tasatargil A (71) 2017 Male Wistar rats 8 rats/group – in total n = 32 Experimental intervention study Nesfatin-1 showed cardioprotective effects in rats by decreasing myocardial apoptosis and inflammation which in turn reduces myocardial infarct size. Selection bias
Vélez EJ (72) 2020 rat GH3 cells, RC-4B/C cells Not indicated Experimental intervention study Nesfatin-1 and NLP showed a direct effect on somatotrophs by downregulating the synthesis of GH via a GPCR through the AC/PKA/CREB signaling pathway, most likely including a G-α-inhibitory subunit.
Wang Q (73) 2014 Male Wistar rats 65-65 rats/experiment – in total n = 246 Experimental intervention study In the central nucleus of the amygdala nesfatin-1 modulated the activity of GD-sensitive neurons and gastric motility. Selection bias
Wu D (74) 2014 Male Sprague-Dawley rats 51 rats/group – in total n = 102 Experimental intervention study Hypothalamic nesfatin-1 was involved in the regulation of glucose homeostasis and hepatic insulin sensitivity, associated with the activation of the mTOR-STAT3 signaling pathway. Selection bias
Xia ZF (75) 2012 Male Sprague-Dawley rats, vagal neurons of Sprague-Dawley rats Not indicated Experimental intervention study Nesfatin-1 inhibited gastric acid secretion stimulated by a central vagal mechanism in rats involving T-Typ Ca2+ channels. Selection bias
Xu L (76) 2017 Male Wistar rats 46-120 rats/experiment – in total approximately 439 Experimental intervention study Nesfatin-1 signaling in the lateral hypothalamic area modulated the activation of GD-responsive neurons, gastric motility and gastric secretion also involving melanin-concentrating hormone signaling. Selection bias
Xu L (77) 2015 Male Wistar rats 6-58 rats/experiment – in total n = 262 Experimental intervention study Nesfatin-1 administration into the BMA increased firing rate of GD-excitatory neurons, while decreasing firing rates of GD-inhibitory neurons. Nesfatin-1 in the BMA is involved in decreasing gastric motility and the Arc may also play a role in this regulating process. Selection bias
Yamawa-ki H (16) 2012 Male Wistar rats 8-23 rats/experiment – in total n = 58 Experimental intervention study Nesfatin-1 modulated peripheral arteria contractility by impairing cGMP release, thus inhibiting the SNP-induced smooth muscle relaxation. Selection bias
Yang M (78) 2012 Male Sprague-Dawley rats 8-40 rats/experiment – in total n = 68 Experimental intervention study Icv injection of nesfatin-1 increased peripheral and hepatic insulin sensitivity by decreasing gluconeogenesis and promoting peripheral glucose uptake through AMPK/AKT/TORC2 pathway. Selection bias
Yin Y (79) 2015 C57BL/6J mice 24-30 mice/experiment, exact number of mice not indicated Experimental intervention study Nesfatin-1 modulated lipid accumulation in hepatocytes via an AMPK-dependent mechanism.
Ying J (80) 2015 Male Wistar rats Not indicated Experimental intervention study Nesfatin-1 inhibited L-type Ca2+ channels via the MC4-R and involved the Gβγ subunit of Gi/o-protein and the downstream PKCθ pathway. Selection bias
Yosten GL (81) 2014 Male Sprague-Dawley rats 5-13 rats/group – in total n = 248 Experimental intervention study The hypertensive effect of nesfatin-1 may require both activation of oxytocinergic neurons and recruitment of CRF neurons. Selection bias
Yuan JH (82) 2017 Male Wistar rats 24-56 rats/experiment, exact number of rats not indicated Experimental intervention study Nesfatin-1 played a role in inhibition of food intake, alteration of the excitability of glucose sensitive neurons in the LPBN and an increase of UCP expression in brown adipose tissue by involving the melanocortin system. Selection bias
Zhang JR (83) 2018 Male Sprague-Dawley rats 6 rats/group, exact number of rats not indicated Experimental intervention study Nesfatin-1 stimulated VSMC proliferation, migration, and phenotype switch from a contractile to a synthetic state. Selection bias
Zhang T (84) 2019 Male Sprague-Dawley rats 6 rats/group – in total n = 54 Experimental intervention study Hypothalamic nesfatin-1 regulated feeding behavior through the MC3/4R-ERK signaling pathway.
Zhang X (85) 2018 Siberian sturgeons 6-8 sturgeons/group – in total n = 45 Experimental intervention study Nesfatin-1 reduced food intake in Siberia sturgeon predominantly via the CCK-CCK1R signaling pathway.
Zhou XP (86) 2016 Male Sprague-Dawley rats 15-18 rats/group, exact number of rats not indicated Experimental intervention study Nesfatin-1/NUCB2 in the amygdala was involved in the pathophysiology of IBS-like visceral hypersensitivity, likely by involving glucocorticoid and mineral corticoid receptor pathways. Selection bias

AC, adenylyl cyclase; AMPK, 5’ AMP-activated protein kinase; BMA, basomedial amygdala; CCK, cholecystokinin; CCK1-R, cholecystokinin1 receptor; cGMP, cyclic guanosine monophosphate; CREB, cAMP response element-binding protein; CRF, corticotropin-releasing factor; CRF1, corticotropin-releasing factor receptor 1; EGF, Epidermal growth factor; ERK, extracellular signal-regulated kinases; GD, gastric distension; GHSR, growth hormone secretagogue receptor; GLUT4, glucose transporter type 4; GPCR, G protein-coupled receptor; H1-R, histamine receptor 1; H3-R, histamine receptor 3; HFD, high-fat diet; HGSMC, human gastrointestinal smooth muscle cells; iBAT, interscapular brown adipose tissue; IBS, irritable bowel syndrome; icv, intracerebroventricular; KATP channel, ATP-sensitive potassium channel; Kv, voltage-gated potassium; LHA, lateral hypothalamic area; LKB1, liver kinase B1; LPBN, lateral parabrachial nucleus; MAP, mean arterial pressure; MAPK, mitogen-activated protein kinase; MC3-R, melanocortin 3 receptor; MC4-R, melanocortin 4 receptor; MEK, MAPK kinase/ERK kinase; mTOR, mammalian target of rapamycin; NLP, nesfatin-1-like peptide; NO, nitric oxide; NPR-A, natriuretic peptide receptor A; NPY, neuropeptide Y; NUCB2, nucleobindin-2; pGC, particulate guanylate cyclase; PKA, protein kinase A; PKC, protein kinase C; PKCθ, protein kinase C theta; PKG, protein kinase G; PVN, paraventricular nucleus; RCC, renal cell carcinoma; SNP, sodium nitroprusside; SPF, Specific-pathogen-free; STAT, signal transducers and activators of transcription; TORC1, target of Rapamycin complex 1; TORC2, target of Rapamycin complex 2; TRH, thyrotropin-releasing hormone; T2DM, type 2 diabetes mellitus; UCP, uncoupling protein; VEC, Vascular endothelial cells; VMH, ventromedial hypothalamus; VSMC, vascular smooth muscle cells; ZEB1, zinc finger E-box-binding homeobox 1.

 3 Results

1,147 articles were identified after searching the databases using the keywords mentioned above. Reviews, surveys, case reports, comments, letters, conference abstracts or posters, as well as economic evaluation and non-English language studies or studies with no full text available, and duplicates were excluded. This deceased the number to 425 articles. Next, title and abstract were screened and studies which deviated from the main topic were excluded; thus, 128 studies required full-text screening. Here, studies not related to the review topic were excluded. Ultimately, 70 articles were selected for this systematic review. The PRISMA flow diagram schematically depicts the article selection process ( Figure 1 ). Table 2 shows the main results of these articles.

Flowchart for article screening and selection.

 3.1 Quality Assessment

The current review consists of observational preclinical and clinical studies or experimental studies, assuming a risk for bias. There are several issues that may contribute to limited comparability between studies and thus limited transferability of study results in general. First, the studies included different species or population, which may lead to limited comparability. Second, the respective study populations differed in sample size, while the study methods, treatments and observation periods used were also very heterogeneous. Furthermore, we only reviewed the abstracts and full texts published in English. Studies in other languages have not been included. Additionally, we searched only three databases for potentially eligible studies. Taken together, bias cannot be ruled out for the studies included in this systematic review; thus, these limitations should be kept in mind when interpreting the results discussed here.

 4 Discussion

The aim of this systematic review was to identify and summarize the state of knowledge on signaling cascades of nesfatin-1 and to shed light on the peptide’s potential receptor. Nesfatin-1 affects multiple sites in the organism and elicits a variety of intracellular effects, which accounts for the pleiotropic nature of this peptide. The multiple intracellular signaling cascades triggered by nesfatin-1 ( Figure 2 ) only reinforce the multifaceted nature of this peptide and highlight that it may be of great importance to understand the exact cascades by further investigating the particular type and localization of the potential receptor in the future.

Putative intracellular signaling cascades initiated by the binding of nesfatin-1 to its receptor.

 4.1 Intracellular Signaling and Potential Receptor

By using autoradiography binding of radiolabeled nesfatin-1 in the gastric mucosa of corpus and antrum, in duodenum, jejunum and ileum and centrally in the cortex, paraventricular nucleus of the hypothalamus, area postrema, dorsal motor nucleus of the vagus nerve and cerebellum was shown, giving rise to respective expression sited of the receptor (62). Since nesfatin-1 is known to be able to cross the blood-brain barrier, peripheral nesfatin-1 might access and then bind to these central receptors (87). In addition, NUCB2/Nesfatin-1 was found to be widely distributed in the central nervous system of mice (88) and rats (3, 89).

4.1.1 AMPK Signaling Pathway

Converging evidence points towards a mediation of nesfatin-1’s effects via a G-protein coupled receptor: Previous results suggest the presence of a nesfatin-1 receptor in hepatocytes whose activation stimulates the phosphorylation of AMPK, reducing hepatic lipid accumulation. These alterations were associated with a significant attenuation of peroxisome proliferator-activated receptor γ (PPARγ) and sterol-regulatory element-binding protein-1 (SREBP1), which are known lipogenesis-related transcription factors (79). Furthermore, in diabetic mice low-dose injection of nesfatin-1 also regulated fatty acid metabolism via activation of an AMPK-ACC pathway (30). The assumption of an influence of nesfatin-1 on AMPK signaling cascades is consistent with recent findings, highlighting that nesfatin-1/NUCB2 enhances invasion, migration, and mesenchymal phenotype in colon cancer via liver kinase B1 (LKB1)/AMPK/target of rapamycin kinase complex I (TORC1)/ZEB1 signaling pathways (44). In line with this, it was further shown that nesfatin-1 suppresses peripheral artery remodeling likely by increasing NO production and LKB1-mediated activation of AMPK in vascular endothelial cells in mice (54). However, in the testis of mice nesfatin-1-induces an increase in G protein-coupled receptor 54 (GPR-54) accompanied by increases in PCNA, Bcl2, androgen receptor (AR), GLUT8, insulin receptor and gonadotropin-releasing hormone receptor (GnRH-R) (64, 65). In addition, a potential role of protein kinase B (AKT) as a signaling mechanism for nesfatin-1-induced glucose uptake and activation of the AMP-activated protein kinase (AMPK)/extracellular signal-regulated kinase 1/2 (ERK1/2) system was found through which nesfatin-1 enhances insulin sensitivity in the testis of mice (64, 66). Supporting these findings, icv injection of nesfatin-1 increased peripheral and hepatic insulin sensitivity by decreasing gluconeogenesis and promoting peripheral glucose uptake through the AMPK/AKT/TORC2 pathway (78).

 4.1.2 MAPK Signaling Pathway

Furthermore, previous results assumed the presence of a nesfatin-1-specific-receptor, likely a Gi/o protein-coupled receptor, on the cell surface of a murine neuroblastoma cell line (NB41A3 cells) and mouse hypothalamus. Here, binding of nesfatin-1 activates the cAMP-response reporter (CRE) and further phosphorylates CREB in these cells by utilizing Ca2+ influx and/or the MAPK signaling pathway (40). Other studies also point to a crucial role of nesfatin-1 in the ERK/MAPK/mechanistic Target of Rapamycin (mTOR) signaling pathway by upregulating endothelial NO synthase (eNOS) levels in human gastrointestinal smooth muscle cells (HGSMC). Here, nesfatin-1 increases pro-apoptotic factors p53 and Fas, thereby accelerating apoptosis in HGSMC. Furthermore, nesfatin-1 led to reduced expression of ERK1/2, p38, MAPK and mTOR in HGSMC (68). Moreover, in adrenocortical cells nesfatin-1 increases apoptosis by involving ERK1/2, p38, c-Jun N-terminal kinase 1/2 (JNK1/2) signaling pathways, Bcl-2-associated X protein (Bax), B-cell lymphoma-extra-large (BCL-XL), and Bcl-2 genes (63). In accordance, nesfatin-1 decreased apoptosis rate in rat chondrocytes also through the Bax/Bcl-2 signaling pathway and further through suppressing both NF-κB and MAPK signaling pathways (43). Furthermore, it was found that nesfatin-1 ameliorates levels of human gene for type H procollagen (CoI2a1) while it decreases the IL-1beta induced expression of matrix metalloproteinases (MMP), a disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS5), cyclooxygenase 2 (COX-2), caspase-3, nitric oxide (NO), inducible nitric oxide synthase (iNOS), prostaglandin E2 (PGE2), and interleukin-6. The nesfatin-1-induced decrease of caspase-3 activity was also detected in the hippocampus accompanied by fewer ionized calcium binding adaptor molecule 1 (Iba-1)-positive cells (32). Interestingly, consecutive intraperitoneal (ip) administration of nesfatin-1 for three weeks decreases brain-derived neurotrophic factor (BDNF) and phosphorylated-ERK levels in the hippocampus and prefrontal cortex (PFC), thereby downregulating the ERK signaling pathway (37). In accordance, it was demonstrated that nesfatin-1 protects dopaminergic neurons from 1-Methyl-4-phenylpyridinium (MPP+)- and 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridin (MPTP)-induced neurotoxicity both in vivo and in vitro, probably via activation of the C-Raf/ERK1/2 signaling cascade (67). Regarding nesfatin-1’s influence on the ERK signaling cascade, it was further found that the peptide regulates the autonomic nervous system through ERK signaling in corticotropin-releasing factor (CRF) positive neurons in the paraventricular nucleus (PVN). Precisely, central nesfatin-1 administration stimulated MAPK activity thereby enhancing ERK1/2 phosphorylation in CRF neurons of the PVN (69). Consistent with these findings, also in human neuroblastoma SH-SY5Y cells, it was observed that the stimulatory effects of nesfatin-1 on synapsin I expression are mediated by CRF1 through the cAMP/MAPK/ERK pathway (29).

 4.1.3 CRF Signaling Pathway

Regarding nesfatin-1’s influence on CRF signaling pathways, gastric distension (GD)-responsive neurons were found in ventromedial hypothalamic nucleus (VMH), whose firing rate was altered by nesfatin-1, most likely through interactions with CRF signaling pathways (35). This hypothesis was strengthened by the observed association of nesfatin-1 and irritable bowel syndrome-like visceral hypersensitivity that is also mediated, at least in part, by CRF/CRF1 signaling pathways in the brain (42). In consistence with these findings, it was reported that nesfatin-1 reduced dark-phase food intake via CRF pathways (18). Furthermore, in neonatal chicks nesfatin-1 used CRF1/CRF2 as well as histamine (H)1 and H3 receptors to mediate its anorexigenic effect. Interestingly, co-injection of nesfatin-1 and chlorpheniramine (H1 antagonist) blunted nesfatin-1-induced hypophagia, while co-administration with thioperamide (H3 antagonist) reinforced the hypophagic effect of nesfatin-1. This divergence in the effects of H1 and H3 receptors can be explained by the fact that H1 is a postsynaptic receptor, while H3 is a presynaptic autoreceptor, leading to the hypothesis that H1 and H3 play a different regulatory role in the feeding behavior influenced by nesfatin-1 (39).

 4.1.4 Melanocortin Signaling Pathway

Using the melanocortin signaling pathway, nesfatin-1 was found to alter firing rates of GD-responsive neurons in the VMH (36), baso-medial amygdala (BMA) (77), arcuate nucleus (49) and central nucleus of the amygdala (73). Also, by involving the melanocortin system nesfatin-1 alters the excitability of glucose sensitive neurons in the lateral parabrachial nucleus (LPBN) and increases the level of uncoupling protein (UCP) expression in brown adipose tissue (BAT) (82). In accordance, it was assumed that nesfatin-1-induced satiety is associated with leptin-independent melanocortin signaling in the hypothalamus (1). This hypothesis was strengthened by a study showing that hypothalamic nesfatin-1 regulates feeding behavior through the MC3/4-ERK signaling pathway. Interestingly, in this study, hypothalamic nesfatin-1 mediates its effects via MC3/4, while not altering expression of MC3/4 (84). Furthermore, through activation of the melanocortin system icv nesfatin-1 treatment increases dry heat loss, interscapular (i) BAT and tail temperature. Moreover, nesfatin-1 administration upregulated the expression of POMC and MC3 mRNA in the hypothalamus along with an elevation of iodothyronine deiodinase 2 (Dio2), UCP1 and PPARγ-1 alpha mRNA in the iBAT (31). Furthermore, the nesfatin-1-induced elevation in the mRNA expression of the cAMP-responsive gene Dio2 strengthens the hypothesis of an activation of the β-adrenergic/cAMP signaling pathway, which is in line with other findings emphasizing the established role of nesfatin-1 in sympathetic nerve activity by activating the central melanocortin system (70). On the other hand, only the midsegment of nesfatin-1 proves effective and leads to a higher activation of c-Fos in the brainstem nucleus of the solitary tract (NTS). Furthermore, administration of the middle segment of nesfatin-1 results in an increase in the expression of proopiomelanocortin (POMC), cocaine- and amphetamine-regulated transcript (CART) mRNA in the NTS (9). In adult ventricular myocytes nesfatin-1 targets MC4, sequentially coupling to the Gβγ subunits of Gi/o, leading to the subsequent activation of the novel protein kinase C (PKC) θ isoform, subsequently resulting in an inhibition of L-Type Ca2+ channels associated with a hyperpolarizing shift in the voltage-dependence of inactivation. Notable the nesfatin-1 mediated inhibition of calcium-influx was not affected by Kt-5720, a PKA antagonist indicating that the cAMP/PKA pathway is not involved in the nesfatin-1-induced L-Type Ca2+ channel response in ventricular myocytes (80). In contrast, it was observed that both nesfatin-1 and nesfatin-1-like peptide directly affect somatotrophs via binding to a GPCR containing a G-α-i subunit and utilizing the adenylyl cyclase (AC)/protein kinase A (PKA)/CREB signaling pathway subunit, thereby downregulating the synthesis of ghrelin hormone (72).

 4.1.5 Ion Currents

However, in cardiac vagal neurons nesfatin-1 may increase cytosolic Ca2+ levels via a Gi/o-coupled mechanism by involving P/Q-type voltage-activated Ca2+ channels (25), while in hypothalamic neurons the peptide might mediate Ca2+ influx also via a GPCR, most likely by affecting both L- and P/Q- Ca2+ channels. Surprisingly, Ca2+ influx was significantly reduced by a PKA blocker, indicating an involvement of PKA in hypothalamic neurons (26). The effects of nesfatin-1 in sensory neurons may be mediated through the participation of a Gi/o protein coupled receptor as it is speculated that the nesfatin-1-induced Ca2+ increase may result from a Ca2+ influx from both extracellular and intracellular sources (58). Furthermore, several other studies proposed an influence of nesfatin-1 on calcium levels in various tissues: Exposure of the isolated and perfused working heart to nesfatin-1 results in positive inotropism mediated through cAMP, PKA, L-type Ca2+ channels, sarcoplasmic/endoplasmic reticulum calcium ATPase 2a (SERCA2a) pumps, ERK1/2 and phospholamban (PLN) (53). On the other hand, it was found that nesfatin-1 leads to increased expression of Atp2a2a mRNA encoding SERCA2a, while there were no changes observed in the expression of ryanodine receptor 1b (RyR1b) encoding mRNA (55). Furthermore, a different study demonstrated that nesfatin-1 induces heart failure during clinical treatments by increasing expression of the cardiac L-type Ca2+ channel a1c subunit (22). Likewise, it was shown that in mice, nesfatin-1 dose-dependently stimulates intracellular Ca2+ levels via L-type Ca2+ channels independently of PKA and phospholipase A2 (PLA2) in beta-cells under elevated plasma glucose concentration (56). One mechanism of the elevated Ca2+ influx could be an increase in membrane Na+ permeability, which depolarizes the membrane to open voltage-gated calcium channels (VDCC) (90), a mechanism used by glucagon-like peptide 1 (GLP-1) (91). Another potential explanation is an involvement of protein kinase C, which has been reported to increase glucose-stimulated Ca2+ influx through VDCC and insulin secretion (92). In contrast, another study reported that peripheral nesfatin-1 stimulates Ca2+ influx through voltage-gated N-type channels, thereby directly activating afferent vagal neurons (41). On the other hand, nesfatin-1 showed an effect on vagal neurons by mediating Ca2+ signaling through T-type channels, which are low-voltage activated channels localized in different areas of the central nervous system (75, 93, 94). The ultimate role of T-type Ca2+ channel activation in the response of vagal neurons to nesfatin-1 and the downstream target/effect of this signaling pathway remain unknown.

However, nesfatin-1 not only regulates the calcium influx via various mechanisms, but also influences the levels of other ions: More precisely, nesfatin-1 directly induces an inhibition of the voltage-dependent potassium (Kv) current by directly binding to Kv2.1 channels to exert its effect on pancreatic beta cells, as these Kv channels have been identified as the major contributors to Kv currents in these cells. Since nesfatin-1 is localized in beta cells, it has been hypothesized that nesfatin-1 may affect beta cell function in an autocrine/paracrine manner (51). Another finding assumes that nesfatin-1 activates KATP channels, thereby inhibiting orexigenic neuropeptide Y (NPY) neurons of the arcuate nucleus and consequently leading to satiety (61).

 4.1.6 NO-cGMP System

Interestingly, nesfatin-1 also targets the NO-cGMP system; again, the particular receptor(s) is/are still unknown and require further research: In atrial tissue nesfatin-1 might increase the sensitivity of smooth muscle to cGMP-mediated relaxing mechanisms rather than increasing the NO levels. Interestingly, these positive chronotropic effects in the atrial tissue were independent of the β1-adrenergic receptor (24). On the other hand, nesfatin-1 also impairs the SNP-induced cGMP production, thereby inhibiting the NO donor-induced smooth muscle relaxations. Since these effects were persistent in the presence of IBMX, a phosphodiesterase (PDE) inhibitor, it can be suggested that these effects may be mediated via inhibition of soluble guanylate cyclase activity rather than activation of PDEs (16). However, other findings indicated that by recruiting guanylyl cyclase-linked receptors, namely natriuretic peptide receptor type A (NPR-A), and thereby involving the cGMP/protein kinase G pathway and ERK1/2, nesfatin-1 mediates negative inotropic and lusitropic effects in rats. Since the use of pertussistoxin did not inhibit the effects of nesfatin-1, the hypothesis that nesfatin-1 binds to a Gi/o cannot be confirmed by these observations (21).

 4.1.7 AKT Signaling Pathway

Also involved in multiple aspects of the effects of nesfatin-1 is the AKT signaling pathway: In the myocardium of mice with myocardial infection, nesfatin-1 increases expressions of phosphorylated-AKT/AKT and phosphorylated-glycogen synthase kinase 3 beta (GSK-3β)/GSK-3β, thereby protecting cardiac tissue (71). Other findings indicate that overexpression of nesfatin-1 in human trophoblasts influences the expression of phosphoinositide-3-kinase (PI3K)/AKT/mTOR and AKT/GSK3β pathway, contributing to trophoblast dysfunction simultaneously suppressing oxidative stress by reducing reactive oxygen species (ROS), malondialdehyde (MDA), and superoxide dismutase (SOD) levels (48). Furthermore, in vascular smoot muscle cells (VSMC) nesfatin-1 modulates the crosstalk between PI3K/AKT/mTOR and Janus kinase 2 (JAK2)/STAT3 signaling, leading to hypertension and vascular remodeling (50). Nesfatin-1 also dose-dependently increased MMP-2 and MMP-9 levels, while it decreased PPARγ gene expression in VSMCS contributing to vascular remodeling and neointimal hyperplasia (83). Regarding STAT3 signaling, hypothalamic nesfatin-1 in rats activates the mTOR-STAT3 pathway, thereby regulating glucose homeostasis and hepatic insulin sensitivity (74). Moreover, studies involving HL-1 cells and cardiomyocytes indicate a nesfatin-1-induced phosphorylation of ERK1/2, AKT and the substrate of AKT, AS160, thereby stimulating peripheral GLUT-4 translocation (34). These findings are in line with the results of a recent study reporting nesfatin-1 to affect glucose metabolism by affecting AKT phosphorylation and GLUT4 membrane translocation in adipose tissue, liver, and skeletal muscle (14). The specific receptor to which nesfatin-1 binds to trigger these effects is still unknown.

 4.2 Colocalization With Other Peptides

Furthermore, PVN neurons in rats are directly depolarized by nesfatin-1, suggesting a mediation of these effects through the activation of a GPCR. Since PVN neurons respond to nesfatin-1 and further produce nesfatin-1, there might be potential interactions between various subgroups of PVN neurons engaged in the control of several autonomic outputs. The specificity of the effects may also arise from the co-expression of other receptors on nesfatin-1-sensitive neurons. An alternative explanation is that multiple nesfatin-1 receptors exist that are separately responsible for hyperpolarizing or depolarizing responses (60). It was shown that in the PVN, nesfatin-1 targets magnocellular and parvocellular Oxt neurons as well as nesfatin-1 neurons themselves, further stimulating Oxt release. Furthermore, the presence of nesfatin-1 specifically in the secretory vesicles of PVN neurons was found, indicating paracrine/autocrine actions of nesfatin-1 (52). On the other hand, it was suggested that the hypertensive effect of nesfatin-1 may require both activation of Oxt neurons and recruitment of CRF neurons (81). Moreover, by targeting ghrelin and Oxt receptors nesfatin-1 suppresses neutrophil infiltration and improves glutathione levels in acute pancreatitis (27) and colitis (59). Interestingly, the effects of nesfatin-1 on myeloperoxidase activity, lipid peroxidation and glutathione level were abrogated by application of melanocortin receptor antagonist. Despite previously demonstrating that nesfatin-1 utilizes the melanocortin signaling pathway for its effects on food intake, these findings indicate that nesfatin-1 may also utilize the receptors mediating its anorexigenic effect for anti-inflammatory effects (59). Since the effects of nesfatin-1 on GD- excitatory neurons and GD-inhibitory neurons in the PVN were attenuated in the presence of H4928, an Oxt receptor antagonist, it can be assumed that nesfatin-1involves Oxt receptors to modulate gastric function (38). Moreover, in goldfish nesfatin-1 inhibits ghrelin mRNA expression in the brain and vice versa, leading to the assumption of a negative feedback inhibition of endogenous ghrelin and nesfatin-1 (45). Another study indicates that peripheral nesfatin-1 most likely exerts part of its effect directly via ghrelin receptor (GHSR) signaling. Furthermore, the results here show that the effects of nesfatin-1 in mice fed a normal chow diet, such as improvement of glucose tolerance, upregulation and phosphorylation of AKT-kinase mRNA and GLUT4 membrane translocation, were dependent on the presence of GHSR. In high-fat diet (HFD) fed mice, nesfatin-1 additionally led to a raise of AKT levels in liver tissues, which is also a GHSR-dependent mechanism (33). Therefore, it is possible that nesfatin-1 acts as an endogenous inverse agonist of the GHSR and influences the structure or activity of the GHSR. Furthermore, it was found that nesfatin-1 inhibits the excitability of dopaminergic neurons in the ventral tegmental area (VTA) (28) and the substantia nigra (47), thereby decreasing dopamine release (28). In addition, nesfatin-1 signaling in the lateral hypothalamic area (LHA) or electric stimulation of the Arc modulate the activation of GD-responsive neurons, gastric motility and gastric secretion involving melanin-concentrating hormone signaling indicating the potential presence of nesfatin-1 specific receptors in these neurons (76). Recent findings also provide evidence that nesfatin-1 administered into the amygdala targets glucocorticoid and mineral corticoid receptor pathways, thereby being involved in the pathophysiology of irritable bowel syndrome (IBS)-like visceral hypersensitivity (86). Lastly, predominantly via the CCK-CCK1R signaling pathway nesfatin-1 reduces food intake in Siberia sturgeon (85).

Involving cholinergic pathways, central administration of nesfatin-1 elevates mean arterial pressure and modulates heart rate in rats. These cardiovascular effects were mediated by both nicotinic and muscarinic receptors. Considering that recent studies have shown that both muscarinic and nicotinic acetylcholine receptors interact with G-coupled proteins (95), it may be that nesfatin-1 mediates its cardiovascular effects via central muscarinic and nicotinic receptors because of its affinity to GPCRs (23).

Furthermore, it was found that central nesfatin-1 can increase peripheral sympathetic outflow and thus β-adrenergic activation, resulting in iBAT thermogenesis and body weight loss. It was demonstrated that the thermogenetic effect of nesfatin-1 mainly depends on β3-adrenergic stimulation. In addition, levels of Dio2 and cell death inducing DFFA like effector A (CIDEA) mRNA were increased in brown adipose tissue after nesfatin-1 administration, which is plausible as both are involved in regulating the thermogenic program (46). Since the direct effects of peripherally injected nesfatin-1 on vascular smooth muscle were attenuated by pretreatment with propranolol, an involvement of the β-adrenergic system can also be suspected here (57).

 4.3 Implications for Future Research

The described various distribution of the nesfatin-1 receptor further supports the assumption that nesfatin-1 may be involved in the regulation of various homeostatic functions, and the various signaling pathways underlying the actions of nesfatin-1 emphasize its multiple effects. The recent discoveries about the diverse effects of nesfatin-1 indicate the importance of evaluating and determining the potential use of nesfatin-1 in a therapeutic context in the future. For this reason, further research is needed to fully understand the exact cascades of the peptide and its complex interplay with other hormones.

 5 Conclusion

This present review highlights nesfatin-1 as a pleotropic peptide that acts at multiple levels in the organism, thereby eliciting a wide variety of effects. As diverse as the effects of the peptide, so are the intracellular signaling pathways and downstream effects summarized here, including the influence of nesfatin-1 on various hormones and their receptors. The identification of the so far unknown nesfatin-1 receptor will represent a major leap forward in our understanding of the physiology of nesfatin-1 and will allow us to better investigate the precise mechanisms underlying the many different effects of the peptide. Further research is needed so we might be able to consider a therapeutic use of nesfatin-1 in the future.

 Data Availability Statement

The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.

 Author Contributions

EW performed the systematic search. SR and EW screened the papers and SR wrote the first draft of the manuscript. AS planned the study and gave critical input throughout the study. All authors contributed to the article and approved the submitted version.

 Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

 Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

 Acknowledgments

We acknowledge support by Deutsche Forschungsgemeinschaft and the Open Access Publishing Fund of the University of Tübingen.

 References Oh-I S Shimizu H Satoh T Okada S Adachi S Inoue K . Identification of Nesfatin-1 as a Satiety Molecule in the Hypothalamus. Nature (2006) 443(7112):709–12. doi: 10.1038/nature05162 Dore R Levata L Lehnert H Schulz C . Nesfatin-1: Functions and Physiology of a Novel Regulatory Peptide. J Endocrinol (2017) 232(1):R45–65. doi: 10.1530/JOE-16-0361 Goebel M Stengel A Wang L Lambrecht NW Taché Y . Nesfatin-1 Immunoreactivity in Rat Brain and Spinal Cord Autonomic Nuclei. Neurosci Lett (2009) 452(3):241–6. doi: 10.1016/j.neulet.2009.01.064 Shimizu H Oh-I S Okada S Mori M . Nesfatin-1: An Overview and Future Clinical Application. Endocr J (2009) 56(4):537–43. doi: 10.1507/endocrj.k09e-117 Prinz P Stengel A . Nesfatin-1: Current Status as a Peripheral Hormone and Future Prospects. Curr Opin Pharmacol (2016) 31:19–24. doi: 10.1016/j.coph.2016.08.011 Gao X Zhang K Song M Li X Luo L Tian Y . Role of Nesfatin-1 in the Reproductive Axis of Male Rat. Sci Rep (2016) 6:32877. doi: 10.1038/srep32877 Wei Y Li J Wang H Wang G . NUCB2/nesfatin-1: Expression and Functions in the Regulation of Emotion and Stress. Prog Neuropsychopharmacol Biol Psychiatry (2018) 81:221–7. doi: 10.1016/j.pnpbp.2017.09.024 Stengel A Goebel-Stengel M Wang L Kato I Mori M Taché Y . Nesfatin-1(30-59) But Not the N- and C-Terminal Fragments, Nesfatin-1(1-29) and Nesfatin-1(60-82) Injected Intracerebroventricularly Decreases Dark Phase Food Intake by Increasing Inter-Meal Intervals in Mice. Peptides (2012) 35(2):143–8. doi: 10.1016/j.peptides.2012.03.015 Shimizu H Oh-I S Hashimoto K Nakata M Yamamoto S Yoshida N . Peripheral Administration of Nesfatin-1 Reduces Food Intake in Mice: The Leptin-Independent Mechanism. Endocrinology (2009) 150(2):662–71. doi: 10.1210/en.2008-0598 Prinz P Teuffel P Lembke V Kobelt P Goebel-Stengel M Hofmann T . Nesfatin-130-59 Injected Intracerebroventricularly Differentially Affects Food Intake Microstructure in Rats Under Normal Weight and Diet-Induced Obese Conditions. Front Neurosci (2015) 9:422. doi: 10.3389/fnins.2015.00422 Stengel A Taché Y . Nesfatin-1-Role as Possible New Potent Regulator of Food Intake. Regul Pept (2010) 163(1-3):18–23. doi: 10.1016/j.regpep.2010.05.002 Mohan H Unniappan S . Ontogenic Pattern of Nucleobindin-2/Nesfatin-1 Expression in the Gastroenteropancreatic Tissues and Serum of Sprague Dawley Rats. Regul Pept (2012) 175(1-3):61–9. doi: 10.1016/j.regpep.2012.02.006 Stengel A Goebel M Yakubov I Wang L Witcher D Coskun T . Identification and Characterization of Nesfatin-1 Immunoreactivity in Endocrine Cell Types of the Rat Gastric Oxyntic Mucosa. Endocrinology (2009) 150(1):232–8. doi: 10.1210/en.2008-0747 Li Z Gao L Tang H Yin Y Xiang X Li Y . Peripheral effects of nesfatin-1 on glucose homeostasis. PLoS One (2013) 8(8):e71513. doi: 10.1371/journal.pone.0071513 Özsavcí D Erşahin M Şener A Özakpinar ÖB Toklu HZ Akakín D . The Novel Function of Nesfatin-1 as an Anti-Inflammatory and Antiapoptotic Peptide in Subarachnoid Hemorrhage-Induced Oxidative Brain Damage in Rats. Neurosurgery (2011) 68(6):1699–708. doi: 10.1227/NEU.0b013e318210f258 discussion 1708. Yamawaki H Takahashi M Mukohda M Morita T Okada M Hara Y . A Novel Adipocytokine, Nesfatin-1 Modulates Peripheral Arterial Contractility and Blood Pressure in Rats. Biochem Biophys Res Commun (2012) 418(4):676–81. doi: 10.1016/j.bbrc.2012.01.076 Atsuchi K Asakawa A Ushikai M Ataka K Tsai M Koyama K . Centrally Administered Nesfatin-1 Inhibits Feeding Behaviour and Gastroduodenal Motility in Mice. Neuroreport (2010) 21(15):1008–11. doi: 10.1097/WNR.0b013e32833f7b96 Stengel A Goebel M Wang L Rivier J Kobelt P Mönnikes H . Central Nesfatin-1 Reduces Dark-Phase Food Intake and Gastric Emptying in Rats: Differential Role of Corticotropin-Releasing Factor2 Receptor. Endocrinology (2009) 150(11):4911–9. doi: 10.1210/en.2009-0578 Angelone T Rocca C Pasqua T . Nesfatin-1 in Cardiovascular Orchestration: From Bench to Bedside. Pharmacol Res (2020) 156:104766. doi: 10.1016/j.phrs.2020.104766 Moher D Liberati A Tetzlaff J Altman DG PRISMA Group . Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement. BMJ (2009) 339:b2535. doi: 10.1136/bmj.b2535 Angelone T Filice E Pasqua T Amodio N Galluccio M Montesanti G . Nesfatin-1 as a Novel Cardiac Peptide: Identification, Functional Characterization, and Protection Against Ischemia/Reperfusion Injury. Cell Mol Life Sci (2013) 70(3):495–509. doi: 10.1007/s00018-012-1138-7 Ayada C Turgut G Turgut S . The Effect of Nesfatin-1 on Heart L-Type Ca²⁺ Channel α1c Subunit in Rats Subjected to Chronic Restraint Stress. Bratisl Lek Listy (2015) 116(5):326–9. doi: 10.4149/bll_2015_061 Aydin B Guvenc G Altinbas B Niaz N Yalcin M . Modulation of Nesfatin-1-Induced Cardiovascular Effects by the Central Cholinergic System. Neuropeptides (2018) 70:9–15. doi: 10.1016/j.npep.2018.05.001 Barutcigil A Tasatargil A . Effects of Nesfatin-1 on Atrial Contractility and Thoracic Aorta Reactivity in Male Rats. Clin Exp Hypertens (2018) 40(5):414–20. doi: 10.1080/10641963.2017.1384487 Brailoiu GC Deliu E Tica AA Rabinowitz JE Tilley DG Benamar K . Nesfatin-1 Activates Cardiac Vagal Neurons of Nucleus Ambiguus and Elicits Bradycardia in Conscious Rats. J Neurochem (2013) 126(6):739–48. doi: 10.1111/jnc.12355 Brailoiu GC Dun SL Brailoiu E Inan S Yang J Chang JK . Nesfatin-1: Distribution and Interaction With a G Protein-Coupled Receptor in the Rat Brain. Endocrinology (2007) 148(10):5088–94. doi: 10.1210/en.2007-0701 Buzcu H Ozbeyli D Yuksel M Cilingir Kaya OT Kasimay Cakir O . Nesfatin-1 Protects From Acute Pancreatitis: Role of Melanocortin Receptors. J Physiol Pharmacol (2019) 70(6):839–48. doi: 10.26402/jpp.2019.6.03 Chen X Shu X Cong ZK Jiang ZY Jiang H . Nesfatin-1 Acts on the Dopaminergic Reward Pathway to Inhibit Food Intake. Neuropeptides (2015) 53:45–50. doi: 10.1016/j.npep.2015.07.004 Chen Z Xu YY Ge JF Chen FH . CRHR1 Mediates the Up-Regulation of Synapsin I Induced by Nesfatin-1 Through ERK 1/2 Signaling in SH-SY5Y Cells. Cell Mol Neurobiol (2018) 38(3):627–33. doi: 10.1007/s10571-017-0509-x Dong J Xu H Xu H Wang PF Cai GJ Song HF . Nesfatin-1 Stimulates Fatty-Acid Oxidation by Activating AMP-Activated Protein Kinase in STZ-Induced Type 2 Diabetic Mice. PloS One (2013) 8(12):e83397. doi: 10.1371/journal.pone.0083397 Dore R Levata L Gachkar S Jöhren O Mittag J Lehnert H . The Thermogenic Effect of Nesfatin-1 Requires Recruitment of the Melanocortin System. J Endocrinol (2017) 235(2):111–22. doi: 10.1530/JOE-17-0151 Erfani S Moghimi A Aboutaleb N Khaksari M . Nesfatin-1 Improve Spatial Memory Impairment Following Transient Global Cerebral Ischemia/Reperfusion via Inhibiting Microglial and Caspase-3 Activation. J Mol Neurosci (2018) 65(3):377–84. doi: 10.1007/s12031-018-1105-3 Fan XT Tian Z Li SZ Zhai T Liu JL Wang R . Ghrelin Receptor Is Required for the Effect of Nesfatin-1 on Glucose Metabolism. Front Endocrinol (2018) 9:633. doi: 10.3389/fendo.2018.00633 Feijóo-Bandín S Rodríguez-Penas D García-Rúa V Mosquera-Leal A Otero MF Pereira E . Nesfatin-1 in Human and Murine Cardiomyocytes: Synthesis, Secretion, and Mobilization of GLUT-4. Endocrinology (2013) 154(12):4757–67. doi: 10.1210/en.2013-1497 Feng H Wang Q Guo F Han X Pang M Sun X . Nesfatin-1 Influences the Excitability of Gastric Distension-Responsive Neurons in the Ventromedial Hypothalamic Nucleus of Rats. Physiol Res (2017) 66(2):335–44. doi: 10.33549/physiolres.933347 Gao S Guo F Sun X Zhang N Gong Y Xu L . The Inhibitory Effects of Nesfatin-1 in Ventromedial Hypothalamus on Gastric Function and Its Regulation by Nucleus Accumbens. Front Physiol (2017) 7:634. doi: 10.3389/fphys.2016.00634 Ge JF Xu YY Qin G Pan XY Cheng JQ Chen FH . Nesfatin-1, a Potent Anorexic Agent, Decreases Exploration and Induces Anxiety-Like Behavior in Rats Without Altering Learning or Memory. Brain Res (2015) 1629:171–81. doi: 10.1016/j.brainres.2015.10.027 Guo FF Xu L Gao SL Sun XR Li ZL Gong YL . The Effects of Nesfatin-1 in the Paraventricular Nucleus on Gastric Motility and its Potential Regulation by the Lateral Hypothalamic Area in Rats. J Neurochem (2015) 132(3):266–75. doi: 10.1111/jnc.12973 Heidarzadeh H Zendehdel M Babapour V Gilanpour H . The Effect of Nesfatin-1 on Food Intake in Neonatal Chicks: Role of CRF1/CRF2 and H1/H3 Receptors. Vet Res Commun (2018) 42(1):39–47. doi: 10.1007/s11259-017-9706-9 Ishida E Hashimoto K Shimizu H Okada S Satoh T Kato I . Nesfatin-1 Induces the Phosphorylation Levels of cAMP Response Element-Binding Protein for Intracellular Signaling in a Neural Cell Line. PloS One (2012) 12):e50918. doi: 10.1371/journal.pone.0050918 Iwasaki Y Nakabayashi H Kakei M Shimizu H Mori M Yada T . Nesfatin-1 Evokes Ca2+ Signaling in Isolated Vagal Afferent Neurons via Ca2+ Influx Through N-Type Channels. Biochem Biophys Res Commun (2009) 390(3):958–62. doi: 10.1016/j.bbrc.2009.10.085 Jia FY Li XL Li TN Wu J Xie BY Lin L . Role of Nesfatin-1 in a Rat Model of Visceral Hypersensitivity. World J Gastroenterol (2013) 19(22):3487–93. doi: 10.3748/wjg.v19.i22.3487 Jiang L Xu K Li J Zhou X Xu L Wu Z . Nesfatin-1 Suppresses Interleukin-1β-Induced Inflammation, Apoptosis, and Cartilage Matrix Destruction in Chondrocytes and Ameliorates Osteoarthritis in Rats. Aging (2020) 12(2):1760–77. doi: 10.18632/aging.102711 Kan JY Yen MC Wang JY Wu DC Chiu YJ Ho YW . Nesfatin-1/Nucleobindin-2 Enhances Cell Migration, Invasion, and Epithelial-Mesenchymal Transition via LKB1/AMPK/TORC1/ZEB1 Pathways in Colon Cancer. Oncotarget (2016) 7(21):31336–49. doi: 10.18632/oncotarget.9140 Kerbel B Unniappan S . Nesfatin-1 Suppresses Energy Intake, Co-Localises Ghrelin in the Brain and Gut, and Alters Ghrelin, Cholecystokinin and Orexin mRNA Expression in Goldfish. J Neuroendocrinol (2012) 24(2):366–77. doi: 10.1111/j.1365-2826.2011.02246.x Levata L Dore R Jöhren O Schwaninger M Schulz C Lehnert H . Nesfatin-1 Acts Centrally to Induce Sympathetic Activation of Brown Adipose Tissue and Non-Shivering Thermogenesis. Horm Metab Res (2019) 51(10):678–85. doi: 10.1055/a-0985-4272 Li C Zhang F Shi L Zhang H Tian Z Xie J . Nesfatin-1 Decreases Excitability of Dopaminergic Neurons in the Substantia Nigra. J Mol Neurosci (2014) 52(3):419–24. doi: 10.1007/s12031-013-0169-3 Li T Wei S Fan C Tang D Luo D . Nesfatin-1 Promotes Proliferation, Migration and Invasion of HTR-8/SVneo Trophoblast Cells and Inhibits Oxidative Stress via Activation of PI3K/AKT/mTOR and AKT/Gsk3β Pathway. Reprod Sci (2021) 28(2):550–61. doi: 10.1007/s43032-020-00324-1 Li ZL Xu L Sun XR Guo FF Gong YL Gao SL . Central Nesfatin-1 Influences the Excitability of Ghrelin-Responsive Gastric Distension Neurons in the Arcuate Nucleus and Reduces Gastric Motility in Rats. Eur J Neurosci (2013) 38(11):3636–43. doi: 10.1111/ejn.12366 Lu QB Wang HP Tang ZH Cheng H Du Q Wang YB . Nesfatin-1 Functions as a Switch for Phenotype Transformation and Proliferation of VSMCs in Hypertensive Vascular Remodeling. Biochim Biophys Acta Mol Basis Dis (2018) 1864(6 Pt A):2154–68. doi: 10.1016/j.bbadis.2018.04.002 Maejima Y Horita S Kobayashi D Aoki M O’hashi R Imai R . Nesfatin-1 Inhibits Voltage Gated K+ Channels in Pancreatic Beta Cells. Peptides (2017) 95:10–5. doi: 10.1016/j.peptides.2017.07.001 Maejima Y Sedbazar U Suyama S Kohno D Onaka T Takano E . Nesfatin-1-Regulated Oxytocinergic Signaling in the Paraventricular Nucleus Causes Anorexia Through a Leptin-Independent Melanocortin Pathway. Cell Metab (2009) 10(5):355–65. doi: 10.1016/j.cmet.2009.09.002 Mazza R Gattuso A Filice M Cantafio P Cerra MC Angelone T . Nesfatin-1 as a New Positive Inotrope in the Goldfish (Carassius Auratus) Heart. Gen Comp Endocrinol (2015) 224:160–7. doi: 10.1016/j.ygcen.2015.08.003 Mori Y Shimizu H Kushima H Saito T Hiromura M Terasaki M . Nesfatin-1 Suppresses Peripheral Arterial Remodeling Without Elevating Blood Pressure in Mice. Endocr Connect (2019) 8(5):536–46. doi: 10.1530/EC-19-0120 Nair N Gerger C Hatef A Weber LP Unniappan S . Ultrasonography Reveals In Vivo Dose-Dependent Inhibition of End Systolic and Diastolic Volumes, Heart Rate and Cardiac Output by Nesfatin-1 in Zebrafish. Gen Comp Endocrinol (2016) 234:142–50. doi: 10.1016/j.ygcen.2016.02.015 Nakata M Manaka K Yamamoto S Mori M Yada T . Nesfatin-1 Enhances Glucose-Induced Insulin Secretion by Promoting Ca(2+) Influx Through L-Type Channels in Mouse Islet β-Cells. Endocr J (2011) 58(4):305–13. doi: 10.1507/endocrj.k11e-056 Osaki A Shimizu H . Peripheral Administration of Nesfatin-1 Increases Blood Pressure in Mice. Hypertens Res (2014) 37(2):185–6. doi: 10.1038/hr.2013.122 Ozcan M Gok ZB Kacar E Serhatlioglu I Kelestimur H . Nesfatin-1 Increases Intracellular Calcium Concentration by Protein Kinase C Activation in Cultured Rat Dorsal Root Ganglion Neurons. Neurosci Lett (2016) 619:177–81. doi: 10.1016/j.neulet.2016.03.018 Ozturk CC Oktay S Yuksel M Akakin D Yarat A Kasimay Cakir O . Anti-Inflammatory Effects of Nesfatin-1 in Rats With Acetic Acid - Induced Colitis and Underlying Mechanisms. J Physiol Pharmacol (2015) 66(5):741–50. Price CJ Hoyda TD Samson WK Ferguson AV . Nesfatin-1 Influences the Excitability of Paraventricular Nucleus Neurones. J Neuroendocrinol (2008) 20(2):245–50. doi: 10.1111/j.1365-2826.2007.01641.x Price CJ Samson WK Ferguson AV . Nesfatin-1 Inhibits NPY Neurons in the Arcuate Nucleus. Brain Res (2008) 1230:99–106. doi: 10.1016/j.brainres.2008.06.084 Prinz P Goebel-Stengel M Teuffel P Rose M Klapp BF Stengel A . Peripheral and Central Localization of the Nesfatin-1 Receptor Using Autoradiography in Rats. Biochem Biophys Res Commun (2016) 470(3):521–7. doi: 10.1016/j.bbrc.2016.01.113 Ramanjaneya M Tan BK Rucinski M Kawan M Hu J Kaur J . Nesfatin-1 Inhibits Proliferation and Enhances Apoptosis of Human Adrenocortical H295R Cells. J Endocrinol (2015) 226(1):1–11. doi: 10.1530/JOE-14-0496 Ranjan A Choubey M Yada T Krishna A . Direct Effects of Neuropeptide Nesfatin-1 on Testicular Spermatogenesis and Steroidogenesis of the Adult Mice. Gen Comp Endocrinol (2019) 271:49–60. doi: 10.1016/j.ygcen.2018.10.022 Ranjan A Choubey M Yada T Krishna A . Immunohistochemical Localization and Possible Functions of Nesfatin-1 in the Testis of Mice During Pubertal Development and Sexual Maturation. J Mol Histol (2019) 50(6):533–49. doi: 10.1007/s10735-019-09846-8 Ranjan A Choubey M Yada T Krishna A . Nesfatin-1 Ameliorates Type-2 Diabetes-Associated Reproductive Dysfunction in Male Mice. J Endocrinol Invest (2020) 43(4):515–28. doi: 10.1007/s40618-019-01136-0 Shen XL Song N Du XX Li Y Xie JX Jiang H . Nesfatin-1 Protects Dopaminergic Neurons Against MPP+/MPTP-Induced Neurotoxicity Through the C-Raf-ERK1/2-Dependent Anti-Apoptotic Pathway. Sci Rep (2017) 7:40961. doi: 10.1038/srep40961 Tan J Jin L Wang Y Cao B Wang S Zhang F . Nesfatin-1 Acts as an Inhibitory Factor in Human Gastrointestinal Smooth Muscle Cells in Diabetes Mellitus-Induced Delayed Gastric Emptying. Int J Clin Exp Pathol (2016) 9(11):11214–21. Tanida M Gotoh H Yamamoto N Wang M Kuda Y Kurata Y . Hypothalamic Nesfatin-1 Stimulates Sympathetic Nerve Activity via Hypothalamic ERK Signaling. Diabetes (2015) 64(11):3725–36. doi: 10.2337/db15-0282 Tanida M Mori M . Nesfatin-1 Stimulates Renal Sympathetic Nerve Activity in Rats. Neuroreport (2011) 22(6):309–12. doi: 10.1097/WNR.0b013e328346107f Tasatargil A Kuscu N Dalaklioglu S Adiguzel D Celik-Ozenci C Ozdem S . Cardioprotective Effect of Nesfatin-1 Against Isoproterenol-Induced Myocardial Infarction in Rats: Role of the Akt/GSK-3β Pathway. Peptides (2017) 95:1–9. doi: 10.1016/j.peptides.2017.07.003 Vélez EJ Unniappan S . Nesfatin-1 and Nesfatin-1-Like Peptide Suppress Growth Hormone Synthesis via the AC/PKA/CREB Pathway in Mammalian Somatotrophs. Sci Rep (2020) 10(1):16686. doi: 10.1038/s41598-020-73840-4 Wang Q Guo F Sun X Gao S Li Z Gong Y . Effects of Exogenous Nesfatin-1 on Gastric Distention-Sensitive Neurons in the Central Nucleus of the Amygdala and Gastric Motility in Rats. Neurosci Lett (2014) 582:65–70. doi: 10.1016/j.neulet.2014.09.003 Wu D Yang M Chen Y Jia Y Ma ZA Boden G . Hypothalamic Nesfatin-1/NUCB2 Knockdown Augments Hepatic Gluconeogenesis That Is Correlated With Inhibition of mTOR-STAT3 Signaling Pathway in Rats. Diabetes (2014) 63(4):1234–47. doi: 10.2337/db13-0899 Xia ZF Fritze DM Li JY Chai B Zhang C Zhang W . Nesfatin-1 Inhibits Gastric Acid Secretion via a Central Vagal Mechanism in Rats. Am J Physiol Gastrointest Liver Physiol (2012) 303(5):G570–7. doi: 10.1152/ajpgi.00178.2012 Xu L Wang H Gong Y Pang M Sun X Guo F . Nesfatin-1 Regulates the Lateral Hypothalamic Area Melanin-Concentrating Hormone-Responsive Gastric Distension-Sensitive Neurons and Gastric Function via Arcuate Nucleus Innervation. Metabolism (2017) 67:14–25. doi: 10.1016/j.metabol.2016.10.010 Xu L Wang Q Guo F Pang M Sun X Gao S . Nesfatin-1 Signaling in the Basom Edial Amygdala Modulates the Gastric Distension-Sensitive Neurons Discharge and Decreases Gastric Motility via Melanocortin 3/4 Receptors and Modified by the Arcuate Nucleus. Eur J Pharmacol (2015) 764:164–72. doi: 10.1016/j.ejphar.2015.07.002 Yang M Zhang Z Wang C Li K Li S Boden G . Nesfatin-1 Action in the Brain Increases Insulin Sensitivity Through Akt/AMPK/TORC2 Pathway in Diet-Induced Insulin Resistance. Diabetes (2012) 61(8):1959–68. doi: 10.2337/db11-1755 Yin Y Li Z Gao L Li Y Zhao J Zhang W . AMPK-Dependent Modulation of Hepatic Lipid Metabolism by Nesfatin-1. Mol Cell Endocrinol (2015) 417:20–6. doi: 10.1016/j.mce.2015.09.006 Ying J Zhang Y Gong S Chang Z Zhou X Li H . Nesfatin-1 Suppresses Cardiac L-Type Ca²⁺ Channels Through Melanocortin Type 4 Receptor and the Novel Protein Kinase C Theta Isoform Pathway. Cell Physiol Biochem (2015) 36(2):555–68. doi: 10.1159/000430120 Yosten GL Samson WK . Neural Circuitry Underlying the Central Hypertensive Action of Nesfatin-1: Melanocortins, Corticotropin-Releasing Hormone, and Oxytocin. Am J Physiol Regul Integr Comp Physiol (2014) 306(10):R722–7. doi: 10.1152/ajpregu.00396.2013 Yuan JH Chen X Dong J Zhang D Song K Zhang Y . Nesfatin-1 in the Lateral Parabrachial Nucleus Inhibits Food Intake, Modulates Excitability of Glucosensing Neurons, and Enhances UCP1 Expression in Brown Adipose Tissue. Front Physiol (2017) 8:235. doi: 10.3389/fphys.2017.00235 Zhang JR Lu QB Feng WB Wang HP Tang ZH Cheng H . Nesfatin-1 Promotes VSMC Migration and Neointimal Hyperplasia by Upregulating Matrix Metalloproteinases and Downregulating Pparγ. BioMed Pharmacother (2018) 102:711–7. doi: 10.1016/j.biopha.2018.03.120 Zhang T Wang M Liu L He B Hu J Wang Y . Hypothalamic Nesfatin-1 Mediates Feeding Behavior via MC3/4R-ERK Signaling Pathway After Weight Loss in Obese Sprague-Dawley Rats. Peptides (2019) 119:170080. doi: 10.1016/j.peptides.2019.04.007 Zhang X Qi J Tang N Wang S Wu Y Chen H . Intraperitoneal Injection of Nesfatin-1 Primarily Through the CCK-CCK1R Signal Pathway Affects Expression of Appetite Factors to Inhibit the Food Intake of Siberian Sturgeon (Acipenser Baerii). Peptides (2018) 109:14–22. doi: 10.1016/j.peptides.2018.09.008 Zhou XP Sha J Huang L Li TN Zhang RR Tang MD . Nesfatin-1/NUCB2 in the Amygdala Influences Visceral Sensitivity via Glucocorticoid and Mineralocorticoid Receptors in Male Maternal Separation Rats. Neurogastroenterol Motil (2016) 28(10):1545–53. doi: 10.1111/nmo.12853 Pan W Hsuchou H Kastin AJ . Nesfatin-1 Crosses the Blood-Brain Barrier Without Saturation. Peptides (2007) 28(11):2223–8. doi: 10.1016/j.peptides.2007.09.005 Goebel-Stengel M Wang L Stengel A Taché Y . Localization of Nesfatin-1 Neurons in the Mouse Brain and Functional Implication. Brain Res (2011) 1396:20–34. doi: 10.1016/j.brainres.2011.04.031 Foo KS Brismar H Broberger C . Distribution and Neuropeptide Coexistence of Nucleobindin-2 mRNA/Nesfatin-Like Immunoreactivity in the Rat CNS. Neuroscience (2008) 156(3):563–79. doi: 10.1016/j.neuroscience.2008.07.054 Kato M Ma HT Tatemoto K . GLP-1 Depolarizes the Rat Pancreatic Beta Cell in a Na(+)-Dependent Manner. Regul Pept (1996) 62(1):23–7. doi: 10.1016/0167-0115(95)00164-6 Hiriart M Matteson DR . Na Channels and Two Types of Ca Channels in Rat Pancreatic B Cells Identified With the Reverse Hemolytic Plaque Assay. J Gen Physiol (1988) 91(5):617–39. doi: 10.1085/jgp.91.5.617 Arkhammar P Juntti-Berggren L Larsson O Welsh M Nånberg E Sjöholm A . Protein Kinase C Modulates the Insulin Secretory Process by Maintaining a Proper Function of the β-Cell Voltage- Activated Ca2+ Channels. J Biol Chem (1994) 269:2743–9. doi: 10.1016/S0021-9258(17)42006-0 Iftinca MC . Neuronal T-Type Calcium Channels: What’s New? Iftinca: T-Type Channel Regulation. J Med Life (2011) 4(2):126–38. Ross WN . Understanding Calcium Waves and Sparks in Central Neurons. Nat Rev Neurosci (2012) 13(3):157–68. doi: 10.1038/nrn3168 Kabbani N Nordman JC Corgiat BA Veltri DP Shehu A Seymour VA . Are Nicotinic Acetylcholine Receptors Coupled to G Proteins? Bioessays (2013) 35(12):1025–34. doi: 10.1002/bies.201300082