Front. Syst. Neurosci.Frontiers in Systems NeuroscienceFront. Syst. Neurosci.1662-5137Frontiers Media S.A.10.3389/fnsys.2022.867875NeuroscienceOriginal ResearchImatinib Mesylate Reduces Voiding Frequency in Female Mice With Acute Cyclophosphamide-Induced CystitisPerkinsMegan E.GirardBeatrice M.CampbellSusan E.VizzardMargaret A.*Department of Neurological Sciences, Larner College of Medicine, University of Vermont, Burlington, VT, United States
Edited by: Pedro L. Vera, Lexington VA Medical Center, United States Department of Veterans Affairs, United States
Reviewed by: Betty Exintaris, Monash University, Australia; Francisco Cruz, University of Porto, Portugal
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Lamina propria interstitial cells that express the tyrosine kinase receptor, platelet-derived growth factor receptor alpha (PDGFRα) may play a role in urinary sensory signaling. Imatinib mesylate, also referred to as imatinib, is a tyrosine kinase inhibitor that can inhibit PDGFRα and has been widely used in urological research. We evaluated the functional effects of imatinib administration (via oral gavage or intravesical infusion) with two different experimental designs (prevention and treatment), in a cyclophosphamide (CYP)-induced cystitis (acute, intermediate, and chronic), male and female rodent model using conscious cystometry and somatic sensitivity testing. Imatinib significantly (0.0001 ≤ p ≤ 0.05) decreased voiding frequency and increased bladder capacity in acute CYP-induced cystitis, by the prevention (females) and treatment (females and males) designs. Imatinib was not effective in preventing or treating intermediate or chronic CYP-induced cystitis in either sex. Interestingly, in the prevention experiments, imatinib administration increased (0.0001 ≤ p ≤ 0.01) voiding frequency and decreased bladder capacity in control mice. However, in the treatment experiments, imatinib administration decreased (0.01 ≤ p ≤ 0.05) voiding frequency and increased bladder capacity in control mice. Bladder function improvements observed with imatinib treatment in acute CYP-induced cystitis mice remained and additionally improved with a second dose of imatinib 24 hours after CYP treatment. Imatinib administration did not affect pelvic somatic sensitivity in female mice with acute CYP-induced cystitis. Our studies suggest that (1) imatinib improves bladder function in mice with acute CYP-induced cystitis with a prevention and treatment design and (2) interstitial cells may be a useful target to improve bladder function in cystitis.
interstitial cystitisinterstitial cellsplatelet-derived growth factor receptor (PDGFR)imatinib mesylateconscious cystometrysomatic sensitivity5R01DK1201081R01DK124580National Institute of Diabetes and Digestive and Kidney Diseases10.13039/100000062Introduction
The storage and release functions of the urinary bladder are highly organized and coordinated by peripheral and central neural pathways involving the spinal cord, brain, afferent and efferent nerves, dorsal root ganglia (DRG), autonomic ganglia and the urinary bladder (Andersson, 2002; de Groat et al., 2015). The urinary bladder is organized into layers: the mucosa, muscularis propria, and the adventitia/serosa. The mucosal layer consists of transitional epithelial (urothelial) cells that line the lumen of the bladder and a lamina propria (LP) (also referred to as the submucosa) beneath the basement membrane of the epithelial cells (Andersson, 2002, 2004; Merrill et al., 2016). The urothelium responds to stimuli and releases various factors including ATP, ACh, and nitric oxide (Birder and Andersson, 2013; Merrill et al., 2016). The urothelium can be compromised with injury or inflammation, allowing toxic substances to reach the suburothelial nerve plexus and muscular layers, contributing to urinary urgency, frequency, and pain during voiding (Birder, 2005; Birder and Andersson, 2013). The LP is composed of loose connective tissue, interstitial cells, vasculature, adipocytes, lymphatic vessels, fibroblasts, nerve fibers and endings and may integrate urothelial and smooth muscle input (Andersson, 2002, 2004; Birder and Andersson, 2013).
Neuro-urological research continues to advance our understanding of the mechanisms underlying bladder function and dysfunction. However, many questions remain concerning the identity of potential treatment targets as well as treatment options for urinary bladder dysfunction. For example, current theories suggest a sensory intermediary function for the LP interstitial cells to mediate signals from the urothelium to afferent nerves and/or the detrusor muscle, to regulate bladder sensation and contractility (Gray et al., 2013; Heppner et al., 2017; Koh et al., 2018). LP interstitial cells in the urinary bladder are positioned near afferent nerve terminals in the suburothelial plexus (Koh et al., 2012; Gabella, 2019) and exhibit cholinergic (Mukerji et al., 2006; Grol et al., 2009), purinergic (Sui et al., 2006; Fry et al., 2012; Lee et al., 2014; Heppner et al., 2017) and nitrergic (Smet et al., 1996; Gillespie et al., 2006; de Jongh et al., 2007) properties (Koh et al., 2018). Other potential roles for LP interstitial cells include: transduction of bladder mechanosensation (Isogai et al., 2016; Heppner et al., 2017; Liu et al., 2018; Steiner et al., 2018; Dalghi et al., 2019), propagation of calcium transients (Heppner et al., 2017) and signal transmission via gap junctions (Ikeda et al., 2007). A subset of LP interstitial cells expresses the tyrosine kinase receptor platelet-derived growth factor receptor alpha (PDGFRα) (Koh et al., 2012; Monaghan et al., 2012; Sancho et al., 2017) and this subpopulation may be important for bladder voiding during early postnatal development before coordinated urinary function (Kanai et al., 2007; Heppner et al., 2017). PDGFRα+ interstitial cells are found in the urinary bladder of human, mouse, rat, guinea pig, and pig, with similar morphology, chemical expression, and organization (Gevaert et al., 2014b,2017; Steiner et al., 2018). Studies suggest that PDGFRα+ LP interstitial cells may also contribute to bladder dysfunction (e.g., interstitial cystitis/bladder pain syndrome, IC/BPS) because preclinical rodent models show increased expression of interstitial cell markers (de Jongh et al., 2007; Kubota et al., 2008; Kim et al., 2011; Abrams et al., 2012; Fry et al., 2012; Johnston et al., 2012; Deng et al., 2015; Kjell et al., 2015; Liu et al., 2017, 2018; Sancho et al., 2017). PDGFRα+ bladder interstitial cells also exhibit morphological and chemical differences in patients with OAB or IC/BPS (Neuhaus et al., 2005; Roosen et al., 2009a,b; Gevaert et al., 2011, 2015; Meng et al., 2015). Additionally, interstitial cells display abnormal electrophysiological properties in IC/BPS and may contribute to the increased and spontaneous contractions observed in the detrusor (Rosenberg et al., 2016; Liu et al., 2017, 2018).
Imatinib mesylate, also referred to as imatinib, is a competitive inhibitor of the ATP-binding site of certain receptor tyrosine kinases including PDGFRα (Buchdunger et al., 1996, 2000; Kilic et al., 2000) and has been commonly used in lower urinary tract (LUT) studies to target PDGFRα+ interstitial cells (Biers et al., 2006; Kubota et al., 2006; Min et al., 2011; Abrams et al., 2012; Deng et al., 2013; Gevaert et al., 2014a; Kjell et al., 2015; Sancho et al., 2017; Giglio et al., 2018). Recent reports indicate that imatinib administration reduces PDGFRα expression and voiding frequency in rodents with IC/BPS (Sancho et al., 2017; Giglio et al., 2018). In this study, we expand upon previous studies (Sancho et al., 2017; Giglio et al., 2018) to determine the functional effects of imatinib mesylate administration (e.g., gavage, intravesical) in a cyclophosphamide (CYP)-induced cystitis (acute, intermediate, chronic) mouse model (male and female) using conscious, unrestrained, open-outlet cystometry. We also assess the mechanical sensitivity of the pelvic region in a CYP-induced cystitis mouse model with and without imatinib treatment (e.g., gavage, intravesical).
Materials and MethodsExperimental Animals
Male and female wildtype (WT), C57BL/6 mice (3–5 months) (Jackson Labs, Bar Harbor, ME, United States) were used in these studies. Mice were bred locally at The Larner College of Medicine, University of Vermont (UVM) animal facilities in standard laboratory conditions, as previously described (Tooke et al., 2019). The UVM Institutional Animal Care and Use Committee (IACUC) approved all experimental procedures involving animal use (IACUC #X9-020). The UVM Office of Animal Care and Management managed animal care in accordance with the American Association for Accreditation of Laboratory Animal Care (AAALAC) and National Institutes of Health (NIH) guidelines. All efforts were taken to minimize animal pain and distress. Mice exhibiting signs of pain and distress that could not be managed with post-operative analgesics were immediately euthanized. Separate cohorts of littermate WT mice were used in these studies. Female mice were primarily used because of the increased IC/BPS prevalence in human females (Hanno et al., 2015). The estrous cycle status of mice was not determined.
Cyclophosphamide Dosing and Administration
Cyclophosphamide treatment groups received CYP injections (i.p.) to induce acute (200 mg/kg, 4 h), intermediate (200 mg/kg, 48 h) or chronic (75 mg/kg, every 72 h for 8 days) urinary bladder inflammation as previously described (Malley and Vizzard, 2002; Bjorling et al., 2011; Guo et al., 2018). Control groups did not receive CYP. After completion of CYP treatment, mice were used for bladder function testing (i.e., cystometry) or tissues (e.g., urinary bladder) were harvested from anesthetized (5% isoflurane in oxygen) mice subsequently euthanized by thoracotomy. Urinary bladders were collected and stored for future experiments.
Imatinib Mesylate Dosing and Administration
The dose and route of imatinib were determined in pilot studies and by using previous reports (Abrams et al., 2012; Kjell et al., 2015; Sancho et al., 2017) as guidance. Imatinib or vehicle (i.e., water or saline) was delivered by two different routes in separate cohorts of mice: (1) systemically by oral gavage (250 mg/kg; 22 gauge/25 mm, stainless steel); or (2) directly by intravesical infusion (50 μM) via an externalized bladder catheter, or by transurethral intravesical infusion (50 μM). Upon cessation of gavage and infusion, mice were used for testing and/or euthanized for tissue collection.
Oral Gavage (Prevention Schedule)
Mice were placed headfirst in a cone shaped, plastic bag with the far corner cut. Alternative handling techniques (i.e., scruff) could not be used because of the intravesical implant surgery with exteriorization at the base of the neck. Mice were monitored constantly to ensure correct gavage needle placement and animal well-being. The same individual performed all gavage procedures at the same time of day (8 a.m.–12 p.m.) to reduce potential variability.
Mice were pre-treated with imatinib (250 mg/kg) for 5 days prior to CYP (i.p.) administration ranging from 5 to 12 days total, depending on the CYP dosing schedule. All groups were gavaged daily throughout the entire experimental period with imatinib or vehicle control, including on surgery, CYP administration and cystometry testing days. On these days, mice were gavaged and left undisturbed in their home cages for at least 30 min prior to surgery, CYP administration or cystometry testing.
Catheter Implant for Intravesical Infusion (Prevention Schedule)
Mice were pre-treated with imatinib (50 μM, 30 min, 0.5 mL, 1X/day) via an externalized bladder catheter for 5 days prior to CYP (4 h, 200 mg/kg, i.p.) administration. Some cohorts additionally received protamine sulfate (PS; 10 mg/kg, 0.5 mL, 30 min) infusions, prior to imatinib. Bladder parameters were assessed using conscious, open outlet cystometry after acute (4 h) CYP.
Catheter Implant for Intravesical Infusion (Treatment Schedule)
Acute (4 h, 200 mg/kg, i.p.) or chronic (every 72 h for 8 days, 75 mg/kg, i.p.) cystitis was induced with CYP as previously described (Guo et al., 2018; Tooke et al., 2019). Bladder parameters were assessed using conscious, open outlet cystometry before and after the imatinib infusion (50 μM, 30 min, 0.5 mL).
Mice were anesthetized with isoflurane in oxygen (3–4%), placed in the supine position on a water mat heating pad and catheterized by inserting lubricated polyethylene tubing (PE-10, Clay Adams, Parsippany, NJ, United States) into the bladder through the urethra. The mice were manually voided before the urethral instillation procedure. Solution (i.e., imatinib or saline) was instilled into the bladder until a full bladder could be palpated (25–400 μL). The catheter was then removed from the urethra while the mice remained anesthetized (30 min).
Intravesical Catheter Implantation
Intravesical catheter implantation was performed as previously described (Schnegelsberg et al., 2010; Gonzalez et al., 2013). Mice received analgesics (carprofen, 0.1 mg/kg, s.c.) before and after (every 24 h for 48 h total) surgery.
Conscious, Open-Outlet Cystometry With Continuous Infusion of Saline
Conscious, open-outlet cystometry with continuous saline infusion was performed as previously described (Guo et al., 2018; Tooke et al., 2019). Three days after surgery, mice were placed, unrestrained, in a wire bottom cage with the dorsal neck tubing exteriorized and connected to the cystometry system (Med Associates, St. Albans, VT, United States). Room temperature saline was infused into the bladder (25 μl/min) to elicit repetitive bladder contractions. After an initial accommodation period (20–30 min), a minimum of 6 consistent micturition cycles were recorded. Urodynamic measures included: minimum pressure (pressure at the beginning of bladder filling), threshold pressure (bladder pressure immediately before micturition), maximum pressure, intermicturition interval (time between micturition events) and infused volume. Bladder capacity is defined as the infused volume necessary to elicit a micturition event. Voided volume was not analyzed as multiple groups (e.g., CYP groups) were unable to be assessed, due to very small volume voids. Non-voiding contractions (NVCs) were also not analyzed because multiple groups did not reliably produce NVCs.
Imatinib (50 μM) was intravesically infused into the bladder for some experiments where mice served as their own controls and were evaluated before and after imatinib treatment. Baseline bladder function testing was conducted with intravesical saline, followed by intravesical imatinib treatment, then bladder function testing was repeated. At least 6, reproducible micturition cycles were obtained before and after imatinib treatment. After cystometry, mice were euthanized by thoracotomy. Urinary bladders were harvested for future experiments.
Pelvic Mechanical Sensitivity Testing
Mechanical sensitivity was assessed in separate groups of mice that did not undergo the intravesical catheter implantation surgery nor cystometry. The imatinib prevention (gavage) and treatment schedules (intravesical infusion) were evaluated. All mice were acclimated to the testing environment for 2 h/day for 2 days prior to Schnegelsberg et al. (2010) and on the test day.
Prevention
Cohorts received daily doses of imatinib or vehicle (water) via oral gavage, 1X/day for 5 days. On the test day (i.e., last day), the cohorts received the final dose of imatinib, followed 30 min later with acute CYP treatment. Mechanical sensitivity was evaluated 4 h after CYP treatment.
Treatment
Cohorts received acute CYP treatment followed 4 h later by an intravesical infusion (transurethral catheter) of imatinib or vehicle (saline) followed (30 min) by mechanical sensitivity testing.
Control mice did not receive CYP treatment. Mice were tested in individual plexiglass chambers with a stainless-steel wire grid floor, using calibrated von Frey microfilaments (0.008–1 g, Semmes Weinstein, Stoelting Co, Wood Dale, IL, United States). Microfilaments were applied in a perpendicular manner, until the hair buckled to the lower pelvic/abdominal region overlying the bladder for 1–3 s with an interstimulus interval of at least 15 s. Positive behaviors included sharp retraction of the abdomen, jumping or immediate licking or scratching of the affected area (May and Vizzard, 2010; Schnegelsberg et al., 2010). Mechanical sensitivity testing was performed in a blinded manner, with mixed treatment and control groups. The groups were decoded following analyses.
Mechanical Sensitivity Analysis
The mechanical force needed to elicit a withdrawal response in 50% of the mice was determined using the up-down method (Deuis et al., 2017). At least four responses were obtained after the first change in von Frey filament direction. The withdrawal threshold was defined as a positive response, followed by a negative response in either direction, repeated at least twice. Two separate evaluators determined the withdrawal thresholds; one evaluator was blinded to all conditions.
Pain Behavioral Assessments
Secondary behavioral assessments that may be indicative of pain or distress were also conducted. Behavior was only assessed in the control and treatment (intravesical) groups also undergoing mechanical sensitivity testing. Mice were acclimated to individual cages 30 min/day, for 2 days before behavioral assessments. On the test day, after microfilament sensitivity testing, mice were immediately placed in individual cages for acclimation (10 min). Mice were then recorded using a video camera for 15 min. An evaluator, blinded to groups, examined the video and determined total time moving and total licking behaviors of the abdominal pelvic area (Boucher et al., 2000; Arras et al., 2007; Yoshikawa et al., 2012).
Exclusionary Criteria
Mice were withdrawn from study because of adverse postoperative events or pain, lethargy, or if distress could not be alleviated by postoperative analgesics. Some cystometry recordings were rendered unusable due excessive behavioral movements (e.g., grooming, standing, walking, defecation, and chewed tubing). Approximately 10% of mice (n = 32) were removed from the study.
Statistical Analyses
All values represent mean ± SEM. When the F ratio exceeded the critical value at α = 0.05, post hoc multiple comparisons tests were performed. Data were analyzed using a two-way analysis of variance (ANOVA) with Bonferroni’s multiple comparisons test, a repeated measures two-way ANOVA with Šídák’s multiple comparisons test, or Student’s paired t-test, as indicated by experimental design. All analyses were performed using GraphPad Prism software (GraphPad Prism version 8.0.0 for Windows, GraphPad Software, San Diego, CA, United States).1
ResultsImatinib Decreases Voiding Frequency and Increases Bladder Capacity in the Acute (4 h) Cyclophosphamide-Induced Cystitis Model: Prevention or Treatment Design
Administration of imatinib significantly (p ≤ 0.001) increased the intermicturition interval (IMI) and the infused volume (IV) in mice with acute (200 mg/kg, i.p., 4 h) CYP-induced cystitis when evaluated in two different drug delivery methods and experimental designs (Figures 1, 2).
Imatinib mesylate pre-treatment via oral gavage significantly alters intermicturition interval (IMI) and infused volume (IV) in an acute (4 h) cyclophosphamide (CYP)-induced cystitis mouse model. (A) Acute CYP-induced cystitis (200 mg/kg, 4 h, i.p.) experimental schedule for imatinib mesylate pre-treatment via oral gavage (250 mg/kg, 5 days, 1X/day). (B,D) Imatinib mesylate pre-treatment significantly increased IMI and IV (p ≤ 0.001) in female mice with acute (4 h) CYP-induced cystitis. (C,E) Imatinib mesylate pre-treatment did not significantly affect bladder measures in male mice with acute CYP-induced cystitis. (B–E) Imatinib pre-treatment alone by gavage, without CYP, significantly (0.01 ≤ p ≤ 0.0001) decreased IMI and IV in both female and male mice, compared to vehicle treatment alone. n = 5–9. Values are mean ± SEM. *p ≤ 0.05; **p ≤ 0.01; ***p ≤ 0.001; ****p ≤ 0.0001 by two-way ANOVA with Bonferroni’s multiple comparisons test. CMG, cystometrogram.
Imatinib mesylate treatment via intravesical infusion significantly increases IMI and IV in an acute (4 h) CYP-induced cystitis mouse model. (A) Acute CYP-induced cystitis (200 mg/kg, 4 h, i.p.) experimental schedule for imatinib mesylate treatment via intravesical infusion (50 μM, 30 min, 0.5 mL). (B–E) Imatinib treatment via intravesical infusion significantly increases the IMI and IV in female (p ≤ 0.0001) and male (p ≤ 0.05) with acute (4 h) CYP-induced cystitis. Imatinib treatment via intravesical infusion significantly increases the IMI and IV in female (p ≤ 0.01) and male (p ≤ 0.05) control (no CYP) mice. Control (no CYP) and 4 h CYP treated mice were separate groups of mice, each tested before and after imatinib infusion. n = 6–10. Values are mean ± SEM. *p ≤ 0.05; **p ≤ 0.01; ****p ≤ 0.0001 by two-way repeated measures ANOVA with Šídák’s multiple comparisons test. CMG, cystometrogram.
Prevention Effects
Mice were pre-treated daily via oral gavage or direct intravesical infusion with imatinib mesylate, followed by induction of CYP-induced cystitis (Figure 1A). Female and male mice with acute (4 h) CYP-induced cystitis exhibited significantly (p ≤ 0.01) decreased IMI and IV compared to controls, as expected (Figures 1B–E, 3A,B). In female mice with acute (4 h) CYP-induced cystitis, imatinib (250 mg/kg, 5 days) administration via oral gavage significantly (p ≤ 0.001) increased IMI and IV compared to vehicle (water) treated mice (Figures 1B,D, 3C,D). However, this imatinib delivery method and treatment schedule did not affect IMI or IV in male mice with CYP-induced cystitis (Figures 1C,E). Imatinib pre-treatment significantly (p ≤ 0.01) increased bladder pressures (minimum, threshold, maximum) in male and female mice with acute CYP-induced cystitis, compared to controls (Table 1).
Representative bladder function cystometry recordings from female mice with acute CYP-induced cystitis, pre-treated with imatinib mesylate or vehicle via oral gavage. (A,B) Mice with 4 h CYP-induced cystitis (200 mg/kg, 4 h, i.p.) pre-treated with vehicle exhibited significantly decreased IMI (p ≤ 0.001) and IV (p ≤ 0.0001), compared to control mice. (C,D) Mice with 4 h CYP-induced cystitis pre-treated with imatinib (250 mg/kg, 5 days, 1X/day) exhibited significantly (p ≤ 0.001) increased IMI and IV, compared to mice with 4 h CYP-induced cystitis pre-treated with vehicle. Recordings are from separate cohorts of mice. n = 5–9. By two-way ANOVA with Bonferroni’s multiple comparisons test. CMG, cystometrogram; BP, bladder pressure.
Mean bladder pressures during conscious, open-outlet cystometry in control (no CYP), acute CYP (4 h, 200 mg/kg, i.p.), or chronic CYP (75 mg/kg every 72 h for 8 days, i.p.) male and female mice pre-treated with imatinib mesylate or vehicle via oral gavage.
Group
Threshold pressure
Minimum pressure
Maximum pressure
Female mice
Vehicle (No CYP)
12.09 ± 0.7
10.23 ± 0.7
27.04 ± 2.1
Vehicle + Acute (4 h) CYP
28.84 ± 2.9**
24.12 ± 2.9**
34.25 ± 3.0
Imatinib (No CYP)
27.35 ± 2.1**
18.9 ± 1.4
38.82 ± 4.0
Imatinib + Acute (4 h) CYP
39.34 ± 3.7+****
32.41 ± 3.0++****
50.83 ± 4.8**
Vehicle (No CYP)
21.71 ± 2.9
13.77 ± 1.1
34.06 ± 3.5
Vehicle + Chronic (8 d) CYP
33.5 ± 2.7+*
27.88 ± 2.8+**
44.87 ± 2.7
Imatinib (No CYP)
22.22 ± 1.5
16.45 ± 1.5
34.68 ± 2.0
Imatinib + Chronic (8 d) CYP
30.45 ± 2.7
26.04 ± 3.1**
42.77 ± 3.6
Male Mice
Vehicle (No CYP)
12.65 ± 0.5
11.82 ± 0.2
28.71 ± 1.3
Vehicle + Acute (4 h) CYP
17.26 ± 0.4++
15.53 ± 0.8
34.22 ± 1.4
Imatinib (No CYP)
26.23 ± 2.1****
20.58 ± 2.0**
38.86 ± 2.9*
Imatinib + Acute (4 h) CYP
24.22 ± 1.7#***
21.13 ± 1.6**
35.37 ± 2.1
n = 5–9. Values are means ± SEM by two-way ANOVA with Bonferroni’s multiple comparisons test.
*p ≤ 0.05; **p ≤ 0.01; ***p ≤ 0.001; ****p ≤ 0.0001 when compared to vehicle control, +p ≤ 0.05; ++p ≤ 0.01; ++++p ≤ 0.0001 when compared to imatinib control, or #p ≤ 0.05; ##p ≤ 0.01; ####p ≤ 0.0001 when compared to vehicle + acute CYP.
The systemic administration of imatinib by gavage may have off-target effects not specifically due to PDGFRα inhibition at the level of the urinary bladder. Thus, we conducted a series of experiments to intravesically infuse imatinib to investigate bladder-specific effects of PDGFRα inhibition. Mice were pre-treated with imatinib (50 μM, 0.5 mL, 30 min) for 5 days and acute cystitis was induced via CYP on day 5. This treatment and dosing schedule resulted in mice exhibiting increased voiding frequency as documented in mice with only CYP-induced cystitis (4 h) (data not shown). We hypothesized that intravesical imatinib was unable to penetrate the intact urothelial barrier to access the LP. Thus, we performed a follow-up study in a separate cohort of mice that received intravesical protamine sulfate (PS) (10 mg/kg, 0.5 mL, 30 min) every other day, prior to imatinib infusions, to disrupt the urothelial lining (Stein et al., 1996). PS does not affect voiding frequency at this concentration (Chuang et al., 2003; Fraser et al., 2003; Klinger and Vizzard, 2008). Urinary bladder function resembled that in CYP-treated mice (without imatinib) but imatinib treatment did not significantly affect IMI or IV, despite PS treatment (data not shown).
Treatment Effects
We then evaluated potential treatment effects of direct intravesical infusion of imatinib in mice with acute CYP-induced cystitis. Mice were treated with imatinib via intrabladder infusion (50 μM, 0.5 mL, 30 min) after induction of acute (4 h) CYP cystitis (Figure 2A). Bladder function was recorded before and after imatinib infusion. Acute CYP treatment significantly (p ≤ 0.01) reduced IMI and IV in female mice (Figures 2B,D). Imatinib treatment significantly increased IMI and IV in female (1.7-fold) (p ≤ 0.0001; Figures 2B,D, 4A–D) and male (1.6-fold) (p ≤ 0.05; Figures 2C,E) mice with acute CYP-induced cystitis. Imatinib treatment significantly (p ≤ 0.05) reduced minimum bladder pressure in female mice with acute CYP-induced cystitis but did not affect bladder pressures in male mice (Table 2). Bladder function changes in mice with imatinib infusion were observed within 30–50 min. Most mice (n = 16/19, 84%) exhibited changes in bladder function following imatinib infusion that persisted until the end of the recording session (i.e., 30–60 min).
Representative bladder function cystometry recordings from a female mouse with acute CYP-induced cystitis, before and after imatinib mesylate treatment via intravesical infusion. (A,B) Before imatinib treatment via intravesical infusion, mice with acute CYP-induced cystitis (200 mg/kg, 4 h, i.p.) exhibited decreased IMI and IV. (C,D) After imatinib treatment via intravesical infusion (50 μM, 30 min, 0.5 ml), mice with 4 h CYP-induced cystitis exhibited significantly (p ≤ 0.0001) increased IMI and IV. Recordings displayed are from the same mouse, before and after imatinib treatment. Mice with 4 h CYP-induced cystitis in these experiments acted as their own controls. n = 6–10. By two-way repeated measures ANOVA with Šídák’s multiple comparisons test. CMG, cystometrogram; BP, bladder pressure.
Mean bladder pressures during conscious, open-outlet cystometry in control (no CYP), acute CYP (4 h or 24 h, 200 mg/kg, i.p.), or chronic CYP (75 mg/kg every 72 h for 8 days, i.p.) male and female mice treated with imatinib mesylate or vehicle (saline) via intravesical bladder infusion.
Group
Threshold pressure
Minimum pressure
Maximum pressure
Female mice
Control (No CYP) Pre-Imatinib
26.3 ± 1.5
17.9 ± 1.9
33.8 ± 2.4
Post-Imatinib
26.5 ± 1.8
15.8 ± 1.4
32.8 ± 1.5
Acute CYP (4 h) Pre-Imatinib
28.9 ± 2.4
17.4 ± 1.7
39.4 ± 2.8
Post-Imatinib
27.0 ± 2.8
13.7 ± 0.8*
38.1 ± 2.8
Acute CYP (4 h) Pre-Imatinib Infusion #1
28.0 ± 3.1
18.1 ± 3.2
38.1 ± 2.8
Post-Imatinib Infusion #1
26.5 ± 3.4
16.5 ± 4.1
35.8 ± 3.4
24 h CYP Pre-Imatinib Infusion #2
29.1 ± 3.4
15.3 ± 2.2
29.1 ± 3.4
Post-Imatinib Infusion #2
29.3 ± 2.7
16.9 ± 2.1
29.3 ± 2.7
Chronic CYP (8 day) Pre-Imatinib
26.6 ± 2.6
16.0 ± 1.4
37.7 ± 2.3
Post-Imatinib
24.6 ± 2.2
15.6 ± 1.7
38.6 ± 2.4
Male Mice
Control (No CYP) Pre-Imatinib
27.1 ± 1.4
18.7 ± 1.9
39.7 ± 2.4
Post-Imatinib
24.0 ± 1.6
16.4 ± 1.1
37.1 ± 1.7
Acute CYP (4 h) Pre-Imatinib
28.9 ± 4.2
24.2 ± 4.4
42.6 ± 4.3
Post-Imatinib
32.0 ± 6.6
25.6 ± 6.8
46.3 ± 6.8
n = 5–10. Values are means ± SEM by Student’s paired t-test (chronic CYP with imatinib infusion experiment) or repeated measures, two-way ANOVA with Bonferroni’s (4 h/24 h CYP with imatinib infusion experiment) or Šídák’s (female and male acute CYP with imatinib infusion experiment) multiple comparisons test. *p ≤ 0.05 when compared to 4 h CYP, pre-imatinib infusion.
Imatinib Is Not Effective in Preventing or Treating Intermediate (48 h) or Chronic (8 Day) Cyclophosphamide-Induced Cystitis
We investigated the effects of PDGFRα blockade with imatinib in mice with intermediate (48 h) and chronic (8 day) CYP-induced cystitis using prevention (i.e., imatinib via oral gavage before CYP treatment) and treatment (i.e., CYP treatment followed by intrabladder infusion of imatinib) methods (Figures 5A, 6A and Supplementary Figure 3).
Imatinib mesylate pre-treatment via gavage does not significantly affect bladder function in mice with chronic (8 day) CYP-induced cystitis. (A) Chronic CYP-induced cystitis (75 mg/kg, every 72 h for 8 days) experimental schedule for imatinib mesylate pre-treatment via oral gavage (250 mg/kg, 1X/day). (B,C) Imatinib pre-treatment via gavage did not significantly affect IMI or IV in female mice with chronic CYP-induced cystitis. n = 7–9. Values are mean ± SEM by two-way ANOVA with Bonferroni’s multiple comparisons test. CMG, cystometrogram.
Imatinib mesylate treatment via intravesical infusion does not significantly affect bladder function in mice with chronic (8 day) CYP-induced cystitis. (A) Chronic CYP-induced cystitis (75 mg/kg, every 72 h for 8 days) experimental schedule for imatinib mesylate treatment via intravesical bladder infusion (50 μM, 30 min, 0.5 mL). (B,C) Imatinib treatment via intravesical bladder infusion did not significantly affect IMI or IV in chronic CYP-induced cystitis, female mice. n = 7–9. Values are mean ± SEM by Student’s paired t-test. CMG, cystometrogram.
Prevention
Before CYP treatment, mice were pre-treated daily with imatinib for 5 days. CYP treatment began on the 5th day for intermediate and chronic schedules. Intermediate CYP treatment consisted of a single CYP injection (200 mg/kg, i.p.) followed by bladder function testing at 48 h (intermediate) after injection. For the chronic cystitis model, mice received 3 CYP injections every 72 h (75 mg/kg, i.p.) followed by bladder function testing on the last day. Daily imatinib administration continued throughout the CYP treatment period for a total of 7 or 12 total days for the intermediate or chronic CYP schedules, respectively. Mice with chronic (75 mg/kg, i.p. every 72 h, 8 days) CYP-induced cystitis exhibited significantly (p ≤ 0.05) decreased IMI and IV compared to controls (Figures 5B,C). Mice pre-treated with imatinib (250 mg/kg, 12 total days) by gavage with chronic CYP treatment, did not exhibit significant differences in IMI or IV compared to chronic CYP groups pre-treated with vehicle (Figures 5B,C). Imatinib pre-treatment significantly (p ≤ 0.01) increased minimum pressure in chronic CYP-induced cystitis female mice, compared to vehicle controls (Table 1). We additionally assessed the effectiveness of imatinib at an intermediate CYP-induced cystitis time point (200 mg/kg, i.p., 48 h) with imatinib pre-treatment (gavage, 250 mg/kg, 7 total days) and found no significant differences in IMI or IV compared to vehicle treated groups or controls (Supplementary Figure 3).
Treatment
Mice were treated by intravesical infusion with imatinib (50 μM, 0.5 mL, 30 min) on the last day of the chronic CYP protocol (Figure 6A; 75 mg/kg, i.p. every 72 h, 8 days). Bladder function was recorded before and after the imatinib intravesical infusion in the same mice. Mice with chronic CYP-induced cystitis treated with imatinib via intrabladder infusion did not exhibit significant differences in bladder function compared to pretreatment function (Figures 6B,C and Table 2).
Use of imatinib mesylate as a prevention or treatment for bladder dysfunction with CYP-induced cystitis was ineffective in intermediate (48 h) or chronic (8 day) CYP treatment protocols. Due to the absence of effect(s) in female mice, studies were not repeated with male cohorts.
Oral Gavage of Imatinib Increases Voiding Frequency and Decreases Bladder Capacity in Control (No Cyclophosphamide) Mice
In prevention studies with imatinib pre-treatment, control (no CYP) groups were necessary and allowed us to assess the effect of PDGFRα inhibition on bladder function before CYP treatment. Control mice were treated with imatinib or vehicle throughout the experimental period (Figures 1A, 5A) and did not receive CYP injections. Female and male control (no CYP) mice treated with imatinib, via gavage, for the acute 5-day schedule, exhibited increased voiding frequency (decreased IMI and IV) (p ≤ 0.01), compared to vehicle treated control (no CYP) mice (Figures 1B–E). In female mice, decreases in IMI and IV were more dramatic in mice with acute CYP-induced cystitis treated with vehicle compared to the imatinib treated control (5 day) group (Figures 1B,D). However, in male mice, the imatinib treated control group (5 day) and 4 h CYP treatment with vehicle groups were not significantly different (Figures 1C,E). Imatinib significantly (p ≤ 0.01) increased bladder pressure for both female (threshold) and male (threshold and minimum) control mice (Table 1). Imatinib treatment in control mice (no CYP) did not significantly affect bladder function with the intermediate (8 day) (Supplementary Figure 3) or chronic (12 day) schedules (Figures 5B,C and Table 1).
Intrabladder Infusion of Imatinib Decreases Voiding Frequency and Increases Bladder Capacity in Male and Female Control (No Cyclophosphamide) Mice
Imatinib treatment, via intrabladder infusion, significantly decreased voiding frequency (increased IMI and IV) in female (p ≤ 0.01) (1.5-fold) and male (p ≤ 0.05) (1.4-fold) control (no CYP) mice but did not affect bladder pressures in either sex (Figures 2B–E and Table 2).
Multiple Treatments With Intrabladder Infusion of Imatinib May Further Improve Bladder Function With Acute (4 h) Cyclophosphamide-Induced Cystitis in Female Mice
We evaluated if an additional treatment with imatinib mesylate would result in a greater improvement in bladder function in the acute CYP-induced cystitis mouse model beyond what was observed with a single intrabladder infusion. In this experiment, mice received imatinib treatment (50 μM, 0.5 mL, 30 min) via intrabladder infusion 4 and 24 h after inducing acute (4 h) cystitis with CYP. Bladder function was recorded before and after imatinib treatment, both 4 and 24 h after CYP administration (Figure 7A). IMI and IV significantly increased (p ≤ 0.01) after the first dose of imatinib treatment with acute (4 h) CYP treatment (Figures 7B,C). Twenty-four hours later, before the second dose of imatinib, significant (p ≤ 0.01) changes in bladder function (e.g., increased IMI and IV) persisted. The second dose of imatinib, 24 h after CYP treatment significantly (p ≤ 0.05) increased IMI and IV compared to acute (4 h) CYP-induced cystitis before (p ≤ 0.001) and after the effects of a single dose of imatinib (p ≤ 0.01; Figures 7B,C). Imatinib treatment did not affect bladder pressures at 4 or 24 h (Table 2). These results suggest that multiple doses of imatinib may improve bladder function outcomes with acute (4 h) CYP-induced cystitis.
Two intravesical infusions with imatinib mesylate significantly increases IMI and IV in female mice with acute (4 h) CYP-induced cystitis. (A) Acute CYP-induced cystitis (200 mg/kg, 4 h, i.p.) experimental schedule for two-dose imatinib mesylate treatment via intravesical bladder infusion (50 μM, 30 min, 0.5 mL). Acute cystitis is induced on the third day. Bladder function with cystometrogram (CMG) is recorded 4 h after the CYP injection, before and after an intravesical bladder infusion of imatinib mesylate, and again, 24 h after the CYP injection on day 4, before and after a second imatinib mesylate intravesical bladder infusion. (B,C) Imatinib mesylate treatment significantly (p ≤ 0.01) increased the IMI and IV in female mice with acute CYP-induced cystitis at 4 and 24 h (p ≤ 0.001) following CYP. n = 4. Values are mean ± SEM. *p ≤ 0.05; **p ≤ 0.01; ***p ≤ 0.001; by two-way repeated measures ANOVA with Bonferroni’s multiple comparisons test. CMG, cystometrogram.
Oral Gavage or Transurethral Infusion of Imatinib Does Not Affect Pelvic Somatic Sensitivity in Female Mice With Acute (4 h) Cyclophosphamide-Induced Cystitis
Acute CYP administration significantly (p ≤ 0.05) increased pelvic somatic sensitivity compared to control (no CYP) (Supplementary Figures 1, 2). In controls (no CYP), imatinib delivery via gavage (prevention protocol) increased pelvic sensitivity (p ≤ 0.05) but no effect was observed with transurethral infusion of imatinib (treatment protocol) (Supplementary Figures 1, 2). In mice with acute CYP-induced cystitis, imatinib treatment (transurethral intrabladder infusion, 50 μM, 0.5 mL, 30 min) or prevention (oral gavage, 250 mg/kg, 5 days) did not affect pelvic somatic sensitivity (Supplementary Figures 1, 2). We additionally scored behaviors in female mice with acute CYP-induced cystitis following transurethral infusion (50 μM, 0.5 mL, 30 min) of imatinib or vehicle. Total licking behaviors were significantly (p ≤ 0.05) increased in mice with 4 h CYP-induced cystitis. However, imatinib treatment did not significantly affect either total time moving or total licking behaviors in control mice or in mice with 4 h CYP-induced cystitis (Supplementary Figure 2).
Discussion
Our studies demonstrate different effects of imatinib treatment depending on its use in control (no CYP), CYP-treated or mice with varying durations of CYP-treatment. Our studies expand upon previous reports investigating the effects of imatinib in the micturition system in a variety of bladder dysfunction models, including: CYP-induced cystitis (Sancho et al., 2017; Liu et al., 2018), radiation-induced cystitis (Giglio et al., 2018); spinal cord injury (SCI)-induced overactive bladder (Abrams et al., 2012; Deng et al., 2013; Kjell et al., 2015), and bladder outlet obstruction (Kim et al., 2011; Preis et al., 2015). Although various in vivo and ex vivo approaches have been used to determine effects of imatinib on rat and guinea pig bladder function (Kubota et al., 2004, 2006; Biers et al., 2006; Kim et al., 2011; Abrams et al., 2012; Deng et al., 2013; Gevaert et al., 2014a; Kjell et al., 2015; Sancho et al., 2017; Giglio et al., 2018; Liu et al., 2018), we believe these studies are the first to use conscious, unrestrained cystometry to assess the effects of imatinib mesylate on urinary bladder function in mice with CYP-induced cystitis. Our results suggest imatinib prevention and treatment improve LUT storage outcomes in female mice with acute (4 h) CYP-induced cystitis but not chronic CYP-induced cystitis. Interestingly, our prevention (gavage) studies in control mice (no CYP) also demonstrate that imatinib treatment can increase voiding frequency suggesting that imatinib and PDGFRα+ interstitial cells may contribute to the development and maintenance of bladder dysfunction (e.g., increased voiding frequency). Although cystometry results demonstrate that intravesical or oral imatinib can improve urinary bladder function in acute (4 h) CYP cystitis, imatinib does not affect mechanical sensitivity of the pelvic region in these mice. The absence of effect of imatinib on mechanical sensitivity may suggest that imatinib will not effectively treat pain symptoms in IC/BPS patients but could be useful for OAB patients. Ultimately, our studies suggest imatinib mesylate given systemically (gavage) or intravesically as a potential therapeutic for LUT storage symptoms in IC/BPS and/or OAB. Imatinib prevention (i.e., gavage, 250 mg/kg, 1X/day, 5 days) increased IV and IMI in female, but not male, mice with acute CYP-induced cystitis. Although imatinib does inhibit the tyrosine kinase receptor PDGFRα, like the majority of other PDGFRα inhibitors, it is not specific (Roskoski, 2018). Imatinib additionally inhibits PDGFRβ, c-KIT and BCR-ABL (Buchdunger et al., 2000; Capdeville et al., 2002). With systemic administration of imatinib, we cannot exclude the possibility that improvements in bladder outcomes were due to blockade of PDGFRα and other receptors throughout the body. Although we are unable to achieve specific PDGFRα inhibition with imatinib given systemically or intravesically, we used intravesical delivery to target the site of action of imatinib to the urinary bladder.
For the intravesical imatinib administration experiments, we initially conducted a preventative design with daily imatinib bladder infusions prior to induction of acute (4 h) CYP-induced cystitis on the last experimental day. However, imatinib prevention via intravesical infusion did not affect LUT outcomes in acute CYP-induced cystitis mice. We next evaluated intravesical treatment studies to examine the effect of imatinib on bladder function after inducing acute CYP cystitis. Intravesical imatinib treatment significantly improved LUT function in female and male mice with acute CYP-induced cystitis. Imatinib prevention and treatment had similar magnitude of effect in increasing IMI and IV in CYP-treated mice. Despite improvements in LUT outcomes, imatinib prevention was associated with increases in bladder pressures, while intravesical infusion of imatinib reduced or had no effect on bladder pressures. If these data can eventually be translated to humans with IC/BPS, the magnitude of effect with route of administration, the ease and convenience of administration, as well as off-target effects will need to be addressed.
Surprisingly, imatinib prevention in control (no CYP) mice increased voiding frequency compared to vehicle treated controls. However, the increased voiding frequency in female controls was less than that observed in female mice with acute CYP-induced cystitis. Increased voiding frequency in control mice treated with systemic (gavage) imatinib treatment may be, in part, due to PDGFRα inhibition of detrusor interstitial cells. Our studies did not directly assess the contribution of detrusor interstitial cells to the increased voiding frequency observed in control mice pre-treated with imatinib. However, studies show that PDGFRα+ detrusor interstitial cells exhibit inhibitory influence over smooth muscle cells (SMCs) to regulate contractions during bladder filling, likely via SK3 channels (Parajuli et al., 2012; Anderson et al., 2013; Lee et al., 2013, 2017; Koh et al., 2018). SK3 agonists enhance outward currents in PDGFRα+ detrusor interstitial cells and reduce detrusor contractions, whereas antagonists block outward currents and increase contractions (Lee et al., 2013, 2014, 2017). Thus, the increased voiding frequency in control mice pre-treated with imatinib may be due imatinib inhibition of PDGFRα+ detrusor interstitial cells, resulting in the release of interstitial cell inhibitory control over detrusor SMCs to produce an increase in voiding frequency. Interestingly, similar results were not observed when control mice were treated with intravesical imatinib administration. Imatinib treatment (50 μM, 0.5 mL, 30 min) increased bladder capacity and reduced voiding frequency in control (non-CYP) female and male mice. These results may, in part, be due to imatinib blockade of PDGFRα expressed by LP interstitial cells. Although we cannot discount an effect of imatinib on detrusor interstitial cells with the treatment design, intravesical infusion of imatinib would likely first act on LP interstitial cells based upon their proximity to the bladder lumen infusion site. As suggested, LP interstitial cells may act as sensory intermediaries to the detrusor and/or afferent nerves (Wiseman et al., 2003; Gray et al., 2013; Heppner et al., 2017; Sancho et al., 2017; Koh et al., 2018). It may be possible that blockade of LP interstitial cells disrupts communication with bladder afferent nerves, resulting in dysregulated sensory signaling, and in turn, increased IMI and IV. However, these ideas should be further researched as our studies do not directly assess the contribution of specific interstitial cells to LUT function in the control or inflamed bladder.
Imatinib was effective at improving bladder function in mice with acute (4 h) CYP-induced cystitis for both the prevention (systemic gavage) and treatment (intravesical) designs, yet imatinib did not affect bladder function in mice with intermediate (48 h; gavage) or chronic (8 day; gavage and intravesical) CYP-induced cystitis. Many significant changes occur throughout the micturition system (e.g., inflammatory mediator expression, peripheral and central sensitization) which contribute to symptom progression and exacerbation with acute, intermediate, and chronic CYP-induced cystitis (Malley and Vizzard, 2002; Arms et al., 2013; Gonzalez et al., 2014; Guo et al., 2018). These nuances increase the complexity of treating urinary bladder dysfunction and may suggest that some treatments may only be effective at certain timepoints. In addition, a combination of therapeutics and treatments may be beneficial when treating the progression of acute to chronic urinary bladder inflammation. Future studies in mice with acute, intermediate, and chronic CYP-induced cystitis that evaluate bladder function effects when imatinib is combined with other treatments (e.g., neuropeptide, cytokine, and chemokine receptor antagonists) should be considered (Arms et al., 2010, 2013; Gonzalez et al., 2013, 2014, 2016; Merrill and Vizzard, 2014; Girard et al., 2016, 2019, 2021; Guo et al., 2018; Tooke et al., 2019). In addition, our results assessing imatinib treatment at 4 and 24 h after CYP treatment, suggest repeated use of imatinib may offer additional improvements in bladder function in acute CYP-induced cystitis and extend symptom relief. Future studies should determine the duration of symptom relief period and if bladder dysfunction can be fully reversed with multiple imatinib treatments.
In addition to LUT symptoms, IC/BPS patients report unpleasant pelvic sensations (e.g., pain, pressure, or discomfort) (Hanno et al., 2015). Thus, we also examined mechanical sensitivity of the abdominal/pelvic region in cystitis with imatinib administration. Our results suggest that imatinib prevention and treatment improves functional bladder outcomes (i.e., IV, IMI), but may not affect pelvic sensation. If clinically translatable to human patients, these results may suggest that imatinib will not effectively treat the pelvic pain component of IC/BPS and that imatinib may be a more suitable treatment for OAB. The therapeutic potential of imatinib for OAB warrants further research as our studies did not assess the effect of imatinib on LUT function in an OAB model. The differential effects on bladder function and pelvic sensitivity were surprising to us because we have evaluated multiple pharmacological agents (Arms et al., 2013; Girard et al., 2016, 2019, 2021; Guo et al., 2018) in rodents with CYP-induced cystitis and have never demonstrated improvements in bladder function without reductions in mechanical sensitivity. However, these results may provide information about the role of LP interstitial cells in the urinary bladder and their potential communication with bladder nerve fibers. Additional studies are planned to evaluate the effect of imatinib on pelvic sensitivity in CYP-induced cystitis using visceromotor responses.
Overexpression and enhanced activity of PDGFs/Rs may indicate pathological processes (e.g., cancerous, fibrotic, inflammatory, and vascular conditions) (Heldin and Westermark, 1999; Andrae et al., 2008). In urinary bladder dysfunction, PDGFs/Rs may contribute to underlying mechanisms that induce or sustain inflammation. Although the PDGFRα LP interstitial cells likely serve important roles in the normal functioning bladder (e.g., communicating bladder fullness to afferent nerves and regulating detrusor muscle contractions) (Heppner et al., 2017), they may also contribute to pathological states by altering the inflammatory milieu of the urinary bladder. In mice with incomplete SCI treated with imatinib mesylate, serum levels of monocyte chemoattractant protein-1, macrophage inflammatory protein (MIP)-3α, and keratinocyte chemoattractant/growth-regulated oncogene (interleukin 8) were significantly increased (Kjell et al., 2015) and yet mice exhibited improvements in bladder function and hindlimb locomotion. Future studies that address mechanisms underlying bladder functional recovery in the presence of, or possibly supported by, an inflammatory activation by imatinib are needed. We are currently examining inflammatory activation in the LUT by imatinib in mice with and without CYP-induced cystitis.
In conclusion, our results suggest imatinib administration improves bladder function (e.g., IMI and IV) in mice with acute CYP-induced cystitis by a prevention (gavage; females) and treatment (intravesical infusion; females and males) experimental design. Bladder function improvements in the acute CYP-induced cystitis model with imatinib administration may be due, at least in part, to inhibition of the PDGFRα+ LP interstitial cells. Furthermore, these studies demonstrated changes in voiding frequency with imatinib administration supporting the suggestion that these cells function as a sensory intermediary role in control as well as the inflamed urinary bladder. The absence of effect of imatinib administration by the prevention (gavage) and treatment (intravesical infusion) on mechanical sensitivity in mice with acute CYP-induced cystitis may suggest that imatinib mesylate may be more appropriate as a treatment for OAB where patients present with urinary storage symptoms (e.g., increased urgency, frequency, nocturia) without pelvic pain, pressure or discomfort reported by IC/BPS patients (Macdiarmid and Sand, 2007). These studies provide some insight into a novel cell population in the urinary bladder that may be an effective target in managing cystitis-induced bladder dysfunction.
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.
Ethics Statement
The animal study was reviewed and approved by the University of Vermont Institutional Animal Care and Use Committee.
Author Contributions
MP, BG, and MV conceived and designed the research, interpreted the results of experiments, and edited and revised the manuscript. MP, SC, and BG performed the experiments. MP analyzed the data, prepared the figures, and drafted the manuscript. MP, BG, SC, and MV approved the final version of manuscript. All authors contributed to the article and approved the submitted version.
Author Disclaimer
The National Institutes of Health had no role in the experiments described, including the design, data collection, and analysis of studies performed in the Vizzard laboratory, decision to publish, or preparation of the manuscript. The contents are solely the responsibility of the authors and do not necessarily represent the official views of the National Institutes of Health.
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.
Funding
This work was funded by National Institute of Diabetes and Digestive and Kidney Diseases Grants 5R01DK120108 and 1R01DK124580 to MV.
We gratefully acknowledge the additional support provided by the Cell and Molecular Core in the Department of Neurological Sciences at the Larner College of Medicine and Vermont Integrative Genomics Resource. We thank Lily Wilkinson and Celia Mcclintock for their tremendous assistance with animal care, handling and observation.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnsys.2022.867875/full#supplementary-material
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(2012). Glycine transporter type 2 (GlyT2) inhibitor ameliorates bladder overactivity and nociceptive behavior in rats.Eur Urol.62704–712. 10.1016/j.eururo.2012.01.04422341128AbbreviationsIC/BPS
interstitial cystitis/bladder pain syndrome
OAB
overactive bladder
SCI
spinal cord injury
LUT
lower urinary tract
WT
wild type
PDGFRα
platelet-derived growth factor receptor alpha
PDGF
platelet-derived growth factors
c-KIT
tyrosine-protein kinase KIT
CML
chronic myeloid leukemia
CYP
cyclophosphamide
PS
protamine sulfate
i.p.
intraperitoneal
s.c.
subcutaneous
LP
lamina propria
DRG
dorsal root ganglia
SMC
smooth muscle cell
ATP
adenosine triphosphate
ACh
acetylcholine
CCL2
C-C motif chemokine ligand 2
MAPK/ERK
mitogen-activated protein kinase/extracellular signal-related kinase