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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Neural Circuits</journal-id>
<journal-title>Frontiers in Neural Circuits</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Neural Circuits</abbrev-journal-title>
<issn pub-type="epub">1662-5110</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fncir.2022.1093711</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Neuroscience</subject>
<subj-group>
<subject>Editorial</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Editorial: The medial septum as a smart clock: New aspects of its function beyond pacemaking</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Hangya</surname> <given-names>Bal&#x000E1;zs</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/16568/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Varga</surname> <given-names>Viktor</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="corresp" rid="c002"><sup>&#x0002A;</sup></xref>
<uri xlink:href="http://loop.frontiersin.org/people/1012295/overview"/>
</contrib>
</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Lend&#x000FC;let Laboratory of Systems Neuroscience, Institute of Experimental Medicine</institution>, <addr-line>Budapest</addr-line>, <country>Hungary</country></aff>
<aff id="aff2"><sup>2</sup><institution>Subcortical Modulation Research Group, Institute of Experimental Medicine</institution>, <addr-line>Budapest</addr-line>, <country>Hungary</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited by: Erika Gyengesi, Western Sydney University, Australia</p></fn>
<corresp id="c001">&#x0002A;Correspondence: Bal&#x000E1;zs Hangya &#x02709; <email>hangya.balazs&#x00040;koki.hu</email></corresp>
<corresp id="c002">Viktor Varga &#x02709; <email>varga.viktor&#x00040;koki.mta.hu</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>13</day>
<month>01</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2022</year>
</pub-date>
<volume>16</volume>
<elocation-id>1093711</elocation-id>
<history>
<date date-type="received">
<day>09</day>
<month>11</month>
<year>2022</year>
</date>
<date date-type="accepted">
<day>30</day>
<month>12</month>
<year>2022</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2023 Hangya and Varga.</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Hangya and Varga</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/"><p>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.</p></license> </permissions>
<related-article id="RA1" related-article-type="commentary-article" xlink:href="https://www.frontiersin.org/research-topics/27654/the-medial-septum-as-a-smart-clock-new-aspects-of-its-function-beyond-pacemaking" ext-link-type="uri">Editorial on the Research Topic <article-title>The medial septum as a smart clock: New aspects of its function beyond pacemaking</article-title></related-article>
<kwd-group>
<kwd>oscillation</kwd>
<kwd>memory</kwd>
<kwd>motion</kwd>
<kwd>motivation</kwd>
<kwd>hippocampus</kwd>
<kwd>theta rhythm</kwd>
<kwd>neuromodulation</kwd>
<kwd>cholinergic</kwd>
</kwd-group>
<counts>
<fig-count count="0"/>
<table-count count="0"/>
<equation-count count="0"/>
<ref-count count="3"/>
<page-count count="3"/>
<word-count count="1441"/>
</counts>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="s1">
<title>Introduction</title>
<p>The medial septum (MS) has long been studied for its role in the generation of hippocampal theta oscillation, the dominant rhythm of the limbic system during information collecting behaviors and REM sleep (Buzs&#x000E1;ki, <xref ref-type="bibr" rid="B1">2002</xref>; Vertes and Kocsis, <xref ref-type="bibr" rid="B2">1997</xref>). Early lesion studies in rats as well as human patients with MS lesions also pointed to the septum&#x00027;s role in episodic memory formation (Yoder and Pang, <xref ref-type="bibr" rid="B3">2005</xref>). However, recent studies suggested key additional roles of the MS in motion control, reinforcement processing and social memory, sparking a renewed interest in septal studies. How the three major MS cell types, that is, cholinergic, GABAergic, and glutamatergic neurons segregate and multiplex these seemingly diverse functions is presently in intense research focus. These novel aspects also raise multiple possibilities of therapeutical interventions targeting the MS in neuropsychiatric diseases. This Research Topic revisits different angles of MS research and points to exciting future directions including potential therapeutical benefits.</p>
<sec>
<title>Motivated states and movement</title>
<p>Exploration of medial septum&#x00027;s involvement in motivated behaviors predates the discovery of its role in hippocampal oscillogenesis. However, following the report of rhythmic bursting medial septal neurons coupled to theta activity in the hippocampus, the main focus shifted to studying how medial septum controls memory-related physiological phenomena. The review by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fncir.2021.699798">Mocellin and Mikulovic</ext-link> attempts to redirect attention back to coordination of affective states and accompanying motor actions by the medial septum. They provide an integrated view of how the medial septal circuit in concert with connected regions supports the correlated functions of theta genesis and modulation of movement during motivated behaviors.</p>
</sec>
<sec>
<title>Cholinergic temporal dynamics and motion control</title>
<p>Glutamatergic MS neurons were shown to potently control locomotive behavior in mice; however, MS cholinergic and GABAergic neurons also show correlations with locomotion, indicating complex MS functions related to animal speed. In an original research article, <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fncir.2022.957441">Kopsick et al.</ext-link> show by using fiber photometry that MS cholinergic neurons&#x00027; activity correlates with the logarithm of movement speed, with fast enough dynamics to serve as a speed signal for the hippocampus. Importantly, this cholinergic speed signal was independent of visual inputs and also reflected the speed of neck movements when mice were stationary.</p>
</sec>
<sec>
<title>Memory functions, impairment, and treatment approaches</title>
<p>MS neurons process motion, reinforcement, memory and attentional information, prompting an update on how the MS participates in mnemonic processing. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fncir.2022.916499">Tsanov</ext-link> provides a systems model for the MS in memory processing that reflects these recent findings and discusses how this updated model may influence treatment strategies of neurodegenerative disorders. These potential interventions include targeting the dopaminergic system, deep brain stimulation in cholinergic areas, vagus nerve stimulation, as well as exercise-based and cognitive enhancement strategies.</p>
</sec>
<sec>
<title>The MS as a potential target in oscillopathies</title>
<p>As noted, the MS orchestrates hippocampal theta oscillations related to learning, memory, and spatial navigation, but also to anxiety and fear in the ventral hippocampus. Additionally, oscillatory control by the MS may go beyond the theta frequency band, and physiological rhythms affected by the MS are often disrupted in pathological conditions. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fncir.2021.701080">Takeuchi et al.</ext-link> review MS stimulation strategies that may alleviate the negative consequences of such &#x0201C;oscillopathies,&#x0201D; stressing the importance of stimulation timing at varying timescales as a key determinant of therapeutical success. Such strategies may eventually prove successful in a broad range of conditions from Alzheimer&#x00027;s disease to schizophrenia to anxiety to pain.</p>
</sec>
<sec>
<title>MS glutamatergric transmission, theta, and nociception</title>
<p>Network mechanisms whereby sensory inputs are transformed into the rhythmic output of the medial septum are still largely unknown. The original research by <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fncir.2021.663633">Ibrahim et al.</ext-link> investigated how intraseptal components of glutamatergic signaling modulates spontaneous and sensory-evoked theta oscillation. They reported a surprising decoupling of theta genesis and motor control in response to NMDA-receptor blockade. Further findings uncovered the antinociceptive effect of AMPA-receptor antagonism that links their paper to the growing number studies exploring the therapeutic potential of medial septum manipulation.</p>
</sec>
<sec>
<title>Consciousness and gamma oscillations</title>
<p><ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fncir.2022.895000">Leung and Ma</ext-link>&#x00027;s review places the medial septum in the intersection of gamma oscillations and consciousness. Information about medial septum&#x00027;s role in extra-theta rhythms is relatively scarce compared to the huge body of theta literature. Likewise, the medial septal control of conscious states, especially in the context of pathological alterations or artificially induced but clinically relevant brain states, is also an understudied field. This review gives a comprehensive survey of studies focusing on the correlated alteration of gamma oscillation and conscious states following seizures or anesthesia. The many cited reports are thought-provoking and by shedding light on our gaps of knowledge may motivate further translatable research of medial septal function.</p>
</sec>
<sec>
<title>Social memory</title>
<p>Recent landmark discoveries unraveled fundamental mechanisms of social memory formation. The medial septum is thought to be a key coordinator of the episodic memory circuit; thus, linking its already known functions with new findings about social learning is the key objective of <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fncir.2022.965172">Griguoli and Pimpinella</ext-link>&#x00027;s review. Many psychopathologies are accompanied by the severe disruption of social life. As thoroughly reviewed in this paper, the medial septum is a key hub not only for episodic but also for social memory formation, that may render it a potential therapeutic target for treating debilitating social psychological impairments.</p></sec></sec>
<sec id="s2">
<title>Summary</title>
<p>We live in exciting times. The methodological revolution of neuroscience research has uncovered countless novel findings and put old discoveries into new light. The medial septum has long been known as a key center for rhythm genesis. Despite decades of research, it remained an enigmatic region holding its secrets tight to its chest. Nonetheless, novel methods enabled cracking many unknown aspects of medial septal functions. Authors of this collection of papers highlighted many new discoveries and placed them into the context of what we already know about the medial septum. Furthermore, connecting basic discoveries with clinical findings raised the intriguing possibility that this region, through its many connections, is in an ideal position whereby lost coordination of activity can be restored. Thus, many new directions of medial septum research may emanate from both long-known facts and new findings, a large part described in this article collection.</p></sec>
<sec sec-type="author-contributions" id="s3">
<title>Author contributions</title>
<p>BH and VV wrote the editorial. All authors contributed to the article and approved the submitted version.</p></sec>
</body>
<back>
<sec sec-type="funding-information" id="s4">
<title>Funding</title>
<p>This work was supported by the NAP3.0 National Program of the Hungarian Academy of Sciences, NKFIH K135561, SPIRITS 2020 of Kyoto University, and the European Research Council Starting Grant no. 715043 to BH and NKFIH K132735 to VV.</p>
</sec>
<sec sec-type="COI-statement" id="conf1">
<title>Conflict of interest</title>
<p>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.</p>
</sec>
<sec sec-type="disclaimer" id="s5">
<title>Publisher&#x00027;s note</title>
<p>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.</p>
</sec>
<ref-list>
<title>References</title>
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</back>
</article>