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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Annals of Clinical and Experimental Neurology</journal-id><journal-title-group><journal-title xml:lang="en">Annals of Clinical and Experimental Neurology</journal-title><trans-title-group xml:lang="ru"><trans-title>Анналы клинической и экспериментальной неврологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2075-5473</issn><issn publication-format="electronic">2409-2533</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">578</article-id><article-id pub-id-type="doi">10.25692/ACEN.2019.1.6</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Original articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Оригинальные статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Unknown</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Integrative functions of the retrosplenial cortex in rats: anatomy, connectomics, and cellular electrophysiology</article-title><trans-title-group xml:lang="ru"><trans-title>Интегративные функции ретросплениальной коры: данные анатомии, коннектомики и клеточной электрофизиологии у крыс</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Mineeva</surname><given-names>Olga A.</given-names></name><name xml:lang="ru"><surname>Минеева</surname><given-names>Ольга Александровна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>o.mineyeva@gmail.com</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Bezryadnov</surname><given-names>Dmitrii V.</given-names></name><name xml:lang="ru"><surname>Безряднов</surname><given-names>Дмитрий Васильевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>o.mineyeva@gmail.com</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Chekhov</surname><given-names>Sergey A.</given-names></name><name xml:lang="ru"><surname>Чехов</surname><given-names>Сергей Александрович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>o.mineyeva@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Svarnik</surname><given-names>Оlga E.</given-names></name><name xml:lang="ru"><surname>Сварник</surname><given-names>Ольга Евгеньевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>o.mineyeva@gmail.com</email><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Anokhin</surname><given-names>Konstantin V.</given-names></name><name xml:lang="ru"><surname>Анохин</surname><given-names>Константин Владимирович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>o.mineyeva@gmail.com</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff4"/><xref ref-type="aff" rid="aff5"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">P.K. Anokhin Institute of Normal Physiology</institution></aff><aff><institution xml:lang="ru">ФГБНУ «Институт нормальной физиологии им. П.К. Анохина»</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Moscow Institute of Physics and Technology</institution></aff><aff><institution xml:lang="ru">ФГАОУ ВО "Московский физико-технический институт"</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Institute of Psychology of Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">ФГБУН «Институт психологии РАН»</institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en">National Research Center "Kurchatov Institute"</institution></aff><aff><institution xml:lang="ru">НИЦ "Курчатовский институт"</institution></aff></aff-alternatives><aff-alternatives id="aff5"><aff><institution xml:lang="en">M.V.Lomonosov Moscow State University</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВО "Московский государственный университет им. М.В.Ломоносова"</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2019-03-15" publication-format="electronic"><day>15</day><month>03</month><year>2019</year></pub-date><volume>13</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>47</fpage><lpage>54</lpage><history><date date-type="received" iso-8601-date="2019-03-17"><day>17</day><month>03</month><year>2019</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2019, Mineeva O.A., Bezryadnov D.V., Chekhov S.A., Svarnik О.E., Anokhin K.V.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2019, Mineeva O.A., Bezryadnov D.V., Chekhov S.A., Svarnik О.E., Anokhin K.V.</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="en">Mineeva O.A., Bezryadnov D.V., Chekhov S.A., Svarnik О.E., Anokhin K.V.</copyright-holder><copyright-holder xml:lang="ru">Mineeva O.A., Bezryadnov D.V., Chekhov S.A., Svarnik О.E., Anokhin K.V.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://annaly-nevrologii.com/pathID/article/view/578">https://annaly-nevrologii.com/pathID/article/view/578</self-uri><abstract xml:lang="en"><p>Current review is focused on the integrative functions of the retrosplenial cortex, which neurons are largely involved in spatial orientation and ambulation of an organism. We discuss anatomy and connectivity of the retrosplenial cortex in rats as well as the most recent findings concerning the behavioral specialization of its neurons observed using multielectrode recordings. Pattern of connections of the retrosplenial cortex allows to consider its interfacing role in linking brain regions specifically involved in spatial navigation and memory with areas of the associative cortex which lack spatial tuning. In this paper, we touch upon that unique anatomical connectivity which is reflected in the peculiar behavioral specialization of the retrosplenial cortex neurons. Complex spatial tuning of retrosplenial neurons is likely to represent the association of spatial and nonspatial information, and provides a clue to principles of information integration in the cerebral cortex.</p></abstract><trans-abstract xml:lang="ru"><p>Обзор посвящен интегративным функциям ретросплениальной коры, значительная доля нейронов которой обладает специализацией относительно положения и перемещения организма в пространстве. Разбираются современные данные об анатомии и связях ретросплениальной коры у крыс, а также о поведенческой специализации ее нейронов, обнаруженной с помощью мультиэлектродной регистрации клеточной активности. Паттерн связей ретросплениальной коры позволяет рассматривать ее как своеобразное связующее звено между областями мозга, специфически ответственными за пространственную навигацию и ассоциативными областями коры, не имеющими пространственной настройки. Этой уникальной особенностью анатомических связей ретросплениальной коры, по-видимому, объясняется присутствие в ней нейронов не только с пространственными, но и с более сложными поведенческими специализациями, которые рассмотрены в данном обзоре. Подобные сложно специализированные клетки вероятно должны ассоциировать комбинацию пространственной и непространственной информации, и раскрытие механизмов этой ассоциации может принести новое в понимание принципов организации когнитивных функций коры головного мозга.</p></trans-abstract><kwd-group xml:lang="en"><kwd>retrosplenial cortex</kwd><kwd>connectomics</kwd><kwd>neuronal activity</kwd><kwd>behavioral specialization of neurons</kwd><kwd>spatial memory</kwd><kwd>information integration</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>ретросплениальная кора</kwd><kwd>коннектомика</kwd><kwd>нейронная активность</kwd><kwd>поведенческая специализация нейронов</kwd><kwd>пространственная память</kwd><kwd>интеграция информации</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Alivisatos A.P. Andrews A.M., Boyden E.S. et al. Nanotools for neuroscience and brain activity mapping. ACS Publications 2013; 7: 1850–1866. DOI: 10.1021/nn4012847. PMID: 23514423.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Kim C.K., Adhikari A., Deisseroth K. Integration of optogenetics with complementary methodologies in systems neuroscience. Nat Rev Neurosci 2017; 18: 222–235. DOI: 10.1038/nrn.2017.15. PMID: 28303019.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Luo L., Callaway E.M., Svoboda K. Genetic dissection of neural circuits: a decade of progress. Neuron 2018; 98: 256–281. DOI: 10.1016/j.neuron.2018.05.004. PMID: 29772206.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Rivnay J., Wang H., Fenno L. et al. Next-generation probes, particles, and proteins for neural interfacing. Sci Adv 2017; 3: P. e1601649. DOI: 10.1126/sciadv.1601649. PMID: 28630894.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Kandel E. A place and a grid in the sun. Cell 2014; 159: 1239–1242. DOI: 10.1016/j.cell.2014.11.033. PMID: 25480286.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Langmoen I.A., Apuzzo M.L. The brain on itself: nobel laureates and the history of fundamental nervous system function. Neurosurgery 2007; 61: 891–908. DOI: 10.1227/01.neu.0000303185.49555.a9. PMID: 18091266.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Yuste R. From the neuron doctrine to neural networks. Nat Rev Neurosci 2015; 16: 487–497. DOI: 10.1038/nrn3962. PMID: 26152865.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>O’Keefe J., Dostrovsky J. The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat. Brain Res 1971; 34: 171–175. DOI: http://dx.doi.org/10.1016/0006-8993(71)90358-1. PMID: 5124915.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Taube J.S., Muller R.U., Ranck J.B. Head-direction cells recorded from the postsubiculum in freely moving rats. I. Description and quantitative analysis. J Neurosci 1990; 10: 420–435. DOI: https://doi.org/10.1523/JNEUROSCI.10-02-00420.1990. PMID: 2303851.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Hafting T., Fyhn M., Molden S. et al. Microstructure of a spatial map in the entorhinal cortex. Nature 2005; 436: 801–806. DOI: 10.1038/nature03721. PMID: 15965463.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Mitchell A.S., Czajkowski R., Zhang N. et al. Retrosplenial cortex and its role in spatial cognition. Brain Neurosci Adv 2018; 2: 2398212818757098. DOI: https://doi.org/10.1177/2398212818757098. PMID: 30221204.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Lavenex P., Amaral D.G. Hippocampal-neocortical interaction: a hierarchy of associativity. Hippocampus 2000; 10: 420–430. DOI: 10.1002/1098-1063(2000)10:4&lt;420::AID-HIPO8&gt;3.0.CO;2-5. PMID: 10985281.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Sewards T.V., Sewards M.A. Input and output stations of the entorhinal cortex: superficial vs. deep layers or lateral vs. medial divisions? Brain Res Brain Res Rev 2003; 42: 243–251. DOI: https://doi.org/10.1016/S0165-0173(03)00175-9. PMID: 12791442.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Harker K.T., Whishaw I.Q. Impaired place navigation in place and matching-to-place swimming pool tasks follows both retrosplenial cortex lesions and cingulum bundle lesions in rats. Hippocampus 2004; 14: 224–231. DOI: 10.1002/hipo.10159. PMID: 15098727.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Pothuizen H.H.J., Davies M., Aggleton J.P., Vann S.D. Effects of selective granular retrosplenial cortex lesions on spatial working memory in rats. Behav Brain Res 2010; 208: 566–575. DOI: 10.1016/j.bbr.2010.01.001. PMID: 20074589.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Vann S.D., Aggleton J.P. Extensive cytotoxic lesions of the rat retrosplenial cortex reveal consistent deficits on tasks that tax allocentric spatial memory. Behav Neurosci 2002; 116: 85–94. DOI: DOI: 10.1037//0735-7044.116.1.85. PMID: 11895186.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Cooper B.G., Mizumori S.J. Retrosplenial cortex inactivation selectively impairs navigation in darkness. Neuroreport 1999; 10: 625–630. PMID: 10208601.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Elduayen C., Save E. The retrosplenial cortex is necessary for path integration in the dark. Behav Brain Res 2014; 272: 303–307. DOI: 10.1016/j.bbr.2014.07.009. PMID: 25026093.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Miller A.M.P., Vedder L.C., Law L.M., Smith D.M. Cues, context, and long-term memory: the role of the retrosplenial cortex in spatial cognition. Front Hum Neurosci 2014; 8: 586. DOI: 10.3389/fnhum.2014.00586. PMID: 25140141.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Epstein R.A., Patai E.Z., Julian J.B., Spiers H.J. The cognitive map in humans: spatial navigation and beyond. Nat Neurosci 2017; 20: 1504–1513. DOI: 10.1038/nn.4656. PMID: 29073650.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Epstein R.A. Parahippocampal and retrosplenial contributions to human spatial navigation. Trends Cogn Sci 2008; 12: 388–396. DOI: 10.1016/j.tics.2008.07.004. PMID: 18760955.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>An Y., Varma V.R., Varma S. et al. Evidence for brain glucose dysregulation in Alzheimer’s disease. Alzheimers Dement. 2018; 14: 318–329. DOI: 10.1016/j.jalz.2017.09.011. PMID: 29055815.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Minoshima S., Giordani B., Berent S. et al. Metabolic reduction in the posterior cingulate cortex in very early Alzheimer’s disease. Ann Neurol 1997; 42: 85–94. DOI: 10.1002/ana.410420114. PMID: 9225689.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Nestor P.J., Fryer T.D., Ikeda M., Hodges J.R. Retrosplenial cortex (BA 29/30) hypometabolism in mild cognitive impairment (prodromal Alzheimer’s disease). Eur J Neurosci 2003; 18: 2663–2667. DOI: https://doi.org/10.1046/j.1460-9568.2003.02999.x. PMID: 14622168.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Pengas G., Hodges J.R., Watson P., Nestor P.J. Focal posterior cingulate atrophy in incipient Alzheimer’s disease. Neurobiol Aging 2010; 31: 25–33. DOI: 10.1016/j.neurobiolaging.2008.03.014. PMID: 18455838.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Pengas G., Williams G.B., Acosta-Cabronero J. et al. The relationship of topographical memory performance to regional neurodegeneration in Alzheimer’s disease. Front Aging Neurosci 2012; 4: 17. DOI: 10.3389/fnagi.2012.00017. PMID: 22783190.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Teipel S., Grothe M.J., Alzheimer’s Disease Neuroimaging Initiative. Does posterior cingulate hypometabolism result from disconnection or local pathology across preclinical and clinical stages of Alzheimer’s disease? Eur J Nucl Med Mol Imaging 2016; 43: 526–536. DOI: 10.1007/s00259-015-3222-3. PMID: 26555082.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Tu S., Wong S., Hodges J.R. et al. Lost in spatial translation — A novel tool to objectively assess spatial disorientation in Alzheimer’s disease and frontotemporal dementia. Cortex J Devoted Study Nerv Syst Behav 2015; 67: 83–94. DOI: 10.1016/j.cortex.2015.03.016. PMID: 25913063.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Villain N., Desgranges B., Viader F. et al. Relationships between hippocampal atrophy, white matter disruption, and gray matter hypometabolism in Alzheimer’s disease. J Neurosci 2008; 28: 6174–6181. DOI: 10.1523/JNEUROSCI.1392-08.2008. PMID: 18550759.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Yasuno F., Kazui H., Yamamoto A. et al. Resting-state synchrony between the retrosplenial cortex and anterior medial cortical structures relates to memory complaints in subjective cognitive impairment. Neurobiol Aging 2015; 36: 2145–2152. DOI: 10.1016/j.neurobiolaging.2015.03.006. PMID: 25862421.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Sugar J., Witter M.P., van Strien N.M., Cappaert N.L. The retrosplenial cortex: intrinsic connectivity and connections with the (para)hippocampal region in the rat. An interactive connectome. Front Neuroinformatics 2011; 5: 7. DOI: 10.3389/fninf.2011.00007. PMID: 21847380.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Paxinos G., Watson C. The Rat Brain in Stereotaxic Coordinates in Stereotaxic Coordinates. London: Elsevier, 2007.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Lau C., Ng L., Thompson C. et al. Exploration and visualization of gene expression with neuroanatomy in the adult mouse brain. BMC Bioinformatics 2008; 9: 153. DOI: 10.1186/1471-2105-9-153. PMID: 18366675.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Wyss J.M., Van Groen T., Sripanidkulchai K. Dendritic bundling in layer I of granular retrosplenial cortex: intracellular labeling and selectivity of innervation. J Comp Neurol 1990; 295: 33–42. DOI: 10.1002/cne.902950104. PMID: 2341634.</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Jones B.F., Groenewegen H.J., Witter M.P. Intrinsic connections of the cingulate cortex in the rat suggest the existence of multiple functionally segregated networks. Neuroscience 2005; 133: 193–207. DOI: 10.1016/j.neuroscience.2005.01.063. PMID: 15893643.</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Shibata H., Honda Y., Sasaki H., Naito J. Organization of intrinsic connections of the retrosplenial cortex in the rat. Anat Sci Int 2009; 84: 280–292. DOI: 10.1007/s12565-009-0035-0. PMID: 19322631.</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Van Groen T., Wyss J.M. Connections of the retrosplenial granular b cortex in the rat. J Comp Neurol 2003; 463: 249–263. DOI: 10.1002/cne.10757. PMID: 12820159.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Van Groen T., Wyss J.M. Connections of the retrosplenial granular a cortex in the rat. J Comp Neurol 1990; 300: 593–606. DOI: 10.1002/cne.903000412. PMID: 2273095.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Miyashita T., Rockland K.S. GABAergic projections from the hippocampus to the retrosplenial cortex in the rat. Eur J Neurosci 2007; 26: 1193–1204. DOI: 10.1111/j.1460-9568.2007.05745.x. PMID: 17767498.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Shibata H. Terminal distribution of projections from the retrosplenial area to the retrohippocampal region in the rat, as studied by anterograde transport of biotinylated dextran amine. Neurosci Res 1994; 20: 331–336. DOI: https://doi.org/10.1016/0168-0102(94)90055-8. PMID: 7532841.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Naber P.A., Witter M.P. Subicular efferents are organized mostly as parallel projections: a double-labeling, retrograde-tracing study in the rat. J Comp Neurol 1998; 393: 284–297. DOI: https://doi.org/10.1002/(SICI)1096-9861(19980413)393:3&lt;284::AID-CNE2&gt;3.0.CO;2-Y. PMID: 9548550.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Köhler C. Intrinsic projections of the retrohippocampal region in the rat brain. I. The subicular complex. J Comp Neurol 1985; 236: 504–522. DOI: 10.1002/cne.902360407. PMID: 3902916.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Vogt B.A., Miller M.W. Cortical connections between rat cingulate cortex and visual, motor, and postsubicular cortices. J Comp Neurol 1983; 216: 192–210. DOI: 10.1002/cne.902160207. PMID: 6863602.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Jun J.J., Steinmetz N.A., Siegle J.H. et al. Fully integrated silicon probes for high-density recording of neural activity. Nature 2017; 551: 232–236. DOI: 10.1038/nature24636. PMID: 29120427.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Beggs J.M., Moyer J.R. Jr, McGann J.P., Brown T.H. Prolonged synaptic integration in perirhinal cortical neurons. J Neurophysiol 2000; 83: 3294–3298. DOI: 10.1152/jn.2000.83.6.3294. PMID: 10848549.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>McGann J.P., Moyer J.R., Brown T.H. Predominance of late-spiking neurons in layer VI of rat perirhinal cortex. J Neurosci 2001; 21: 4969–4976. DOI: https://doi.org/10.1523/JNEUROSCI.21-14-04969.2001. PMID: 11438572.</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Kurotani T., Miyashita T., Wintzer M. et al. Pyramidal neurons in the superficial layers of rat retrosplenial cortex exhibit a late-spiking firing property. Brain Struct Funct 2013; 218: 239–254. DOI: 10.1007/s00429-012-0398-1. PMID: 22383041.</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Alexander A.S., Nitz D.A. Retrosplenial cortex maps the conjunction of internal and external spaces. Nat Neurosci 2015; 18: 1143–1151. DOI: 10.1038/nn.4058. PMID: 26147532.</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Chen L.L., Lin L.H., Green E.J. et al. Head-direction cells in the rat posterior cortex. I. Anatomical distribution and behavioral modulation. Exp Brain Res 1994; 101: 8–23. DOI: https://doi.org/10.1007/BF00243212. PMID: 7843305.</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Chen L.L., Lin L.H., Barnes C.A., McNaughton B.L. Head-direction cells in the rat posterior cortex. II. Contributions of visual and ideothetic information to the directional firing. Exp Brain Res 1994; 101: 24–34. DOI: 10.1007/BF00243213. PMID: 7843299.</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Cho J., Sharp P.E. Head direction, place, and movement correlates for cells in the rat retrosplenial cortex. Behav Neurosci 2001; 115: 3–25. PMID: 11256450.</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Jacob P.-Y., Casali G., Spieser L. et al. An independent, landmark-dominated head-direction signal in dysgranular retrosplenial cortex. Nat Neurosci 2017; 20: 173–175. DOI: 10.1038/nn.4465. PMID: 27991898.</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Alexander A.S., Nitz D.A. Spatially periodic activation patterns of retrosplenial cortex encode route sub-spaces and distance traveled. Curr Biol 2017; 27: 1551–1560.e4. DOI: 10.1016/j.cub.2017.04.036. PMID: 28528904.</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Smith D.M., Barredo J., Mizumori S.J.Y. Complimentary roles of the hippocampus and retrosplenial cortex in behavioral context discrimination. Hippocampus 2012; 22: 1121–1133. DOI: 10.1002/hipo.20958. PMID: 21630374.</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Navratilova Z., Hoang L.T., Schwindel C.D. et al. Experience-dependent firing rate remapping generates directional selectivity in hippocampal place cells. Front Neural Circuits 2012; 6: 6. DOI: 10.3389/fncir.2012.00006. PMID: 22363267.</mixed-citation></ref></ref-list></back></article>
