[Emergent role of astrocytes in oxytocin-mediated modulatory control of neuronal circuits and brain functions].

Rôle émergent des astrocytes dans le contrôle des circuits neuronaux et des fonctions cérébrales modulés par l’ocytocine.

Journal

Biologie aujourd'hui
ISSN: 2105-0686
Titre abrégé: Biol Aujourdhui
Pays: France
ID NLM: 101544020

Informations de publication

Date de publication:
2022
Historique:
received: 22 09 2022
entrez: 6 2 2023
pubmed: 7 2 2023
medline: 9 2 2023
Statut: ppublish

Résumé

The neuropeptide oxytocin has been in the focus of scientists for decades due to its profound and pleiotropic effects on physiology, activity of neuronal circuits and behaviors. Until recently, it was believed that oxytocinergic action exclusively occurs through direct activation of neuronal oxytocin receptors. However, several studies demonstrated the existence and functional relevance of astroglial oxytocin receptors in various brain regions in the mouse and rat brain. Astrocytic signaling and activity are critical for many important physiological processes including metabolism, neurotransmitter clearance from the synaptic cleft and integrated brain functions. While it can be speculated that oxytocinergic action on astrocytes predominantly facilitates neuromodulation via the release of gliotransmitters, the precise role of astrocytic oxytocin receptors remains elusive. In this review, we discuss the latest studies on the interaction between the oxytocinergic system and astrocytes, and give details of underlying intracellular cascades. Rôle émergent des astrocytes dans le contrôle des circuits neuronaux et des fonctions cérébrales modulés par l’ocytocine. L’ocytocine est un neuropeptide au centre de l’attention des scientifiques depuis des décennies, en raison de ses effets puissants et pléiotropes tant sur le plan physiologique que sur l’activité des circuits neuronaux, modulant ainsi nos comportements. Jusqu’à une date récente, on pensait que l’action de l’ocytocine était induite exclusivement par l’activation directe de ses récepteurs neuronaux. Cependant, plusieurs études ont démontré l’existence et la pertinence fonctionnelle des récepteurs astrogliaux de l’ocytocine dans diverses régions du cerveau de la souris et du rat. La signalisation et l’activité astrocytaires sont essentielles à de nombreux processus physiologiques importants, notamment le métabolisme, l’élimination des neurotransmetteurs de la fente synaptique et les fonctions cérébrales intégrées. Bien que l’on puisse supposer que l’action de l’ocytocine sur les astrocytes facilite principalement la neuromodulation via la libération de gliotransmetteurs, le rôle précis des récepteurs astrocytaires de l’ocytocine reste difficile à cerner. Dans cette revue, nous discutons des dernières études sur l’interaction entre le système ocytocinergique et les astrocytes, et décrivons les cascades intracellulaires mises en jeu.

Autres résumés

Type: Publisher (fre)
Rôle émergent des astrocytes dans le contrôle des circuits neuronaux et des fonctions cérébrales modulés par l’ocytocine.

Identifiants

pubmed: 36744981
doi: 10.1051/jbio/2022022
pii: jbio220022
doi:

Substances chimiques

Oxytocin 50-56-6
Receptors, Oxytocin 0

Types de publication

Review English Abstract Journal Article

Langues

fre

Sous-ensembles de citation

IM

Pagination

155-165

Informations de copyright

© Société de Biologie, 2023.

Références

Alanazi, M.M., Havranek, T., Bakos, J., Cubeddu, L.X., Castejon, A.M. (2020). Cell proliferation and anti-oxidant effects of oxytocin and oxytocin receptors: role of extracellular signal-regulating kinase in astrocyte-like cells. Endocr Regul, 54, 172-182.
Althammer, F., Eliava, M., Grinevich, V. (2021). Central and peripheral release of oxytocin: Relevance of neuroendocrine and neurotransmitter actions for physiology and behavior. Handb Clin Neurol, 180, 25-44.
Althammer, F., Krause, E.G., de Kloet, A.D., Smith, J., Grinevich, V., Charlet, A., Stern, J.E. (2022a). Identification and three-dimensional reconstruction of oxytocin receptor expressing astrocytes in the rat and mouse brain. STAR Protoc, 3, 101160.
Althammer, F., Roy, R.K., Lefevre, A., Najjar, R.S., Schoenig, K., Bartsch, D., Eliava, M., Feresin, R., Hammock, E.A.D., Murphy, A.Z., Charlet, A., Grinevich, V., Stern, J.E. (2022b). Altered PVN-to-CA2 hippocampal oxytocin pathway and reduced number of oxytocin-receptor expressing astrocytes in heart failure rats. J Neuroendocrinol, 34, e13166.
Amato, S., Averna, M., Guidolin, D., Pedrazzi, M., Pelassa, S., Capraro, M., Passalacqua, M., Bozzo, M., Gatta, E., Anderlini, D., Maura, G., Agnati, L.F., Cervetto, C., Marcoli, M. (2022). Heterodimer of A2A and oxytocin receptors regulating glutamate release in adult striatal astrocytes. Int J Mol Sci, 23, 2326.
Anagnostou, E., Soorya, L., Brian, J., Dupuis, A., Mankad, D., Smile, S., Jacob, S. (2014). Intranasal oxytocin in the treatment of autism spectrum disorders: a review of literature and early safety and efficacy data in youth. Brain Res, 1580, 188-198.
Araque, A., Carmignoto, G., Haydon, P.G., Oliet, S.H., Robitaille, R., Volterra, A. (2014). Gliotransmitters travel in time and space. Neuron, 81, 728-739.
Augusto-Oliveira, M., Arrifano, G.P., Takeda, P.Y., Lopes-Araujo, A., Santos-Sacramento, L., Anthony, D.C., Verkhratsky, A., Crespo-Lopez, M.E. (2020). Astroglia-specific contributions to the regulation of synapses, cognition and behaviour. Neurosci Biobehav Rev, 118, 331-357.
Bakos, J., Srancikova, A., Havranek, T., Bacova, Z. (2018). Molecular mechanisms of oxytocin signaling at the synaptic connection. Neural Plast, 2018, 4864107.
Bazargani, N., Attwell, D. (2016). Astrocyte calcium signaling: the third wave. Nat Neurosci, 19, 182-189.
Brown, C.H., Bains, J.S., Ludwig, M., Stern, J.E. (2013). Physiological regulation of magnocellular neurosecretory cell activity: integration of intrinsic, local and afferent mechanisms. J Neuroendocrinol, 25, 678-710.
Brown, C.H., Ludwig, M., Tasker, J.G., Stern, J.E. (2020). Somato-dendritic vasopressin and oxytocin secretion in endocrine and autonomic regulation. J Neuroendocrinol, 32, e12856.
Buijs, R.M. (1983). Vasopressin and oxytocin – Their role in neurotransmission. Pharmacol Ther, 22, 127-141.
Busnelli, M., Chini, B. (2018). Molecular basis of oxytocin receptor signalling in the brain: What we know and what we need to know. Curr Top Behav Neurosci, 35, 3-29.
Busnelli, M., Sauliere, A., Manning, M., Bouvier, M., Gales, C., Chini, B. (2012). Functional selective oxytocin-derived agonists discriminate between individual G protein family subtypes. J Biol Chem, 287, 3617-3629.
Chatterjee, O., Patil, K., Sahu, A., Gopalakrishnan, L., Mol, P., Advani, J., Mukherjee, S., Christopher, R., Prasad, T.S. (2016). An overview of the oxytocin-oxytocin receptor signaling network. J Cell Commun Signal, 10, 355-360.
Coyle, J.T., Balu, D., Wolosker, H. (2020). D-Serine, the shape-shifting NMDA receptor co-agonist. Neurochem Res, 45, 1344-1353.
Dale, H.H. (1906). On some physiological actions of ergot. J Physiol, 34, 163-206.
Di Scala-Guénot, D., Strosser, M.T. (1992). Oxytocin receptors on cultured astroglial cells. Kinetic and pharmacological characterization of oxytocin-binding sites on intact hypothalamic and hippocampic cells from foetal rat brain. Biochem J, 284, 491-497.
Di Scala-Guénot, D., Mouginot, D., Strosser, M.T. (1994). Increase of intracellular calcium induced by oxytocin in hypothalamic cultured astrocytes. Glia, 11, 269-276.
Domes, G., Heinrichs, M., Kumbier, E., Grossmann, A., Hauenstein, K., Herpertz, S.C. (2013). Effects of intranasal oxytocin on the neural basis of face processing in autism spectrum disorder. Biol Psychiatry, 74, 164-171.
Eliava, M., Melchior, M., Knobloch-Bollmann, H.S., Wahis, J., da Silva Gouveia, M., Tang, Y., Ciobanu, A.C., Triana del Rio, R., Roth, L.C., Althammer, F., Chavant, V., Goumon, Y., Gruber, T., Petit-Demoulière, N., Busnelli, M., Chini, B., Tan, L.L., Mitre, M., Froemke, R.C., Chao, M.V., Giese, G., Sprengel, R., Kuner, R., Poisbeau, P., Seeburg, P.H., Stoop, R., Charlet, A., Grinevich, V. (2016). A new population of parvocellular oxytocin neurons controlling magnocellular neuron activity and inflammatory pain processing. Neuron, 89, 1291-1304.
Evrard, M.E., Strosser, M.T., Di Scala-Guénot, D. (1997). Pharmacological characterization of oxytocin-binding sites in rat spinal cord membranes: comparison with embryonic cultured spinal cord neurones and astrocytes. J Neuroendocrinol, 9, 553-560.
Fiacco, T.A., McCarthy, K.D. (2018). Multiple lines of evidence indicate that gliotransmission does not occur under physiological conditions. J Neurosci, 38, 3-13.
Foo, L.C., Allen, N.J., Bushong, E.A., Ventura, P.B., Chung, W.S., Zhou, L., Cahoy, J.D., Daneman, R., Zong, H., Ellisman, M.H., Barres, B.A. (2011). Development of a method for the purification and culture of rodent astrocytes. Neuron, 71, 799-811.
Ford, C.L., Young, L.J. (2022). Refining oxytocin therapy for autism: context is key. Nat Rev Neurol, 18, 67-68.
Frijling, J.L., (2017). Preventing PTSD with oxytocin: effects of oxytocin administration on fear neurocircuitry and PTSD symptom development in recently trauma-exposed individuals. Eur J Psychotraumatol, 8, 1302652.
Frijling, J.L., van Zuiden, M., Koch, S.B., Nawijn, L., Goslings, J.C., Luitse, J.S., Biesheuvel, T.H., Honig, A., Bakker, F.C., Denys, D., Veltman, D.J., Olff, M. (2014). Efficacy of oxytocin administration early after psychotrauma in preventing the development of PTSD: study protocol of a randomized controlled trial. BMC Psychiatry, 14, 92.
Froemke, R.C., Young, L.J. (2021). Oxytocin, neural plasticity, and social behavior. Annu Rev Neurosci, 44, 359-381.
Fuxe, K., Borroto-Escuela, D.O., Romero-Fernandez, W., Ciruela, F., Manger, P., Leo, G., Diaz-Cabiale, Z., Agnati, L.F. (2012). On the role of volume transmission and receptor-receptor interactions in social behaviour: focus on central catecholamine and oxytocin neurons. Brain Res, 1476, 119-131.
Gautvik, K.M., de Lecea, L., Gautvik, V.T., Danielson, P.E., Tranque, P., Dopazo, A., Bloom, F.E., Sutcliffe, J.G. (1996). Overview of the most prevalent hypothalamus-specific mRNAs, as identified by directional tag PCR subtraction. Proc Natl Acad Sci USA, 93, 8733-8738.
Gimpl, G., Fahrenholz, F., (2001). The oxytocin receptor system: structure, function, and regulation. Physiol Rev, 81, 629-683.
Gordon, I., Vander Wyk, B.C., Bennett, R.H., Cordeaux, C., Lucas, M.V., Eilbott, J.A., Zagoory-Sharon, O., Leckman, J.F., Feldman, R., Pelphrey, K.A. (2013). Oxytocin enhances brain function in children with autism. Proc Natl Acad Sci USA, 110, 20953-20958.
Gould, B.R., Zingg, H.H. (2003). Mapping oxytocin receptor gene expression in the mouse brain and mammary gland using an oxytocin receptor-LacZ reporter mouse. Neuroscience, 122, 155-167.
Grandes, P., Kq, K.Q.D., Morino, P., Cuenod, M., Streit, P. (1991). Homocysteate, an excitatory transmitter candidate localized in glia. Eur J Neurosci, 3, 1370-1373.
Gravati, M., Busnelli, M., Bulgheroni, E., Reversi, A., Spaiardi, P., Parenti, M., Toselli, M., Chini, B. (2010). Dual modulation of inward rectifier potassium currents in olfactory neuronal cells by promiscuous G protein coupling of the oxytocin receptor. J Neurochem, 114, 1424-1435.
Grinevich, V., Knobloch-Bollmann, H.S., Eliava, M., Busnelli, M., Chini, B. (2016). Assembling the puzzle: Pathways of oxytocin signaling in the brain. Biol Psychiatry, 79, 155-164.
Grinevich, V., Neumann, I.D. (2020). Brain oxytocin: how puzzle stones from animal studies translate into psychiatry. Mol Psychiatry, 26, 265-279.
Guastella, A.J., Einfeld, S.L., Gray, K.M., Rinehart, N.J., Tonge, B.J., Lambert, T.J., Hickie, I.B., (2010). Intranasal oxytocin improves emotion recognition for youth with autism spectrum disorders. Biol Psychiatry, 67, 692-694.
Gwee, P.C., Tay, B.H., Brenner, S., Venkatesh, B. (2009). Characterization of the neurohypophysial hormone gene loci in elephant shark and the Japanese lamprey: Origin of the vertebrate neurohypophysial hormone genes. BMC Evol Biol, 9, 47.
Hasan, M.T., Althammer, F., Silva da Gouveia, M., Goyon, S., Eliava, M., Lefevre, A., Kerspern, D., Schimmer, J., Raftogianni, A., Wahis, J., Knobloch-Bollmann, H.S., Tang, Y., Liu, X., Jain, A., Chavant, V., Goumon, Y., Weislogel, J.M., Hurlemann, R., Herpertz, S.C., Pitzer, C., Darbon, P., Dogbevia, G.K., Bertocchi, I., Larkum, M.E., Sprengel, R., Bading, H., Charlet, A., Grinevich, V. (2019). A fear memory engram and its plasticity in the hypothalamic oxytocin system. Neuron, 103, 133-146.
Hatton, G.I., Perlmutter, L.S., Salm, A.K., Tweedle, C.D. (1984). Dynamic neuronal-glial interactions in hypothalamus and pituitary: implications for control of hormone synthesis and release. Peptides, 5(Suppl 1), 121-138.
Havranek, T., Lestanova, Z., Mravec, B., Strbak, V., Bakos, J., Bacova, Z. (2017). Oxytocin modulates expression of neuron and glial markers in the rat hippocampus. Folia Biol (Praha), 63, 91-97.
Henneberger, C., Bard, L., Panatier, A., Reynolds, J.P., Kopach, O., Medvedev, N.I., Minge, D., Herde, M.K., Anders, S., Kraev, I., Heller, J.P., Rama, S., Zheng, K., Jensen, T.P., Sanchez-Romero, I., Jackson, C.J., Janovjak, H., Ottersen, O.P., Nagelhus, E.A., Oliet, S.H.R., Stewart, M.G., Nagerl, U.V., Rusakov, D.A. (2020). LTP induction boosts glutamate spillover by driving withdrawal of perisynaptic astroglia. Neuron, 108, 919-936.
Hoare, S., Copland, J.A., Strakova, Z., Ives, K., Jeng, Y.J., Hellmich, M.R., Soloff, M.S. (1999). The proximal portion of the COOH terminus of the oxytocin receptor is required for coupling to G(q), but not G(i). Independent mechanisms for elevating intracellular calcium concentrations from intracellular stores. J Biol Chem, 274, 28682-28689.
Hu, N.Y., Chen, Y.T., Wang, Q., Jie, W., Liu, Y.S., You, Q.L., Li, Z.L., Li, X.W., Reibel, S., Pfrieger, F.W., Yang, J.M., Gao, T.M. (2020). Expression patterns of inducible Cre recombinase driven by differential astrocyte-specific promoters in transgenic mouse lines. Neurosci Bull, 36, 530-544.
Inoue, T., Yamakage, H., Tanaka, M., Kusakabe, T., Shimatsu, A., Satoh-Asahara, N. (2019). Oxytocin suppresses inflammatory responses induced by lipopolysaccharide through inhibition of the eIF-2-ATF4 pathway in mouse microglia. Cells, 8, 527.
Insel, T.R., Young, L.J., 2001. The neurobiology of attachment. Nat Rev Neurosci, 2, 129-136.
Ivanov, A.D., Mothet, J.P. (2019). The plastic D-serine signaling pathway: Sliding from neurons to glia and vice-versa. Neurosci Lett, 689, 21-25.
Jurek, B., Neumann, I.D. (2018). The oxytocin receptor: From intracellular signaling to behavior. Physiol Rev, 98, 1805-1908.
Knobloch, H.S., Charlet, A., Hoffmann, L.C., Eliava, M., Khrulev, S., Cetin, A.H., Osten, P., Schwarz, M.K., Seeburg, P.H., Stoop, R., Grinevich, V. (2012). Evoked axonal oxytocin release in the central amygdala attenuates fear response. Neuron, 73, 553-566.
Kuo, J., Hariri, O.R., Micevych, P. (2009). An interaction of oxytocin receptors with metabotropic glutamate receptors in hypothalamic astrocytes. J Neuroendocrinol, 21, 1001-1006.
Landgraf, R., Neumann, I.D. (2004). Vasopressin and oxytocin release within the brain: a dynamic concept of multiple and variable modes of neuropeptide communication. Front Neuroendocrinol, 25, 150-176.
Langle, S.L., Poulain, D.A., Theodosis, D.T. (2003). Induction of rapid, activity-dependent neuronal-glial remodelling in the adult rat hypothalamus in vitro. Eur J Neurosci, 18, 206-214.
Lee, H.J., Macbeth, A.H., Pagani, J.H., Young, W.S., 3rd. (2009). Oxytocin: the great facilitator of life. Prog Neurobiol, 88, 127-151.
Leng, G., Ludwig, M. (2008). Neurotransmitters and peptides: whispered secrets and public announcements. J Physiol, 586, 5625-5632.
Ludwig, M., Leng, G. (2006). Dendritic peptide release and peptide-dependent behaviours. Nat Rev Neurosci, 7, 126-136.
Ludwig, M., Stern, J. (2015). Multiple signalling modalities mediated by dendritic exocytosis of oxytocin and vasopressin. Philos Trans R Soc Lond B Biol Sci, 370(1762), 20140182.
Maicas-Royo, J., Leng, G., MacGregor, D.J. (2018). A predictive, quantitative model of spiking activity and stimulus-secretion coupling in oxytocin neurons. Endocrinology, 159, 1433-1452.
Mairesse, J., Zinni, M., Pansiot, J., Hassan-Abdi, R., Demene, C., Colella, M., Charriaut-Marlangue, C., Rideau Batista Novais, A., Tanter, M., Maccari, S., Gressens, P., Vaiman, D., Soussi-Yanicostas, N., Baud, O. (2019). Oxytocin receptor agonist reduces perinatal brain damage by targeting microglia. Glia, 67, 345-359.
McKay, E.C., Beck, J.S., Khoo, S.K., Dykema, K.J., Cottingham, S.L., Winn, M.E., Paulson, H.L., Lieberman, A.P., Counts, S.E. (2019). Peri-infarct upregulation of the oxytocin receptor in vascular dementia. J Neuropathol Exp Neurol, 78, 436-452.
Meyer-Lindenberg, A., Domes, G., Kirsch, P., Heinrichs, M. (2011). Oxytocin and vasopressin in the human brain: social neuropeptides for translational medicine. Nat Rev Neurosci, 12, 524-538.
Mitre, M., Marlin, B.J., Schiavo, J.K., Morina, E., Norden, S.E., Hackett, T.A., Aoki, C.J., Chao, M.V., Froemke, R.C. (2016). A distributed network for social cognition enriched for oxytocin receptors. J Neurosci, 36, 2517-2535.
Mitre, M., Minder, J., Morina, E.X., Chao, M.V., Froemke, R.C. (2018). Oxytocin modulation of neural circuits. Curr Top Behav Neurosci, 35, 31-53.
Newmaster, K.T., Nolan, Z.T., Chon, U., Vanselow, D.J., Weit, A.R., Tabbaa, M., Hidema, S., Nishimori, K., Hammock, E.A.D., Kim, Y., (2020). Quantitative cellular-resolution map of the oxytocin receptor in postnatally developing mouse brains. Nat Commun, 11, 1885.
Olff, M., Langeland, W., Witteveen, A., Denys, D. (2010). A psychobiological rationale for oxytocin in the treatment of posttraumatic stress disorder. CNS Spectr, 15, 522-530.
Oliet, S.H., Panatier, A., Piet, R., Mothet, J.P., Poulain, D.A., Theodosis, D.T. (2008). Neuron-glia interactions in the rat supraoptic nucleus. Prog Brain Res, 170, 109-117.
Owen, S.F., Tuncdemir, S.N., Bader, P.L., Tirko, N.N., Fishell, G., Tsien, R.W. (2013). Oxytocin enhances hippocampal spike transmission by modulating fast-spiking interneurons. Nature, 500, 458-462.
Palanisamy, A., Kannappan, R., Xu, Z., Martino, A., Friese, M.B., Boyd, J.D., Crosby, G., Culley, D.J. (2018). Oxytocin alters cell fate selection of rat neural progenitor cells in vitro. PLoS One, 13, e0191160.
Panaro, M.A., Benameur, T., Porro, C. (2020). Hypothalamic neuropeptide brain protection: Focus on oxytocin. J Clin Med, 9, 1534.
Panatier, A., Gentles, S.J., Bourque, C.W., Oliet, S.H. 2006. Activity-dependent synaptic plasticity in the supraoptic nucleus of the rat hypothalamus. J Physiol, 573, 711-721.
Papouin, T., Henneberger, C., Rusakov, D.A., Oliet, S.H.R. (2017). Astroglial versus neuronal D-serine: Fact checking. Trends Neurosci, 40, 517-520.
Parent, A.S., Rasier, G., Matagne, V., Lomniczi, A., Lebrethon, M.C., Gerard, A., Ojeda, S.R., Bourguignon, J.P. (2008). Oxytocin facilitates female sexual maturation through a glia-to-neuron signaling pathway. Endocrinology, 149, 1358-1365.
Parpura, V., Basarsky, T.A., Liu, F., Jeftinija, K., Jeftinija, S., Haydon, P.G. (1994). Glutamate-mediated astrocyte-neuron signalling. Nature, 369, 744-747.
Phaneuf, S., Europe-Finner, G.N., Varney, M., MacKenzie, I.Z., Watson, S.P., Lopez Bernal, A. (1993). Oxytocin-stimulated phosphoinositide hydrolysis in human myometrial cells: involvement of pertussis toxin-sensitive and -insensitive G-proteins. J Endocrinol, 136, 497-509.
Rimoldi, V., Reversi, A., Taverna, E., Rosa, P., Francolini, M., Cassoni, P., Parenti, M., Chini, B. (2003). Oxytocin receptor elicits different EGFR/MAPK activation patterns depending on its localization in caveolin-1 enriched domains. Oncogene, 22, 6054-6060.
Rosso, L., Peteri-Brunback, B., Vouret-Craviari, V., Deroanne, C., Van Obberghen-Schilling, E., Mienville, J.M. (2002). Vasopressin and oxytocin reverse adenosine-induced pituicyte stellation via calcium-dependent activation of Cdc42. Eur J Neurosci, 16, 2324-2332.
Salm, A.K., Smithson, K.G., Hatton, G.I. (1985). Lactation-associated redistribution of the glial fibrillary acidic protein within the supraoptic nucleus. An immunocytochemical study. Cell Tissue Res, 242, 9-15.
Savtchouk, I., Volterra, A. (2018). Gliotransmission: Beyond black-and-white. J Neurosci, 38, 14-25.
Shigetomi, E., Kracun, S., Khakh, B.S. (2010a). Monitoring astrocyte calcium microdomains with improved membrane targeted GCaMP reporters. Neuron Glia Biol, 6, 183-191.
Shigetomi, E., Kracun, S., Sofroniew, M.V., Khakh, B.S. (2010b). A genetically targeted optical sensor to monitor calcium signals in astrocyte processes. Nat Neurosci, 13, 759-766.
Sloan, S.A., Barres, B.A. (2014). Looks can be deceiving: reconsidering the evidence for gliotransmission. Neuron, 84, 1112-1115.
Stifter, S.A., Greter, M. (2020). STOP floxing around: Specificity and leakiness of inducible Cre/loxP systems. Eur J Immunol, 50, 338-341.
Stoop, R. (2012). Neuromodulation by oxytocin and vasopressin. Neuron, 76, 142-159.
Strakova, Z., Copland, J.A., Lolait, S.J., Soloff, M.S. (1998). ERK2 mediates oxytocin-stimulated PGE2 synthesis. Am J Physiol, 274, E634-641.
Swaab, D.F. (1997). Prader-Willi syndrome and the hypothalamus. Acta Paediatr Suppl, 423, 50-54.
Swaab, D.F., Purba, J.S., Hofman, M.A. (1995). Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons (putative satiety cells) in Prader-Willi syndrome: a study of five cases. J Clin Endocrinol Metab, 80, 573-579.
Tasker, J.G., Oliet, S.H., Bains, J.S., Brown, C.H., Stern, J.E. (2012). Glial regulation of neuronal function: from synapse to systems physiology. J Neuroendocrinol, 24, 566-576.
Tauber, M., Boulanouar, K., Diene, G., Cabal-Berthoumieu, S., Ehlinger, V., Fichaux-Bourin, P., Molinas, C., Faye, S., Valette, M., Pourrinet, J., Cessans, C., Viaux-Sauvelon, S., Bascoul, C., Guedeney, A., Delhanty, P., Geenen, V., Martens, H., Muscatelli, F., Cohen, D., Consoli, A., Payoux, P., Arnaud, C., Salles, J.P. (2017). The use of oxytocin to improve feeding and social skills in infants with Prader-Willi syndrome. Pediatrics, 139, e20162976.
Tauber, M., Mantoulan, C., Copet, P., Jauregui, J., Demeer, G., Diene, G., Roge, B., Laurier, V., Ehlinger, V., Arnaud, C., Molinas, C., Thuilleaux, D. (2011). Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients with Prader-Willi syndrome: a randomised placebo-controlled trial in 24 patients. Orphanet J Rare Dis, 6, 47.
Theodosis, D.T., Chapman, D.B., Montagnese, C., Poulain, D.A., Morris, J.F. (1986a). Structural plasticity in the hypothalamic supraoptic nucleus at lactation affects oxytocin-, but not vasopressin-secreting neurones. Neuroscience, 17, 661-678.
Theodosis, D.T., Montagnese, C., Rodriguez, F., Vincent, J.D., Poulain, D.A. (1986b). Oxytocin induces morphological plasticity in the adult hypothalamo-neurohypophysial system. Nature, 322, 738-740.
Theofanopoulou, C., Gedman, G., Cahill, J.A., Boeckx, C., Jarvis, E.D. (2021). Universal nomenclature for oxytocin-vasotocin ligand and receptor families. Nature, 592, 747-755.
Tirko, N.N., Eyring, K.W., Carcea, I., Mitre, M., Chao, M.V., Froemke, R.C., Tsien, R.W. (2018). Oxytocin transforms firing mode of CA2 hippocampal neurons. Neuron, 100, 593-608.
Tobin, V., Leng, G., Ludwig, M. (2012). The involvement of actin, calcium channels and exocytosis proteins in somato-dendritic oxytocin and vasopressin release. Front Physiol, 3, 261.
Verkhratsky, A., Nedergaard, M. (2018). Physiology of astroglia. Physiol Rev, 98, 239-389.
von Bartheld, C.S., Bahney, J., Herculano-Houzel, S., (2016). The search for true numbers of neurons and glial cells in the human brain: A review of 150 years of cell counting. J Comp Neurol, 524, 3865-3895.
Wahis, J., Baudon, A., Althammer, F., Kerspern, D., Goyon, S., Hagiwara, D., Lefevre, A., Barteczko, L., Boury-Jamot, B., Bellanger, B., Abatis, M., Da Silva Gouveia, M., Benusiglio, D., Eliava, M., Rozov, A., Weinsanto, I., Knobloch-Bollmann, H.S., Kirchner, M.K., Roy, R.K., Wang, H., Pertin, M., Inquimbert, P., Pitzer, C., Siemens, J., Goumon, Y., Boutrel, B., Lamy, C.M., Decosterd, I., Chatton, J.Y., Rouach, N., Young, W.S., Stern, J.E., Poisbeau, P., Stoop, R., Darbon, P., Grinevich, V., Charlet, A. (2021). Astrocytes mediate the effect of oxytocin in the central amygdala on neuronal activity and affective states in rodents. Nat Neurosci, 24, 529-541.
Wang, P., Qin, D., Wang, Y.F. (2017). Oxytocin rapidly changes astrocytic GFAP plasticity by differentially modulating the expressions of pERK 1/2 and protein kinase A. Front Mol Neurosci, 10, 262.
Wang, Y.F., Hatton, G.I. (2006). Mechanisms underlying oxytocin-induced excitation of supraoptic neurons: prostaglandin mediation of actin polymerization. J Neurophysiol, 95, 3933-3947.
Wang, Y.F., Hatton, G.I. (2007). Interaction of extracellular signal-regulated protein kinase 1/2 with actin cytoskeleton in supraoptic oxytocin neurons and astrocytes: role in burst firing. J Neurosci, 27, 13822-13834.
Wang, Y.F., Hatton, G.I. (2009). Astrocytic plasticity and patterned oxytocin neuronal activity: dynamic interactions. J Neurosci, 29, 1743-1754.
Young, L.J., Wang, Z. (2004). The neurobiology of pair bonding. Nat Neurosci, 7, 1048-1054.
Young, W.S., Song, J. (2020). Characterization of oxytocin receptor expression within various neuronal populations of the mouse dorsal hippocampus. Front Mol Neurosci, 13, 40.
Zatkova, M., Bacova, Z., Puerta, F., Lestanova, Z., Alanazi, M., Kiss, A., Reichova, A., Castejon, A.M., Ostatnikova, D., Bakos, J. (2018). Projection length stimulated by oxytocin is modulated by the inhibition of calcium signaling in U-87MG cells. J Neural Transm, 125, 1847-1856.
Zhang, J.M., Wang, H.K., Ye, C.Q., Ge, W., Chen, Y., Jiang, Z.L., Wu, C.P., Poo, M.M., Duan, S. (2003). ATP released by astrocytes mediates glutamatergic activity-dependent heterosynaptic suppression. Neuron, 40, 971-982.

Auteurs

Angel Baudon (A)

Centre National de la Recherche Scientifique et Université de Strasbourg, Institut des Neurosciences Cellulaires et Intégratives, 8 allée du Général Rouvillois, 67000 Strasbourg, France.

Etienne Clauss Creusot (E)

Centre National de la Recherche Scientifique et Université de Strasbourg, Institut des Neurosciences Cellulaires et Intégratives, 8 allée du Général Rouvillois, 67000 Strasbourg, France.

Alexandre Charlet (A)

Centre National de la Recherche Scientifique et Université de Strasbourg, Institut des Neurosciences Cellulaires et Intégratives, 8 allée du Général Rouvillois, 67000 Strasbourg, France.

Articles similaires

Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell
Animals TOR Serine-Threonine Kinases Colorectal Neoplasms Colitis Mice
Animals Tail Swine Behavior, Animal Animal Husbandry

Classifications MeSH