Electrophysiological Identification of the Functional Presynaptic Nerve Terminals on an Isolated Single Vasopressin Neurone of the Rat Supraoptic Nucleus
Release of arginine vasopressin (AVP) and oxytocin from magnocellular neurosecretory cells (MNCs) of the supraoptic nucleus (SON) is under the control of glutamate‐dependent excitation and GABA‐dependent inhibition. The possible role of the synaptic terminals attached to SON neurones has been invest...
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Veröffentlicht in: | Journal of neuroendocrinology 2010-05, Vol.22 (5), p.413-419 |
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description | Release of arginine vasopressin (AVP) and oxytocin from magnocellular neurosecretory cells (MNCs) of the supraoptic nucleus (SON) is under the control of glutamate‐dependent excitation and GABA‐dependent inhibition. The possible role of the synaptic terminals attached to SON neurones has been investigated using whole‐cell patch‐clamp recording in in vitro rat brain slice preparations. Recent evidence has provided new insights into the repercussions of glial environment modifications on the physiology of MNCs at the synaptic level in the SON. In the present study, excitatory glutamatergic and inhibitory GABAergic synaptic inputs were recorded from an isolated single SON neurone cultured for 12 h, using the whole‐cell patch clamp technique. Neurones expressed an AVP‐enhanced green fluorescent protein (eGFP) fusion gene in MNCs. In addition, native synaptic terminals attached to a dissociated AVP‐eGFP neurone were visualised with synaptic vesicle markers. These results suggest that the function of presynaptic nerve terminals may be evaluated directly in a single AVP‐eGFP neurone. These preparations would be helpful in future studies aiming to electrophysiologically distinguish between the functions of synaptic terminals and glial modifications in the SON neurones. |
doi_str_mv | 10.1111/j.1365-2826.2010.01979.x |
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The possible role of the synaptic terminals attached to SON neurones has been investigated using whole‐cell patch‐clamp recording in in vitro rat brain slice preparations. Recent evidence has provided new insights into the repercussions of glial environment modifications on the physiology of MNCs at the synaptic level in the SON. In the present study, excitatory glutamatergic and inhibitory GABAergic synaptic inputs were recorded from an isolated single SON neurone cultured for 12 h, using the whole‐cell patch clamp technique. Neurones expressed an AVP‐enhanced green fluorescent protein (eGFP) fusion gene in MNCs. In addition, native synaptic terminals attached to a dissociated AVP‐eGFP neurone were visualised with synaptic vesicle markers. These results suggest that the function of presynaptic nerve terminals may be evaluated directly in a single AVP‐eGFP neurone. 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These preparations would be helpful in future studies aiming to electrophysiologically distinguish between the functions of synaptic terminals and glial modifications in the SON neurones.</description><subject>Animals</subject><subject>Arginine Vasopressin - genetics</subject><subject>Arginine Vasopressin - physiology</subject><subject>green fluorescent protein</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Male</subject><subject>Neurons - physiology</subject><subject>Patch-Clamp Techniques</subject><subject>Presynaptic Terminals - physiology</subject><subject>Rats</subject><subject>Rats, Transgenic</subject><subject>supraoptic nucleus</subject><subject>Supraoptic Nucleus - physiology</subject><subject>vasopressin neurone</subject><subject>whole-cell patch-clamp</subject><issn>0953-8194</issn><issn>1365-2826</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcFy0zAQhjUMDA0pr8DoxslBsmzZOnBgStIG2pRJWuCmke11q6BYrmRD8ii8LTJucwVddlf7f79m9COEKZnRcN5tZ5TxNIrzmM9iEm4JFZmY7Z-hyXHxHE2ISFmUU5GcoFfebwmhWcrIS3QSGM5SKibo99xA2Tnb3h-8tsbe6VIZvKyg6XQd-k7bBtsad_eAF31TDnMQfHHgD41qO13iFbifgG_A7XRYeRwA1eClt0Z1UOGNbu4M4K_K2zZQXjeB6J1t4Ml3rTq86Vun7OjXlwZ6f4pe1MEOXj_WKbpdzG_OLqLL6_Pl2YfLqExJIqKYM8FpxlWq8ioRokiZyEWcsCKmhIs6z1VVKFErChnhhAV5XHPOkqJIipwBm6K3o2_r7EMPvpM77UswRjVgey-zJOHhH1P-byVjcZ6wUKYoH5Wls947qGXr9E65g6REDgnKrRyCkkNQckhQ_k1Q7gP65vGRvthBdQSfIguC96PglzZw-G9j-Wk1H7rARyOvfQf7I6_cD8kzlqXy2-pcbj5frb-vP17IBfsD3n27Tw</recordid><startdate>201005</startdate><enddate>201005</enddate><creator>Ohbuchi, T.</creator><creator>Yokoyama, T.</creator><creator>Fujihara, H.</creator><creator>Suzuki, H.</creator><creator>Ueta, Y.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>201005</creationdate><title>Electrophysiological Identification of the Functional Presynaptic Nerve Terminals on an Isolated Single Vasopressin Neurone of the Rat Supraoptic Nucleus</title><author>Ohbuchi, T. ; Yokoyama, T. ; Fujihara, H. ; Suzuki, H. ; Ueta, Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5049-26396176a5a8d499b53989243b21069f88adba9fa1e706036392f6634bb4b83e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Arginine Vasopressin - genetics</topic><topic>Arginine Vasopressin - physiology</topic><topic>green fluorescent protein</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Male</topic><topic>Neurons - physiology</topic><topic>Patch-Clamp Techniques</topic><topic>Presynaptic Terminals - physiology</topic><topic>Rats</topic><topic>Rats, Transgenic</topic><topic>supraoptic nucleus</topic><topic>Supraoptic Nucleus - physiology</topic><topic>vasopressin neurone</topic><topic>whole-cell patch-clamp</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ohbuchi, T.</creatorcontrib><creatorcontrib>Yokoyama, T.</creatorcontrib><creatorcontrib>Fujihara, H.</creatorcontrib><creatorcontrib>Suzuki, H.</creatorcontrib><creatorcontrib>Ueta, Y.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>Journal of neuroendocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ohbuchi, T.</au><au>Yokoyama, T.</au><au>Fujihara, H.</au><au>Suzuki, H.</au><au>Ueta, Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrophysiological Identification of the Functional Presynaptic Nerve Terminals on an Isolated Single Vasopressin Neurone of the Rat Supraoptic Nucleus</atitle><jtitle>Journal of neuroendocrinology</jtitle><addtitle>J Neuroendocrinol</addtitle><date>2010-05</date><risdate>2010</risdate><volume>22</volume><issue>5</issue><spage>413</spage><epage>419</epage><pages>413-419</pages><issn>0953-8194</issn><eissn>1365-2826</eissn><abstract>Release of arginine vasopressin (AVP) and oxytocin from magnocellular neurosecretory cells (MNCs) of the supraoptic nucleus (SON) is under the control of glutamate‐dependent excitation and GABA‐dependent inhibition. The possible role of the synaptic terminals attached to SON neurones has been investigated using whole‐cell patch‐clamp recording in in vitro rat brain slice preparations. Recent evidence has provided new insights into the repercussions of glial environment modifications on the physiology of MNCs at the synaptic level in the SON. In the present study, excitatory glutamatergic and inhibitory GABAergic synaptic inputs were recorded from an isolated single SON neurone cultured for 12 h, using the whole‐cell patch clamp technique. Neurones expressed an AVP‐enhanced green fluorescent protein (eGFP) fusion gene in MNCs. In addition, native synaptic terminals attached to a dissociated AVP‐eGFP neurone were visualised with synaptic vesicle markers. These results suggest that the function of presynaptic nerve terminals may be evaluated directly in a single AVP‐eGFP neurone. These preparations would be helpful in future studies aiming to electrophysiologically distinguish between the functions of synaptic terminals and glial modifications in the SON neurones.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>20163519</pmid><doi>10.1111/j.1365-2826.2010.01979.x</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Arginine Vasopressin - genetics Arginine Vasopressin - physiology green fluorescent protein Green Fluorescent Proteins - genetics Male Neurons - physiology Patch-Clamp Techniques Presynaptic Terminals - physiology Rats Rats, Transgenic supraoptic nucleus Supraoptic Nucleus - physiology vasopressin neurone whole-cell patch-clamp |
title | Electrophysiological Identification of the Functional Presynaptic Nerve Terminals on an Isolated Single Vasopressin Neurone of the Rat Supraoptic Nucleus |
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