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Release of [3H]5-hydroxytryptamine from the intermediate area of rat thoracic spinal cord is modulated by presynaptic autoreceptors

✍ Scribed by Ling Yang; Henry M. Jacocks III; Cinda J. Helke


Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
762 KB
Volume
18
Category
Article
ISSN
0887-4476

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✦ Synopsis


Abstract

Serotonin (5‐HT) nerve terminals innervate sympathetic preganglionic neurons of the intermediolateral cell column (IML); however, neither the depolarization‐induced release of 5‐HT nor the presence of presynaptic modulatory autoreceptors have been directly studied in this system. We used in vitro superfusion of the microdissected intermediate area (including the intermediolateral cell column, intercalated nucleus, and central autonomic nucleus) of the rat thoracic spinal cord to measure basal and stimulated release of preloaded [^3^H]5‐HT. Elevated K^+^ evoked a concentration‐ and Ca^2+^ dependent release of [^3^H]5‐HT. Exogenous 5‐HT and the 5‐HT~1B~ agonist, CGS‐12066B, both decreased the K^+^‐stimulated release of [^3^H]5‐HT. A 5‐HT~1B~ antagonist (methiothepin) blocked the 5‐HT‐ and the CGS‐12066B‐induced inhibition of K^+^‐evoked release of [^3^H]5‐HT. A 5‐HT~1A~ antagonist (NAN‐190) did not alter the inhibitory actions of exogenous 5‐HT. Moreover, a 5‐HT~1A~ agonist (8‐OH‐DPAT), a 5‐HT~2A/2C~ agonist [(+/‐)‐DOI hydrochloride], and a 5‐HT~3~ agonist (2‐methyl‐5‐HT) did not alter the K^+^ evoked release of [^3^H]5‐HT. These data demonstrate that 5‐HT is released from the intermediate area of the rat thoracic spinal cord. The 5‐HT receptor subtype involved in the inhibition of the evoked release of [^3^H]5‐HT is of the 5‐HT~1B~ subtype. These findings may help clarify the complex role of 5‐HT in spinal regulation of the sympathetic nervous system. © 1994 Wiley‐Liss, IncThis article is US Government work and, as such, is in the public domain in the United States of America.


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