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EFFECTS OF SEROTONIN AND THE 5-HT(2/1C) RECEPTOR AGONIST DOI ON NEURONS OF THE CEREBELLAR DENTATE INTERPOSITUS NUCLEI - POSSIBLE INVOLVEMENT OF A GABAERGIC INTERNEURON
被引:26
|作者:
CUMMINGHOOD, PA
STRAHLENDORF, HK
STRAHLENDORF, JC
机构:
[1] TEXAS TECH UNIV, HLTH SCI CTR, DEPT PHYSIOL, LUBBOCK, TX 79430 USA
[2] TEXAS TECH UNIV, HLTH SCI CTR, DEPT MED & SURG NEUROL, LUBBOCK, TX 79430 USA
关键词:
5-HT;
(5-HYDROXYTRYPTAMINE;
SEROTONIN);
DOI (1-(2,5-DIMETHOXY-4-IODOPHENYL)-2-AMINOPROPANE);
DENTATE INTERPOSITUS;
CEREBELLUM;
GABA(GAMMA-AMINOBUTYRIC ACID);
5-HT(2/1C) RECEPTORS;
D O I:
10.1016/0014-2999(93)90485-Z
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The present study was designed to examine the effects of iontophoretically applied serotonin (5-HT) on neurons of the cerebellar dentate/interpositus nuclei in an in vitro slice preparation and to determine if the 5-HT2/1c receptor subtype could be responsible for mediating any effects noted with 5-HT. 5-HT and the 5-HT2/1C-selective agonist 1-(2,5-dimethoxy-4-iodophenyl)2-aminopropane hydrochloride (DOI) were iontophoretically applied alone and during superfusion of the 5-HT2/1C-selective antagonist, ritanserin. 5-HT and DOI elicited either inhibition or excitation of the spontaneous activity of dentate/interpositus neurons. An inhibitory response was induced by both compounds in the majority of cells responding. Ritanserin significantly attenuated the inhibitory response elicited by both 5-HT and DOI. In addition, the inhibitory response to DOI was significantly attenuated by the gamma-aminobutyric acid (GABA) antagonists, bicuculline and picrotoxin. Our results suggest that the 5-HT2/1C receptor subtype may be partially responsible for mediating 5-HT-induced inhibition of dentate/interpositus neurons, possibly via activation of GABAergic interneurons.
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页码:457 / 465
页数:9
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