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伏隔核或尾状核中的多巴胺受体阻断对注射到背侧或中缝正中的8-OH-DPAT诱导的进食有不同影响。

Dopamine receptor blockade in nucleus accumbens or caudate nucleus differentially affects feeding induced by 8-OH-DPAT injected into dorsal or median raphe.

作者信息

Fletcher P J

机构信息

Section of Biopsychology, Clarke Institute of Psychiatry, Toronto, Ont., Canada.

出版信息

Brain Res. 1991 Jun 28;552(2):181-9. doi: 10.1016/0006-8993(91)90082-7.

DOI:10.1016/0006-8993(91)90082-7
PMID:1833034
Abstract

The 5-hydroxytryptamine (5-HT)1A receptor agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) elicits a variety of behaviours including feeding in rats. These effects are accompanied by a reduction in 5-HT neurotransmission resulting from activation of somatodendritic 5-HT receptors located in the midbrain raphe nuclei. Previous work showing that dopamine receptor antagonists attenuate 8-OH-DPAT-induced feeding indicates that a facilitation of dopamine activity, secondary to reduced 5-HT activity, is involved in the expression of this effect. Microinjection studies were conducted to explore further the nature of this 5-HT-dopamine interaction. Injection of 8-OH-DPAT (0.125-2 micrograms) into either dorsal or median raphe induced dose-dependent increases in 1 h food intake in non-deprived rats. Pretreatment with haloperidol (0.05 and 0.1 mg/kg s.c.) attenuated the effect induced by median raphe 8-OH-DPAT (0.5 microgram) complementing previous results with dorsal raphe 8-OH-DPAT. The feeding resulting from dorsal raphe (1 microgram) or median raphe (0.5 microgram) 8-OH-DPAT was attenuated by alpha-flupenthixol (1.25 and 2.5 micrograms) injected into the nucleus accumbens. alpha-Flupenthixol in either the dorsolateral or ventrolateral aspects of the caudate nucleus attenuated also the feeding response to dorsal raphe, but not median raphe, 8-OH-DPAT. However, alpha-flupenthixol in the dorsomedial caudate failed to alter feeding resulting from dorsal raphe 8-OH-DPAT.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

5-羟色胺(5-HT)1A受体激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)能引发多种行为,包括大鼠进食。这些效应伴随着中脑缝际核中树突体5-HT受体激活导致的5-HT神经传递减少。先前的研究表明多巴胺受体拮抗剂可减弱8-OH-DPAT诱导的进食,这表明5-HT活性降低继发的多巴胺活性增强参与了该效应的表达。进行了微量注射研究以进一步探究这种5-HT-多巴胺相互作用的本质。向未剥夺食物的大鼠的背侧或中缝际注射8-OH-DPAT(0.125 - 2微克)会导致1小时食物摄入量呈剂量依赖性增加。用氟哌啶醇(0.05和0.1毫克/千克皮下注射)预处理可减弱中缝际8-OH-DPAT(0.5微克)诱导的效应,这与先前背侧缝际8-OH-DPAT的结果相符。向伏隔核注射α-氟奋乃静(1.25和2.5微克)可减弱背侧缝际(1微克)或中缝际(0.5微克)8-OH-DPAT引起的进食。尾状核背外侧或腹外侧的α-氟奋乃静也可减弱对背侧缝际8-OH-DPAT的进食反应,但对中缝际8-OH-DPAT无效。然而,尾状核背内侧的α-氟奋乃静未能改变背侧缝际8-OH-DPAT引起的进食。(摘要截选至250字)

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