Prast H, Prast M, Philippu A
Department of Pharmacology and Toxicology, University of Innsbruck, Austria.
Agents Actions. 1994 Jun;41 Spec No:C64-5. doi: 10.1007/BF02007769.
To investigate the modulation of histamine release by autoreceptors and heteroreceptors, the rat anterior hypothalamus was superfused through a push-pull cannula with agonists or antagonists of histamine and acetylcholine muscarinic receptors. Superfusion with the H3 receptor agonist (R)-alpha-methylhistamine inhibited, while superfusion with thioperamide (H3 antagonist) enhanced histamine release. Superfusion with carbachol (a mixed M1, M2, M3 agonist) inhibited the release of histamine. The release of endogenous histamine was enhanced on superfusion with atropine (a mixed M1, M2, M3 antagonist). The M3 muscarinic antagonist 4-diphenylacetoxy-N-methylpiperidine enhanced the release rate of histamine. It is concluded that in the anterior hypothalamus the release of endogenous histamine is modulated by H3 autoreceptors. Moreover, acetylcholine released from cholinergic neurons also modulates the release of histamine via M1 and/or M3 heteroreceptors.
为研究自身受体和异源受体对组胺释放的调节作用,通过推挽式套管用组胺和乙酰胆碱毒蕈碱受体激动剂或拮抗剂对大鼠下丘脑前部进行灌流。用H3受体激动剂(R)-α-甲基组胺灌流可抑制组胺释放,而用硫代哌啶(H3拮抗剂)灌流则增强组胺释放。用卡巴胆碱(一种M1、M2、M3混合激动剂)灌流可抑制组胺释放。用阿托品(一种M1、M2、M3混合拮抗剂)灌流可增强内源性组胺释放。M3毒蕈碱拮抗剂4-二苯基乙酰氧基-N-甲基哌啶可提高组胺释放速率。得出结论:在下丘脑前部,内源性组胺释放受H3自身受体调节。此外,胆碱能神经元释放的乙酰胆碱也通过M1和/或M3异源受体调节组胺释放。