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儿茶酚胺受体活性在调节大鼠打哈欠发生率中的作用。

Involvement of catecholamine receptor activities in modulating the incidence of yawning in rats.

作者信息

Kimura H, Yamada K, Nagashima M, Furukawa T

机构信息

Department of Pharmacology, School of Medicine, Fukuoka University, Japan.

出版信息

Pharmacol Biochem Behav. 1996 Apr;53(4):1017-21. doi: 10.1016/0091-3057(95)02154-x.

Abstract

Possible involvement of catecholamine receptor activities in modulating the incidence of yawning, which involves activation of dopaminergic-cholinergic linked neuronal mechanism, was investigated in rats. Subcutaneous injection of talipexole (B-HT 920), a selective dopamine D2-receptor-agonist, elicited yawning behavior. This behavior was increased by prazosin and bunazosin, alpha 1-adrenoceptor antagonists, and by pindolol, a beta-adrenoceptor antagonist. The yawning induced by physostigmine, an anticholinesterase agent, and pilocarpine, a direct muscarinic receptor agonist, was increased by pindolol, but was unaffected by prazosin and bunazosin. In addition, the yawning induced by the dopaminergic agonists, but not by the cholinergic agonists, was markedly suppressed by ST587, an alpha 1-adrenoceptor agonist. All the yawning responses to dopaminergic and cholinergic agents were reduced not only by scopolamine, a muscarinic receptor antagonist, but also by idazoxan, rauwolscine, and yohimbine, alpha 2-adrenoceptor antagonists. The results suggest that catecholamine receptor activities seem to play different roles in inhibitory modulation of the occurrence of yawning caused by dopaminergic and cholinergic stimulation.

摘要

在大鼠中研究了儿茶酚胺受体活性在调节打哈欠发生率中的可能作用,打哈欠涉及多巴胺能-胆碱能连接的神经元机制的激活。皮下注射选择性多巴胺D2受体激动剂他利克索(B-HT 920)会引发打哈欠行为。这种行为会被α1肾上腺素能受体拮抗剂哌唑嗪和布那唑嗪以及β肾上腺素能受体拮抗剂吲哚洛尔增强。抗胆碱酯酶药毒扁豆碱和直接毒蕈碱受体激动剂毛果芸香碱诱导的打哈欠会被吲哚洛尔增强,但不受哌唑嗪和布那唑嗪影响。此外,多巴胺能激动剂诱导的打哈欠(而非胆碱能激动剂诱导的打哈欠)会被α1肾上腺素能受体激动剂ST587显著抑制。对多巴胺能和胆碱能药物的所有打哈欠反应不仅会被毒蕈碱受体拮抗剂东莨菪碱降低,还会被α2肾上腺素能受体拮抗剂咪唑克生、育亨宾碱和利血平降低。结果表明,儿茶酚胺受体活性似乎在抑制由多巴胺能和胆碱能刺激引起的打哈欠发生中发挥不同作用。

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