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α-肾上腺素能受体在唾液分泌中的生理作用。

Physiological role of alpha-adrenoceptors in salivary secretion.

作者信息

Elverdin J C, Kaniucki M O, Stefano F J, Perec C J

机构信息

School of Dentistry, University of Buenos Aires, Argentina.

出版信息

Acta Odontol Latinoam. 1990;5(1):31-8.

PMID:1963779
Abstract

The submaxillary gland (SM) of rat is innervated by both branches of the autonomic nervous system. Secretion is mediated by the activation of both muscarinic-cholinergic and alpha/beta adrenergic receptors. Studies of the relative affinity of pharmacological agonists and antagonists have warranted a subclassification of alpha adrenoceptors into types alpha 1 and alpha 2. Our studies involve an analysis of the physiologic role of both types of alpha adrenoceptors in salivary secretion. Dose response curves (DRC) to noradrenaline (NA) following administration of alpha adrenoceptor antagonists, i.e. prazosin (alpha 1 antagonist), yohimbine (alpha 2 antagonist) and phentolamine (alpha 1-alpha 2 antagonist) were constructed. Our results demonstrate that prazosin is 100 times more effective than yohimbine in blocking NA-induced salivary secretion. The alpha 2 agonist clonidine (10 micrograms/Kg) blocked the DRCs to methacholine, noradrenaline and substance P-but failed to modify the DRC to isoproterenol. Our results reveal that the subtypes of alpha adrenergic receptors play antagonistic roles in salivary secretion. Alpha 1 stimulation elicits profuse salivary secretion whereas alpha 2 stimulation inhibits salivary secretion induced by 3 different types of agonists, i.e. alpha 1, muscarinic-cholinergic and neurokininergic without affecting beta receptor mediated responses.

摘要

大鼠的颌下腺(SM)由自主神经系统的两个分支支配。分泌是由毒蕈碱 - 胆碱能受体和α/β肾上腺素能受体的激活介导的。对药理学激动剂和拮抗剂相对亲和力的研究使得α肾上腺素能受体可细分为α1和α2型。我们的研究涉及分析这两种类型的α肾上腺素能受体在唾液分泌中的生理作用。构建了在给予α肾上腺素能受体拮抗剂(即哌唑嗪(α1拮抗剂)、育亨宾(α2拮抗剂)和酚妥拉明(α1 - α2拮抗剂)后对去甲肾上腺素(NA)的剂量反应曲线(DRC)。我们的结果表明,在阻断NA诱导的唾液分泌方面,哌唑嗪比育亨宾有效100倍。α2激动剂可乐定(10微克/千克)阻断了对乙酰甲胆碱、去甲肾上腺素和P物质的DRC,但未能改变对异丙肾上腺素的DRC。我们的结果表明,α肾上腺素能受体的亚型在唾液分泌中起拮抗作用。α1刺激引发大量唾液分泌,而α2刺激抑制由3种不同类型激动剂(即α1、毒蕈碱 - 胆碱能和神经激肽能)诱导的唾液分泌,而不影响β受体介导的反应。

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