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失神经支配的人腮腺对毛果芸香碱和阿托品的反常唾液分泌反应比较

Comparison of paradoxical salivatory responses to chlorosyle and atropine in a denervated human parotid gland.

作者信息

Levin S L

出版信息

Int J Clin Pharmacol Res. 1985;5(5):363-7.

PMID:3934088
Abstract

In the case of the denervated human parotid gland, atropine is a cholinopositive agent that causes an extremely intense and prolonged (up to 3-5 h) salivation. An attempt was made to find out the extent to which the "weight increase" principle had an effect on such a gland, i.e. whether larger analogues of atropine which has a relative molecular mass of 289.4 would stimulate or inhibit the paradoxical salivation. The studies involving chlorosyle of a mass of 355.89 were carried out in seven subjects during the last three years. The cholinopositive activity of chlorosyle, as a ligand with increased weight on both poles, on a denervated gland, was several times lower than that of atropine. With the increase of the ligand's dosage, the cholinoexciting activity of chlorosyle decreased sharply and was just restricted by the initial cholinomimetic excitement transforming into a blockade, which may be compared with the action of depolarizing myorelaxants. The data obtained may provide a foundation for conceptualization of the expansion of a response-active cholinopositive zone in a cholinoreceptor deprived of nervous control, which, probably, results from relocation of hydrophobic segments to the macromolecular periphery or, more precisely, to the synthesis of receptors with another part of the zone. The chlorosyle radicals with increased length and weight, while contacting the hydrophobic segments, conditioned the occurrence of cholinoblocking activity and inhibition of the cholinoexciting effect.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在去神经支配的人腮腺的情况下,阿托品是一种胆碱阳性剂,可引起极其强烈且持久(长达3 - 5小时)的唾液分泌。人们试图弄清楚“重量增加”原理对这样一个腺体的影响程度,即相对分子质量为289.4的阿托品的较大类似物是否会刺激或抑制这种反常的唾液分泌。在过去三年中,对7名受试者进行了涉及质量为355.89的氯西雷的研究。氯西雷作为一种在两极重量都增加的配体,其在去神经支配腺体上的胆碱阳性活性比阿托品低几倍。随着配体剂量的增加,氯西雷的胆碱兴奋活性急剧下降,并且仅受最初的拟胆碱兴奋转变为阻断作用的限制,这可与去极化肌松剂的作用相比较。所获得的数据可为概念化在缺乏神经控制的胆碱能受体中反应活性胆碱阳性区的扩展提供基础,这可能是由于疏水片段重新定位到大分子外围,或者更准确地说,是由于与该区域另一部分的受体合成。长度和重量增加的氯西雷基团在与疏水片段接触时,导致胆碱阻断活性的出现并抑制胆碱兴奋作用。(摘要截取自250字)

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