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[乙酰胆碱对垂体后叶素诱导的水通过蛙膀胱壁的渗透流动的影响]

[Effect of acetylcholine on the pituitrin induced osmotic flow of water through the wall of the frog urinary bladder].

作者信息

Bagrov Ia Iu, Manusova N B

出版信息

Biull Eksp Biol Med. 1978 Sep;86(9):321-4.

PMID:81076
Abstract

The role of intercellular pathways in the ADH-dependent water transport was studied on the frog urinary bladder by means of acetylcholine (AC) and other cholinergic compounds. AC (10(-3) M) was found to cause a strong suppression of the pituitrin-stimulated water flow. Analogous effect was produced by AC on the osmotic flow stimulated by cyclic adenosine monophosphate (cAMP) and theolin. The antipituitrin effect was not reproduced either by nicotine, nor by potent M-cholinomimetic agents (methylfurmetide and F-2268), and was not prevented by M- and N-cholynolytic drugs (atropine, metacin, flaxedil, hexamethonium). However, the antipituitrin effect of AC was completely removed by the anticholinesterase drugs with different mode of action (eserine, proserine, armin, acridine iodmethylate, GD-42) in concentrations of 10(-6)--10(-3) M. It was concluded that the smooth muscles contraction with the subsequent closure of the intercellular spaces was not responsible for the antipituitrinic action of AC. This effect appears to be connected with cholinesterase activation. A possible role of the phosphoinositides in the water permeability regulation of the urinary bladder wall is discussed.

摘要

利用乙酰胆碱(AC)和其他胆碱能化合物,在蛙膀胱上研究了细胞间途径在抗利尿激素(ADH)依赖性水转运中的作用。发现AC(10⁻³M)可强烈抑制垂体后叶素刺激的水流动。AC对环磷酸腺苷(cAMP)和茶碱刺激的渗透流动产生类似作用。尼古丁和强效M胆碱模拟剂(甲呋酰胺和F - 2268)均未再现抗垂体后叶素作用,M和N胆碱能阻断药物(阿托品、麦他西平、三碘季铵酚、六甲铵)也不能阻止该作用。然而,浓度为10⁻⁶ - 10⁻³M的不同作用方式的抗胆碱酯酶药物(毒扁豆碱、前丝氨酸、阿米林、碘化甲基吖啶、GD - 42)可完全消除AC的抗垂体后叶素作用。得出的结论是,平滑肌收缩及随后细胞间隙的关闭并非AC抗垂体后叶素作用的原因。该作用似乎与胆碱酯酶激活有关。讨论了磷酸肌醇在膀胱壁水通透性调节中的可能作用。

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