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豚鼠回肠肌间神经丛中3H-乙酰胆碱的分泌可被8-溴腺苷3',5'-环磷酸增强,但不受8-溴鸟苷3',5'-环磷酸的影响。

Secretion of 3H-acetylcholine from guinea-pig ileum myenteric plexus is enhanced by 8-Br adenosine 3', 5'-cyclic monophosphate but not changed by 8-Br guanosine 3', 5'-cyclic monophosphate.

作者信息

Alberts P, Stjärne L

出版信息

Acta Physiol Scand. 1982 Jun;115(2):269-72. doi: 10.1111/j.1748-1716.1982.tb07075.x.

Abstract

The acetylcholine (ACh) stores of cholinergic neurons of the myenteric plexus of guinea-pig ileum were labelled by preincubation with 3H-(methyl)-choline. The secretion of labelled transmitter evoked by electrical field stimulation at 1 Hz in the presence of eserine increased by 55% after addition of 0.5 mM 8-Br adenosine 3', 5'-cyclic monophosphate (8-Br cAMP). Atropine further enhanced the secretory response, but not more than in the absence of 8-Br cAMP. 8-Br guanosine 3', 5'-cyclic monophosphate (8-Br cGMP, 0.5 mM) did not change the secretory response to 0.5 or 1 Hz stimulation, either at 1.8 mM or at 0.6 mM calcium, in the absence of eserine. Nor did 1 mM 8-Br cGMP alter the effects of atropine or of oxotremorine. Activation of guanylate cyclase by 0.1 mM N-methyl-N'-nit-ro-N-nitroso guanidine failed to alter the secretory response to 0.5 Hz stimulation in the absence of eserine, or to influence the depression of the secretion caused by oxotremorine. The phosphodiesterase inhibitor 3-isobutyl-l-methylxanthine (a mM) neither altered the secretory response in the presence of eserine, nor the enhancing effect of atropine. The results suggest that cyclic nucleotides are probably not critically involved as "second messengers" in the muscarinic "autoinhibition" of ACh secretion from cholinergic myenteric neurons of guinea-pig ileum.

摘要

豚鼠回肠肌间神经丛胆碱能神经元的乙酰胆碱(ACh)储备通过与3H-(甲基)胆碱预孵育进行标记。在毒扁豆碱存在的情况下,1Hz电场刺激诱发的标记递质分泌在加入0.5mM 8-溴腺苷3',5'-环磷酸(8-溴cAMP)后增加了55%。阿托品进一步增强了分泌反应,但增强程度不超过未添加8-溴cAMP时。在无毒扁豆碱的情况下,无论是在1.8mM还是0.6mM钙浓度下,0.5mM的8-溴鸟苷3',5'-环磷酸(8-溴cGMP)均未改变对0.5或1Hz刺激的分泌反应。1mM 8-溴cGMP也未改变阿托品或氧化震颤素的作用。0.1mM N-甲基-N'-硝基-N-亚硝基胍激活鸟苷酸环化酶未能改变在无毒扁豆碱时对0.5Hz刺激的分泌反应,也未影响氧化震颤素引起的分泌抑制。磷酸二酯酶抑制剂3-异丁基-1-甲基黄嘌呤(1mM)既未改变毒扁豆碱存在时的分泌反应,也未改变阿托品的增强作用。结果表明,环核苷酸可能并非作为“第二信使”在豚鼠回肠胆碱能肌间神经元乙酰胆碱分泌的毒蕈碱样 “自身抑制 ”中起关键作用。

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