White T D, Al-Humayyd M
J Neurochem. 1983 Apr;40(4):1069-75. doi: 10.1111/j.1471-4159.1983.tb08094.x.
The effects of cholinergic agonists and antagonists on the release of ATP from isolated myenteric varicosities were studied using a firefly luciferin-luciferase technique. In a previous study, acetylcholine and nicotine released ATP from isolated myenteric varicosities, whereas the muscarinic agonist bethanechol did not. In the present study, release of ATP by acetylcholine was shown to be Ca2+ dependent. d-Tubocurarine competitively antagonized the release of ATP by either acetylcholine or nicotine. Maximal release of ATP by acetylcholine (10(-3) M) was approximately 24% that observed with the depolarizing drug veratridine (5 X 10(-5) M), suggesting either that not all of the varicosities capable of releasing ATP possess nicotinic receptors or that acetylcholine does not depolarize the varicosities to the degree that veratridine does. Tetrodotoxin slightly but significantly reduced ATP release induced by acetylcholine or nicotine, indicating some involvement of Na+ channels in the release process. Finally, 6-hydroxydopamine pretreatment produced a 48% reduction in the acetylcholine-evoked release of ATP, suggesting that much, but possibly not all, of the ATP release occurs from noradrenergic varicosities present in the preparation.
利用萤火虫荧光素 - 荧光素酶技术,研究了胆碱能激动剂和拮抗剂对离体肠肌层曲张体释放ATP的影响。在先前的一项研究中,乙酰胆碱和尼古丁可使离体肠肌层曲张体释放ATP,而毒蕈碱激动剂氨甲酰甲胆碱则不能。在本研究中,乙酰胆碱诱导的ATP释放显示为Ca2+依赖性。d - 筒箭毒碱竞争性拮抗乙酰胆碱或尼古丁诱导的ATP释放。乙酰胆碱(10(-3) M)诱导的ATP最大释放量约为去极化药物藜芦碱(5×10(-5) M)诱导释放量的24%,这表明要么并非所有能够释放ATP的曲张体都具有烟碱受体,要么乙酰胆碱对曲张体的去极化程度不如藜芦碱。河豚毒素轻微但显著降低了乙酰胆碱或尼古丁诱导的ATP释放,表明Na+通道在释放过程中有所参与。最后,6 - 羟基多巴胺预处理使乙酰胆碱诱发的ATP释放减少了48%,这表明该制剂中存在的去甲肾上腺素能曲张体释放了大部分但可能不是全部的ATP。