Blandizzi C, Doda M, Tarkovács G, Del Tacca M, Vizi E S
Institute of Medical Pharmacology, University of Pisa, Italy.
Eur J Pharmacol. 1991 Dec 3;205(3):311-3. doi: 10.1016/0014-2999(91)90916-e.
The effects of alpha 2-adrenoceptor ligands on electrically stimulated [3H]acetylcholine release from longitudinal muscle strips of guinea-pig ileum were examined. Xylazine or oxymetazoline reduced the release of [3H]acetylcholine in a concentration-dependent manner, both these actions being antagonized by idazoxan, CH 38083, or WB 4101. Prazosin, considered as an alpha 2B-adrenoceptor antagonist, failed to modify the inhibitory effects of xylazine or oxymetazoline. It is concluded that the alpha 2-adrenoceptors involved in the modulation of acetylcholine release from cholinergic axon terminals of guinea-pig ileum are of the alpha 2A subtype.
研究了α2-肾上腺素能受体配体对豚鼠回肠纵肌条电刺激释放[3H]乙酰胆碱的影响。赛拉嗪或羟甲唑啉以浓度依赖性方式降低[3H]乙酰胆碱的释放,这两种作用均被咪唑克生、CH 38083或WB 4101拮抗。被认为是α2B-肾上腺素能受体拮抗剂的哌唑嗪未能改变赛拉嗪或羟甲唑啉的抑制作用。得出的结论是,参与调节豚鼠回肠胆碱能轴突终末乙酰胆碱释放的α2-肾上腺素能受体属于α2A亚型。