Brown B S, Gorczynski R J, Reynolds R D, Shaffer J E
Br J Pharmacol. 1986 Jan;87(1):87-95. doi: 10.1111/j.1476-5381.1986.tb10160.x.
ACC-9358 (N-[(3,5-di(pyrrolidinylmethyl)-4-hydroxy)benzoyl]aniline) is a newly developed analogue of changrolin, an antiarrhythmic agent used in the Peoples Republic of China. Since changrolin and other antiarrhythmic agents exert parasympatholytic activity which may limit their clinical usefulness, it was of interest to examine the parasympatholytic effects of ACC-9358. For comparative purposes we also studied the parasympatholytic activity of disopyramide. In guinea-pig isolated ileal strips, disopyramide, 3-30 microM, and ACC-9358, 100-300 microM, competitively antagonized carbachol-induced contractions with pA2 values of 5.78 and 4.17, respectively. In guinea-pig isolated right atria, disopyramide 3-30 microM, competitively antagonized methacholine-induced slowing of spontaneous beating with a pA2 value of 5.99 whereas ACC-9358, 3-300 microM, produced no significant muscarinic blockade in this preparation. Disopyramide (1.9-15 mg kg-1, i.v.), but not ACC-9358 (7.5-1.5 mg kg-1, i.v.), significantly increased rat pupil diameter in vivo. Disopyramide and ACC-9358 blocked vagal-induced reductions in heart rate in dogs anaesthetized with pentobarbitone. ED50 values were approximately 0.65 and 11.25 mg kg-1, respectively. We conclude that ACC-9358 possesses significantly less parasympatholytic activity than disopyramide.
ACC - 9358(N - [(3,5 - 二(吡咯烷基甲基)- 4 - 羟基)苯甲酰基]苯胺)是新开发的常咯啉类似物,常咯啉是一种在中国使用的抗心律失常药物。由于常咯啉和其他抗心律失常药物具有副交感神经阻滞活性,这可能会限制它们的临床应用,因此研究ACC - 9358的副交感神经阻滞作用具有重要意义。为了进行比较,我们还研究了丙吡胺的副交感神经阻滞活性。在豚鼠离体回肠肌条中,3 - 30微摩尔/升的丙吡胺和100 - 300微摩尔/升的ACC - 9358竞争性拮抗卡巴胆碱诱导的收缩,其pA2值分别为5.78和4.17。在豚鼠离体右心房中,3 - 30微摩尔/升的丙吡胺竞争性拮抗乙酰甲胆碱诱导的自发搏动减慢,pA2值为5.99,而3 - 300微摩尔/升的ACC - 9358在该制剂中未产生明显的毒蕈碱阻断作用。丙吡胺(1.9 - 15毫克/千克,静脉注射),但不是ACC - 9358(7.5 - 1.5毫克/千克,静脉注射),在体内显著增加大鼠瞳孔直径。丙吡胺和ACC - 9358阻断了戊巴比妥麻醉犬迷走神经诱导的心率降低。ED50值分别约为0.65和11.25毫克/千克。我们得出结论,ACC - 9358的副交感神经阻滞活性明显低于丙吡胺。