Leeling J, Bare J, Phillips B, Medon P
Arzneimittelforschung. 1976;26(9):1665-8.
The effects of 1-methyl-3-keto-4-phenylquinuclidinium bromide (MA540) on tissue monoamine levels in male rats have been compared to those of guanethidine. Neither compound influenced norepinephrine (NE) or 5-hydroxytryptamine (5-HT) levels in brain or epinephrine (E) levels in adrenal medulla. MA540 is about twice as potent as guanethidine as a heart NE depleting agent at both 8 and 24 h after drug administration. The durations of action of the compounds are similar. Unlike guanethidine, MA540 does not deplete NE in small intestine, which suggests that the drug may not elicit guanethidine-like intestinal side effects.
已将1-甲基-3-酮-4-苯基喹核溴化物(MA540)对雄性大鼠组织单胺水平的影响与胍乙啶的影响进行了比较。这两种化合物均未影响大脑中的去甲肾上腺素(NE)或5-羟色胺(5-HT)水平,也未影响肾上腺髓质中的肾上腺素(E)水平。在给药后8小时和24小时,MA540作为心脏NE耗竭剂的效力约为胍乙啶的两倍。这两种化合物的作用持续时间相似。与胍乙啶不同,MA540不会消耗小肠中的NE,这表明该药物可能不会引发类似胍乙啶的肠道副作用。