Schayer R W, Reilly M A
Agents Actions. 1975 May;5(2):119-24. doi: 10.1007/BF02027351.
A method for determining the histamine-methylating enzyme (HME) using crude enzyme, and minute quantities of the substrate, was applied to tissues of mice, guinea-pigs and rats. Since high levels of endogenous histamine can affect the results, tissue homogenates were dialyzed prior to incubation. Findings were compared with in vivo data on methylating ability of individual tissues; most of this in vivo data is published but a new test of guinea-pig tissues was made using amodiaquine as an inhibitor. The correlation was good, better than that obtained by other procedures. It was observed that dialysis caused an increase in HME for some guinea-pig tissues, but a loss for some mouse tissues. Possible explanations are considered. Quinacrine N-mustard, a derivative of a known HME inhibitor, was tested in mice; it altered the distribution of injected 14C-histamine but showed no evidence of HME inhibition.
一种使用粗酶和微量底物测定组胺甲基化酶(HME)的方法被应用于小鼠、豚鼠和大鼠的组织。由于内源性组胺的高水平会影响结果,因此在孵育前对组织匀浆进行了透析。将结果与各组织甲基化能力的体内数据进行了比较;大部分体内数据已发表,但使用阿莫地喹作为抑制剂对豚鼠组织进行了一项新测试。相关性良好,优于其他方法获得的结果。观察到透析使一些豚鼠组织的HME增加,但使一些小鼠组织的HME减少。考虑了可能的解释。对已知HME抑制剂的衍生物喹吖因氮芥在小鼠中进行了测试;它改变了注射的14C-组胺的分布,但没有显示出HME抑制的证据。