Kobayashi M, Ohata K
Jpn J Pharmacol. 1984 Oct;36(2):169-75. doi: 10.1254/jjp.36.169.
Four uterine-contractile substances (a, b, c and d) and three uterine-contractile substances (a', c' and d') were obtained from the reaction mixture of rat plasma kininogen with the kinin-forming enzyme in rat stomach and the homogenate of the rat stomach with 0.2% acetic acid, respectively. By high performance liquid chromatography with a Zorbax ODS reversed-phase column, the retention times of materials a, c and d were found to be equal to those of materials a', c' and d', and they were not equal to those of kallidin, methionyl-lysyl-bradykinin (MLBK) and bradykinin (BK). The retention time of material b was equal to that of BK. The uterine-contractile activities of the materials a, b, c, d, a', c' and d' were all abolished by chymotrypsin, but not by trypsin treatment. These materials all relaxed the isolated rat duodenum in the presence of atropine, dibenamine, diphenhydramine and propranolol, and they produced a fall in rabbit blood pressure after administration of atropine, dibenamine and propranolol. The content ratios of a: b: c: d and a': c': d' were 4: 4: 67: 25 and 65: 19: 16, respectively, as calculated from the uterine-contractile activities of these materials.
分别从大鼠血浆激肽原与大鼠胃中的激肽形成酶的反应混合物以及用0.2%乙酸处理的大鼠胃匀浆中获得了四种子宫收缩物质(a、b、c和d)和三种子宫收缩物质(a'、c'和d')。使用Zorbax ODS反相柱进行高效液相色谱分析时,发现物质a、c和d的保留时间与物质a'、c'和d'的保留时间相等,且它们与胰激肽、甲硫氨酰 - 赖氨酰 - 缓激肽(MLBK)和缓激肽(BK)的保留时间不相等。物质b的保留时间与BK的保留时间相等。物质a、b、c、d、a'、c'和d'的子宫收缩活性均被胰凝乳蛋白酶消除,但胰蛋白酶处理则无此效果。在存在阿托品、苄胺唑啉、苯海拉明和普萘洛尔的情况下,这些物质均可使离体大鼠十二指肠松弛,并且在给予阿托品、苄胺唑啉和普萘洛尔后,它们会使兔血压下降。根据这些物质的子宫收缩活性计算得出,a:b:c:d和a':c':d'的含量比分别为4:4:67:25和65:19:16。