Kobayashi M, Shikimi T, Miyata S, Ohata K
Jpn J Pharmacol. 1980 Oct;30(5):701-10. doi: 10.1254/jjp.30.701.
A bradykinin (BK)-like substance (P1) in the rat stomach was extracted with acetic acid, n-butanol, distilled water and methanol. The gradient and equilibrium chromatography were carried out on SP-Sephadex C-25 columns with the extract containing P1. P1 had a different retention time from BK, kallidin and methionyl-lysyl-bradykinin (MLBK), on the equilibrium chromatography. The apparent molecular weight of P1 estimated by gel chromatography was over 1,300. P1 was classified as a biologically BK-like peptide of mammalian origin which is distinct from BK, kallidin and MLBK. Another kind of biologically active substance (P2) which contracts the isolated rat uterus and duodenum was detected during the course of the extraction and purification of P1. The contractile activity of P2 was abolished by the presence of dibenamine or methysergide, but was not influenced by chymotrypsin, trypsin or papain digestion. The hypotensive effect of P2 on rabbit blood pressure was similar to that of serotonin (5-HT). The retention times of P2 on the equilibrium chromatography on the SP-Sephadex C-25 column, and on the gel chromatography were the same as those of 5-HT. P2 proved to be 5-HT.
用乙酸、正丁醇、蒸馏水和甲醇从大鼠胃中提取出一种类缓激肽物质(P1)。采用梯度洗脱和平衡色谱法,在SP - Sephadex C - 25柱上对含有P1的提取物进行分析。在平衡色谱中,P1的保留时间与缓激肽、胰激肽和甲硫氨酰 - 赖氨酰 - 缓激肽(MLBK)不同。通过凝胶色谱法估算,P1的表观分子量超过1300。P1被归类为一种源自哺乳动物的具有生物学活性的类缓激肽肽,它与缓激肽、胰激肽和MLBK不同。在P1的提取和纯化过程中,检测到另一种能使离体大鼠子宫和十二指肠收缩的生物活性物质(P2)。P2的收缩活性可被苄胺或甲基麦角新碱消除,但不受胰凝乳蛋白酶、胰蛋白酶或木瓜蛋白酶消化的影响。P2对兔血压的降压作用与5 - 羟色胺(5 - HT)相似。P2在SP - Sephadex C - 25柱上的平衡色谱以及凝胶色谱中的保留时间与5 - HT相同。结果证明P2就是5 - HT。