Kim S, Hosoi M, Nakajima K, Yamamoto K
Department of Pharmacology, Osaka City University Medical School, Japan.
Can J Physiol Pharmacol. 1991 Sep;69(9):1350-4. doi: 10.1139/y91-199.
Using immunological techniques, we have demonstrated that about half the trypsin-activatable renin in normal rat plasma is prorenin, while the other is not, and that inactive renin in nephrectomized rat plasma is not prorenin. In the present study, the trypsin-induced angiotensin I generating activity not related to prorenin from normal rat plasma disappeared after HPLC on G3000SW. HPLC analysis of trypsin-treated plasma showed the generation of active renin by trypsin for normal rat plasma, while it did not for nephrectomized rat plasma. These results indicate that trypsin treatment of crude plasma results in the generation of angiotensin I generating activity not due to prorenin, as well as activation of prorenin. HPLC on G3000SW is a useful tool for the determination of plasma prorenin.
运用免疫学技术,我们已经证明,正常大鼠血浆中约一半可被胰蛋白酶激活的肾素是肾素原,而另一半则不是,并且肾切除大鼠血浆中的无活性肾素不是肾素原。在本研究中,正常大鼠血浆中与肾素原无关的胰蛋白酶诱导的血管紧张素I生成活性在G3000SW柱上进行高效液相色谱分析后消失。对经胰蛋白酶处理的血浆进行高效液相色谱分析表明,胰蛋白酶可使正常大鼠血浆产生活性肾素,而对肾切除大鼠血浆则无此作用。这些结果表明,用胰蛋白酶处理粗制血浆会导致产生并非由肾素原引起的血管紧张素I生成活性,以及激活肾素原。在G3000SW柱上进行高效液相色谱分析是测定血浆肾素原的一种有用工具。