G Evin, J Gardes, C Kreft, B Castro, P Corvol, J Menard
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引用次数: 0
摘要
1. 几个胃抑素A衍生物的合成是为了增加水溶性而不改变抑制肾素-血管紧张素原反应的能力。2. 体外、体内研究了胃抑素精氨酸- o -甲酯,并与胃抑素A及胃抑素A精氨酸盐进行了比较。该化合物在体外抑制纯化猪肾素与合成肾素n -乙酰四肽或天然大鼠肾素底物的反应。抑菌常数与抑菌素A. 4在同一数量级。在肾性高血压大鼠中,大剂量注射胃抑素精氨酸- o -甲基酯或胃抑素精氨酸盐降低血压的效果与大剂量注射Sar1, ala8 -血管紧张素II相同。
Soluble pepstatins: a new approach to blockade in vivo of the renin-angiotensin system.
1. Synthesis of several pepstatin A derivatives was performed with the aim of increasing water solubility without altering the capacity to inhibit the renin-angiotensinogen reaction. 2. Pepstatinyl-arginine-O-methyl ester was studied in vitro and in vivo and compared with pepstatin A and with the arginine salt of pepstatin A. 3. This compound inhibited in vitro the reaction between purified hog renin and the synthetic renin N-acetyl-tetradecapeptide or the natural rat renin substrate. The inhibitory constant was of the same order of magnitude as that of pepstatin A. 4. In renal hypertensive rats, the bolus injection of pepstatinyl-arginine-O-methyl-ester or of the arginine salt of pepstatin decreased blood pressure to the same extent as a bolus injection of Sar1, Ala8-angiotensin II.