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肾素抑制对清醒灵长类动物食蟹猴的影响。

Effects of renin inhibition in the conscious primate Macaca fascicularis.

作者信息

Hui K Y, Knight D R, Nussberger J, Hartley L H, Vatner S F, Haber E

机构信息

Massachusetts General Hospital, Boston 02114.

出版信息

Hypertension. 1989 Nov;14(5):480-7. doi: 10.1161/01.hyp.14.5.480.

DOI:10.1161/01.hyp.14.5.480
PMID:2680962
Abstract

Pro-His-Pro-Phe-His-Statine-Ile-Phe-NH2 (R-Pep-27), a potent renin inhibitory peptide, was infused into the conscious, sodium-depleted Macaca fascicularis at doses of 0, 0.1, 1, 4, 16, and 32 micrograms/kg/min for 10 minutes. At all doses greater than 0.1 microgram/kg/min, there was a parallel decrease in mean arterial pressure (MAP), plasma renin activity, and plasma angiotensin II (Ang II) concentration. On the other hand, assays with monoclonal antibodies specific for total renin and active renin demonstrated that the peptide's inhibition of circulating active renin stimulated the release of both. The maximal effective R-Pep-27 dose was approximately 16 micrograms/kg/min, which reduced MAP by an average of 15.8 +/- 1.4 mm Hg (n = 14) and plasma renin activity and plasma Ang II concentration to 3% (n = 9) and 15% (n = 5), respectively, of the pretreatment values. At 0.1 microgram/kg/min, there was no significant decrease in MAP; however, measurement of plasma renin activity showed an average decrease in activity of 42% (n = 3). No significant change in the heart rate was observed at all the doses studied. For comparison, intravenous captopril (400 micrograms/kg bolus) was administered after the MAP of the monkeys had recovered from the peptide experiments, and it reduced MAP by 25.1 +/- 2.4 mm Hg (n = 10) without significantly changing plasma renin activity. As anticipated, injection of angiotensin I (80-160 ng/kg bolus) into sodium-depleted monkeys during peptide infusion caused a transient rise in MAP of 14.8 +/- 5.4 mm Hg (n = 4) above the mean pretreatment value.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

脯氨酸 - 组氨酸 - 脯氨酸 - 苯丙氨酸 - 组氨酸 - 抑肽酶 - 异亮氨酸 - 苯丙氨酸 - 氨基(R - Pep - 27)是一种强效肾素抑制肽,以0、0.1、1、4、16和32微克/千克/分钟的剂量注入清醒、缺钠的食蟹猴体内,持续10分钟。在所有大于0.1微克/千克/分钟的剂量下,平均动脉压(MAP)、血浆肾素活性和血浆血管紧张素II(Ang II)浓度均呈平行下降。另一方面,用针对总肾素和活性肾素的单克隆抗体进行的检测表明,该肽对循环活性肾素的抑制作用刺激了两者的释放。R - Pep - 27的最大有效剂量约为16微克/千克/分钟,可使MAP平均降低15.8±1.4毫米汞柱(n = 14),血浆肾素活性和血浆Ang II浓度分别降至预处理值的3%(n = 9)和15%(n = 5)。在0.1微克/千克/分钟时,MAP没有显著下降;然而,血浆肾素活性测量显示活性平均下降42%(n = 3)。在所研究的所有剂量下,心率均未观察到显著变化。为作比较,在猴子的MAP从肽实验中恢复后,静脉注射卡托普利(400微克/千克推注),它使MAP降低了25.1±2.4毫米汞柱(n = 10),而血浆肾素活性没有显著变化。正如预期的那样,在肽输注期间向缺钠猴子注射血管紧张素I(80 - 160纳克/千克推注)导致MAP短暂升高14.8±5.4毫米汞柱(n = 4),高于预处理平均值。(摘要截于250字)

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