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一种新合成的内皮素拮抗剂BQ-123在遗传性高血压模型中的降压作用。

Antihypertensive effect of a newly synthesized endothelin antagonist, BQ-123, in a genetic hypertensive model.

作者信息

Nishikibe M, Tsuchida S, Okada M, Fukuroda T, Shimamoto K, Yano M, Ishikawa K, Ikemoto F

机构信息

New Drug Discovery Research Laboratories, Tsukuba Research Institute, Banyu Pharmaceutical Co., Ltd., Ibaraki, Japan.

出版信息

Life Sci. 1993;52(8):717-24. doi: 10.1016/0024-3205(93)90233-s.

Abstract

A newly synthesized ET(A)-selective antagonist, BQ-123, was examined with respect to its anti-endothelin(ET) action in vitro and in vivo and its effect on blood pressure in Wistar Kyoto rats (WKY), spontaneously hypertensive rats (SHR) and stroke-prone spontaneously hypertensive rats (SHRSP). In isolated porcine coronary arteries, BQ-123 (0.07 microM to 6.0 microM) shifted the concentration-response curve for ET-1 to the right without affecting the maximal response of ET-1, its pA2 value being 7.35. Intravenous infusion of BQ-123 at a rate of 1.2 and 30 mg/kg/hr produced a significant decrease in blood pressure in 20- to 29-week-old SHRSP, but did not alter blood pressure in 13- to 16-week-old WKY or in 18- to 19-week-old and 40-week-old SHR. The hypotensive effect of BQ-123 depended on the pretreatment blood pressure level. These results suggest that ET-1 is involved in part in the maintenance of high blood pressure in malignant hypertension, as exemplified by SHRSP.

摘要

一种新合成的ET(A)选择性拮抗剂BQ-123,在体外和体内对其抗内皮素(ET)作用以及对Wistar Kyoto大鼠(WKY)、自发性高血压大鼠(SHR)和易卒中型自发性高血压大鼠(SHRSP)血压的影响进行了研究。在离体猪冠状动脉中,BQ-123(0.07微摩尔/升至6.0微摩尔/升)使ET-1的浓度-反应曲线右移,而不影响ET-1的最大反应,其pA2值为7.35。以1.2和30毫克/千克/小时的速率静脉输注BQ-123,可使20至29周龄的SHRSP血压显著降低,但对13至16周龄的WKY或18至19周龄及40周龄的SHR血压无影响。BQ-123的降压作用取决于预处理时的血压水平。这些结果表明,ET-1部分参与了恶性高血压(如SHRSP)中高血压的维持。

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