Benetos A, Gavras I, Gavras H
Hypertension. 1986 Nov;8(11):1089-92. doi: 10.1161/01.hyp.8.11.1089.
The purpose of these experiments was to study the possible contribution of bradykinin to normal blood pressure maintenance. The bradykinin analogue B4146, a competitive antagonist-partial agonist of bradykinin, was used in three groups of normotensive unanesthetized Wistar rats. Two intra-aortic injections of B4146 (1 mg in 0.2 ml of dextrose) were given 5 minutes apart (i.e., well after return of blood pressure to baseline, which occurred within 68 +/- 19 seconds). One group had been pretreated with the angiotensin converting enzyme inhibitor HOE 498, 1 mg/kg (Hoechst), and one received only dextrose as the first injection to serve as controls. The bradykinin antagonist produced an average increase in mean arterial pressure of approximately 13 mm Hg for all groups. In five animals, however, the first injection of B4146 produced a hypotensive effect, whereas the second one consistently produced a rise in blood pressure. Pretreatment with the angiotensin converting enzyme inhibitor did not affect the magnitude of the subsequent blood pressure increase in response to B4146. Since smaller doses of B4146, sufficient to block exogenous bradykinin, do not cause changes in normal blood pressure, we conclude that endogenous bradykinin does contribute to normal blood pressure maintenance, but its effect can be demonstrated only if very high doses of its antagonist are injected, maybe because a high concentration of the compound is necessary to displace not only circulating but possibly tissue receptor-bound bradykinin as well.
这些实验的目的是研究缓激肽对维持正常血压可能产生的作用。缓激肽类似物B4146,一种缓激肽的竞争性拮抗剂-部分激动剂,被用于三组未麻醉的血压正常的Wistar大鼠。每隔5分钟进行两次主动脉内注射B4146(1毫克溶于0.2毫升葡萄糖中)(即,在血压恢复到基线水平之后很久,血压在68±19秒内恢复到基线)。一组预先用血管紧张素转换酶抑制剂HOE 498,1毫克/千克(赫斯特公司)进行预处理,另一组第一次注射仅给予葡萄糖作为对照。缓激肽拮抗剂使所有组的平均动脉压平均升高约13毫米汞柱。然而,在五只动物中,第一次注射B4146产生了降压作用,而第二次注射则持续使血压升高。用血管紧张素转换酶抑制剂进行预处理并不影响随后对B4146反应时血压升高的幅度。由于足以阻断外源性缓激肽的较小剂量的B4146不会引起正常血压的变化,我们得出结论,内源性缓激肽确实有助于维持正常血压,但只有在注射非常高剂量的其拮抗剂时才能证明其作用,这可能是因为需要高浓度的该化合物不仅要置换循环中的缓激肽,而且可能还要置换与组织受体结合的缓激肽。