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转换酶抑制对血管紧张素诱导的血管加压素释放的影响。

Influence of converting enzyme inhibition on the release of vasopressin induced by angiotensin.

作者信息

Knepel W, Meyer D K

出版信息

Br J Pharmacol. 1980;71(1):337-41. doi: 10.1111/j.1476-5381.1980.tb10944.x.

Abstract

1 The effects of intravenous infusion of angiotensin I, II and (des-1-Asp) angiotensin II (angiotensin III) on the plasma vasopressin levels, with and without converting enzyme inhibition, were investigated in conscious rats by use of a specific radioimmunoassay. 2 All three peptides caused a dose-dependent increase in vasopressin release, angiotensin III infusion being less effective than angiotensin I or II. 3 The converting enzyme inhibitor, SQ 20881 (Pyr-Trp-Pro-Arg-Pro-Gln-Ile-Pro-Pro) (1.0 mg/kg, i.v.), had no effect on the plasma vasopressin concentrations in bilaterally nephrectomized rats, but increased them in intact or sham-operated animals. 4 SQ 20881 potentiated vasopressin release, elicited by angiotensin I, leaving that elicited by angiotensin II unchanged. The receptor antagonist, saralasin, prevented the angiotensin-induced increase in plasma vasopressin concentration, even after pretreatment with SQ 20881. 5 These data support the assumption that the renin-angiotensin system may be involved in the control of vasopressin release, and indicate that in addition to angiotensin II, angiotensin I and III may also contribute, acting in concert.

摘要
  1. 采用特异性放射免疫分析法,在清醒大鼠中研究了静脉输注血管紧张素I、II和(去-1-天冬氨酸)血管紧张素II(血管紧张素III)对血浆血管加压素水平的影响,以及有无转换酶抑制时的情况。2. 所有三种肽均引起血管加压素释放呈剂量依赖性增加,血管紧张素III输注的效果低于血管紧张素I或II。3. 转换酶抑制剂SQ 20881(吡咯-色氨酸-脯氨酸-精氨酸-脯氨酸-谷氨酰胺-异亮氨酸-脯氨酸-脯氨酸)(1.0毫克/千克,静脉注射)对双侧肾切除大鼠的血浆血管加压素浓度无影响,但在完整或假手术动物中使其升高。4. SQ 20881增强了血管紧张素I引起的血管加压素释放,而血管紧张素II引起的释放不变。受体拮抗剂沙拉新即使在经SQ 20881预处理后也能阻止血管紧张素诱导的血浆血管加压素浓度升高。5. 这些数据支持肾素-血管紧张素系统可能参与血管加压素释放控制的假设,并表明除血管紧张素II外,血管紧张素I和III也可能协同发挥作用。

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Pharmacology of angiotensin.血管紧张素的药理学
Pharmacol Rev. 1974 Jun;26(2):69-123.

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