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缓激肽对离体、血液灌流犬心房的变时性和变力性作用。

Chronotropic and inotropic effects of bradykinin on isolated, blood-perfused canine atrium.

作者信息

Kobayashi M, Furukawa Y, Chiba S

出版信息

Jpn Heart J. 1980 Jan;21(1):121-9. doi: 10.1536/ihj.21.121.

Abstract

Effects of bradykinin on SA node pacemaker activity and atrial contractility were studied, using isolated, blood-perfused dog atrium preparations. Bradykinin (0.1--100 micrograms) caused a slightly but consistently positive chronotropic action, although it did not produce a consistent inotropic action. When successive doses of bradykinin were given in a short period, these preparations displayed tachphylaxis. Bradykinin-induced action was not suppressed by a potent beta-adrenoceptor blocking agent, carteolol. In addition, kallikrein (0.1--3 units), was administered into the sinus node artery to investigate the effect of endogenous kinins. Kallikrein had no effect on SA node pacemaker activity nor atrial contractility at any examined doses. On the other hand, a kallikrein inhibitor, aprotinin, induced dose-relatedly a negative inotropic and chronotropic effect at a dose range from 100 to 3,000 units. These negative actions of aprotinin were not blocked by an adequate dose of atropine. From these results, it is concluded that bradykinin has a slight direct positive chronotropic effect, and that aprotinin has direct negative inotropic and chronotropic effects in the isolated, blood-perfused canine atrium in a wide dose range.

摘要

利用离体、血液灌注的犬心房标本,研究了缓激肽对窦房结起搏活动和心房收缩性的影响。缓激肽(0.1 - 100微克)引起轻微但持续的正性变时作用,尽管它未产生一致的变力作用。当在短时间内连续给予缓激肽剂量时,这些标本表现出快速耐受性。缓激肽诱导的作用未被强效β - 肾上腺素能受体阻滞剂 carteolol 抑制。此外,将激肽释放酶(0.1 - 3单位)注入窦房结动脉以研究内源性激肽的作用。在所检测的任何剂量下,激肽释放酶对窦房结起搏活动和心房收缩性均无影响。另一方面,激肽释放酶抑制剂抑肽酶在100至3000单位的剂量范围内剂量依赖性地诱导负性变力和变时作用。抑肽酶的这些负性作用未被足量阿托品阻断。从这些结果得出结论,缓激肽具有轻微的直接正性变时作用,且抑肽酶在离体、血液灌注的犬心房中在宽剂量范围内具有直接负性变力和变时作用。

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