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普萘洛尔处理大鼠后,α1 -肾上腺素能受体亚型改变介导心脏功能。

Altered alpha 1-adrenoceptor subtypes mediated cardiac function after treatment of propranolol to rats.

作者信息

Li W, Zhang Y, Wang X L

机构信息

Department of Pharmacology, Chinese Academy of Medical Sciences, Beijing, China.

出版信息

Zhongguo Yao Li Xue Bao. 1997 May;18(3):237-40.

Abstract

AIM

To study inotropic and chronotropic effects mediated by alpha 1A- and alpha 1B-adrenoceptors after 5-d propranolol (Pro) treatment.

METHODS

The positive inotropic and chronotropic effects mediated by alpha 1A and alpha 1B subtypes were determined on isolated left ventricular papillary muscles and right atrium in Pro- and NaCl-treated rats.

RESULTS

The basic contractility of papillary muscles induced by phenylephrine (Phe) was 90 +/- 18 mg in Pro-treated rats and 53 +/- 17 mg in control group (P < 0.05). The increment on force of contraction was 20 +/- 12 mg in Pro-pretreated rats and 5 +/- 5 mg in NaCl-treated rats (P < 0.05). After preincubated with chloroethylclonidine, the increment on force of contraction was reduced in Pro-treated rats, but was not much changed in control group. Phe in presence of 5-methylurapidil induced positive inotropic effect with 13 +/- 5 mg in Pro-treated group, but not in NaCl-treated rats. Under the normal and the inhibited cardiac state, the maximal increment in beat rate mediated by alpha 1B showed no difference between the Pro-treated and NaCl-treated rats.

CONCLUSION

After chronic treatment of Pro, alpha 1-adrenoceptor-mediated positive inotropic effect in rat heart was improved, which was mainly induced by stimulation of alpha 1B when beta-adrenoceptors were blocked.

摘要

目的

研究普萘洛尔(Pro)治疗5天后,α1A和α1B肾上腺素能受体介导的变力性和变时性效应。

方法

在Pro处理组和NaCl处理组大鼠的离体左心室乳头肌和右心房上,测定α1A和α1B亚型介导的正性变力性和变时性效应。

结果

苯肾上腺素(Phe)诱导的Pro处理组大鼠乳头肌基础收缩力为90±18mg,对照组为53±17mg(P<0.05)。Pro预处理组大鼠收缩力增加20±12mg,NaCl处理组为5±5mg(P<0.05)。用氯乙可乐定预孵育后,Pro处理组大鼠收缩力增加幅度降低,而对照组变化不大。在5-甲基尿嘧啶存在下,Phe在Pro处理组诱导的正性变力性效应为13±5mg,而NaCl处理组大鼠未出现该效应。在正常和心脏抑制状态下,α1B介导的Pro处理组和NaCl处理组大鼠心率最大增加幅度无差异。

结论

长期使用Pro后,大鼠心脏中α1肾上腺素能受体介导的正性变力性效应增强,这主要是在β肾上腺素能受体被阻断时由α1B的刺激引起的。

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