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去甲肾上腺素诱导清醒犬外周β1-肾上腺素能血管舒张

Norepinephrine-induced beta 1-adrenergic peripheral vasodilation in conscious dogs.

作者信息

Vatner S F, Knight D R, Hintze T H

出版信息

Am J Physiol. 1985 Jul;249(1 Pt 2):H49-56. doi: 10.1152/ajpheart.1985.249.1.H49.

Abstract

Norepinephrine (NE) elicits alpha-adrenergic vasoconstriction and beta 1-adrenergic increases in heart rate and myocardial contractility. To determine whether NE can also elicit peripheral beta 1-adrenergic vasodilation, conscious dogs were studied after recovery from instrumentation for the measurement of cardiac output, arterial pressure, and left ventricular (LV) pressure and calculations of LV dP/dt and total peripheral resistance (TPR). NE, after pretreatment with hexamethonium and phentolamine, reduced mean arterial pressure 40 +/- 5% from 117 +/- 9 mmHg and TPR 60 +/- 5% from 0.058 +/- 0.007 mmHg X ml-1 X min and increased cardiac output 55 +/- 11% from 2,159 +/- 188 ml/min. beta 1-Adrenergic blockade with atenolol reversed the vasodilation induced by NE completely, while at this time isoproterenol was still able to reduce peripheral resistance further, by 67 +/- 7%, indicating that beta 2-adrenergic receptors were not blocked. Administration of phentolamine to intact dogs caused a fall in mean arterial pressure (23 +/- 5%) and TPR (34 +/- 5.4%) and an endogenous increase in plasma NE (2,987 +/- 905 pg/ml) and epinephrine (584 +/- 92 pg/ml). These increases in cardiac output and decreases in TPR were also reversed by atenolol (0.5 mg/kg). Moreover, this dose of atenolol blocked the increases in iliac blood flow induced by local injection of NE in the limb. Thus, in the presence of alpha-adrenergic receptor blockade, either administration of NE or release of endogenous NE elicits potent peripheral vasodilation, which appears to involve a beta 1-adrenergic receptor mechanism.

摘要

去甲肾上腺素(NE)可引起α-肾上腺素能血管收缩以及β1-肾上腺素能介导的心率加快和心肌收缩力增强。为了确定NE是否也能引起外周β1-肾上腺素能血管舒张,在对清醒犬进行用于测量心输出量、动脉压和左心室(LV)压力以及计算LV dP/dt和总外周阻力(TPR)的仪器植入术后恢复后,对其进行了研究。在用六甲铵和酚妥拉明预处理后,NE使平均动脉压从117±9 mmHg降低了40±5%,使TPR从0.058±0.007 mmHg·ml-1·min降低了60±5%,并使心输出量从2159±188 ml/min增加了55±11%。用阿替洛尔进行β1-肾上腺素能阻断可完全逆转NE诱导的血管舒张,而此时异丙肾上腺素仍能够使外周阻力进一步降低67±7%,这表明β2-肾上腺素能受体未被阻断。对完整的犬给予酚妥拉明会导致平均动脉压下降(23±5%)和TPR下降(34±5.4%),以及血浆NE(2987±905 pg/ml)和肾上腺素(584±92 pg/ml)内源性增加。心输出量的这些增加和TPR的降低也被阿替洛尔(0.5 mg/kg)逆转。此外,该剂量的阿替洛尔阻断了局部注射NE于肢体所诱导的髂血流量增加。因此,在存在α-肾上腺素能受体阻断的情况下,给予NE或内源性NE的释放均会引起有效的外周血管舒张,这似乎涉及β1-肾上腺素能受体机制。

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