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β-肾上腺素能阻滞剂布新洛尔内在拟交感活性的选择性

Selectivity of the intrinsic sympathomimetic activity of the beta-adrenergic blocking drug bucindolol.

作者信息

Leff A R, Garrity E R, Munoz N M, Tallet J, Cavigelli M, Deitchman D, Rajfer S I

出版信息

J Cardiovasc Pharmacol. 1984 Sep-Oct;6(5):859-66. doi: 10.1097/00005344-198409000-00019.

Abstract

We studied the comparative effects of beta-adrenergic blockade with propranolol (PROP) and bucindolol (BUC), a beta-adrenergic agonist having both alpha-adrenergic blocking properties and intrinsic sympathomimetic activity (ISA) on airway and cardiovascular responses, in 38 mongrel dogs in situ. Intravenous infusion of 0.6 mg/kg + 6 micrograms/kg/min BUC and 2.0 mg/kg + 20 micrograms/kg/min PROP caused identical shifts in the isoproterenol (ISO) EC50 for chronotropic and hypotensive arterial blood pressure responses. After PROP administration, resting heart rate (HR) decreased from 188 +/- 15 to 142 +/- 12 beats/min (p less than 0.02); BUC caused no decrease in HR. In contrast, the effects of BUC and PROP on mean arterial blood pressure response to ISO were similar. No change in bronchomotor tone was observed after bolus injection of either BUC or PROP. Beta-Adrenergic relaxation to ISO and alpha-adrenergic contraction to norepinephrine (NE) were studied simultaneously in tracheal and bronchial airways using chronotropically equivalent beta-adrenoceptor blocking doses of PROP and BUC. Comparable inhibition of ISO-induced airway relaxation after contraction with 120 micrograms/kg/min i.v. serotonin was demonstrated in both PROP (n = 5) and BUC (n = 5) groups (p less than 0.01 for doses greater than 5 X 10(-11) mol/kg). Similarly, both BUC (n = 5) and PROP (n = 5) blocked beta-adrenergic relaxation and caused identical alpha-adrenergic airway contraction to intravenous NE. We conclude that the ISA of the beta-adrenergic blocking drug BUC can be demonstrated on the spontaneous rate of the heart but not on the activity of bronchial smooth muscle. BUC neither augments ISO-induced relaxation nor inhibits NE-induced contraction of airways after effective chronotropic blockade.

摘要

我们在38只处于原位的杂种犬中,研究了普萘洛尔(PROP)和布新洛尔(BUC)(一种兼具α-肾上腺素能阻断特性和内在拟交感活性(ISA)的β-肾上腺素能激动剂)对气道和心血管反应的比较效应。静脉输注0.6mg/kg + 6μg/kg/min的BUC和2.0mg/kg + 20μg/kg/min的PROP,可使异丙肾上腺素(ISO)对变时性和降压性动脉血压反应的半数有效浓度(EC50)发生相同的偏移。给予PROP后,静息心率(HR)从188±15次/分钟降至142±12次/分钟(p<0.02);BUC未使HR降低。相比之下,BUC和PROP对ISO引起的平均动脉血压反应的影响相似。推注BUC或PROP后,未观察到支气管运动张力的变化。使用变时等效的β-肾上腺素能受体阻断剂量的PROP和BUC,在气管和支气管气道中同时研究了对ISO的β-肾上腺素能舒张作用和对去甲肾上腺素(NE)的α-肾上腺素能收缩作用。在PROP组(n = 5)和BUC组(n = 5)中,静脉注射120μg/kg/min血清素收缩后,对ISO诱导的气道舒张具有可比的抑制作用(剂量大于5×10⁻¹¹mol/kg时,p<0.01)。同样,BUC组(n = 5)和PROP组(n = 5)均阻断了β-肾上腺素能舒张作用,并对静脉注射NE引起了相同的α-肾上腺素能气道收缩。我们得出结论,β-肾上腺素能阻断药物BUC的ISA可在心脏的自发频率上表现出来,但在支气管平滑肌的活性上则不然。在有效的变时性阻断后,BUC既不增强ISO诱导的舒张作用,也不抑制NE诱导的气道收缩。

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