Wang S N, Fontenot H J, Kennedy R H
Department of pharmacology & Toxicology, University of Arkansas for Medical Sciences, Little Rock 72205, USA.
Eur J Pharmacol. 1997 Feb 19;321(1):39-43. doi: 10.1016/s0014-2999(97)00003-4.
This study was designed to determine if the positive inotropic action of alpha 1-adrenergic stimulation in rat heart is mediated via alpha 1D-adrenoceptors. Isolated left atrial and papillary muscle were suspended in oxygenated Krebs-Henseleit buffer (37 degrees C) containing 1 microM nadolol and paced at 3.0 Hz. Isometric tension was continuously monitored. Cumulative concentration-response curves for phenylephrine were obtained in the presence and absence of BMY 7378 (8-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]-8-azaspirol[4.5] decane-7,9-dione), a selective competitive alpha 1D-adrenoceptor antagonist. BMY 7378 at concentrations up to 30 nM did not significantly affect the positive inotropic response to phenylephrine. In contrast, as reported by other investigators, alpha 1D-adrenoceptor-selective concentrations of this antagonist (3 and 10 nM) did elicit a concentration-dependent right-ward shift in the vasoconstrictor response to phenylephrine in rat abdominal aorta. These data suggest that alpha 1D-adrenoceptors do not play a major role in the positive inotropic action of alpha-adrenoceptor stimulation in rat cardiac muscle.
本研究旨在确定大鼠心脏中α1 - 肾上腺素能刺激的正性肌力作用是否通过α1D - 肾上腺素能受体介导。将离体左心房和乳头肌悬挂于含1微摩尔纳多洛尔的氧合Krebs - Henseleit缓冲液(37℃)中,以3.0赫兹频率起搏。连续监测等长张力。在有和无BMY 7378(8 - [2 - [4 - (2 - 甲氧基苯基)-1 - 哌嗪基]乙基]-8 - 氮杂螺[4.5]癸烷 - 7,9 - 二酮)(一种选择性竞争性α1D - 肾上腺素能受体拮抗剂)存在的情况下,获得去氧肾上腺素的累积浓度 - 反应曲线。浓度高达30纳摩尔的BMY 7378对去氧肾上腺素的正性肌力反应无显著影响。相比之下,正如其他研究者所报道的,该拮抗剂的α1D - 肾上腺素能受体选择性浓度(3和10纳摩尔)确实在大鼠腹主动脉中引起了对去氧肾上腺素的血管收缩反应呈浓度依赖性的右移。这些数据表明,α1D - 肾上腺素能受体在大鼠心肌中α - 肾上腺素能受体刺激的正性肌力作用中不发挥主要作用。