首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Effects of chronic intravenous infusions of dopexamine and isoprenaline to rats on D1- beta 1- and beta 2-receptor-mediated responses.
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Effects of chronic intravenous infusions of dopexamine and isoprenaline to rats on D1- beta 1- and beta 2-receptor-mediated responses.

机译:慢性多巴胺和异丙肾上腺素静脉滴注对大鼠的D1β1和β2受体介导的反应的影响。

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摘要

1. Rats received intravenous infusions of dopexamine, an agonist with selectivity for D1-dopamine receptors and beta 2-adrenoceptors (240 micrograms kg-1 h-1), isoprenaline, a beta 1- and beta 2-adrenoceptor agonist (40 micrograms kg-1 h-1) or vehicle (isotonic saline at pH 2.5) for 7 days via subcutaneously implanted osmotic minipumps. Tissues were then removed for determination of functional responsiveness to beta 1-adrenoceptor, beta 2-adrenoceptor and dopamine D1-receptor stimulation. 2. The beta 1-adrenoceptor-mediated responses of the spontaneously beating right atrium (increase in rate) and paced left atrium (increase in tension) showed significant reductions in sensitivity to isoprenaline following isoprenaline infusion. The EC50 values were significantly increased from 5.6 to 17.7 nM in right atria and from 7.4 to 27.1 nM in left atria. The maximum rate increase of right atria was also significantly less after isoprenaline infusion compared with controls (164.0 and 251.9 beats min-1, respectively) but the maximum tension responses of left atria were not significantly different. After infusion with dopexamine, however, there was no change in sensitivity of the left or right atria to beta 1-adrenoceptor stimulation by isoprenaline. 3. beta 2-Adrenoceptor-mediated relaxation responses to isoprenaline of the pulmonary artery, constricted with noradrenaline (6 x 10(-8) M), showed no significant difference in maximum response or EC50 in tissue from isoprenaline- or dopexamine-infused rats compared with vehicle-infused controls. beta 2-Adrenoceptor-mediated vasodilator responses were also examined in the kidney perfused with the thromboxane A2 analogue, U46619 (7.1 x 10(-8) M) to raise perfusion pressure.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.大鼠接受多巴沙胺静脉滴注,多巴沙胺是一种对D1-多巴胺受体和β2肾上腺素受体具有选择性的激动剂(240微克kg-1 h-1),异丙肾上腺素,β1和β2肾上腺素受体激动剂(40微克kg) -1 h-1)或溶媒(pH 2.5的等渗盐水)通过皮下植入的渗透微型泵持续7天。然后取出组织以确定对β1肾上腺素能受体,β2肾上腺素能受体和多巴胺D1受体刺激的功能反应性。 2.β1肾上腺素受体介导的自发跳动的右心房反应(速率增加)和起搏的左心房反应(张力增加)显示,在输注异丙肾上腺素后,对异丙肾上腺素的敏感性显着降低。右心房的EC50值从5.6 nM显着增加,左心房从7.4到27.1 nM。异丙肾上腺素输注后,右心房的最大增速也明显低于对照组(分别为164.0和251.9次min-1),但左心房的最大张力反应无显着差异。但是,在输注多巴沙明后,左心房或右心房对异丙肾上腺素对β1肾上腺素受体刺激的敏感性没有变化。 3.β2-肾上腺素受体介导的对肺动脉中异丙肾上腺素的舒张反应,用去甲肾上腺素(6 x 10(-8)M收缩),在异丙肾上腺素或多巴沙胺注入的大鼠的最大反应或EC50中无显着差异与注入车辆的控件相比。还用灌注血栓素A2类似物U46619(7.1 x 10(-8)M)的肾脏检查了β2肾上腺素受体介导的血管舒张反应,以提高灌注压力。(摘要截断为250字)

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