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Cardioprotective and β-adrenoceptor antagonistic activity of a newly synthesized aryloxypropanolamine derivative PP-36

机译:新合成的芳氧基丙醇胺衍生物PP-36的心脏保护作用和β-肾上腺素受体拮抗活性

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摘要

The present study was performed to evaluate the cardioprotective effects and pharmacological characterization of newly synthesized β-adrenoreceptor antagonists 3-(3-tert-butylamino-2-hydroxypropoxy)-4-methoxybenzaldehyde (PP-36) in the rat model of coronary artery occlusion and reperfusion. Pre-ischemic administration (20 minutes before coronary occlusion) of PP-36 showed cardioprotective effects against ischemia/reperfusion injury in rats. PP-36 (6 mg kg−1) significantly reduced arrhythmia score (6.33 ± 0.55, P < 0.05), infarct size/left ventricle size (38.9 ± 3.2, P < 0.05) and no mortality compared to vehicle-treated control group (14.17 ± 1.83, 44.9 ± 4.6 and 17% respectively). In-vitro studies in rat isolated right atria, guinea-pig trachea and rat distal colon preparations, were carried out to investigate the potency of PP-36 towards different β-adrenoceptor subtypes. pA2/pKB values of PP-36 for β1-β2-and β3-adrenoceptors were 6.904 ± 0.190, 6.44 ± 0.129 and 5.773 ± 0.129, respectively. In conclusion, PP-36 is a β-adrenoceptor antagonist possessing potent anti-arrhythmic and cardioprotective effects against ischemia/reperfusion injury in rats.
机译:进行本研究以评估新合成的β-肾上腺素受体拮抗剂3-(3-叔丁基氨基-2-羟基丙氧基)-4-甲氧基苯甲醛(PP-36)在冠状动脉闭塞大鼠模型中的心脏保护作用和药理特性和再灌注。 PP-36缺血前给药(冠状动脉闭塞前20分钟)显示对大鼠缺血/再灌注损伤具有心脏保护作用。 PP-36(6 mg kg −1 )显着降低了心律失常评分(6.33±0.55,P <0.05),梗死面积/左心室面积(38.9±3.2,P <0.05)并且无死亡率接受媒介物治疗的对照组(分别为14.17±1.83、44.9±4.6和17%)。在大鼠离体右心房,豚鼠气管和大鼠远端结肠制剂中进行了体外研究,以研究PP-36对不同的β-肾上腺素受体亚型的效力。 PP1-36对β1-β2-和β3-肾上腺素能受体的pA2 / pKB值分别为6.904±0.190、6.44±0.129和5.773±0.129。总之,PP-36是一种β-肾上腺素受体拮抗剂,对大鼠缺血/再灌注损伤具有有效的抗心律失常和心脏保护作用。

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