Evaluation of the antihypertensive activity and alpha adrenergic receptor interaction of cleistanthins A and B.

R P Priyadharsini, S Parasuraman, R Raveendran
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引用次数: 5

Abstract

Hypertension was induced in male Sprague Dawley rats with twice weekly administration of deoxycorticosterone acetate (DOCA) salt (20 mg/kg s.c) for 4 weeks. They were divided into eight groups of six animals each viz., hypertensive control, standard (prazosin 1 mg/kg), cleistanthin A 12.5, 25, 50 mg/kg and cleistanthin B 12.5, 25 mg/kg, and 50 mg/kg. One more group served as normal control. The hypertension was induced in 4 weeks, and the animals were given assigned treatment in 5(th) week. The alteration in blood pressure (BP) was recorded weekly using a rodent noninvasive blood pressure system. At the end of the experiment alpha-adrenergic receptor response of drugs like adrenaline, nor adrenaline, dopamine (doses 1 μg and 2 μg) was recorded invasively. Two-way repeated measures ANOVA followed by Bonferroni post-hoc test was used to analyze the data. The systolic BP and diastolic BP of test groups rose to a higher level after DOCA administration and fell to the normal range (P < 0.05) following the administration of cleistanthins A and B. There were no differences in the weekly heart rate among the groups. In the test group animals pretreated with prazosin and cleistanthins, adrenaline, noradrenaline and dopamine failed to raise the mean arterial pressure and the end-diastolic pressure from baseline (P > 0.05) cleistanthins A and B exert a significant antihypertensive effect through alpha-adrenergic receptor blockade similar to prazosin.

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清肠素A和B抗高血压活性及α肾上腺素能受体相互作用的评价。
用醋酸脱氧皮质酮(DOCA)盐(20 mg/kg s.c),每周2次,连续4周诱导雄性Sprague Dawley大鼠高血压。将其分为8组,每组6只,分别为高血压对照组、标准组(吡唑嗪1 mg/kg)、清肠素A 12.5、25、50 mg/kg和清肠素B 12.5、25、50 mg/kg。另一组作为正常对照组。第4周诱导高血压,第5周给药。每周使用啮齿动物无创血压系统记录血压(BP)变化。实验结束时,有创记录肾上腺素、非肾上腺素、多巴胺(剂量分别为1 μg和2 μg)对α -肾上腺素能受体的反应。采用双向重复测量方差分析和Bonferroni事后检验对数据进行分析。各组患者的收缩压、舒张压均在给药后升高,在给药后降至正常范围(P < 0.05)。各组周心率差异无统计学意义。实验组动物经prazosin和clestanthins预处理后,肾上腺素、去甲肾上腺素和多巴胺均未能使平均动脉压和舒张末压较基线升高(P > 0.05), clestanthins A和B与prazosin类似通过阻断α -肾上腺素能受体发挥显著降压作用。
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