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首页> 外文期刊>Japanese Journal of Pharmacology >MODIFICATIONS OF RESPONSES TO ADRENERGIC DRUGS IN ARTERIAL STRIPS BY TREATMENT IN VIVO WITH EPHEDRINE AND RESERPINE
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MODIFICATIONS OF RESPONSES TO ADRENERGIC DRUGS IN ARTERIAL STRIPS BY TREATMENT IN VIVO WITH EPHEDRINE AND RESERPINE

机译:上皮肾上腺素和利血平在体内对动脉带中抗肾上腺皮质药物的反应的改变

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摘要

References(42) The aim of the present experiment was to investigate effects of ephedrine and reserpine, administered in vivo, on responses of dog isolated arterial strips to adrenergic drugs, and to study a possible mechanism involved in the reversal of blood pressure responses to dopamine. Dose-dependent contractile responses to adrenaline (A), dopamine (DA) and ephedrine (ED) were depressed in the femoral strips isolated from the ED-treated dogs as compared with those isolated from the untreated dogs. Those to noradrenaline (NA) were potentiated in low concentration and inhibited in high concentration, though those to tyramine (TY) were not altered. Relaxing and contractile responses to isoprenaline (IP) were inhibited. DA did not induce a relaxing effect but a contractile one even in the strips brought to a state of moderate tone with ED or phelypressin. In the strips isolated from the reserpine-treated dogs, contractile responses were to some extent potentiated by NA, A and DA, and significantly by ED, while those to TY were inhibited. Relaxing responses to IP were reduced and contractile responses potentiated. In the strips extirpated from the reserpine and ED-treated dogs, contractile responses to NA and A were potentiated in low concentration and inhibited in high concentration. Those to TY were inhibited in low concentration and tended to be potentiated in high concentration whereas those to DA and ED were not affected. Dose-dependent relaxing effects of DA in the dog renal and mesenteric strips contracted previously by KCl after phenoxy-benzamine were attenuated by treatment with ephedrine in vivo. The results suggested that the dopamine reversal in the blood pressure may be mainly due to actions other than its peripheral effect on the blood vessels.
机译:参考文献(42),本实验的目的是研究体内施用的麻黄碱和利血平对狗分离的动脉条对肾上腺素药物的反应的影响,并研究与多巴胺引起的血压反应逆转有关的可能机制。与未经治疗的狗相比,从经ED治疗的狗分离出的股骨条中,对肾上腺素(A),多巴胺(DA)和麻黄碱(ED)的剂量依赖性收缩反应得到抑制。去甲肾上腺素(NA)的那些在低浓度下被增强,而在高浓度下被抑制,而酪胺(TY)的那些未改变。对异丙肾上腺素(IP)的松弛和收缩反应被抑制。 DA不会引起松弛作用,但是即使在条带中,收缩性的作用也使ED或苯丙氨酸加压素达到中度状态。从利血平治疗的狗中分离出的条带中,NA,A和DA在一定程度上增强了收缩反应,而ED则显着增强,而对TY的收缩反应则受到抑制。对IP的放松反应减少,收缩反应增强。从利血平和ED处理的狗中去除的条带中,对NA和A的收缩反应在低浓度下增强而在高浓度下受到抑制。 TY的那些在低浓度时受到抑制,高浓度时趋于增强,而DA和ED的那些不受影响。在体内用麻黄碱治疗后,苯氧基-苯扎明使KCl收缩的狗肾和肠系膜条中DA的剂量依赖性舒张作用。结果表明,血压中的多巴胺逆转可能主要是由于其对血管的外围作用以外的其他作用。

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