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对一种结构上与肼屈嗪相关的新型抗高血压药物恩屈嗪在大鼠身上进行的研究。

Studies in the rat on endralazine, a new antihypertensive drug structurally related to hydralazine.

作者信息

Oates H F, Stoker L M

出版信息

Clin Exp Pharmacol Physiol. 1981 Mar-Apr;8(2):133-9. doi: 10.1111/j.1440-1681.1981.tb00144.x.

Abstract
  1. The effects on blood pressure, heart rate and plasma renin activity of a new hydralazine congener, endralazine, were evaluated in anaesthetized rats. Dose-response relationships for endralazine, hydralazine and diazoxide, administered intravenously, were compared, and the interactions of endralazine with the ganglionic blocking agent, pentolinium, or with adrenaline, noradrenaline and angiotensin II were examined. 2. In the dose range 0.05 to 1.0 mg/kg, endralazine produced prompt dose-related reductions in systolic and diastolic blood pressure, with relatively little effect on heart rate. The drug had a pronounced dose-related renin stimulating effect. 3. Endralazine retained approximately 80% of its hypotensive activity after pretreatment with pentolinium, and caused no significant attenuation of pressor responses to adrenaline, noradrenaline or angiotensin II. 4. Endralazine was an effective hypotensive agent, with a prompt onset of action, a prolonged and stable effect, and a potency at least twice that of hydralazine and 20 to 25 times that of diazoxide. The data are consistent with a predominantly direct vasodilator mode of action.
摘要
  1. 在麻醉大鼠中评估了一种新型肼屈嗪同类物恩屈嗪对血压、心率和血浆肾素活性的影响。比较了静脉注射恩屈嗪、肼屈嗪和二氮嗪的剂量-反应关系,并研究了恩屈嗪与神经节阻断剂潘托铵或与肾上腺素、去甲肾上腺素和血管紧张素II的相互作用。2. 在0.05至1.0mg/kg的剂量范围内,恩屈嗪可迅速产生与剂量相关的收缩压和舒张压降低,对心率影响相对较小。该药物具有明显的与剂量相关的肾素刺激作用。3. 用潘托铵预处理后,恩屈嗪保留了约80%的降压活性,且对肾上腺素、去甲肾上腺素或血管紧张素II的升压反应无明显减弱。4. 恩屈嗪是一种有效的降压药,起效迅速,作用持久且稳定,效力至少是肼屈嗪的两倍,是二氮嗪的20至25倍。数据与主要为直接血管舒张作用模式一致。

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