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首页> 外文期刊>European journal of drug metabolism and pharmacokinetics >Comparative study of effects of angiotensin II receptor antagonist, KD3-671, and angiotensin converting enzyme inhibitor, enalaprilat, on cough reflex in guinea pig.
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Comparative study of effects of angiotensin II receptor antagonist, KD3-671, and angiotensin converting enzyme inhibitor, enalaprilat, on cough reflex in guinea pig.

机译:血管紧张素Ⅱ受体拮抗剂KD3-671和血管紧张素转化酶抑制剂依那普利拉对豚鼠咳嗽反射影响的比较研究。

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Angiotensin converting enzyme (ACE) inhibitor prevents the inactivation of bradykinin by inhibiting ACE activity, leading to side effects such as dry cough and angioedema. KD3-671 is a novel nonpeptide angiotensin II antagonist which is expected to exhibit persistent hypotensive action without these side effects. In this study, we investigated the relationship between the pharmacokinetics and cough-inducing effect of this drug in guinea-pig, compared with that of an ACE inhibitor, enalaprilat. KD3-671 was not significantly different from the vehicle treatment in the ability to induce coughing, whereas enalaprilat significantly enhanced coughing compared with the vehicle treatment. Thus, as expected from its mechanism of pharmacological action, KD3-671 did not induce coughing. We suggest that the citric acid-induced guinea pig coughing model will be useful in preclinical studies to examine the effect of drug on pulmonary function.
机译:血管紧张素转换酶(ACE)抑制剂通过抑制ACE活性来防止缓激肽失活,从而导致诸如干咳和血管性水肿等副作用。 KD3-671是新型的非肽血管紧张素II拮抗剂,有望表现出持续的降压作用而没有这些副作用。在这项研究中,我们研究了该药物在豚鼠中的药代动力学与诱导咳嗽之间的关系,与ACE抑制剂依那普利拉相比。 KD3-671在诱导咳嗽的能力方面与媒介物治疗没有显着差异,而依那普利拉则与媒介物治疗相比明显增强了咳嗽。因此,如从其药理作用机理所预期的那样,KD3-671不会引起咳嗽。我们建议柠檬酸诱导的豚鼠咳嗽模型将在临床前研究中有用,以检查药物对肺功能的影响。

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