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首页> 外文期刊>Research in Pharmaceutical Sciences >Effects of lisinopril, captopril and losartan alone or in combination with morphine in light tail flick analgesic test
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Effects of lisinopril, captopril and losartan alone or in combination with morphine in light tail flick analgesic test

机译:赖诺普利,卡托普利和氯沙坦单独使用或与吗啡合用在轻尾甩打镇痛试验中的作用

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摘要

There are controversial reports about the effect of captopril on pain modulation. Also while captopril may potentiate morphine analgesia, enalapril has not such an effect and interaction of morphine with angiotensin II receptor antagonists and other angiotensin converting enzyme inhibitors has not been studied yet. Therefore, this study was designed to assess the effect of captopril, lisinopril and losartan on pain sensation and the possible modifying effect of these drugs on morphine antinociception. Male Swiss mice (25-35 g) in groups of 6 animals per each received vehicle (10 ml/kg), captopril (20 mg/kg), lisinopril (10 mg/kg) and losartan (10 mg/kg) alone or in combination with morphine (5 mg/kg, i.p.) and analgesic response was assessed using light tail flick test. Reaction latencies to a light beam were recorded at 15 minute intervals until 2 hours. The maximum possible analgesic effect was calculated and compared. Lisinopril and captopril when administered alone could not change the pain response but losartan per se induced a hyperalgesic state. Pretreatment with captopril potentiated morphine analgesic response and losartan and lisinopril did not modify morphine analgesia. It is concluded that although angiotensin converting enzyme inhibitors have the same mechanism of action on renin-angiotensin system but they do not have the same interaction with morphine. Also since losartan, an antagonist of angiotensin receptor type 1 did not alter morphine response, it seems that these receptors are not involved in captopril potentiation of morphine analgesia.
机译:关于卡托普利对疼痛调节的作用有争议的报道。同样,尽管卡托普利可以增强吗啡镇痛作用,但依那普利没有这种作用,并且尚未研究吗啡与血管紧张素II受体拮抗剂和其他血管紧张素转化酶抑制剂的相互作用。因此,本研究旨在评估卡托普利,赖诺普利和氯沙坦对疼痛感的作用以及这些药物对吗啡抗伤害感受的可能的调节作用。每只接受的媒介物(10 ml / kg),卡托普利(20 mg / kg),赖诺普利(10 mg / kg)和氯沙坦(10 mg / kg)的雄性Swiss小鼠(25-35 g)每组6只动物,或与吗啡(5 mg / kg,腹膜内)联合使用,使用轻尾甩尾试验评估镇痛反应。以15分钟的间隔记录对光束的反应潜伏期,直到2小时。计算并比较了最大可能的止痛效果。单独使用时,利诺普利和卡托普利不能改变疼痛反应,但氯沙坦本身会引起痛觉过敏状态。卡托普利增强的吗啡镇痛反应以及氯沙坦和赖诺普利的预处理未改变吗啡镇痛作用。结论是,尽管血管紧张素转化酶抑制剂对肾素-血管紧张素系统具有相同的作用机理,但它们与吗啡的相互作用并不相同。同样,由于1型血管紧张素受体的拮抗剂氯沙坦不会改变吗啡反应,因此似乎这些受体不参与吗啡镇痛的卡托普利增强作用。

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