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氨氯地平的镇痛作用及其与吗啡和酮咯酸诱导镇痛的相互作用。

Analgesic effects of amlodipine and its interaction with morphine and ketorolac-induced analgesia.

作者信息

Doğrul A, Yeşilyurt O, Deniz G, Işimer A

机构信息

Department of Pharmacology, Faculty of Medicine, Gülhane Medical Military Academy, Ankara, Turkey.

出版信息

Gen Pharmacol. 1997 Nov;29(5):839-45. doi: 10.1016/s0306-3623(97)00003-7.

Abstract
  1. The antinociceptive effects of amlodipine, administered subcutaneously (s.c.), intracerebroventricularly (i.c.v.) and intrathecally (i.t.) were examined with the acetic acid writhing and tail-flick tests in mice. Amlodipine was also tested in combination with morphine and ketorolac. Isobolographic analyses were used to define the nature of functional interactions between amlodipine and morphine or ketorolac. 2. The s.c. (0.1, 1.25, 2.5, 5 and 10 mg/kg), i.c.v. (2.5, 5, 10 and 20 micrograms/mice) and i.t. (2.5, 5, 10 and 20 micrograms/mice) administration of amlodipine exhibited a dose-dependent antinociceptive effect in the writhing test but had no effect on the tail-flick latency. Isobolographic analyses revealed an additive interaction between amlodipine and morphine or ketorolac in the writhing test. 3. These results suggest that amlodipine induces antinociception and increases antinociceptive action of morphine and ketorolac, possibly through a decrease in cellular calcium availability.
摘要
  1. 通过小鼠醋酸扭体试验和甩尾试验,研究了皮下(s.c.)、脑室内(i.c.v.)和鞘内(i.t.)注射氨氯地平的抗伤害感受作用。氨氯地平还与吗啡和酮咯酸联合进行了测试。采用等效应线图分析来确定氨氯地平与吗啡或酮咯酸之间功能相互作用的性质。2. 皮下注射(0.1、1.25、2.5、5和10 mg/kg)、脑室内注射(2.5、5、10和20微克/只小鼠)和鞘内注射(2.5、5、10和20微克/只小鼠)氨氯地平在扭体试验中呈现剂量依赖性抗伤害感受作用,但对甩尾潜伏期无影响。等效应线图分析显示在扭体试验中氨氯地平与吗啡或酮咯酸之间存在相加相互作用。3. 这些结果表明,氨氯地平诱导抗伤害感受,并增强吗啡和酮咯酸的抗伤害感受作用,可能是通过降低细胞内钙的可利用性实现的。

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