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κ-激动剂布马佐辛的呼吸抑制和镇痛作用的比较研究

A comparative study of the respiratory depressant and analgesic effects of bremazocine, a kappa-agonist.

作者信息

Pazos A, Tristán C, Flórez J

出版信息

Life Sci. 1983;33 Suppl 1:579-81. doi: 10.1016/0024-3205(83)90569-6.

Abstract

The respiratory depression and analgesia induced by a kappa-agonist, bremazocine, were studied by the ED50 ratios and the apparent pA2 values of the interaction with naloxone. The ratio between the ED50 in respiratory depression and analgesia (i.c.v.) was very high compared to that of other mu- and delta-agonists, indicating its small activity on the respiratory center. pA2 values were 7.33 and 7.20 for analgesia and respiratory depression, respectively, after i.c.v. administration. After s.c. injection, the pA2 value for analgesia was 6.16. The results confirm the involvement of different opiate receptors in the mediation of supraspinal and spinal analgesia. The results suggest that bremazocine may induce analgesia by interacting with different types of receptors located at different levels of the CNS. This property and the low activity on the respiratory center make drugs like bremazocine good candidates in the search for safer opiate analgesics.

摘要

通过ED50比值以及与纳洛酮相互作用的表观pA2值,研究了κ-激动剂布瑞马佐辛诱导的呼吸抑制和镇痛作用。与其他μ-和δ-激动剂相比,布瑞马佐辛在呼吸抑制和镇痛(脑室内给药)方面的ED50比值非常高,表明其对呼吸中枢的活性较小。脑室内给药后,镇痛和呼吸抑制的pA2值分别为7.33和7.20。皮下注射后,镇痛的pA2值为6.16。结果证实了不同阿片受体参与了脊髓上和脊髓镇痛的介导。结果表明,布瑞马佐辛可能通过与位于中枢神经系统不同水平的不同类型受体相互作用而诱导镇痛。这种特性以及对呼吸中枢的低活性使得像布瑞马佐辛这样的药物成为寻找更安全阿片类镇痛药的良好候选药物。

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