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吗啡与一种新的α2-肾上腺素受体激动剂在小鼠体内的相互作用。

Interaction of morphine with a new alpha2-adrenoceptor agonist in mice.

机构信息

Programa de Desenvolvimento de Fármacos, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Brazil.

出版信息

J Pain. 2010 Jan;11(1):71-8. doi: 10.1016/j.jpain.2009.08.001. Epub 2009 Oct 22.

Abstract

UNLABELLED

Finding new chemicals or adjuvants with analgesic effects in the central nervous system is clinically relevant due to the limited number of drugs with these properties. Here, we present PT-31, which is chemically related to 3-benzyl-imidazolidine, with an analgesic profile that results from alpha(2)-adrenoceptor activation. Intraperitoneal administration of PT-31 dose-dependently produced antinociception in the hot plate test, and interacted synergistically with morphine. This effect was completely reversed by yohimbine, a non-selective antagonist of alpha(2)-adrenoceptors, and by BRL 44408, a selective alpha(2A)-adrenoceptor antagonist. The combination of morphine and PT-31 produced greater antinociceptive activity than either alone, and isobolographic analysis revealed a synergistic interaction between these compounds. Docking results confirm the high affinity of the PT-31 ligand at the alpha(2A)-adrenoceptor.

PERSPECTIVE

This study introduces a new analgesic compound (PT-31) that acts via alpha(2A)-adrenoceptor activation. A significant increase in analgesia was observed when co-administered with morphine. PT-31 is an interesting new substance for pain therapy.

摘要

未标记

由于具有这些特性的药物数量有限,因此在中枢神经系统中寻找具有镇痛作用的新化学物质或佐剂在临床上具有重要意义。在这里,我们介绍了 PT-31,它在化学上与 3-苄基-咪唑烷有关,其镇痛作用是通过 α2-肾上腺素受体激活产生的。PT-31 腹腔给药剂量依赖性地产生热板试验中的镇痛作用,并与吗啡产生协同作用。这种作用被非选择性 α2-肾上腺素受体拮抗剂育亨宾和选择性 α2A-肾上腺素受体拮抗剂 BRL 44408 完全逆转。吗啡和 PT-31 的联合使用产生的镇痛作用大于单独使用任何一种药物,等辐射分析显示这些化合物之间存在协同相互作用。对接结果证实了 PT-31 配体与 α2A-肾上腺素受体的高亲和力。

观点

本研究介绍了一种通过 α2A-肾上腺素受体激活起作用的新型镇痛化合物(PT-31)。当与吗啡联合使用时,观察到镇痛作用显著增加。PT-31 是一种用于疼痛治疗的有趣的新型物质。

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