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强效阿片肽 AM94 的抗伤害感受特性,其为具有非肼连接基团的二肽啡肽的氟化类似物。

Antinociceptive profile of potent opioid peptide AM94, a fluorinated analogue of biphalin with non-hydrazine linker.

机构信息

Dipartimento di Farmacia, Università di Chieti-Pescara G. d'Annunzio, Chieti, Italy.

出版信息

J Pept Sci. 2013 Apr;19(4):233-9. doi: 10.1002/psc.2465. Epub 2012 Nov 8.

Abstract

AM94 is a fluorinated analog of biphalin with non-hydrazine linker that has an in vitro affinity for μ-opioid and δ-opioid receptors tenfold higher than biphalin. Furthermore, in vivo evaluation in rats showed that AM94 has in hot plate test - after both intracerebroventricular and intravenous administrations - a greater and more durable efficacy than biphalin. Here, the antinociceptive profile of AM94 is further evaluated by following two different administration routes, intrathecal and subcutaneous, and two different animal species, rats and mice. The analgesic potency of AM94 is compared with that of both the parent peptide biphalin and morphine. Results show that in rats (tail flick test) and in mice (formalin test), AM94 has a higher and more durable analgesic effect than biphalin after intrathecal and subcutaneous administrations. Conformational properties of biphalin and AM94 were also investigated by variable-temperature (1)H NMR and energy minimization.

摘要

AM94 是一种氟代双啡烷类似物,具有非肼连接子,其对 μ-阿片受体和 δ-阿片受体的体外亲和力比双啡烷高十倍。此外,在大鼠体内评估表明,AM94 在热板试验中——无论是鞘内还是静脉给药后——比双啡烷具有更大和更持久的疗效。在这里,通过以下两种不同的给药途径(鞘内和皮下)和两种不同的动物物种(大鼠和小鼠)进一步评估了 AM94 的镇痛特征。比较了 AM94 的镇痛效力与母体肽双啡烷和吗啡的镇痛效力。结果表明,在大鼠(尾巴闪烁试验)和小鼠(福尔马林试验)中,鞘内和皮下给药后,AM94 的镇痛效果比双啡烷更高、更持久。还通过变温(1)H NMR 和能量最小化研究了双啡烷和 AM94 的构象特性。

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