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[阿片受体激动剂和拮抗剂对动物耐低氧性缺氧的影响]

[Effect of opiate receptor agonists and antagonists on the resistance of animals to hypoxic hypoxia].

作者信息

Zakusov V V, Iasnetsov V V, Ostrovskaia R U, Chukaev V V, Motin V G

出版信息

Biull Eksp Biol Med. 1984 Dec;98(12):680-2.

PMID:6095953
Abstract

The effects of morphine, a series of synthetic enkephalin analogs and antagonists of narcotic analgesics on the animals' survival rate under hypoxic hypoxia were studied in experiments on mice, rabbits, and cats. It was shown that the agonists of mu-opiate receptors, morphine, FK 33-824 (Tyr-D-Ala-Gly-MePhe-Met-(O)-ol, Tyr-D-Ala-Gly-Phe-(NO2)-NH2 and Tyr-D-Ala-Gly-MePhe-Gly-ol increase the survival rate in a hermetic chamber and that this effect is arrested by naloxone, nalorphine, and TRH. Tyr-D-Ala-Gly-D-Leu, an agonist of delta-opiate receptors has no antihypoxic properties. The data obtained point to the involvement of opiate receptors (at least of those of the mu-type) in realization of the reactions that increase the resistance to hypoxia. Bicuculline was shown to be able to remove the antihypoxic effect of the agonists of opiate receptors, suggesting the GABAergic modulation of this effect.

摘要

在小鼠、兔子和猫身上进行的实验研究了吗啡、一系列合成脑啡肽类似物以及麻醉性镇痛药拮抗剂对动物在低氧性缺氧条件下存活率的影响。结果表明,μ-阿片受体激动剂吗啡、FK 33-824(酪氨酰-D-丙氨酰-甘氨酰-甲硫苯丙氨酰-甲硫氨酸-(O)-醇)、酪氨酰-D-丙氨酰-甘氨酰-苯丙氨酸-(NO₂)-NH₂和酪氨酰-D-丙氨酰-甘氨酰-甲硫苯丙氨酰-甘氨醇可提高密闭舱内的存活率,且这种作用可被纳洛酮、烯丙吗啡和促甲状腺激素阻断。δ-阿片受体激动剂酪氨酰-D-丙氨酰-甘氨酰-D-亮氨酸没有抗缺氧特性。所获数据表明阿片受体(至少是μ型受体)参与了增强对缺氧抵抗力反应的实现。已证明荷包牡丹碱能够消除阿片受体激动剂的抗缺氧作用,提示该作用存在γ-氨基丁酸能调节。

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