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[阿片类拮抗剂在实验性创伤性休克中的作用机制]

[The mechanism of action of opiate antagonists in experimental traumatic shock].

作者信息

Sherman D M, Mikuliak I V, Kolomiĭtsev V I

出版信息

Farmakol Toksikol. 1990 Mar-Apr;53(2):64-6.

PMID:2369960
Abstract

Acute experiments on 86 adult rabbits have shown that in the early period of Cannon's traumatic shock nalophine and naloxone relieve torpidity, restore motor activity and responses to standard stimuli. This prolongs the animal life (nalorphine) and increases the survivability (naloxone). However in some rabbits a premature relief of torpidity (0.5 mg/kg of nalorphine) precipitates the animal death. It is concluded that in the late period the drugs exert no effect on the shock outcome and that inactivation of opioid suppression system can either trigger the mechanism of shock withdrawal or promote a reduction of its severity.

摘要

对86只成年兔子进行的急性实验表明,在坎农创伤性休克的早期,纳洛芬和纳洛酮可缓解迟钝状态,恢复运动活性以及对标准刺激的反应。这可延长动物的存活时间(纳洛芬)并提高存活率(纳洛酮)。然而,在一些兔子中,过早缓解迟钝状态(0.5毫克/千克纳洛芬)会促使动物死亡。得出的结论是,在后期这些药物对休克结局没有影响,并且阿片样物质抑制系统的失活既可以触发休克消退机制,也可以促进减轻其严重程度。

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