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[γ-氨基丁酸能物质对大鼠吗啡镇痛作用的影响]

[Effect of GABA-ergic substances on the analgesic effect of morphine in rats].

作者信息

Ostrovskaia R U, Bulaev V M

出版信息

Biull Eksp Biol Med. 1979 Jul;88(7):35-7.

PMID:380685
Abstract

The effect of GABA-ergic compounds on morphine-induced analgesia was studied to reveal probable interaction of GABA and opiates. As an index for morphine effect the reaction of vocalization in response to electrical stimulation of the rat tail was used. It was shown that thiosemicarbazide, the inhibitor of glutamate decarboxylase and bicuculline, GABA-ergic receptor blocking agent, which were proposed to be joined in a group of GABA-negative compounds, reduce and shorten the effect of morphine. Depakine, the inhibitor of alpha-ketoglutarate-GABA-transaminase, as well as GABA itself administered in high doses (GABA-positive actions) make morphine analgesia more pronounced and longer. Probable causes of the described interrelationship between GABA and opiates are discussed.

摘要

研究了γ-氨基丁酸(GABA)能化合物对吗啡诱导镇痛的影响,以揭示GABA与阿片类药物之间可能的相互作用。作为吗啡作用的指标,采用了大鼠尾巴电刺激引起的发声反应。结果表明,硫代氨基脲(谷氨酸脱羧酶抑制剂)和荷包牡丹碱(GABA能受体阻断剂,它们被认为属于GABA阴性化合物组)可降低并缩短吗啡的作用。丙戊酸(α-酮戊二酸-GABA转氨酶抑制剂)以及高剂量给予的GABA本身(GABA阳性作用)可使吗啡镇痛作用更明显且持续时间更长。文中讨论了GABA与阿片类药物之间上述相互关系的可能原因。

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