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关于γ-氨基丁酸(GABA)参与巴氯芬、蝇蕈醇和吗啡产生的镇痛作用。

On the involvement of GABA in the analgesia produced by baclofen, muscimol and morphine.

作者信息

Sawynok J, LaBella F S

出版信息

Neuropharmacology. 1982 May;21(5):397-403. doi: 10.1016/0028-3908(82)90022-3.

Abstract

In the mouse hot-plate test (50 degrees C), muscimol produced analgesia which was blocked by bicuculline but not by picrotoxin. Analgesia produced by baclofen was dose-dependent and stereoselective, but was not blocked by bicuculline, picrotoxin or naloxone. Morphine-induced analgesia was not altered by bicuculline. The inhibitors of GABA-transaminase, amino-oxyacetic acid, gamma-acetylenic GABA and gamma-vinyl GABA, produced analgesia which was much more prolonged than that observed with muscimol, baclofen or morphine. The analgesic action of these agents was not significantly altered by bicuculline. At a higher plate temperature (55 degrees C), GABA-transaminase inhibitors produced minimal analgesia but significantly enhanced the analgesic action of baclofen. gamma-Vinyl GABA markedly increased both the peak effect and the duration of analgesia but gamma-acetylenic GABA and amino-oxyacetic acid caused smaller increases. In the mouse hot-plate test, bicuculline-sensitive GABA receptors appear to mediate the analgesic action fo muscimol. Analgesia produced by baclofen, morphine and inhibitors of GABA-transaminase may involve another class of GABA receptors which are insensitive to bicuculline.

摘要

在小鼠热板试验(50摄氏度)中,蝇蕈醇产生的镇痛作用可被荷包牡丹碱阻断,但不能被印防己毒素阻断。巴氯芬产生的镇痛作用具有剂量依赖性和立体选择性,但不能被荷包牡丹碱、印防己毒素或纳洛酮阻断。吗啡诱导的镇痛作用不受荷包牡丹碱影响。γ-氨基丁酸转氨酶抑制剂,如氨基氧乙酸、γ-乙炔基氨基丁酸和γ-乙烯基氨基丁酸,产生的镇痛作用比蝇蕈醇、巴氯芬或吗啡观察到的作用持续时间长得多。这些药物的镇痛作用不受荷包牡丹碱的显著影响。在较高的热板温度(55摄氏度)下,γ-氨基丁酸转氨酶抑制剂产生的镇痛作用最小,但能显著增强巴氯芬的镇痛作用。γ-乙烯基氨基丁酸显著增加了镇痛的峰值效应和持续时间,但γ-乙炔基氨基丁酸和氨基氧乙酸引起的增加较小。在小鼠热板试验中,对荷包牡丹碱敏感的γ-氨基丁酸受体似乎介导了蝇蕈醇的镇痛作用。巴氯芬、吗啡和γ-氨基丁酸转氨酶抑制剂产生的镇痛作用可能涉及另一类对荷包牡丹碱不敏感的γ-氨基丁酸受体。

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