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首页> 外文期刊>Japanese Journal of Pharmacology >The Possible Involvement of GABAA Systems in the Antinarcotic Effect of Majonoside-R2, a Major Constituent of Vietnamese Ginseng, in Mice
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The Possible Involvement of GABAA Systems in the Antinarcotic Effect of Majonoside-R2, a Major Constituent of Vietnamese Ginseng, in Mice

机译:GABAA系统可能参与了越南人参主要成分Majonoside-R2的抗麻醉作用

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References(13) Cited-By(7) The effect of majonoside-R2 on morphine and U-50, 488H-induced antinociception was examined by the tail-pinch test in mice and compared with that of diazepam. Majonoside-R2 and diazepam inhibited the morphine and U-50, 488H-induced antinociception, and the actions were antagonized by the benzodiazepine receptor antagonist flumazenil and the GABA-gated Cl- channel blocker picrotoxin. Diazepam but not majonoside-R2 exhibited a protective activity against convulsion caused by the GABAA antagonists bicuculline and picrotoxin. These results indicate that GABAA systems are involved in the effect of majonoside-R2 on the opioid-induced antinociception and suggest that the mechanisms of action of majonoside-R2 may differ from those of diazepam.
机译:参考文献(13)引用了(7)鼠尾苷R2对吗啡和U-50、488H诱导的镇痛作用在小鼠中进行了尾捏试验,并与地西epa进行了比较。 Majonoside-R2和地西epa抑制吗啡和U-50、488H诱导的抗伤害感受,苯二氮卓受体拮抗剂氟马西尼和GABA门控的Cl通道阻滞剂微毒素拮抗作用。地西p,而不是马洛糖苷-R2,对由GABAA拮抗剂双小分子和苦瓜毒素引起的惊厥具有保护作用。这些结果表明,GABAA系统参与了majonoside-R2对阿片样物质诱导的抗伤害感受的作用,并表明majonoside-R2的作用机制可能与地西epa不同。

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