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首页> 外文期刊>Journal of Ginseng Research >Morphine dependence is attenuated by red ginseng extract and ginsenosides Rh2, Rg3, and compound K
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Morphine dependence is attenuated by red ginseng extract and ginsenosides Rh2, Rg3, and compound K

机译:红参提取物和人参皂苷Rh2,Rg3和化合物K减弱了吗啡依赖性

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Background Red ginseng and ginsenosides have shown plethoric effects against various ailments. However, little is known regarding the effect of red ginseng on morphine-induced dependence and tolerance. We therefore investigated the effect of red ginseng extract (RGE) and biotransformed ginsenosides Rh2, Rg3, and compound K on morphine-induced dependence in mice and rats. Methods While mice were pretreated with RGE and then morphine was injected intraperitoneally, rats were infused with ginsenosides and morphine intracranially for 7 days. Naloxone-induced morphine withdrawal syndrome was estimated and conditioned place preference test was performed for physical and psychological dependence, respectively. Western blotting was used to measure protein expressions. Results Whereas RGE inhibited the number of naloxone-precipitated jumps and reduced conditioned place preference score, it restored the level of glutathione in mice. Likewise, ginsenosides Rh2, Rg3, and compound K attenuated morphine-dependent behavioral patterns such as teeth chattering, grooming, wet-dog shake, and escape behavior in rats. Moreover, activated N-methyl-D-aspartate acid receptor subunit 1 and extracellular signal-regulated kinase in the frontal cortex of rats, and cultured cortical neurons from mice were downregulated by ginsenosides Rh2, Rg3, and compound K despite their differential effects. Conclusion RGE and biotransformed ginsenosides could be considered as potential therapeutic agents against morphine-induced dependence. Keywords: biotransformation, ginsenosides, morphine dependence, red ginseng extract.
机译:背景红参和人参皂苷已显示出对多种疾病的多效作用。但是,关于红参对吗啡诱导的依赖性和耐受性的影响知之甚少。因此,我们研究了红参提取物(RGE)和生物转化人参皂甙Rh2,Rg3和化合物K对吗啡诱导的小鼠和大鼠依赖性的作用。方法用RGE预处理小鼠,然后腹腔注射吗啡,然后给大鼠颅内注射人参皂甙和吗啡7天。估计了纳洛酮诱发的吗啡戒断综合征,并分别针对身体和心理依赖性进行了条件场所偏爱测试。蛋白质印迹法用于测量蛋白质表达。结果尽管RGE抑制了纳洛酮沉淀的跳跃次数并降低了条件位置偏爱评分,但它恢复了小鼠中的谷胱甘肽水平。同样,人参皂甙Rh2,Rg3和化合物K减弱了吗啡依赖性的行为模式,例如大鼠的牙齿颤动,修饰,湿狗摇动和逃逸行为。此外,人参皂苷Rh2,Rg3和化合物K尽管有不同的作用,但在大鼠额叶皮层中激活的N-甲基-D-天冬氨酸酸受体亚基1和细胞外信号调节激酶以及小鼠培养的皮质神经元均被下调。结论RGE和生物转化的人参皂苷可被视为对抗吗啡诱导的依赖性的潜在治疗剂。关键词:生物转化人参皂苷吗啡依赖红参提取物

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