...
首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Crude saponin extracted from Vietnamese ginseng and its major constituent majonoside-R2 attenuate the psychological stress- and foot-shock stress-induced antinociception in mice.
【24h】

Crude saponin extracted from Vietnamese ginseng and its major constituent majonoside-R2 attenuate the psychological stress- and foot-shock stress-induced antinociception in mice.

机译:从越南人参中提取的粗皂苷及其主要成分majonoside-R2可减轻小鼠的心理应激和足部震荡引起的抗伤害感受。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Effects of Vietnamese ginseng (VG) crude saponin and majonoside-R2, a major saponin constituent, on the psychological stress- and foot shock stress-induced antinociception in the tail pinch test were examined in mice. VG crude saponin (6.2, 12.5, and 25 mg/kg, P.O.) attenuated psychological stress- but not foot shock stress-induced antinociceptive response, whereas majonoside-R2 (3, 6.2, and 12.5 mg/kg, P.O. and i.p.), as well as naloxone (2 mg/kg, i.p.), suppressed both psychological stress- and foot shock stress-induced antinociception. Pretreatment with the crude saponin (12.5 mg/kg, P.O.) or majonoside-R2 (6.2 mg/kg, P.O.) for 5 days followed by the treatment in combination with stress for next 5 days did not affect the development of adaptation to foot shock stress, but they significantly suppressed the antinociceptive action of the stress measured on the first, second, and third day during the stress exposure period. Majonoside-R2 (6.2 mg/kg, P.O.) but not the crude saponin (12.5 mg/kg, P.O.) significantly blocked the development of adaptation to psychological stress. These results suggest that VG crude saponin has the suppressing effect on psychological stress- and foot shock stress-induced antinociception and that majonoside-R2 is important for the action of the saponin.
机译:在小鼠的尾巴捏合试验中,研究了越南人参粗皂苷和主要皂苷成分majonoside-R2对心理应激和足部休克应激诱导的抗伤害感受的影响。 VG粗皂苷(6.2、12.5和25 mg / kg,PO)减轻了心理压力,但并未减弱足部休克压力引起的抗伤害感受反应,而majonoside-R2(3、6.2和12.5 mg / kg,PO和ip),以及纳洛酮(2 mg / kg,腹腔注射)抑制了心理压力和脚底冲击压力引起的抗伤害感受。用粗皂苷(12.5 mg / kg,PO)或majonoside-R2(6.2 mg / kg,PO)预处理5天,然后再与压力相结合进行接下来5天的治疗,不会影响对足部休克的适应压力,但它们显着抑制了在压力暴露期间第一天,第二天和第三天测得的压力的镇痛作用。 Majonoside-R2(6.2 mg / kg,P.O.)而非粗皂苷(12.5 mg / kg,P.O.)显着阻碍了对心理压力的适应性发展。这些结果表明,VG粗皂苷对心理应激和足部休克应激诱导的抗伤害感受具有抑制作用,而魔芋皂苷R2对皂苷的作用很重要。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号