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Antinociceptive Effects of Ginsenoside Rg3 in a Rat Model of Incisional Pain

机译:人参皂苷Rg3在切口痛大鼠模型中的镇痛作用

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Background: Ginsenoside Rg3 is an extract of total ginseng saponins, which accounts for 4.7% of all saponins. This study aimed to identify the mechanisms of the antinociceptive effects of ginsenoside Rg3. Methods: Rats were randomly divided into six groups, which were treated with vehicle or 0.5, 1, 1.5, 2, or 4 mg/kg of ginsenoside Rg3 intraperitoneally 2 h after a plantar incision was made. To evaluate the mechanisms of antinociceptive effects, the rats were intraperitoneally injected with naloxone 5 mg/kg, atropine 1 mg/kg, yohimbine 2 mg/kg, mecamylamine 1 mg/kg, prazosin 1 mg/kg, and dexmedetomidine 5 mu g/kg. Hyperalgesia produced by the plantar incision was assessed using von Frey filaments 1 day before the incision (BI) and 2 h after the plantar incision (AP); this measurement was repeated at 15, 30, 45, 60, 80, 100 and 120 min, and 24 and 48 h after the injection of ginsenoside Rg3. Serum interleukin-1 beta (IL-1 beta) and interleukin-6 (IL-6) levels were measured 1 day before incision and 120 min, 24 h, and 48 h after the injection of ginsenoside Rg3 or vehicle. Results: The mechanical withdrawal threshold (MWT) significantly increased in the group that received ginsenoside Rg3. The dose-MWT response showed a curvilinear, bell-shaped relationship. The maximum MWT was found with the administration of ginsenoside Rg3 at 1.5 mg/kg; MWT decreased to 2 and 4 mg/kg. Yohimbine diminished the analgesic effect of ginsenoside Rg3. Prazosin and dexmedetomidine increased the analgesic effect of ginsenoside Rg3. IL-1 beta and IL-6 appeared significantly lower relative to control group. Conclusions: Ginsenoside Rg3 has an analgesic effect with a curvilinear dose-response relationship. Alpha 2 adrenergic receptor appeared to be related to the analgesic effect of ginsenoside Rg3. Also, the anti-inflammatory effect of ginsenoside Rg3 could be related to its analgesic effect. (C) 2016 S. Karger AG, Basel
机译:背景:人参皂苷Rg3是人参总皂苷的提取物,占所有皂苷的4.7%。这项研究旨在确定人参皂苷Rg3的抗伤害感受机制。方法:将大鼠随机分为六组,分别在足底切开后2 h腹腔内施用媒介物或0.5、1、1.5、2或4 mg / kg人参皂苷Rg3。为了评估抗伤害作用的机制,给大鼠腹膜内注射纳洛酮5 mg / kg,阿托品1 mg / kg,育亨宾2 mg / kg,美加明胺1 mg / kg,哌唑嗪1 mg / kg和右美托咪定5μg / kg。公斤。切口前1天(BI)和the切口(AP)后2 h使用von Frey丝评估足底切口产生的痛觉过敏。注射人参皂苷Rg3后15、30、45、60、80、100和120分钟,24和48小时重复此测量。在切开前1天以及注射人参皂苷Rg3或赋形剂后120分钟,24小时和48小时,测量血清白细胞介素1β(IL-1 beta)和白细胞介素6(IL-6)的水平。结果:接受人参皂苷Rg3的组的机械退缩阈值(MWT)显着增加。剂量-MWT反应显示出曲线的钟形关系。人参皂苷Rg3的剂量为1.5 mg / kg时发现最大的MWT。 MWT降至2和4 mg / kg。育亨宾减弱了人参皂苷Rg3的镇痛作用。哌唑嗪和右美托咪定可增强人参皂苷Rg3的镇痛作用。相对于对照组,IL-1β和IL-6明显降低。结论:人参皂苷Rg3具有止痛作用,且具有曲线剂量反应关系。 Alpha 2肾上腺素受体似乎与人参皂苷Rg3的镇痛作用有关。此外,人参皂苷Rg3的抗炎作用可能与其镇痛作用有关。 (C)2016 S.Karger AG,巴塞尔

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