首页> 外文期刊>The American journal of Chinese medicine >A Chinese Herbal Decoction, Shaoyao-Gancao Tang, Exerts Analgesic Effect by Down-Regulating the TRPV1 Channel in a Rat Model of Arthritic Pain
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A Chinese Herbal Decoction, Shaoyao-Gancao Tang, Exerts Analgesic Effect by Down-Regulating the TRPV1 Channel in a Rat Model of Arthritic Pain

机译:中药汤少药-甘草汤通过下调关节炎大鼠模型的TRPV1通道发挥镇痛作用

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Shaoyao-Gancao Tang (SGT) is one of the most frequently used compound formulas in the treatment of pain-related diseases in the medical practice of traditional Chinese medicine (TCM). To investigate the anti-inflammatory and antinociceptive effects, as well as to uncover the molecular mechanism of SGT, the rat pain model of arthritis was experimentally induced by single unilateral injection of rats' left hind paw with Freund's complete adjuvant (FCA). SGT was orally administered to the rats daily at three doses individually for a period of 16 days post-model induction. Swollen degrees and pain thresholds of the rats in different groups were measured for evaluation of the anti-inflammatory and anti-nociceptive effects of SGT. Furthermore, the mRNA and protein expression levels of transient receptor potential ion channel protein vanilloid receptor 1 (TRPV1) channel as well as its calcium-mediating function in the isolated DRG neurons were further detected to provide indexes for exploration of the molecular mechanisms mediating anti-arthritic activities of SGT. As a result, FCA injection induced significant allodynia, inflammation and edema, accompanied by a significant increase in both expression and calcium-mediating function of the TRPV1 channel. Pharmacologically, oral administration of SGT at a high or middle dose demonstrated a significant relief from the above-mentioned pathological conditions in a dose-dependent manner. Simultaneously the mRNA and protein expressional levels of TRPV1 channel, as well as its calcium-mediating function, were down-regulated greatly. These findings suggest that SGT possesses a significant analgesic and anti-inflammatory effect on arthritis rats; its therapeutic activities might be achieved through reversing the elevated expression and function of TRPV1 channel evoked by FCA.
机译:少药-甘草汤(SGT)是中药医学实践中治疗疼痛相关疾病最常用的复方之一。为了研究抗炎和镇痛作用,并揭示SGT的分子机制,通过单侧注射弗氏完全佐剂(FCA)实验性地诱导大鼠左后足关节炎模型。在模型诱导后的16天内,每天以三剂分别口服给予大鼠SGT。测量不同组大鼠的肿胀程度和疼痛阈值,以评估SGT的抗炎和抗伤害感受作用。此外,还进一步检测了瞬时受体电位离子通道蛋白香草受体1(TRPV1)通道的mRNA和蛋白表达水平,以及其在分离的DRG神经元中的钙介导功能,为探索介导抗反式分子的分子机制提供了指标。 SGT的关节炎活动。结果,FCA注射诱导了明显的异常性疼痛,炎症和水肿,并伴随着TRPV1通道的表达和钙介导功能的显着增加。在药理上,以高剂量或中剂量口服SGT证明以剂量依赖性方式显着缓解了上述病理状况。同时,TRPV1通道的mRNA和蛋白表达水平及其钙介导功能也被下调。这些发现表明,SGT对关节炎大鼠具有明显的镇痛和抗炎作用。它的治疗活性可以通过逆转FCA引起的TRPV1通道的升高表达和功能来实现。

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