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Effects of Danggui Sini decoction on neuropathic pain: experimental studies and clinical pharmacological significance of inhibiting glial activation and proinflammatory cytokines in the spinal cord

机译:Dangui Sini汤对神经性疼痛的影响:抑制脊髓胶质激活和促炎细胞因子的实验研究和临床药理学意义

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Aim: Neuropathic pain responds poorly to drug treatments. Partial relief is achieved in only about half of the patients. Danggui Sini decoction (DSD), an aqueous extract of Angelica sinensis, Ramulus Cinnamomi, and Radix Puerariae, has been used extensively in China to treat inflammatory and ischemic diseases. The current study examined the putative effects of DSD on neuropathic pain. Method: We used two commonly-used animal models: chronic constriction injury (CCI) and diabetic neuropathy for the study. And we examined effects of DSD on pain response, activation of microglia and astroglia in spinal dorsal horn, and expression of proinflammatory cytokines in the spinal cord. Results: Consecutive intragastric administration of DSD (25 - 100 mg/kg) for 10 days inhibited the mechanical and thermal nociceptive response induced by CCI and diabetes without interfering with the normal pain response. Meanwhile, in both models, DSD inhibited the over-expression of specific markers for microglia (Iba-1) and astroglia (GFAP) activation in the spinal dorsal horn. DSD also reduced the elevated nuclear NF-kappa B level and inhibited the up-regulation of proinflammatory cytokines, such as IL-6, IL-1 beta, and TNF-alpha, in the spinal cord. Conclusion: DSD can alleviate CCI and diabetes-induced neuropathic pain, and its effectiveness might be due to the inhibition of neuroinflammation in the spinal dorsal horn. The anti-inflammation effect of DSD may be related to the suppression of spinal NF-kappa B activation and/or cytokines expression.
机译:目的:神经性疼痛对药物治疗造成的良差。部分浮雕只在大约一半的患者中实现。 Danggui Sini汤(DSD),Angelica Sinensis,Raculus Cinnamomi和Nadix Puerariae的含水提取物,在中国已经广泛使用,以治疗炎症和缺血性疾病。目前的研究检测了DSD对神经性疼痛的推定作用。方法:我们使用了两种常用的动物模型:慢性收缩损伤(CCI)和该研究的糖尿病神经病变。并且我们检测了DSD对脊髓背角中疼痛反应,激活的微胶质胶质胶质胶质菌和脊髓中促炎细胞因子的表达。结果:DSD(25-100mg / kg)的连续胃内给药10天抑制CCI和糖尿病诱导的机械和热伤害反应,而不会干扰正常的疼痛反应。同时,在两种模型中,DSD抑制了脊椎背角中的微胶质细胞(IBA-1)和星形胶蛋白(GFAP)活化的特定标志物的过表达。 DSD还减少了核NF-κB水平的升高,并抑制了脊髓中促炎细胞因子的上调,例如IL-6,IL-1β和TNF-α。结论:DSD可以缓解CCI和糖尿病诱导的神经性疼痛,其有效性可能是由于脊髓背角中神经炎症的抑制。 DSD的抗炎效应可能与抑制脊髓NF-Kappa B激活和/或细胞因子表达有关。

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