Liu Ming, Qiang Qiu Hong, Ling Qian, Yu Chang Xi, Li Xuejun, Liu Suhuan, Yang Shuyu
Int J Clin Pharmacol Ther. 2017 May;55(5):453-464. doi: 10.5414/CP202613.
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 and , has been used extensively in China to treat inflammatory and ischemic diseases. The current study examined the putative effects of DSD on neuropathic pain.
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.
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-κB level and inhibited the up-regulation of proinflammatory cytokines, such as IL-6, IL-1β, and TNF-α, 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-κB activation and/or cytokines expression. .
神经性疼痛对药物治疗反应不佳。仅约一半的患者能获得部分缓解。当归四逆汤(DSD),一种由[具体药材1]和[具体药材2]制成的水提取物,在中国已被广泛用于治疗炎症性和缺血性疾病。本研究探讨了DSD对神经性疼痛的假定作用。
我们使用了两种常用的动物模型:慢性压迫损伤(CCI)模型和糖尿病性神经病变模型进行研究。我们检测了DSD对疼痛反应、脊髓背角小胶质细胞和星形胶质细胞的激活以及脊髓中促炎细胞因子表达的影响。
连续10天胃内给予DSD(25 - 100mg/kg)可抑制由CCI和糖尿病诱导的机械性和热性伤害性反应,而不干扰正常的疼痛反应。同时,在两种模型中,DSD均抑制了脊髓背角小胶质细胞(Iba-1)和星形胶质细胞(GFAP)激活的特异性标志物的过度表达。DSD还降低了脊髓中升高的核NF-κB水平,并抑制了促炎细胞因子如IL-6、IL-1β和TNF-α的上调。
DSD可减轻CCI和糖尿病诱导的神经性疼痛,其有效性可能归因于对脊髓背角神经炎症的抑制。DSD的抗炎作用可能与抑制脊髓NF-κB激活和/或细胞因子表达有关。