Danggui‐shaoyao‐san, a traditional Chinese medicine prescription, alleviates the orthodontic pain and inhibits neuronal and microglia activation
Danggui‐shaoyao‐san, a traditional Chinese medicine prescription, alleviates the orthodontic pain and inhibits neuronal and microglia activation
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DOI:
10.3760/cma.j.issn.0366-6999.20141589
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发表时间:
2014-10
影响因子:
6.1
通讯作者:
Hongshi Li;Z. Gu;Li'an Wu;Liang Xia;Kecheng Zhou;L. E;Dongsheng Wang;J. Kou;Hongchen Liu
中科院分区:
文献类型:
--
作者:
Hongshi Li;Z. Gu;Li'an Wu;Liang Xia;Kecheng Zhou;L. E;Dongsheng Wang;J. Kou;Hongchen Liu
Background The pain caused by orthodontic treatment has been considered as tough problems in orthodontic practice. Danggui‐shaoyao‐san (DSS) is a traditional Chinese medicine (TCM) prescription which has long been used for pain treatment and possesses antioxidative, cognitive enhancing and antidepressant effects. We raise the hypothesis that DSS exerts analgesic effect for orthodontic pain via inhibiting the activations of neuron and microglia. Methods DSS was given twice a day from day 5 prior to experimental tooth movement (ETM). Directed face grooming and vacuous chewing movements (VCM) were evaluated. Immunofluorescent histochemistry and Western blot analysis were used to quantify the Iba‐1 (microglia activation) and Fos (neuronal activation) expression levels in the trigeminal spinal nucleus caudalis (Vc). Results ETM significantly increased directed face grooming and VCM which reached the peak at post‐operative day (POD) 1 and gradually decreased to the baseline at POD 7. However, a drastic peak increase of Fos expression in Vc was observed at 4 hours and gradually decreased to baseline at POD 7; while the increased Iba‐1 level reached the peak at POD 1 and gradually decreased to baseline at POD 7. Furthermore, pre‐treatment with DSS significantly attenuated the ETM induced directed face grooming and VCM as well as the Fos and Iba‐1 levels at POD 1. Conclusion Treatment with DSS had significant analgesic effects on ETM‐induced pain, which was accompanied with inhibition of both neuronal and microglial activation.