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藁本内酯通过抑制大鼠脊髓c-Jun氨基末端激酶/c-Jun通路的激活来缓解完全弗氏佐剂诱导的机械性痛觉过敏。

Ligustilide Relieves Complete Freund's Adjuvant-induced Mechanical Hyperalgesia through Inhibiting the Activation of Spinal c-Jun N-terminal Kinase/c-Jun Pathway in Rats.

作者信息

Wang Yi-Rui, Xu Hui, Tao Min, Xu Li-Hua, Fu Xin-Chun

机构信息

Department of Anesthesiology, Huangyan Hospital, Wenzhou Medical University, Taizhou 318020, China.

出版信息

Pharmacogn Mag. 2017 Oct-Dec;13(52):634-638. doi: 10.4103/pm.pm_546_16. Epub 2017 Nov 13.

Abstract

BACKGROUND

Ligustilide, an active ingredient in a traditional Chinese medicine, has anti-inflammatory and analgesic effects. The underlying mechanisms of the anti-inflammatory pain effects of ligustilide are not completely understood.

OBJECTIVE

The aim of this study to investigate whether ligustilide conducts its analgesic effects on the complete Freund's adjuvant (CFA)-induced inflammatory pain through regulating the c-Jun N-terminal kinase (JNK)/c-Jun pathway in the spinal cord.

MATERIALS AND METHODS

Paw withdrawal thresholds (PWTs) and paw withdrawal latencies (PWLs) were tested to examine the analgesic effect of ligustilide on CFA-induced inflammatory pain in rats. The change of spinal JNK/c-Jun activation was detected by western blotting after CFA injection with or without consecutive intrathecal ligustilide administration. After SP600125 (JNK inhibitor) was intrathecally injected in CFA rats, PWTs and PWLs were tested to investigate the change of ligustilide's analgesic effect.

RESULTS

Repeated intravenous injection of ligustilide could attenuate the pain hypersensitivity induced by CFA. CFA caused increased activation of spinal JNK/c-Jun, which could be inhibited by ligustilide administration. Intrathecal injection of JNK inhibitor inhibited the CFA-induced mechanical hyperalgesia.

CONCLUSION

Ligustilide could inhibit the upregulation of spinal p-JNK/p-c-Jun caused by CFA, and the inhibition of JNK/c-Jun activation is closely related to its anti-mechanical hyperalgesia effect in inflammatory pain.

SUMMARY

Ligustilide, an active ingredient in a popular traditional Chinese medicine, has effective anti-inflammatory and analgesic effects. Ligustilide inhibits the complete Freund's adjuvant-induced activation of spinal c-Jun N-terminal kinase-(JNK)/c-Jun pathway in rats. The inhibition of JNK/c-Jun activation is closely related to the anti-mechanical hyperalgesia effect of ligustilide. CFA: Complete Freund's adjuvant, JNK: c-Jun N-terminal kinase, MAPK: Mitogen-activated protein kinase, PWT: Paw withdrawal threshold, PWL: Paw withdrawal latency.

摘要

背景

藁本内酯是一种中药活性成分,具有抗炎和镇痛作用。藁本内酯抗炎镇痛作用的潜在机制尚未完全明确。

目的

本研究旨在探讨藁本内酯是否通过调节脊髓中的c-Jun氨基末端激酶(JNK)/c-Jun信号通路,对完全弗氏佐剂(CFA)诱导的炎性疼痛发挥镇痛作用。

材料与方法

通过检测大鼠的 paw withdrawal thresholds(PWTs)和 paw withdrawal latencies(PWLs),以考察藁本内酯对CFA诱导的大鼠炎性疼痛的镇痛效果。在注射CFA前后连续鞘内注射或不注射藁本内酯后,通过蛋白质免疫印迹法检测脊髓中JNK/c-Jun的激活变化。在CFA诱导的大鼠中鞘内注射SP600125(JNK抑制剂)后,检测PWTs和PWLs,以研究藁本内酯镇痛效果的变化。

结果

反复静脉注射藁本内酯可减轻CFA诱导的疼痛超敏反应。CFA可导致脊髓JNK/c-Jun的激活增加,而藁本内酯给药可抑制这种激活。鞘内注射JNK抑制剂可抑制CFA诱导的机械性痛觉过敏。

结论

藁本内酯可抑制CFA引起的脊髓p-JNK/p-c-Jun上调,且抑制JNK/c-Jun激活与其在炎性疼痛中抗机械性痛觉过敏作用密切相关。

总结

藁本内酯是一种常用中药的活性成分,具有有效的抗炎和镇痛作用。藁本内酯可抑制完全弗氏佐剂诱导的大鼠脊髓c-Jun氨基末端激酶-(JNK)/c-Jun信号通路激活。抑制JNK/c-Jun激活与藁本内酯的抗机械性痛觉过敏作用密切相关。CFA:完全弗氏佐剂,JNK:c-Jun氨基末端激酶,MAPK:丝裂原活化蛋白激酶,PWT: paw withdrawal threshold,PWL:paw withdrawal latency 。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e43/5701403/1f1ee9bf3bcb/PM-13-634-g002.jpg

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