Spinal miR-34a regulates inflammatory pain by targeting SIRT1 in complete Freund's adjuvant mice

被引:15
作者
Chen, Shuangdong [1 ]
Gu, Yixiao [1 ]
Dai, Qinxue [1 ]
He, Yanshu [1 ]
Wang, Junlu [1 ,2 ]
机构
[1] WenZhou Med Univ, Affiliated Hosp 1, Dept Anesthesiol, 2 FuxueLane, Wenzhou 325000, Zhejiang, Peoples R China
[2] Wencheng Cty Peoples Hosp, Wenzhou, Zhejiang, Peoples R China
关键词
SIRT1; miR-34a; Inflammatory pain; Spinal cord; ATTENUATES NEUROPATHIC PAIN; ACTIVATION; MICRORNA-34A; RNAS;
D O I
10.1016/j.bbrc.2019.07.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sirtuin1 (SIRT1), which is regulated by microRNA-34a (miR-34a), can modulate pathophysiology processes, including nonalcoholic fatty liver disease and intestinal ischemia/reperfusion injury. We previously reported that SIRT1, an NAD(+)-dependent deacetylase, plays a vital role in the development of neuropathic pain. However, the role of miR-34a/SIRT1 in complete Freund's adjuvant (CFA)-induced inflammatory pain remains unclear. In the present study, we examined miR-34a and SIRT1 in CFA mice. MiR-34a levels increased, while SIRT1 decreased in the spinal cord. Inhibiting miR-34a by intrathecal injection of miR-34a antagomir attenuated CFA-induced pain behavior. Moreover, miR-34a antagomir inhibited the CFA-induced SIRT1 decrease in the spinal cord. Furthermore, the analgesic effect of miR-34a antagomir was abrogated by the SIRT1 inhibitor EX-527. Our data provide support that the underlying mechanisms of miR-34a in promoting inflammatory pain may involve negative regulation of SIRT1. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:1196 / 1203
页数:8
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