Wen Wanshun, Wang Jinlin, Zhang Biyu, Wang Jun
Department of Rehabilitation Medicine, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, Zhejiang Province, China.
Department of Anesthesiology, Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China.
PPAR Res. 2020 Dec 14;2020:6661642. doi: 10.1155/2020/6661642. eCollection 2020.
Inflammation caused by neuropathy contributes to the development of neuropathic pain (NP), but the exact mechanism still needs to be understood. Peroxisome proliferator-activated receptor (PPAR), an important inflammation regulator, might participate in the inflammation in NP. To explore the role of PPAR in NP, the effects of PPAR agonist WY-14643 on chronic constriction injury (CCI) rats were evaluated. The results showed that WY-14643 stimulation could decrease inflammation and relieve neuropathic pain, which was relative with the activation of PPAR. In addition, we also found that the SIRT1/NF-B pathway was involved in the WY-14643-induced anti-inflammation in NP, and activation of PPAR increased SIRT1 expression, thus reducing the proinflammatory function of NF-B. These data suggested that WY-14643 might serve as an inflammation mediator, which may be a potential therapy option for NP.
神经病变引发的炎症会促使神经性疼痛(NP)的发展,但其确切机制仍有待明确。过氧化物酶体增殖物激活受体(PPAR)作为一种重要的炎症调节因子,可能参与了NP中的炎症反应。为探究PPAR在NP中的作用,我们评估了PPAR激动剂WY-14643对慢性缩窄性损伤(CCI)大鼠的影响。结果显示,WY-14643刺激可减轻炎症并缓解神经性疼痛,这与PPAR的激活相关。此外,我们还发现SIRT1/NF-κB通路参与了WY-14643诱导的NP抗炎作用,PPAR的激活增加了SIRT1的表达,从而降低了NF-κB的促炎功能。这些数据表明,WY-14643可能作为一种炎症介质,这或许是NP的一种潜在治疗选择。