Rosiglitazone Alleviates Mechanical Allodynia of Rats with Bone Cancer Pain through the Activation of PPAR-γ to Inhibit the NF-κB/NLRP3 Inflammatory Axis in Spinal Cord Neurons.

IF 3.5 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
PPAR Research Pub Date : 2021-08-25 eCollection Date: 2021-01-01 DOI:10.1155/2021/6086265
Jie Fu, Baoxia Zhao, Chaobo Ni, Huadong Ni, Longsheng Xu, Qiuli He, Miao Xu, Chengfei Xu, Ge Luo, Jianjun Zhu, Jiachun Tao, Ming Yao
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引用次数: 9

Abstract

Bone cancer pain (BCP) is a serious clinical problem that affects the quality of life of cancer patients. However, the current treatment methods for this condition are still unsatisfactory. This study investigated whether intrathecal injection of rosiglitazone modulates the noxious behaviors associated with BCP, and the possible mechanisms related to this effect were explored. We found that rosiglitazone treatment relieved bone cancer-induced mechanical hyperalgesia in a dose-dependent manner, promoted the expression of peroxisome proliferator-activated receptor-γ (PPAR-γ) in spinal cord neurons, and inhibited the activation of the nuclear factor-kappa B (NF-κB)/nod-like receptor protein 3 (NLRP3) inflammatory axis induced by BCP. However, concurrent administration of the PPAR-γ antagonist GW9662 reversed these effects. The results show that rosiglitazone inhibits the NF-κB/NLRP3 inflammation axis by activating PPAR-γ in spinal neurons, thereby alleviating BCP. Therefore, the PPAR-γ/NF-κB/NLRP3 signaling pathway may be a potential target for the treatment of BCP in the future.

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罗格列酮通过激活PPAR-γ抑制脊髓神经元NF-κB/NLRP3炎症轴减轻骨癌性疼痛大鼠机械异常性痛
骨癌疼痛是影响肿瘤患者生活质量的严重临床问题。然而,目前对这种情况的治疗方法仍然令人不满意。本研究探讨鞘内注射罗格列酮是否能调节BCP相关的有害行为,并探讨其可能的作用机制。我们发现罗格列酮以剂量依赖的方式缓解骨癌引起的机械性痛觉过敏,促进脊髓神经元中过氧化物酶体增殖物激活受体-γ (PPAR-γ)的表达,抑制BCP诱导的核因子-κB (NF-κB)/淋巴结样受体蛋白3 (NLRP3)炎症轴的激活。然而,同时给予PPAR-γ拮抗剂GW9662逆转了这些作用。结果表明,罗格列酮通过激活脊髓神经元PPAR-γ抑制NF-κB/NLRP3炎症轴,从而减轻BCP。因此,PPAR-γ/NF-κB/NLRP3信号通路可能是未来治疗BCP的潜在靶点。
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来源期刊
PPAR Research
PPAR Research MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
6.20
自引率
3.40%
发文量
17
审稿时长
12 months
期刊介绍: PPAR Research is a peer-reviewed, Open Access journal that publishes original research and review articles on advances in basic research focusing on mechanisms involved in the activation of peroxisome proliferator-activated receptors (PPARs), as well as their role in the regulation of cellular differentiation, development, energy homeostasis and metabolic function. The journal also welcomes preclinical and clinical trials of drugs that can modulate PPAR activity, with a view to treating chronic diseases and disorders such as dyslipidemia, diabetes, adipocyte differentiation, inflammation, cancer, lung diseases, neurodegenerative disorders, and obesity.
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