College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
Division of Neurology, King Abdulaziz Medical City, Ministry of the National Guard Health Affairs, Riyadh, Saudi Arabia.
Eur J Med Res. 2024 Feb 9;29(1):113. doi: 10.1186/s40001-024-01700-2.
Multiple sclerosis (MS) is the most frequent inflammatory and demyelinating disease of the central nervous system (CNS). The underlying pathophysiology of MS is the destruction of myelin sheath by immune cells. The formation of myelin plaques, inflammation, and injury of neuronal myelin sheath characterizes its neuropathology. MS plaques are multiple focal regions of demyelination disseminated in the brain's white matter, spinal cords, deep grey matter, and cerebral cortex. Fenofibrate is a peroxisome proliferative activated receptor alpha (PPAR-α) that attenuates the inflammatory reactions in MS. Fenofibrate inhibits differentiation of Th17 by inhibiting the expression of pro-inflammatory signaling. According to these findings, this review intended to illuminate the mechanistic immunoinflammatory role of fenofibrate in mitigating MS neuropathology. In conclusion, fenofibrate can attenuate MS neuropathology by modulating different pathways, including oxidative stress, autophagy, mitochondrial dysfunction, inflammatory-signaling pathways, and neuroinflammation.
多发性硬化症(MS)是中枢神经系统(CNS)最常见的炎症性和脱髓鞘疾病。MS 的潜在病理生理学是免疫细胞对髓鞘的破坏。髓鞘斑块的形成、炎症和神经元髓鞘的损伤是其神经病理学的特征。MS 斑块是多发性脱髓鞘病灶,散布在大脑白质、脊髓、深部灰质和大脑皮层。非诺贝特是过氧化物酶体增殖物激活受体α(PPAR-α),可减轻 MS 中的炎症反应。非诺贝特通过抑制促炎信号的表达来抑制 Th17 的分化。根据这些发现,本综述旨在阐明非诺贝特在减轻 MS 神经病理学中的免疫炎症作用机制。总之,非诺贝特可以通过调节不同的途径来减轻 MS 神经病理学,包括氧化应激、自噬、线粒体功能障碍、炎症信号通路和神经炎症。