别嘌呤醇
高尿酸血症
癫痫
尿酸
医学
黄嘌呤氧化酶
炎症
神经炎症
氧化应激
星形胶质增生
内科学
神经科学
生物
中枢神经系统
生物化学
精神科
酶
作者
Ali Abdullah AlAseeri,Hayder M. Al‐kuraishy,Ali I. Al‐Gareeb,Naif H. Ali,Αθανάσιος Αλεξίου,Marios Papadakis,Mostafa M. Bahaa,Mubarak Alruwaili,Gaber El‐Saber Batiha
标识
DOI:10.1016/j.brainresbull.2024.110973
摘要
Epilepsy is a common neurological disease characterized by the recurrent, paroxysmal, and unprovoked seizures. It has been shown that hyperuricemia enhances and associated with the development and progression of epilepsy through induction of inflammation and oxidative stress. In addition, uric acid is released within the brain and contributes in the development of neuronal hyperexcitability and epileptic seizure. Brain uric acid acts as damage associated molecular pattern (DAMP) activates the immune response and induce the development of neuroinflammation. Therefore, inhibition of xanthine oxidase by allopurinol may reduce hyperuricemia-induced epileptic seizure and associated oxidative stress and inflammation. However, the underlying mechanism of allopurinol in the epilepsy was not fully elucidated. Therefore, this review aims to revise from published articles the link between hyperuricemia and epilepsy, and how allopurinol inhibits the development of epileptic seizure.
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