Ma Jiashu, Zheng Yunshao, Sun Fengxia, Fan Yunli, Fan Yunming, Su Xianbiao, Wang Zhongbao, Weng Ning, Li Ranran
School of Mental Health, Jining Medical University, Jining Shandong 272067.
Department of Psychiatry, Shandong Mental Health Center, Jinan 250014.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2023 Oct 28;48(10):1529-1538. doi: 10.11817/j.issn.1672-7347.2023.230029.
Antipsychotic medications are commonly used to treat schizophrenia, but they can have negative effects on lipid metabolism, leading to an increased risk of cardiovascular diseases, reduced life expectancy, and difficulties with treatment adherence. The specific mechanisms by which antipsychotics disrupt lipid metabolism are not well understood. Sterol regulatory element-binding proteins (SREBPs) are important transcriptional factors that regulate lipid metabolism. Proprotein convertase subtilisin/kexin type 9 (), a gene regulated by SREBPs, plays a critical role in controlling levels of low-density lipoprotein cholesterol (LDL-C) and has become a focus of research on lipid-lowering drugs. Recent studies have shown that antipsychotic drugs can affect lipid metabolism through the SREBP/PCSK9 pathway. A deep understanding of the mechanism for this pathway in antipsychotic drug-related metabolic abnormalities will promote the prevention of lipid metabolism disorders in patients with schizophrenia and the development and application of new drugs.
抗精神病药物常用于治疗精神分裂症,但它们可能对脂质代谢产生负面影响,导致心血管疾病风险增加、预期寿命缩短以及治疗依从性困难。抗精神病药物扰乱脂质代谢的具体机制尚不完全清楚。固醇调节元件结合蛋白(SREBPs)是调节脂质代谢的重要转录因子。前蛋白转化酶枯草溶菌素/kexin 9型(PCSK9)是一个受SREBPs调节的基因,在控制低密度脂蛋白胆固醇(LDL-C)水平方面起关键作用,并已成为降脂药物研究的焦点。最近的研究表明,抗精神病药物可通过SREBP/PCSK9途径影响脂质代谢。深入了解该途径在抗精神病药物相关代谢异常中的机制,将有助于预防精神分裂症患者的脂质代谢紊乱以及新药的研发和应用。