[Elucidating the Mechanisms of Lipid Accumulation in the Liver and Evaluating Potential Drug Targets].

IF 0.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Takayuki Koga
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引用次数: 0

Abstract

Fatty liver is defined as a condition in which fat accumulates excessively in the liver. It is characterized by either more than 30% of hepatocytes being fatty or over 5% of the total liver weight attributable to fat. The mechanisms behind hepatic fat accumulation are not fully understood, and no curative treatments have been established; thus, most treatments are symptomatic. Recent studies have focused on the mechanisms involving peroxisome proliferator-activated receptors (PPARs) α and γ, which are central to most research in lipid metabolism and inflammation. However, the development of drugs targeting PPARβ/δ, another isoform, has not progressed as much as for other PPARs. PPARβ/δ is known to play a critical role in maintaining homeostasis in lipid and glucose metabolism, differentiation, and inflammation, similar to other PPAR isoforms, making it a promising target for drug discovery. This review summarizes the potential of PPARβ/δ as a therapeutic target for fatty liver treatment, suggesting that it could be a valuable drug target given its roles in fundamental regulatory mechanisms.

[阐明肝脏脂质积聚机制及评估潜在药物靶点]。
脂肪肝被定义为脂肪在肝脏中过度积聚的一种疾病。其特征是超过30%的肝细胞是脂肪性的,或超过5%的肝脏总重量可归因于脂肪。肝脏脂肪堆积背后的机制尚不完全清楚,也没有有效的治疗方法;因此,大多数治疗都是对症治疗。最近的研究集中在涉及过氧化物酶体增殖物激活受体(PPARs) α和γ的机制上,它们是大多数脂质代谢和炎症研究的核心。然而,针对PPARβ/δ(另一种亚型)的药物开发进展不如其他ppar。已知PPARβ/δ在维持脂质和糖代谢、分化和炎症的稳态中发挥关键作用,类似于其他PPAR异构体,使其成为药物发现的有希望的靶点。这篇综述总结了PPARβ/δ作为脂肪肝治疗靶点的潜力,表明它可能是一个有价值的药物靶点,因为它在基本的调节机制中起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
169
审稿时长
1 months
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