Species differences of fatty liver diseases: comparisons between human and feline.

IF 3.1 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM American journal of physiology. Endocrinology and metabolism Pub Date : 2025-01-01 Epub Date: 2024-12-05 DOI:10.1152/ajpendo.00014.2024
Like Ling, Ruilin Li, Mengqiong Xu, Junjie Zhou, Manli Hu, Xin Zhang, Xiao-Jing Zhang
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Abstract

Nonalcoholic fatty liver disease (NAFLD) has emerged as the most widespread chronic liver disease that poses significant threats to public health due to changes in dietary habits and lifestyle patterns. The transition from simple steatosis to nonalcoholic steatohepatitis (NASH) markedly increases the risk of developing cirrhosis, hepatocellular carcinoma, and liver failure in patients. However, there is only one Food and Drug Administration-approved therapeutic drug in the world, and the clinical demand is huge. There is significant clinical heterogeneity among patients with NAFLD, and it is challenging to fully understand human NAFLD using only a single animal model. Interestingly, felines, like humans, are particularly prone to spontaneous fatty liver disease. This review summarized and compared the etiology, clinical features, pathological characteristics, and molecular pathogenesis between human fatty liver and feline hepatic lipidosis (FHL). We analyzed the key similarities and differences between those two species, aiming to provide theoretical foundations for developing effective strategies for the treatment of NAFLD in clinics.

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脂肪肝疾病的物种差异:人与猫的比较。
非酒精性脂肪性肝病(NAFLD)已成为最广泛的慢性肝病,由于饮食习惯和生活方式的改变,对公众健康构成重大威胁。从单纯性脂肪变性到非酒精性脂肪性肝炎(NASH)的转变显著增加了患者发生肝硬化、肝细胞癌和肝功能衰竭的风险。然而,世界上只有一种FDA批准的治疗药物,临床需求巨大。NAFLD患者存在显著的临床异质性,仅使用单一动物模型来充分了解人类NAFLD是具有挑战性的。有趣的是,猫科动物和人类一样,特别容易患上自发性脂肪肝疾病。本文综述并比较了人脂肪肝和猫肝性脂质病的病因、临床特点、病理特点及分子发病机制。我们分析了这两个物种的主要异同点,旨在为临床制定有效的治疗策略提供理论依据。
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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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