Department of Psychiatry, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 83301, Taiwan.
Liver Transplantation Center, Department of Surgery, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 83301, Taiwan.
Int J Mol Sci. 2021 Dec 27;23(1):256. doi: 10.3390/ijms23010256.
The liver plays a central role in energy metabolism. Dysregulated hepatic lipid metabolism is a major cause of non-alcoholic fatty liver disease (NAFLD), a chronic liver disorder closely linked to obesity and insulin resistance. NAFLD is rapidly emerging as a global health problem with currently no approved therapy. While early stages of NAFLD are often considered benign, the disease can progress to an advanced stage that involves chronic inflammation, with increased risk for developing end-stage disease including fibrosis and liver cancer. Hence, there is an urgent need to identify potential pharmacological targets. Ca is an essential signaling molecule involved in a myriad of cellular processes. Intracellular Ca is intricately compartmentalized, and the Ca flow is tightly controlled by a network of Ca transport and buffering proteins. Impaired Ca signaling is strongly associated with endoplasmic reticulum stress, mitochondrial dysfunction and autophagic defects, all of which are etiological factors of NAFLD. In this review, we describe the recent advances that underscore the critical role of dysregulated Ca homeostasis in lipid metabolic abnormalities and discuss the feasibility of targeting Ca signaling as a potential therapeutic approach.
肝脏在能量代谢中起着核心作用。肝脂代谢失调是导致非酒精性脂肪性肝病(NAFLD)的主要原因,NAFLD 是一种与肥胖和胰岛素抵抗密切相关的慢性肝脏疾病。NAFLD 迅速成为一个全球性的健康问题,目前尚无批准的治疗方法。虽然 NAFLD 的早期阶段通常被认为是良性的,但该疾病可能会进展到晚期,涉及慢性炎症,发生纤维化和肝癌等终末期疾病的风险增加。因此,迫切需要确定潜在的药物靶点。钙是一种参与多种细胞过程的必需信号分子。细胞内钙被精细地分隔,钙流由钙转运和缓冲蛋白网络严格控制。钙信号受损与内质网应激、线粒体功能障碍和自噬缺陷密切相关,所有这些都是 NAFLD 的病因因素。在这篇综述中,我们描述了最近的进展,强调了钙稳态失调在脂质代谢异常中的关键作用,并讨论了靶向钙信号作为一种潜在治疗方法的可行性。