Department of Pharmacology, Toxicology and Therapeutic Chemistry, School of Pharmacy and Food Science, University of Barcelona, Avda Joan XXIII 27-31, 08028 Barcelona, Spain.
Institute of Biomedicine, University of Barcelona, 08028 Barcelona, Spain.
Nutrients. 2020 Oct 23;12(11):3240. doi: 10.3390/nu12113240.
Non-alcoholic fatty liver disease is a highly prevalent condition without specific pharmacological treatment, characterized in the initial stages by hepatic steatosis. It was suggested that lipid infiltration in the liver might be reduced by caffeine through anti-inflammatory, antioxidative, and fatty acid metabolism-related mechanisms. We investigated the effects of caffeine (CAF) and green coffee extract (GCE) on hepatic lipids in lean female rats with steatosis. For three months, female Sprague-Dawley rats were fed a standard diet or a cocoa butter-based high-fat diet plus 10% liquid fructose. In the last month, the high-fat diet was supplemented or not with CAF or a GCE, providing 5 mg/kg of CAF. Plasma lipid levels and the hepatic expression of molecules involved in lipid metabolism were determined. Lipidomic analysis was performed in liver samples. The diet caused hepatic steatosis without obesity, inflammation, endoplasmic reticulum stress, or hepatic insulin resistance. Neither CAF nor GCE alleviated hepatic steatosis, but GCE-treated rats showed lower hepatic triglyceride levels compared to the CAF group. The GCE effects could be related to reductions of hepatic (i) mTOR phosphorylation, leading to higher nuclear lipin-1 levels and limiting lipogenic gene expression; (ii) diacylglycerol levels; (iii) hexosylceramide/ceramide ratios; and (iv) very-low-density lipoprotein receptor expression. In conclusion, a low dose of CAF did not reduce hepatic steatosis in lean female rats, but the same dose provided as a green coffee extract led to lower liver triglyceride levels.
非酒精性脂肪性肝病是一种普遍存在的疾病,目前尚无特异性的药物治疗方法,其特征是在初期存在肝脂肪变性。有研究表明,咖啡因可能通过抗炎、抗氧化和脂肪酸代谢相关机制减少肝脏内的脂质浸润。本研究旨在观察咖啡因(CAF)和绿原酸(GCE)对瘦型脂肪性肝病大鼠肝脏脂质的影响。雌性 Sprague-Dawley 大鼠三个月内给予标准饮食或可可脂基高脂肪饮食(添加 10%液体果糖)。最后一个月,高脂饮食分别或不添加 CAF 或 GCE(提供 5mg/kg 的 CAF)。检测各组大鼠的血脂水平和肝脏脂质代谢相关分子的表达,并进行肝脏脂质组学分析。结果显示,高脂饮食导致大鼠肝脏脂肪变性而无肥胖、炎症、内质网应激或肝胰岛素抵抗。CAF 和 GCE 均不能减轻肝脂肪变性,但 GCE 组大鼠的肝甘油三酯水平低于 CAF 组。GCE 的作用可能与降低肝脏以下水平有关:(i)mTOR 磷酸化,导致核脂肪素-1水平升高,限制了脂肪生成基因的表达;(ii)二酰基甘油水平;(iii)己糖神经酰胺/神经酰胺比值;(iv)极低密度脂蛋白受体表达。综上所述,低剂量 CAF 不能减轻瘦型雌性大鼠的肝脂肪变性,但相同剂量的 GCE 可降低大鼠肝脏的甘油三酯水平。