Effects of a Low Dose of Caffeine Alone or as Part of a Green Coffee Extract, in a Rat Dietary Model of Lean Non-Alcoholic Fatty Liver Disease without Inflammation

Nutrients. 2020 Oct 23;12(11):3240. doi: 10.3390/nu12113240.

Abstract

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.

Keywords: caffeine; coffee; dietary supplements; hepatic steatosis; non-alcoholic fatty liver disease.

MeSH terms

  • Animals
  • Caffeine / administration & dosage*
  • Coffee*
  • Diet, High-Fat / adverse effects
  • Dietary Fats
  • Dietary Supplements*
  • Disease Models, Animal
  • Female
  • Fructose / administration & dosage
  • Insulin Resistance
  • Lipid Metabolism
  • Lipids / blood
  • Lipogenesis / drug effects
  • Liver / metabolism
  • Non-alcoholic Fatty Liver Disease / etiology
  • Non-alcoholic Fatty Liver Disease / therapy*
  • Plant Extracts / administration & dosage*
  • Rats
  • Rats, Sprague-Dawley
  • Triglycerides / metabolism

Substances

  • Coffee
  • Dietary Fats
  • Lipids
  • Plant Extracts
  • Triglycerides
  • Fructose
  • Caffeine
  • cocoa butter