A Combination of Coffee Compounds Shows Insulin-Sensitizing and Hepatoprotective Effects in a Rat Model of Diet-Induced Metabolic Syndrome

Nutrients. 2017 Dec 22;10(1):6. doi: 10.3390/nu10010006.

Abstract

Since coffee may help to prevent the development of metabolic syndrome (MetS), we aimed to evaluate the short- and long-term effects of a coffee-based supplement on different features of diet-induced MetS. In this study, 24 Sprague Dawley rats were divided into control or nutraceuticals groups to receive a high-fat/high-fructose diet with or without a mixture of caffeic acid (30 mg/day), trigonelline (20 mg/day), and cafestol (1 mg/day) for 12 weeks. An additional 11 rats were assigned to an acute crossover study. In the chronic experiment, nutraceuticals did not alter body weight or glycemic control, but improved fed hyperinsulinemia (mean difference = 30.80 mU/L, p = 0.044) and homeostatic model assessment-insulin resistance (HOMA-IR) (mean difference = 15.29, p = 0.033), and plasma adiponectin levels (mean difference = -0.99 µg/mL, p = 0.048). The impact of nutraceuticals on post-prandial glycemia tended to be more pronounced after acute administration than at the end of the chronic study. Circulating (mean difference = 4.75 U/L, p = 0.014) and intrahepatocellular alanine transaminase activity was assessed by hyperpolarized-13C nuclear magnetic resonance NMR spectroscopy and found to be reduced by coffee nutraceuticals at endpoint. There was also a tendency towards lower liver triglyceride content and histological steatosis score in the intervention group. In conclusion, a mixture of coffee nutraceuticals improved insulin sensitivity and exhibited hepatoprotective effects in a rat model of MetS. Higher dosages with or without caffeine deserve to be studied in the future.

Keywords: adiponectin; coffee; dietary supplements; hyperpolarized magnetic resonance spectroscopy; metabolic syndrome X; non-alcoholic fatty liver disease.

MeSH terms

  • Alkaloids / blood
  • Alkaloids / isolation & purification
  • Alkaloids / pharmacology*
  • Animals
  • Blood Glucose / drug effects
  • Blood Glucose / metabolism
  • Caffeic Acids / blood
  • Caffeic Acids / isolation & purification
  • Caffeic Acids / pharmacology*
  • Carbon-13 Magnetic Resonance Spectroscopy
  • Coffea* / chemistry
  • Cytokines / blood
  • Diet, High-Fat*
  • Dietary Sucrose*
  • Dietary Supplements*
  • Disease Models, Animal
  • Diterpenes / blood
  • Diterpenes / isolation & purification
  • Diterpenes / pharmacology*
  • Insulin / blood
  • Insulin Resistance*
  • Lipids / blood
  • Liver / drug effects*
  • Liver / metabolism
  • Liver / pathology
  • Metabolic Syndrome / blood
  • Metabolic Syndrome / etiology
  • Metabolic Syndrome / pathology
  • Metabolic Syndrome / prevention & control*
  • Non-alcoholic Fatty Liver Disease / blood
  • Non-alcoholic Fatty Liver Disease / etiology
  • Non-alcoholic Fatty Liver Disease / pathology
  • Non-alcoholic Fatty Liver Disease / prevention & control*
  • Rats, Sprague-Dawley
  • Seeds
  • Time Factors

Substances

  • Alkaloids
  • Blood Glucose
  • Caffeic Acids
  • Cytokines
  • Dietary Sucrose
  • Diterpenes
  • Insulin
  • Lipids
  • trigonelline
  • cafestol
  • caffeic acid