4.1 Article

Daily Coffee Intake Inhibits Pancreatic Beta Cell Damage and Nonalcoholic Steatohepatitis in a Mouse Model of Spontaneous Metabolic Syndrome, Tsumura-Suzuki Obese Diabetic Mice

期刊

METABOLIC SYNDROME AND RELATED DISORDERS
卷 15, 期 4, 页码 170-177

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/met.2016.0114

关键词

coffee intake; nonalcoholic steatohepatitis; beta cell failure; animal model; hepatocellular carcinoma

资金

  1. JSPS KAKENHI [24390181, 25340121, 15K15098]
  2. All Japan Coffee Association
  3. Grants-in-Aid for Scientific Research [24390181, 15K15098] Funding Source: KAKEN

向作者/读者索取更多资源

Background: Metabolic syndrome is one of the most important health issues worldwide. Obesity causes insulin resistance, hyperlipidemia, diabetes, and various diseases throughout the body. The liver phenotype, which is called nonalcoholic steatohepatitis (NASH), frequently progresses to hepatocellular carcinoma. We recently established a new animal model, Tsumura-Suzuki obese diabetic (TSOD) mice, which spontaneously exhibit obesity, diabetes, hyperlipidemia, and NASH with liver nodules. Methods: We examined the effects of coffee intake on various conditions of the metabolic syndrome using TSOD mice. The daily volume of coffee administered was limited so that it reflected the appropriate quantities consumed in humans. To clarify the effects of the specific components, animals were divided into two coffee-intake groups that included with and without caffeine. Results: Coffee intake did not significantly affect obesity and hyperlipidemia in TSOD mice. In contrast, coffee intake caused various degrees of improvement in the pancreatic beta cell damage and steatohepatitis with liver carcinogenesis. Most of the effects were believed to be caused by a synergistic effect of caffeine with other components such as polyphenols. However, the antifibrotic effects of coffee appeared to be due to the polyphenols rather than the caffeine. Conclusions: A daily habit of drinking coffee could possibly play a role in the prevention of metabolic syndrome.

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