Age-dependent sex difference of non-alcoholic fatty liver disease in TSOD and db/db mice

PLoS One. 2022 Dec 14;17(12):e0278580. doi: 10.1371/journal.pone.0278580. eCollection 2022.

Abstract

According to previous clinical studies, the prevalence of non-alcoholic fatty liver disease (NAFLD) is higher in men than women only during the reproductive age. Animal models of NAFLD that reflect sex differences in humans have not been established. In this study, we examined sex differences in the hepatic lesions of Tsumura Suzuki obese diabetes (TSOD) and db/db mice, which are representative genetic models of NAFLD. Male and female TSOD and db/db mice were fed with a normal diet and tap water ad libitum. Six male and female mice of each strain were sacrificed at the ages of 3 and 9 months, respectively, and serum biochemical, pathological, and molecular analyses were performed. Serum aspartate aminotransferase (AST) levels were significantly higher in male than female mice of both strains at the age of 3 months; however, at 9 months, significant sex differences were not observed. Similarly, alanine aminotransferase (ALT) levels were significantly higher in male mice than in female TSOD mice at the age of 3 months; however, at 9 months, significant sex differences were not observed. Image analysis of histological slides revealed that the frequency of the steatotic area was significantly higher in male than female db/db mice at the age of 3 months; however, significant sex differences were not observed at 9 months. The frequency of Sirius red-positive fibrotic area was significantly higher in male than female mice in both strains at the age of 3 months; however, significant sex differences were not observed at 9 months. Serum AST and ALT levels and hepatic steatosis and fibrosis in TSOD and db/db mice showed age-dependent sex differences consistent with those observed in human NAFLD. These mice may be suitable for studying sex differences of the disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase
  • Animals
  • Diabetes Mellitus* / pathology
  • Disease Models, Animal
  • Female
  • Humans
  • Infant
  • Liver / pathology
  • Male
  • Mice
  • Mice, Inbred Strains
  • Mice, Obese
  • Non-alcoholic Fatty Liver Disease* / pathology
  • Obesity / pathology
  • Sex Characteristics

Substances

  • Alanine Transaminase

Grants and funding

This work was supported by the Japan Society for the Promotion of Science (JSPS) KAKENHI Grant (18K11053) to Y. Takahashi. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.