Chinese Journal of Pharmacovigilance ›› 2023, Vol. 20 ›› Issue (3): 273-276.
DOI: 10.19803/j.1672-8629.20220559

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Evaluation of a KKAy animal model of type 2 diabetes mellitus combined with nonalcoholic fatty liver disease

WANG Shan1, HUANG Jukai1, WU Honghui1, WEN Yalu1, ZHANG Li2, WANG Jianhua3, YANG Xiaohui1,*   

  1. 1Department of Nephrology and Endocrinology, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, Beijing 100700, China;
    2Scientific Research Department, Dongfang Hospital Affiliated to Beijing University of Chinese Medicine, Beijing 100078, China;
    3Capital Institute of Pediatrics, Beijing 100020, China
  • Received:2022-09-22 Online:2023-03-15 Published:2023-03-17

Abstract: Objective To explore the age of onset and stability of a KKAY animal model of type 2 diabetes mellitus combined with nonalcoholic fatty liver disease. Methods Eighteen twelve-week-old C57BL/6J mice were assigned to the control group that was fed with normal diets while another 18 twelve-week-old KKAy mice served as the model group that was fed with high-fat diets. Six mice in control and model group were randomly killed at the 14,18,22 weeks of age, respectively. Blood glucose, weight, serum liver function and lipid levels were monitored and the pathological changes of hepatic tissues were observed. Results Compared with the control group, the body mass, liver mass, liver index and blood glucose level of the model group increased significantly (P< 0.05) from the 14th week. The results of serology showed that the ALT, AST, CHOL, HDL-C and LDL-C levels were significantly increased compared with the control group (P< 0.05), but no significant difference was found in TG levels between the two groups (P> 0.05). Pathological staining showed both steatosis of hepatocytes in the 14th week and inflammatory cell infiltration in the 22nd week. Conclusion The 14-week-old KKAy mice treated with high fat diets can serve as a stable mouse model of type 2 diabetes mellitus combined with nonalcoholic fatty liver disease.

Key words: type 2 diabetes mellitus, nonalcoholic fatty liver disease, KKAy mice, animal model

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