Hu, Q and Chen, H and Zuo, Y and He, Q and He, X and Simpson Jr, S and Huang, W and Yang, H and Zhang, H and Lin, R, Role of PCK1 gene on oil tea-induced glucose homeostasis and type 2 diabetes: An animal experiment and a case-control study, Nutrition & Metabolism, 16, (1) Article 12. ISSN 1743-7075 (2019) [Refereed Article]
Methods: Twenty seven db/db mice were gavaged with saline, metformin and oil tea for 8 weeks with measurement of biochemical profiles. A real-time2 (RT2) profiler polymerase chain reaction (PCR) array comprising 84 genes involved in glucose metabolism was measured and validated by quantitative PCR (qPCR). The association between the candidate genes and type 2 diabetes were further analyzed in a case-control study in the Chinese minority population.
Results: Oil tea treatment facilitated glucose homeostasis by decreasing fasting blood glucose and total cholesterol, and improving glucose tolerance. Suppressing phosphoenolpyruvate carboxykinase 1 (PCK1) expression was observed in the oil tea treatment group and the expression was significantly correlated with fasting blood glucose levels. Target prediction and functional annotation by WEB-based GEne SeT AnaLysis Toolkit (WebGestalt) revealed that PCK1 mainly involved in the glycolysis/gluconeogenesis pathway among the top Kyoto Encyclopedia of Genes and Genomes (KEGG) database pathways. Both rs707555 and rs2071023 in PCK1 were significantly associated with type 2 diabetes in the minority population of Guangxi.
Conclusion: Our findings indicated oil tea improved glucose homeostasis via down-regulation of PCK1 and PCK1 may be a genetic marker for the treatment of type 2 diabetes.
|Item Type:||Refereed Article|
|Keywords:||fasting blood glucose, glucose tolerance, glycolysis/gluconeogenesis pathway, oil tea, PCK1, RT2 profiler PCR array, SNP, Type 2 diabetes|
|Research Division:||Biological Sciences|
|Research Group:||Biochemistry and Cell Biology|
|Research Field:||Cell Metabolism|
|Objective Group:||Clinical Health (Organs, Diseases and Abnormal Conditions)|
|UTAS Author:||Simpson Jr, S (Dr Steve Simpson JR)|
|Deposited By:||Menzies Institute for Medical Research|
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