亚临床感染
内分泌学
内科学
脂质代谢
血脂异常
甲状腺
新陈代谢
小RNA
激素
实时聚合酶链反应
医学
生物
基因
生物化学
糖尿病
作者
Liya Zhang,Wenyu Jia,Yunyun Xu,Xiaoming Zhou,Rui Yang,Ling Gao,Jiajun Zhao
出处
期刊:Chinese Journal of Endocrinology and Metabolism
日期:2018-05-25
卷期号:34 (5): 410-415
标识
DOI:10.3760/cma.j.issn.1000-6699.2018.05.010
摘要
Objective
To obtain a non-invasive subclinical hypothyroidism (SCH) mouse model, and to explore microRNAs profile related to lipid metabolism in the model mice.
Methods
C57BL/6 male mice (8 weeks) were treated with methimazole (MMI, 0.08 mg/kg BW/d) to construct SCH mouse model. MicroRNAs profiling analysis was performed by real-time quantitative polymerase chain reaction (qRT-PCR).
Results
Compared with the control group, the serum thyroid stimulating hormone (TSH) in subclinical hypothyroidism group increased significantly (P 0.05), which was in line with the diagnostic criteria of SCH. SCH mice was accompanied by dyslipidemia and liver lipid metabolism disorders. Four lipid metabolism related miRNAs, miR-33, miR-122, miR-199a-5p, and miR-375 in the liver of SCH mice were significantly decreased compared with those of control(P<0.05).
Conclusion
The noninvasive SCH model generated by MMI and miRNAs profile provide an animal model and a molecular basis for the study of SCH related lipid metabolism disorders. (Chin J Endocrinol Metab, 2018, 34: 410-415)
Key words:
Subclinical hypothyroidism; Methimazole; MicroRNAs; Lipid metabolism
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