Affiliation:
1. Department of Pediatric Endocrinology and Metabolic Disease, Anhui
Provincial Children's Hospital, Hefei, China
Abstract
AbstractHyperlipidemia is a common metabolic disorder that can lead to cardiovascular
disease. PDK4 is a key enzyme that regulates glucose and fatty acid metabolism
and homeostasis. The aim of this study is to explore the correlation between
PDK4 expression and dyslipidemia in obese children, and to find new therapeutic
targets for hyperlipidemia in children. The expression of PDK4 in serum was
detected by qRT-PCR. Receiver operating characteristic curve was used to analyze
the relationship between PDK4 and dyslipidemia. Upstream miRNAs of PDK4 were
predicted by the database and verified by dual luciferase reporter gene assay
and detected by qRT-PCR. The hyperlipidemia mouse model was established by
high-fat diet (HFD) feeding, and the metabolic disorders of mice were detected.
PDK4 is poorly expressed in the serum of obese children. The upstream of PDK4
may be inhibited by miR-107, miR-27a-3p, and miR-106b-5p, which are highly
expressed in the serum of obese children. Overexpression of PDK4 improves lipid
metabolism in HFD mice. miR-27a-3p silencing upregulates PDK4 to improve lipid
metabolism. In conclusion, PDK4 has a diagnostic effect on dyslipidemia in
children, while lipid metabolism in hyperlipidemic mice could be mitigated by
upregulation of PDK4, which was inhibited by miR-107, miR-27a-3p and miR-106b-5p
on upstream.
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by
1 articles.
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