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Jiye Aa

Researcher at China Pharmaceutical University

Publications -  101
Citations -  2337

Jiye Aa is an academic researcher from China Pharmaceutical University. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 24, co-authored 88 publications receiving 1600 citations. Previous affiliations of Jiye Aa include Yantai University.

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CD147 reprograms fatty acid metabolism in hepatocellular carcinoma cells through Akt/mTOR/SREBP1c and P38/PPARα pathways.

TL;DR: It is demonstrated that CD147 is a critical regulator of fatty acid metabolism, which provides a strong line of evidence for this molecule to be used as a drug target in cancer treatment.
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Differences in metabolite profile between blood plasma and serum.

TL;DR: Because incubation affected the analyte peak areas less in serum than in plasma, the results highlight the importance in choosing serum or plasma as the analytical sample and in stipulating the incubation time.
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Orally Administered Berberine Modulates Hepatic Lipid Metabolism by Altering Microbial Bile Acid Metabolism and the Intestinal FXR Signaling Pathway.

TL;DR: BBR prevented the development of high-fat-diet–induced obesity and ameliorated triglyceride accumulation in livers of WT, but not FXRint−/− mice, and results indicate that BBR may exert its lipid-lowering effect primarily in the gut by modulating the turnover of bile acids and subsequently the ileal FXR signaling pathway.
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Curcumin regulates endogenous and exogenous metabolism via Nrf2-FXR-LXR pathway in NAFLD mice.

TL;DR: Findings indicate that the Nrf2/FXR/LXRα pathway might synergistically regulate both endogenous and exogenous metabolism in NAFLD mice and LXRα may be a novel therapeutic target of curcumin for the prevention and treatment of NAFLd.
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GC/TOFMS analysis of metabolites in serum and urine reveals metabolic perturbation of TCA cycle in db/db mice involved in diabetic nephropathy

TL;DR: To probe potential markers and the underlying mechanism ofDN, an animal model of DN, the db/db mice, was used and serum and urine metabolites were profiled using gas chromatography/time-of-flight mass spectrometry to suggest perturbations in the tricarboxylic acid cycle, lipid metabolism, glycolysis, and amino acid turnover.