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Bingbing Jiang

Researcher at Boston University

Publications -  13
Citations -  2740

Bingbing Jiang is an academic researcher from Boston University. The author has contributed to research in topics: AMP-activated protein kinase & Nitric oxide synthase. The author has an hindex of 12, co-authored 12 publications receiving 2389 citations. Previous affiliations of Bingbing Jiang include Brigham and Women's Hospital.

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AMPK phosphorylates and inhibits SREBP activity to attenuate hepatic steatosis and atherosclerosis in diet-induced insulin-resistant mice.

TL;DR: It is demonstrated that AMPK interacts with and directly phosphorylates sterol regulatory element binding proteins (SREBP-1c and -2) and AMPK-dependent phosphorylation of SREBP may offer therapeutic strategies to combat insulin resistance, dyslipidemia, and atherosclerosis.
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SIRT1 Regulates Hepatocyte Lipid Metabolism through Activating AMP-activated Protein Kinase *

TL;DR: It is shown that polyphenols, including resveratrol and the synthetic polyphenol S17834, increase SIRT1 deacetylase activity, LKB1 phosphorylation at Ser428, and AMPK activity, which suggests that Sirt1 functions as a novel upstream regulator for L KB1/AMPK signaling and plays an essential role in the regulation of hepatocyte lipid metabolism.
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Temporal Control of NF-κB Activation by ERK Differentially Regulates Interleukin-1β-induced Gene Expression

TL;DR: Although NF-κB activation was essential for interleukin-1β induction of each of the proteins studied, gene expression was differentially regulated by ERK and by the duration of NF-kkB activation.
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AMPK Activation by Metformin Suppresses Abnormal Extracellular Matrix Remodeling in Adipose Tissue and Ameliorates Insulin Resistance in Obesity.

TL;DR: Treatment with the antidiabetic drug metformin inhibits excessive ECM deposition in WAT of ob/ob mice and mice with diet-induced obesity, as evidenced by decreased collagen deposition surrounding adipocytes and expression of fibrotic genes including the collagen cross-linking regulator LOX.
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Persistent Activation of Nuclear Factor-κB by Interleukin-1β and Subsequent Inducible NO Synthase Expression Requires Extracellular Signal-Regulated Kinase

TL;DR: Data suggest that ERK activity is required for persistent NF-&kgr;B activation by IL-1&bgr; that is necessary for iNOS gene expression.