Jing Luo
Virginia Tech
11 Papers
3 Citations
Jing Luo is an academic researcher from Virginia Tech. The author has contributed to research in topics: Biology & Internal medicine. The author has an hindex of 8, co-authored 11 publications. Previous affiliations of Jing Luo include Sun Yat-sen University.
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Papers
Does GPER Really Function as a G Protein-Coupled Estrogen Receptor in vivo?
Jing Luo,Jing Luo,Dongmin Liu +2 more
TL;DR: There is still lack of evidence that GPER plays a significant role in mediating endogenous estrogen action in vivo, but opportunities for the development of new therapeutic strategies to strengthen the benefits of estrogen while limiting the potential side effects are provided.
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Dietary Anti-Aging Polyphenols and Potential Mechanisms.
TL;DR: In this paper, the authors highlight the potential anti-aging mechanisms of polyphenols, including antioxidant signaling, preventing cellular senescence, targeting microRNA, influencing NO bioavailability, and promoting mitochondrial function.
Kaempferol ameliorates hyperglycemia through suppressing hepatic gluconeogenesis and enhancing hepatic insulin sensitivity in diet-induced obese mice.
Hana Alkhalidy,William T. Moore,Aihua Wang,Jing Luo,Ryan P. McMillan,Yao Wang,Wei Zhen,Matthew W. Hulver,Dongmin Liu +8 more
TL;DR: Oral administration of kaempferol significantly improved blood glucose control in obese mice, which was associated with reduced hepatic glucose production and improved whole-body insulin sensitivity without altering body weight gain, food consumption or adiposity.
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Baicalein Protects against Type 2 Diabetes via Promoting Islet β-Cell Function in Obese Diabetic Mice.
TL;DR: It is shown that dietary supplementation of baicalein, a flavone isolated from the roots of Chinese herb Scutellaria baicalensis, improved glucose tolerance and enhanced glucose-stimulated insulin secretion (GSIS) in high-fat diet (HFD-) induced middle-aged obese mice, and demonstrate that baicalsein may be a naturally occurring antidiabetic agent by directly modulating pancreatic β-cell function.
Estradiol signaling mediates gender difference in visceral adiposity via autophagy.
Zhipeng Tao,Louise D. Zheng,Cayleen Smith,Jing Luo,Alex Robinson,Fabio A. Almeida,Zongwei Wang,Aria F. Olumi,Dongmin Liu,Zhiyong Cheng +9 more
TL;DR: This study suggests that the lower visceral adiposity in the females (vs. the males) arises from a more active estradiol-ERα signaling, which tunes down autophagy and adipogenesis.