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L

L.B. Chen

Researcher at Wuhan University

Publications -  6
Citations -  171

L.B. Chen is an academic researcher from Wuhan University. The author has contributed to research in topics: Hypothalamic–pituitary–adrenal axis & Glucocorticoid. The author has an hindex of 5, co-authored 6 publications receiving 152 citations.

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Nicotine-induced over-exposure to maternal glucocorticoid and activated glucocorticoid metabolism causes hypothalamic-pituitary-adrenal axis-associated neuroendocrine metabolic alterations in fetal rats

TL;DR: Prenatal nicotine exposure causes HPA axis-associated neuroendocrine metabolic alterations in fetal rats and the underlying mechanism may involve activated glucocorticoid metabolism in various fetal tissues.
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Prenatal nicotine exposure induced a hypothalamic–pituitary–adrenal axis-associated neuroendocrine metabolic programmed alteration in intrauterine growth retardation offspring rats

TL;DR: It is suggested that prenatal nicotine exposure induced an HPA axis-associated neuroendocrine metabolic programmed alteration in adult offspring, which might be attributed to hippocampal functional injury in utero.
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The chronic effects of low lead level on the expressions of Nrf2 and Mrp1 of the testes in the rats

TL;DR: Mrp1 might play important roles in lead detoxification by Nrf2 in rats' testes, and significant increases were observed in the expressions of Mrp1 and NRF2 in two lead groups.
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The accumulation and efflux of lead partly depend on ATP-dependent efflux pump–multidrug resistance protein 1 and glutathione in testis Sertoli cells

TL;DR: Results indicate that lead excretion may be mediated by Mrp1 and GSH in TM4 cells, and could be one of the important intervention points for lead detoxification.
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Effects of individual and multiple fatty acids (palmitate, oleate and docosahaexenoic acid) on cell viability and lipid metabolism in LO2 human liver cells

TL;DR: The results indicate that the type, concentration and mixture ratios of FAs are all important in determining the cell viability and lipid metabolism-related gene expression in LO2 hepatocytes.