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- W2005770022 abstract "This study tested the effect of ginsenoside Rg1 (G-Rg1) in cyclosporin A (CsA)-induced endoplasmic reticulum (ER) stress on renal tubular cell apoptosis in a rat model of chronic CsA nephropathy. Twenty-two Sprague-Dawley rats were randomized into 3 groups: a control group, a model group (CsA 25 mg/kg per day), and a G-Rg1 treatment group (CsA 25 mg/kg per day and G-Rg1 20 mg/kg per day). We examined the effects of G-Rg1 on histopathology, terminal deoxynucleotidyl transferase dUTP nick-end labeling staining, and expression of glucose-regulated protein 78, CCAAT/enhancer-binding protein homologous protein, and caspase-3 by using Western blot analysis. G-Rg1 attenuated CsA-induced tubulointerstitial fibrosis and reduced tubular epithelial cell apoptosis as assessed by terminal deoxynucleotidyl transferase dUTP nick-end labeling staining and caspase-3 expression. Compared with the model group, it reduced the expression of glucose-regulated protein 78 and CCAAT/enhancer-binding protein homologous protein (0.12 ± 0.03 vs 0.48 ± 0.05 [P < .01]; 0.55 ± 0.11 vs 1.08 ± 0.07 [P < .05]), respectively. G-Rg1 mitigates the progression of chronic CsA nephropathy, at least in part, through inhibition of ER stress–triggered tubular cell apoptosis." @default.
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- W2005770022 date "2015-03-01" @default.
- W2005770022 modified "2023-10-18" @default.
- W2005770022 title "Ginsenoside Rg1 Protects Chronic Cyclosporin A Nephropathy From Tubular Cell Apoptosis by Inhibiting Endoplasmic Reticulum Stress in Rats" @default.
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- W2005770022 doi "https://doi.org/10.1016/j.transproceed.2014.10.047" @default.
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