RÉSUMÉ
AIM: To investigate the protective effects of quercetin on nephrotoxicity induced by cyclosporine A(CsA)in rats. METHODS: Male Sprague-Dawley (SD) rats were divided into four groups of seven rats each. Control group, quercetin (40 mg/kg) group, CsA (40mg/kg) group, CsA (40 mg/kg) plus quercetin (40 mg/kg) group. The all groups were administered once day respectively for 15 days. Twenty-four hour urines were collected at the 10th and 14th day respectively after administration to measure the content of urinary protein and urinary N-acetyl-?-D-glucosaminidase(NAG). The animals in all groups were sacrificed 4 h after the last administration. Blood samples were collected to measure serum creatinine(SCr), blood urea nitrogen(BUN). Kidneys were removed rapidly, excised and sectioned for histological analysis. Other kiney tissues were utilized for biochemical analysis. RESULTS: Quercetin prevented urinary protein, SCr, BUN, NAG, and kidneys histological alterations.Quercetin significantly decreased malondialdehyde(MDA) content while significantly increased glutathione(GSH) content and glutathione-S-transferase(GST), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), catalase(CAT) activities of kidneys tissues in the rats treated with CsA. CONCLUSION: Quercetin can effectively attenuate the nephrotoxicity induced by CsA.
RÉSUMÉ
AIM : To investigate the effects of tetramethylpyrazine (TMP) on the proliferation of rat glomerular mesangial cells (GMCs) induced by LPS and the levels of intercellular adhesion molecule-1 (I CAM-1). METHODS : Different concentrations of TMP were put in the cultured rat GMCs in vitro after induced by LPS. Cell proliferation was assessed by MTT colorimetric assay and cell cycle was analyzed by flow cytometry. The levels of ICAM-1 were detected by immunohistology. RESULTS : The proliferation of MC induced by LPS was inhibited significantly by TMP with a dose-dependant manner. In the cell cycle, TMP increased the cells in G 0/G 1 phase and decreased the cells in S phase, and the ICAM-1 expression level was decreased. CONCLUSION : LPS-induced proliferation of MC is inhabited significantly by TMP. It blocks G 0/G 1 phase into S phase and inhibited the ICAM-1 expression.
RÉSUMÉ
AIM To investigate the protective effects and mechanisms of TMP on accelerated anti-glomerulus basement membrane(GBM) antibody nephritis of rats. METHODS Model of accelerated anti-GBM nephritis was established in rats and TMP was administrated 120 mg?kg -1 ?d -1 by ip since the day before the model established, consecutively for 15 days. Content of 24h urine protein was detected after model established and rats were killed on d 7 and d 14. Contents of blood urine nitrogen (BUN) and serum creatinine (SCr) were detected. Renal cortex cytoplasm and mitochondria were produced and change of content of lipid peroxidation products malondialdehyde(MDA), activities of glutathione peroxidase(GSH-Px) and catalase(CAT) and superoxide dismutase(SOD) were investigated. RESULTS Compared with model group, TMP group showed significant inhibition in changes of proteinuria and BUN, SCr(P