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CHEN Ni, HAN Pengding, CHEN Wen. et al. Investigation the Inhibitory Effects of Kaempferol on Rat Renalmesangial Cells Proliferation under High [J]. Journal of Sichuan University (Medical Sciences), 2017, 48(4): 526-530.
Citation: CHEN Ni, HAN Pengding, CHEN Wen. et al. Investigation the Inhibitory Effects of Kaempferol on Rat Renalmesangial Cells Proliferation under High [J]. Journal of Sichuan University (Medical Sciences), 2017, 48(4): 526-530.

Investigation the Inhibitory Effects of Kaempferol on Rat Renalmesangial Cells Proliferation under High 

  • Objective To investigate the protective effects of kaempferol on rat renal mesangial cells under high glucose condition and explore its mechanism. Methods The HBZY-1 cells were divided into normal glucose group (5.5 mmol/L), high glucose group (25 mmol/L), 10 μmol/L kaempferol+high glucose group, and 30 μmol/L kaempferol+high glucose group. Cell proliferative ability was measured by MTT; cell cycle was analyzed by flow cytometry; mRNA and protein levels were determined by Real-time PCR and Western blot, respectively. Results Kaempferol had no effect on the proliferative ability of rat renal mesangial cells under normal glucose (5.5 mmol/L) condition. High glucose (25 mmol/L) enhanced the cell proliferative ability, and this effect was antagonized by kaempferol (10-30 μmol/L) treatment. High glucose reduced the cell population at G0 /G1 2/M phase; and kaempferol treatment restored high glucose-induced changes in cell cycle. Kaempferol also prevented high glucose-induced increase in fibronectin and connective tissue growth factor mRNA and protein expression levels. Kaempferol also prevented high glucose-induced increase in fibronectin and connective tissue growth factor mRNA and protein expression levels. Further, high glucose caused an increase in protein level of phosphorylated p38 mitogen-activated protein kinases (p38 MAPK), which was antagonized by kaempferol treatment. Conclusion Our results suggest that kaempferol exerts its protective effect on rat renal mesangial cells under high glucose condition via p38 MAPK signaling pathway.
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