Abstract
Aim:
Increased expression of c-fos, c-jun and type IV collagen (CoIV) in glomerular mesangial cells (GMC) are important characteristics of diabetic nephropathy. Both c-fos and c-jun regulate the gene expression of extracellular matrix components, and CoIV is the main component of the extracellular matrix. It has been reported that puerarin inhibits aggregation of the extracellular matrix in diabetic rats by an as yet unknown mechanism. The aim of this study is to investigate the effect of puerarin on c-fos, c-jun and CoIV expression in GMC cultured in medium containing 5.6 or 27.8 mmol/L glucose.
Methods:
The expressions of c-fos and c-jun were measured at the protein level using flow cytometry. CoIV content was detected using radioimmunoassay. Protein kinase C (PKC) activity was measured using liquid scintillation counting.
Results:
Puerarin (10−5 mmol/L) significantly ameliorated the high-glucose effect on c-fos, c-jun and CoIV expression. This effect is accompanied by a reduced PKC activity in these cells.
Conclusion:
Our results suggest that reduced PKC activity and expression of c-fos and c-jun in GMC might participate in the mechanisms underlying the therapeutic effect of puerarin on diabetic nephropathy.
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References
Gao YJ, Yue ZJ, Yan LJ, Nan CH, Li DM . Effects of high glucose condition on expression of extracellular matrix of glomerular mesangial cells in rats. Sect Clin Biochem & Lab Med Foreign Med Sci 2004; 25: 99–101.
Kikkawa R, Koya D, Haneda M . Progression of diabetic nephropathy. Am J Kidney Dis 2003; 41: S19–21.
Haneda M, Koya D, Kikkawa R . Cellular mechanisms in the development and progression of diabetic nephropathy: activation of the DAG-PKC-ERK pathway. Am J Kidney Dis 2001; 38: 178–81.
Zhang L, Zhang L, Zhao GS . The regulation of AP-1 on mitosin activating protein kinase signaling pathway. Pathophysiol Clin Med 2002; 20: 32–5.
Mao CP, Gu ZL . Researches of puerarin on pharmacological effect and clinical application. Chin J Hemorh 2004; 14: 138–42.
Mei CL, Zhang LM, Chen L . Establish and identify rat mesangial cells. J Nephro Dial Transplant 1996; 5: 90–2.
Mao CP, Gu ZL, Cao L . Experimental studies on the effects and mechanisms of puerarin in diabetic uninephrectomized rats. Jiangsu Med J 2005; 31: 223–5.
Shankland SJ, Scholey JW . Expression of growth-related protooncogenes during diabetic renal hypertrophy. Kidney Int 1995; 47: 782–8.
Murphy M, McGinty A, Godson C . Protein kinase C: potential targets for intervention in diabetic nephropathy. Curr Opin Nephrol Hypertens 1998; 7: 563–70.
Koya D, King GL . Protein kinase C activation and the development of diabetic complications. Diabetes 1998; 47: 859–66.
Pariat M, Salvat C, Bebien M, Brockly F, Altieri E, Carillo S, et al. The sensitivity of c-Jun and c-Fos proteins to calpains depends on conformational determinants of the monomers and not on formation of dimers. Biochem J 2000; 345: 129–38.
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Mao, Cp., Gu, Zl. Puerarin reduces increased c-fos, c-jun, and type IV collagen expression caused by high glucose in glomerular mesangial cells. Acta Pharmacol Sin 26, 982–986 (2005). https://doi.org/10.1111/j.1745-7254.2005.00133.x
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DOI: https://doi.org/10.1111/j.1745-7254.2005.00133.x
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