Skip to main content
Erschienen in: Inflammation 4/2012

01.08.2012

Rosiglitazone Ameliorates Diabetic Nephropathy by Reducing the Expression of Chemerin and ChemR23 in the Kidney of Streptozotocin-Induced Diabetic Rats

verfasst von: Wenchao Hu, Qian Yu, Jie Zhang, Demin Liu

Erschienen in: Inflammation | Ausgabe 4/2012

Einloggen, um Zugang zu erhalten

Abstract

Chemerin is shown to be associated with inflammation which is involved in the pathogenesis of diabetic nephropathy. This study aims to determine whether rosiglitazone and pioglitazone ameliorate renal function through an effect on the expression of chemerin and ChemR23 in streptozotocin-induced diabetic rats. The rats were randomized to control, diabetic, rosiglitazone-, and pioglitazone-treated groups. The expression level of chemerin and ChemR23 in the renal tissues was significantly elevated in the diabetic group compared with the control group. Rosiglitazone inhibited the overexpression of chemerin and ChemR23, while pioglitazone inhibited the overexpression of ChemR23 in the kidney of diabetic rats. In addition, chemerin expression level was positively correlated with transforming growth factor-β1, connective tissue growth factor, tumor necrosis factor-α, and intracellular cell adhesion molecule-1 expression in diabetic rats. Rosiglitazone ameliorates diabetic nephropathy by reducing the expression of chemerin and ChemR23 in diabetic rats.
Literatur
1.
Zurück zum Zitat Wagman, A.S., and J.M. Nuss. 2001. Current therapies and emerging targets for the treatment of diabetes. Current Pharmaceutical Design 7(6): 417–450.PubMedCrossRef Wagman, A.S., and J.M. Nuss. 2001. Current therapies and emerging targets for the treatment of diabetes. Current Pharmaceutical Design 7(6): 417–450.PubMedCrossRef
2.
Zurück zum Zitat Pfau, D., A. Bachmann, U. Lössner, J. Kratzsch, M. Blüher, M. Stumvoll, and M. Fasshauer. 2010. Serum levels of the adipokine chemerin in relation to renal function. Diabetes Care 33(1): 171–173.PubMedCrossRef Pfau, D., A. Bachmann, U. Lössner, J. Kratzsch, M. Blüher, M. Stumvoll, and M. Fasshauer. 2010. Serum levels of the adipokine chemerin in relation to renal function. Diabetes Care 33(1): 171–173.PubMedCrossRef
3.
Zurück zum Zitat Yamamoto, T., A.R. Qureshi, B. Anderstam, O. Heimbürger, P. Bárány, B. Lindholm, P. Stenvinkel, and J. Axelsson. 2010. Clinical importance of an elevated circulating chemerin level in incident dialysis patients. Nephrology, Dialysis, Transplantation 25(12): 4017–4023.PubMedCrossRef Yamamoto, T., A.R. Qureshi, B. Anderstam, O. Heimbürger, P. Bárány, B. Lindholm, P. Stenvinkel, and J. Axelsson. 2010. Clinical importance of an elevated circulating chemerin level in incident dialysis patients. Nephrology, Dialysis, Transplantation 25(12): 4017–4023.PubMedCrossRef
4.
Zurück zum Zitat Hu, W., and P. Feng. 2010. Elevated serum chemerin concentrations are associated with renal dysfunction in type 2 diabetic patients. Diabetes Research and Clinical Practice 91(2): 159–163.PubMedCrossRef Hu, W., and P. Feng. 2010. Elevated serum chemerin concentrations are associated with renal dysfunction in type 2 diabetic patients. Diabetes Research and Clinical Practice 91(2): 159–163.PubMedCrossRef
5.
Zurück zum Zitat Lehrke, M., A. Becker, M. Greif, R. Stark, R.P. Laubender, F. von Ziegler, C. Lebherz, J. Tittus, M. Reiser, C. Becker, B. Göke, A.W. Leber, K.G. Parhofer, and U.C. Broedl. 2009. Chemerin is associated with markers of inflammation and components of the metabolic syndrome but does not predict coronary atherosclerosis. European Journal of Endocrinology 161(2): 339–344.PubMedCrossRef Lehrke, M., A. Becker, M. Greif, R. Stark, R.P. Laubender, F. von Ziegler, C. Lebherz, J. Tittus, M. Reiser, C. Becker, B. Göke, A.W. Leber, K.G. Parhofer, and U.C. Broedl. 2009. Chemerin is associated with markers of inflammation and components of the metabolic syndrome but does not predict coronary atherosclerosis. European Journal of Endocrinology 161(2): 339–344.PubMedCrossRef
6.
Zurück zum Zitat Weigert, J., M. Neumeier, J. Wanninger, M. Filarsky, S. Bauer, R. Wiest, S. Farkas, M.N. Scherer, A. Schäffler, C. Aslanidis, J. Schölmerich, and C. Buechler. 2010. Systemic chemerin is related to inflammation rather than obesity in type 2 diabetes. Clinical Endocrinology 72(3): 342–348.PubMedCrossRef Weigert, J., M. Neumeier, J. Wanninger, M. Filarsky, S. Bauer, R. Wiest, S. Farkas, M.N. Scherer, A. Schäffler, C. Aslanidis, J. Schölmerich, and C. Buechler. 2010. Systemic chemerin is related to inflammation rather than obesity in type 2 diabetes. Clinical Endocrinology 72(3): 342–348.PubMedCrossRef
7.
Zurück zum Zitat King, G.L. 2008. The role of inflammatory cytokines in diabetes and its complications. Journal of Periodontology 79(8 Suppl): 1527–1534.PubMedCrossRef King, G.L. 2008. The role of inflammatory cytokines in diabetes and its complications. Journal of Periodontology 79(8 Suppl): 1527–1534.PubMedCrossRef
8.
Zurück zum Zitat Roh, S.G., S.H. Song, K.C. Choi, K. Katoh, V. Wittamer, M. Parmentier, and S. Sasaki. 2007. Chemerin–a new adipokine that modulates adipogenesis via its own receptor. Biochemical and Biophysical Research Communications 362(4): 1013–1038.PubMedCrossRef Roh, S.G., S.H. Song, K.C. Choi, K. Katoh, V. Wittamer, M. Parmentier, and S. Sasaki. 2007. Chemerin–a new adipokine that modulates adipogenesis via its own receptor. Biochemical and Biophysical Research Communications 362(4): 1013–1038.PubMedCrossRef
9.
Zurück zum Zitat Yoshimura, T., and J.J. Oppenheim. 2011. Chemokine-like receptor 1 (CMKLR1) and chemokine (C-C motif) receptor-like 2 (CCRL2); two multifunctional receptors with unusual properties. Experimental Cell Research 317(5): 674–684.PubMedCrossRef Yoshimura, T., and J.J. Oppenheim. 2011. Chemokine-like receptor 1 (CMKLR1) and chemokine (C-C motif) receptor-like 2 (CCRL2); two multifunctional receptors with unusual properties. Experimental Cell Research 317(5): 674–684.PubMedCrossRef
10.
Zurück zum Zitat Lebovitz, H.E., and M.A. Banerji. 2001. Insulin resistance and its treatment by thiazolidinediones. Recent Progress in Hormone Research 56: 265–294.PubMedCrossRef Lebovitz, H.E., and M.A. Banerji. 2001. Insulin resistance and its treatment by thiazolidinediones. Recent Progress in Hormone Research 56: 265–294.PubMedCrossRef
11.
Zurück zum Zitat Zheng, M., S. Ye, Z. Zhai, Y. Chen, X. Li, G. Yang, A. Fan, and Y. Wang. 2009. Rosiglitazone protects diabetic rats against kidney disease through the suppression of renal moncyte chemoattractant protein-1 expression. Journal of Diabetes and its Complications 23(2): 124–129.PubMedCrossRef Zheng, M., S. Ye, Z. Zhai, Y. Chen, X. Li, G. Yang, A. Fan, and Y. Wang. 2009. Rosiglitazone protects diabetic rats against kidney disease through the suppression of renal moncyte chemoattractant protein-1 expression. Journal of Diabetes and its Complications 23(2): 124–129.PubMedCrossRef
12.
Zurück zum Zitat Kim, H.J., S.K. Kim, W.S. Shim, J.H. Lee, K.Y. Hur, E.S. Kang, C.W. Ahn, S.K. Lim, H.C. Lee, and B.S. Cha. 2008. Rosiglitazone improves insulin sensitivity with increased serum leptin levels in patients with type 2 diabetes mellitus. Diabetes Research and Clinical Practice 81(1): 42–49.PubMedCrossRef Kim, H.J., S.K. Kim, W.S. Shim, J.H. Lee, K.Y. Hur, E.S. Kang, C.W. Ahn, S.K. Lim, H.C. Lee, and B.S. Cha. 2008. Rosiglitazone improves insulin sensitivity with increased serum leptin levels in patients with type 2 diabetes mellitus. Diabetes Research and Clinical Practice 81(1): 42–49.PubMedCrossRef
13.
Zurück zum Zitat Majuri, A., M. Santaniemi, K. Rautio, A. Kunnari, J. Vartiainen, A. Ruokonen, Y.A. Kesäniemi, J.S. Tapanainen, O. Ukkola, and L. Morin-Papunen. 2007. Rosiglitazone treatment increases plasma levels of adiponectin and decreases levels of resistin in overweight women with PCOS: A randomized placebo-controlled study. European Journal of Endocrinology 156(2): 263–269.PubMedCrossRef Majuri, A., M. Santaniemi, K. Rautio, A. Kunnari, J. Vartiainen, A. Ruokonen, Y.A. Kesäniemi, J.S. Tapanainen, O. Ukkola, and L. Morin-Papunen. 2007. Rosiglitazone treatment increases plasma levels of adiponectin and decreases levels of resistin in overweight women with PCOS: A randomized placebo-controlled study. European Journal of Endocrinology 156(2): 263–269.PubMedCrossRef
14.
Zurück zum Zitat Aso, Y., K. Hara, N. Ozeki, C. Yatsuka, T. Nakano, S. Matsumoto, M. Suetsugu, T. Nakamachi, K. Takebayashi, K. Haruki, and T. Inukai. 2009. Low-dose pioglitazone increases serum high molecular weight adiponectin and improves glycemic control in Japanese patients with poorly controlled type 2 diabetes. Diabetes Research and Clinical Practice 85(2): 147–152.PubMedCrossRef Aso, Y., K. Hara, N. Ozeki, C. Yatsuka, T. Nakano, S. Matsumoto, M. Suetsugu, T. Nakamachi, K. Takebayashi, K. Haruki, and T. Inukai. 2009. Low-dose pioglitazone increases serum high molecular weight adiponectin and improves glycemic control in Japanese patients with poorly controlled type 2 diabetes. Diabetes Research and Clinical Practice 85(2): 147–152.PubMedCrossRef
15.
Zurück zum Zitat Pfützner, A., N. Marx, D. Walcher, M. Löbig, D. Seidel, and T. Forst. 2008. Impact of rosiglitazone on visfatin and adiponectin plasma concentrations in patients with type 2 diabetes and coronary artery disease. Clinical Laboratory 54(7–8): 237–241.PubMed Pfützner, A., N. Marx, D. Walcher, M. Löbig, D. Seidel, and T. Forst. 2008. Impact of rosiglitazone on visfatin and adiponectin plasma concentrations in patients with type 2 diabetes and coronary artery disease. Clinical Laboratory 54(7–8): 237–241.PubMed
16.
Zurück zum Zitat Goralski, K.B., T.C. McCarthy, E.A. Hanniman, B.A. Zabel, E.C. Butcher, S.D. Parlee, S. Muruganandan, and C.J. Sinal. 2007. Chemerin, a novel adipokine that regulates adipogenesis and adipocyte metabolism. Journal of Biological Chemistry 282(38): 28175–28188.PubMedCrossRef Goralski, K.B., T.C. McCarthy, E.A. Hanniman, B.A. Zabel, E.C. Butcher, S.D. Parlee, S. Muruganandan, and C.J. Sinal. 2007. Chemerin, a novel adipokine that regulates adipogenesis and adipocyte metabolism. Journal of Biological Chemistry 282(38): 28175–28188.PubMedCrossRef
17.
Zurück zum Zitat Stejskal, D., M. Karpisek, Z. Hanulova, and M. Svestak. 2008. Chemerin is an independent marker of the metabolic syndrome in a Caucasian population–a pilot study. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 152(2): 217–221.PubMed Stejskal, D., M. Karpisek, Z. Hanulova, and M. Svestak. 2008. Chemerin is an independent marker of the metabolic syndrome in a Caucasian population–a pilot study. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 152(2): 217–221.PubMed
18.
Zurück zum Zitat Bozaoglu, K., D. Segal, K.A. Shields, N. Cummings, J.E. Curran, A.G. Comuzzie, M.C. Mahaney, D.L. Rainwater, J.L. VandeBerg, J.W. MacCluer, G. Collier, J. Blangero, K. Walder, and J.B. Jowett. 2009. Chemerin is associated with metabolic syndrome phenotypes in a Mexican-American population. Journal of Clinical Endocrinology and Metabolism 94(8): 3085–3088.PubMedCrossRef Bozaoglu, K., D. Segal, K.A. Shields, N. Cummings, J.E. Curran, A.G. Comuzzie, M.C. Mahaney, D.L. Rainwater, J.L. VandeBerg, J.W. MacCluer, G. Collier, J. Blangero, K. Walder, and J.B. Jowett. 2009. Chemerin is associated with metabolic syndrome phenotypes in a Mexican-American population. Journal of Clinical Endocrinology and Metabolism 94(8): 3085–3088.PubMedCrossRef
19.
Zurück zum Zitat Derosa, G., and P. Maffioli. 2011. Thiazolidinediones plus metformin association on body weight in patients with type 2 diabetes. Diabetes Research and Clinical Practice 91(3): 265–270.PubMedCrossRef Derosa, G., and P. Maffioli. 2011. Thiazolidinediones plus metformin association on body weight in patients with type 2 diabetes. Diabetes Research and Clinical Practice 91(3): 265–270.PubMedCrossRef
20.
Zurück zum Zitat Sarafidis, P.A., P.C. Stafylas, P.I. Georgianos, A.N. Saratzis, and A.N. Lasaridis. 2010. Effect of thiazolidinediones on albuminuria and proteinuria in diabetes: A meta-analysis. American Journal of Kidney Diseases 55(5): 835–847.PubMedCrossRef Sarafidis, P.A., P.C. Stafylas, P.I. Georgianos, A.N. Saratzis, and A.N. Lasaridis. 2010. Effect of thiazolidinediones on albuminuria and proteinuria in diabetes: A meta-analysis. American Journal of Kidney Diseases 55(5): 835–847.PubMedCrossRef
21.
Zurück zum Zitat Toblli, J.E., G. Cao, J.F. Giani, M. Angerosa, F.P. Dominici, and N.F. Gonzalez-Cadavid. 2011. Antifibrotic effects of pioglitazone at low doses on the diabetic rat kidney are associated with the improvement of markers of cell turnover, tubular and endothelial integrity, and angiogenesis. Kidney & Blood Pressure Research 34(1): 20–33.CrossRef Toblli, J.E., G. Cao, J.F. Giani, M. Angerosa, F.P. Dominici, and N.F. Gonzalez-Cadavid. 2011. Antifibrotic effects of pioglitazone at low doses on the diabetic rat kidney are associated with the improvement of markers of cell turnover, tubular and endothelial integrity, and angiogenesis. Kidney & Blood Pressure Research 34(1): 20–33.CrossRef
22.
Zurück zum Zitat Muruganandan, S., S.D. Parlee, J.L. Rourke, M.C. Ernst, K.B. Goralski, and C.J. Sinal. 2011. Chemerin, a novel peroxisome proliferator-activated receptor gamma (PPARgamma) target gene that promotes mesenchymal stem cell adipogenesis. Journal of Biological Chemistry 286(27): 23982–23995.PubMedCrossRef Muruganandan, S., S.D. Parlee, J.L. Rourke, M.C. Ernst, K.B. Goralski, and C.J. Sinal. 2011. Chemerin, a novel peroxisome proliferator-activated receptor gamma (PPARgamma) target gene that promotes mesenchymal stem cell adipogenesis. Journal of Biological Chemistry 286(27): 23982–23995.PubMedCrossRef
23.
Zurück zum Zitat Han, D.C., B.B. Hoffman, S.W. Hong, J. Guo, and F.N. Ziyadeh. 2000. Therapy with antisense TGF-beta1 oligodeoxynucleotides reduces kidney weight and matrix mRNAs in diabetic mice. American Journal of Physiology. Renal Physiology 278: F628–F634.PubMed Han, D.C., B.B. Hoffman, S.W. Hong, J. Guo, and F.N. Ziyadeh. 2000. Therapy with antisense TGF-beta1 oligodeoxynucleotides reduces kidney weight and matrix mRNAs in diabetic mice. American Journal of Physiology. Renal Physiology 278: F628–F634.PubMed
24.
Zurück zum Zitat Yamamoto, T., T. Nakamura, N.A. Noble, E. Ruoslahti, and W.A. Border. 1993. Expression of transforming growth factor beta is elevated in human and experimental diabetic nephropathy. Proceedings of the National Academy of Sciences of the United States of America 90(5): 1814–1818.PubMedCrossRef Yamamoto, T., T. Nakamura, N.A. Noble, E. Ruoslahti, and W.A. Border. 1993. Expression of transforming growth factor beta is elevated in human and experimental diabetic nephropathy. Proceedings of the National Academy of Sciences of the United States of America 90(5): 1814–1818.PubMedCrossRef
25.
Zurück zum Zitat Connolly, S.B., D. Sadlier, N.E. Kieran, P. Doran, and H.R. Brady. 2003. Transcriptome profiling and the pathogenesis of diabetic complications. Journal of the American Society of Nephrology 14: S279–S283.PubMedCrossRef Connolly, S.B., D. Sadlier, N.E. Kieran, P. Doran, and H.R. Brady. 2003. Transcriptome profiling and the pathogenesis of diabetic complications. Journal of the American Society of Nephrology 14: S279–S283.PubMedCrossRef
26.
Zurück zum Zitat Wahab, N.A., L. Schaefer, B.S. Weston, O. Yiannikouris, A. Wright, A. Babelova, R. Schaefer, and R.M. Mason. 2005. Glomerular expression of thrombospondin-1, transforming growth factor beta and connective tissue growth factor at different stages of diabetic nephropathy and their interdependent roles in mesangial response to diabetic stimuli. Diabetologia 48(12): 2650–2660.PubMedCrossRef Wahab, N.A., L. Schaefer, B.S. Weston, O. Yiannikouris, A. Wright, A. Babelova, R. Schaefer, and R.M. Mason. 2005. Glomerular expression of thrombospondin-1, transforming growth factor beta and connective tissue growth factor at different stages of diabetic nephropathy and their interdependent roles in mesangial response to diabetic stimuli. Diabetologia 48(12): 2650–2660.PubMedCrossRef
27.
Zurück zum Zitat Yeo, E.S., J.Y. Hwang, J.E. Park, Y.J. Choi, K.B. Huh, and W.Y. Kim. 2010. Tumor necrosis factor (TNF-alpha) and C-reactive protein (CRP) are positively associated with the risk of chronic kidney disease in patients with type 2 diabetes. Yonsei Medical Journal 51(4): 519–525.PubMedCrossRef Yeo, E.S., J.Y. Hwang, J.E. Park, Y.J. Choi, K.B. Huh, and W.Y. Kim. 2010. Tumor necrosis factor (TNF-alpha) and C-reactive protein (CRP) are positively associated with the risk of chronic kidney disease in patients with type 2 diabetes. Yonsei Medical Journal 51(4): 519–525.PubMedCrossRef
28.
Zurück zum Zitat Chen, L., J. Zhang, Y. Zhang, Y. Wang, and B. Wang. 2008. Improvement of inflammatory responses associated with NF-kappa B pathway in kidneys from diabetic rats. Inflammation Research 57(5): 199–204.PubMedCrossRef Chen, L., J. Zhang, Y. Zhang, Y. Wang, and B. Wang. 2008. Improvement of inflammatory responses associated with NF-kappa B pathway in kidneys from diabetic rats. Inflammation Research 57(5): 199–204.PubMedCrossRef
29.
Zurück zum Zitat Chow, F.Y., D.J. Nikolic-Paterson, E. Ozols, R.C. Atkins, and G.H. Tesch. 2005. Intercellular adhesion molecule-1 deficiency is protective against nephropathy in type 2 diabetic db/db mice. Journal of the American Society of Nephrology 16(6): 1711–1722.PubMedCrossRef Chow, F.Y., D.J. Nikolic-Paterson, E. Ozols, R.C. Atkins, and G.H. Tesch. 2005. Intercellular adhesion molecule-1 deficiency is protective against nephropathy in type 2 diabetic db/db mice. Journal of the American Society of Nephrology 16(6): 1711–1722.PubMedCrossRef
30.
Zurück zum Zitat Hart, R., and D.R. Greaves. 2010. Chemerin contributes to inflammation by promoting macrophage adhesion to VCAM-1 and fibronectin through clustering of VLA-4 and VLA-5. Journal of Immunology 185(6): 3728–3739.CrossRef Hart, R., and D.R. Greaves. 2010. Chemerin contributes to inflammation by promoting macrophage adhesion to VCAM-1 and fibronectin through clustering of VLA-4 and VLA-5. Journal of Immunology 185(6): 3728–3739.CrossRef
31.
Zurück zum Zitat Sell, H., A. Divoux, C. Poitou, A. Basdevant, J.L. Bouillot, P. Bedossa, J. Tordjman, J. Eckel, and K. Clément. 2010. Chemerin correlates with markers for fatty liver in morbidly obese patients and strongly decreases after weight loss induced by bariatric surgery. Journal of Clinical Endocrinology and Metabolism 95(6): 2892–2896.PubMedCrossRef Sell, H., A. Divoux, C. Poitou, A. Basdevant, J.L. Bouillot, P. Bedossa, J. Tordjman, J. Eckel, and K. Clément. 2010. Chemerin correlates with markers for fatty liver in morbidly obese patients and strongly decreases after weight loss induced by bariatric surgery. Journal of Clinical Endocrinology and Metabolism 95(6): 2892–2896.PubMedCrossRef
Metadaten
Titel
Rosiglitazone Ameliorates Diabetic Nephropathy by Reducing the Expression of Chemerin and ChemR23 in the Kidney of Streptozotocin-Induced Diabetic Rats
verfasst von
Wenchao Hu
Qian Yu
Jie Zhang
Demin Liu
Publikationsdatum
01.08.2012
Verlag
Springer US
Erschienen in
Inflammation / Ausgabe 4/2012
Print ISSN: 0360-3997
Elektronische ISSN: 1573-2576
DOI
https://doi.org/10.1007/s10753-012-9440-y

Weitere Artikel der Ausgabe 4/2012

Inflammation 4/2012 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.