Inhibition of renin activity by aliskiren ameliorates diabetic nephropathy in type 1 diabetes mouse model

Abstract

Renin is the rate-limiting enzyme of the reninangiotensin system (RAS). In addition to its enzymatic activity to generate angiotensin I, renin also signals through the (pro)renin receptor to exert angiotensin II-independent effects. In this study we examined the effect of renin inhibition on the development of diabetic nephropathy. Male DBA/2J mice were induced to diabetes with streptozotocin, and the diabetic mice were treated for 16 weeks with saline or aliskiren, a renin enzymatic inhibitor. Aliskiren treatment had little effects on blood glucose and blood pressure in diabetic mice. Saline-treated mice developed progressive albuminuria and glome-rulosclerosis, and aliskiren treatment effectively alleviated albumiuria and glomerulosclerosis. Morphologically aliskiren treatment prevented the thickening of the glomerular basement membrane and reduced podocyte loss. At the molecular levels, aliskiren prevented the decline of slit diaphragm proteins and blocked the synthesis of extracellular matrix and pro-fibrotic factors in the diabetic kidney. Aliskiren treatment results in compensatory renin increase in the glomeruli due to blockade of the negative feedback loop, and also partially suppressed the intracellular signaling mediated by the (pro)renin receptor activated in hyperglycemia. These observations suggest that the therapeutic activity of aliskiren to prevent diabetic renal injury is contributed by inhibition of both the angiotensin II-dependent and -independent pathways. Taken together, it is concluded that inhibition of renin enzymatic activity ameliorates diabetic renal injury in type 1 diabetes, and support the use of aliskiren in diabetes kidney disease.

Share and Cite:

Zhang, Y. , Wang, Y. , Chen, Y. , K. Deb, D. , Sun, T. , Zhao, Q. and Chun Li, Y. (2012) Inhibition of renin activity by aliskiren ameliorates diabetic nephropathy in type 1 diabetes mouse model. Journal of Diabetes Mellitus, 2, 353-360. doi: 10.4236/jdm.2012.23055.

Conflicts of Interest

The authors declare no conflicts of interest.

References

[1] Nguyen, G., Delarue, F., Burckle, C., Bouzhir, L., Giller, T. and Sraer, J.D. (2002) Pivotal role of the renin/prorenin receptor in angiotensin II production and cellular responses to renin. Journal of Clinical Investigation, 109, 1417-1427.
[2] Anderson, S., Jung, F.F. and Ingelfinger, J.R. (1993) Renal renin-angiotensin system in diabetes: Functional, immunohistochemical, and molecular biological correlations. American Journal of Physiology, 265, 477-486.
[3] Zimpelmann, J., Kumar, D., Levine, D.Z., Wehbi, G., Imig, J.D., Navar, L.G. and Burns, K.D. (2000) Early diabetes mellitus stimulates proximal tubule renin mRNA expression in the rat. Kidney International, 58, 2320-2330. doi:10.1046/j.1523-1755.2000.00416.x
[4] Gilbert, R.E., Krum, H., Wilkinson-Berka, J. and Kelly, D.J. (2003) The renin-angiotensin system and the long-term complications of diabetes: Pathophysiological and therapeutic considerations. Diabetic Medicine, 20, 607-621. doi:10.1046/j.1464-5491.2003.00979.x
[5] Carey, R.M. and Siragy, H.M. (2003) The intrarenal reninangiotensin system and diabetic nephropathy. Trends in Endocrinology & Metabolism, 14, 274-281. doi:10.1016/S1043-2760(03)00111-5
[6] Huang, Y., Wongamorntham, S., Kasting, J., McQuillan, D., Owens, R.T., Yu, L., Noble, N.A. and Border, W. (2006) Renin increases mesangial cell transforming growth factor-beta1 and matrix proteins through receptor-mediated, angiotensin II-independent mechanisms. Kidney International, 69, 105-113. doi:10.1038/sj.ki.5000011
[7] Chan, J.C., Ko, G.T., Leung, D.H., Cheung, R.C., Cheung, M.Y., So, W.Y., Swaminathan, R., Nicholls, M.G., Critchley, J.A. and Cockram, C.S. (2000) Long-term effects of angiotensin-converting enzyme inhibition and metabolic control in hypertensive type 2 diabetic patients. Kidney International, 57, 590-600. doi:10.1046/j.1523-1755.2000.00879.x
[8] Lewis, E.J., Hunsicker, L.G., Clarke, W.R., Berl, T., Pohl, M.A., Lewis, J.B., Ritz, E., Atkins, R.C., Rohde, R., and Raz, I. (2001) Renoprotective effect of the angiotensin-receptor antagonist irbesartan in patients with nephropathy due to type 2 diabetes. The New England Journal of Medicine, 345, 851-860. doi:10.1056/NEJMoa011303
[9] Brenner, B.M., Cooper, M.E., de Zeeuw, D., Keane, W.F., Mitch, W.E., Parving, H.H., Remuzzi, G., Snapinn, S.M., Zhang, Z. and Shahinfar, S. (2001) Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy. The New England Journal of Medicine, 345, 861-869. doi:10.1056/NEJMoa011161
[10] Parving, H.H., Lehnert, H., Brochner-Mortensen, J., Gomis, R., Andersen, S., and Arner, P. (2001) The effect of irbesartan on the development of diabetic nephropathy in patients with type 2 diabetes. The New England Journal of Medicine, 345, 870-878. doi:10.1056/NEJMoa011489
[11] Andersen, S., Tarnow, L., Rossing, P., Hansen, B.V. and Parving, H.H. (2000) Renoprotective effects of angiotensin II receptor blockade in type 1 diabetic patients with diabetic nephropathy. Kidney International, 57, 601-606. doi:10.1046/j.1523-1755.2000.00880.x
[12] Ichihara, A., Hayashi, M., Kaneshiro, Y., Suzuki, F., Nakagawa, T., Tada, Y., Koura, Y., Nishiyama, A., Okada, H., Uddin, M.N., Nabi, A.H., Ishida, Y., Inagami, T. and Saruta, T. (2004) Inhibition of diabetic nephropathy by a decoy peptide corresponding to the “handle” region for nonproteolytic activation of prorenin. Journal of Clinical Investigation, 114, 1128-1135. doi:10.1172/JCI21398
[13] Zhang, Z., Zhang, Y., Ning, G., Deb, D.K., Kong, J. and Li, Y.C. (2008) Combination therapy with AT1 blocker and vitamin D analog markedly ameliorates diabetic nephropathy: Blockade of compensatory renin increase. Proceedings of the National Academy of Sciences USA, 105, 15896-15901. doi:10.1073/pnas.0803751105
[14] Zhang, Y., Deb. K.D., Kong, J., Ning, G., Wong, Y., Li, G., Chen, Y., Zhang, Z., Strugnell, S., Sabbagh, Y., Arbeeny, C. and Li, Y.C. (2009) Long-Term Therapeutic Effect of Vitamin D Analog Doxercalciferol on Diabetic Nephropathy: Strong Synergism with AT1 Receptor Antagonist. American Journal of Physiology Renal Physiology, 297, F791-F801. doi:10.1152/ajprenal.00247.2009
[15] Wood, J.M., Maibaum, J., Rahuel, J., Grutter, M.G., Cohen, N.C., Rasetti, V., Ruger, H., Goschke, R., Stutz, S., Fuhrer, W., Schilling, W., Rigollier, P., Yamaguchi, Y., Cumin, F., Baum, H.P., Schnell, C.R., Herold, P., Mah, R., Jensen, C., O’Brien, E., Stanton, A. and Bedigian, M.P. (2003) Structure-based design of aliskiren, a novel orally effective renin inhibitor. Biochemical and Biophysical Research Communications, 308, 698-705. doi:10.1016/S0006-291X(03)01451-7
[16] Parving, H.H., Persson, F., Lewis, J.B., Lewis, E.J. and Hollenberg, N.K. (2008) Aliskiren combined with losartan in type 2 diabetes and nephropathy. The New England Journal of Medicine, 358, 2433-2446. doi:10.1056/NEJMoa0708379
[17] Persson, F., Lewis, J.B., Lewis, E.J., Rossing, P., Hollenberg, N.K. and Parving, H.H. (2011) Aliskiren in combination with losartan reduces albuminuria independent of baseline blood pressure in patients with type 2 diabetes and nephropathy. Clinical Journal of the American Society of Nephrology, 6, 1025-1031. doi:10.2215/CJN.07590810
[18] Lu, H., Rateri, D.L., Feldman, D.L.Jr.R.J., Fukamizu, A., Ishida, J., Oesterling, E.G., Cassis, L.A. and Daugherty, A. (2008) Renin inhibition reduces hypercholesterolemia-induced atherosclerosis in mice. Journal of Clinical Investigation, 118, 984-993.
[19] Zhang, Z., Sun, L., Wang, Y., Ning, G., Minto, A.W., Kong, J., Quigg, R.J. and Li, Y.C. (2008) Renoprotective role of the vitamin D receptor in diabetic nephropathy. Kidney International, 73, 163-171. doi:10.1038/sj.ki.5002572
[20] Li, Y.C., Kong, J., Wei, M., Chen, Z.F., Liu, S.Q. and Cao, L.P. (2002) 1,25-Dihydroxyvitamin D(3) is a negative endocrine regulator of the renin-angiotensin system. Journal of Clinical Investigation, 110, 229-238.
[21] Taneda, S., Pippin, J.W., Sage, E.H., Hudkins, K.L., Takeuchi, Y., Couser, W.G. and Alpers, C.E. (2003) Amelioration of diabetic nephropathy in SPARC-null mice. Journal of the American Society of Nephrology, 14, 968-980. doi:10.1097/01.ASN.0000054498.83125.90
[22] Takemoto, M., Asker, N., Gerhardt, H., Lundkvist, A., Johansson, B.R., Saito, Y. and Betsholtz, C. (2002) A new method for large scale isolation of kidney glomeruli from mice. American Journal of Pathology, 161, 799-805. doi:10.1016/S0002-9440(10)64239-3
[23] Li, Y.C., Bolt, M.J.G., Cao, L.-P. and Sitrin, M.D. (2001) Effects of vitamin D receptor inactivation on the expression of calbindins and calcium metabolism. American Journal of Physiology—Endocrinology and Metabolism, 281, 558-564.
[24] Qi, Z., Fujita, H., Jin, J., Davis, L.S., Wang, Y., Fogo, A.B. and Breyer, M.D. (2005) Characterization of susceptibility of inbred mouse strains to diabetic nephropathy. Diabetes, 54, 2628-2637. doi:10.2337/diabetes.54.9.2628
[25] Li, Y.C. (2007) Inhibition of renin: An updated review of the development of renin inhibitors. Current Opinion in Investigational Drugs, 8, 750-757.
[26] Nussberger, J., Wuerzner, G., Jensen, C. and Brunner, H.R. (2002) Angiotensin II suppression in humans by the orally active renin inhibitor Aliskiren (SPP100): Comparison with enalapril. Hypertension, 39, 1-8. doi:10.1161/hy0102.102293
[27] Feldman, D.L., Jin, L., Xuan, H., Contrepas, A., Zhou, Y., Webb, R.L., Mueller, D.N., Feldt, S., Cumin, F., Maniara, W., Persohn, E., Schuetz, H., Jan Danser, A.H. and Nguyen, G. (2008) Effects of aliskiren on blood pressure, albuminuria, and (pro)renin receptor expression in diabetic TG(mRen-2)27 rats. Hypertension, 52, 130-136. doi:10.1161/HYPERTENSIONAHA.107.108845
[28] Muller, D.N. and Luft, F.C. (2006) Direct renin inhibition with aliskiren in hypertension and target organ damage. Clinical Journal of the American Society of Nephrology, 1, 221-228. doi:10.2215/CJN.01201005
[29] Azizi, M., Menard, J., Bissery, A., Guyenne, T.T., Bura-Riviere, A., Vaidyanathan, S. and Camisasca, R.P. (2004) Pharmacologic demonstration of the synergistic effects of a combination of the renin inhibitor aliskiren and the AT1 receptor antagonist valsartan on the angiotensin II-renin feedback interruption. Journal of the American Society of Nephrology, 15, 3126-3133. doi:10.1097/01.ASN.0000146686.35541.29
[30] Durvasula, R.V. and Shankland, S.J. (2008) Activation of a local renin angiotensin system in podocytes by glucose. American Journal of Physiology—Renal Physiology, 294, 830-839. doi:10.1152/ajprenal.00266.2007
[31] Vidotti, D.B., Casarini, D.E., Cristovam, P.C., Leite, C.A., Schor, N. and Boim, M.A. (2004) High glucose concentration stimulates intracellular renin activity and angiotensin II generation in rat mesangial cells. American Journal of Physiology—Renal Physiology, 286, 1039-1045. doi:10.1152/ajprenal.00371.2003
[32] Yoo, T.H., Li, J.J., Kim, J.J., Jung, D.S., Kwak, S.J., Ryu, D.R., Choi, H.Y., Kim, J.S., Kim, H.J., Han, S.H., Lee, J.E., Han, D.S. and Kang, S.W. (2007) Activation of the renin-angiotensin system within podocytes in diabetes. Kidney International, 71, 1019-1027. doi:10.1038/sj.ki.5002195
[33] Yuan, W., Pan, W., Kong, J., Zheng, W., Szeto, F.L., Wong, K.E., Cohen, R., Klopot, A., Zhang, Z. and Li, Y.C.(2007) 1,25-Dihydroxyvitamin D3 suppresses renin gene transcription by blocking the activity of the cyclic AMP Response element in the renin gene promoter. The Journal of Biological Chemistry, 282, 29821-29830. doi:10.1074/jbc.M705495200
[34] Ichihara, A., Suzuki, F., Nakagawa, T., Kaneshiro, Y., Takemitsu, T., Sakoda, M., Nabi, A.H., Nishiyama, A., Sugaya, T., Hayashi, M. and Inagami, T. (2006) Prorenin receptor blockade inhibits development of glomerulosclerosis in diabetic angiotensin II type 1a receptor-deficient mice. Journal of the American Society of Nephrology, 17, 1950-1961. doi:10.1681/ASN.2006010029
[35] Feldt, S., Batenburg, W.W., Mazak, I., Maschke, U., Wellner, M., Kvakan, H., Dechend, R., Fiebeler, A., Burckle, C., Contrepas, A., Jan Danser, A.H., Bader, M., Nguyen, G., Luft, F.C. and Muller, D.N. (2008) Prorenin and renin-induced extracellular signal-regulated kinase 1/2 activation in monocytes is not blocked by aliskiren or the handle-region peptide. Hypertension, 51, 682-688. doi:10.1161/HYPERTENSIONAHA.107.101444

Copyright © 2024 by authors and Scientific Research Publishing Inc.

Creative Commons License

This work and the related PDF file are licensed under a Creative Commons Attribution 4.0 International License.