C-peptide replacement therapy as an emerging strategy for preventing diabetic vasculopathy

被引:63
作者
Bhatt, Mahendra Prasad [1 ]
Lim, Young-Cheol [1 ]
Ha, Kwon-Soo [1 ]
机构
[1] Kangwon Natl Univ, Sch Med, Dept Mol & Cellular Biochem, Chunchon 200701, Kangwon Do, South Korea
关键词
C-peptide; Diabetic vasculopathy; C-peptide replacement therapy; Insulin; GLUCOSE-INDUCED APOPTOSIS; ACTIVATED PROTEIN-KINASE; NITRIC-OXIDE SYNTHASE; VASCULAR RISK-FACTORS; K+-ATPASE ACTIVITY; NF-KAPPA-B; HUMAN PROINSULIN; ENDOTHELIAL-CELLS; RENAL-FUNCTION; BLOOD-FLOW;
D O I
10.1093/cvr/cvu211
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Lack of C-peptide, along with insulin, is the main feature of Type 1 diabetes mellitus (DM) and is also observed in progressive beta-cell loss in later stage of Type 2 DM. Therapeutic approaches to hyperglycaemic control have been ineffective in preventing diabetic vasculopathy, and alternative therapeutic strategies are necessary to target both hyperglycaemia and diabetic complications. End-stage organ failure in DM seems to develop primarily due to vascular dysfunction and damage, leading to two types of organ-specific diseases, such as micro- and macrovascular complications. Numerous studies in diabetic patients and animals demonstrate that C-peptide treatment alone or in combination with insulin has physiological functions and might be beneficial in preventing diabetic complications. Current evidence suggests that C-peptide replacement therapy might prevent and ameliorate diabetic vasculopathy and organ-specific complications through conservation of vascular function, as well as prevention of endothelial cell death, microvascular permeability, vascular inflammation, and neointima formation. In this review, we describe recent advances on the beneficial role of C-peptide replacement therapy for preventing diabetic complications, such as retinopathy, nephropathy, neuropathy, impaired wound healing, and inflammation, and further discuss potential beneficial effects of combined C-peptide and insulin supplement therapy to control hyperglycaemia and to prevent organ-specific complications.
引用
收藏
页码:234 / 244
页数:11
相关论文
共 134 条
[91]   The clotting system - a major player in wound healing [J].
Monroe, Dougald M. ;
Hoffman, Maureane .
HAEMOPHILIA, 2012, 18 :11-16
[92]   Cellular mechanisms by which proinsulin C-peptide prevents insulin-induced neointima formation in human saphenous vein [J].
Mughal, R. S. ;
Scragg, J. L. ;
Lister, P. ;
Warburton, P. ;
Riches, K. ;
O'Regan, D. J. ;
Ball, S. G. ;
Turner, N. A. ;
Porter, K. E. .
DIABETOLOGIA, 2010, 53 (08) :1761-1771
[93]   Solution structure of human proinsulin C-peptide [J].
Munte, CE ;
Vilela, L ;
Kalbitzer, HR ;
Garratt, RC .
FEBS JOURNAL, 2005, 272 (16) :4284-4293
[94]   In Vivo Quantitative Visualization Analysis of the Effect of C-Peptide on Glomerular Hyperfiltration in Diabetic Rats by Using Multiphoton Microscopy [J].
Nakamoto, Hiroshi ;
Kajiya, Fumihiko .
MICROCIRCULATION, 2013, 20 (05) :425-433
[95]   Macrophages and angiogenesis: a role for Wnt signaling [J].
Newman, Andrew C. ;
Hughes, Christopher C. W. .
VASCULAR CELL, 2012, 4
[96]   The C-peptide fragment EVARQ reduces glomerular hyperfiltration in streptozotocin-induced diabetic rats [J].
Nordquist, Lina ;
Moe, Erika ;
Sjoquist, Mats .
DIABETES-METABOLISM RESEARCH AND REVIEWS, 2007, 23 (05) :400-405
[97]   Proinsulin C-peptide prevents type-1 diabetes-induced decrease of renal Na+-K+-ATPase α1-subunit in rats [J].
Nordquist, Lina ;
Shimada, Kohei ;
Ishii, Tatsuya ;
Furuya, Daniela Tomie ;
Kamikawa, Akihiro ;
Kimura, Kazuhiro .
DIABETES-METABOLISM RESEARCH AND REVIEWS, 2010, 26 (03) :193-199
[98]   Proinsulin C-peptide reduces diabetes-induced glomerular hyperfiltration via efferent arteriole dilation and inhibition of tubular sodium reabsorption [J].
Nordquist, Lina ;
Brown, Russell ;
Fasching, Angelica ;
Persson, Patrik ;
Palm, Fredrik .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2009, 297 (05) :F1265-F1272
[99]   Differential effects of proinsulin C-peptide fragments on Na+, K+-ATPase activity of renal tubule segments [J].
Ohtomo, Y ;
Bergman, T ;
Johansson, BL ;
Jörnvall, H ;
Wahren, J .
DIABETOLOGIA, 1998, 41 (03) :287-291
[100]   A review of anti-VEGF agents for proliferative diabetic retinopathy [J].
Osaadon, P. ;
Fagan, X. J. ;
Lifshitz, T. ;
Levy, J. .
EYE, 2014, 28 (05) :510-520