Role of C-peptide in human physiology

被引:217
作者
Wahren, J [1 ]
Ekberg, K
Johansson, J
Henriksson, M
Pramanik, A
Johansson, BL
Rigler, R
Jörnvall, H
机构
[1] Karolinska Hosp, Sect Clin Physiol A2 01, Dept Surg Sci, SE-17176 Stockholm, Sweden
[2] Karolinska Inst, Dept Med Biochem & Biophys, SE-17177 Stockholm, Sweden
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2000年 / 278卷 / 05期
关键词
sodium-potassium-adenosine 5 '-triphosphatase; endothelial nitric oxide synthase; renal function; autonomic nerve function; G protein;
D O I
10.1152/ajpendo.2000.278.5.E759
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The C-peptide of proinsulin is important for the biosynthesis of insulin but has for a long time been considered to be biologically inert. Data now indicate that C-peptide in the nanomolar concentration range binds specifically to cell surfaces, probably to a G protein-coupled surface receptor, with subsequent activation of Ca2+-dependent intracellular signaling pathways. The association rate constant, K-ass, for C-peptide binding to endothelial cells, renal tubular cells, and fibroblasts is similar to 3.10(9) M-1. The binding is stereospecific, and no cross-reaction is seen with insulin, proinsulin, insulin growth factors I and II, or neuropeptide Y. C-peptide stimulates Na+-K+-ATPase and endothelial nitric oxide synthase activities. Data also indicate that C-peptide administration is accompanied by augmented blood flow in skeletal muscle and skin, diminished glomerular hyperfiltration, reduced urinary albumin excretion, and improved nerve function, all in patients with type 1 diabetes who lack C-peptide, but not in healthy subjects. The possibility exists that C-peptide replacement, together with insulin administration, may prevent the development or retard the progression of long-term complications in type 1 diabetes.
引用
收藏
页码:E759 / E768
页数:10
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