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Cellular and physiological effects of C-peptide
Claire E Hills1, Nigel J Brunskill
1Department of Infection, Immunity and Inflammation, University of Leicester School of Medicine, Leicester LE1 7RH, UK.
Proinsulin C-peptide, once thought inert, actively binds cell receptors, triggering signaling pathways. This suggests Type 1 diabetes may be a dual-hormone deficiency, warranting C-peptide replacement alongside insulin.
Area of Science:
- Endocrinology
- Molecular Biology
- Diabetology
Background:
- Traditionally, C-peptide was considered biologically inert, serving only as a marker for insulin production.
- Emerging evidence highlights significant biological functions of C-peptide beyond its role as an insulin surrogate.
Purpose of the Study:
- To investigate the biological functions and therapeutic potential of proinsulin C-peptide.
- To re-evaluate the role of C-peptide in Type 1 diabetes management.
Main Methods:
- Investigated C-peptide's interaction with cell membrane receptors, likely G-protein-coupled receptors.
- Analyzed C-peptide-induced intracellular signaling pathways and gene transcription.
- Evaluated C-peptide's effects on glucose metabolism and diabetic complications in animal models and Type 1 diabetic patients.
Main Results:
- C-peptide binds cell membranes with high affinity, activating signaling pathways and altering cell phenotype.
- Short-term studies show C-peptide enhances glucose disposal and metabolic control in diabetic models and patients.
- Evidence suggests C-peptide ameliorates diabetic nephropathy and neuropathy in preclinical and clinical studies.
Conclusions:
- C-peptide possesses significant biological activity, challenging its traditional inert status.
- Type 1 diabetes may be viewed as a dual-hormone deficiency disease.
- C-peptide replacement therapy, in conjunction with insulin, should be considered for managing Type 1 diabetes.
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