C‐peptide in diabetes: A player in a dual hormone disorder?

Author:

Dakroub Ali1,Dbouk Ali2,Asfour Aref3,Nasser Suzanne A.4,El‐Yazbi Ahmed F.56,Sahebkar Amirhossein78ORCID,Eid Assaad A.9,Iratni Rabah10,Eid Ali H.11ORCID

Affiliation:

1. St. Francis Hospital and Heart Center Roslyn New York USA

2. Department of Medicine, Saint‐Joseph University Medical School Hotel‐Dieu de France Hospital Beirut Lebanon

3. Leeds Teaching Hospitals NHS Trust West Yorkshire United Kingdom

4. Keele University Staffordshire UK

5. Faculty of Pharmacy Alamein International University (AIU) Alamein City Egypt

6. Department of Pharmacology and Toxicology Faculty of Pharmacy, Alexandria University Alexandria Egypt

7. Applied Biomedical Research Center Mashhad University of Medical Sciences Mashhad Iran

8. Biotechnology Research Center, Pharmaceutical Technology Institute Mashhad University of Medical Sciences Mashhad Iran

9. Department of Anatomy, Cell Biology and Physiological Sciences, Faculty of Medicine American University of Beirut Beirut Lebanon

10. Department of Biology, College of Science United Arab Emirates University Al Ain UAE

11. Department of Basic Medical Sciences, College of Medicine, QU Health Qatar University Doha Qatar

Abstract

AbstractC‐peptide, a byproduct of insulin synthesis believed to be biologically inert, is emerging as a multifunctional molecule. C‐peptide serves an anti‐inflammatory and anti‐atherogenic role in type 1 diabetes mellitus (T1DM) and early T2DM. C‐peptide protects endothelial cells by activating AMP‐activated protein kinase α, thus suppressing the activity of NAD(P)H oxidase activity and reducing reactive oxygen species (ROS) generation. It also prevents apoptosis by regulating hyperglycemia‐induced p53 upregulation and mitochondrial adaptor p66shc overactivation, as well as reducing caspase‐3 activity and promoting expression of B‐cell lymphoma‐2. Additionally, C‐peptide suppresses platelet‐derived growth factor (PDGF)‐beta receptor and p44/p42 mitogen‐activated protein (MAP) kinase phosphorylation to inhibit vascular smooth muscle cells (VSMC) proliferation. It also diminishes leukocyte adhesion by virtue of its capacity to abolish nuclear factor kappa B (NF‐kB) signaling, a major pro‐inflammatory cascade. Consequently, it is envisaged that supplementation of C‐peptide in T1DM might ameliorate or even prevent end‐organ damage. In marked contrast, C‐peptide increases monocyte recruitment and migration through phosphoinositide 3‐kinase (PI‐3 kinase)‐mediated pathways, induces lipid accumulation via peroxisome proliferator‐activated receptor γ upregulation, and stimulates VSMC proliferation and CD4+ lymphocyte migration through Src‐kinase and PI‐3K dependent pathways. Thus, it promotes atherosclerosis and microvascular damage in late T2DM. Indeed, C‐peptide is now contemplated as a potential biomarker for insulin resistance in T2DM and linked to increased coronary artery disease risk. This shift in the understanding of the pathophysiology of diabetes from being a single hormone deficiency to a dual hormone disorder warrants a careful consideration of the role of C‐peptide as a unique molecule with promising diagnostic, prognostic, and therapeutic applications.

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Physiology

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