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Reduction Levels and the Effects of High-Molecular-Weight Adiponectin via AMPK/eNOS in Chinese Type 2 Diabetes

Authors :
C Xia
W Li
Qiuhe Ji
F Yi
S Guo
Kun Lian
Q Huang
X Guo
Haichang Wang
Ling Tao
Rutao Wang
Yan Li
Jingyi Liu
Z Tan
Source :
Experimental and Clinical Endocrinology & Diabetes. 124:541-547
Publication Year :
2016
Publisher :
Georg Thieme Verlag KG, 2016.

Abstract

Aim: This study was to investigate the change of high-molecula-weight (HMW) adiponectin (APN) isoform, the association between type 2 diabetes mellitus (T2DM) and HMW APN isoform, the variation of Disulfide-bond A oxidoreductase-like protein (DsbA-L), the effect of HMW APN isoform on AMP-dependent protein kinase (AMPK) and endothelial nitric oxide synthase (eNOS) in Chinese T2DM. Method: 169 patients aged at (48.7±9.4) years and 107 healthy control subjects aged at (42.6±7.8) years took part in this study. Anthropometric measures of the characters were assayed and different APN isoforms, DsbA-L, AMPK and eNOS levels were determined. Results: Ln(sRAGE) and Ln(Adiponectin) were significantly lower and significantly higher for the other characteristics in T2DM. Ln(Adiponectin) was negatively and significantly correlated with WHR, Ln(triglycerides), fasting plasma glucose, HbA1c (%) in control subjects and T2DM patients. Plasma and adipose tissue total APN and HMW APN were significantly reduced in newly diagnosed T2DM patients. DsbA-L was markedly down-regulated in diabetic adipose tissue. HMW APN caused significant decreases in AMPK and eNOS phosphorylation levels of human umbilical vein endothelial cells (HUVECs). Conclusions: Our results demonstrated that total APN levels was closely related to the risk of T2DM and HMW APN reduction was involved in the diabetic vascular AMPK/eNOS signal pathway. The findings will provide insight into novel therapeutic approaches for reducing the elevated cardiovascular risk associated with T2DM.

Details

ISSN :
14393646 and 09477349
Volume :
124
Database :
OpenAIRE
Journal :
Experimental and Clinical Endocrinology & Diabetes
Accession number :
edsair.doi.dedup.....2464e32f09cdcd220affb146e6cf1654
Full Text :
https://doi.org/10.1055/s-0042-109262