Association of monocyte chemoattractant protein-1 with adipocyte number, insulin resistance and liver function markers

Background  Monocyte chemoattractant protein‐1 (MCP‐1) is an inflammatory chemokine known to induce adipocyte dedifferentiation and insulin resistance. Inflammation, insulin resistance, and obesity have been implicated in the pathogenesis of non‐alcoholic fatty liver disease (NAFLD). Methods  Fastin...

Full description

Saved in:
Bibliographic Details
Published inJournal of medical primatology Vol. 38; no. 6; pp. 418 - 424
Main Authors Bose, Tanushree, Alvarenga, Juan Carlos Lopez, Tejero, M. Elizabeth, Voruganti, V. Saroja, Proffitt, J. Michael, Freeland-Graves, Jeanne H., Cole, Shelley A., Comuzzie, Anthony G.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.12.2009
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background  Monocyte chemoattractant protein‐1 (MCP‐1) is an inflammatory chemokine known to induce adipocyte dedifferentiation and insulin resistance. Inflammation, insulin resistance, and obesity have been implicated in the pathogenesis of non‐alcoholic fatty liver disease (NAFLD). Methods  Fasting plasma from 43 baboons were assayed for MCP‐1, insulin, glucose, alanine aminotransferase (ALT), and aspartate aminotransferase (AST). Adipocyte number and volume were measured via biopsies of omental adipose tissue. The homeostatic model assessment method (HOMA) was used to estimate systemic insulin resistance. Results  Sex and age adjusted correlations were significant for MCP‐1 with adipocyte number (r = −0.42; P = 0.01), adipocyte volume (r = 0.38; P = 0.02), HOMA (r = 0.45; P = 0.004), ALT (r = 0.46; P = 0.03) and AST (r = 0.45; P = 0.03). Conclusions  These results suggest that MCP‐1 is related with adipocyte dedifferentiation and systemic insulin resistance, thereby potentially contributing to the development of NAFLD.
Bibliography:ArticleID:JMP379
ark:/67375/WNG-TX3PV2C0-K
istex:B706271867D5FCEE972C78AB284F7A2B5202845A
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0047-2565
1600-0684
DOI:10.1111/j.1600-0684.2009.00379.x