Document Detail


Implication of low level inflammation in the insulin resistance of adipose tissue at late pregnancy.
MedLine Citation:
PMID:  21914778     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Insulin resistance is a characteristic of late pregnancy, and adipose tissue is one of the tissues that most actively contributes to the reduced maternal insulin sensitivity. There is evidence that pregnancy is a condition of moderate inflammation, although the physiological role of this low-grade inflammation remains unclear. The present study was designed to validate whether low-grade inflammation plays a role in the development of insulin resistance in adipose tissue during late pregnancy. To this end, we analyzed proinflammatory adipokines and kinases in lumbar adipose tissue of nonpregnant and late pregnant rats at d 18 and 20 of gestation. We found that circulating and tissue levels of adipokines, such as IL-1β, plasminogen activator inhibitor-1, and TNF-α, were increased at late pregnancy, which correlated with insulin resistance. The observed increase in adipokines coincided with an enhanced activation of p38 MAPK in adipose tissue. Treatment of pregnant rats with the p38 MAPK inhibitor SB 202190 increased insulin-stimulated tyrosine phosphorylation of the insulin receptor (IR) and IR substrate-1 in adipose tissue, which was paralleled by a reduction of IR substrate-1 serine phosphorylation and an enhancement of the metabolic actions of insulin. These results indicate that activation of p38 MAPK in adipose tissue contributes to adipose tissue insulin resistance at late pregnancy. Furthermore, the results of the present study support the hypothesis that physiological low-grade inflammation in the maternal organism is relevant to the development of pregnancy-associated insulin resistance.
Authors:
J de Castro; J Sevillano; J Marciniak; R Rodriguez; C González-Martín; M Viana; O H Eun-suk; S Hauguel de Mouzon; E Herrera; M P Ramos
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2011-09-13
Journal Detail:
Title:  Endocrinology     Volume:  152     ISSN:  1945-7170     ISO Abbreviation:  Endocrinology     Publication Date:  2011 Nov 
Date Detail:
Created Date:  2011-10-24     Completed Date:  2011-12-08     Revised Date:  2013-06-27    
Medline Journal Info:
Nlm Unique ID:  0375040     Medline TA:  Endocrinology     Country:  United States    
Other Details:
Languages:  eng     Pagination:  4094-105     Citation Subset:  AIM; IM    
Affiliation:
Facultad de Farmacia, Universidad San Pablo-CEU, Carretera Boadilla del Monte, km 5.3, 28668 Madrid, Spain.
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MeSH Terms
Descriptor/Qualifier:
Adipokines / metabolism*
Adipose Tissue / metabolism*,  physiopathology
Animals
Female
Inflammation / metabolism*,  physiopathology
Insulin / metabolism
Insulin Receptor Substrate Proteins / metabolism
Insulin Resistance / physiology*
Phosphorylation / physiology
Pregnancy
Rats
Rats, Sprague-Dawley
Receptor, Insulin / metabolism
Tumor Necrosis Factor-alpha / metabolism
p38 Mitogen-Activated Protein Kinases / metabolism
Grant Support
ID/Acronym/Agency:
HD 057236/HD/NICHD NIH HHS
Chemical
Reg. No./Substance:
0/Adipokines; 0/Insulin; 0/Insulin Receptor Substrate Proteins; 0/Irs1 protein, rat; 0/Tumor Necrosis Factor-alpha; EC 2.7.10.1/Receptor, Insulin; EC 2.7.11.24/p38 Mitogen-Activated Protein Kinases
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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