Document Detail


Uremia attenuates growth hormone-stimulated insulin-like growth factor-1 expression, a process worsened by inflammation.
MedLine Citation:
PMID:  20375991     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Growth hormone (GH) resistance is common in uremia and together with resistance to insulin-like growth factor-1 (IGF-1) contributes to uremic growth retardation and muscle wasting. Previously, we found decreased GH-stimulated janus-kinase 2-signal transducers and activators of transcription 5 (STAT5) phosphorylation and nuclear translocation in uremia; however, it is unclear whether there are more distal defects. Therefore, we tested whether the binding of phosphorylated STAT5b to DNA is intact in uremia. Using uremic rats we found that in addition to impaired hepatic STAT5b phosphorylation, the binding of available phospho-STAT5b to DNA is decreased thus contributing to impaired IGF-1 gene expression. As sepsis-induced inflammation causes a loss of body protein and as Gram-negative infections are relatively common in uremia, we also characterized mechanisms in which acute inflammation might contribute to GH resistance in uremia. Endotoxin-induced inflammation markedly increased the resistance to GH-mediated STAT5b signaling, and further decreased STAT5b binding to DNA and IGF-1 gene expression. These perturbations appear to be related to increased cytokine expression. Thus, our findings indicate that hepatic resistance to GH-induced IGF-1 expression in uremia arises due to defects in STAT5b phosphorylation and its impaired binding to DNA, processes further aggravated by inflammation.
Authors:
Yu Chen; Jaclyn Biada; Sumita Sood; Ralph Rabkin
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.     Date:  2010-04-07
Journal Detail:
Title:  Kidney international     Volume:  78     ISSN:  1523-1755     ISO Abbreviation:  Kidney Int.     Publication Date:  2010 Jul 
Date Detail:
Created Date:  2010-06-16     Completed Date:  2010-09-22     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0323470     Medline TA:  Kidney Int     Country:  United States    
Other Details:
Languages:  eng     Pagination:  89-95     Citation Subset:  IM    
Affiliation:
Department of Medicine, Stanford University, Stanford, California, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
DNA / genetics,  metabolism
Gene Expression / drug effects
Growth Hormone / genetics,  metabolism,  pharmacology*
Human Growth Hormone / genetics,  metabolism
Inflammation / genetics,  metabolism
Insulin-Like Growth Factor I / genetics,  metabolism*
Janus Kinase 2 / genetics,  metabolism
Liver / metabolism
Male
Phosphorylation
Rats
Rats, Sprague-Dawley
STAT5 Transcription Factor
Signal Transduction / drug effects,  genetics,  physiology
Uremia / genetics,  metabolism*
Grant Support
ID/Acronym/Agency:
R01 DK 068517/DK/NIDDK NIH HHS
Chemical
Reg. No./Substance:
0/STAT5 Transcription Factor; 0/STAT5B protein, human; 12629-01-5/Human Growth Hormone; 67763-96-6/Insulin-Like Growth Factor I; 9002-72-6/Growth Hormone; 9007-49-2/DNA; EC 2.7.10.1/Janus Kinase 2

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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