Document Detail


Improving insulin sensitivity via activation of PPAR-gamma increases telomerase activity in the heart of OLETF rats.
MedLine Citation:
PMID:  19855065     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
This study was conducted to examine telomere biology in terms of improving insulin sensitivity in a type 2 diabetic animal model: Otsuka Long-Evans Tokushima fatty (OLETF) rats. To improve insulin sensitivity, pioglitazone (PG; 10 mg.kg(-1).day(-1)) was administrated to OLETF rats from 20 to 40 wk of age, and the effects of treatment were compared with those in untreated OLETF or control Long-Evans Tokushima Otsuka fatty rats. At the end of the study, the homeostasis model assessment of insulin resistance significantly increased in OLETF rats but decreased in OLETF rats treated with PG. No shortening of telomere length was observed in the heart tissue of OLETF rats, whereas telomerase activity was decreased in OLETF heart tissue. The mRNA expression of both telomerase reverse transcriptase and telomere repeat binding factor 2 was downregulated in the hearts of OLETF rats. The protein expression of phospho-Akt, insulin-like growth factor, and endothelial nitric oxide synthase was reduced in OLETF rats. On the other hand, myocardial matrix metalloproteinase-9 expression was elevated in OLETF rats. The changes observed in OLETF rats were inhibited by PG treatment. However, protein and mRNA expression of Sirt1, a lifespan modulator, were attenuated in OLETF rat hearts, although they were enhanced in OLETF rats with PG treatment. Myocardial fibrosis was less extensive and diastolic dysfunction more greatly ameliorated in PG-treated OLETF rats than in OLETF rats. These findings suggest that improving insulin sensitivity via the activation of peroxisom proliferator-activated receptor-gamma may exert regulatory effects on cardiac telomere biology and may have desirable morphological and functional effects on the diabetic heart.
Authors:
Naoki Makino; Toyoki Maeda; Jun-ichi Oyama; Yosihiro Higuchi; Koji Mimori
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2009-10-23
Journal Detail:
Title:  American journal of physiology. Heart and circulatory physiology     Volume:  297     ISSN:  1522-1539     ISO Abbreviation:  Am. J. Physiol. Heart Circ. Physiol.     Publication Date:  2009 Dec 
Date Detail:
Created Date:  2009-11-25     Completed Date:  2010-02-17     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100901228     Medline TA:  Am J Physiol Heart Circ Physiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  H2188-95     Citation Subset:  IM    
Affiliation:
Division of Molecular and Clinical Gerontology, Department of Molecular and Cellular Biology, Medical Institute of Bioregulation, Kyushu University, 4546 Tsurumihara, Beppu 874-0838, Japan. makinon@beppu.kyushu-u.ac.jp
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MeSH Terms
Descriptor/Qualifier:
Adipose Tissue / enzymology
Animals
Diabetes Mellitus, Type 2 / drug therapy*,  enzymology,  genetics,  physiopathology
Disease Models, Animal
Fibrosis
Hypoglycemic Agents / administration & dosage,  pharmacology*
Insulin Resistance*
Liver / enzymology
Male
Matrix Metalloproteinase 9 / metabolism
Muscle, Skeletal / enzymology
Myocardial Contraction / drug effects
Myocardium / enzymology*,  pathology
Nitric Oxide Synthase Type III / metabolism
PPAR gamma / agonists*
Phosphorylation
Proto-Oncogene Proteins c-akt / metabolism
RNA, Messenger / metabolism
Rats
Rats, Inbred OLETF
Sirtuin 1 / metabolism
Somatomedins / metabolism
Telomerase / genetics,  metabolism*
Telomeric Repeat Binding Protein 2 / metabolism
Thiazolidinediones / administration & dosage,  pharmacology*
Up-Regulation
Chemical
Reg. No./Substance:
0/Hypoglycemic Agents; 0/PPAR gamma; 0/RNA, Messenger; 0/Somatomedins; 0/Telomeric Repeat Binding Protein 2; 0/Thiazolidinediones; 111025-46-8/pioglitazone; EC 1.14.13.39/Nitric Oxide Synthase Type III; EC 1.14.13.39/Nos3 protein, rat; EC 2.7.11.1/Proto-Oncogene Proteins c-akt; EC 2.7.7.49/Telomerase; EC 3.4.24.35/Matrix Metalloproteinase 9; EC 3.5.1.-/Sirt1 protein, rat; EC 3.5.1.-/Sirtuin 1

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