کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1907397 | 1046353 | 2006 | 12 صفحه PDF | دانلود رایگان |

Werner Syndrome (WS) is a rare disorder characterized by the premature onset of a number of age-related diseases. The gene responsible for WS encodes a DNA helicase/exonuclease protein. Previously, we generated a mouse model lacking part of the helicase domain of the murine Wrn homologue. Mutant WrnΔhel/Δhel mice developed severe cardiac interstitial fibrosis in addition to tumors. Further analyses of these mice on the pure C57Bl/6 genetic background revealed abnormal increases in visceral fat deposition, fasting blood triglyceride and cholesterol levels followed by insulin resistance and high blood glucose levels. These phenotypes were more severe in mutant females than mutant males. In addition, adult mice had clear hemodynamic signs of aortic stenosis. All these symptoms appeared before the onset of cardiomyopathy and are known to cause heart failure. Interestingly, WrnΔhel/Δhel adult mice (but not juveniles) showed higher levels of serum and cardiac tissue reactive oxygen species followed in time by an increase in cardiac oxidative DNA damage, all this prior to cardiac fibrosis.
Journal: Experimental Gerontology - Volume 41, Issue 2, February 2006, Pages 157–168