Morphological alterations and NO-synthase expression in the heart after continuous light exposure of rats
Language English Country Czech Republic Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
17824804
DOI
10.33549/physiolres.931400
PII: 1400
Knihovny.cz E-resources
- MeSH
- Time Factors MeSH
- Fibrosis MeSH
- Myocytes, Cardiac enzymology pathology radiation effects MeSH
- Collagen Type III metabolism MeSH
- Collagen Type I metabolism MeSH
- Rats MeSH
- Rats, Wistar MeSH
- Light * MeSH
- Nitric Oxide Synthase Type II metabolism MeSH
- Nitric Oxide Synthase Type III MeSH
- Body Weight radiation effects MeSH
- Organ Size radiation effects MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Collagen Type III MeSH
- Collagen Type I MeSH
- Nos2 protein, rat MeSH Browser
- Nos3 protein, rat MeSH Browser
- Nitric Oxide Synthase Type II MeSH
- Nitric Oxide Synthase Type III MeSH
Although exposure to continuous light is associated with hypertension and modulates the outcome of ischemia-reperfusion injury, less attention has been paid to its effects on cardiac morphology. We investigated whether 4-week exposure of experimental rats to continuous 24 h/day light can modify cardiac morphology, with focus on heart weight, fibrosis and collagen I/III ratio in correlation with NO-synthase expression. Two groups of male adult Wistar rats were studied: controls exposed to normal light/dark cycle (12 h/day light, 12 h/day dark) and rats exposed to continuous light. After 4 weeks of treatment the absolute and the relative heart weights were determined and myocardial fibrosis and collagen type I/III ratio were evaluated using picrosirius red staining. Endothelial and inducible NO-synthase expression was detected immunohistochemically. The exposure of rats to continuous light resulted in an increase of body weight with proportionally increased heart weight. Myocardial fibrosis remained unaffected but collagen I/III ratio increased. Neither endothelial nor inducible NO-synthase expression was altered in light-exposed rats. We conclude that the loss of structural homogeneity of the myocardium in favor of collagen type I might increase myocardial stiffness and contribute to functional alterations after continuous light exposure.
References provided by Crossref.org
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