Effect of captopril and melatonin on fibrotic rebuilding of the aorta in 24 hour light-induced hypertension
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24329693
DOI
10.33549/physiolres.932592
PII: 932592
Knihovny.cz E-zdroje
- MeSH
- antifibrinolytika aplikace a dávkování MeSH
- antihypertenziva aplikace a dávkování MeSH
- aorta účinky léků patofyziologie MeSH
- fibrilární kolageny metabolismus MeSH
- hypertenze etiologie patofyziologie prevence a kontrola MeSH
- kaptopril aplikace a dávkování MeSH
- krysa rodu Rattus MeSH
- melatonin aplikace a dávkování MeSH
- potkani Wistar MeSH
- světelná stimulace škodlivé účinky MeSH
- světlo škodlivé účinky MeSH
- tuhost cévní stěny účinky léků MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antifibrinolytika MeSH
- antihypertenziva MeSH
- fibrilární kolageny MeSH
- kaptopril MeSH
- melatonin MeSH
Chronic continuous light exposure leads to melatonin deficiency along with complex neurohumoral activation resulting in hypertension development in rats. The aim of this study was to show, whether continuous light induces fibrotic rebuilding of the aorta and whether the treatment with melatonin or angiotensin converting enzyme inhibitor captopril can prevent these potential alterations. In a six-week experiment, 3-month-old Wistar rats were divided into 4 groups (ten per group): controls, rats exposed to continuous light, exposed to continuous light plus treated with captopril (100 mg/kg/24 h) and exposed to continuous light plus treated with melatonin (10 mg/kg/24 h). Systolic blood pressure (SBP) and collagen type I and III in the media of thoracic aorta were measured. Continuous light induced hypertension and fibrotic rebuilding of the aorta in terms of enhancement of collagen I and III concentration in the aortic media. Both captopril and melatonin prevented SBP rise and reduced collagen III concentration in the aorta. However, only melatonin reduced collagen I and the sum of collagen I and III in the aortic tissue. We conclude that in continuous light-induced hypertension, administration of melatonin, along with SBP reduction, decreases collagen I and III concentration in the aorta. It is suggested that antifibrotic effect of melatonin may reduce the stiffness of the aorta and small arteries and beneficially influence the nature of the pulse wave and peripheral vascular resistance.
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