Effect of captopril and melatonin on fibrotic rebuilding of the aorta in 24 hour light-induced hypertension
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24329693
DOI
10.33549/physiolres.932592
PII: 932592
Knihovny.cz E-resources
- MeSH
- Antifibrinolytic Agents administration & dosage MeSH
- Antihypertensive Agents administration & dosage MeSH
- Aorta drug effects physiopathology MeSH
- Fibrillar Collagens metabolism MeSH
- Hypertension etiology physiopathology prevention & control MeSH
- Captopril administration & dosage MeSH
- Rats MeSH
- Melatonin administration & dosage MeSH
- Rats, Wistar MeSH
- Photic Stimulation adverse effects MeSH
- Light adverse effects MeSH
- Vascular Stiffness drug 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
- Antifibrinolytic Agents MeSH
- Antihypertensive Agents MeSH
- Fibrillar Collagens MeSH
- Captopril 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.
References provided by Crossref.org
Lactacystin-induced kidney fibrosis: Protection by melatonin and captopril
Ivabradine Ameliorates Kidney Fibrosis in L-NAME-Induced Hypertension