Different effects of 7-nitroindazole and L-NAME administered both individually and together on the cardiovascular system of the rat
Language English Country Czech Republic Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
25194127
DOI
10.33549/physiolres.932777
PII: 932777
Knihovny.cz E-resources
- MeSH
- Aorta, Thoracic drug effects enzymology physiopathology ultrastructure MeSH
- Carotid Arteries drug effects enzymology physiopathology ultrastructure MeSH
- Hypertension drug therapy enzymology pathology physiopathology MeSH
- Indazoles pharmacology MeSH
- Enzyme Inhibitors pharmacology MeSH
- Cardiomegaly enzymology pathology physiopathology prevention & control MeSH
- Coronary Vessels drug effects enzymology physiopathology ultrastructure MeSH
- Blood Pressure drug effects MeSH
- Disease Models, Animal MeSH
- NG-Nitroarginine Methyl Ester pharmacology MeSH
- Rats, Inbred SHR MeSH
- Rats, Wistar MeSH
- Vascular Remodeling drug effects MeSH
- Ventricular Remodeling drug effects MeSH
- Heart Ventricles drug effects enzymology pathology physiopathology MeSH
- Nitric Oxide Synthase antagonists & inhibitors metabolism MeSH
- Vasodilation drug effects MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- 7-nitroindazole MeSH Browser
- Indazoles MeSH
- Enzyme Inhibitors MeSH
- NG-Nitroarginine Methyl Ester MeSH
- Nitric Oxide Synthase MeSH
We evaluated the effects of N(G)-nitro-L-arginine methylester (L-NAME) (50 mg/kg/day) and 7-nitroindazole (7NI) (10 mg/kg/day) administered from 10th-16th week of age either individually or together on cardiovascular system of Wistar rats and SHR. Systolic blood pressure (sBP) was measured weekly by the plethysmographic method. For morphological studies, the animals (n=10) were perfused with a fixative (120 mm Hg), and thoracic aorta and carotid and coronary arteries were processed for electron microscopy. For functional investigation (n=10), aortic rings were used in an organ bath. In Wistar rats, L-NAME evoked an increase of sBP; hypertrophy of the heart and arterial walls; an increase in cross-sectional areas (CSA) of endothelial cells (EC), muscle cells (SMC), extracellular matrix (ECM), and a decrease in acetylcholine-induced endothelial-dependent relaxation (EDR). 7NI evoked sBP-independent hypotrophy of the heart and arterial walls, a decrease in CSA of EC and SMC without affecting the CSA of ECM, and a mild decrease in acetylcholine-induced EDR. 7NI and L-NAME administered together evoked lower effect on BP and trophicity of the heart and all arteries, and a similar decrease in acetylcholine-induced EDR compared to L-NAME alone. In SHR, 7NI did not evoke any effect on the studied parameters.
References provided by Crossref.org
Age-dependent redox status in the brain stem of NO-deficient hypertensive rats