EFFECT OF LONG-TERM ISRADIPINE TREATMENT ON THE MORPHOLOGY OF THE ENDOTHELIUM IN THE AORTA OF SPONTANEOUSLY HYPERTENSIVE RATS

Citation
F. Ferrante et al., EFFECT OF LONG-TERM ISRADIPINE TREATMENT ON THE MORPHOLOGY OF THE ENDOTHELIUM IN THE AORTA OF SPONTANEOUSLY HYPERTENSIVE RATS, Clinical and experimental hypertension, 16(6), 1994, pp. 865-880
Citations number
32
Categorie Soggetti
Pharmacology & Pharmacy","Cardiac & Cardiovascular System
ISSN journal
10641963
Volume
16
Issue
6
Year of publication
1994
Pages
865 - 880
Database
ISI
SICI code
1064-1963(1994)16:6<865:EOLITO>2.0.ZU;2-Q
Abstract
The influence of hypertension and of treatment with the dihydropyridin e calcium channel blocker isradipine on the morphology of the thoracic aorta and of the aortic tunica intima were studied. Three experimenta l groups of male spontaneously hypertensive rats (SHR) of 10 weeks of age were used. Two groups were treated with a daily oral dose of 0.01 mg/Kg or of 0.1 mg/Kg of isradipine respectively. A third group of SHR was left untreated and served as control. Age-matched normotensive Wi star-Kyoto (WKY) rats were used as a reference group. Animals were all owed to survive for 12 weeks and were killed at 22 weeks of age. Systo lic pressure values which did not change in WKY rats, significantly in creased in SHR as a function of age. The dose of 0.1 mg/Kg/day isradip ine reduced systolic pressure to normotensive values after the first w eek of treatment, whereas the lower one was ineffective. The area of t he wall, the area of the tunica media and the wall-to-lumen ratio of t he aorta significantly increased in SHR and decreased either with the antihypertensive and non-antihypertensive doses of isradipine. Transmi ssion and scanning electron microscope analysis of the tunica intima r evealed hypertrophy of the endothelial cells with an increase in sub e ndothelial space in SHR. An improvement of the endothelial morphology and a decrease in sub endothelial space was noticeable in isradipine-t reated SHR. Although the hypotensive dose of the compound was the most effective, the non-hypotensive dose was active as well. The above res ults suggest that isradipine treatment may counter structural changes of the aorta of SHR and has a protective action on the hypertension-de pendent modifications of the endothelium. The endothelial effects are probably dependent only in part by the hypotensive activity of the com pound.