A LIPOPROTEIN-LIPASE ACTIVATOR, NO-1886, IMPROVES ENDOTHELIUM-DEPENDENT RELAXATION OF RAT AORTA ASSOCIATED WITH AGING

Citation
T. Hara et al., A LIPOPROTEIN-LIPASE ACTIVATOR, NO-1886, IMPROVES ENDOTHELIUM-DEPENDENT RELAXATION OF RAT AORTA ASSOCIATED WITH AGING, European journal of pharmacology, 350(1), 1998, pp. 75-79
Citations number
29
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
00142999
Volume
350
Issue
1
Year of publication
1998
Pages
75 - 79
Database
ISI
SICI code
0014-2999(1998)350:1<75:ALANIE>2.0.ZU;2-E
Abstract
Endothelial function is closely related to development of atherosclero sis and is impaired with aging. The novel compound NO-1886, osphorylme thyl-N-(4-bromo-2-cyanophenyl)benzamide, is a lipoprotein lipase activ ator and its long term administration protects against the development of experimental atherosclerosis in animals. The aim of this study was to ascertain whether NO-1886 ameliorates the impaired endothelium-dep endent relaxation of rat aorta associated with aging. NO-1886 (50 mg/k g p.o.) was administered to 7-month old rats for 3 months. Plasma lipi d, glucose and insulin levels in old control rats (10 months of age) w ere significantly higher than those of young rats (2 months of age). N O-1886 decreased plasma triglyceride levels told rats, 233 +/- 10 mg/d l; old rats + NO-1886, 172 +/- 16 mg/dl, P < 0.01) and increased plasm a high density lipoprotein (HDL) cholesterol level told rats, 72 +/- 6 mg/dl; old rats + NO-1886, 142 +/- 6 mg/dl, P < 0.001) in old rats, b ut had no effects on plasma glucose or insulin. The endothelium-depend ent relaxation of the thoracic aorta caused by histamine was significa ntly impaired in old rats (% relaxation at 10(-5.5) M histamine: young rats 25.4 +/- 3.1%; old rats 14.1 +/- 1.9%, P < 0.01), an effect comp letely prevented by NO-1886 told rats + NO-1886; 22.8 +/- 2.8%, P < 0. 05 vs. old rats). In contrast, NO-1886 showed no effect on the endothe lium-independent relaxation by sodium nitroprusside. These results ind icate that NO-1886 improves impaired endothelium-dependent relaxation of rat aorta associated with aging, possibly by correcting lipid metab olism. (C) 1998 Elsevier Science B.V. All lights reserved.