Nitric oxide does not participate in the metabolic effects of exogenous bradykinin in fructose-fed rats

Citation
Y. Erlich et al., Nitric oxide does not participate in the metabolic effects of exogenous bradykinin in fructose-fed rats, AM J HYPERT, 14(1), 2001, pp. 3-6
Citations number
24
Categorie Soggetti
Cardiovascular & Respiratory Systems
Journal title
AMERICAN JOURNAL OF HYPERTENSION
ISSN journal
08957061 → ACNP
Volume
14
Issue
1
Year of publication
2001
Pages
3 - 6
Database
ISI
SICI code
0895-7061(200101)14:1<3:NODNPI>2.0.ZU;2-Z
Abstract
The study was carried out to demonstrate the effects of bradykinin (BK) on hypertension, hyperinsulinemia, and hypertriglyceridemia in fructose-fed ra ts, and to determine whether these actions are mediated through nitric-oxid e (NO) formation. Eighteen rats, rendered hypertensive, hyperinsulinemic, and hypertriglyceri demic by a fructose-enriched diet, were studied. BK (0.2 mg/day) was infuse d intravenously using osmotic pumps attached by a catheter to the jugular v ein of 12 rats for 12 days. BK was administered either alone (n = 6) or wit h concomitant inhibition of NO synthase (n = 6). Six untreated rats served as control. Measurements of systolic blood pressure (indirect method) and l evels of insulin and triglyceride in serum were taken every second day. BK infused chronically, induced a marked fall in all parameters as early as th e second day of infusion: in blood pressure from 152 +/- 7 to 126 +/- 12 mm Hg, in insulin from 8.7 +/- 2.9 to 4.6 +/- 5.4 pg/mL, and in triglyceride f rom 308 +/- 94 to 76 +/- 19 mg/dL. No such reduction was seen in untreated animals. When BK was administered concurrently with NO synthase inhibitor, blood pressure rose significantly, reaching very high values at the end of treatment. However, the reduction in insulin and triglyceride levels induce d by BK was not affected. The capacity of BK to enhance reduction in hyperinsulinemia and hypertrigly ceridemia in the fructose-fed rats is not mediated by NO formation. Whether this action of BK is related to a direct effect of this peptide remains to be determined. (C) 2001 American Journal of Hypertension, Ltd.