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Research ArticleCARDIOVASCULAR

Female Rats Fed a High-Fat Diet Were Associated with Vascular Dysfunction and Cardiac Fibrosis in the Absence of Overt Obesity and Hyperlipidemia: Therapeutic Potential of Resveratrol

Marie-Claude Aubin, Claude Lajoie, Robert Clément, Hugues Gosselin, Angelino Calderone and Louis P. Perrault
Journal of Pharmacology and Experimental Therapeutics June 2008, 325 (3) 961-968; DOI: https://doi.org/10.1124/jpet.107.135061
Marie-Claude Aubin
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Claude Lajoie
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Robert Clément
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Hugues Gosselin
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Angelino Calderone
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Louis P. Perrault
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Abstract

It remains presently unknown whether vascular reactivity is impaired and whether maladaptive cardiac remodeling occurs before the onset of overt obesity and in the absence of hyperlipidemia. Normal female rats were fed a high-fat diet for 8 weeks and were associated with a modest nonsignificant increase of body weight (standard diet, 300 ± 10, versus high-fat diet, 329 ± 14 g) and a normal plasma lipid profile. In rats fed a high-fat diet, systolic (171 ± 7 mm Hg) and diastolic blood pressures (109 ± 3) were increased compared to a standard diet (systolic blood pressure, 134 ± 8; diastolic blood pressure, 96 ± 5 mm Hg), and acetylcholine-dependent relaxation of isolated aortic rings (high-fat diet, 22 ± 5%, versus standard diet, 53 ± 8%) was significantly reduced. Furthermore, perivascular fibrosis was detected in the heart of rats fed a high-fat diet. The exogenous addition of resveratrol (trans-3,5,4′-trihydroxystilbene) (0.1 μM) to aortic rings isolated from rats fed a high-fat diet restored acetylcholine-mediated relaxation (47 ± 9%). The administration of resveratrol (20 mg/kg/day for 8 weeks) to rats fed a high-fat diet prevented the increase in blood pressure and preserved acetylcholine-dependent relaxation of isolated aortic rings. However, resveratrol therapy failed to attenuate the perivascular fibrotic response. These data have demonstrated that a high-fat diet fed to normal female rats can elicit a hypertensive response and induce perivascular fibrosis before the development of overt obesity and in the absence of hyperlipidemia. Resveratrol therapy can prevent the hypertensive response in female rats fed a high-fat diet but is without effect on the progression of perivascular fibrosis.

Footnotes

  • This work was supported by the Heart and Stroke Foundation of Canada and Quebec, Canadian Institutes of Health Research, and “Fonds de la Recherche de l'Institut de Cardiologie de Montréal” (FRICM).

  • M.-C.A. is a Ph.D. student funded by the Heart and Stroke Foundation of Canada.

  • L.P.P. is a Chercheur-Boursier Senior of the “Fonds de la Recherche en Santé du Québec” (FRSQ).

  • A.C. is a Chercheur-Boursier National of the FRSQ.

  • Article, publication date, and citation information can be found at http://jpet.aspetjournals.org.

  • doi:10.1124/jpet.107.135061.

  • ABBREVIATIONS: LV, left ventricle; ANP, atrial natriuretic peptide; TGF, transforming growth factor; PCR, polymerase chain reaction; SERCA2, sarcoplasmic reticulum Ca2+-ATPase 2; ANOVA, analysis of variance.

    • Received December 5, 2007.
    • Accepted March 19, 2008.
  • The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics: 376 (2)
Journal of Pharmacology and Experimental Therapeutics
Vol. 376, Issue 2
1 Feb 2021
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Research ArticleCARDIOVASCULAR

Female Rats Fed a High-Fat Diet Were Associated with Vascular Dysfunction and Cardiac Fibrosis in the Absence of Overt Obesity and Hyperlipidemia: Therapeutic Potential of Resveratrol

Marie-Claude Aubin, Claude Lajoie, Robert Clément, Hugues Gosselin, Angelino Calderone and Louis P. Perrault
Journal of Pharmacology and Experimental Therapeutics June 1, 2008, 325 (3) 961-968; DOI: https://doi.org/10.1124/jpet.107.135061

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Research ArticleCARDIOVASCULAR

Female Rats Fed a High-Fat Diet Were Associated with Vascular Dysfunction and Cardiac Fibrosis in the Absence of Overt Obesity and Hyperlipidemia: Therapeutic Potential of Resveratrol

Marie-Claude Aubin, Claude Lajoie, Robert Clément, Hugues Gosselin, Angelino Calderone and Louis P. Perrault
Journal of Pharmacology and Experimental Therapeutics June 1, 2008, 325 (3) 961-968; DOI: https://doi.org/10.1124/jpet.107.135061
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