Revista argentina de cardiología
versión On-line ISSN 1850-3748
RENNA, Nicolás et al. Vascular Expression of Proinflammatory Transcription Factors in a Model of Metabolic Syndrome. Rev. argent. cardiol. [online]. 2007, vol.75, n.1, pp. 36-41. ISSN 1850-3748.
With the goal of assessing the expression of redox-sensitive transcription factors in the arteries of an experimental model of hypertension associated to metabolic syndrome (FFHR), we studied Wistar Kyoto rats (WKY) and spontaneously hypertensive 30-day male rats (SHR), which were randomly distributed in 4 groups (n=8 in each group). Group 1: WKY (control rats), Group 2: FFR: rats that received 10% W/V fructose in drinking water during a 10-week period, Group 3: SHR rats, and Group 4: FFHR: 2+3, i.e., SHR rats treated like Group 2. With the glucose tolerance test, groups FFR and FFHR had HOMA (homeostasis assessment model) and area under the curve (AUC) values that were characteristic of insulinresistance. They also showed significant differences in triglyceride and HDL cholesterol levels compared to controls, and increased their systolic blood pressure. Oxidative stress, as assessed by NAD(P)H oxidase and TBARS (thiobarbituric acid reactive substances) activity was significantly higher in FFR and FFHR groups, whereas in these same groups eNOS activity decreased markedly. Relative cardiac weight increased in FFR and FFHR groups, with a larger myocyte area in the left ventricular free wall. Sections of the left carotid artery exhibited eutrophic growth of the middle layer in FFHR. Mean optical density for anti-c-fos, anti-NF-kB and anti-VCAM-1 antibodies was greater in resistance renal arteries and in the carotid artery of FFHR and FFR groups. The data confirm the findings of the pathological experimental model and suggest that oxidative stress and the subsequent activation of genes that participate in the inflammatory process are actively involved in the development of vascular remodeling.
Palabras llave : Remodeling; Metabolic Syndrome X; Inflammation; Transcription, genetic.