Arginine and aerobic training prevent endothelial and metabolic alterations in rats at high risk for the development of the metabolic syndrome. Issue 1 (11th August 2017)

• Record Type: Journal Article
• Authors: Medeiros, Renata F.; Gaique, Thaiane G.; Bento-Bernardes, Thais; Kindlovits, Raquel; Gomes, Tamiris M. B.; Motta, Nadia Alice V.; Brito, Fernanda Carla; Fernandes-Santos, Caroline; Oliveira, Karen J.; Nóbrega, Antonio Claudio L.
• Is Part Of: British journal of nutrition. Volume 118:Issue 1(2017)
• Page Start: 1
• Page End: 10
• Publication Date: 2017-08-11
• Subjects: Metabolic syndrome, -- Fructose, -- Aerobic training, -- Arginine supplementation; Nutrition -- Periodicals; 572.4
• DOI: 10.1017/S0007114517001702
• Languages: English
• ISSNs: 0007-1145

Abstract

Abstract: Endothelial function is a key mechanism in the development of CVD. Arginine and exercise are important non-pharmacological strategies for mitigating the impact of metabolic changes in the metabolic syndrome, but the effect of their combined administration is unknown. Thus, the aim of this study was to investigate the isolated and combined effects of aerobic training and arginine supplementation on metabolic variables and vascular reactivity in rats at high risk for developing the metabolic syndrome. Wistar rats were divided into two groups: control and fructose (F – water with 10 % fructose). After 2 weeks, the F group was divided into four groups: F, fructose+arginine (FA, 880 mg/kg per d ofl -arginine), fructose+training (FT) and fructose+arginine+training (FTA); treatments lasted for 8 weeks, and no difference was observed in body mass gain. Arginine did not improve the body protein content, and both the FA and FT groups show a reversal of the increase in adipose tissue. Insulin increase was prevented by training and arginine, without additive effect, and the increase in serum TAG was prevented only by training. The F group showed impaired endothelium-dependent vasodilation and hyperreactivity to phenylephrine, but arginine and training were capable of preventing these effects, even separately. Higher nitric oxide level was observed in the FA and FT groups, and no potentiating effect was detected. Thus, only training was able to prevent the increase in TAG and improve the protein mass, and training and arginine exert similar effects on fat content, insulin and endothelial function, but these effects are not additive.