Ketmanee Senaphan1, Weerapon Sangartit1, Poungrat Pakdeechote1, Veerapol Kukongviriyapan2, Patchareewan Pannangpetch2, Supawan Thawornchinsombut3, Stephen E Greenwald4, Upa Kukongviriyapan5. 1. Department of Physiology, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand. 2. Department of Pharmacology, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand. 3. Department of Food Technology, Faculty of Technology, Khon Kaen University, Khon Kaen, 40002, Thailand. 4. Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, E1 2ES, UK. 5. Department of Physiology, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand. upa_ku@kku.ac.th.
Abstract
PURPOSE: Rice bran protein hydrolysates (RBPH) contain highly nutritional proteins and antioxidant compounds which show benefits against metabolic syndrome (MetS). Increased arterial stiffness and the components of MetS have been shown to be associated with an increased risk of cardiovascular disease. This study aimed to investigate whether RBPH could alleviate the metabolic disorders, arterial stiffening, vascular remodeling, and oxidative stress in rats fed a high-carbohydrate and high-fat (HCHF) diet. METHODS: Male Sprague-Dawley rats were fed either a standard chow and tap water or a HCHF diet and 15 % fructose solution for 16 weeks. HCHF rats were treated orally with RBPH (250 or 500 mg/kg/day) for the final 6 weeks of the experimental period. RESULTS: Rats fed with HCHF diet had hyperglycemia, insulin resistance, dyslipidemia, hypertension, increased aortic pulse wave velocity, aortic wall hypertrophy and vascular remodeling with increased MMP-2 and MMP-9 expression. RBPH supplementation significantly alleviated these alterations (P < 0.05). Moreover, RBPH reduced the levels of angiotensin-converting enzyme (ACE) and tumor necrosis factor-alpha in plasma. Oxidative stress was also alleviated after RBPH treatment by decreasing plasma malondialdehyde, reducing superoxide production and suppressing p47phox NADPH oxidase expression in the vascular tissues of HCHF rats. RBPH increased plasma nitrate/nitrite level and up-regulated eNOS expression in the aortas of HCHF-diet-fed rats, indicating that RBPH increased NO production. CONCLUSION: RBPH mitigate the deleterious effects of HCHF through potential mechanisms involving enhanced NO bioavailability, anti-ACE, anti-inflammatory and antioxidant properties. RBPH could be used as dietary supplements to minimize oxidative stress and vascular alterations triggered by MetS.
PURPOSE:Rice bran protein hydrolysates (RBPH) contain highly nutritional proteins and antioxidant compounds which show benefits against metabolic syndrome (MetS). Increased arterial stiffness and the components of MetS have been shown to be associated with an increased risk of cardiovascular disease. This study aimed to investigate whether RBPH could alleviate the metabolic disorders, arterial stiffening, vascular remodeling, and oxidative stress in rats fed a high-carbohydrate and high-fat (HCHF) diet. METHODS: Male Sprague-Dawley rats were fed either a standard chow and tapwater or a HCHF diet and 15 % fructose solution for 16 weeks. HCHF rats were treated orally with RBPH (250 or 500 mg/kg/day) for the final 6 weeks of the experimental period. RESULTS:Rats fed with HCHF diet had hyperglycemia, insulin resistance, dyslipidemia, hypertension, increased aortic pulse wave velocity, aortic wall hypertrophy and vascular remodeling with increased MMP-2 and MMP-9 expression. RBPH supplementation significantly alleviated these alterations (P < 0.05). Moreover, RBPH reduced the levels of angiotensin-converting enzyme (ACE) and tumor necrosis factor-alpha in plasma. Oxidative stress was also alleviated after RBPH treatment by decreasing plasma malondialdehyde, reducing superoxide production and suppressing p47phox NADPH oxidase expression in the vascular tissues of HCHF rats. RBPH increased plasma nitrate/nitrite level and up-regulated eNOS expression in the aortas of HCHF-diet-fed rats, indicating that RBPH increased NO production. CONCLUSION:RBPH mitigate the deleterious effects of HCHF through potential mechanisms involving enhanced NO bioavailability, anti-ACE, anti-inflammatory and antioxidant properties. RBPH could be used as dietary supplements to minimize oxidative stress and vascular alterations triggered by MetS.
Entities:
Keywords:
Arterial stiffness; High-carbohydrate and high-fat diet; Metabolic syndrome; Oxidative stress; Rice bran protein hydrolysates; Vascular remodeling
Authors: Maria Luisa Justo; Manila Candiracci; Ana Paula Dantas; Maria Alvarez de Sotomayor; Juan Parrado; Elisabet Vila; Maria Dolores Herrera; Rosalia Rodriguez-Rodriguez Journal: J Nutr Biochem Date: 2013-03-01 Impact factor: 6.048
Authors: Flavia M Gonçalves; Anna L B Jacob-Ferreira; Valeria A Gomes; Antonio Casella-Filho; Antonio C P Chagas; Andrea M Marcaccini; Raquel F Gerlach; Jose E Tanus-Santos Journal: Clin Chim Acta Date: 2009-02-28 Impact factor: 3.786