Rice bran protein hydrolysates reduce arterial stiffening, vascular remodeling and oxidative stress in rats fed a high-carbohydrate and high-fat diet

被引:34
作者
Senaphan, Ketmanee [1 ]
Sangartit, Weerapon [1 ]
Pakdeechote, Poungrat [1 ]
Kukongviriyapan, Veerapol [2 ]
Pannangpetch, Patchareewan [2 ]
Thawornchinsombut, Supawan [3 ]
Greenwald, Stephen E. [4 ]
Kukongviriyapan, Upa [1 ]
机构
[1] Khon Kaen Univ, Fac Med, Dept Physiol, Khon Kaen 40002, Thailand
[2] Khon Kaen Univ, Fac Med, Dept Pharmacol, Khon Kaen 40002, Thailand
[3] Khon Kaen Univ, Fac Technol, Dept Food Technol, Khon Kaen 40002, Thailand
[4] Queen Mary Univ London, Barts & London Sch Med & Dent, Blizard Inst, London E1 2ES, England
关键词
Arterial stiffness; High-carbohydrate and high-fat diet; Metabolic syndrome; Rice bran protein hydrolysates; Oxidative stress; Vascular remodeling; PULSE-WAVE VELOCITY; METABOLIC SYNDROME; MATRIX METALLOPROTEINASES; ENDOTHELIAL FUNCTION; INSULIN-RESISTANCE; CARDIOVASCULAR RISK; ANGIOTENSIN-II; FERULIC ACID; ANTIOXIDANT; STIFFNESS;
D O I
10.1007/s00394-016-1311-0
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
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 p47(phox) 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.
引用
收藏
页码:219 / 230
页数:12
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