An SOD rich melon extract Extramel® prevents aortic lipids and liver steatosis in diet-induced model of atherosclerosis

被引:36
作者
Decorde, K. [1 ]
Ventura, E. [1 ]
Lacan, D. [2 ]
Ramos, J. [3 ]
Cristol, J. -P. [1 ,4 ]
Rouanet, J. -M. [1 ]
机构
[1] Univ Montpellier 1&2, UMR Prevent Malnutr & Pathol Associees 204, F-34095 Montpellier 05, France
[2] Bionov Sarl, Avignon, France
[3] CHU Guy De Chauliac, Serv Anat Pathol, Montpellier, France
[4] CHU Lapeyronie, Serv Biochim, Montpellier, France
关键词
Atherosclerosis; Melon extract; Fatty liver; Hamsters; Superoxide dismutase; LOW-DENSITY-LIPOPROTEIN; SUPEROXIDE-DISMUTASE; OXIDATIVE-STRESS; NADPH-OXIDASE; FATTY LIVER; IN-VIVO; ANTIOXIDANT; SUPPLEMENTATION; CONSUMPTION; HAMSTERS;
D O I
10.1016/j.numecd.2009.04.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and aims: Oxidative stress has been involved in the early steps of atherosclerosis and previous studies on hypercholesterolemic hamsters have shown that nonenzymatic antioxidant could prevent fatty streak formation. Therefore, we investigated whether a melon juice extract (Extramel (R)) rich in superoxide dismutase (SOD) would prevent the development of early atherosclerosis. Methods and results: The effects of Extramel (R) on plasma cholesterol, aortic fatty streak formation, hepatic steatosis, superoxide anion tissue production and NAD(P)H oxidase expression were studied in hamsters fed with an atherogenic diet (HF), receiving by gavage either water or Extramel (R) at 0.7, 2.8 or 5.6 mg/d. After 12 weeks of oral administration, Extramel (R) lowered plasma cholesterol and non-HDL cholesterol and induced blood and liver SOD activities. It also strongly reduced the area of aortic fatty streak by 49-85%, cardiac (45%) and liver (67%) production of superoxide anion and liver p22(phox) subunit of NAD(P)H oxidase expression by 66%, and attenuated the development of hepatic steatosis. Conclusion: These findings support the view that chronic consumption of melon juice extract rich in SOD has potential beneficial effects with respect to the development of atherosclerosis and liver steatosis, emphasizing its use as potential dietary therapy. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:301 / 307
页数:7
相关论文
共 36 条
[1]   Recent concepts in non-alcoholic fatty liver disease [J].
Adams, LA ;
Angulo, P .
DIABETIC MEDICINE, 2005, 22 (09) :1129-1133
[2]   dExtracts enriched in different polyphenolic families normalize increased cardiac NADPH oxidase expression while having differential effects on insulin resistance, hypertension, and cardiac hypertrophy in high-fructose-fed rats [J].
Al-Awwadi, NA ;
Araiz, C ;
Bornet, A ;
Delbosc, S ;
Cristol, JP ;
Linck, N ;
Azay, J ;
Teissedre, PL ;
Cros, G .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2005, 53 (01) :151-157
[3]  
[Anonymous], 2002, Nutrition Clinique et Metabolisme, DOI DOI 10.1016/S0985-0562(02)00166-8
[4]   Dietary wine phenolics catechin, quercetin, and resveratrol efficiently protect hypercholesterolemic hamsters against aortic fatty streak accumulation [J].
Auger, C ;
Teissedre, PL ;
Gérain, P ;
Lequeux, N ;
Bornet, A ;
Serisier, S ;
Besançon, P ;
Caporiccio, B ;
Cristol, JP ;
Rouanet, JM .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2005, 53 (06) :2015-2021
[5]   Red wine phenolic compounds reduce plasma lipids and apolipoprotein B and prevent early aortic atherosclerosis in hypercholesterolemic golden Syrian hamsters (Mesocricetus auratus) [J].
Auger, C ;
Caporiccio, B ;
Landrault, N ;
Teissedre, PL ;
Laurent, C ;
Cros, G ;
Besançon, P ;
Rouanet, JM .
JOURNAL OF NUTRITION, 2002, 132 (06) :1207-1213
[6]   Systemic levels of lipid peroxidation and its metabolic and dietary correlates in patients with nonalcoholic steatohepatitis [J].
Chalasani, N ;
Deeg, MA ;
Crabb, DW .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2004, 99 (08) :1497-1502
[7]   Fruit and vegetable consumption and risk of coronary heart disease: A meta-analysis of cohort studies [J].
Dauchet, Luc ;
Amouyel, Philippe ;
Hercberg, Serge ;
Dallongeville, Jean .
JOURNAL OF NUTRITION, 2006, 136 (10) :2588-2593
[8]   Oxidative stress in alcoholic liver disease: Role of NADPH oxidase complex [J].
De Minicis, Samele ;
Brenner, David A. .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2008, 23 :S98-S103
[9]  
Dini L, 1996, CELL MOL BIOL, V42, P269
[10]  
FOLCH J, 1957, J BIOL CHEM, V226, P497