Oxidative stress as a mechanism of diabetes in diabetic BB prone rats: Effect of secoisolariciresinol diglucoside (SDG)

被引:76
作者
Prasad, K [1 ]
机构
[1] Univ Saskatchewan, Coll Med, Dept Physiol, Saskatoon, SK S7N 0W0, Canada
关键词
Type I diabetes; malondialdehyde; pancreatic antioxidant reserve; antioxidant; flaxseed; secoisolariciresinol diglucoside; oxidative stress;
D O I
10.1023/A:1007079802459
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Secoisolariciresinol diglucoside (SDG) isolated from flaxseed has antioxidant activity and has been shown to prevent hypercholesterolemic atherosclerosis. An investigation was made of the effects of SDG on the development of diabetes in diabetic prone BioBreeding rats (BBdp rats), a model of human type I diabetes [insulin dependent diabetes mellitus (IDDM)] to determine if this type of diabetes is due to oxidative stress and if SDG can prevent the incidence of diabetes. The rats were divided into three groups: Group I, BioBreeding normal rats (BBn rats) (n = 10); group II, BBdp untreated (n = 11); and group III, BBdp treated with SDG 22 mg/kg body wt, orally) (n = 14). Oxidative stress was determined by measuring lipid peroxidation product malondialdehyde (MDA) an index of level of reactive oxygen species in blood and pancreas; and pancreatic chemiluminescence (Pancreatic-CL), a measure of antioxidant reserve. Incidence of diabetes was 72.7% in untreated and 21.4% in SDG-treated group as determined by glycosuria and hyperglycemia. SDG prevented the development of diabetes by approximately 71%. Development of diabetes was associated with an increase in serum and pancreatic MDA and a decrease in antioxidant reserve. Prevention in development of diabetes by SDG was associated with a decrease in serum and pancreatic-MDA and an increase in antioxidant reserve. These results suggest that IDDM is mediated through oxidative stress and that SDG prevents the development of diabetes.
引用
收藏
页码:89 / 96
页数:8
相关论文
共 47 条
[1]   PARTIAL PROTECTION AGAINST STREPTOZOTOCIN-INDUCED HYPERGLYCEMIA BY SUPEROXIDE-DISMUTASE LINKED TO POLYETHYLENE-GLYCOL [J].
ASPLUND, K ;
GRANKVIST, K ;
MARKLUND, S ;
TALJEDAL, IB .
ACTA ENDOCRINOLOGICA, 1984, 107 (03) :390-394
[2]   CELL-MEDIATED AUTOIMMUNITY IN TYPE-I DIABETES [J].
BARBOSA, J ;
BACH, FH .
DIABETES-METABOLISM REVIEWS, 1987, 3 (04) :981-1004
[3]   GAMMA-INTERFERON IS ABLE TO ENHANCE THE OXIDATIVE-METABOLISM OF HUMAN-NEUTROPHILS [J].
BERTON, G ;
ZENI, L ;
CASSATELLA, MA ;
ROSSI, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 138 (03) :1276-1282
[4]   ROLE OF CYTOKINES AND PLATELET-ACTIVATING FACTOR IN MICROVASCULAR IMMUNE INJURY [J].
BRAQUET, P ;
HOSFORD, D ;
BRAQUET, M ;
BOURGAIN, R ;
BUSSOLINO, F .
INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1989, 88 (1-2) :88-100
[5]  
CADENAS E, 1982, EUR J BIOCHEM, V124, P349
[6]   OXYGEN-INDUCED OR ORGANIC HYDROPEROXIDE-INDUCED CHEMI-LUMINESCENCE OF BRAIN AND LIVER HOMOGENATES [J].
CADENAS, E ;
VARSAVSKY, AI ;
BOVERIS, A ;
CHANCE, B .
BIOCHEMICAL JOURNAL, 1981, 198 (03) :645-654
[7]   LOW-LEVEL CHEMI-LUMINESCENCE OF ISOLATED HEPATOCYTES [J].
CADENAS, E ;
WEFERS, H ;
SIES, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1981, 119 (03) :531-536
[8]   ADMINISTRATION OF SILICA PARTICLES OR ANTI-LYT2 ANTIBODY PREVENTS BETA-CELL DESTRUCTION IN NOD MICE GIVEN CYCLOPHOSPHAMIDE [J].
CHARLTON, B ;
BACELJ, A ;
MANDEL, TE .
DIABETES, 1988, 37 (07) :930-935
[9]  
Cornall A.G., 1949, J BIOL CHEM, V177, P751
[10]   SELECTIVE ANTAGONISM OF PLATELET-ACTIVATING-FACTOR (PAF)-INDUCED AGGREGATION AND SECRETION IN WASHED RABBIT PLATELETS BY CV-3988, L-652731, TRIAZOLAM AND ALPRAZOLAM [J].
COX, CP ;
WOOD, KL .
THROMBOSIS RESEARCH, 1987, 47 (03) :249-257