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Protective effects of broccoli (Brassica oleracea) against oxidative damage in vitro and in vivo

Authors
Cho, Eun JuLee, Young A.Yoo, Hye HyunYokozawa, Takako
Issue Date
Dec-2006
Publisher
Center for Academic Publications Japan
Keywords
broccoli; antioxidative activity; oxidative stress; diabetes; streptozotocin
Citation
Journal of Nutritional Science and Vitaminology, v.52, no.6, pp 437 - 444
Pages
8
Indexed
SCIE
SCOPUS
Journal Title
Journal of Nutritional Science and Vitaminology
Volume
52
Number
6
Start Page
437
End Page
444
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/44468
DOI
10.3177/jnsv.52.437
ISSN
0301-4800
1881-7742
Abstract
The antioxidative effect and protective potential against diabetes of the broccoli flower were investigated both in vitro and in a diabetic rat model. Among fractions of MeOH, CH2Cl2, BuOH, and H2O, the BuOH fraction exerted the strongest inhibitory activities on 1,1-diphenyl-2-picrylhydrazyl radical, radical-induced protein oxidation, and nitric oxide generation by sodium nitroprusside. The in vitro results suggest that the BuOH fraction from the broccoli flower has a protective potential against oxidative stress. The rat model with diabetes induced by streptozotocin was employed to evaluate the protective effect of the BuOH fraction in vivo. Diabetic rats showed reduced body weight gain and heavier kidney and liver weights than normal rats, while oral administration of the BuOH fraction at,an oral dose of 100 or 200 mg/kg body weight/d for 20 d attenuated the physiological changes induced by diabetes. In addition, oral administration of the BuOH fraction to diabetic rats led to significant decreases in serum glucose and glycosylated protein, while it resulted in the increase of serum albumin, implying that the BuOH fraction improves the abnormal metabolism of glucose and protein that leads to oxidative stress. Moreover, it significantly reduced thiobarbituric acid-reactive substance levels in serum, hepatic and renal mitochondria. This suggests that the BuOH fraction would alleviate the oxidative stress associated with diabetes through the inhibition of lipid peroxidation. The present study demonstrates that the BuOH fraction has an antioxidative effect in vitro and it protects against oxidative stress induced by diabetes in an in vivo model.
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