Hesperidin Supplementation Alleviates Oxidative DNA Damage and Lipid Peroxidation in Type 2 Diabetes: A Randomized Double-Blind Placebo-Controlled Clinical Trial

被引:64
作者
Homayouni, Fatemeh [1 ]
Haidari, Fatemeh [1 ]
Hedayati, Mehdi [2 ]
Zakerkish, Mehrnoosh [3 ]
Ahmadi, Kambiz [4 ]
机构
[1] Ahvaz Jundishapur Univ Med Sci, Fac Paramed Sci, Dept Nutr, Nutr & Metab Dis Res Ctr, Ahvaz 6135715794, Iran
[2] Shahid Beheshti Univ Med Sci, Res Inst Endocrine Sci, Cellular & Mol Endocrine Res Ctr, Tehran, Iran
[3] Ahvaz Jundishapur Univ Med Sci, Dept Endocrinol & Metab, Diabet Res Ctr, Ahvaz, Iran
[4] Ahvaz Jundishapur Univ Med Sci, Fac Publ Hlth, Dept Stat & Epidemiol, Ahvaz, Iran
关键词
hesperidin; oxidative stress; oxidative DNA damage; lipid peroxidation; type; 2; diabetes; STRESS; ANTIOXIDANT; MALONDIALDEHYDE; HYPERGLYCEMIA; 8-OHDG;
D O I
10.1002/ptr.5881
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
This study aimed to examine the effects of hesperidin supplement on the glycemic parameters, oxidative DNA damage, and lipid peroxidation in patients with type 2 diabetes. Sixty-four patients were randomly allocated to receive 500 mg/day hesperidin or placebo capsules for 6 weeks. Data on glycemic parameters, total antioxidant capacity (TAC), 8-hydroxydeoxyguanosine (8-OHDG), and malondialdehyde (MDA) were collected at the baseline and at the end of the study. In hesperidin group, TAC increased (0.74 +/- 0.16 vs. 0.82 +/- 0.18), while serum froctoseamin (5.79 +/- 5.86 vs. 5.01 +/- 4.95; p = 0.001), 8-OHDG (14.32 +/- 6.4 vs. 11.00 +/- 7.0; p = 0.000), and MDA (5.78 +/- 1.76 vs. 4.60 +/- 0.75; p = 0.000) decreased in comparison with the baseline values. There was a significant difference in percent change of TAC (13.35 +/- 19.21 vs. 3.13 +/- 10.02; p = 0.043), froctoseamin (-10.10 +/- 16.84 vs. 4.27 +/- 34.646), 8-OHDG (-25.11 +/- 28.23 vs. 8.69 +/- 35.41; p = 0.000), and MDA (-16.46 +/- 18.04 vs. -1.82 +/- 22.63; p = 0.007) between hesperidin and control groups following intervention in adjusted models. These results suggest that hesperidin may improve TAC and alleviate serum froctoseamin, 8-OHDG, and MDA levels in type 2 diabetes. Copyright (C) 2017 John Wiley & Sons, Ltd.
引用
收藏
页码:1539 / 1545
页数:7
相关论文
共 30 条
[1]
Protective effect of alpha glucosyl hesperidin (G-hesperidin) on chronic vanadium induced testicular toxicity and sperm nuclear DNA damage in male Sprague Dawley rats [J].
Bharathi, B. Vijaya ;
Prakash, G. Jaya ;
Krishna, K. M. ;
Krishna, C. H. Ravi ;
Sivanarayana, T. ;
Madan, K. ;
Raju, G. A. Rama ;
Annapurna, A. .
ANDROLOGIA, 2015, 47 (05) :568-578
[2]
Bhutia Yazum, 2011, J Nat Sci Biol Med, V2, P107, DOI 10.4103/0976-9668.82309
[3]
Hesperidin, an antioxidant flavonoid, prevents acrylonitrile-induced oxidative stress in rat brain [J].
El-Sayed, El-Sayed M. ;
Abo-Salem, Osama M. ;
Abd-Ellah, Mohamed F. ;
Abd-Alla, Gamil M. .
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2008, 22 (04) :268-273
[4]
El-Shafey MM, 2014, INT J PHARM SCI, V4, P554
[5]
Oxidative stress and stress-activated signaling pathways: A unifying hypothesis of type 2 diabetes [J].
Evans, JL ;
Goldfine, ID ;
Maddux, BA ;
Grodsky, GM .
ENDOCRINE REVIEWS, 2002, 23 (05) :599-622
[6]
Oxidative Stress and Diabetic Complications [J].
Giacco, Ferdinando ;
Brownlee, Michael .
CIRCULATION RESEARCH, 2010, 107 (09) :1058-1070
[7]
The International Physical Activity Questionnaire (IPAQ):: a study of concurrent and construct validity [J].
Hagstromer, Maria ;
Oja, Pekka ;
Sjostrom, Michael .
PUBLIC HEALTH NUTRITION, 2006, 9 (06) :755-762
[8]
Evaluation of antioxidative and anti-inflammatory potential of hesperidin and naringin on the rat air pouch model of inflammation [J].
Jain, Mandipika ;
Parmar, Hamendra Singh .
INFLAMMATION RESEARCH, 2011, 60 (05) :483-491
[9]
Evaluation of antioxidant activity of hesperidin and its protective effect on H2O2 induced oxidative damage on pBR322 DNA and RBC cellular membrane [J].
Kalpana, K. B. ;
Srinivasan, M. ;
Menon, Venugopal P. .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2009, 323 (1-2) :21-29
[10]
Kang Dong Soo, 2015, Ann Pediatr Endocrinol Metab, V20, P21, DOI 10.6065/apem.2015.20.1.21