High fat diet induced oxidative DNA damage estimated by 8-oxo-7,8-dihydro-2′-deoxyguanosine excretion in rats

被引:35
|
作者
Loft, S
Thorling, EB
Poulsen, HE
机构
[1] Univ Copenhagen, Panum Inst, Dept Pharmacol, Inst Publ Hlth, DK-2200 Copenhagen, Denmark
[2] Univ Aarhus, Inst Environm & Occupat Med, Danish Canc Soc, DK-8000 Aarhus C, Denmark
[3] Copenhagen Univ Hosp, Rigshosp, Dept Clin Pharmacol, Copenhagen, Denmark
关键词
8-OxodG; dietary fat; rats; metabolism; oxidative DNA damage;
D O I
10.1080/10715769800300641
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The role of dietary fats and energy in carcinogenesis has been partly related to oxidative damage to DNA. We have investigated the effect of dietary fat content and saturation on the urinary excretion of 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG) in male and female rats. Groups of Fischer F344 rats (n = 6-10) were fed control chow (3.4% fat) or diets containing 21.8% corn oil or 19.8% coconut oil + 2% corn oil for 12-15 weeks. At the end of the diet intervention period 24 h urine was collected for determination of 8-oxodG by HPLC. In the male groups fed control, corn oil and coconut oil diet the excretion of 8-oxodG was 403 +/- 150, 932 +/- 198 and 954 +/- 367 pmol/kg 24 h, respectively (p < 0.05). In the female groups fed control and corn oil diet the excretion of 8-oxodG was 752 +/- 80 and 2206 +/- 282 pmol/kg 24 h, respectively (p < 0.05). Calculated per whole animal the excretion was 137 +/- 51, 324 +/- 70 and 328 +/- 128 pmol/24 h in the control, corn and coconut oil male groups and 156 +/- 21 and 464 +/- 56 pmol/24 h in the control and corn oil female groups, respectively(p < 0.05). Thus, per animal or per consumed energy there was much less difference in 8-oxodG excretion between the corresponding male and female groups and only significant difference between the high fat groups. There was a close correlation (r = 0.7; p < 0.05) between 8-oxodG excretion and the energy intake. The present study suggests that a high fat diet increases oxidative DNA modification substantially irrespective of the saturation level of the fat. Energy intake appears to be the major determinant of the rate of modification.
引用
收藏
页码:595 / 600
页数:6
相关论文
共 50 条
  • [31] 8-Oxo-7,8-dihydro-2′-deoxyguanosine Forms a Relatively Unstable Tetrameric Structure Compared with 2′-Deoxyguanosine
    Iwahashi, Hideo
    JOURNAL OF CLINICAL BIOCHEMISTRY AND NUTRITION, 2009, 44 (01) : 57 - 61
  • [32] Structural Insights into the Specificity of 8-Oxo-7,8-dihydro-2′-deoxyguanosine Bypass by Family X DNA Polymerases
    Kaminski, Andrea M.
    Kunkel, Thomas A.
    Pedersen, Lars C.
    Bebenek, Katarzyna
    GENES, 2022, 13 (01)
  • [33] Induction of 8-oxo-7,8-dihydro-2'-deoxyguanosine by ultraviolet radiation in calf thymus DNA and HeLa cells
    Zhang, XS
    Rosenstein, BS
    Wang, Y
    Lebwohl, M
    Mitchell, DM
    Wei, HC
    PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1997, 65 (01) : 119 - 124
  • [34] Renal excretion of 8-oxo-7,8-dihydro-2′-deoxyguanosine in Wistar rats with increased O2 consumption due to cold stress
    Topp, H
    Lengger, C
    Schöch, G
    Werner, J
    Mietzsch, E
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 376 (02) : 328 - 332
  • [35] Nucleotide excision repair of oxidised genomic DNA is not a source of urinary 8-oxo-7,8-dihydro-2′-deoxyguanosine
    Evans, Mark D.
    Mistry, Vilas
    Singh, Rajinder
    Gackowski, Daniel
    Rozalski, Rafal
    Siomek-Gorecka, Agnieszka
    Phillips, David H.
    Zuo, Jie
    Mullenders, Leon
    Pines, Alex
    Nakabeppu, Yusaku
    Sakumi, Kunihiko
    Sekiguchi, Mutsuo
    Tsuzuki, Teruhisa
    Bignami, Margherita
    Olinski, Ryszard
    Cooke, Marcus S.
    FREE RADICAL BIOLOGY AND MEDICINE, 2016, 99 : 385 - 391
  • [36] Quantitative Detection of 8-Oxo-7,8-dihydro-2′-deoxyguanosine Using Chemical Tagging and qPCR
    Bajacan, John Ernest Vallarta
    Hong, In Seok
    Penning, Trevor W.
    Greenberg, Marc M.
    CHEMICAL RESEARCH IN TOXICOLOGY, 2014, 27 (07) : 1227 - 1235
  • [37] Human and Methodological Sources of Variability in the Measurement of Urinary 8-Oxo-7,8-dihydro-2′-deoxyguanosine
    Barregard, Lars
    Moller, Peter
    Henriksen, Trine
    Mistry, Vilas
    Koppen, Gudrun
    Rossner, Pavel, Jr.
    Sram, Radim J.
    Weimann, Allan
    Poulsen, Henrik E.
    Nataf, Robert
    Andreoli, Roberta
    Manini, Paola
    Marczylo, Tim
    Lam, Patricia
    Evans, Mark D.
    Kasai, Hiroshi
    Kawai, Kazuaki
    Li, Yun-Shan
    Sakai, Kazuo
    Singh, Rajinder
    Teichert, Friederike
    Farmer, Peter B.
    Rozalski, Rafal
    Gackowski, Daniel
    Siomek, Agnieszka
    Saez, Guillermo T.
    Cerda, Concha
    Broberg, Karin
    Lindh, Christian
    Hossain, Mohammad Bakhtiar
    Haghdoost, Siamak
    Hu, Chiung-Wen
    Chao, Mu-Rong
    Wu, Kuen-Yuh
    Orhan, Hilmi
    Senduran, Nilufer
    Smith, Raymond J.
    Santella, Regina M.
    Su, Yali
    Cortez, Czarina
    Yeh, Susan
    Olinski, Ryszard
    Loft, Steffen
    Cooke, Marcus S.
    ANTIOXIDANTS & REDOX SIGNALING, 2013, 18 (18) : 2377 - 2391
  • [38] Effects of natural compounds on the accuracy of 8-oxo-7,8-dihydro-2′- deoxyguanosine translesion synthesis
    Amandine, Nachtergael
    Deborah, Lanterbecq
    Martin, Spanoghe
    Alexandra, Belayew
    Pierre, Duez
    PLANTA MEDICA, 2021, 87 (15) : 1244 - 1244
  • [39] Evidence for attenuated cellular 8-oxo-7,8-dihydro-2′-deoxyguanosine removal in cancer patients
    Cooke, MS
    Rozalski, R
    Dove, R
    Gackowski, D
    Siomek, A
    Evans, MD
    Olinski, R
    BIOLOGICAL CHEMISTRY, 2006, 387 (04) : 393 - 400
  • [40] Optimization of the workup procedure for the analysis of 8-oxo-7,8-dihydro-2′-deoxyguanosine with electrochemical detection
    Hofer, T
    Möller, L
    CHEMICAL RESEARCH IN TOXICOLOGY, 2002, 15 (03) : 426 - 432