Caffeine Increases Apolipoprotein A-1 and Paraoxonase-1 but not Paraoxonase-3 Protein Levels in Human-Derived Liver (HepG2) Cells

被引:3
|
作者
Ozgun, Gulben Sayilan [1 ]
Ozgun, Eray [1 ]
Tabakcioglu, Kiymet [2 ]
Gokmen, Selma Suer [1 ]
Eskiocak, Sevgi [1 ]
Cakir, Erol [1 ]
机构
[1] Trakya Univ, Sch Med, Dept Med Biochem, Edirne, Turkey
[2] Trakya Univ, Sch Med, Dept Med Biol, Edirne, Turkey
关键词
Caffeine; apolipoprotein A-1; paraoxonase-1; paraoxonase-3; HepG2; cells; HIGH-DENSITY-LIPOPROTEIN; COFFEE; ATHEROSCLEROSIS; CHOLESTEROL; ANTIOXIDANTS; CONSUMPTION; TOXICITY; GENE;
D O I
10.4274/balkanmedj.2016.1217
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Apolipoprotein A-1, paraoxonase-1 and paraoxonase-3 are antioxidant and anti-atherosclerotic structural high-density lipoprotein proteins that are mainly synthesized by the liver. No study has ever been performed to specifically examine the effects of caffeine on paraoxonase enzymes and on liver apolipoprotein A-1 protein levels. Aims: To investigate the dose-dependent effects of caffeine on liver apolipoprotein A-1, paraoxonase-1 and paraoxonase-3 protein levels. Study Design: In vitro experimental study. Methods: HepG2 cells were incubated with 0 (control), 10, 50 and 200 mu M of caffeine for 24 hours. Cell viability was evaluated by 3-(4,5-Dimethyl-2-thiazolyl)-2,5diphenyl-2H-tetrazolium bromide assay. Apolipoprotein A-1, paraoxonase-1 and paraoxonase-3 protein levels were measured by western blotting. Results: We observed a significant increase on apolipoprotein A-1 and paraoxonase-1 protein levels in the cells incubated with 50 mu M of caffeine and a significant increase on paraoxonase-1 protein level in the cells incubated with 200 mu M of caffeine. Conclusion: Our study showed that caffeine does not change paraoxonase-3 protein level, but the higher doses used in our study do cause an increase in both apolipoprotein A-1 and paraoxonase-1 protein levels in liver cells.
引用
收藏
页码:534 / 539
页数:6
相关论文
共 50 条
  • [41] Interleukin-1β and interleukin-6 increase levels of apolipoprotein B mRNA and decrease accumulation of its protein in culture medium of HepG2 cells
    Yokoyama, K
    Ishibashi, T
    Liang, YQ
    Nagayoshi, A
    Teramoto, T
    Maruyama, Y
    JOURNAL OF LIPID RESEARCH, 1998, 39 (01) : 103 - 113
  • [42] Inhibition of aflatoxin B1 genotoxicity in human liver-derived HepG2 cells by kolaviron biflavonoids and molecular mechanisms of action
    Nwankwo, JO
    Tahnteng, JG
    Emerole, GO
    EUROPEAN JOURNAL OF CANCER PREVENTION, 2000, 9 (05) : 351 - 361
  • [43] HMGB1 release by human liver L02 and HepG2 cells induced by lipopolysaccharide
    Huang, Ze-Bing
    Dai, Xia-Hong
    Xiao, Mei-Fang
    Zhou, Rong-Rong
    Zhao, Shu-Shan
    Zhang, Bao-Xin
    Yi, Pan-Pan
    Chen, Ruo-Chan
    Li, Wen-Ting
    Yaser, Ai-Madhagi
    Huang, Yan
    Fan, Xue-Gong
    MOLECULAR MEDICINE REPORTS, 2013, 8 (01) : 103 - 112
  • [44] Claudin-1 silencing increases sensitivity of liver cancer HepG2 cells to 5-fluorouracil by inhibiting autophagy
    Tong, Hui
    Li, Tao
    Qiu, Weihua
    Zhu, Zhecheng
    ONCOLOGY LETTERS, 2019, 18 (06) : 5709 - 5716
  • [45] Structurally related mycotoxins ochratoxin A, ochratoxin B, and citrinin differ in their genotoxic activities and in their mode, of action in human-derived liver (HepG2) cells:: Implications for risk assessment
    Knasmüller, S
    Cavin, C
    Chakraborty, A
    Darroudi, F
    Majer, BJ
    Huber, WW
    Ehrlich, VA
    NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 2004, 50 (02): : 190 - 197
  • [46] Uptake and metabolism of 3,5,3'-triiodothyronine and 3,3',5'-triiodothyronine by human liver-derived cells: HepG2 cells as a model for thyroid hormone handling by human liver
    vanStralen, PGJ
    vanderHoek, HJ
    Docter, R
    deJong, M
    Krenning, EP
    Everts, ME
    Hennemann, G
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (01): : 244 - 248
  • [47] Overexpression of acyl-CoA synthetase-1 increases lipid deposition in hepatic (HepG2) cells and rodent liver in vivo
    Parkes, Heidi A.
    Preston, Elaine
    Wilks, Donna
    Ballesteros, Mercedes
    Carpenter, Lee
    Wood, Leonie
    Kraegen, Edward W.
    Furler, Stuart M.
    Cooney, Gregory J.
    AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2006, 291 (04): : E737 - E744
  • [48] Arsenite down-regulates cytochrome P450 1A1 at the transcriptional and posttranslational levels in human HepG2 cells
    Anwar-Mohamed, Anwar
    El-Kadi, Ayman O. S.
    FREE RADICAL BIOLOGY AND MEDICINE, 2010, 48 (10) : 1399 - 1409
  • [49] Hepatitis C core protein increases sensitivity of HepG2 cells to oxidants and down-regulates heme oxygenase-1.
    Wen, F
    Abdalla, MY
    Aloman, C
    Icardi, M
    McCormick, ML
    Branch, AD
    Walewski, J
    LaBrecque, DR
    Voigt, M
    Brown, KE
    Britigan, BE
    Schmidt, WN
    HEPATOLOGY, 2003, 38 (04) : 236A - 236A
  • [50] Cadmium cation increases the production and mRNA levels of insulin-like growth factor-binding protein-1 in HepG2
    Oishi, Yuichi
    Ohnishi, Motoko
    Kobayashi-Hattori, Kazuo
    Takita, Toshichika
    Noguchi, Tadashi
    BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2007, 71 (05) : 1334 - 1337