Apple juice intervention modulates expression of ARE-dependent genes in rat colon and liver

Eur J Nutr. 2011 Mar;50(2):135-43. doi: 10.1007/s00394-010-0124-9. Epub 2010 Jul 22.

Abstract

Background: The risk of cancer and other degenerative diseases is inversely correlated with consumption of fruits and vegetables. This beneficial effect is mainly attributed to secondary plant constituents such as polyphenols, supposed to play a major role in protection against ROS (reactive oxygen species)-associated toxicity.

Aim of the study: To elucidate the potential of differently manufactured apple juices (clear AJ/cloudy AJ/smoothie, in comparison with a polyphenol-free control juice) to modulate expression of ARE-dependent genes.

Methods: In male Sprague-Dawley rats (n = 8/group; 10d juice intervention, 4d wash-out; 4 treatment cycles), expression of target genes (superoxide dismutase, SOD1/SOD2; glutathione peroxidase, GPX1/GPX2; γ-glutamylcysteine ligase, GCLC/GCLM; glutathione reductase, GSR; catalase, CAT; NAD(P)H:quinone oxidoreductase-1, NQO1 and transcription factor erythroid-derived 2-like-2, Nrf2) was quantified with duplex RT-PCR, using glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as control.

Results: In colon and liver of rats consuming polyphenol-free control juice, rather similar basic expressions were observed (relative GAPDH ratios ranging from 2 to 0.7 and 2.5-0.3, respectively). In the distal colon, apple juice intervention slightly but significantly induced most genes (e.g. GPX2, GSR, CAT, Nrf2; p < 0.001), whereas in the liver only GPX1 and NQO1 mRNA were up-regulated; other hepatic target genes were not affected or down-regulated (SOD1, SOD2, GCLC/M, GSR), concomitant with the absence of Nrf2 induction. Induction of antioxidant gene expression differed with juice type (cloudy AJ > clear AJ ~ smoothie).

Conclusion: Taken together, the results underline the potential of polyphenol-rich apple juice to increase the expression of ARE-dependent antioxidant genes.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Beverages / analysis*
  • Catalase / genetics
  • Catalase / metabolism
  • Colon / metabolism*
  • Dipeptides / genetics
  • Dipeptides / metabolism
  • Flavonoids / pharmacology*
  • Fruit / chemistry
  • Glutathione Peroxidase / genetics
  • Glutathione Peroxidase / metabolism
  • Glutathione Peroxidase GPX1
  • Liver / metabolism*
  • Male
  • Malus / chemistry*
  • NAD(P)H Dehydrogenase (Quinone) / genetics
  • NAD(P)H Dehydrogenase (Quinone) / metabolism
  • Oxidative Stress
  • Phenols / pharmacology*
  • Polyphenols
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species
  • Reverse Transcriptase Polymerase Chain Reaction
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Superoxide Dismutase-1
  • Up-Regulation
  • Vegetables / chemistry

Substances

  • Antioxidants
  • Dipeptides
  • Flavonoids
  • Phenols
  • Polyphenols
  • Reactive Oxygen Species
  • Catalase
  • Glutathione Peroxidase
  • glutathione peroxidase 2, rat
  • Sod1 protein, rat
  • Superoxide Dismutase
  • Superoxide Dismutase-1
  • superoxide dismutase 2
  • NAD(P)H Dehydrogenase (Quinone)
  • NQO1 protein, rat
  • gamma-glutamylcysteine
  • Glutathione Peroxidase GPX1