A circadian study of liver antioxidant enzyme systems of female Fischer-344 rats subjected to dietary restriction for six weeks.

E T Oriaku, F Chen, V G Desai, J L Pipkin, J G Shaddock, R Weindruch, R W Hart, R J Feuers
Author Information

Abstract

We examined the influences of dietary restriction (DR) on the circadian profile of liver catalase (CAT), glutathione peroxidase (GPx), and interacting systems required for removal of H2O2 (support systems), in 18-week old female Fischer 344 rats fed 60% of their ad libitum (AL) diet for six weeks. Food was presented to the DR animals during the early light-span. Regardless of diet, enzyme levels were generally consistent with circadian patterns. In CR animals, maximum activities often occurred at the time of food presentation. CAT and GPx activities generally were significantly higher in DR animals than in AL animals at the time of feeding. When assessing glucose-6-phosphate dehydrogenase (G6PDH) activity using saturating substrate (NADP(+)) concentrations, higher activities were seen at all times of day in the AL animals; however, when activity was measured in the presence of lower (i.e., physiologic) NADP(+) concentrations, the reverse was true. In contrast, glutathione reductase (GR) activity was not influenced by DR. Cytosolic levels of NADPH peaked and were higher in DR than in AL rodents prior to feeding. NADH levels were not influenced by diet, but did manifest a significant circadian pattern with a maximum occurring toward the middle of the dark span. These data suggest that even at a young age and following only a relatively brief duration of DR, there exists an enhanced enzymatic capability in rats subjected to DR to remove free radicals generated as a consequence of normal oxidative metabolism. Further, these data support emerging trends suggesting metabolic regulation of antioxidant defense systems in response to free radical generation.

References

  1. Life Sci. 1994;55(25-26):2097-103 [PMID: 7997068]
  2. Sci Am. 1996 Jan;274(1):46-52 [PMID: 8533065]
  3. Anal Biochem. 1980 Jan 1;101(1):123-30 [PMID: 7356121]
  4. Mech Ageing Dev. 1989 May;48(2):117-33 [PMID: 2661930]
  5. Mech Ageing Dev. 1989 May;48(2):179-89 [PMID: 2661933]
  6. Mutat Res. 1993 Dec;295(4-6):191-200 [PMID: 7507557]
  7. Aust N Z J Ophthalmol. 1995 Feb;23(1):3-7 [PMID: 7619452]
  8. J Lab Clin Med. 1991 Jul;118(1):3-4 [PMID: 2066640]
  9. Biochim Biophys Acta. 1991 May 24;1074(1):195-200 [PMID: 2043671]
  10. Age (Omaha). 1997 Oct;20(4):215-20 [PMID: 23604323]
  11. Methods Enzymol. 1984;105:121-6 [PMID: 6727660]
  12. Mutat Res. 1992 Sep;275(3-6):257-66 [PMID: 1383768]
  13. Biochem Soc Symp. 1995;61:1-31 [PMID: 8660387]
  14. Proc Natl Acad Sci U S A. 1981 Nov;78(11):7124-8 [PMID: 6947277]
  15. Nutrition. 1989 May-Jun;5(3):155-71; discussion 172 [PMID: 2520283]
  16. Mutat Res. 1996 May;316(5-6):209-36 [PMID: 8649456]
  17. Biochem J. 1991 May 15;276 ( Pt 1):245-50 [PMID: 2039474]
  18. Pathol Biol (Paris). 1996 Jan;44(1):14-24 [PMID: 8734295]
  19. J Am Geriatr Soc. 1984 Apr;32(4):296-300 [PMID: 6707410]
  20. Physiol Rev. 1979 Jul;59(3):527-605 [PMID: 37532]
  21. Med Lab Sci. 1992 Dec;49(4):313-8 [PMID: 1339935]
  22. Ann N Y Acad Sci. 1992 Nov 21;663:74-84 [PMID: 1482104]
  23. J Nutr. 1961 Oct;75:197-210 [PMID: 14494200]
  24. J Nutr. 1990 Jun;120(6):602-9 [PMID: 2352034]
  25. Anal Biochem. 1990 Feb 1;184(2):193-9 [PMID: 2327564]
  26. Biochem Biophys Res Commun. 1974 Jul 10;59(1):406-13 [PMID: 4152246]
  27. J Nutr. 1987 Feb;117(2):361-7 [PMID: 3031254]
  28. Clin Geriatr Med. 1995 Nov;11(4):553-65 [PMID: 8556686]
  29. Haematologia (Budap). 1995;26(4):177-89 [PMID: 7590512]
  30. J Biol Chem. 1951 Nov;193(1):265-75 [PMID: 14907713]

Word Cloud

Created with Highcharts 10.0.0DRanimalscircadiansystemsALratsdietlevelsactivitieshigheractivitydietaryrestrictionliverCATglutathioneGPxsupportfemalesixweeksenzymegenerallymaximumtimefeedingNADP+concentrationsinfluenceddatasubjectedfreeantioxidantexaminedinfluencesprofilecatalaseperoxidaseinteractingrequiredremovalH2O218-weekoldFischer344fed60%adlibitumFoodpresentedearlylight-spanRegardlessconsistentpatternsCRoftenoccurredfoodpresentationsignificantlyassessingglucose-6-phosphatedehydrogenaseG6PDHusingsaturatingsubstrateseentimesdayhowevermeasuredpresenceloweriephysiologicreversetruecontrastreductaseGRCytosolicNADPHpeakedrodentspriorNADHmanifestsignificantpatternoccurringtowardmiddledarkspansuggestevenyoungagefollowingrelativelybriefdurationexistsenhancedenzymaticcapabilityremoveradicalsgeneratedconsequencenormaloxidativemetabolismemergingtrendssuggestingmetabolicregulationdefenseresponseradicalgenerationstudyFischer-344

Similar Articles

Cited By

No available data.