Skip to main content
Log in

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

  • Published:
AGE Aims and scope Submit manuscript

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.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. McCay CM, Crowell MR and Maynard LA: The effect of retarded growth upon the length of the life span and upon the ultimate body size. J. Nutr. 10:63–79, 1935.

    CAS  Google Scholar 

  2. Tannenbaum A: The genesis and growth of tumors. II. Effects of caloric restriction per se. Cancer Res. 2: 460–467, 1942.

    CAS  Google Scholar 

  3. Ross MH: Length of life and nutrition in the rat. J. Nutr. 75:197–210, 1961.

    PubMed  CAS  Google Scholar 

  4. Masoro EJ: Food restriction and the aging process. J. Am. Geriatr. Soc. 32:296–300, 1984.

    PubMed  CAS  Google Scholar 

  5. Weindruch R and Walford RL: The retardation of aging and disease by dietary restriction. Springfield, IL; Charles C. Thomas, 1988.

    Google Scholar 

  6. Harman D: Free radical theory of aging: role of free radical in the origination and evolution of life, aging and disease processes, in Free Radicals, Aging, and Degenerative Diseases, edited by Johnson JE Jr, Walford R, Harman D and Miquel J, New York, Liss, 1986, pp. 3–49.

    Google Scholar 

  7. Harman D: The aging process. Proc. Natl. Acad. Sci. USA 78:7124–7128, 1981.

    PubMed  CAS  Google Scholar 

  8. Rikans LE, Moore DR and Snowden CD: Sex-dependent differences in the effects of aging on antioxidant defense mechanisms of rat liver. Biochimica et Biophysica Acta, 1074:195–200, 1991.

    PubMed  CAS  Google Scholar 

  9. Harman D: Free radical therory of aging. Mutation Res. 275:257–266, 1992.

    Article  PubMed  CAS  Google Scholar 

  10. Gutteridge JM: Aging and free radicals. Medical Lab. Sci. 49:313–318, 1992.

    CAS  Google Scholar 

  11. Sohal RS and Orr WC: Relationship between antioxidants, prooxidants, and the aging process. Annals of the New York Acad. Sci. 663:74–84, 1992.

    CAS  Google Scholar 

  12. Kowald A and Kirkwood TB: A network theory of aging: the interactions of defective mitochondria, aberrant proteins, free radicals and scavengers in the aging process. Mutation Res. 316:209–236, 1996.

    Article  PubMed  CAS  Google Scholar 

  13. Carney JM and Carney AM: Role of protein oxidation in aging and in age-associated neuro-degenerative diseases. Life Sci. 55:2097–2103, 1994.

    Article  PubMed  CAS  Google Scholar 

  14. Florence TM: The role of free radicals in disease. Australian and New Zealand J. Ophthalmology 23: 3–7, 1995.

    CAS  Google Scholar 

  15. Feuers R J, Weindruch R and Hart RW: Caloric restriction, aging and antioxidant enzymes. Mutation Res. 295:191–200, 1993.

    Article  PubMed  CAS  Google Scholar 

  16. McCarter RJ: Role of caloric restriction in the prolongation of life. Clinics in Geriatr. Med. 11: 553–565, 1995.

    CAS  Google Scholar 

  17. Weindruch R: Caloric restriction and aging. Scientific American 274:46–52, 1996.

    Article  PubMed  CAS  Google Scholar 

  18. Hollan S: Free radicals in health and disease. Haematologia 26:177–189, 1995.

    PubMed  CAS  Google Scholar 

  19. Davis KJ: Oxidative stress: the paradox of aerobic life. Biochemical Soc. Symposia 61:1–31, 1995.

    Google Scholar 

  20. Laval J: Role of DNA repair enzymes in the cellular resistance to oxidative stress. Pathologie Biologie 44:14–24, 1996.

    PubMed  CAS  Google Scholar 

  21. Chance B, Sies H and Boveris A: Hydroperoxide metabolism in mammalian organs. Physiol. Revs. 59: 527–605, 1979.

    CAS  Google Scholar 

  22. Flora AD, Morelli A and Liuliano F: Human erythrocyte glucose-6-phosphate dehydrogenase. Content of bound coenzyme. Biochem Biophys. Res. Comm. 59:406–413, 1974.

    Article  PubMed  Google Scholar 

  23. Koizumi A, Weindruch R and Walford RL: Influences of dietary restriction and age on liver enzyme activities and lipid peroxidation in mice. J. Nutr. 117:361–367, 1987.

    PubMed  CAS  Google Scholar 

  24. Rao G, Xia E, Nadakavukaren MJ and Richardson A: Effect of dietary restriction on the age-dependent changes in the expression of antioxidant enzymes in rat liver. J. Nutr. 120:602–609, 1990.

    PubMed  CAS  Google Scholar 

  25. Feuers R J, Delongchamp RR, Casciano DA, Burkhart JG and Mohrenweiser HW: Assay for mouse tissue enzymes: Levels of activity and statistical variation for 29 enzymes of liver or brain. Anal. Biochem. 101:123–130, 1980.

    Article  PubMed  CAS  Google Scholar 

  26. Lowry OH, Rosebrough NJ, Farr AL and Randall RJ: Protein measurement with the Folin phenol reagent. J. Biol. Chem. 193:265–275, 1951.

    PubMed  CAS  Google Scholar 

  27. Bergmeyer HU, Crewehn K and Corassl M: Enzymes as biochemical reagents, in Methods of Enzymatic Analysis. 2nd Ed., Vol. 1, edited by Bergmeyer, HU, New York, Academic Press, Inc., 1974, pp. 458–459.

    Google Scholar 

  28. Aebi H: Catalase in vitro. Methods Enzymol. 105:121–126, 1984.

    Article  PubMed  CAS  Google Scholar 

  29. Wheeler CR, Salzman JA, Elsayed NM, Omaye ST and Korle DW Jr: Automated assays for superoxide dismutase, catalase, gluthathione reductase activity. Anal. Biochem. 184:193–199, 1990.

    Article  PubMed  CAS  Google Scholar 

  30. Klingenberg M: Nicotinamide-adenine dinucleotides (NAD, NADP, NADH, NADPH) spectrophotometric and fluorimetric methods, in Methods of Enzymatic Analysis, 2nd Ed., Vol. IV, edited by Bergmeyer HU, New York, Academic Press, Inc., 1974, pp. 2045–2059.

    Google Scholar 

  31. Halberg F, Johnson EA, Nelson W, Runge W and Sothern R: Autorhythemometry-procedures for physiological self-measurements and their analysis. Physiol. Teach. 1:1–11,1972.

    Google Scholar 

  32. Feuers RJ, Duffy PH, Chen F, Desai V, Oriaku E, Shaddock JG, Pipkin JL, Weindruch R and Hart RW: Intermediary Metabolism and Antioxidant Systems, in Dietary Restriction: Implications for the Design and Interpretation of Toxicity and Carcinogenicity Studies, edited by Hart R, Neumann, D and Robertson, R, Wash., DC, ILSI Press, 1995, pp. 181–195.

    Google Scholar 

  33. Duffy PH, Feuers RJ, Leakey JEA, Nakamura KD, Turturro A and Hart RW: Effect of chronic caloric restriction on the physiological variables related to energy metabolism in the male Fischer 344 rat. Mech. Ageing Dev. 48: 117–133, 1989.

    Article  PubMed  CAS  Google Scholar 

  34. Feuers RJ, Duffy PH, Leakey JEA, Turturro A, Mittelstaedt RA and Hart RW: Effect of chronic caloric restriction on hepatic enzymes of intermediary metabolism in the male Fischer 344 rat. Mech Ageing Dev. 48: 179–189, 1989.

    Article  PubMed  CAS  Google Scholar 

  35. Manos, P, Nakayama, R, and Holten, D: Regulation of glucose-6-phosphate dehydrognease synthesis and mRNA abundance in cultured rat hepatocytes. Biochem. J. 276:245–250, 1991.

    PubMed  CAS  Google Scholar 

  36. Feuers RJ, Weindruch R, Leakey, JEA, Duffy, PH and Hart, RW: Increased effective activity of rat liver catalase by dietary restriction. Age 20: 215–220, 1997.

    CAS  Google Scholar 

  37. Eaton JW: Catalases and peroxidases and glutathione and hydrogen peroxide: Mysteries of the bestiary. J Lab Clin Med. 118:3–4, 1991.

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

About this article

Cite this article

Oriaku, E.T., Chen, F., Desai, V.G. et al. A circadian study of liver antioxidant enzyme systems of female Fischer-344 rats subjected to dietary restriction for six weeks.. AGE 20, 221–228 (1997). https://doi.org/10.1007/s11357-997-0022-0

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11357-997-0022-0

Keywords

Navigation