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Effects of copper deficiency on hepatic and cardiac antioxidant enzyme activities in lactose- and sucrose-fed rats

Published online by Cambridge University Press:  09 March 2007

S. M. Lynch
Affiliation:
Biomedical Sciences Research Centre, University of Ulster at Jordanstown, Newtownabbey, Co. Antrim BT37 0QB, Northern Ireland
J. J. Strain
Affiliation:
Biomedical Sciences Research Centre, University of Ulster at Jordanstown, Newtownabbey, Co. Antrim BT37 0QB, Northern Ireland
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Abstract

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1. A number of dietary sugars are known to mediate the effects of copper deficiency. The effects of lactose (compared with sucrose) and a dietary Cu deficiency on hepatic and cardiac antioxidant enzyme activities and tissue mineral element status were investigated in the rat.

2. Groups (n 6) of male weanling Wistar rats were provided ad lib. with deionized water and diets containing sucrose (580 g/kg) or sucrose and lactose (387 g/kg and 193 g/kg respectively) with either control (12.0 mg/kg) or deficient (1.5 mg/kg) quantities of Cu for 77 d.

3. Animals consuming the low-Cu diets exhibited significantly decreased tissue Cu levels (P < 0.01), hepatic and cardiac cytochrome c oxidase (EC 1.9.3.1, CCO) activities (P < 0.01 and P < 0.001 respectively) and hepatic Cu-zinc superoxide dismutase (EC 1.15.1.1, CuZnSOD) activity (P < 0.05). The low-Cu diets also significantly decreased cardiac manganese superoxide dismutase (EC 1.15.1.1, MnSOD), catalase (EC 1.11.1.6) and glutathione peroxidase (EC 1.11.1.9, GSH-Px) activities (P < 0.01, P < 0.05 and P < 0.001 respectively).

4. Hepatic Mn was significantly increased in both lactose-fed (P < 0.001) and Cu-deficient (P < 0.01) animals. These increases were unrelated to hepatic MnSOD activity. Cardiac Zn was significantly (P < 0.01) increased in Cu-deficient animals.

5. Lactose feeding resulted in significantly increased cardiac CCO activity (P < 0.001) but significantly decreased hepatic CuZnSOD (P < 0.05), catalase (P < 0.01) and GSH-Px (P < 0.001) activities.

6. The activities of lactose dehydrogenase (EC 1.1.1.27, LDH) and glucose-6-phosphate dehydrogenase (EC 1.1.1.49, G6PDH) were found to be significantly (P < 0.05 and P < 0.01 respectively) increased in Cu-deficient animals and G6PDH activity was significantly (P < 0.01) decreased as a result of lactose consumption.

7. The observed changes in antioxidant enzyme activities associated with both Cu deficieny and lactose consumption may have important implications for the development of free radical mediated cell damage. However, no significant differences in either hepatic or cardiac levels of thiobarbituric acid reactive substances, a measure of lipid peroxidation, were found.

Type
Research Article
Copyright
Copyright © The Nutrition Society 1989

References

Aebi, H. (1974). Catalase. In Methods of Enzymatic Analysis, pp. 673684 [Bergmeyer, H. U., editor]. New York: Academic Press.CrossRefGoogle Scholar
Beynen, A. C., den Engelsman, G., Scholz, K. E. & West, C. E. (1983) Casein-induced hypercholesterolaemia in rabbits: distribution of cholesterol, triglycerides and phospholipids between serum and liver. Annals of Nutrition and Metabolism 27, 117124.Google Scholar
Blake, D. R., Allen, R. E. & Lunec, J. (1987) Free radicals in biological systems — a review orientated to inflammatory processes. British Medical Bulletin 43, 371385.Google Scholar
Bradford, M. M. (1976) Rapid and sensitive method for quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72, 248254.Google Scholar
Briggs, R. D., Rosenberg, M. L., O'Neal, R. M., Thomas, W. A. & Hartroft, W. S. (1960) Myocardial infarction in patients treated with Sippy and other high-milk diets. Circulation 21, 538542.CrossRefGoogle ScholarPubMed
Cooperstein, S. J. & Lazarow, A. (1951) A microspectrophotometric method for the determination of cytochrome oxidase. Journal of Biological Chemistry 189, 665670.Google Scholar
Fields, M., Ferretti, R. J., Reiser, S. & SmithJ. C. Jr, J. C. Jr, (1984) The severity of copper deficiency in rats is determined by the type of dietary carbohydrate. Proceedings of the Society for Experimental Biology and Medicine 175, 530537.Google Scholar
Flohe, L. & Otting, F. (1984) Superoxide dismutase assays. Methods in Enzymology 105, 93104.Google Scholar
Fridovich, I. (1975) Superoxide dismutases. Annual Review of Biochemistry 44, 147159.CrossRefGoogle Scholar
Gray, G. M. (1971) Intestinal digestion and maldigestion of dietary carbohydrates. Annual Review of Medicine 22, 391404.Google Scholar
Gruden, N. (1976) The effect of milk diet on manganese transport through the rat's duodenal wall. Nutrition Reports International 14, 515520.Google Scholar
Holbrook, J., Fields, M., Smith, J. C. Jr, Reiser, S. & Los, Alamos, Medical, Research Group (1986) Tissue distribution and excretion of copper-67 intraperitoneally administered to rats fed fructose or starch. Journal of Nutrition 116, 831838.Google ScholarPubMed
Jannson, L. T., Perkkio, M. V., Willis, W. T., RefinoC. J., C. J., & Dallman, P. R. (1985) Red cell superoxide dismutase is increased in iron deficiency anemia. Acta Haematologica 74, 218221.Google Scholar
Johnson, M. A. & Hove, S. S. (1986) Development of anemia in copper-deficient rats fed high levels of dietary iron and sucrose. Journal of Nutrition 116, 12251238.Google Scholar
Kincaid, S. A. & Carlton, W. W. (1982) Experimental copper deficiency in laboratory mice. Laboratory Animal Science 32, 491494.Google Scholar
King, B. D., Lassiter, J. W., Neathery, M. W., Miller, W. J. & Gentry, R. P. (1979) Manganese retention in rats fed different diets and chemical forms of manganese. Journal of Animal Science 49, 12351241.Google Scholar
King, B. D., Lassiter, J. W., Neathery, M. W., Miller, W. J. & Gentry, R. P. (1980) Effect of lactose, copper and iron on manganese retention and tissue distribution in rats fed dextrose and casein diets. Journal of Animal Science 50, 452458.Google Scholar
Klevay, L. M. (1983) Copper and ischemic heart disease. Biological Trace Element Research 5, 245255.CrossRefGoogle Scholar
Kornberg, A., Horecker, B. L. & Smyriot, P. Z. (1955) Glucose-6-phosphate dehydrogenase - 6-Phosphogluconic dehydrogenase. Methods in Enzymology 1, 323327.Google Scholar
Lember, M. & Tamm, A. (1988) Lactose absorption and milk-drinking habits in Estonians with myocardial infarction. British Medical Journal 296, 9596.Google Scholar
Lynch, S. M. & Strain, J. J. (1988) Effects of dietary copper deficiency on hepatic antioxidant enzymes in male and female rats. Nutrition Reports International 37, 11271134.Google Scholar
Majno, G., Jorris, I. & Zand, T. (1985) Atherosclerosis: new horizons. Human Pathology 16, 35.Google Scholar
Michaelis, O. E. IV & Szepesi, B. (1973) Effect of various sugars on hepatic glucose-6-phosphate dehydrogenase, malic enzyme and total liver lipid of the rat. Journal of Nutrition 103, 697705.Google Scholar
Morrison, E. S., Scott, R. F., Kroms, M. & Frick, J. (1972) Glucose degradation in normal and atherosclerosic aortic intima-media. Atherosclerosis 16, 175184.CrossRefGoogle Scholar
Murthy, L., Klevay, L. M. & Petering, H. G. (1974) Interrelationships of zinc and copper nutriture in the rat. Journal of Nutrition 104, 14581465.Google Scholar
Oberley, L. W. & Spitz, D. R. (1984) Assay of superoxide dismutase activity in tumor tissue. Methods in Enzymology 105, 457464.Google Scholar
Ohkawa, H., Ohishi, N. & Yagi, K. (1979) Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry 95, 351358.Google Scholar
Paglia, D. E. & Valentine, W. N. (1967) Studies on quantitative and qualitative characterization of erythrocyte glutathione peroxidase. Journal of Laboratory and Clinical Medicine 70, 158160.Google Scholar
Paynter, D. I. (1980) The role of dietary copper, manganese, selenium, and vitamine E in lipid peroxidation in tissues of the rat. Biological Trace Element Research 2, 121135.Google Scholar
Pearce, R. J. (1984) Correlation of coronary heart disease with milk consumption: is protein or some other factor involved? Medical Hypotheses 14, 259260.Google ScholarPubMed
Petering, H. G., Murthy, L., Stemmer, K. L., Finelli, V. N. & Menden, E. E. (1986) Effects of copper deficiency on the cardiovascular system of the rat. Biological Trace Element Research 9, 251270.CrossRefGoogle Scholar
Segall, J. J. (1980) Hypothesis. Is milk a dietary risk factor for ischaemic heart disease? International Journal of Epidemiology 9, 271276.Google Scholar
Slater, T. F. (1984) Overview of methods used for detecting lipid peroxidation. Methods in Enzymology 105, 283293.Google Scholar
Stange, E. & Papenberg, J. (1978) Changes in chemical and metabolic properties of rabbit aorta by dietary cholesterol and saturated and poly-unsaturated fats. Atherosclerosis 29, 467476.CrossRefGoogle Scholar
Stemmer, K. L., Petering, H. G., Murthy, L., Finelli, V. N. & Menden, E. E. (1985) Copper deficiency effects on cardiovascular system and lipid metabolism in the rat; the role of dietary proteins and excessive zinc. Annals of Nutrition and Metabolism 29, 332347.Google Scholar
Strain, J. J. (1988) Milk consumption, lactose and copper in the aetiology of ischaemic heart disease. Medical Hypotheses 25, 99101.Google Scholar
Thuesen, L., Nielsen, T. T., Thomassen, A. & Bagger, J. P. (1984) Beneficial effect of a low-fat low-calorie diet on myocardial energy metabolism in patients with angina pectoris. Lancet ii, 5962.CrossRefGoogle Scholar
Trayhurn, P. & Jennings, G. (1987) Functional atrophy of brown adipose tissue during lactation in mice. Biochemical Journal 248, 273276.Google Scholar
Wroblewski, F. & LaDue, J. S. (1955) Lactic dehydrogenase activity in blood. Proceedings of the Society for Experimental Biology and Medicine 90, 210213.CrossRefGoogle Scholar