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Journal of Nutrition Vol. 116 No. 6 June 1986, pp. 1054-1060
Copyright © 1986 by American Society for Nutrition
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Effect of Dietary Zinc on Endogenous Free Radical Production in Rat Lung Microsomes1

Tammy M. Bray2, Stan Kubow3 and William J. Bettger

Department of Nutrition, College of Biological Science, University of Guelph, Guelph, Ontario, Canada NIG 2W1

The objective of this study was to investigate the effect of dietary zinc on endogenous production of free radicals in lung and liver microsomes. Male weanling rats were fed a zinc-deficient basal diet containing <1.1 ppm zinc, or were pair-fed or fed ad libitum a zinc-adequate diet supplemented with 100 ppm zinc. The isolated microsomes (100,000 x g precipitate) of lung and liver were incubated with 0.1 M PBN (spin trap) and 0.3 mM NADPH (cofactor) at 37°C for 1.0 h. A carboncentered free radical (aN = 16.0 G, aFormula = 3.4 G) was trapped in both lung and liver microsomes. There was a significant increase in the concentration of carbon-centered free radicals generated in lung microsomes in animals fed a zinc-deficient diet. Dietary zinc status did not significantly affect the concentration of free radicals in liver microsomes. The amount of free radicals generated is proportional to microsomal protein concentration and is linear with protein concentration between 5 and 20 mg per milliliter of incubate. The free radicals formed in the microsomal system were dependent on the presence of NADPH. Carbon monoxide inhibited 40–50% of the free radical production in both lung and liver microsomes. The results suggest that dietary zinc deficiency stimulates the production of endogenous free radicals in rat lung microsomes by an NADPH- and cytochrome P-450-dependent system.


KEY WORDS: • zinc • free radicals • rat lung • cytochrome P-450

1 Presented in part at the XIII International Congress of Nutrition, Brighton, United Kingdom, August 18–23, 1985. This work is supported by National Heart, Lung and Blood Institute grant HL 33491-01 and OMAF, Canada.

2 Author to whom requests for reprints should be addressed.

3 Present address: Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario, Canada N1G 2W1.

Manuscript received 10 October 1985. Revision accepted 10 February 1986.




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Increased Glutathione Synthesis through an ARE-Nrf2-Dependent Pathway by Zinc in the RPE: Implication for Protection against Oxidative Stress.
Invest. Ophthalmol. Vis. Sci., June 1, 2006; 47(6): 2709 - 2715.
[Abstract] [Full Text] [PDF]




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