Friday, May 26, 2017

Dietary Sources and Availability of Zinc

Reference from the joint report of FAO/WHO expert consultation on Human Vitamins and Minerals verbatim.

19. Sian, L., Mingyan, X., Miller, L.V., Tong, L., Krebs, N.F. & Hambidge, K.M. 1996. Zinc absorption and intestinal losses of endogenous zinc in young Chinese women with marginal zinc intakes. Am. J. Clin. Nutr., 63: 348-53.

23. Knudsen, E., Jensen, M., Solgaard, P., Sørensen, S.S. & Sandström, B. 1995. Zinc absorption estimated by fecal monitoring of zinc stable isotopes validated by comparison with whole-body retention of zinc radioisotopes in Humans. J. Nutr., 125: 1274-1282.

25. Hunt, J.R., Gallagher, S.K., Johnson, L.K. & Lykken, G.I. 1995. High- versus low-meat diets: effects on zinc absorption, iron status, and calcium, copper, iron, magnesium, manganese, nitrogen, phosphorus, and zinc balance in postmenopausal women. Am. J. Clin. Nutr., 62: 621-32.

32. AO/IAEA/WHO. 1996. Trace elements in Human nutrition and health. Geneva, World
Health Organization.



20. Sandström, B. 1989. Dietary pattern and zinc supply. In: Zinc in Human biology. Mills C.F. ed. p. 350-363. Devon , U.K., Springer-Verlag.

Lean red meat, whole-grain cereals, pulses, and legumes provide the highest concentrations of zinc 25-50 mg/kg (380-760 μmol/kg) raw weight. Processed cereals with low extraction ratespolished rice, and lean meat or meat with high fat content have a moderate zinc content 10-25 mg/kg (150-380 μmol/kg). Fish, roots and tubers, green leafy vegetables, and fruits are only modest sources of zinc <10 mg/kg (<150 μmol/kg) (20).
21. Sandström, B. & Lönnerdal, B. 1989. Promoters and antagonists of zinc absorption. In: Zinc in Human biology. Mills C.F. ed. p.57-78. Devon , U.K., Springer-Verlag. 
Separated fats and oils, sugar, and alcohol have a very low zinc content. The utilisation of zinc depends on the overall composition of the diet. Experimental studies have identified a number of dietary factors as potential promoters or antagonists of zinc absorption (21).
Soluble low-molecular-weight organic substances, such as amino and hydroxy acids, facilitate zinc absorption. In contrast, organic compounds forming stable and poorly soluble complexes with zinc can impair absorption. In addition, competitive interactions between zinc and other ions with similar physicochemical properties can affect the uptake and intestinal absorption of zinc.
The risk for competitive interactions seems mainly to be related to high doses in the form of supplements or in aqueous solutions. However, at levels present in food and at realistic fortification levels, zinc absorption appears not to be affected, for example, by iron and copper (21).
Isotope studies with human subjects have identified two factors which together with the total zinc content of the diet are major determinants of absorption and utilisation of dietary zinc. The first is the content of inositol hexaphosphate (phytate) and the second is the level and source of dietary protein. Phytates are present in whole-grain cereals and legumes and in smaller amounts in other vegetables. They have a strong potential for binding divalent cations and their depressive effect on zinc absorption has been demonstrated in humans (21).
20. Sandström, B. 1989. Dietary pattern and zinc supply. In: Zinc in Human biology. Mills C.F. ed. p. 350-363. Devon , U.K., Springer-Verlag.
The molar ratio between phytates and zinc in meals or diets is a useful indicator of the effect of phytates in depressing zinc absorption. At molar ratios above the range of 6–10, zinc absorption starts to decline; at ratios above 15 absorption is typically less than 15 percent (20).
22. Petterson, D., Sandström, B. & Cederblad, Å. 1994. Absorption of zinc from lupin (Lupinus angustifolius) - based foods. Br. J. Nutr., 72: 865-71.
The effect of phytate is, however, modified by the source and amount of dietary proteins consumed. Animal proteins improve zinc absorption from a phytate-containing diet. Zinc absorption from some legume-based diets is comparable with that from animal-protein-based diets despite a higher phytate content in the former. High dietary calcium potentiated the antagonistic effects of phytates on zinc absorption in experimental studies. The results from human studies are less consistent and any effects seem to depend on the source of calcium and the composition of the diet (22).
Some examples of recently published absorption studies illustrate the effect of zinccontent and diet composition on fractional zinc absorption (Table 53) (19, 23- 25).
24. Hunt, J.R., Matthys, L.A. & Johnson, L.K. 1998. Zinc absorption, mineral balance, and blood lipids in women consuming controlled lactoovovegetarian and omnivorous diets for 8 wk. Am. J. Clin. Nutr., 67: 421-30.

25. Hunt, J.R., Gallagher, S.K., Johnson, L.K. & Lykken, G.I. 1995. High- versus low-meat diets: effects on zinc absorption, iron status, and calcium, copper, iron, magnesium, manganese, nitrogen, phosphorus, and zinc balance in postmenopausal women. Am. J. Clin. Nutr., 62: 621-32.

20. Sandström, B. 1989. Dietary pattern and zinc supply. In: Zinc in Human biology. Mills C.F. ed. p. 350-363. Devon , U.K., Springer-Verlag.
The results from the total diet studies, where all main meals of a day’s intake have been extrinsically labelled, show a remarkable consistency in fractional absorption despite relatively large variations in meal composition and zinc content. Thus, approximately twice as much zinc was absorbed from a non-vegetarian or high-meat diet (24, 25) than from a diet in rural China based on rice and wheat flour (20).
26. Nävert, B., Sandström, B. & Cederblad, Å. 1985. Reduction of the phytate content of bran by leavening in bread and its effect on absorption of zinc in man. Br. J. Nutr., 53: 47 53.

27. Sandström, B. & Sandberg, A.S. 1992. Inhibitory effects of isolated inositol phosphates on zinc absorption in Humans. J Trace Elem Electrolyte Health Dis., 6: 99-103.
Data are lacking on zinc absorption from typical diets of developing countries, which usually have a high phytate content. The availability of zinc from the diet can be improved by reductions in the phytate content and inclusion of animal protein sources. Lower extraction rates of cereal grains will result in lower phytate content but at the same time the zinc content is reduced, so that the net effect on zinc supply is limited. The phytate content can be reduced by activating the phytase present in most phytate-containing foods or through the addition of microbial or fungal phytases. Phytases hydrolyse the phytate to lower inositol phosphates, resulting in an improved zinc absorption (26, 27).
28. Gibson, R.S., Yeudall, F., Drost, N., Mtitimuni, B. & Cullinan, T. 1998. Dietary interventions to prevent zinc deficiency. Am. J. Clin. Nutr., 68(suppl.): 484S-487S.
The activity of phytases in tropical cereals such as maize and sorghum is lower than that in wheat and rye (28). Germination of cereals and legumes increases phytase activity and addition of some germinated flour to ungerminated maize or sorghum followed by soaking at ambient temperature for 12–24 hours can reduce the phytate content substantially (28). 
Additional reduction can be achieved by the fermentation of porridge for weaning foods or doughs for bread making. Commercially available phytase preparations could also be used but may not be economically accessible in many populations.

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