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Are all steaks created equal?

Published online by Cambridge University Press:  08 March 2011

Hartmut H. Glossmann*
Affiliation:
Institute for Biochemical Pharmacology, Peter Mayrstrasse 1, A-6020 Innsbruck, Austria
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Abstract

Type
Letter to the Editor
Copyright
Copyright © The Author 2011

Madam

In a recent analysis of plasma concentrations of 25-hydroxyvitamin D (25(OH)D) in meat eaters, fish eaters, vegetarians and vegans(Reference Crowe, Steur and Allen1), the authors reported that the magnitude of difference of 2·4 μg/d in calculated dietary vitamin D intake between meat eaters (3·1 μg/d) and vegans (0·7 μg/d) and the overall difference in the plasma concentration of 25(OH)D of 21 nmol/l were surprising. One could even conclude that eating meat accounts for more than 25 % of the total circulating pro-hormone in this cohort, although meat eaters may also consume other good sources (fish, dairy and eggs) of vitamin D. The difference was considerably larger (by a factor of four to eight) than could be predicted by vitamin D intervention studies which relate intake of vitamin D to plasma levels of the pro-hormone. Vitamin D intake was calculated from the amount of food and the nutrient content from food composition tables. The findings are of considerable interest as meat eaters had a higher BMI than vegans and less vigorous exercise but equal summer outdoor activity, excluding cutaneous biosynthesis of vitamin D3 via UV-B as a major factor for the difference. Furthermore, the data suggested that more meat consumption is accompanied by higher 25(OH)D levels. Considering the current debate about the relationship between vitamin D status and health, the results are new, perhaps provocative and need confirmation.

One possible explanation, in addition to other factors such as calcium intake or supplements considered by the authors, is that the calculated vitamin D content from food tables(2) does not reflect the true intake, as many data are from specimens analysed decades ago. A survey of the more recent literature on vitamin D content of animal feeds is interesting in this context. The poultry and cattle industries appear to have optimized their feeds with respect to vitamin D. For example, chicken feed is recommended to contain between 35 and 70 μg vitamin D3/kg to optimize egg production and other parameters for health(Reference Atencio, Edwards and Pesti3). Although the vitamin D content of the optimized hen eggs(Reference Mattila, Lehikoinen and Kiiskinen4) is reported, I could not find any recent data on meat from these chickens. A special case is beef. Because of a long standing interest of the meat industry in the tenderness of beef(Reference Montgomery, Carr and Kerth5), vitamin D3 and more recently 25(OH)D3(Reference Foote, Horst and Huff-Lonergan6, Reference Carnagey, Huff-Lonergan and Lonergan7) have been investigated as treatments for cattle before slaughter. The hypothesis behind these supplementations is that by increasing the calcium content in muscles post mortem, myofibril proteolysis could be faster. Although one does not know for sure if as a consequence of these experiments (which suggested some but variable success with respect to tenderness) such regimens are currently implemented by the cattle industry, they offer insight into levels of vitamin D3 and 25(OH)D3 in tissues (muscle and liver) and serum of control (not supplemented) animals. The vitamin D3 content of steaks obtained from seven publications between 2000 and 2008 (not shown) varied between 0.76 and 10 ng/g fresh tissue. An almost neglected constituent of meat is 25(OH)D3(Reference Ovesen, Brot and Jakobsen8). In nine publications from the same time period (not shown) levels in steaks between 0.2 and 25 ng/g fresh tissue are reported. The latter, very high value deserves a special comment later. 25(OH)D3 has some remarkable properties: in contrast to vitamin D3 the serum increase of 25(OH)D3 is directly proportional to oral input(Reference Barger-Lux, Heaney and Dowell9) and its biological activity, calculated as a function of serum 25(OH)D3 increase, is between four(Reference Barger-Lux, Heaney and Dowell9) and nine times higher(Reference Stamp, Haddad and Twigg10) than that of vitamin D3. In food composition tables(2) the vitamin D level of meat is calculated as D3 plus five times 25(OH)D3. In addition to some debate on the exact correction factor to convert 25(OH)D3 into vitamin D, seasonal variation and different cattle-raising practices (housed or unhoused) may contribute to error in these tables.

The much higher oral bioavailability and the shorter half-life of the pro-hormone(Reference Vicchio, Yergey and O'Brien11) compared with vitamin D3 are currently being explored for rapid supplementation of vitamin D-deficient intensive-care patients(Reference Mata-Granados, Vargas-Vasserot and Ferreiro-Vera12).

In contrast to the above supplementation experiments where a tendency towards lower values (plasma, meat) for animals kept in shelters compared with pasture is apparent, little is known – and controversy exists – about how cows acquire vitamin D3.

The role of UV-B for vitamin D status in cows was recently investigated. Vitamin D-depleted dairy cows were covered with UV-protection horse blankets, udder covers or both and exposed for 28 d to natural summer (July to August) sunlight (on pasture) for 5 h daily(Reference Hymøller and Jensen13). Plasma concentrations of 25(OH)D3 reached peak levels of 40.7 ng/ml in no-cover (‘natural’) cows, whereas covered cows responded in strict correlation to the average surface area exposed. The authors concluded that cows are similar to man with respect to cutaneous biosynthesis of vitamin D3. Indeed, in Angus cows which were on pasture from the time of calving until August, the plasma concentration of the pro-hormone was 75 ng/ml and this was accompanied by the above-mentioned very high content of 25 ng 25(OH)D3/g fresh muscle tissue(Reference Carnagey, Huff-Lonergan and Lonergan7). On the other hand, animals housed in shelters had only between 0.5 to 1.68 ng/g in steaks(Reference Foote, Horst and Huff-Lonergan6, Reference Carnagey, Huff-Lonergan and Trenkle14). Given that sunlight exposure is the main determinant for the pro-hormone content of beef, one must conclude that meat from cattle on pasture and slaughtered at the end of summer has a much higher content of the metabolite than meat from cows housed in shelters or slaughtered in winter. If an average meat eater consumes the equivalent of 100 g of fresh beef daily (equivalent to 2.5 μg/g) from pasture-kept cattle (slaughtered late in summer and having the above content of 25(OH)D3), the increase in serum 25(OH)D3 steady-state levels in nmol/l can be calculated from a formula(Reference Barger-Lux, Heaney and Dowell9) to be about 10 nmol/l or even more. One cannot exclude that many of the meat eaters analysed by Crowe et al.(Reference Crowe, Steur and Allen1) consumed such ‘naturally fortified’ beef. The very high content of 25(OH)D3 in muscle from unsupplemented and unhoused cattle(Reference Carnagey, Huff-Lonergan and Lonergan7) is a good argument for biological farming, e.g. considering alpine regions where cattle are kept unhoused at high altitudes with up to 50 % more UV-B compared with sea level from the end of April to October.

References

1. Crowe, FL, Steur, M, Allen, NE et al. (2010) Plasma concentrations of 25-hydroxyvitamin D in meat eaters, fish eaters, vegetarians and vegans: results from the EPIC–Oxford study. Public Health Nutr [Epublication ahead of print version].Google ScholarPubMed
2. Food Standards Agency (2002) McCance and Widdowson's The Composition of Foods integrated dataset (CoF IDS). http://www.food.gov.uk/science/dietarysurveys/dietsurveys/ (accessed October 2010).Google Scholar
3. Atencio, A, JrEdwards, HM, Pesti, GM et al. (2006) The vitamin D3 requirement of broiler breeders. Poult Sci 85, 674692.Google Scholar
4. Mattila, P, Lehikoinen, K, Kiiskinen, T et al. (1999) Cholecalciferol and 25-hydroxycholecalciferol content of chicken egg yolk as affected by the cholecalciferol content of feed. J Agric Food Chem 47, 40894092.Google Scholar
5. Montgomery, JL, Carr, MA, Kerth, CR et al. (2002) Effect of vitamin D3 supplementation level on the postmortem tenderization of beef from steers. J Anim Sci 80, 971981.CrossRefGoogle ScholarPubMed
6. Foote, MR, Horst, RL, Huff-Lonergan, EJ et al. (2004) The use of vitamin D3 and its metabolites to improve beef tenderness. J Anim Sci 82, 242249.CrossRefGoogle ScholarPubMed
7. Carnagey, KM, Huff-Lonergan, EJ, Lonergan, SM et al. (2008) Use of 25-hydroxyvitamin D3 and dietary calcium to improve tenderness of beef from the round of beef cows. J Anim Sci 86, 16371648.CrossRefGoogle ScholarPubMed
8. Ovesen, L, Brot, C & Jakobsen, J (2003) Food contents and biological activity of 25-hydroxyvitamin D: a vitamin D metabolite to be reckoned with? Ann Nutr Metab 47, 107113.CrossRefGoogle Scholar
9. Barger-Lux, MJ, Heaney, RP, Dowell, S et al. (1998) Vitamin D and its major metabolites: serum levels after graded oral dosing in healthy men. Osteoporos Int 8, 222230.CrossRefGoogle ScholarPubMed
10. Stamp, TC, Haddad, JG & Twigg, CA (1997) Comparison of oral 25-hydroxycholecalciferol, vitamin D, and ultraviolet light as determinants of circulating 25-hydroxyvitamin D. Lancet 1, 13411343.Google Scholar
11. Vicchio, D, Yergey, A, O'Brien, K et al. (1993) Quantification and kinetics of 25-hydroxyvitamin D3 by isotope dilution liquid chromatography/thermospray mass spectrometry. Biol Mass Spectrom 22, 5358.Google Scholar
12. Mata-Granados, JM, Vargas-Vasserot, J, Ferreiro-Vera, C et al. (2010) Evaluation of vitamin D endocrine system (VDES) status and response to treatment of patients in intensive care units (ICUs) using an on-line SPE–LC–MS/MS method. J Steroid Biochem Mol Biol 121, 452455.Google Scholar
13. Hymøller, L & Jensen, SK (2010) Vitamin D(3) synthesis in the entire skin surface of dairy cows despite hair coverage. J Dairy Sci 93, 20252029.Google Scholar
14. Carnagey, KM, Huff-Lonergan, EJ, Trenkle, A et al. (2008) Use of 25-hydroxyvitamin D3 and vitamin E to improve tenderness of beef from the longissimus dorsi of heifers. J Anim Sci 86, 16491657.Google Scholar