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Interspecies Differences in Plasma Concentrations of 25-hydroxyvitamin D3 and Dermal Vitamin D Synthesis of Kiwi (Apteryx Mantelli), Tuatara (Sphenodon Punctatus), and New Zealand Sea Lions (Phocarctos Hookeri)

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Date 2017 Jul 30
PMID 28755031
Citations 2
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Abstract

Vitamin D plays a central role in calcium homeostasis of most vertebrates, and is obtained in different species through diet, dermal synthesis, or a combination of both. The aim of this study was to determine the predominant routes of Vitamin D synthesis in three disparate species, brown kiwi (Apteryx mantelli), tuatara (Sphenodon punctatus), and New Zealand sea lions (Phocarctos hookeri). We surveyed plasma concentrations of 25-hydroxyvitamin D and D, analysed environmental conditions and life history factors, and determined the ability of skin samples to synthesise Vitamin D on exposure to ultraviolet-B radiation. There was variation in the plasma/serum 25-hydroxyvitamin D concentrations between and within the species studied, with wild kiwi having the lowest concentrations and NZ sea lions the highest. Kiwi skin produced small but measurable amounts of Vitamin D, while tuatara skin produced Vitamin D concentrations higher than that of kiwi. New Zealand sea lion skin produced the highest amount of Vitamin D and differed from the other two species in this study in that Vitamin D was present in skin before UV-B exposure. The results from this study show that all three species studied retained the ability to use both dietary and dermal sources of Vitamin D, although there was interspecies variation in the magnitude of dermal synthesis. Comparisons between these species show that there are differences in their Vitamin D pathways, but suggest that there are more factors contributing to these pathways than might be expected solely from life history characteristics.

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References
1.
Holick M, MacLAUGHLIN J, Doppelt S . Regulation of cutaneous previtamin D3 photosynthesis in man: skin pigment is not an essential regulator. Science. 1981; 211(4482):590-3. DOI: 10.1126/science.6256855. View

2.
Holick M . Vitamin D: evolutionary, physiological and health perspectives. Curr Drug Targets. 2010; 12(1):4-18. DOI: 10.2174/138945011793591635. View

3.
Thorp B . Skeletal disorders in the fowl: a review. Avian Pathol. 1994; 23(2):203-36. DOI: 10.1080/03079459408418991. View

4.
Olds J, Burrough E, Madison D, Ensley S, Horst R, Janke B . Clinical investigation into feed-related hypervitaminosis D in a captive flock of budgerigars (Melopsittacus undulatus): morbidity, mortalities, and pathologic lesions. J Zoo Wildl Med. 2015; 46(1):9-17. DOI: 10.1638/2013-0062R2.1. View

5.
How K, Hazewinkel H, Mol J . Dietary vitamin D dependence of cat and dog due to inadequate cutaneous synthesis of vitamin D. Gen Comp Endocrinol. 1994; 96(1):12-8. DOI: 10.1006/gcen.1994.1154. View