Effects of sunlight on behavior and 25-hydroxyvitamin D levels in two species of Old World fruit bats

It has long been accepted that most vertebrate animals meet their vitamin D requirements from exposure of skin to UV-B (UV-B) radiation. Many factors affect this endogenous synthesis of vitamin D, including season, latitude, time of day, age, presence of hair, and degree of skin pigmentation. Most bats roost in dark places by day and forage at night, and thus have little or no potential for sunlight exposure. Notwithstanding, some tropical species are diurnal and are known to roost in the canopy of trees where they may be exposed to sunlight for up to 12 h each day. In this study, two species of captive tropical bats (both species are active at night but one, Rousettus aegyptiacus, roosts in caves, tombs, and buildings, whereas the other, Pteropus hypomelanus, roosts in trees) were evaluated for their ability to endogenously synthesize vitamin D. Following timed periods of sunlight exposure, blood plasma was analyzed using a competitive protein binding assay (CPBA) to determine concentrations of 25-hydroxyvitamin D [25(OH)D], the major circulating vitamin D metabolite. The ability to photoconvert provitamin D (7-dehydrocholesterol, 7-DHC) in the sub-tropical winter was determined using sunlight exposed borosilicate samples of 7-DHC in hourly increments. Finally, both species were evaluated in their preference for a roost site by the release of individuals into sunlight or shade in timed trials. Our results support the hypotheses: (1) when exposed to natural sunlight, both species exhibited an ability to endogenously synthesize vitamin D, although significant differences were found between the two, (2) photoconversion of 7-DHC to previtamin D3 is possible during the mid-day hours of a sub-tropical winter day and (3) captive, cave roosting R. aegyptiacus will choose shaded roost sites while captive P. hypomelanus will show no preference for either shade or sun.

[1]  M. Holick,et al.  Photobiology of Vitamin D , 2010 .

[2]  T. Kunz,et al.  Variation in Serum 25-Hydroxyvitamin D in Free-Ranging New-World Tropical Bats , 2009 .

[3]  H. Pols,et al.  Vitamin D , 1928, Calcified Tissue International.

[4]  M. Holick,et al.  Prevalence of Vitamin D inadequacy among postmenopausal North American women receiving osteoporosis therapy. , 2005, The Journal of clinical endocrinology and metabolism.

[5]  J. Pettifor,et al.  Vitamin D metabolism in a frugivorous nocturnal mammal, the Egyptian fruit bat (Rousettus aegyptiacus). , 2003, General and comparative endocrinology.

[6]  N. Paul,et al.  Ecological roles of solar UV radiation: towards an integrated approach , 2003 .

[7]  M. Holick Vitamin D: the underappreciated D-lightful hormone that is important for skeletal and cellular health , 2002 .

[8]  G. Kwiecinski,et al.  Observations on serum 25-hydroxyvitamin D and calcium concentrations from wild-caught and captive neotropical bats, Artibeus jamaicensis. , 2001, General and comparative endocrinology.

[9]  E. Dierenfeld,et al.  PLASMA FAT-SOLUBLE VITAMIN AND MINERAL CONCENTRATIONS IN RELATION TO DIET IN CAPTIVE PTEROPODID BATS , 2000, Journal of zoo and wildlife medicine : official publication of the American Association of Zoo Veterinarians.

[10]  Thomas H. Kunz,et al.  Pteropus hypomelanus , 2000 .

[11]  T. Kunz,et al.  Thermoregulatory behavior in the small island flying fox, Pteropus hypomelanus (Chiroptera: Pteropodidae) , 1999 .

[12]  M. Holick Chapter 5 – Vitamin D Metabolism and Biological Function , 1998 .

[13]  M. Holick,et al.  Determination of vitamins D, A, and E in sera and vitamin D in milk from captive and free-ranging polar bears (Ursus maritimus), and 7-dehydrocholesterol levels in skin from captive polar bears , 1998 .

[14]  M. Holick,et al.  The effect of season and latitude on in vitro vitamin D formation by sunlight in South Africa. , 1996, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde.

[15]  J. Mol,et al.  Dietary vitamin D dependence of cat and dog due to inadequate cutaneous synthesis of vitamin D. , 1994, General and comparative endocrinology.

[16]  M. Holick,et al.  McCollum Award Lecture, 1994: vitamin D--new horizons for the 21st century. , 1994, The American journal of clinical nutrition.

[17]  M. Holick,et al.  Photosynthesis of Previtamin D3, in Cities Around the World , 1992 .

[18]  David A. Bender,et al.  Nutritional Biochemistry of the Vitamins , 1992 .

[19]  S. Yahav,et al.  Cholecalciferol has no effect on calcium and inorganic phosphorus balance in a naturally cholecalciferol-deplete subterranean mammal, the naked mole rat (Heterocephalus glaber). , 1991, The Journal of endocrinology.

[20]  R. Buffenstein,et al.  Is vitamin D3 essential for mineral metabolism in the Damara mole-rat (Cryptomys damarensis)? , 1991, General and comparative endocrinology.

[21]  J. Speakman Why do insectivorous bats in Britain not fly in daylight more frequently , 1991 .

[22]  T. Chen,et al.  A method for the determination of the circulating concentration of 1,25-dihydroxyvitamin D. , 1990, The Journal of nutritional biochemistry.

[23]  T. Chen,et al.  Methods for the determination of the circulating concentration of 25-hydroxyvitamin D. , 1990, The Journal of nutritional biochemistry.

[24]  M. Holick,et al.  Sunlight regulates the cutaneous production of vitamin D3 by causing its photodegradation. , 1989, The Journal of clinical endocrinology and metabolism.

[25]  L. Mcdowell Vitamins in Animal Nutrition: Comparative Aspects to Human Nutrition , 1989 .

[26]  M. Holick,et al.  Influence of season and latitude on the cutaneous synthesis of vitamin D3: exposure to winter sunlight in Boston and Edmonton will not promote vitamin D3 synthesis in human skin. , 1988, The Journal of clinical endocrinology and metabolism.

[27]  R. Horst,et al.  The biological assessment of vitamin D3 metabolites produced by rumen bacteria. , 1988, Journal of steroid biochemistry.

[28]  R. L. Boland Plants as a source of vitamin D3 metabolites. , 2009, Nutrition reviews.

[29]  M. Holick,et al.  Aging Decreases the Capacity of Human Skin to Produce Vitamin D3 , 1986 .

[30]  M. Schreibman,et al.  Vertebrate endocrinology : fundamentals and biomedical implications , 1986 .

[31]  M. Holick,et al.  Aging decreases the capacity of human skin to produce vitamin D3. , 1985, The Journal of clinical investigation.

[32]  P. Maderson Skin: biochemistry and physiology of the skin. , 1984, Science.

[33]  T. Kunz Roosting Ecology of Bats , 1982 .

[34]  Thomas H. Kunz,et al.  Ecology of Bats , 1984, Springer US.

[35]  M. Holick,et al.  Regulation of cutaneous previtamin D3 photosynthesis in man: skin pigment is not an essential regulator. , 1981, Science.

[36]  H. DeLuca William C. Rose lectureship in biochemistry and nutrition. Some new concepts emanating from a study of the metabolism and function of Vitamin D. , 2009, Nutrition reviews.

[37]  R. Anderson,et al.  Photosynthesis of previtamin D3 in human skin and the physiologic consequences. , 1980, Science.

[38]  T. Oppé,et al.  Vitamin D deficiency. , 1979, British medical journal.

[39]  J. Haddad,et al.  COMPETITIVE PROTEIN-BINDING RADIOASSAY FOR 25-HYDROXYCHOLECALCIFEROL1 , 1971 .

[40]  J. Haddad,et al.  Competitive protein-binding radioassay for 25-hydroxycholecalciferol. , 1971, The Journal of clinical endocrinology and metabolism.