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2006 | 15 | 2 |

Tytuł artykułu

Contents of calcium, magnesium, and phosphorus in antlers and cranial bones of the European red deer [Cervus elaphus] from different regions in Western Poland

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Annual shedding of antlers by males is a characteristic feature of most deer species. Regrowth is very fast, reaching 2 cm/day for some species and making them an interesting model for studying tissue regeneration processes. The aim of this study was to compare the contents of calcium, magnesium, and phosphorus in antlers and cranial bones of European red deer from Western Pomerania, Poland. We obtained 30 antlers from three forestry districts that differed in the extent of environmental pollution with fluorine compounds, SO₂, NOx, CO, and CO₂ (Trzebież, Rokita and Gryfino). Deer were assigned to two age groups: from 2 to 4 years, and from 6 to 8 years. Powdered samples of cranial bones and antler base obtained with a dental drill were dissolved in nitric acid. Calcium and magnesium contents were measured by atomic absorption spectroscopy, while phosphorus was determined colorimetrically. The content of calcium was higher in antlers - (mean 133.96 mg/g) hardly surprising given the higher calcified cartilage and immature bone content in antler as opposed to cranial bone (mean 123.79 mg/g). Phosphorus content was slightly higher in bones than in antlers (84.62 mg/g and 83.58 mg/g, respectively), which suggests that Ca:P ratios are different in the mineral phase or that there is more P in bone compared to the antler matrix. No difference in magnesium content was noted (5.23 to 5.46 mg/g). Statistical analysis revealed significant differences depending on age of the animal and level of industrial pollution in the animal's habitat.

Wydawca

-

Rocznik

Tom

15

Numer

2

Opis fizyczny

p.297-301,fig.,ref.

Twórcy

autor
  • Pomeranian Medical University, Powstancow Wlkp.72, 70-111 Szczecin, Poland
autor
autor
autor
autor

Bibliografia

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  • 2. JACZEWSKI Z. Deer antler (In Polish); PWRiL: Warszawa, 1981.
  • 3. VAN DER EEMS K., BRON R., GUNDBERG C. Circulating levels of 1,25 dihydroxyvitamin D, alkaline phosphatase, hydroxyproline and osteocalcin associated with antler growth in white-tailed deer. Acta Endocrinologica (Copenh) 118, 407, 1988.
  • 4. BANKS W.J. JR., EPLING G.P., KAINER R.A., DAVIS R.W. Antler growth and osteoporosis. II. Gravimetric and chemical changes in the costal compacta during the antler growth cycle. Anat Rec. Dec; 162(4), 399, 1968.
  • 5. BANKS W.J. JR., EPLING G.P., KAINER R.A., DAVIS R.W. Antler growth and osteoporosis. I. Morphological and morphometric changes in the costal compacta during the antler growth cycle. Anat Rec. Dec; 162(4), 387, 1968.
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  • 8. KIERDORF U., STOFFELS E., STOFFELS D., KIERDORF H., SZUWART T., CLEMEN G. Histological studies of bone formation during pedicle restoration and early antler regeneration in roe deer and fallow deer. Anat. Rec. 273A (2), 741, 2003.
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  • 13. SAMUJŁO D., MACHOY-MOKRZYŃSKA A., DĄBROWSKA E., NOWICKA W., PATERKOWSKI W. Fluoride accumulation in European deer antlers. Environ. Sci. 2(4), 189, 1994.
  • 14. PAWLUS G., GUTOWSKA I., MACHOY Z., MACHALIŃSKI B. Quantitative relationships between magnesium and calcium in human tooth buds and teeth. (In Polish) J. Elementol. 8(2), 75, 2003.
  • 15. DOŁĘGOWSKA B., MACHOY Z., CHLUBEK D. Dynamics of changes in the calcium, magnesium, and phosphate content in the chicken femoral bones. (In Polish) Biul. Magnezol. 6(2), 125, 2001.
  • 16. KIERDORF U., KIERDORF H., SCHULTZ M., ROLF H.J. Histological structure of antlers in castrated male fallow deer (Dama dama). Anat. Rec. 281A(2), 1352, 2004.
  • 17. GOSS R., VAN PRAAGH A., BREWER P. The mechanism of antler casting in the follow deer. J. Exp. Zool. 264(4), 429, 1992.
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  • 19. DĄBKOWSKA E. An attempt to evaluate the risk of forest animals expose to industrial emissions on the basis of changes in mineral composition of the masticatory organ in deer from Western Pomerania regions. (In Polish) Ann. Acad. Med. Stetin. 34, 37, 1988.
  • 20. SCHULTZ S.R., JOHNSON M.K., FEAGLEY S.E., SOUTHERN L.L., WARD T.L. Mineral content of Louisiana white-tailed deer. J. Wild. Disease 30(1), 77, 1994.
  • 21. FAUCHEUX C., NESBITT S., HORTON M., PRICE J. Cells in regenerating deer antler cartilage provide a microenvironment that supports osteoblast differentiation. J. Exp. Biol. pp. 443-455, 2004.
  • 22. BAXTER B.J., ANDREWS R.N., BARRELL G.K. Bone turnover associated with antler growth in red deer (Cervus elaphus). Anat. Rec. 256(1), 14, 1999.
  • 23. BROCKSTEDT RASMUSSEN H., SORENSEN P.L., EWALD H., MELSEN F. The rhythmic relation between antler and bone porosity in Danish deer. Bone. 8(1), 19, 1987.
  • 24. BUBENIK GA, SEMPERE AJ, HAMR J. Developing antler, a model for endocrine regulation of bone growth. Concentration gradient of T3, T4 and alkaline phosphatase in the antler, jugular, and the saphenous veins. Calcif. Tissue. Int. 41(1), 38, 1987.
  • 25. SZUWART T., KIERDORF H., KIERDORF U., ALTHOFF J., CLEMEN G. Tissue differentiation and correlated changes in enzymatic activities during primary antler development in fallow deer (Dama dama). Anat Rec. 243(4), 413, 1995.
  • 26. PIOTROWSKA S. Schedding and rebuilding of antlers is an interesting biological phenomenon. (In polish) Wszechświat 106(4-6), 144, 2005.

Typ dokumentu

Bibliografia

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