RESEARCH PAPER
Biochemical bone metabolism markers and morphometric, densitometric and biomechanical properties of femur and tibia in female and gonadectomised male Polish Landrace pigs
 
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1
Department of Animal Physiology, Faculty of Veterinary Medicine, University of Life Sciences, Lublin, Poland
 
2
II Department of Radiology, Medical University, Lublin, Poland
 
3
Department of Conservative Dentistry, Medical University, Lublin, Poland
 
4
Department of Animal Anatomy, Faculty of Veterinary Medicine, University of Life Sciences, Lublin, Poland
 
 
Corresponding author
Marcin R. Tatara   

Department of Animal Physiology, University of Life Sciences, Akademicka 12, 20-950 Lublin, Poland.
 
 
J Pre Clin Clin Res. 2012;6(1):14-19
 
KEYWORDS
ABSTRACT
Estrogens and androgens are critical regulators of bone metabolism and maintain bone mass throughout live in humans and animals. The aim of the presented study was to compare biochemical bone turnover markers and hormones influencing bone tissue metabolism and skeletal properties in female and orchidectomised male pigs at slaughter age. To achieve this aim, femur and tibia from 6-month-old pigs were investigated in terms of morphometric, densitometric and biomechanical properties. Serum evaluation of osteocalcin (OC), bone-specific alkaline phosphatase (BAP), growth hormone (GH), insulin-like growth factor-1 (IGF-1) and cotrisol in newborn and 90-day-old pigs was performed. This study shows a significantly higher growth rate and final body weight gain in orchidectomised males when compared to females (p<0.05). The obtained results have not shown statistically significant differences in weight, length, volumetric bone mineral density of the trabecular and cortical bone, vertical and horizontal diameters of the mid-shaft, cross-sectional area, second moment of inertia, mean relative wall thickness, cortical index, maximum elastic strength and ultimate strength of femur and tibia in females and orchidectomised males (p>0.05). Bone formation markers such as BAP and OC assessed in serum were not significantly different between both the investigated groups (p>0.05). Furthermore, serum concentrations of GH, IGF-1 and cortisol were not gender-differentiated (p>0.05). In conclusion, the differences in body weight gain were not influenced by gender-differentiated serum concentrations of GH, IGF-1 and cortisol. Lack of significant differences of morphological, densitometric and biomechanical properties of femur and tibia between the groups was related to very similar levels of OC, BAP, GH, IGF-1 and cortisol. The data obtained provide novel physiological information on bone metabolism markers and regulators, as well as properties of femur and tibia in female and gonadectomised male pigs. The results obtained in this study may therefore be useful in experimental approaches for studying the effects of physiological, nutritional, pharmacological, toxicological and environmental factors on bone metabolism and skeletal system properties in pigs.
REFERENCES (41)
1.
Ishimi Y, Yoshida M, Wakimoto S, Wu J, Chiba H, Wang X, Takeda K, Miyaura C. Genistein, a soybean isoflavone, affects bone marrow lymphopoiesis and prevents bone loss in castrated male mice. Bone. 2002; 31: 180-185.
 
2.
Matsumoto C, Inada M, Toda K, Miyaura C. Estrogen and androgen play distinct roles in bone turnover in male mice before and after reaching sexual maturity. Bone. 2006; 38: 220-226.
 
3.
Ross RW, Small EJ. Osteoporosis in men treated with androgen deprivation therapy for prostate cancer. J Urol. 2002; 167: 1952-1956.
 
4.
Vanderschueren D, Vandenput L. Androgens and osteoporosis. Andrologia 2000; 32: 125-130.
 
5.
Anderson FH, Francis RM, Peaston RT, Wastell HJ. Androgen supplementation in eugonadal men with osteoporosis: effects of six months’ treatment on markers of bone formation and resorption. J Bone Miner Res. 1997; 12: 472-478.
 
6.
Harada N, Utsumi T, Takagi Y. Tissue-specific expression of the human aromatase cytochrome P-450 gene by alternative use of multiple exons 1 and promoters, and switching of tissue-specific exons 1 in carcinogenesis. Proc Natl Acad Sci. USA 1993; 90: 11312-1136.
 
7.
Simpson ER, Maahendroo MS, Means GD, Kilgore MW, Hinshelwood MM, Graham-Lorence S, et al. Aromatase cytochrome P450, the enzyme responsible for estrogen biosynthesis. Endocr Rev. 1994; 15: 342-355.
 
8.
Terashima M, Toda K, Kawamoto T, Kuribayashi I, Ogawa Y, Maeda T, Shizuta Y. Isolation of a full-length cDNA encoding mouse aromatase P450. Arch Biochem Biophys. 1991; 285: 231-287.
 
9.
Bilezikian JP, Morishima A, Bell J, Grumbach MM. Increased bone mass as a result of estrogen therapy in a man with aromatase deficiency. N Engl J Med. 1998; 339: 599-603.
 
10.
Carani C, Qin K, Simoni M, Faustini-Fustini M, Serpente S, Boyd J, Korach KS, Simpson ER. Effect of testosterone and estradiol in a man with aromatase deficiency. N Engl J Med. 1997; 337: 91-95.
 
11.
Kowalik S, Śliwa E, Tatara MR, Krupski W, Majcher P, Studziński T. Influence of alpha-ketoglutarate on mineral density and geometrical and mechanical parameters of femora during postnatal life in piglets. Bull Vet Inst Pulawy 2005; 49: 107-111.
 
12.
Tatara MR, Brodzki A, Krupski W, Śliwa E, Silmanowicz P, Majcher P, Pierzynowski SG, Studziński T. Effects of α-ketoglutarate on bone homeostasis and plasma amino acids in turkeys. Poult Sci. 2005; 84: 1604-1609.
 
13.
Tatara MR, Silmanowicz P, Majcher P, Krupski W, Studziński T. Influence of alpha-ketoglutarate on cortical bone atrophy after denervation of the humerus in turkey. Bull Vet Inst Pulawy 2005; 49: 113-116.
 
14.
Andersen NK, Tatara MR, Krupski W, Majcher P, Harrison AP. The long-term effect of α-ketoglutarate, given early in postnatal life, on both growth and various bone parameters in pigs. J Anim Physiol Anim Nutr. 2008; 92: 519-528.
 
15.
Harrison AP, Tygesen MP, Sawa-Wojtanowicz B, Husted S, Tatara MR. α-Ketoglutarate treatment early in postnatal life improves bone density in lambs at slaughter. Bone. 2004; 35: 204-209.
 
16.
Tatara MR, Śliwa E, Krupski W. Prenatal programming of skeletal development in the offspring: effects of maternal treatment with β-hydroxy-β-methylbutyrate (HMB) on femur properties in pigs at slaughter age. Bone. 2007; 40: 1615-1622.
 
17.
Tatara MR, Tygesen MP, Sawa-Wojtanowicz B, Krupski W, Majcher P, Harrison AP. Bone development: the effect of short term alphaketoglutarate administration on long term mechanical properties of ribs in ram lambs. Small Rum Res. 2007; 67: 179-183.
 
18.
Williams J, Abumrad N, Barbul A. Effect of a specialized amino acid mixture on human collagen deposition. Ann Surg. 2002; 236: 369-375.
 
19.
Tatara MR. Neonatal programming of skeletal development in sheep is mediated by somatotrophic axis function. Exp Physiol. 2008; 93: 763-772.
 
20.
Ferretti JL, Capozza RF, Mondelo N, Montuori E, Zanchetta JR. Determination of femur structural properties by geometric and material variables as a function of body weight in rats. Evidence of sexual dimorphism. Bone.1993; 14: 265-270.
 
21.
Ferretti JL, Capozza RF, Mondelo N, Zanchetta JR. Interrelationships between densitometric, geometric and mechanical properties of rat femora: inferences concerning mechanical regulation of bone modelling. J Bone Miner Res. 1993; 8: 1389-1395.
 
22.
Tatara MR, Krupski W, Majcher P, Studziński T. Long-term denervation of the humerus in turkeys as an experimental model for osteopenia. Poult Sci. 2005; 84: 718-722.
 
23.
Fall C, Hindmarsh P, Dennison E, Kellingray S, Barker D, Cooper C. Programming of growth hormone secretion and bone mineral density in elderly men: a hypothesis. J Clin Endocrinol Metab. 1998; 83: 135-139.
 
24.
Fowden AL, Giussani DA, Forhead AJ. Endocrine and metabolic programming during intrauterine development. Early Hum Dev. 2005; 81: 723-734.
 
25.
Rizzoli R, Bonjour J-P, Ferrari SL. Osteoporosis, genetics and hormones. J Mol Endocrinol. 2001; 26: 79-94.
 
26.
Ueland T. Bone metabolism in relation to alterations in systemic growth hormone. Growth Horm IGF Res. 2004; 14: 404-417.
 
27.
Falorni A, Bini V, Cabiati G, Papi F, Arzano S, Celi F, Sanasi M. Serum levels of type I procollagen C-terminal propeptide, insulin-like growth factor-I (IGF-I), and IGF binding protein-3 in obese children and adolescents: relationship to gender, pubertal development, growth, insulin, and nutritional status. Metabolism 1997; 46: 862-871.
 
28.
Leger J, Mercat I, Alberti C, Chevenne D, Armoogum P, Tichet J, Czernichow P. The relationship between the GH/IGF-I axis and serum markers of bone turnover metabolism in healthy children. Eur J Endocrinol. 2007; 157: 685-692.
 
29.
Brabant G, von zur Muhlen A, Wuster C, Ranke MB, Kratzsch J, Kiess W, Ketelslegers JM, Wilhelmsen L, Hulthen L, Saller B, Mattsson A, Wilde J, Schemer R, Kann P; German KIMS Board. Serum insulinlike growth factor I reference values for an automated chemiluminescence immunoassay system: results from a multicenter study. Horm Res. 2003; 60: 53-60.
 
30.
Rauchenzauner M, Schmid A, Heinz-Erian P, Kapelari K, Falkensammer G, Griesmacher A, Finkenstedt G, Hogler W. Sex- and age-specific reference curves for serum markers of bone turnover in healthy children from 2 months to 18 years. J Clin Endocrinol Metab. 2007; 92: 443-449.
 
31.
Yan L, Prentice A, Zhou B, Zhang H, Wang X, Stirling DM, Laidlaw A, Han Y, Laskey A. Age- and gender-related differences in bone mineral status and biochemical markers of bone metabolism in Northern Chinese men and women. Bone. 2002; 30: 412-415.
 
32.
Buonomo FC, Klindt J. Ontogeny of growth hormone (GH), insulinlike growth factors (IGF-I and IGF-II) and IGF binding protein-2 (IGFBP-2) in genetically lean and obese swine. Domest Anim Endocrinol. 1993; 10: 257-265.
 
33.
Suzuki K, Nakagawa M, Katoh K, Kadowaki H, Shibata T, Uchida H, Obara Y, Nishida A. Genetic correlation between serum insulinlike growth factor-1 concentration and performance and meat quality traits in Duroc pigs. J Anim Sci. 2004; 82: 994-999.
 
34.
Nyberg L, Lundstrom K, Edfors-Lilja I, Rundgren M. Effects of transport stress on concentrations of cortisol, corticosteroid-binding globulin and glucocorticoid receptors in pigs with different halothane genotypes. J Anim Sci. 1988; 66: 1201-1211.
 
35.
Carroll JA, Veum TL, Matteri RL. Endocrine responses to weaning and changes in post-weaning diet in the young pig. Domest Anim Endocrinol. 1998; 15: 183-194.
 
36.
Ahamed Y. Sex-specific changes in bone structure and strength during growth: pQCT analysis of the mid-tibia. MS Thesis. British Columbia University, 2007.
 
37.
Gilsanz V. Phenotype and genotype of osteoporosis. Trends Endocrinol Metab. 1998; 9: 184-190.
 
38.
Gilsanz V, Gibbens DT, Roe TF, Carlson M, Senac MO, Boechat MI, Huang HK, Schulz EE, Libanati CR, Cann CC. Vertebral body density in children: effect of puberty. Radiology 1988; 166: 847-850.
 
39.
Gilsanz V, Roe TF, Mora S, Costin G, Goodman WG. Changes in vertebral bone density in black girls and white girls during childhood and puberty. N Engl J Med. 1991; 325: 1597-600.
 
40.
Trotter M, Dixon BB. Sequential changes in weight, density, and percentage ash weight of human skeletons from an early fetal period through old age. Anat Rec. 1974; 179: 1-18.
 
41.
Crenshaw TD, Peo ER, Lewis AJ Jr, Moser BD, Olson D. Influence of age, sex and calcium and phosphorus levels on the mechanical properties of various bones in swine. J Anim Sci. 1981; 52: 1319-1329.
 
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