INFLUENCE OF TWO OPTIONS OF DOSED ALIMENTARY DEPRIVATION ON THE INORGANIC AND ORGANIC BONE TISSUE MATRIX YA YOUNG RATS
I.G. Litovka1, S.P. Vesselsky2, S.Magomedov3, C.P. Bogomolets4, R.V. Yanko1, V.Ya. Berezovsky1
- Bogomolets Institute of Physiology National Academy of Sciences of Ukraine
- Taras Shevchenko Kyiv National University
- The Institute of Traumatology and Orthopaedics of NAMSU of Ukraine
- Bogomolets National Medical University, Kyiv, Ukraine
DOI: https://doi.org/10.15407/fz66.01.010
Abstract
The effect of 28-day 30% restriction of nutrition and periodic
fasting (after every 2 days) on inorganic and organic bone
tissue of 3-month-old Wistar male rats was studied. All results
were compared with the control group (digestive diet).
The tendency to a decrease the concentration of calcium and
magnesium in the diaphysis of the femur in rats of both experimental
groups was revealed. The content of phosphorus in the
bone tissue of rats under the 28-day 30% restriction of nutrition
probably decreased by 26.1%. Alkaline phosphatase activity
decreased by 37.3% in serum and by 31.1% in bone tissue.
During the period of daily fasting, this indicator decreased by
36.7% in serum and by 30.2% in bone tissue. The activity of
acid phosphatase in serum decreased in rats of both groups by
36.2 and 37.5%, and in bone tissue by 47.4 and 37.7%, respectively.
The concentration of glycosaminoglycans increased by
101.7% in the serum of rats under a 28-day 30% restriction of
nutrition and by 35.6% under conditions of periodic fasting.
A significant decrease in the concentration of uronic acids in
the bone tissue of rats was found under conditions of 28-day
30% restriction of nutrition. In both experimental groups the
concentration of free amino acids, lysine, cystine, alanine
and methionine, which are directly involved in the synthesis
of bone collagen, increased. Thus, under 30% restriction of nutrition and periodic starvation in early ontogeny (puberty)
lead to adverse changes in biochemical markers of metabolism
of inorganic and organic matrix and inhibit bone remodeling.
Keywords:
bone tissue; markers of bone remodeling; dietary restriction
References
- Villareal DT, Fontana L, Das SK, et.al. Effect of two-year caloric restriction on bone metabolism and bone mineral density in non-obese younger adults: a randomized clinical trial. J Bone Mineral Res. 2016;31(1):40-51.
CrossRef
PubMed PubMedCentral
- Zibellini J, Seimon RV, Lee CM, et al. Does diet-induced weight loss lead to bone loss in overweight or obese adults? A systematic review and meta-analysis of clinical trials. J Bone Mineral Res. 2015;30(12): 2168-78.
CrossRef
PubMed
- Guedes PMSG, Zamarioli A, Botega II, et.al. Undernutrition impairs the quality of growth plate and trabecular and cortical bones in growing rats1. Acta Cir b Bras. 2019;34(3):e201900301.
CrossRef
PubMed PubMedCentral
- McCay CM, Maynard LA, Sperling G, Osgood HS. Nutritional requirements during the latter half of life: one figure. J Nutrition. 1941;21(Issue 1):45-60.
CrossRef
- Reeve J. PTH: a future role in manage men to fosteoporosis? J Bone Mineralres. 1996;11(4):440-5.
CrossRef
PubMed
- Pop LC, Sukumar D, Tomaino K. Moderate weight loss in obese and overweight men preserves bone quality. Am J Clin Nutrition. 2015;101(3):659-67.
CrossRef
PubMed PubMedCentral
- Mattson MP, Longo VD, Harvie M. Impact of intermittent fasting on health and disease processes. Ageing Res Rev. 2017;39:46-58.
CrossRef
PubMed PubMedCentral
- Hisatomi Y, Kugino K. Changes in bone density and bone quality caused by single fasting for 96 hours in rats. Peer J. 2019;6: e6161.
CrossRef
PubMed PubMedCentral
- Povoroznyuk VV, Hopkalova IV, Grigorieva NV. Features of changes in bone mineral density in white Wistar rats depending on age and sex. Probl Aging and Longevity. 2011;20(4):391-401. [Russian].
- Klyatskin SA, Lifshitz RI. Determination of glycosaminoglycans by ortsin method in patients' blood. Lab Work. 1989;10:51-3. [Russian].
- Leontiev VK, Petrovich YA. Biochemical methods in clinical and experimental dentistry. Omsk. 1976. [Russian].
- Sharaev PN, Strelkov NS, Guncha VV, Sosulina LL. Determination of hyaluronidase activity in biological fluids. Clin Lab Diagnost. 1996;3:21-2. [Russian].
- Veselskiy SP, Lyaschenko PS, Kostenko SI, et.al. Way of sample preparation of bioliquids detecting in lipids determination. Pryroda. Ukrainian Patent 33564A, 2001, Feb.
- Kaznacheeva AI, Zlydnev NZ. The content of free aminoacids in healthy blood plasma, erythrocytes and urine. Lab Work.1976;8:479-80. [Russian].
- Zainabadi K, Liu CJ, Caldwell ALM, Guarente L. SIRT1 is a positive regulator of in vivo bone mass and a therapeutic target for osteoporosis. PLoS One. 2017;12(9):1-12.
CrossRef
PubMed PubMedCentral
- Sørensen KU, Kruger MC, Hansen-Møller J, Poulsen HD. Bone biochemical markers for assessment of bone responses to differentiated phosphorus supply in growingfinishing pigs. J Animal Sci. 2018;96(11):4693-703.
CrossRef
PubMed
- WadaT, NakashimaT, Hiroshi N, Penninger JM. RANKLRANK signaling in osteoclastogenesis and bone disease. Trends Mol Med. 2006;12(1):17-25.
CrossRef
PubMed
- Kenkre JS, Bassett JHD. The bone remodelling cycle. Ann Clin Biochem. 2018;55:308-27.
CrossRef
PubMed
- Henriksen K, Bollerslev J, Everts V, Karsdal MA. Osteoclast activity and subtypes as a function of physiology and pathology. Implications for future treatments of osteoporosis. Endocrin Rev. 2011;32(1):31-63.
CrossRef
PubMed
- Shlikova VO, Levanda OM. Income, nutritional conditions, and life span of the population: A comparative analysis of Ukraine and EU. Countries Demography and Soc Econ. 2018;1(32):140-52.
CrossRef
|