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3+ 4/2002 - Společnost pro pojivové tkáně

3+ 4/2002 - Společnost pro pojivové tkáně

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unit of LM than controls in <strong>pro</strong>portion with<br />

the reduction observed in LM, reaching<br />

very low BMC or FA-BMC values in the<br />

extreme cases.<br />

Results suggest that l. dialysed men and<br />

pre-MP women show a normal control of<br />

bone mass by muscle mass; 2. however, the<br />

metabolic interference from CAPD/HD<br />

reduces the BMC/LM <strong>pro</strong>portionality regardless<br />

of the patient's fat mass, and 3. this situation<br />

is further affected by menopause, after<br />

which the BMC control seems to be<br />

impaired in <strong>pro</strong>portion with the reduction<br />

in mechanical usage (muscle mass reduction).<br />

This would confirm that dialysisinduced<br />

systemic factors affected the bone<br />

mechanostat setpoint over the natural<br />

endocrine influences in these patients.<br />

BIOCHEMICAL PROCESSES IN THE<br />

CORTICAL BONE DURING THE<br />

STRESS/STRAIN CHANGES<br />

M. Petrtýl, and J. Danešová<br />

Laboratory of Biomechanics and Biomaterial Engineering,<br />

Department of Structural Mechanics, Faculty of<br />

Civ. Eng., Czech Technical University,Thákurova 7,<br />

Prague 6, 160 00, Czech Republic<br />

E-mail: petrtyl@fsv.cvut.cz<br />

Aim of the study: The bone tissue<br />

remodelling is controlled in a dominant<br />

way by biomechanical remodelling initiators<br />

(i.e. by spherical strain tensors) and by<br />

biomechanical speed regulators of metabolic<br />

remodelling <strong>pro</strong>cesses (i.e. by deviators<br />

of the stress/strain tensors).<br />

The bone tissue remodelling is relatively<br />

avery slow <strong>pro</strong>cess. In physiologically<br />

„normal“ conditions, it tends towards the<br />

state of remodelling equilibrium in which<br />

the coincidence of the first dominant principal<br />

stress/strain direction, and the direction<br />

of the first principaI axis of anisotropy,<br />

104<br />

LOCOMOTOR SYSTEM vol. 9, <strong>2002</strong>, No. <strong>3+</strong>4<br />

and the principal directions of the structure<br />

(longitudinal axes of osteons) is<br />

reached at the point of macrostructure.The<br />

presented theory is concerned to the exact<br />

formulations of the mechanical (i.e.<br />

stress/strain fields) effects on the biochemical<br />

metabolic <strong>pro</strong>cesses.<br />

Materials and methods: On the basis<br />

of the up-to-now recognized and available<br />

knowledge of biochemical <strong>pro</strong>cesses related<br />

to the creation of a new bone, the kinetics<br />

of chemical substances (molecular mixtures)<br />

can be expressed by five global<br />

stoichiometric equations of bone remodelling.<br />

In regard to the stoichiometric equations,<br />

it is necessary to point out that they<br />

express global metabolic <strong>pro</strong>cesses which<br />

.are initiated by mechanical loading effects<br />

in the cases of dominant biomechanical<br />

activities.The biochemical reactions related<br />

to the cortical bone remodeling and<br />

expressed by stoichiometric equations <strong>pro</strong>ceed<br />

at certain speeds that depend on the<br />

speed constants and on the concentrations<br />

of individual substrates Di.<br />

Results: The fundamental kinetic equations<br />

of bone remodelling present the relations<br />

between the time change and the concentrations<br />

of molar substances. The speed<br />

remodelling constants with speed remodelling<br />

functions depend on the mechanical<br />

stress, resp. on the spheric stress tenzor.<br />

Conclusions: the biochemical reactions<br />

are initiated by the deviator of the<br />

stress/strain tensor. Shear stresses (the components<br />

of stress tensor deviator) deform<br />

the microelements of bone tissue and the<br />

flow of extracelular liquid mechanochemically<br />

(with the direct activity of integrins a,<br />

b) starting the <strong>pro</strong>duction of <strong>pro</strong>staglandin<br />

E which initiates bone compartment<br />

resorption (Klein-Nulend, E. H. Burger).

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