2013, Number 1
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Rev Invest Clin 2013; 65 (1)
Operational mechanism modification of bone mechanostat in an animal model of nutritional stress: effect of propranolol
Pintos PM, Lezón CE, Bozzini C, Friedman SM, Boyer PM
Language: Spanish
References: 41
Page: 39-51
PDF size: 267.22 Kb.
ABSTRACT
Introduction. Propranolol (P) treatment exerts a preventive
effect against the detrimental consequences to bone status in
mildly chronically food-restricted growing rats (NGR) by an
increment in cortical bone and by improving its spatial distribution.
Objective. To study the effect of β-blocker on operational
mechanism of bone mechanostat in an animal
model of nutritional stress.
Material and methods. Weanling
male Wistar rats were randomly assigned to four
groups: control (C), C + P (CP), NGR and NGR + P (NGRP).
C and CP rats were fed freely with the standard diet. NGR
and NGRP rats received, for 4 weeks, 80% of the amount of
food consumed by C and CP respectively, the previous day,
corrected by body weight. Propranolol (7 mg/kg/day) was injected
ip 5 days per week, for four weeks in CP and NGRP
rats. C and NGR received saline injections at an identical
dosage regimen. Body weight and length were determined
during the experimental period. Dietary intake was registered
daily. Animals were sacrificed after 4 weeks of food restriction.
Immediately, cuadriceps, femur and tibiae from
each animal were dissected and weighed, and histomorphometric
and mechanical studies were performed. Serum
α-CTX, osteocalcin, intact PTH, calcium and phosphorous
were determined. Body protein (% prot) was measured in all
groups.
Results. Food restriction induced detrimental
effects on body and femoral growth, load-bearing capacity
(Wf), % prot and cuadriceps weight in NGR
vs. C (p ‹ 0.01).
β-blocker did not modify anthropometric and bone morphometric
parameters in NGRP and CP
vs. NGR and C, respectively
(p › 0.05). However, Wf NGRP
vs. NGR was
significantly higher (p ‹ 0.01). a-CTX was significantly higher
in NGR
vs. C (p ‹ 0.01). No significant differences were
observed in α-CTX levels between CP, NGRP and C (p ›
0.05). Serum osteocalcin, intact PTH, calcium and phospho-
rous showed no significant difference between groups (p ›
0.05).
Conclusion. These results suggest that modeling increase
in bone mass and strength in NGRP rats could be due
to an anticatabolic interaction of the β -blocker propranolol
on operational mechanism of bone mechanostat in an animal
model of nutritional stress.
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