Improved bone status by the beta-blocker propranolol in an animal model of nutritional growth retardation.

The aim of the present research was to study if the beta-blocker propranolol, which is known to increase bone mass, could reverse the adverse skeletal effects of mild chronic food restriction in weanling rats. Male Wistar rats were divided into four groups: control, control+propranolol (CP), nutritional growth retardation (NGR) and nutritional growth retardation+propranolol (NGRP). Control 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 the control and CP rats, respectively. Results were expressed as mean values and sem. Food restriction induced detrimental effects on body and femur weight and length (P < 0.05) and bone structural and geometrical properties (P < 0.001), confirming results previously shown in our laboratory. However, the beta-blocker overcame the deleterious effect of nutritional stress on load-bearing capacity, yielding load, bone stiffness, cross-sectional cortical bone area and second moment of inertia of the cross-section in relation to the horizontal axis without affecting anthropometric, histomorphometric and bone morphometric parameters. The results suggest that propranolol administration to mildly chronically undernourished rats markedly attenuates the impaired bone status in this animal model of growth retardation.

Mandibular bone stiffening and increased bone calcium mass in rats permanently stunted by hypophysectomy.

OBJECTIVE: This investigation was designed to obtain information on the changes induced by hypophysectomy on biometric parameters, bone calcium mass, and material and architectural properties during ontogenesis of the rat mandible. DESIGN: Female Sprague-Dawley rats were hypophysectomised (HX) at 30 days of age. A "basal control group" (BC) was sacrificed on the same day surgery was performed. An "age-matched intact control group" (CON) was also included. HX and CON rats were sacrificed when aged 6 months. Body weight was monitored weekly. Mandibular growth was estimated directly on the right hemimandible by taking measurements between stable anatomical points. Its mechanical properties were determined using a three-point bending mechanical test. Load was applied transversely to the bone axis at a point immediately posterior to the posterior surface of the third molar. The left hemimandibles were ashed in a muffle furnace at 600 degrees C for 18h and the ash weight obtained. Calcium content in the ashes was determined by atomic absorption spectrophotometry. It was taken as the mandibular calcium mass. Histomorphometric studies were performed on decalcified hemimandibles: total interradicular bone, bone volume, and height of the periodontal ligament were measured. CONCLUSIONS: Morphometric studies indicated that hypophysectomy in juvenile rats induced mandibular growth cessation, which was limited to the posterior part of the bone. Thus, the mandible maintained its juvenile proportions and showed an important deformation relative to age. In spite of the reduced bone size, both the mandibular weight and the calcium bone mass increased more than two times in ontogenia. Histomorphometric studies revealed that the interradicular bone volume was markedly increased. These findings strongly suggest that the bone that forms the mandible of the hypophysectomised rat under the conditions of the present study showed a higher than normal density. As evidenced from biomechanical studies, these bone properties, plus the significant stiffening of bone material tissue, were presumably responsible for the unnecessary and marked increment in the "load capacity" suffered by the mandible of the hypophysectomised rat during ontogenesis.

Evidence from catch-up growth and hoarding behavior of rats that exposure to hypobaric air lowers the body-mass set point.

The depression of body growth rate and the reduction of body mass for chronological age and gender in growing experimental animals exposed to hypobaric air (simulated high altitude = SHA) have been associated with hypophagia because of reduced appetite. Catch-up growth during protein recovery after a short period of protein restriction only occurs if food intake becomes super-normal, which should not be possible under hypoxic conditions if the set-point for appetite is adjusted by the level of SHA. The present investigation was designed to test the hypothesis that growth retardation during exposure to SHA is due to an alteration of the neural mechanism for setting body mass size rather than a primary alteration of the central set-point for appetite. One group of female rats aged 35 d were exposed to SHA (5460m) in a SHA chamber for 27 d (HX rats). Other group was maintained under local barometric pressure conditions (NX rats). One half of both NX and HX rats were fed a protein-free diet for the initial 9 d of the experimental period. From this time on, they were fed a diet containing 20% protein, as were the remaining rats of both groups during the entire experimental period. The growth rates of both mass and length of the body were significantly depressed in well-nourished rats exposed to SHA during the entire observation period when compared to normoxic ones. At its end, body mass and body length were 24% and 21% less in HX than in NX rats. Growth rates were negatively affected by protein restriction in both NX and HX rats. During protein recovery, they reached supernormal values in response to supernormal levels of energy intake that allowed a complete catch-up of both body mass and length. The finding that energy intake during the period of protein rehabilitation in HX rats previously stunted by protein restriction was markedly higher than in HX control ones at equal levels of hypoxia demonstrates that the degree of hypoxia does not determine directly the degree of appetite and energy intake. Furthermore, the finding that catch-up growth in the stunted HX rats returns the animal only to the stunted size appropriate for the hypoxic animal supports the hypothesis that hypoxia lowers the set-point for body mass size, which is reached by inhibition of appetite. Confirmation of the hypothesis was done by assessment of the set-point of body mass by the behavioral method of the weight threshold to hoard food. It was lowered by 17.0% in HX rats.

Effect of protein-energy malnutrition in early life on the dimensions and bone quality of the adult rat mandible.

Morphological and biomechanical features of the mandible are negatively affected by protein-energy malnutrition, whose effects are apparently dependent on the time of life of application. The aim here was to investigate, in neonatal rats nursed by dams put on a protein-free diet to depress milk production and thus create a state of protein-energy malnutrition in the offspring, subsequent growth and long-term effects by analyzing mandibular dimensions and bone quality in adulthood. Pregnant Wistar rats were fed a 20% protein diet (control) or a protein-free diet (malnourished) to obtain normal or subnormal milk production, respectively. After weaning, the offspring (males) were fed a 20% protein diet for 70 days. The dimensions of their excised mandibles were measured directly between anatomical points; the geometry and material quality of mandibular bone were assessed by peripheral quantitative computed tomography. Pups suckling from malnourished dams weighed 49.4% of those suckling from control dams at weaning; the actual difference between control and malnourished pups was 25.1g, which persisted until day 91 of age, indicating the absence of catch-up growth. As with body size, the mandibular base length, height and area (an index of mandibular size) were significantly smaller in malnourished than control rats at the end of the study. The mandibular cortical area, volumetric cortical bone mineral content and volumetric cortical bone mineral density assessed by peripheral quantitative computed tomography were similar in both groups of rats at the end of the observation period, but there was a significant reduction in the cortical axial moment of inertia in malnourished rats at this time of postnatal life. These findings suggest that catch-up growth was incomplete in rats malnourished during the suckling period and that the adaptation of mandibular bone architecture to body growth was apparently insufficient to attain normal values, thus not allowing complete compensation in mechanical competence at the end of the study because of an inadequate spatial distribution of resistive material through its cross-section rather than qualitative or quantitative impairment of cortical bone.

The development of bone mass and bone strength in the mandible of the female rat.

The present study provides baseline data for a number of mandibular growth dimensions, specially on bone mass and bone strength, that were collected between the 21st and the 180th days of postnatal life, which are intended as a reference for researchers designing experimental studies, specially on mandibular catch-up growth, and as an aid for clinicians who must evaluate results from published animal studies for validity and potential extrapolation to the human clinical situation. Fifty weanling female Wistar (Hsd:Wi) rats were fed ad libitum a diet previously shown to allow normal, undeformed mandibular growth. Five of them were randomly selected at different times between 21 and 180 d of life. Mandibular growth was estimated directly on the right hemimandible by taking measurements between anatomical points; mandibular bone mass (calcium mass) was estimated from the mg of calcium, determined by atomic absorption spectrophotometry, present in the ashes of the left hemimandible; and mechanical properties of the right hemimandible were determined using three-point bending mechanical test. Dimensions, bone calcium mass and bone strength of the female rat mandible increased linearly from day 21 to approximately day 90. Bone growth, as expected, was more than twice when assessed from bone weight than when derived from mandibular area, length or height when the parameters were expressed as the relative increase from the mean infant condition. The growth rate of the posterior part of the mandible (behind the third molar) was almost five times greater than that of the anterior part. The rates of growth of the studied parameters showed a marked decline after day 90. ANOVA indicated that no statistical differences were found between day 90 and day 120 values. It could be concluded that the female rat mandible attains its adult size, peak bone calcium mass and bone structural mechanical properties at some point between 90 and 120 d of postnatal life. Because of the extremely high positive correlation between mandibular bone calcium mass and both mandibular area and mandibular weight, it was possible to calculate the mandibular peak bone mass from the relations 7.69 mgCa/cm2 and 0.19 mgCa/mg bone.

Permanent reduction of mandibular size and bone stiffness induced in post-weaning rats by cyclophosphamide.

It has been previously reported that several doses of cyclophosphamide (CPA) reduce body weight gain, diaphyseal torsional strength and longitudinal femoral growth in the growing rat. The present study was thus designed to estimate both the initial and the possible long-term effects of CPA treatment, by analyzing mandibular dimensions and biomechanical performance of the bone in adulthood in rats treated with the drug around weaning. Female Sprague-Dawley rats (N=20), 26 d of age, received 100mg/kg of CPA by the intraperitoneal route during days 0, 7 and 21 of the experimental period. Controls (C) received saline. Groups of rats were sacrificed at day 28 to estimate initial changes induced by the drug and on day 126 in order to determine long-term effects. The dimensions of the excised mandibles were measured directly between anatomical points; the geometry and material biomechanical quality of mandibular bone were assessed using a three-point bending mechanical test in an Instron Universal Testing Machine model 4442. CPA reduced body weight, body length and mandibular size (posterior part of the bone) significantly, when the parameters were measured at day 28. They did not recover with time, which means that catch-up growth did not occur and that the overall growth of the body was permanently affected by the drug. CPA treatment was also associated with a marked depression of the natural increase in the mandibular bone mass (cross-sectional area). The bending cross-sectional moment of inertia of the fracture sections (xCSMI) was also negatively affected by treatment. Significant decreases of both ultimate load and stiffness were also observed. The above structural parameters did not recover enough with time to attain control values at the end of the study. The intrinsic stiffness (E) of the mandibular bone was not affected by treatment. These findings suggest that CPA treatment during early postnatal life causes permanent changes in mandibular morphology and affects the adaptation of mandibular bone architecture to body growth, thus not allowing complete compensation at the end of the study because of an inadequate distribution of the resistive material through its cross-section rather than a qualitative impairment of cortical bone.

Long-term exposure to hypobaric hypoxia in rat affects femur cross-sectional geometry and bone tissue material properties.

Hypoxia leads to an increase in erythropoiesis, which induces hypertrophy of the erythropoietic marrow and may induce bone resorption. This study investigates the effect of chronic hypobaric hypoxia (simulated high altitude, SHA) on the biomechanics of rat femurs by mechanical tests of diaphyseal stiffness and strength and calculation of some indicators of bone material properties. Adult female rats were exposed to SHA (5500 m, 23.5h/d for 60 d =HX rats; NX=normoxic). This treatment induced reticulocytosis and polycythemia. Bone mineral content did not differ between NX and HX rats at the end of the study. To determine cortical bone mechanical properties, the right femur was assessed using a 3-point bending test. Endosteum and periosteum moved away from the central axis in HX rats as deduced by an increase in the cross-sectional moment of inertia. The two indicators of bone material properties, the elastic modulus and stress at the yielding point, were significantly reduced. However, the strength of the femur as an intact organ ("load capacity" parameters) was not compromised by exposure to SHA. It is thus proposed that the negative effect of SHA on bone material quality was completely offset by an improvement in diaphyseal cross-sectional design, thus allowing a normal biomechanical response to bending of the femur as a whole.

Biomechanical performance of diaphyseal shafts and bone tissue of femurs from hypothyroid rats.

The bone changes in hypothyroidism are characterized by a low bone turnover with a reduced osteoid apposition and bone mineralization rate, and a decreased osteoclastic resorption in cortical bone. These changes could affect the mechanical performance of bone. The evaluation of such changes was the object of the present investigation. Hypothyroidism was induced in female rats aged 21 days through administration of propylthiouracil in the drinking water for 70 days (HT group). Controls were untreated rats (C group). Right femur mechanical properties were tested in 3-point bending. Structural (load bearing capacity and stiffness), geometric (cross-sectional area and moment of inertia) and material (modulus of elasticity) properties were evaluated. The left femur was ashed for calcium content determination. Plasma T(4) concentration was significantly decreased in HT rats. Body and femur weight and length in HT rats were also reduced. Femoral calcium concentration in ash was higher in HT than in C rats. However, the femoral calcium mass was significantly lower in HT than in C rats because of the reduced femoral size seen in the former. The stiffness of bone material was higher in HT than in C rats, while the bone geometric properties were significantly lower. The "load capacity" was between 30 and 50% reduced in the HT group, although, the differences disappeared when the values were normalized per 100-g body weight. The lowered biomechanical ability observed in the femoral shafts of HT rats seems to be the expression of a diminished rate of growth. Qualitative alterations in the intrinsic mechanical properties of bone tissue were observed in HT rats, probably because the mineral content and the modulus of elasticity were positively affected. The cortical bone of the HT rat thus appears as a bone with a higher than normal strength and stiffness relative to body weight, probably due to improvement of bone material quality due to an increased matrix calcification.

Bone status in an animal model of chronic sub-optimal nutrition: a morphometric, densitometric and mechanical study.

In children, inappropriate eating habits can induce a disease known as nutritional dwarfing (ND). Due to the link between nutritional condition and bone growth, the effects induced by a 20 % reduction of food intake on bone competence were assessed in an animal model of ND. Bone status during catch-up growth was also analysed. Male Wistar rats were divided into control (C) and ND groups. C rats were fed ad libitum. ND received 80 % of the diet consumed by C for 4 weeks (T4); thereafter, they were fed ad libitum for 8 weeks. Results, expressed as mean (SEM) for ND v. C, were as follows. At T4, body weight (g) and length (cm) and femur weight (g) and length (mm) were 97.35 (SEM 5.89) v. 199.07 (SEM 9.24), 16.91 (SEM 0.41) v. 20.26 (SEM 0.31), 0.30 (SEM 0.01) v. 0.46 (SEM 0.01) and 23.09 (SEM 0.29) v. 26.98 (SEM 0.26), respectively (P<0.001); bone mineral content (g) and density (g/cm(2)) were 0.014 (SEM 0.002) v. 0.030 (SEM 0.002) and 0.061 (SEM 0.004) v. 0.080 (SEM 0.003), respectively (P<0.001); load-bearing capacity (N), yielding load (N) and elastic stiffness (N/mm) were 25.06 (SEM 1.24) v. 50.34 (SEM 2.94), 23.72 (SEM 1.02) v. 46.97 (SEM 1.75) and 65.98 (SEM 4.42) v. 115.07 (SEM 3.85), respectively (P<0.001); cross-sectional area (mm(2)) and moment of inertia (mm(4)) were 2.86 (SEM 0.19) v. 4.54 (SEM 0.17) and 1.27 (SEM 0.08) v. 3.03 (SEM 0.16), respectively (P<0.001). Significant effects were not evident in material properties. Parameters assessed normalized during re-feeding. These results suggest that the impaired mechanical femur competence in ND rats could be due to an altered bone mass and architectural distribution rather than to intrinsic quality. Re-feeding caused a reversal of the effects of food restriction on growth and bone parameters in ND rats.

Enanismo por desnutricion: cronodinamia de los procesos metabolicos en ratas / Nutrition dwarfing: longitudinal analysis of anthropometric and metabolic parameters in rats

El enanismo por desnutrición es una enfermedad no orgánica, cuya causa es la reducción voluntaria o no intencional de la ingesta de alimentos, debida a hábitos alimentarios inapropiados, insatisfacción en el peso corporal o a inadecuadas dietas para adelgazar. Los pacientes con retardo en el crecimiento debido a una causa nutricional logram alcanzar un crecimiento que es el equilibrio entre el potencial genético para el crecimiento y la ingesta de nutrientes. Esta desaceleración en el crecimiento produce una adaptación metabólica que no se refleja en los parámetros bioquímicos tradicionales utilizados como marcados de malnutrición. El objetivo de nuestro trabajo fue comparar en un modelo experimental en ratas en crecimineto las posibles modificaciones en la utilización de sustrato endógeno (CC), el consumo de oxígeno (VO2) y la velocidad de crecimiento. Se emplearon 30 ratas macho de la cepa Wistar que al momento del destete se subdividieron en 3 grupos: control (C) y experimentales: E4 y E8. El grupo C recibió una dieta stock ad libitum. El E4 y E8 recibieron por cada 100 gr de peso corporal un 80 por ciento de la misma dieta durante 4 y 8 semanas, respectivamente. Durante el período de depleción nutricional se midieron los siguientes parámetros: 1) peso (P) y talla (T) corporales en función de la edad, 2) P/T Z Score, 3) Composición corporal (CC) por el EM-SCAN, TOBEC modelo SA 3000/3076, Springfield, USA, 4) VO2 por calorimetría indirecta (ECO-OXYMAX, Columbus Instruments). Se obtuvieron los siguientes resultados a las 4 y 8 semanas, respectivamente: 1) La categoría antropométrica (CA) de delgado (P/T Z Score: -0.70 + 0.43) y de desnutrido (P/T Z Score: -1.44 + 0.32), respectivamente, 2) La reserva lipídica fluctuó dentro del rango normal con una cronodinamia significativamente diferente respecto de la del C. 3) No hubo diferencia significativa del VO2 entre C, E4 y E8. Los resultados obtenidos sugieren que la ingesta crónica de una cantidad subóptima (80 por ciento) de una dieta balanceada afecta el crecimiento corporal sin alterar el desarrollo del individuo.