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Biomedical subjects

H Talpaz

Publications and source records attributed to H Talpaz.

14 recordsLinked to original sources

The effect of dietary protein level on the lysine and arginine requirements of growing chickens.

Comparisons were made of the growth and carcass fat responses to dietary lysine and of the lysine requirements of 1-wk-old broiler chickens receiving diets containing either 18, 20, 23 or 25% protein. Similar comparisons were made of the responses elicited by dietary arginine in diets containing 18 or 23% dietary protein. The responses to lysine supplementation and the lysine requirements of chicks receiving 23 or 25% protein diets were similar. In comparing the 18 or 20% to the 23% protein diet, the initial responses of growth and feed efficiency to dietary lysine were augmented, but the maximal weight gain diminished as dietary protein decreased, leading to a decrease in the lysine requirements. The amounts of extractable carcass fat or abdominal fat pad increased as dietary protein was lowered and, in general, were reduced either by lysine or arginine supplementation. Percentage of pectoral muscle increased slightly with dietary arginine and protein supplementation. The results suggest that when total dietary amino acid level is reduced, the requirements for the individual amino acid decrease due to growth retardation resulting from single or multiple amino acid deficiencies. Single amino acid supplementation of low protein diet is more effective in improving the amino acid balance than supplementation of high protein diets, resulting in a further decrease in the requirements.

Animal Nutritional Physiological Phenomena↗

Calcium metabolism and requirements of chickens are affected by growth.

The interaction between growth and calcium homeostasis was studied by comparing the responses of (a) fast-growing broiler chickens (Cobb) and slow-growing Leghorns, and (b) fast-growing chickens (Cobb) fed either high energy (12.13 kJ/g) or low energy (9.2 kJ/g) diets, to dietary calcium concentration ranging between 4 and 20 g/kg). Plasma calcium increased as dietary calcium increased, reaching an apparent plateau between 0.8 and 1.5% dietary calcium, regardless of basal growth rate. Dietary calcium levels of 1.5% and higher induced hypercalcemia and hypophosphatemia in fast- but not in slow-growing chickens. Weight gain was unaffected by dietary calcium in the slow-growing Leghorns, but followed a bell-shaped response pattern in the fast-growing Cobb chickens. Growth inhibition by feeding of low energy diets changed the response pattern from a quadratic form to that of an increase towards a plateau. The response of bone ash to dietary calcium was characterized as quadratic in fast-growing chicks, changing to a pattern of increase towards a plateau in slow-growing chicks. Intestinal calbindin was suppressed by dietary calcium and was higher in the fast-growing than in the slow-growing chicks. An increase in dietary phosphorus resulted in a shift in the response curves of weight gain and bone ash and an increase in the calcium requirements. The results indicate that the response of chicks to dietary calcium and calcium requirements is markedly modified by growth rate.

Analysis of Variance↗

Growth hormone therapy in normal short children induces a transitory decrease in plasma growth hormone releasing hormone levels and in human growth hormone responsiveness to exogenous growth hormone releasing hormone.

A three-month study of the effect of growth hormone (hGH) therapy (0.1 U/kg/day sc) on plasma levels of GH releasing hormone (GHRH), somatostatin and insulin-like growth factor I (IGF-I) and on the hGH responsiveness to exogenous GHRH was carried out in 32 prepubertal short-stature children with normal GH secretion. Blood samples were collected prior to initiation of therapy, and at 5, 30 and 90 days of onset of therapy, as well as 2 and 90 days after termination of therapy. The nonconventional hGH therapy induced an increase in serum IGF-I levels which lasted as long as therapy was continued. Plasma GHRH levels showed an early transitory decrease after five days of therapy, whereas plasma somatostatin levels were unaltered. A slight suppression in hGH responsiveness to exogenous GHRH was found at 2 but not at 90 days after termination of hGH therapy. It is concluded that nonconventional hGH treatment does not cause permanent changes in physiological hGH secretion.

Adolescent↗

Regulation of calbindin mRNA and calbindin turnover in intestine and shell gland of the chicken.

A synthetic oligonucleotide was used as a probe for measurement of calbindin mRNA in the shell gland and intestine of chickens. The half time of calbindin mRNA in the duodenum and shell gland was estimated at 2 and 3.6 h and that of calbindin at 13.9 and 32.6 h, respectively. The formation rates of calbindin mRNA were 0.37 and 0.17 pmol.h-1.g-1 and the rate of calbindin formation was 0.099 and 0.031 microgram.pmol mRNA-1.h-1 in the duodenum and shell gland, respectively. In the shell gland, calbindin mRNA and calbindin appeared at the time of sexual maturation during calcification of the first egg shell. Calbindin mRNA fluctuated markedly during the daily egg cycle, in close temporal association with egg shell calcification. When Ca2+ deposition was eliminated by expulsion of the ovum, the rise in calbindin mRNA was prevented. An indirect suppression of Ca2+ deposition by administration of the carbonic anhydrase inhibitor acetazolamide also resulted in a decrease in calbindin mRNA. The results are consistent with a possible role of Ca2+ flux in the regulation of calbindin mRNA appearance in the shell gland of chickens.

Animals↗

Characterization of growth and development of male British United turkeys.

Body weight and the size of various organs (tibia, pectoral muscle, leg muscle, liver, spleen, and testes) were monitored in growing male turkeys (British United Turkeys) in an effort to characterize their growth pattern. The results were fitted with either a single- or a double-component Gompertz equation, describing single and diphasic growth patterns, respectively, using an iterative nonlinear estimation algorithm. The diphasic model with an early and a late growth component provided a better description of the body weight function than the single-phase model. The start of sexual maturation, evidenced by testicular development, marked the transition age between the early and the late phases of growth. A single-component Gompertz equation was sufficient to describe growth of various individual organs. Growth of bone and liver appeared to follow the early growth component, whereas the path of muscle development appeared to be closer to the later growth component. The results suggest that the diphasic growth behavior of male turkeys is caused by a differential growth rate of various organs, rather than by a periodicity in the overall growth rate.

Animals↗

Calcium dynamics: a model system approach.

A computerized model used to simulate calcium metabolism in growing chicks combines growth equations with differential equations that account for the amount and action of various components of the plasma calcium regulating subsystems--intestine, kidney and bone. These in turn are modulated by the calcium-regulating hormones: parathyroid hormone and 1,25-dihydroxycholecalciferol. Simulation with this model indicated oscillations in the plasma calcium concentration in growing chicks under normal dietary conditions. The oscillations diminish in amplitude and finally disappear when dietary calcium concentrations are either reduced or elevated. These oscillations, triggered by the perturbation imposed by growth, are the result of the dual action of parathyroid hormone on bone on the one hand and on intestinal calcium absorption via the 1,25-dihydroxycholecalciferol synthesizing system on the other and the difference in the response time between the two subsystems. Simulation also predicts that at high or low intakes of calcium, the capacity of the control systems is exceeded and oscillation in plasma. calcium diminish and finally disappear. Bone calcium, simulated for different calcium concentrations, mimics documented experimental results.

Animals↗

Model of plasma calcium regulation: system oscillations induced by growth.

The process of growth was included in a model for simulation of calcium homeostasis in the chick, using data of carcass composition and a model of growth and energy intake. Computer simulations, made for chickens between 0 and 10 wk of age, predicted oscillations in plasma calcium and its major regulatory systems. Analysis of the oscillations indicated a periodicity of approximately 55 h. The oscillations were proportionally dependent on the rate of growth, disappearing almost completely when growth rate was made equal to zero. Subject to the validity of the model, it is suggested that the oscillations in plasma calcium and some of the components of the regulatory systems are induced by a continuous perturbation (growth) resulting in a dual response to the main regulatory hormone, parathyroid hormone, one rapid with a response time of minutes (bone), and one delayed, with a response time of hours (calcium absorption via the metabolism of 1,25-dihydroxychole-calciferol). It is also suggested that some of the normal variance and some of the rhythmicity observed previously in various components of the calcium regulatory system may be the results of spontaneous oscillations.

Animals↗

Differential responses to dietary carbohydrates and fat of turkeys kept at various environmental temperatures.

Interactions between environmental temperature and dietary energy sources were evaluated in 6 to 9-wk and 9 to 12-wk-old turkeys using weight gain, feed efficiency, and carcass fat as response criteria. The dietary variables (soybean oil or glucose) were added in five or six increments at the expense of each other or of the fiber supplements, keeping the minima for protein and amino acid/energy constant. The resulting diets were fed to birds kept at 10 and 27 C. Duplicate experiments were conducted for each mode of dietary variable addition. Parallel increases in body weight gain and feed efficiency were obtained at the two temperatures when fat replaced carbohydrates or fiber, thereby raising dietary energy density. Some responses of weight gain and feed efficiency at the two temperatures were obtained also with a graded isocaloric addition of fat but the response was significant only at 27 C and not at 10 C. A greater response of gain and feed efficiency to energy supplied by dietary glucose was obtained at 10 C as compared with 27 C. Dietary fat supplementation resulted in increased deposition of carcass fat when given together with energy or isocalorically regardless of environmental temperature. Carcass fat was increased by glucose-energy at the low temperature only.

Adipose Tissue↗

Parameter estimation for ligand binding systems kinetics applied to 1,25-dihydroxycholecalciferol.

A mathematical analysis of the kinetics of the hormone-receptor interaction was applied to the 1,25-dihydroxycholecalciferol-intestinal receptor system. The exact analytical solution and the numerical integration of the kinetic equation were installed in a Statistical Analysis System (SAS) computer program to estimate the rate constants of the reaction. Estimates of the parameters obtained by these two methods are similar, demonstrating that the numerical integration can be combined with the nonlinear regression procedure for least-squares parameter fitting using a simple SAS program. This enables estimation of kinetics rate constants when the kinetic equation cannot be solved analytically. The ratio of the rate constants (ka/kd) found by the nonlinear procedure is close to the independently determined equilibrium (Scatchard) constant in the nonlinear analysis.

Animals↗

Calcium metabolism in birds: computer simulation of response to 1,25-dihydroxycholecalciferol.

A simulation model of calcium metabolism in the chick has been used to evaluate the response of the systems that regulate plasma calcium to a continuous input of 1,25-dihydroxycholecalciferol [1,25(OH)2D3] from the intestine. The results of simulation showed that the concentration of the vitamin D metabolite in the intestine increased during the first 24 h and thereafter decreased slightly due to suppression of endogenous hormone production. Metabolite accumulation was accompanied by an increase in calcium absorption, with a lag period of about 4 h. Most of the increase in absorbed calcium was excreted in the urine, with a lesser change in net bone calcium uptake. Plasma calcium increased with time, in proportion to the intake of the exogenous hormone. The validity of the predicted steady-state plasma calcium levels, and bone and kidney calcium flows, is discussed. The results of the simulation demonstrate the importance of the vitamin D-intestinal axis in regulation of plasma calcium.

Animals↗

Simulation of calcium homeostasis: modeling and parameter estimation.

The system that regulates plasma calcium in the bird has been formalized into a model based on a series of differential equations and solved by computer simulation. Bone, kidney, and intestine have been considered as the control subsystems, with parathyroid hormone and 1,25-dihydroxycholecalciferol as the regulating hormones. The parameters used in the simulation model have been computed either from published results or by specifically designed experiments described here. For the estimation of parameters, an iterative procedure has been developed that was designed to minimize the sum of square errors between observed and system-simulated values. Parameters of 1,25-dihydroxycholecalciferol metabolism were experimentally obtained from the kinetic behavior of the 3H-labeled hormone in rachitic birds after a single dose. Model parameters have been adjusted using the results of in vivo calcium loading and validated by an EDTA infusion experiment. The simulation model has been used to study the hierarchy of the activities of the three control subsystems and of the regulating hormones, at different calcium intakes. Positive or negative errors in plasma calcium resulted in an asymmetry in the activities of the controlling systems, bone and kidney, whereas the intestine is characterized by its relatively long response time.

Animals↗

The response of growing turkeys to dietary nutrient density.

The response to diets of different nutrient densities was evaluated in male turkeys. In 2-week experiments with 1-week-old and 14-week-old turkeys the growth response to nutrient density appeared to be biphasic with an accelerated response at the lower and a much smaller response at the upper range of nutrient density. Results suggest that the upper limit of nutrient density for obtaining the accelerated growth response was higher for older (14-week-old) than for younger (1-week-old) birds. In two additional experiments, the growth response at the upper energy range was estimated at 1 to 2% per 100 kcal. In 14-week-old turkeys, abdominal fat did not change with nutrient density.

Age Factors↗

The amino acid requirements of growing turkeys. 2. Experimental validation of model-calculated requirements for sulfur amino acids and lysine.

The response to protein and the requirements for sulfur amino acids and lysine have been evaluated in male turkeys throughout the growth period as an experimental validation of model-calculated requirements (Hurwitz et al., 1983). The sulfur amino acid requirements were 3.4 and 3.1 mg/kcal for 1- and 5-week-old turkeys, respectively. The requirements for lysine were 4.8, 2.7, and 2.2 mg/kcal for 1-, 12-, and 16-week-old turkeys, respectively, which were in close agreement with the model predictions. Dietary protein in diets calculated on the basis of the model was sufficient to maintain maximal growth and feed efficiency. The results were the basis for accepting the general validity of the model-calculated requirements (Hurwitz et al., 1983).

Aging↗