Growth Development and Aging最新文献

This study was done to compare the accuracy of prediction of growth parameters using the Gompertz model when (1) data was collected infrequently, (2) data collection was truncated, and (3) data was missing. Initial growth rate and rate of decay were reduced by half when the model was fitted to data collected biweekly compared to data collected weekly. This reduction led to an increase in age of maximum growth and subsequently over-predicted the asymptotic body weight. When only part of the growth duration was used for prediction, both the initial growth rate and rate of decay were reduced. The degree of data truncation also affected sexual dimorphism of the parameters estimated. Using pre-asymptotic data for growth parameter prediction does not allow the intrinsic efficiency of growth to be determined accurately. However, using growth data with body weights missing at different phases of the growth curve does not seem to significantly affect the predicted growth parameters. Speculative or diagnostic conclusions on intrinsic growth should be done with data collected at short intervals to avoid potential inaccuracies in the prediction of initial growth rate, exponential decay rate, age of maximum growth and asymptotic weight.

In slowly metabolizing tissue such as tooth, bone and ocular lens, D-amino acids converted from L-amino acids accumulate with age and thus reflect the tissue turnover rate. To investigate whether D-amino acids play a role in determining the bone remodeling rate, we measured the accumulation of D-aspartic acid, which has the fastest rate of racemization, in various areas of the mandible. The level of D-aspartic acid was higher in the ramus than in the body (P < 0.01), and within the body, the level was higher in the basal area than in the alveolar area (P < 0.01). Within the alveolar area, the level of D-aspartic acid was higher in the molar region than in the incisal region (P: 0.05-0.01). No correlation was found between the accumulated level of D-aspartic acid with age, because all the specimens were obtained from elderly people with only a few years difference in age. There was also no correlation between D-aspartic acid and sex. In conclusion, we suggest that accumulation of D-aspartic acid in the mandibular bone reflects the differences in remodeling associated with occlusion. The incisal portion of the alveolar area of the mandible (above the mandibular canal), shows the greatest evidence of active remodeling.

Objective: To compare bone mass in newborn infants of First Nations, white and Asian mothers while accounting for vitamin D status. Fifty infants born healthy at term age were measured for bone mass using dual energy x-ray absorptiometry (DXA) within 15 days of life. Vitamin D status was measured as 25(OH)D in cord plasma. White infants were separated based on 25(OH)D concentrations into sufficient and insufficient (< 32.5 nmol/L) to match for vitamin D status of the Asian infants and the First Nations group. Differences among groups were tested using ANOVA and post hoc testing with Bonferroni multiple comparisons test. There were no differences in whole body, spine or femur BMC between the white sufficient and insufficient infants. However, the Asian infants had lower (P < 0.01) spine BMC compared to the white infants and the First Nations infants were intermediate. No differences among the ethnic groups were observed for whole body or femur BMC. These data suggest that white and First Nations newborn infants have comparable bone mass. Asian infants have lower spine bone mass which is more than a factor of body size and independent of vitamin D status at birth.

Prenatal development is highly sensitive to the effects of environmental contaminants. 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) is an environmental toxicant that at very low levels causes teratogenic effects such as irregular tooth development. Variations in susceptibility to TCDD's effects have been attributed primarily to differences at the Ahr locus. There is some evidence, however, that genes at other loci may be involved in mediating TCDD's effects on various endpoints. Our hypothesis therefore was that the effect of TCDD on molar development would differ even among inbred mouse strains possessing similar Ahr alleles. To test this, geometric morphometric techniques were used to evaluate the effects of several different levels of TCDD on molar size, shape and asymmetry in the offspring of dosed females from five different inbred strains of mice bearing TCDD-sensitive Ahr alleles. The results indicated that a maternal dose of 1 microg TCDD/kg body weight on gestation day 13 altered the shape (but not the size or asymmetry) of the first two molars in mice from the C3H/HeJ and CBA/J strains of mice, but not in mice from the other strains. The C3H/HeJ and CBA/J strains appeared to be the most sensitive to the disruption of molar development via TCDD and the C57BL/6J strain appeared to be the least sensitive.

Available techniques for determining age from human cranial remains are limited. This study examines the efficacy of Meindl and Lovejoy's (1985) method of determining age based on ectocranial suture closure patterns as compared to a baseline of ages developed from a multifactorial approach employing various age determining factors from across the skull. What makes this study different is that the sample upon which this comparison is performed contains a large number of artificially deformed crania. Our hypothesis is that aging techniques that rely on suture closure patterns as markers are complicated by the results of artificial modification of the cranial vault. The study is conducted on adult, human crania from prehispanic archaeological sites in South America. Results demonstrate a significant difference between the two aging methods, more particularly when applied to deformed skulls. We conclude that when a skull is deformed age should be estimated utilizing multiple factors that exclude Meindl and Lovejoy's ectocranial suture aging technique.

Three growth models were used to examine the effects of prenatal exposure to aspirin on the postnatal development of brain parts. A total of 60 pregnant rats which were divided into three experimental groups and a control group were exposed to aspirin doses of 12.5, 25, 37.5 mg/kg, and distilled water, respectively. The brain parts of 200 rat pups starting from the first week after birth until the fifth week were weighted and the length and width of the cerebrum and cerebellum were measured to determine the parameters of the growth models. The results indicated that the three models successfully predicted the growth of the different brain parts and that aspirin decreased the total brain weight, cerebrum length and width, and decreased the cerebellum length and width at aspirin dose of 37.5 mg/kg. Further analysis is needed to investigate if aspirin effects were carried out through its role in inhibiting prostaglandin production and consequently affecting the activity of the hypothalamus-pituitary axis.

Over expression of the pro domain of myostatin (MLC-pro) interferes with myostatin function, thus promoting muscle growth. The purpose of this study was to use dual energy X-ray absorptiometry (DXA) to monitor, in vivo, the course of changes in body composition of control and MLC-pro transgenic (TG) mice between 10 and 91 days of age. MLC-pro TG (n = 32) and littermate control (n = 28) mice were produced by mating G-3 male TG mice with non-TG females. At days 10, 20 and weekly thereafter to day 62, and finally at day 91, the mice were anesthetized and scanned by DXA. By day 34, the body weight of the male TG mice was more than that of the control mice and was accompanied by a larger lean mass (LM) and a lower percentage of fat (%F) (P < 0.05). At day 91, the male TG mice had 15.6% greater body weight, 19.4% more LM, 22.4% lower %F, 11.5% more bone mineral, and 4.4% higher bone density (P < 0.05). The lower %F in the TG mice was due mainly to an increase in LM, rather than reduced FM. Measurements of the TG female mice were not different (P > 0.05) from those of control female mice. A region-of-interest analysis was used to provide a separate measure of the hind limb. By using DXA, this study determined the onset and degree of differences in body composition of MLC-pro TG and littermate control mice.

A growth trial was conducted with the Ross 708 broiler chicken to corroborate the relationships between changes in the growth curve (7 to 35 days) and in vitro metabolic parameters. These in vitro parameters also included estimates of the expression of certain genes regulating proteins implicated with regulation of lipogenesis. Birds were fed diets containing 24% protein from 0 to 14 days of age, 21% from 14 to 26 days of age and 18% protein until 35 days of age. Birds were selected and killed at ages corresponding to protein changes. Dual X-ray absorptiometry (DXA) was used to approximate body composition of birds at day 35. The switch from the starter protein level of 24% crude protein to the only slightly lower protein grower diet (21% crude protein) increased both in vitro lipogenesis and malic enzyme activity. A similar observation was noted when the birds were switched to the 18% crude protein finisher diet. These same switches also elicited initial increases in malic enzyme, fatty acids synthase and acetyl CoA carboxylase gene expression that were not sustained following adaptation to the dietary change. Data also show that DXA can be used to estimate body composition of this type of bird.

Most studies of malnutrition focus on adult size, or limited durations of malnutrition. Little is known about the impact of life-long maternal malnutrition on young, pre-weaning offspring, in part because working with such infants is difficult. We created a maternal generation of malnourished dams by feeding female Sprague-Dawley rats, from weaning, either a control diet high in protein (CT) or an isocaloric low protein diet (LPT). The offspring of matings between these dams and control fathers were weighed daily and radiographed three times before sacrifice at 22d, when several visceral organs and muscles were dissected out and weighed. We compared lengths of craniofacial and limb bones, and organ and muscle weights, between the two diet treatments. Allometric cancellation was used to assess integration of growth among organs and muscles. The offspring of LPT dams had body, organ and muscle weights smaller than the offspring of CT dams. When scaled to body mass, some organs of the LPT offspring were relatively larger. Although the CT offspring skeletons were significantly larger than the LPT skeletons, considerable variation existed in the patterns of growth between the two treatments. The CT offspring had a higher level of correlation among muscles, and most organs, than did the offspring of LPT dams. The organs that did maintain a correlation in growth, or linkage, were pairs of organs more likely to be protected (heart-lung or eye-brain) from the insult of protein malnutrition. The ability to protect some organs may be the result of their tighter developmental program, one that is more resistant to differences in available nutrition.

Ontogenetic growth can be described by mathematical equations constructed on the goodness of fit. Recently, the biological mechanism underlying mathematical growth equations has been explored using basic cellular properties. Here, we derive a general statistical model for understanding the genetic regulation of ontogenetic growth by integrating those biologically-proven meaningful growth equations into a quantitative trait locus (QTL) mapping framework. We can characterize the dynamic patterns of effects of QTL governing growth curves and estimate the global effect of the underlying QTL throughout the entire course of growth. The model provides the basis for deciphering genetic relationships for growth rates and the timing of life history events for any kind of organisms.