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Biomedical subjects

T C Peng

Publications and source records attributed to T C Peng.

At least 37 records · Page 2Linked to original sources

Interrelationships of bone ash and whole bone properties in the lactating and parous rat.

Several investigators have studied the mechanical properties of long bones of rats and have found that bone strength may be associated with bone mineral content. In this study we examined further the interrelationships of whole bone properties and bone ash weight of the rat femur. Using a 3-point bending test, the bones were evaluated during lactation and after one to three pregnancy + lactation periods--experiments in which bone ash was significantly reduced. A relationship was established between the time of lactation and the ash weight, stiffness, strength, and toughness but not the ductility. Using all of the experimental data, a highly significant relationship was observed between ash weight and stiffness. A similar significant correlation was revealed between bone ash and strength or toughness, although drawing individual lines for each experiment rather than a common line for all the experiments appeared more appropriate. Given the inherent inaccuracies in the material property measurements of bone, the results suggest that routine measurements of whole bone properties provide an important and sensitive way to evaluate bone quality and that these properties correlate significantly with the bone ash weight.

Animals↗

Cytochemical bioassay of circulating concentrations of rat parathyroid hormone: application to a study of age and sex.

We have found that the cytochemical bioassay (CBA) method, originally developed to measure circulating levels of biologically active parathyroid hormone (bioPTH) in humans, also can measure endogenous concentrations of PTH in rats. Therefore, we have applied this assay method to examine the relationships between age and sex and the circulating levels of bioPTH, calcium, and phosphorus in Fischer rats. The concentration of bioPTH increased in both males and females from 5 to 15 months of age (p less than .001) with no significant sex-related difference. Mean bioPTH values ranged from 2.3 to 3.6 pg (human PTH equivalents)/ml; these values were much lower (1 to 2 orders-of-magnitude) than those reported by others who used radioimmunoassays for PTH that do not discriminate between biologically active and inert PTH fragments. The CBA values for bioPTH were also 1/4-1/5 those obtained in rat serum by newer, more sensitive methods, the N-terminal specific PTH radioimmunoassay and the bioassay based on stimulation of chick renal adenylate cyclase. Regression analysis did not reveal any significant correlation between serum calcium and age. However, serum inorganic phosphorus decreased significantly (p less than .001) from 5 to 15 months of age in both male and female rats and was much lower in females than in males (p less than .001). The fall in serum phosphorus was negatively correlated with the rise in bioPTH (p less than .001). This study, the first to our knowledge to use a CBA to detect physiological changes in the circulating levels of bioPTH in rats, demonstrates the usefulness of the assay in experiments in this species.

Aging↗

Secretion of calcitonin gene-related peptide from baby rat thyroid glands in vitro.

Thyroid glands from 8-day-old rat pups were incubated in serum-free medium for 6 hr. Both calcitonin (CT) and calcitonin gene-related peptide (CGRP) released into medium were measured by radioimmunoassay. In 6 separate experiments CGRP was easily detected in medium in ng/ml concentrations. In 4 of the 6 experiments, where CT release was stimulated by high medium [Ca], the concentration of CGRP in medium showed a positive, significant correlation with the medium CT concentration (r = 0.41-0.69, p less than .05- less than .01). The results are in concert with reports describing the presence of CGRP in the C-cell, and they further show that CGRP, as well as CT, can be secreted by C-cell.

Animals↗

Serum calcitonin, calcium and thyroxine in young and old Zucker fatty rats (fa/fa).

We determined the serum levels of calcitonin (CT), calcium (Ca), and thyroxine (Ti) in lean (?/+) and fatty (fa/fa) male Zucker rats 10 weeks and 10-12 months of age. The most dramatic finding was a high level of serum CT (3.24 +/- 1.18 ng/ml) in young fatties whereas sera from young leans were all below the limit of assay detection (less than 0.120 ng/ml, p less than 0.01). Young fat rats also had elevated levels of both Ca (11.2 +/- 0.2 vs. 9.7 +/- 0.2 mg/dl, p less than 0.001) and Ti (6.7 +/- 0.48 vs. 4.72 +/- 0.28 micrograms/dl, p less than 0.01). In older animals the mean serum level of CT increased further in the fatties and became readily measurable in leans (5.67 +/- 1.94 vs. 1.49 +/- 0.55, p less than 0.01). Thyroid C-cells, identified immunohistochemically, were abundant in both leans and fatties at this age but were substantially more numerous in the fat rats (p less than 0.001). Calcium levels increased somewhat in the older leans, but still remained higher in the fat rats (p less than 0.05). Thyroxine values were essentially the same for old animals of both genotypes (5.07 +/- 0.61 vs. 5.54 +/- 0.88). Age effects were not significant for any measure in the fat animals, but in the leans there were significant age-related increases in CT (p less than 0.02) and serum Ca (p less than 0.05).

Age Factors↗

Evidence of a toxic effect of ethanol on bone in rats.

Tibiae from rats treated chronically for 12 days with enough ethanol to induce physical dependence were found to have an increased incidence of fracture during dissection and cleaning (7 of 12 or 58%) compared to control animals (1 of 12 or 8%). The site of the fractures, the proximal end of the tibia, showed an increased opacity to X-rays, and the dried bones were distinctly darker in appearance than similarly prepared control bones. The effects noted in our study suggest that the rat model could be useful for the study of the mechanisms by which alcohol affects bone growth, remodeling, and strength. These studies might shed new light on the pathogenesis of increased bone fragility in alcoholics.

Alcohol Drinking↗

Age-associated C-cell hyperplasia in the human thyroid.

C cells in 26 normal human thyroids from forensic autopsies were identified by immunoperoxidase staining for calcitonin. C-cell concentrations and total C-cell numbers were determined with the use of morphometric techniques. There was great variation in C-cell density within a given gland and among individuals, although C cells tended to concentrate about one third of the way down the vertical axis of the lateral lobes. Densities of 1-2000 cells/cu mm were found in the third and later decades. In addition there was a statistically significant (P less than 0.01) positive Spearman correlation between total C-cell numbers and age in males. C-cell hyperplasia appears to be an age-related phenomenon that may have physiologic significance and must be taken into consideration in evaluation of thyroid glands for the diagnosis of premalignant lesions of C cells.

Adolescent↗

C-cell nodules in adult human thyroid. A common autopsy finding.

This study was designed to examine the morphologic features and distribution of calcitonin-producing cells (C-cells) in normal adults and in a general autopsy population. Random or serial sections from thyroid glands in forensic and general autopsies were examined by an immunoperoxidase stain for calcitonin to identify C-cells. Six glands out of 30 cases contained large C-cell nodules (85-343 C-cell nuclei per nodule). Five of the nodules were in patients over 50 years of age. C-cell nodules in thyroid sections may represent age-related hyperplasia or a normal variation of ontogeny. This study underscores the importance of serially sectioning the thyroid to evaluate nodular C-cell hyperplasia in preneoplastic or nonneoplastic functional disorders.

Adult↗

Sex difference in serum calcitonin level in rats as related to feeding, fasting, and age.

Serum calcitonin (CT) was measured in male and female Fischer fasted and fed rats from 1-24 months of age. Previous findings by ourselves and others that serum CT rises with advancing age and is higher in females than in males were confirmed and extended. The effects of feeding were examined with the use of three different protocols, overnight fasting then feeding for 1 h, feeding ad libitum, and feeding rats for 2 h after they had been on a fixed feeding schedule for 4 weeks. At 1 month of age serum CT was too low to measure in either sex, fed or fasted. From 2-24 months of age, feeding increased serum immunoreactive CT much more in females than in males. The increase in serum CT was accompanied by a slight decrease in serum calcium. We concluded that the release of CT in rats after eating is sex related.

Aging↗

Calcitonin-like immunoreactivity in rat and human pituitary glands: histochemical, in vitro, and in vivo studies.

This study was designed to determine whether pituitary glands contain an immunoreactive material which reacts with antisera to calcitonin (CT) and, if so, whether secretion of the material could be demonstrated. Testing 15 antisera to rat and human CT and using an immunoperoxidase method, we found 2 antisera to human CT which stained rat pituitaries and several which stained human pituitaries. Essentially all cells in the rat intermediate lobe and scattered cells in the rat and human anterior lobes showed staining, and staining was not entirely abolished by prior adsorption of antisera with rat or human CT. The 2 antisera which stained rat pituitaries showed cross-reactivity with several synthetic human CT fragments (1-18, 11-23 and 22-32) but not with ACTH-(1-39), ACTH-(1-24), beta-endorphin, alpha- or beta MSH, or bovine lipotropin. Crude extracts of pituitaries from 2 strains of young rats showed CT-like immunoreactivity which could be measured easily by RIA (0.2-0.3 ng/gland). In vivo, an antiserum which stained pituitaries and 1 which did not were compared using young rats made hypercalcemic (15-20 mg/dl) with iv Ca. In rats with thyroids, both antisera showed an increase in serum CT of more than 15-fold whether the pituitary was present or absent. In thyroidectomized rats, serum CT remained undetectable (less than 50 to 100 pg/ml) during hypercalcemia even if the pituitary was present. In vitro, rat pituitaries in a serum-free medium did not release measurable amounts of immunoreactive CT-like material even when medium contained high Ca (2.5 mM), high K (25 mM), or TRH (10(-6) M). Therefore, the findings agree with other reports of a CT-like material in the pituitary, but no secretion of the material could be demonstrated. We hypothesize that the material is not authentic CT but is, rather a related peptide sequence probably contained in the 31 K precursor protein of ACTH-beta-lipotropin.

Amino Acid Sequence↗

Hypercalcitoninemia associated with return of serum calcium concentration toward normal in chronically parathyroidectomized rats.

In chronically parathyroidectomized male Fischer and Holtzman rats, we found a progressive rise in the levels of serum immunoreactive calcitonin (CT) despite hypocalcemia. The rise was preceded by an increase in the thyroidal CT concentration (determined by RIA) and hyperplasia of C cells (determined by the immunoperoxidase bridge technique). In association with the rise in serum CT, we also observed a return of serum Ca toward normal levels, which the evidence suggests was not due to compensatory regeneration of parathyroid remnants after incomplete parathyroidectomy. It also is unlikely that ectopic parathyroid tissue was responsible for the return of serum Ca toward normal. Since the increase in serum CT after parathyroidectomy coincided with the return of serum Ca toward normal, we postulate that a gradual rise in serum Ca in chronically parathyroidectomized rats might stimulate the "CT-saturated" thyroid glands to release CT, thus leading to a progressive increase in serum CT. Alternatively, it is possible that the increase in serum CT after parathyroidectomy may be due in part simply to nonspecific leakage of CT from the "CT-saturated" thyroid glands.

Animals↗