Biomedical subjects
Publications and source records attributed to M Bryant.
Electromyography and biofeedback techniques are well established in the disciplines of physical medicine for the retraining of muscle groups to approximate functional performance. This report documents the application of biofeedback techniques to the treatment of swallowing dysfunction in a selected dysphagic patient.
To determine whether particle size of CaCO3 influences the hen's response to sodium zeolite A (ZA), two experiments were conducted. In Experiment 1, hens were fed 0, .75, and 1.50% ZA for 6 wk with and without a Na correction. At the end of the 4th wk, pullet-sized limestone was substituted for 50% of the added fine granular limestone in the diet containing no ZA. In Experiment 2, hens were fed diets containing 0, .68, and 1.36 ZA for 8 wk with and without one-half of the added fine granular limestone substituted for oyster shell. No correction for Na was made. A dietary calcium concentration of 2.75% was used in Experiment 1 and 3.5% in Experiment 2. Egg specific gravity, egg production, feed consumption, and egg weight were measured. Sodium zeolite A increased egg specific gravity, and the beneficial effects of ZA were maintained during Weeks 5 and 6 when pullet-sized limestone was added to the control diet containing no ZA (Experiment 1). Oyster shell and ZA improved egg specific gravity in Experiment 2 and the effect was additive. Dietary treatments had no effect on egg production or egg weight in Experiments 1 or 2 and there was no effect on feed consumption (Experiment 1). Feed consumption was reduced by ZA, when hens were fed oyster shell, but not when they were fed ZA with fine granular limestone (Experiment 2). It was concluded that the beneficial effect of ZA on egg specific gravity was independent of particle size of CaCO3 in the diet.
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Male CD rats were injected with single i.p. doses of benzo(a)pyrene (B(a)P), and peripheral blood lymphocytes (PBLs), livers, and lungs were removed at various times after administration. DNA adducts were analyzed in each tissue by 32P postlabeling with nuclease P1 enhancement. Sister chromatid exchange frequencies were concomitantly measured in cultured whole blood. B(a)P-DNA adducts were observed in all three tissues from animals sacrificed between 1 and 56 days after injection. Maximal adduction levels occurred at about 4 days after administration, followed by a gradual loss of adducts over the period examined. The apparent half-lives of total DNA adducts were 15 days in liver, 17 days in PBLs, and 22 days in lung. Induced sister chromatid exchanges were linearly related to the amount of DNA adducts remaining in the PBLs at the time of harvest up to 56 days and were significantly elevated above concurrent controls up to 14 days. One of the major adducts found in each tissue was N2-(10 beta-[7 beta,8 alpha,9 alpha-trihydroxy-7,8,9,10-tetrahydrobenzo(a) pyrene]yl)deoxyguanosine. An additional novel major adduct was found in the liver DNA and is derived from the further metabolism of B(a)P-trans-7,8-dihydrodiol. A second major novel B(a)P adduct was found in the DNA of lung tissues and accounts for about 40% of the total adducts present. Experimental evidence suggests that this adduct is derived from a metabolic pathway that includes the formation of 9-hydroxy-B(a)P.
Covalent linkage of myristic acid to the N-terminal glycine residue of Pr55gag, the precursor of the major structural proteins of human immunodeficiency virus 1 (HIV-1), facilitates an essential step in virus assembly and propagation. Substitution of the myristoyl-acceptor glycine with alanine, in a functional clone of HIV-1, eliminates virus replication. Complementation of this defect, in trans, restores infectious particle production. The nonmyristoylated (myr-) gag precursor accumulates in infected cells and is not processed into the mature capsid components of the intact virion. However, myr- Pr55gag can be processed by purified HIV protease in vitro, demonstrating that the myristoyl moiety is not required for cleavage by the protease. Myristoylation of Pr55gag is not necessary for localization but is required for stable membrane association and assembly of HIV-1.
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The ability of the Pediatric Trauma Score (PTS) to accurately predict the degree of injury severity of the injured child was assessed by comparing two separate groups of pediatric trauma victims. The first group consisted of 110 patients evaluated at a regional pediatric trauma center whose data was collected and assessed by a single investigator. The second group consisted of a similar matched cohort of 120 patients from the National Pediatric Trauma Registry whose data was collated from multiple participating institutions. In both cases, a linear relationship between PTS and Injury Severity Score (ISS) was documented that was statistically significant to P less than .001. The linear regression coefficients of each group were similar as was the distribution of PTS and ISS. This study documents the validity of the PTS as an initial assessment tool and confirms its reliability as a predictor of injury severity.
The degree of elevation and the duration of induced fever following endotoxin treatment of pregnant golden hamsters were examined. A radiothermistor was surgically implanted in the abdomen of each animal on day 6 of pregnancy. The animals were intravenously treated with a bolus injection of saline or endotoxin (1, 10, 20, or 200 micrograms/kg) on the morning of day 8 of gestation. Abdominal temperatures were monitored at 15-minute intervals on days 8 and 9 and at 1-hour intervals on days 10 through 14 of gestation. The mean temperature of the saline-treated control animals was 37.2 degrees C with a range from 36.5 to 38.2 degrees C. The total number of viable fetuses, and the mean fetal weight of the 1-microgram/kg group were not significantly different from those of the saline controls, although a statistically significant monophasic temperature elevation did occur between 3 and 9 hr post-treatment. Three of seven females that received 10 micrograms/kg had viable litters and exhibited a monophasic fever. The remaining four animals exhibited a biphasic fever and total resorption of all implanted fetuses. The first phase began 2.5 hr post-treatment and lasted for 3-6 hr. The second phase began 12-15 hr post-treatment and lasted for 15 to 25 hr. All animals receiving 20 or 200 micrograms/kg demonstrated similar multiple temperature elevations. Treatment of animals with greater than 20 micrograms/kg resulted in total resorption of all implanted fetuses and maternal weight loss. Nonpregnant females treated with 20 micrograms/kg of endotoxin exhibited a biphasic temperature elevation; thus the second phase of the fever response can not be attributed to embryo death and resorption.
A primary malignant carcinoid in the testis of a 76-year-old man was studied. The clinical indication was the appearance of extensive, papular cutaneous metastases. A markedly enlarged, indurated left testis was discovered during evaluation of the skin lesions. There were no clinical features of carcinoid syndrome. Histochemically, the tumor cells were argyrophilic but nonreactive to an argentaffin stain. Electron microscopy revealed numerous round, neurosecretory-type granules that ranged from 70 to 300 nm. At the time of autopsy, metastases were found in the heart, lungs, and the opposite testis. Review of the laterature failed to uncover any previous reports of a primary malignant carcinoid in the testis.
After repair, nerve stains of skin and subcutaneous tissue biopsies of 23 fingertips contained identifiable axons in all patients. The level of recovery was more advanced in some patients than in others, as manifested by identifiable nerve in various plexuses and receptors. Meissner's corpuscles were observed to be reinnervated in 12 of 17 patients and in 16 of 23 fingertips. The degree and level of reinnervation did not correlate with clinical testing or subjective impression of the result. The authors conclude that sensibility is the result of several factors active in the peripheral and central nervous system. Axonal regrowth is but one of these.
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Histochemical and chemical studies demonstrated a significant increase in the lipods of articular cartilage with advancing age. Triglycerides, cholesterol, and phospholipids were identified chemically and were shown by comparative staining procedures to be present in intracellular and extracellular lipids. The distribution and the composition of the extracellular lipids were interpreted as indicating that the extracellular lipids are of cellular origin. Glycolipids were extracted from cartilage of all ages and were shown to account for a portion of the increase in total lipid with age. Glycolipids extracted from aged cartilage were partially characterized. Cerebrosides, sulfatides, and gangliosides were detected. Glycolipids were estimated to comprise from 5 to 10% of the total lipid of articular cartilage. Arachidonic acid concentrations increased maredly with age in the surface of cartilage but were present in trace amounts in deep cartilage, demonstrating clear-cut differences in the levels as well as the location of this fatty acid precursor of the prostaglandins (PGE2 and PGF2alpha).