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Biomedical subjects

S M Wilson

Publications and source records attributed to S M Wilson.

At least 127 records · Page 7Linked to original sources
PubMed1990

Gender comparisons of college students' attitudes toward sexual behavior.

Questionnaires were distributed to 641 undergraduates at a large southeastern university to elicit opinions concerning various forms of premarital sexual behavior. Hypotheses were developed to determine whether there were differences between the attitudes of males and females. Significant differences were found between males' and females' attitudes toward premarital sex when the couple is casually acquainted, and attitudes toward extramarital sex, oral-genital sex, and anal sex. However, significant differences were not found between males' and females' attitudes toward premarital sex when the couple is in love, attitudes toward premarital sex when the couple is engaged, and attitudes toward masturbation, homosexuality, and sexual fantasizing. Males' attitudes toward various forms of sexual behavior were more liberal than those of females.

Adolescent↗
PubMed1989

Evidence for a factor in normal human serum that induces human neutrophilic granulocyte end-stage maturation in vitro.

The end-stage maturation of neutrophilic granulocyte precursor cells isolated from normal human bone marrow by Ficoll density centrifugation was studied in a liquid culture assay system used previously to study the maturation of guinea pig granulocyte precursors. Dialyzed normal human serum induced end-stage morphological maturation of human granulocyte precursors and this induction was proportional to a serum level of up to 5.0% in the assay medium. At serum concentrations greater than 5.0% a pronounced inhibition of maturation was observed. Passage of serum through a DEAE-Fractogel 650S column equilibrated with 0.01 M phosphate buffer (pH 7.0) resulted in the binding of the end-stage granulocyte maturation factor to the column. The activity eluted from the column in a fraction containing 17% of the starting serum protein that was inhibitor-free and was also capable of inducing the appearance of granulocyte alkaline phosphatase, a specific biochemical marker for granulocyte end-stage maturation. GMF is most likely a protein since it was destroyed by protease digestion. The data also indicate that neither purified human transferrin nor human recombinant granulocyte colony-stimulating factor can substitute for human serum GMF as a granulocyte end-stage maturation factor in this assay system. It was observed, however, that purified human transferrin greatly potentiated the effect of GMF suggesting that transferrin plays a supporting role in the end-stage maturation of human granulocytes in vitro. To our knowledge the evidence presented here indicates for the first time the existence of a neutrophilic granulocyte end-stage maturation factor in normal human serum.

Alkaline Phosphatase↗
PubMed1989

The control of potassium (86Rb+) efflux in the isolated human sweat gland.

Sweat glands, isolated from strips of human skin and pre-loaded with 86Rb+, a marker of potassium transport, were superfused with physiological saline and rate constants for 86Rb+ efflux calculated. The rate of efflux during superfusion with Ca2+-free saline was lower than that measured in the presence of calcium (2.56 mM). Acetylcholine increased the rate of 86Rb+ efflux and this response could be resolved into two components: an initial transient phase which was Ca2+-independent and a slowly declining Ca2+-dependent phase. Adrenaline only caused a Ca2+-dependent increase in efflux. It is suggested that the potassium permeability of the secretory cells increases during activity.

Acetylcholine↗
PubMed1989

Potassium (86Rb+) efflux from the rat submandibular gland under sodium-free conditions in vitro.

1. Fragments of rat submandibular gland were pre-loaded with 86Rb+, an isotopic marker of potassium transport, and rate constants for 86Rb+ efflux were determined during superfusion with a physiological salt solution. 2. In sodium-containing solutions acetylcholine evoked a rapid and immediate increase in efflux rate. After reaching a peak value, the efflux rate initially declined rapidly, but a second, slowly declining phase to the response was also evident. The response could be resolved into Ca2(+)-independent and Ca2(+)-dependent phases. 3. The basal efflux rate was elevated during superfusion with solutions in which sodium had been replaced with either lithium or N-methyl-D-glucammonium (NMDG+). Although lithium had a greater effect, which was absent under calcium-free conditions, addition of calcium to initially calcium-free, lithium-containing solutions did not affect the rate of efflux. 4. In the presence of calcium the response to acetylcholine was augmented during exposure to lithium-containing, sodium-free solutions but, in contrast, slightly inhibited when NMDG+ was used as a sodium substituent. 5. The transient, calcium-independent component of the response to acetylcholine was unaffected by exposure to lithium, whereas the calcium-dependent phase of the response was inhibited. 6. Responsiveness to acetylcholine was reduced during superfusion with a calcium-free, NMDG+-containing solution. The response normally observed when extracellular Ca2+ was subsequently elevated, in the continued presence of acetylcholine, was also inhibited. Sensitivity to acetylcholine was retained, however, when the tissue was initially exposed to a solution containing approximately 20 mumol l-1 Ca2+. The response was smaller than that evoked in sodium-containing solutions. 7. The use of lithium as a sodium substituent presents special problems, possibly related to the effects of this ion on the metabolic cycling of phosphatidylinositol-4,5-bisphosphate metabolites.

Acetylcholine↗
PubMed1988

Effects of stimulation on the ultrastructure and Na, K, Cl composition of the fundus of the rat plantar sweat gland.

Initial stimulation of the rat plantar sweat gland with pilocarpine caused a variable degree of distension of the apical membrane of the secretory cell. This appeared to be a process of filtration of secretory cell cytoplasm through the apical terminal web. Further stimulation resulted in luminal dilatation, cytoplasmic depletion, and morbidity of some cells. These morphological changes in the footpad gland, which thus can no longer be considered as eccrine, were accompanied by a fall in potassium and a rise in sodium concentration within the secretory cells. The mode of secretion induced by pharmacological stimulation was fundamentally the same as that in the glands of species responsive to thermal stimulation.

Animals↗
PubMed1988

The effects of thermally-induced activity in vivo upon the ultrastructure and Na, K and Cl composition of the epithelial cells of sweat glands from patients with cystic fibrosis.

The secretory cells of the fundus of sweat glands from cystic fibrosis (CF) patients had higher Na and Cl contents and showed more granule depletion, cellular disruption and dilated intercellular canaliculi than normal. The cells of the coiled duct also had higher cytoplasmic levels of Na and Cl but were structurally normal. Thermal stimulation produced ultrastructural changes in the CF fundus comparable to normal, including further dilatation of the basolateral clefts, but did not induce the marked changes in the coiled duct which normally occur. The elevated Na and fall in K in the fundus and raised Na and Cl in the coiled duct upon activation, were not observed in the CF glands in which no significant changes were detected.

Chlorides↗
PubMed1988

Effects of thermal stimulation on intracellular sodium, potassium and chlorine in the sweat glands of the cow, sheep and goat.

The intracellular concentrations of electrolyte elements in the sweat glands of the cow, sheep and goat provide evidence of altered secretory activity upon thermal stimulation in the cow but give no indication of such change in the sheep and goat. The results support the view that increased secretory function contributes to the pattern of sweat output in the cow.

Animals↗
PubMed1987

Effects of topically-applied antiperspirant on sweat gland function.

In subjects exposed to a hot environment, short-term topical pretreatment with aluminium zirconium tetrachlorhydrate delayed the onset of visible sweating although it failed to prevent the response. The delay was considered most probably to be due to the occlusive action, in the duct within the upper epidermis, of aluminium-containing conglomerates, which disappear after continuous sweating. However, microanalytical evidence indicated that ionic transport within the fundus secretory cells was also modified.

Administration, Topical↗
PubMed1986

Autoradiographic localization of transported neutral amino acids in epithelia of cat submandibular and sublingual salivary glands.

Light-microscopic autoradiography was used to localize the cellular sites for neutral amino acid uptake in submandibular and sublingual salivary gland epithelia. The vasculature of isolated glands was perfused for 3-5 min with either L-(3-3H)serine or L-(4-3H)phenylalanine and then fixed by perfusion with buffered glutaraldehyde. In the submandibular gland the small neutral amino acid L-serine and the aromatic amino acid L-phenylalanine were localized to central acinar cells, demilunar cells and ductal cells. In the sublingual gland silver grains associated with each of these tritiated amino acids were localized to central acinar and ductal cells. Perfusion of both submandibular and sublingual glands with unlabelled L-serine (25 mM) or L-phenylalanine (30 mM) resulted in a significant decrease in the silver grain density associated with each labelled amino acid. The absence of silver grains in the lumina of acinar and ductal cells and the presence of tight junctions near the apical surface of the epithelium strongly suggest that the initial uptake of these amino acids was mediated by basolateral plasma membrane carriers.

Amino Acids↗
PubMed1986

Transferrin induces maturation of neutrophil granulocyte precursors in vitro.

Previous studies showed that dialyzed serum from guinea pigs contained a factor which induces guinea pig granulocyte precursors to form mature neutrophil granulocytes in vitro. We show here that this maturation inducing activity of serum is associated primarily with transferrin. This activity is not species specific since both guinea pig and human transferrin serve equally well in this capacity. These findings raise the possibility that transferrin could serve as a physiological regulator of granulocyte maturation.

Animals↗
PubMed1986

In extremis use of a Foley catheter in a cardiac stab wound.

A case is discussed of a patient who presented in extremis after a stab wound to the right ventricle. He underwent successful resuscitation using a Foley catheter both for hemostasis and for administration of resuscitation fluids. While not commonly employed in cardiac trauma management, this technique may permit increased salvage due to its simplicity and speed.

Adult↗
PubMed1985

The effect of autonomic agonists and nerve stimulation on protein secretion from the rat submandibular gland.

Saliva samples were obtained from the cannulated duct of the rat submandibular gland following intravenous administration of the autonomic agonists, acetyl beta-methyl choline (methacholine), phenylephrine and isoprenaline and by stimulating sympathetically at 5 and 20 Hz. Phenylephrine and isoprenaline produced a saliva approximately 50-fold richer in protein than that induced by methacholine. Protease activity was greatest in saliva induced by phenylephrine. Methacholine, phenylephrine and isoprenaline caused the secretion of markedly different protein populations, determined by separation on SDS-polyacrylamide gradient gels followed by staining with Coomassie Brilliant Blue R250. Many species in the molecular weight range 10000-40000 were secreted in response to phenylephrine and isoprenaline. Methacholine produced a saliva poor in protein and the resulting electrophoretic banding patterns were faint. Staining with periodic acid-Schiff's reagent showed that the largest protein species (mol. wt. 150000) secreted in response to isoprenaline was glycosylated and that small quantities of a similar protein were present in saliva produced by methacholine and phenylephrine but were not visualized by staining with Coomassie Brilliant Blue R250. Phosphorylated proteins of molecular weights 30000-35000 and 38000-45000 were detected in saliva produced by isoprenaline but not in saliva produced by methacholine or phenylephrine. Stimulation of the cervical sympathetic trunk at 5 Hz yielded a population of salivary proteins, many of which behaved similarly on electrophoresis to proteins secreted in response to isoprenaline. At 20 Hz a different population was secreted, resembling that present in phenylephrine-induced saliva.

Adrenergic Agonists↗