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Biomedical subjects

C Nolan

Publications and source records attributed to C Nolan.

At least 55 records · Page 3Linked to original sources

An outbreak of Yersinia enterocolitica infections caused by contaminated tofu (soybean curd).

The authors investigated 50 Yersinia enterocolitica infections during an outbreak of illness due to contaminated tofu (soybean curd) in Washington State between December 15, 1981 and February 22, 1982. The most common clinical syndrome (36 patients) was gastrointestinal infection for which two patients underwent appendectomies and one a partial colectomy. Of the remaining 14 patients, six had extraintestinal infections, two had fever alone, and six were asymptomatic. The patients with enteric infections were younger (median age three years) than those with extraintestinal infections (median age 28 years). In a case-control study of enteritis patients, illness was associated with ingestion of one brand of tofu (p less than 0.01). Ninety-two per cent of patients with gastrointestinal infections and 33% with extraintestinal infections recalled having eaten the implicated product. Y. enterocolitica serotype O:8, the most common serotype isolated from patients, was also isolated from tofu and the plant's untreated spring water. There was little clinical or laboratory evidence of secondary spread to family members who did not eat tofu. The outbreak demonstrates the transmission of Y. enterocolitica from nature to man and the potential of "natural" foods as vehicles for environmental pathogens.

Adolescent↗

Survey of plasmids and resistance factors in Campylobacter jejuni and Campylobacter coli.

A total of 688 isolates of Campylobacter jejuni and Campylobacter coli were screened for the presence of plasmid DNA by agarose gel electrophoresis and were tested for susceptibility to ampicillin, chloramphenicol, erythromycin, streptomycin, and tetracycline. Of the isolates examined, 32% were noted to harbor plasmid DNA, ranging in size from 2.0 to 162 kilobases. Only tetracycline resistance was noted to correlate with the presence of plasmids. Plasmids capable of transferring tetracycline resistance via conjugation ranged in size from 42 to 100 kilobases. The Bg/II and Bc/I restriction endonuclease profiles of 31 plasmids examined showed marked diversity in their banding patterns. Although a high degree of DNA-DNA homology was noted among the Campylobacter spp. plasmids, no homology was noted between these plasmids and tetracycline R factors commonly found in the family Enterobacteriaceae.

Anti-Bacterial Agents↗

Animal models of male infertility: mice bearing single-gene mutations that induce infertility.

Genetically defined mouse models of male infertility are described in the present report. The mice were rendered infertile by one of the following gene mutations: Ames dwarf, dwarf, flipper-arm, hightail, hypothyroid, little, pygmy, stubby. The effects of each gene mutation on testicular steroidogenesis and spermatogenesis were elucidated by a comparison of the mutant mice to their normal siblings. Testicular steroidogenesis was assessed directly by determining steroid secretion by testes perfused in vitro. The study provides the first comprehensive assessment of testicular function in the mutant mice. The eight gene mutations can be classified into two groups based on the results. One group of gene mutations (Ames dwarf, dwarf, flipper-arm, pygmy) specifically depress spermatogenesis and testicular steroidogenesis. The infertility of these mutant mice can be linked to the lowered total sperm production. The second group of gene mutations (hightail, hypothyroid, little, stubby) do not specifically depress either spermatogenesis or testosterone secretion. Subsequently, the etiology of the male infertility of the second group of mutant mice is unknown. We propose that these mutant mice provide valuable experimental tools for the study of male infertility and male reproduction.

Animals↗

Quantitative metabolic profiling of testicular steroid secretions with bonded-phase capillary gas chromatography.

A procedure is described for quantitative metabolic profiling of nine steroids secreted by mouse testes. The procedure incorporates Celite column chromatography and a gas chromatograph equipped with a bonded-phase capillary column. Validation tests demonstrated that the procedure is precise, efficient, sensitive, and capable of providing information about the spectrum of steroids secreted by testes perfused in vitro. The procedure was used to determine the effect of the hemimelic extra toes gene mutation on the steroidogenic potential of inbred mouse testes perfused in vitro.

Animals↗

Heavy metal uptake and intracellular binding in isolated gill preparations of Mytilus galloprovincialis L.

An in vitro study was performed on the uptake and subsequent binding to protein of heavy metals in isolated gill preparations of Mytilus galloprovincialis. The metals used in the study were Cd, Zn, Hg, V, Cr, Te, Tl, As and Tc. Experiments were conducted for one hour and the disappearance of metals from the water correlated with final gill-metal concentrations. Distribution of metal between 105,000 g cytosol and pellet was determined, as was the association of each metal with cytosol protein following gel-filtration chromatography. Results indicate that all metals are accumulated by the gills but that the uptake kinetics vary with each metal. Similarly, the association of each metal to protein varied for each type.

Animals↗

Leydig cell function in the absence of an intact Y chromosome.

Sex-reversed mice (X/X Sxr) provide a unique opportunity to study Leydig cell function in the absence of an intact Y chromosome. We determined the impact that the absence of an intact Y chromosome has on Leydig cell function by comparing the steroid secretion profiles of in vitro perfused testes from X/X Sxr and X/Y mice. All the testes were maximally stimulated with luteinizing hormone (LH). Nine steroids were extracted from the venous effluent of the in vitro perfused testes and quantified by capillary gas chromatography. A radioimmunoassay was employed to determine the estradiol secretion rate. Secretion rates (ng/h . testis) of seven steroids, including testosterone, did not differ significantly. Testes from X/X Sxr mice secreted more (P less than 0.05) dehydroepiandrosterone and androstenedione than X/Y mouse testes. Importantly, X/X Sxr and X/Y mouse testes secreted the same total amount of steroids, although X/X Sxr mouse testes weigh 17 mg while X/Y mouse testes weigh 110 mg. Histological studies established an increase in the relative mass of Leydig cells and the complete absence of germ cells in X/X Sxr mouse testes. The results suggest that the normal differentiation of steroidogenic pathways occurs in X/X Sxr mouse tests in the absence of an intact Y chromosome.

Animals↗

Persistent Campylobacter jejuni infection in an immunocompromised patient.

Recurrent bacteremia and enteritis due to a specific serotype of Campylobacter jejuni occurred over a 12-month period in a patient on hemodialysis with systemic lupus erythematosus who was also deficient in serum IgA and IgM. A bactericidal defect in the patient's sera for C. jejuni was shown. A role for immunoglobulins in the host response to C. jejuni is suggested, in that the IgA deficiency may have predisposed the patient to chronic gastrointestinal carriage and because the resolution of the bacteremia corresponded with the delayed appearance in the blood of IgG specific for the infecting strain.

Adult↗

Insulin-induced glucose utilization influences triglyceride metabolism.

1. We have investigated the possibility that the effect of insulin on triglyceride metabolism is related to the individual's responsiveness to insulin-mediated glucose utilization. Changes in plasma triglyceride levels were determined during 2 h infusions of insulin with glucose that maintained euglycaemia in 17 subjects, some of whom were overweight and/or hypertriglyceridaemic. 2. Plasma triglyceride concentrations fell in most subjects (mean +/- SD: 19.9 +/- 13.0%). The percentage fall in plasma triglyceride was inversely related to body mass index (r = -0.64, P less than 0.01) and to basal triglyceride concentration (r = -0.69, P less than 0.005), but directly to insulin sensitivity (r = +0.48, P less than 0.05), and was unrelated to plasma free fatty acid concentration. 3. Since insulin sensitivity was also related to body mass index and basal triglyceride level stepwise regression analysis was carried out to determine the influence of these three variables on insulin-mediated lowering of plasma triglyceride. The percentage fall in plasma triglyceride remained independently related to insulin sensitivity (P less than 0.05) and to body mass index (P less than 0.05), and these two variables accounted for 44% of the fall in triglyceride. 4. Resistance to insulin (in terms of glucose utilization) may therefore be one significant, independent factor determining the plasma triglyceride concentration.

Adult↗

Monoclonal antibodies to human estrogen receptor.

Extranuclear estrogen receptor protein (estrophilin) of MCF-7 human breast cancer cells was purified by passage of the cytosol fraction of a cell homogenate through an affinity column of estradiol linked to Sepharose by a substituted di-n-propyl sulfide bridge in the 17 alpha position. Elution with 50 micro M [3H]estradiol in 10% (vol/vol) dimethyl formamide/0.5 M sodium thiocyanate gave 40% recovery of [3H]estradiol-estrophilin showing 14% of the specific radioactivity expected for the pure complex. Serum from a Lewis rat immunized with this partially purified estradiol-receptor complex contained antiestrophilin antibodies that reacted not only with nuclear and extranuclear estradiol-receptor complexes from MCF-7 cells but also with estrophilin from rat, calf, and monkey uterus, hen oviduct, and human breast cancers. Splenic lymphocytes from the immunized rat were fused with cells of two different mouse myeloma lines (P3-X63-Ag8 and Sp2/0-Ag14) to yield hybridoma cultures, 2% of which produced antibodies to estrophilin. After cloning by limiting dilution, three hybridoma lines secreting antiestrophilin were expanded in suspension culture and as ascites tumors in athymic mice to provide substantial quantities of monoclonal antibodies that recognize mammalian but not avian estrophilin and that show different degrees of reactivity with receptor from nonprimate sources. By growing the clone from Sp2/0 in the presence of [35S]methionine, radiolabeled monoclonal IgG has been prepared. These monoclonal antibodies should prove useful in the study of estrogen receptors of human reproductive tissues, in particular for the radioimmunochemical assay and immunocytochemical localization of receptors in breast cancers.

Animals↗

Erythema chronicum migrans with purpura and polymorphonuclear infiltrates.

Erythema chronicum migrans with an intensely purpuric border developed in a 70-year-old woman. A biopsy specimen, in addition to showing the usual perivascular mononuclear infiltrate, demonstrated numerous polymorphonuclear leukocytes associated with leukocytoclasis. Immunofluorescence study showed vascular deposition of IgM and C3.

Aged↗

Plasminogen activator from human embryonic kidney cell cultures. Evidence for a proactivator.

The nature of the trypsin-activatable plasminogen activator produced by kidney cell cultures (Bernik, M.B (1973), J. Clin. Invest. 52, 823-834) was investigated using human embryonic kidney (HEK) cell cultures in serum-free medium. Plaminogen activator activity ratios (trypsin-activated/ untreated controls) in HEK cell-conditioned media were maximal (up to 3) during the first week of culture and remained nearly constant at approximatley 2 for the next 3-5 weeks, while the total plasminogen activator titer increased in a nearly linear manner. Therefore, coincident with progressive cell degeneration and death, the ratios decreased to near unity due to "spontaneous" activation of the enzyme, which was inhibited in cell-free conditioned media by the pancreatic trypsin inhibitor Kunitz and benzamidine. Since the activator is not inhibited by the trypsin inhibitor, it is concluded that a protease other than the plasminogen activator is responsible for the activation. Increases in the plasminogen activator titers (about 2-fold) were similarly obtained by culturing the cells in medium containing low concentrations (0.05-0.10 mug/ml) of trypsin for up to about 6 weeks. The presence of the trypsin inhibitor in HEK cells cultures decreased the rate of activation, resulting in higher activity ratios (up to 6), and the total plasminogen activator activity was reduced only minimally (less than 20%), if at all, by the highest concentration of the trypsin inhibitor (100 mug/ml) tested. Affinity chromatography of conditioned media with activity ratios of 1.6--2 separated the plasminogen activator into an active fraction and a fraction which was activated a minimum of 200-fold by trypsin and contained no measurable activity prior to activation. Gel filtration of crude conditioned media or partially purified activator separated the plasminogen activator into two peaks; both were trypsin-activatable, and their relative proportions varied with the isolated conditions. The results indicate the occurrence of a proenzyme form of the plasminogen activator in the culture media.

Antibodies↗

Immunologic similarities of thrombopoietin from different sources.

Thrombopoietin (TSF) has been detected in kidney cell culture media and human urine fractions by both a bioassay and an immunoassay using antisera raised against TSF-rich kidney cell culture medium and human urinary thrombopoietin. Both antisera cross-reacted with the 2 sources of TSF and gave essentially the same results in the HAI assay, a finding that suggests similarities in immunologic determinants of these 2 thrombopoietin preparations.

Biological Assay↗