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Biomedical subjects

J Berger

Publications and source records attributed to J Berger.

At least 343 records · Page 19Linked to original sources

A comparison of benflurone effects after intravenous infusion or oral administration. A study on laboratory rats.

The effects of oral administration and intravenous infusion of benflurone were compared using the single dose of 100 mg/kg b.w. Oral administration of benflurone induced more moderate changes in both white and red blood picture than the equal dose of orally administered cyclophosphamide. In contrast to oral benflurone administration, intravenous benflurone induced deep anaemia, deep reticulocytopenia, transient neutrophilia and slight decrease in small lymphocyte counts. The recovery from intravenous benfluorone effects was rapid.

Administration, Oral↗

HEMA-particles phagocytosis of rat neutrophils.

A micromethod for testing of phagocytosis employing synthetic hydrophilic HEMA particles seems to be suitable for an examination of rat neutrophils. The normal phagocytic activity was 53.7 +/- 1.4%, phagocytic index 8.2 +/- 0.7, and the number of phagocytosing neutrophils was found to be 74 +/- 5.10(6)/l. Using HEMA particles, an experimentally induced depression of rat neutrophil phagocytosis after cyclophosphamide or benflurone was well detected and quantified.

Animals↗

Comparative potency of atropine sulphate and glycopyrrolate on heart rate in man.

Disagreement as to the effect of glycopyrrolate and atropine sulphate at various dosages on heart rate has been reported in the literature. Of particular interest is the question of whether small doses of glycopyrrolate cause bradycardia. Three groups of subjects were studied. The QRS complexes of the electrocardiogram were continuously recorded on a microcomputer. Group 1 consisted of 10 healthy volunteers who were given two doses of atropine sulphate 1.25 micrograms kg-1 and glycopyrrolate 0.75 micrograms kg-1, in random order at two different times, i.v. Monitoring continued until heart rate returned to baseline. Group 2 consisted of 24 women, ASA class I or II, scheduled for gynaecological operations. Each patient received fractionated i.v. doses of either atropine sulphate 2.5, 2.5 and 5 micrograms kg-1 or glycopyrrolate 1.5, 1.5 and 3.0 micrograms kg-1 at 3-min intervals. Heart rate was measured continuously for 1 h before drug injection and for 10 min after the last dose. Group 3 consisted of six volunteers given both drugs in the same dose and time schedule as Group 2, but heart rate was monitored for 180 min after the last dose. In Group 1, the incidence of bradycardia and increases in heart rate after the first dose were statistically significant for both atropine sulphate and glycopyrrolate when compared with baseline values. In Group 2, both drugs significantly increased the heart rate and had similar times to peak effect. In Group 3, bradycardia occurred only with atropine sulphate. Increases in heart rate, peak heart rate and duration of action were similar with both drugs.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗

A double-blind evaluation of ciladopa in Parkinson's disease.

We evaluated 32 patients with Parkinson's disease in a double-blind, parallel group, placebo-controlled study with ciladopa (a troponylpiperazine derivative). The dosages administered were 5 mg b.i.d. and 15 mg b.i.d. Significant improvement was found in the gait scores and in the total disability scores in the high dose group (p less than 0.05). In addition, there was a trend toward improvement, though not significant, in the bradykinesia and rigidity scores in the high dose group and in the disability scores in the low dose group. Four patients in the low dose group and five patients in the high dose group decreased their Sinemet doses while no patients increased their Sinemet dose. There were no adverse effects observed in this study. These findings suggest that ciladopa may be an efficacious agent in Parkinson's disease. The low incidence of adverse effects with this agent suggests that higher doses may be utilized and may prove to be more effective.

Aged↗

Distribution pattern of peripheral lymphocyte subsets in localized and generalized form of onchocerciasis.

The relationship of peripheral lymphocyte subpopulations to the generalized and localized form of onchocerciasis has been studied in 43 Liberian (West African) patients. Typing revealed a significantly increased proportion of lymphocytes expressing interleukin 2 or transferrin receptors in the localized form of onchocerciasis (African sowda) when compared to subjects with a generalized form and those without signs of onchocerciasis. Patients with African sowda showed a higher number of helper/inducer T cells, a greater ratio of helper/inducer: suppressor/cytotoxic T cells, and an increased number of DR antigen-positive cells and lymphocytes with a natural killer cell phenotype. Furthermore, the serum concentrations of immunoglobulins, particularly IgE an IgG, and antifilarial antibodies were significantly elevated in sowda patients in comparison to the generalized form and the controls. These results indicate that both forms of onchocerciasis represent different immunological types of host responsiveness and that African sowda might be associated with an increased compartment of activated T lymphocytes.

Antibodies, Monoclonal↗

Expression of active, membrane-bound human placental alkaline phosphatase by transfected simian cells.

Human placental alkaline phosphatase (PALPase) has been transiently expressed in simian (COS) cells by transfection with a eukaryotic expression vector containing the corresponding cDNA. The level of expression of PALPase was high, and it was produced in an enzymatically active form. The bulk of PALPase was associated with the cell membrane as shown by immunocytochemistry and subcellular fractionation studies. The PALPase produced by transfected COS cells, like PALPase in human tissue, was specifically released from the intact cells in a hydrophilic form by phosphatidylinositol-specific phospholipase C and is, therefore, apparently attached to the outer membrane by means of a phosphatidylinositol-glycan. Transfected COS cells appear to be an excellent model for elucidating the mechanism of attachment of this phosphatidylinositol-glycan to a protein moiety.

Alkaline Phosphatase↗

Characterization of the phosphatidylinositol-glycan membrane anchor of human placental alkaline phosphatase.

Placental alkaline phosphatase [orthophosphoric-monoester phosphohydrolase (alkaline optimum), EC 3.1.3.1] is a member of a diverse group of membrane proteins whose attachment to the lipid bilayer is mediated by a phosphatidylinositol-glycan. To investigate structural aspects of the glycolipid anchor, cultured WISH cells were used because we found that they produce the enzyme in abundant quantities. When cell suspensions were incubated with purified phosphatidylinositol-specific phospholipase C, most of the placental alkaline phosphatase was released from membranes in a hydrophilic form. On incubation of the cells with [14C]ethanolamine, [14C]myristic acid, or myo-[3H]inositol, each was incorporated into the phosphatase near the carboxyl terminus, showing that these components, which are found in other phosphatidylinositol membrane-linked proteins, are also present in placental alkaline phosphatase.

Alkaline Phosphatase↗

Cloning and sequencing of human intestinal alkaline phosphatase cDNA.

Partial protein sequence data obtained on intestinal alkaline phosphatase indicated a high degree of homology with the reported sequence of the placental isoenzyme. Accordingly, placental alkaline phosphatase cDNA was cloned and used as a probe to clone intestinal alkaline phosphatase cDNA. The latter is somewhat larger (3.1 kilobases) than the cDNA for the placental isozyme (2.8 kilobases). Although the 3' untranslated regions are quite different, there is almost 90% homology in the translated regions of the two isozymes. There are, however, significant differences at their amino and carboxyl termini and a substitution of an alanine in intestinal alkaline phosphatase for a glycine in the active site of the placental isozyme.

Alkaline Phosphatase↗

Chemical immobilization of free-ranging North American bison (Bison bison) in Badlands National Park, South Dakota.

Twenty-six free-ranging North American bison (Bison bison) (22 adult bulls, one yearling male and three adult females) were immobilized using a combination of carfentanil and xylazine. For carfentanil the dose range (mean +/- SD) was 1.8-5.0 micrograms/kg (2.4 +/- 0.7 micrograms/kg) and for xylazine 0.004-0.125 mg/kg (0.07 +/- 0.03 mg/kg). Induction time (mean +/- SE) was 14.2 +/- 2.9 min (median 8 min), while the total mean reversal time after administration of a narcotic antagonist was 9.0 +/- 1.4 min (median 8 min). Only one animal that received the highest initial dose of carfentanil (2.5 mg) showed evidence of becoming "re-narcotized." Five animals required two or more doses of carfentanil before becoming immobilized. Overall, small volumes of drug used (mean = 0.62 ml for carfentanil, 0.53 ml for xylazine) enabled the use of 1 to 2 ml darts, increasing both accuracy and impact safety. Darting success approached 100%.

Anesthesia, General↗

Haematological preclinical recording of adverse drug reactions--current status, problems, and needs. Part I: Standardization of experiments in relation to haematological examination.

The influences of sampling factors, such as age, health of laboratory animals, environmental conditions, and procedures on the standardization of haematological tests in safety drug evaluations performed on animals are discussed. Problems concerning formation and interpretation of haematology reference data are briefly analysed.

Age Factors↗

Age-related sensitivity of rats to induction of anaemia.

The intensity of symptoms of experimental anaemia significantly depended on the age of animals. It increased in elder rats after administration of substances with haemolytic potential (phenylhydrazine, phenacetin, 3-chloro-4-benzyloxyphenylacetic acid, nitrobenzene) whereas it decreased after cyclophosphamide-induced erythropoietic suppression.

Age Factors↗