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Biomedical subjects

J Eapen

Publications and source records attributed to J Eapen.

At least 19 recordsLinked to original sources

The plastic envelope method, a simplified technique for culture diagnosis of trichomoniasis.

Although culture of Trichomonas vaginalis is more sensitive than wet mounts in the diagnosis of trichomoniasis, the lack of convenience of culture prevents it from being widely used. To improve the acceptability of diagnosis by culture, a plastic envelope method (PEM) was devised. PEM permits both immediate examination and culture in one self-contained system. The medium consists of dry ingredients that are reconstituted with water before use. The effectiveness of immediate examinations by PEM was compared with that of wet mounts, and the effectiveness of culture by PEM was compared with that of culture in Trichomonas Medium No. 2 (Oxoid). Of 710 vaginal secretion specimens from symptomatic and asymptomatic women that were tested by the four methods, 62 (9%) were positive for T. vaginalis. The sensitivity was 66% by wet mount, 66% by immediate examination by PEM, 89% by cultures in Oxoid medium, and 97% by culture by PEM. The two culture methods had equivalent sensitivities but were significantly (P less than 0.0001) more sensitive than the two immediate methods. The combined immediate examination by PEM plus culture was more convenient to use than wet mounts plus culture in Oxoid medium. The long shelf-life of PEM's dry medium and its anticipated low cost are additional advantages.

Animals↗

Differences in lipid peroxidation of rat liver rough and smooth microsomes.

The rough and smooth microsomes of rat liver show significant differences in lipid peroxidation induced by both NADPH and ascorbate. The parameters studied include kinetics, response towards cofactors and sensitivity to inhibitors. Smooth microsomes are more prone to lipid peroxidation with increasing concentrations of NADPH, Fe3+, ascorbate and Fe2+, and are more susceptible to inhibitors than rough microsomes. Smooth microsomes also contain higher amounts of ascorbic acid, NADPH cytochrome c reductase and total lipids, besides possessing a higher degree of unsaturation in lipids, all of which promote lipid peroxidation. Our results suggest that, although smooth microsomes are more sensitive to lipid peroxidation, they are compensated for by being more sensitive to inhibitors of lipid peroxidation.

Animals↗

Age-related effect of cycloheximide on lipid peroxidation in rough and smooth microsomes of rat liver.

Cycloheximide, at a nonlethal dose of 2 mg/kg body weight, has different effects on microsomal in vivo lipid peroxidation in different age groups. In general, the antibiotic increases microsomal lipid peroxidation in newborn and 1-year-old rats, but decreases it in 15- and 75-day-old rats. Low doses of cycloheximide induces lipid peroxidation in vitro whereas higher doses cause inhibition. The degree of change differs in the two microsomal fractions. The sucklings are more susceptible to such a change than the older rats. In vivo lipid peroxidation in rat liver homogenate and rough and smooth microsomes declines as a function of age. Smooth microsomes show more lipid peroxidation than the rough in the different age groups.

Aging↗

Effect of cycloheximide on hepatic microsomal lipids as a function of age in rats.

Cycloheximide, at a non-lethal dose of 2 mg/kg body weight, increases the level of total lipids and major lipid fractions in total, rough and smooth liver microsomes obtained from suckling, adult and old rats, but not in the newborns. The rates of increase differ in the different age-groups and fractions. Total lipids and phosphatidyl choline of rough and smooth microsomes in adult rats reach control levels at 6 h after the antibiotic treatment. Phospholipid fractions of old rats tend to approach control levels by 6 h after treatment whereas cholesterol levels remain relatively high. Total lipids, phosphatidyl choline and phosphatidyl ethanolamine of total, rough and smooth microsomes show significant quantitative differences during development.

Aging↗

Effect of cycloheximide on deciduoma morphogenesis and implantation in rats.

Intraperitoneal administration of cycloheximide (1 mg/kg body weight) to rats immediately after an artificial deciduoma induction inhibits the development of decidual tissue. Besides inhibiting the differentiation of stromal to decidual cells, wet weight and levels of uterine protein and RNA are low following the antibiotic treatment. Injection of the drug (1 mg/kg body weight) into pregnant rats, either on the eve of Day 4 or in the morning of Day 5 of pregnancy, does not prevent implantation but interferes with the growth of embryos.

Animals↗

Effect of whole-body x-irradiation on the morphogenesis of rat deciduoma.

Exposure of rats to whole-body X-irradiation (600 R) within 30 minutes of artificial induction of deciduoma resulted in impaired growth of deciduoma involving both endometrium and myometrium. Protein synthesis in endometrium was low 2 days after X-irradiation when compared with unirradiated controls. In addition, levels of RNA and DNA were low in the endometrium of irradiated rats. Development of metrial gland was inhibited in the irradiated rats. The number and morphology of antimesometrial and mesometrial decidual cells were altered in the irradiated animals. Endometrial and myometrial soluble proteins of irradiated rats resolved into fewer bands than those of unirradiated animals.

Animals↗

Protein anabolism in endometrium and myometrium during the growth of induced deciduoma in rats.

Protein anabolism in the endometrium and myometrium was studied during the growth of induced deciduoma in terms of incorporation of [14C]-leucine into proteins. The data show that the specific activity of the proteins was highest 2 days after decidualisation. Protein synthesis in the endometrium studied on that day as a function of time after injection of the labelled amino acid showed a steady increase during the first 2 h. Cycloheximide (2 mg/kg b.wt) administration produced nearly 95% inhibition of protein synthesis in endometrium as well as in myometrium.

Animals↗

The metabolic fate of [35S]-diallyl disulphide in mice.

Diallyl disulphide (DADS) is a major constituent of garlic oil. Uptake of [35S]-labelled diallyl disulphide by mouse liver is highest at 90 min after treatment with [35S]-DADS, 70% of the radioactivity is present in the liver cytosol of which 80% is metabolized to sulphate.

Allyl Compounds↗