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Biomedical subjects

J Itzkovitz

Publications and source records attributed to J Itzkovitz.

3 recordsLinked to original sources

Ovarian hyperstimulation in rats.

Induction of a mild hyperstimulation syndrome in the female rat, and the possible effect of the induction on prolactin, were studied using light and electron microscopy as well as radioimmunoassay. Five days of human menopausal gonadotropin (HMG) treatment were followed by human chorionic gonadotropin (HCG) administration. Ovarian hyperstimulation was observed in all treated rats, as attested to by the weight increase and by histological studies. Ovaries were enlarged 3-4 times as compared with controls, and consisted mostly of corpora lutea follicular cysts and hemorrhagic cysts. Other visceral organs remained unaffected, except for slight edematous changes observed in the lungs of the treated rats. Electron microscopic examination of the hypophysis of the treated group tends to indicate increased synthesis and secretory activity of the prolactin cells. However, serum prolactin levels of treated and non-treated groups were not different. Augmented doses of the gonadotropins did not change the findings, and only mild grade 2 ovarian hyperstimulation, according to Schenker and Weinstein (1978), could be produced in the mature rat. Thus, the rat experimental model does not seem to be comparable with the situation in the human, and cannot be used to study the pathogenesis of the disorder in the human.

Animals↗

Factors affecting sperm motility. IV. Incubation of human semen with caffeine, kallikrein, and other metabolically active compounds.

The effect of six metabolically active compounds, namely caffeine, kallikrein, cyclic adenosine 3':5'-monophosphate, prostaglandin E, triiodothyronine, and insulin on spermatozoal motility was investigated. Hypokinetic and normokinetic semen specimens from fertile and infertile patients were incubated with various concentrations of these compounds. Spermatozoal velocity and percentage of motility were determined periodically with the objective multiple exposure photography (MEP) method before and during the following 4 to 8 hours. No significant differences was found between experimental and control specimens as to these parameters under the influence of the tested compounds, with the exception of caffeine. Caffeine immediately increased the percentage of motile spermatozoa by 30% to 50% of initial values in approximately two-thirds of cases. No influence on sperm velocity was detected during this period. By using the combined MEP and supravital staining techniques it was found that nonmotile live spermatozoa were activated by caffeine without any effect on the percentage of dead sperm. Some practical implications of these findings, the difference between our results and those reported by others, and the mechanism of action of these compounds are reviewed and discussed.

Caffeine↗