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Biomedical subjects

G Csaba

Publications and source records attributed to G Csaba.

At least 469 records · Page 26Linked to original sources

The triiodothyronine antagonistic effect of gamma-L-glutamyl-taurine (litoralon).

A recently recognized bioactive substance of the parathyroid glands, gamma-L-glutamyl-taurine antagonises the metamorphosis enhancing effect of triiodothyronine. Shortening of the body-length of tadpoles is significantly delayed by the substance. The experimental results imply that it fulfills the role of a balance hormone.

Animals↗

Localization of 3H-histamine in the nucleus of Tetrahymena.

3H-histamine was incorporated by Tetrahymena partly into membrane-associated structures (cilia), partly into intra-cytoplasmic localizations, and above all into food vacuoles. A considerable amount appeared in the nucleus, in practically exclusive association with the heterochromatin.

Animals↗

Effect of oestrogenic, and androgenic and gestagenic hormones on the gametogenesis (oogenesis and spermatogenesis) in the snail Helix pomatia.

In the ovotestis of Helix pomatia both oogenesis and spermatogenesis were influenced by treatments with steroid hormones produced in the gonads of higher vertebrates. Testosterone influenced gametogenesis to a small degree. Progesterone and oestrone-acetate at first stimulated ovogenesis, but they also acted on spermatogenesis. All three hormones examined influenced oogenesis in a conspicuous and significant way, while their effect on spermatogenesis was indistinct.

Animals↗

Long-lasting effect of single ecdysone injections in newborn rats.

Single injections of ecdysone to newborn rats were followed by increases in the weights of the adrenals and decreases in the weights of the thymuses in the adults. No change was registered in body weights and in the weights of the gonads. The plasma androsterone levels seemed to decrease; however, the interindividual differences proved to be too great to draw definite conclusions.

Adrenal Glands↗

The binding of 125I-TSH to thyroid cell receptors previously deformed (in neonatal age) by gonadotropin treatment.

Single gonadotropin treatment of newborn rats caused a 63-71% decrease of TSH-binding on isolated thyroid cells prepared from thyroid glands of both 6- and 13-month-old animals. This fact points out that: (1) in newborn animals the hormone receptors are still plastic and deformable and (2) the damaging effect of the analogous hormone manifests itself at the receptor level.

Age Factors↗

Effects of H1 and H2 receptor antagonists on Tetrahymena.

In Tetrahymena pyriformis the phagocytotic rate increases in response to histamine, but neither the H1 antagonist phenindamine nor the H2 antagonist metiamide stimulate phagocytosis. The H1 antagonist counteracts the effect of histamine, whereas the H2 antagonist does not. The histamine receptor of Tetrahymena is of H1-type, since it cannot distinguish between histamine and antagonists which are closely related to it chemically. It does, however, distinguish between histamine and the chemically unrelated H1 antagonist, phenindamine. The H2 antagonist does not interact with the receptor.

Animals↗

Effects of steroids on Tetrahymena.

Phagocytosis of Tetrahymena is inhibited by prednisolone-sodium-succinate and deoxy-corticosterone-glucoside, and stimulated by dexamethasone and prednisolone. Dexamethasone and estradiol enter the cells and are localized first in food vacuoles, and later on in the cytosol. They were never found in the nucleus. The demonstration by biochemical methods of a specific glucocorticoid binding protein failed in all three subcellular fractions examined.

Animals↗

Cyclic AMP and its functional relationship in Tetrahymena: a comparison between phagocytosis and glucose uptake.

In Tetrahymena, an increase in the level of cAMP is accompanied by an increased phagocytotic rate, whereas increased sugar uptake is parallelled by a decreased cAMP level. The increase in cAMP level seems to be decisive with respect to phagocytosis as a basic phenomenon of life. In the action of epinephrine, however, some mechanism other than cAMP mediation may be involved. Depending on concentration, one hormone may provoke either an increase or a decrease in cAMP level, and this in turn triggers the corresponding function.

Animals↗

Effects of epinephrine, glucagon and insulin on glucose metabolism of planaria.

Epinephrine and insulin increased glucose uptake in Planaria, but epinephrine did so to a much grater extent. Glucagon proved to be without effect. The experiments support earlier results according to which in unicellular and invertebrate organisms membrane patterns can be found, which are similar to those of higher organisms and behave like receptors.

Epinephrine↗