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Biomedical subjects

K F Soliman

Publications and source records attributed to K F Soliman.

At least 73 records · Page 4Linked to original sources

Effect of peripheral cholinergic activation on the adrenal cortex function.

The adrenocortical response to cholinergic agonist and antagonist agents were investigated in intact, hypophysectomized and medullectomized rats. The administration of peripherally active compound neostigmine, was found to cause a significant rise of corticosterone in the intact, and the hypophysectomized animals but not in the medullectomized animals. Meanwhile, the centrally and peripherally active cholinergic agent physostigmine caused a significant rise in the intact, hypophysectomized and medullectomized animals. The results also show that the administration of the ganglionic blocker (e.g. tetraethylammonium or hexamethonium), the muscarinic agonist (pilocarpin) or the muscarinic antagonist (atropin) did not result in any significant changes in corticosterone levels. The results of these experiments might indicate that peripheral cholinergic pathway is involved in the regulation of the adrenal cortex function.

Adrenal Cortex↗

In vitro response of the regenerating adrenal gland to epinephrine.

In this experiment, the adrenal medulla was removed from male rats and after 11 days, animals were sacrificed and the adrenal glands were incubated. Addition of epinephrine to the regenerating gland resulted in significant increase in corticosterone content in the gland. However, no significant changes were observed in the intact glands after epinephrine administration. The results of this experiment suggest that epinephrine may be playing a role in the adrenal cortex function.

Adrenal Glands↗

Tissue distribution of 3H-corticosterone in response to stress.

The level and distribution of 3H-corticosterone (3H-B) was investigated in adult male Sprague-Dawley rats in response to diethyl ether stress, epinephrine (EP) and/or dexamethasone (DXM) administration. Diethyl ether stress caused a significant increase in the 3H-B counts by some of the body tissues and brain regions studied. Plasma 3H-B counts in the stressed rats were found to be twice as much as in the control animals. When EP (1.0 mg/kg) was injected, the tissue-plasma ratios(TPR) of 3H-B were significantly lower (P less than 0.05) than those of the dexamethasone (1.0 mg/kg) treated animals or the control group. The high 3H-B count in the plasma in response to diethyl ether stress or EP may indicate a decline in rate of corticosterone metabolism.

Animals↗

Dexamethasone protection against the acute lethality of ethanol in mice.

The administration of dexamethasone (DXM, 2.00 mg/kg) 1 h prior to the injection of lethal doses of ethanol was found to offer complete protection against ethanol toxicity at doses up to 5.25 g/kg and partial protection using higher doses. It is suggested that DXM central action might be involved in the protection against ehanol toxicity.

Animals↗

Pentylenetetrazol effect on adrenocortical maturation in the rat.

The effect of pentylenetetrazol on adrenal cortex maturation was investigated. Two different groups of weanling Sprague-Dawley female rats were used. At the ages of 23 and 29 days, the animals were treated with pentylenetetrazol (10 mg/kg) for 3 days. Results indicated that pentylenetetrazol decreased plasma corticosterone levels of both age groups. This treatment abolished the corticosterone diurnal variation of the 23-day-old rats, but not that of the 29-day-old rats. An increase in uterine weight was also observed in the pentylenetetrazol-treated animals. Results from this study suggest that CNS stimulation with pentylenetetrazol can alter the adrenal cortex maturation.

Adrenal Cortex↗

Diurnal rhythm of ethanol metabolism in the rat.

Male Sprague-Dawley rats injected with 2.0 g/kg of ethanol and analyzed 1 h later at 8 specific times of the day showed diurnal rhythms for alcohol concentrations in the blood, urine, brain and liver tissues. The circadian fluctuation noted for the concentrations of blood and tissue ethanol might indicate a diurnal variation in the enzymatic metabolism of ethanol.

Animals↗

The involvement of serotonin in induced ovulation in the immature rat.

In pregnant mare's serum gonadotropin (PMS) treated immature rats the cortex, cerebellum, caudate nucleus and hypothalamus were isolated and analyzed for their serotonin (5-HT) content at 6-h intervals for 72 h. Results showed a general trend of significant variation occurring in days 1 and 3 after PMS injection with no major variations observed on the second day. The results obtained suggest a possible involvement of 5-HT in the control of ovulation.

Animals↗

CNS stimulation effect on the sexual maturation of the female rat.

In the immature rat, CNS stimulants administration to pregnant mare serum gonadotropin (PMSG) primed rats resulted in significant (p less than 0.01) ovarian and uterine hypertrophy when compared to animals treated with PMSG only. Meanwhile precocious puberty was produced by pentylenetetrazol treatment alone. The results of this experiment may indicate that administration of CNS stimulants has a specific action on the release of endogenous gonadotropin.

Animals↗

Ovarian serotonin content in relation to ovulation.

In the mature cyclic female rat, analysis for ovarian serotonin content reveals comparatively high serotonin content. Fluctuation of serotonin content was observed; peak for serotonin was observed at estrus. In gonadotropin-treated immature rats, there was no detected ovarian serotonin using this procedure. It was concluded that ovaries from gonadotropin-treated immature rats are physiologically different from ovaries taken from mature cyclic rats.

Aging↗

Dexamethasone suppression of ovulation in PMS-treated immature rats.

A single injection of 2.0 mg/kg dexamethasone (DXM) administered at 51 h after pregnant mare serum gonadatropin (PMS) treatment inhibited both ovulation and luteinization. S.c. injection of human chorionic gonadotropin (HGG) caused ovulation and luteinization in DXM-PMS-treated rats, whereas treatment with ACTH failed to overcome the DXM inhibitory effect. These findings are interpreted to indicate that DXM inhibits ovulation through a mechanism which might involve the central nervous system.

Adrenocorticotropic Hormone↗

Ovarian LDH activity in gonadotropin-treated immature rats.

Lactate dehydrogenase (LDH) activity was studied in the ovaries of immature rats treated with pregnant mare serum gonadotropin (PMS). LDH activity increased sharply at 36 h after PMS injection in the ovarian tissue as well as in the blood. It was suggested that the increase of LDH activity in the ovary may be related to its increasing ability to secrete estrogen.

Animals↗

Effect of serotonin on ovulation in the fowl.

Serotonin (5-hydroxytryptamine) injected 8 hours before the expected time of ovulation effectively blocked ovulation (90%). When serotonin was administered for 10 days, the ovarian weight number follicles, adrenal weights, and ovulation rate were significantly changed (p less than or equal to .05). Serotonin or reserpine treatment induced premature oviposition if the egg was in the genital tract. It was suggested from this study that there is stimulation for ovulation at 8 hour before ovulation which can be inhibited by serotonin.

Adrenal Glands↗

Avian postovulatory follicle homogenate effect on the genital tract motility.

The recently ruptured follicles of the avian ovaries were found to contain an oxytocic substance. The substance was found to be heat-labile, nondialyzable and not extractable by lipid solvents. The crude homogenate stimulated the frequency and amplitude of the chicken infundibulum, uterus and uterovaginal junction, if they were taken from hens 2 h before predicted oviposition. The homogenate was found to induce premature oviposition and to stimulate the uterine contractions of rats treated with progesterone. Uterine tissues taken from estrogen-treated rats either did not respond to the homogenate or were inhibited. Addition of phenoxybenzamine or propanolol did not inhibit the stimulatory effect of the homogenate. It is possible that this factor might be involved in regulating oviposition in the hen.

Animals↗