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The aim of this study was to determine the influence of unilateral, intraovarian infusions of Escherichia coli endotoxin (LPS, lipopolysaccharide, serotyp 055:B5) on the concentration of progesterone (P4), testosterone (T), estradiol-17ß (E2) and luteinizing hormone (LH) in peripheral and ovarian blood plasma of gilts. The morphology of ovaries was also estimated. Fourteen sexually matured gilts with controlled estrous cycle were used. The animals were randomly divided into two groups: I (treated; n=7), and II (control; n=7). In the group I, 2 mg of LPS in 1 ml of saline was infused into the hilus of one ovary from the 15th to the 19lh day of the estrous cycle, twice a day (at 06:00 and 18:00). At the same time, 1 ml of saline was infused into the hilus of the contralateral ovary and into both ovaries of the control gilts (Gr. II). From the 15lh to the 7th day of the next estrous cycle blood samples from the jugular vein were collected with various frequency. Additionally, on the 7th day, during the laparotomy, blood samples from the utero-ovarian vein of each ovary were collected and then both ovaries were dissected out to estimate their morphology. Plasma hormone concentrations were determined by radioimmunoassay (RIA). Macroscopic investigation revealed the presence of cysts in both ovaries after unilateral, intraovarian LPS infusions but the number of cysts in the LPS-treated ovaries was higher (P < 0.05) than that in the contralateral ones. In LPS-infused ovaries, numbers of follicles and corpora lutea were lower (P < 0.05) than those in the contralateral and control ovaries. In LPS-treated gilts, P4 concentrations in peripheral blood was increased (P < 0.05-0.001) as compared to that found in the control group in the period from the 21lh to the 7lh day of the next estrous cycle. After LPS infusions, the level of P4 in blood plasma from the utero-ovarian vein of both ovaries was higher (P < 0.05) than that observed in the control group. Moreover, the concentration of P4 was higher (P < 0.05) in LPS-infused ovary than that found in the contralateral one. During the consecutive days of the study, the T level in peripheral and ovarian blood remained unchanged in both the control and LPS-treated groups. In the gilts receiving LPS, the peripheral level of E2 decreased (P < 0.01-0.001) as compared to that found in the control animals from the 20th to the 7lh day of the next estrous cycle. On the 7lh day, the plasma concentration of E2 in the utero-ovarian vein was lower in LPS-treated gilts (P < 0.05) than that found in the control group. This study revealed that infusions of LPS into the hilus of one ovary in gilts caused morphological changes in both ovaries and deviations from normal plasma hormonal profiles. These disturbances partly depended on the location of LPS infusions. The results obtained suggest that the pathologically changed ovary can affect the pituitary function and steroidogenesis of the contralateral ovary what leads to disturbances in the physiologic rythm of the estrous cycle in females.
The present study was designed to examine the influence of Escherichia coli endotoxin (LPS, lipopolysac- charide) on the concentration of gonadotrophin-releasing hormone (GnRH) in the hypothalamus and luteinizing hormone (LH) in the pituitary as well as LH, prolactin (PRL), Cortisol (CI), and sex steroids in blood plasma of prepurtal gilts. In the ovaries, LH/human chorionic gonadotropin (hCG) receptors content was also estimated. The experiment was performed on 10 prepubertal gilts (Large White x Landrace) at the age of 156 ± 2 days (body weight 65.7 ± 3.56 kg, mean + SD). The animals were randomly assigned to one of two groups: 1) treated with Escherichia coli endotoxin (serotype 055:B5; n = 5), and 2) control gilts receiving saline (n = 5). 2 mg of LPS was administered i.m., twice a day (at 08:05 and 20:05) for 4 days. Blood samples from the jugular vein were collected every hour for 12 h (08:00/time 0 - 20:00), for 4 days of the study and more frequently during 4 h (08:00/time 0 - 12:00) sampling periods every day of the experiment. All the gilts were slaughtered on the next day, after the last LPS or saline injections were performed and then, the ovaries, hypothalamus and pituitary were immediately dissected out. Plasma and tissue hormone concentrations were analysed by radioimmunoassay (RIA). During the experimental period, rectal temperature in LPS-treated gilts was higher (on the 1st' and 2nd day - P < 0.001, on the 3th and 4th day - P < 0.05) than that found in the controls. During the whole experiment mean concentrations of CI in the gilts treated with LPS were higher (P < 0.05 - P < 0.001) in comparison to those observed in the controls. In the gilts receiving LPS, plasma LH was lower (P < 0.01, P < 0.001) than that found in the control animals on days 1-4 of the study. Injections of LPS did not affect the frequency, amplitude or duration of LH peaks. In LPS-treated group, plasma PRL was decreased (P < 0.05, P < 0.01) on the 4th day of the experiment in comparison to that found in the control group. During the consecutive days of the study, the levels of androstenedione (A4), testosterone (T) and estradiol-17ß (E2) remained unchanged in both control and LPS-treated gilts and no significant differences between both groups were found. GnRH content in the hypothalamus and LH in the pituitary varied insignificantly between the groups showing tendency to a slight decrease in the gilts receiving LPS. In the ovaries of LPS-treated animals, the concentration of LH/hCG receptors slightly decreased as compared with that found in the control gilts. The results obtained indicate that administration of LPS to prepubertal gilts causes a decrease in plasma LH and PRL concentrations, an increase in Cortisol level and a slight decrease in numbers of LH/hCG receptors in the ovaries. These findings suggest also that pathological states altering secretion of the pituitary hormones can impair processes leading to puberty in a female.
The subject of this wprk was the investigation of luteinizing hormone, progesterone, testosterone and total estrogens concentration in the peripheral plasma of 56 gilts with experimentally-induced hypo- and hyperthyroidism and with ovarian cystic degeneration. The blood samples were collected from the cannulated jugular vein at 19-23 days after last natural estrus, 5-10 times daily. The experiments resulted in significant deviations in plasma hormone profile during the periestrous period. The hypothyroid gilts showed a significant increase but hyperthyroid animals a decrease in level of LH accompanied by a significant peak of estrogens on the 22nd day of cycle. The cyst-bearing gilts exhibited a decreased level of LH, an increased concentration of progesterone and a changeable content of estrogens. It may be suggested that abnormalities in hormonal pattern in experimental gilts were caused by derangement of functional interrelationships in the pituitary-thyroid-ovarian axis which influence sex hormone synthesis and release.
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