Ograniczanie wyników

Czasopisma help
Autorzy help
Lata help
Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników

Znaleziono wyników: 50

Liczba wyników na stronie
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 3 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników

Wyniki wyszukiwania

help Sortuj według:

help Ogranicz wyniki do:
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 3 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników
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 nerve growth factor (NGF) is a polypeptide belonging to the family of trophic factors, influencing not only the population of neurons of both the central and peripheral nervous system, but also cells of the immunological and endocrine systems. The expression of NGF and/or its two types of membrane receptors (NTRK1 and TFRSF1B) was found in cells of ovaries, uterus, oviduct, fetal membranes and placenta. NGF is an important element of the regulation of the ovary functioning in sexually immature and mature females. NGF contributes to the development of the innervation of ovarian structures, stimulates proliferation of steroidogenic cells and synthesis of steroids, as well as participates in the maturation of oocytes and in ovulatory process. Moreover, NGF and neurotransmitters released by adrenergic fibres can play an important role in the formation and/or the course of polycystic ovary syndrome. During the estrous cycle, besides pregnancy NGF stimulates proliferation of uterine cells which lead to the increase of the mass of the uterus. Decreased in the middle and late period of the pregnancy, the expression of this factor in the uterus contributes to neurodegenerative changes whose effect is the reduction of contractions of the uterus. In turn the augmentation of NGF production after parturition leads to the restoration of innervation in this organ. The implication of NGF and its receptors in the functioning of the oviduct, fetal membranes and placenta has not yet been recognized.
The autonomic and sensory subdivision of the peripheral nervous system plays an important role in the control of ovarian functions, which is guaranteed by the location of nerve endings within the close vicinity of all ovarian structures. Noradrenaline participates in regulating follicle growth, ovulation and, through acting on β-adrenergic receptors, is able to increase the activity of enzymes participating in the synthesis of steroids and oxytocin, thus augmenting their production in ovarian cells. Acetylcholine, similarly to noradrenalin, also participates in the ovulation process and increases the synthesis of steroid hormones. The effect of particular neuropeptides on ovarian steroid genesis and/or ovulation may be either stimulatory or inhibitory, depending on the type of cell and steroid. It has been suggested that neurotransmitters of adrenergic, cholinergic and peptidergic nerve fibers can also influence the steroidogenic activity of ovarian cells indirectly, i.e. by regulating ovarian blood flow. The crucial role of peripheral nerve fibers in the control of particular ovarian functions has been further substantiated by results of studies related to the de-nerving of the gonad: serious disturbances in follicular development, ovulation and steroid-genesis were observed following the disruption of the intra-ovarian nerve fibers. Moreover, the prominent role of nerve growth factors in regulating ovarian functions (both the growth and maturation of follicles, as well as steroid-genesis) has recently also been emphasized. The latter, along with neurotransmitters released from adrenergic nerve fibers, may be of great importance during the course of polycystic ovary syndrome.
The study was performed on sexually mature male rats divided randomly into six groups: I – control rats; II and III – ozonized rats and receiving im injections of vitamin C at doses, respectively, 20 and 40 mg/rat, and IV and V – rats did not expose to ozone, treated with mentioned above doses of vitamin C, VI – animals only ozonized, without vitamin injections. On the ground obtained results can ascertain that oxidation stress caused by ozone disturbs process of steroidogenesis in testes leading to a decrease in the content of enzymes – P450scc and 3β-HSD, and consequently the concentrations of testosterone (T) and estradiol-17β (E₂) in gonadal tissue (in spite the elevated content P450arom) Vitamin C distinctly increases the 3β-HSD content in testes restoring the physiological T and E₂ concentrations.
In the present study, the pattern of cyclooxygenase-2 (COX-2) expression in health and inflamed porcine uteri was analyzed using real-time reverse transcriptase-polymerase chain reaction (RT-PCR),Western blot and immunohistochemistry. On day 3 of the estrous cycle, 50 ml of saline or 50 ml of Escherichia coli (E. coli) suspension containing 10⁹ colony-forming units/ml, were injected into each uterine horn of the control (n=6) and experimental gilts (n=7), respectively. This latter procedure lead to a moderately (n=3) or severely intense (n=4) acute endometritis after eight days. Expression of both the COX-2 mRNA and protein was increased in the endometrium (ENDO) of animals suffering from the moderate (P<0.05, P<0.01, respectively) and severe (P<0.01) acute endometritis, as compared to the control tissues. Moreover, COX-2 mRNA level and protein content were higher (P<0.05) in the ENDO of animals with severe than with a moderately acute endometritis. An elevation in the COX-2 gene (P<0.05) and protein (P<0.001) expression was also observed in the myometrium (MYO) of animals suffering from severe endometritis, when compared with the levels observed in MYO of both the health and moderate intensely inflamed uteri. However, both the COX-2 mRNA and protein levels were similar in MYO of the control and moderately inflamed organs. The luminal epithelium, some of uterine glands and circular layer of the MYO were more intensely stained for COX-2 in animals with severe endometritis, than in animals with healthy or moderately inflamed uteri. Nonetheless, stronger COX-2 reaction was found in some of the uterine glands in latter group, when compared to that observed in uteri of the control animals. While positive COX-2-labeling was observed in the muscular layer of all arteries supplying the health and inflamed uteri, such staining was exclusively present in the endothelium of some arteries in inflamed organs. Likewise, some arteries in uteri of the animals with severe endometritis displayed immunoreaction stronger than that found in uteri of the animals with moderate inflammation. The present study revealed an up-regulation of COX-2 mRNA and protein in the inflamed porcine uterus, which was directly related to the intensity of the organ inflammation. An increase in the COX-2 expression in the uterus challenged by E. coli-induced inflammation indicates that this enzyme is crucial for elevated prostaglandins production in the inflamed organ.
The aim of this study was to investigate whether unilateral, intraovarian infusions of bacteria might have induced morphological changes in the contralateral ovary. Eleven sexually matured gilts with controlled estrous cycle were used. The animals were randomly divided into two groups: I (Gr. I, treated; n = 4), and II (Gr. II, control; n = 7). In Gr. I, 1 ml of bacterial suspension (103 colony forming units/ml of saline of Escherichia coli, Staphylococcus aureus and Corynebacterium pyogenes, in proportion 1:1:1) was infused into the hilus of one ovary from the 15th to the 19th day of the estrous cycle. 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. On the 7th day of the next cycle, the ovaries were dissected out. There were no significant differences in the number of follicles and corpora lutea (CL) as well as in weight and size between the bacteria-infused, contralateral and control ovaries. The microscopic observations of the bacteria-infused ovaries revealed the presence of focal infiltrations of neutrophils in the softened stroma, especially around dilated blood vessels filled with erythrocytes. In the contralateral ovaries, the number of regularly distributed neutrophils in the softened stroma was greater than that found in the bacteria-treated ovaries. CL of the bacteria-infused ovaries had more numerous, dilated blood vessels than CL observed in the contralateral gonads. More neutrophils were found in CL of both ovaries in Gr. I as compared to those observed in Gr. II. In Gr. II, single neutrophils were found also in the stroma where the tip of the cannula was inserted. This study revealed that in gilts, unilateral, intraovarian administration of bacteria did not change the number of ovarian structures, the weight and size of the bacteria-infused and contralateral ovary, but induced inflammatory changes in both ovaries.
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 3 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.