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The aim of the study was to determine an in vitro effect of specific agonists of opioid receptors on basal prolactin secretion and in the presence of dopamine or thyreoliberin (TRH) by porcine anterior pituitary cells. The cells were isolated from anterior pituitaries of gilts on days 8–10, 15–17 and 19–21 of the oestrous cycle and submitted to in vitro culture with mu-, delta- and kappaopioid receptor agonists – FK 33-824, DPLPE and U 50,488, respectively. Differentiated effects of the opioid agonists on prolactin secretion by isolated pituitary cells of gilts in chosen days of the oestrous cycle were shown. In the midluteal phase (days 8–10), a reduced prolactin secretion was demonstrated after activation of mu-, delta- and kappa-opioid receptors under all tested conditions. In the early follicular phase (days 15–17), the activation of mu-, delta- and kappa-opioid receptors increased prolactin secretion under basal conditions, as well as mu- and delta-opioid receptors – in the presence of TRH, but the stimulation of mu- and kappa-opioid receptors reduced the hormone secretion in the presence of dopamine. In the late follicular phase (days 19–21), kappa-opioid receptor agonist stimulated prolactin secretion under all tested conditions. The activation of mu- and delta-opioid receptors increased prolactin secretion under basal conditions and in the presence of dopamine, but decreased – in the presence of TRH. The results suggest a possibility of diverse participation of endogenous opioids, depending on stage of the oestrous cycle, in the modulation of prolactin secretion at the pituitary level in gilts during the oestrous cycle.
The expression of mu (μ), delta (δ) and kappa (κ) opioid receptors was determined in vitro under the basal conditions as well as in the presence of cytokines (interleukin (IL)-1β, IL-6 and tumor necrosis factor α (TNFα)) in the endometrium of gilts on days 10–11, 12–13 and 15–16 of the oestrous cycle and pregnancy. These days were chosen due to their importance for the establishment of pregnancy in pigs. During the oestrous cycle, the basal expression of μ opioid receptor mRNA in endometrial explants was greater on days 10–11 than on days 12–13 and 15–16, during pregnancy its expression was greater on days 12–13 than on days 10–11 and 15–16. The expression of δ opioid receptor mRNA did not change during the cycle, but during pregnancy it was the greatest on days 10–11. The expression of κ opioid receptors did not significantly change during studied periods. The cytokines affected the expression of μ and δ, but not κ opioid receptors in endometrial explants. The expression of μ opioid receptor mRNA was significantly decreased by IL-1β on days 10–11, but IL-6 increased and decreased it on days 12–13 and 15–16 of the cycle, respectively. During pregnancy, the expression of μ opioid receptor mRNA in endometrial explants was increased by IL-1β, IL-6 and TNFα on days 10–11, decreased by IL-1β on days 12–13, and increased by TNFα on days 15–16. During the oestrous cycle, the expression of δ opioid receptor mRNA was elevated by IL-1β on all studied days, by IL-6 on days 10–11 and 12–13, and by TNFα on days 15–16. During pregnancy, IL-1β increased the expression of δ opioid receptor transcript on days 12–13. These data suggest that opioid receptors participate in a local regulation of uterine functions in gilts during the oestrous cycle and early pregnancy and their endometrial expression can be modulated by cytokines.
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