Ledwozyw A, Kadziołka A
Zakład Patofizjologii Wydziału Weterynaryjnego AR w Lublinie.
Pol Arch Weter. 1989;29(3-4):79-92.
Cysteinyl leukotrienes C4, D4 and E4 elicited concentration-dependent contractile response of pregnant and non-pregnant pig uterine strips during incubation in De Jalon solution in concentrations between 1 x 10(-9)M and 1 x 10(-5)M for LTC4 and LTD4, and between 1 x 10(-8)M and 1 x 10(-5)M for LTE4. The maximum contractions elicited by leukotrienes were 77.5 +/- 3.0%, 86.0 +/- 2.6% and 37.5 +/- 2.5% of these elicited by histamine 1 x 10(-5)M for LTC4, LTD4 and LTE4, respectively. FPL 55712, leukotriene end-organ antagonist, antagonized the uterine contractile response to cysteinyl leukotrienes in dose-dependent manner. Indomethacin, an inhibitor of cyclooxygenase pathway of arachidonic acid metabolism also antagonized leukotriene-induced contractions of pig uterus. Pregnant uteri were more susceptible to leukotriene action than non-pregnant uteri, and response increased parallelly with advancement of pregnancy. These results demonstrate that LTC4, LTD4 and LTE4 possess significant uterine contractile activity in domestic pig, which may partially be mediated indirectly via cyclooxygenase products of arachidonic acid metabolism.
在德哈隆溶液中孵育期间,半胱氨酰白三烯C4、D4和E4在1×10⁻⁹M至1×10⁻⁵M(LTC4和LTD4)以及1×10⁻⁸M至1×10⁻⁵M(LTE4)的浓度范围内,引起妊娠和未妊娠猪子宫条的浓度依赖性收缩反应。白三烯引起的最大收缩分别为1×10⁻⁵M组胺引起的收缩的77.5±3.0%、86.0±2.6%和37.5±2.5%,分别对应LTC4、LTD4和LTE4。白三烯终末器官拮抗剂FPL 55712以剂量依赖性方式拮抗子宫对半胱氨酰白三烯的收缩反应。吲哚美辛,一种花生四烯酸代谢环氧化酶途径的抑制剂,也拮抗白三烯诱导的猪子宫收缩。妊娠子宫比未妊娠子宫对白三烯作用更敏感,且反应随妊娠进展而平行增加。这些结果表明,LTC4、LTD4和LTE4在家猪中具有显著的子宫收缩活性,这可能部分通过花生四烯酸代谢的环氧化酶产物间接介导。