Pakrasi P L, Dey S K
Prostaglandins Leukot Med. 1985 Jun;18(3):347-52. doi: 10.1016/0262-1746(85)90067-8.
In the present investigation, experiments were undertaken to determine whether a relationship does exist between cyclooxygenase and 5-lipoxygenase pathways in rabbit endometrial cells on day 6 of pregnancy. Endometrial single-cell suspensions were incubated in RPM1-1640 for 1 h under a gas phase of 95% O2 + 5% CO2 at 37 degrees C for 1 h in the presence and absence of indomethacin, a known inhibitor of cyclooxygenase or nordihydroguaiaretic acid (NDGA), a preferential inhibitor of 5-lipoxygenase. Prostaglandins (PGF2 alpha, PGE2 and 6-keto-PGF1 alpha) and 5 (S)-hydroxy-6,8,11,14-eicosatetraenoic acid (5-HETE) were measured in the media by radioimmunoassay. Indomethacin or NDGA at all concentrations used suppressed the release of PGs or 5-HETE, respectively. However, NDGA at the lowest dose (15 microM) stimulated, but at higher doses (30-60 microM) suppressed the release of PGs. On the other hand, indomethacin at both the concentrations (55 microM and 110 microM) used stimulated the release of 5-HETE. The results suggest the existence of an inverse relationship between the two pathways in the preimplantation rabbit endometrial cells.
在本研究中,进行了实验以确定妊娠第6天兔子宫内膜细胞中环氧合酶和5-脂氧合酶途径之间是否确实存在关联。将子宫内膜单细胞悬液在95% O₂ + 5% CO₂ 的气相条件下于37℃在RPMI-1640中孵育1小时,分别在存在和不存在吲哚美辛(一种已知的环氧合酶抑制剂)或去甲二氢愈创木酸(NDGA,一种5-脂氧合酶的优先抑制剂)的情况下进行。通过放射免疫分析法测定培养基中的前列腺素(PGF2α、PGE2和6-酮-PGF1α)以及5-(S)-羟基-6,8,11,14-二十碳四烯酸(5-HETE)。所用的所有浓度的吲哚美辛或NDGA分别抑制了PGs或5-HETE的释放。然而,最低剂量(15μM)的NDGA刺激了PGs的释放,但较高剂量(30 - 60μM)则抑制了PGs的释放。另一方面,所用的两种浓度(55μM和110μM)的吲哚美辛均刺激了5-HETE的释放。结果表明在植入前兔子宫内膜细胞中这两条途径之间存在负相关关系。