Wojciechowska A, Młynarczuk J, Kotwica J
Department of Pathophysiology, School of Medicine, University of Warmia and Mazury, Olsztyn, Poland.
Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Tuwima 10, 10-757 Olsztyn, Poland.
Pol J Vet Sci. 2018 Dec;21(4):721-729. doi: 10.24425/124311.
Polychlorinated biphenyls (PCBs), dichlorodiphenyltrichloroethane (DDT) and its metabo- lite, dichlorodiphenyldichloroethylene (DDE) can disturb the secretory function of the ovary and both contractions and secretory function of the uterus during the estrus cycle and pregnancy. Additionally, PCBs can pass through the placental barrier into allantoic and amniotic fluid. The presence of PCBs in these fluids is associated with higher frequency of spontaneous abortions and premature births in humans and animals. Therefore, the effect of PCBs, DDT and DDE on the connexins (Cx26, Cx32 and Cx43) and keratin 8 (KRT8) expression in bovine placentomes was investigated. The placentome slices from the second trimester of pregnancy were incubated with PCB153, 126, 77, DDT and DDE (each at doses of 1, 10 or 100 ng/ml) for 48 h. Then, the slices were stained using immunohistochemistry. The density of Cxs staining was measured with Axio- Vision Rel. 4.8 software in fetal-maternal connections and binuclear cells (BNC). None of the tested xenobiotics (XBs) affected the localization of Cxs and KRT8 in the fetal-maternal connec- tion area, but the XBs affected the density of Cxs in fetal-maternal connections and binuclear cells (BNCs). Depend on the doses, in fetal-maternal connections all used PCBs changed the protein expression of different Cxs, while in BNCs, all tested XBs except DDT increased the ex- pression of Cxs. None of investigated XBs affected on KRT8 expression. In summary, used XBs affect the expression of Cxs and change the quantitative relationships between them. Therefore, XBs can unfavorably influence function of the utero-placental barrier in cows.
多氯联苯(PCBs)、二氯二苯三氯乙烷(DDT)及其代谢物二氯二苯二氯乙烯(DDE)会干扰发情周期和孕期卵巢的分泌功能以及子宫的收缩和分泌功能。此外,多氯联苯可穿过胎盘屏障进入尿囊液和羊水。这些液体中多氯联苯的存在与人类和动物自然流产和早产的高发生率相关。因此,研究了多氯联苯、滴滴涕和滴滴伊对牛胎盘小叶中连接蛋白(Cx26、Cx32和Cx43)和角蛋白8(KRT8)表达的影响。将妊娠中期的胎盘小叶切片与多氯联苯153、126、77、滴滴涕和滴滴伊(各剂量为1、10或100 ng/ml)孵育48小时。然后,使用免疫组织化学对切片进行染色。使用Axio-Vision Rel. 4.8软件测量胎儿-母体连接和双核细胞(BNC)中连接蛋白染色的密度。所测试的外源性物质(XBs)均未影响连接蛋白和角蛋白8在胎儿-母体连接区域的定位,但外源性物质影响了胎儿-母体连接和双核细胞(BNCs)中连接蛋白的密度。根据剂量不同,在胎儿-母体连接中,所有使用的多氯联苯都改变了不同连接蛋白的蛋白表达,而在双核细胞中,除滴滴涕外的所有测试外源性物质都增加了连接蛋白的表达。所研究的外源性物质均未影响角蛋白8的表达。总之,所使用的外源性物质影响连接蛋白的表达并改变它们之间的定量关系。因此,外源性物质可能对奶牛子宫-胎盘屏障的功能产生不利影响。