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N-acetylcysteine alleviates cadmium-induced placental endoplasmic reticulum stress and fetal growth restriction in mice

机译:N-乙酰半胱氨酸减轻了小鼠镉诱导的胎盘内质网应激和胎儿生长受限

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摘要

Cadmium (Cd) is a developmental toxicant that induces fetal growth restriction (FGR). Placental endoplasmic reticulum (ER) stress is associated with FGR. This study investigated the effects of N-acetylcysteine (NAC) on Cd-induced placental ER stress and FGR. Pregnant mice were intraperitoneally injected with CdCl2 daily from gestational day (GD)13 to GD17. As expected, Cd reduced fetal weight and crown-rump length. Cd decreased the internal space of blood vessels in the placental labyrinth layer and inhibited placental cell proliferation. Several genes of growth factors, such as Vegf-a, placental growth factor, Igf1 and Igf1r, and several genes of nutrient transport pumps, such as Glut1, Fatp1 and Snat2, were down-regulated in placenta of Cd-treated mice. Moreover, Cd evoked placental ER stress. Of interest, NAC alleviated Cd-induced FGR. Additional experiment showed that NAC inhibited Cd-induced impairment of placental development and placental ER stress. Therefore, NAC may be exploited for prevention of Cd-induced placental insufficiency and FGR.
机译:镉(Cd)是一种发育毒性物质,可引起胎儿生长受限(FGR)。胎盘内质网(ER)应激与FGR相关。这项研究调查了N-乙酰半胱氨酸(NAC)对Cd诱导的胎盘ER应激和FGR的影响。从妊娠天(GD)13至GD17,每天腹膜内给CdCl2怀孕的小鼠注射。正如预期的那样,镉可减少胎儿体重和冠臀长度。 Cd减少了胎盘迷宫层血管的内部空间并抑制了胎盘细胞的增殖。在Cd处理过的小鼠的胎盘中,一些生长因子的基因,例如Vegf-a,胎盘生长因子,Igf1和Igf1r,以及营养运输泵的一些基因,例如Glut1,Fatp1和Snat2,均被下调。此外,镉诱发胎盘内质网应激。有趣的是,NAC减轻了Cd诱导的FGR。附加实验表明,NAC抑制了Cd诱导的胎盘发育损伤和胎盘ER应激。因此,NAC可用于预防Cd引起的胎盘功能不全和FGR。

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