Brien M, Berthiaume L, Rudkowska I, Julien P, Bilodeau J F
Axe endocrinologie et néphrologie, Centre de recherche du CHU de Québec-Université Laval, et Centre de recherche en endocrinologie, métabolisme et inflammation (CREMI), Université Laval, Québec G1V 4G2, Canada.
Axe endocrinologie et néphrologie, Centre de recherche du CHU de Québec-Université Laval, et Centre de recherche en endocrinologie, métabolisme et inflammation (CREMI), Université Laval, Québec G1V 4G2, Canada; Département de Kinésiologie, Faculté de médecine, Université Laval, Québec G1K 7P4, Canada.
Placenta. 2017 Mar;51:82-88. doi: 10.1016/j.placenta.2017.01.129. Epub 2017 Feb 2.
Preeclampsia (PE) was shown to affect the placental content and the transfer of polyunsaturated fatty acids (PUFA) to the fetus. Plasmalogens, a type of phospholipids with a vinyl-ether link at the sn-1 position, play an antioxidant role and are specifically enriched in PUFA at the sn-2 position. In this study, we characterized plasmalogen-derived dimethyl acetal (DMA) fatty acid derivatives, 16:0 DMA, 18:0 DMA, 9c-/11c-18:1 DMA and PUFA in the placenta of normotensive (n = 20) and PE (n = 20) pregnancies, according to the sampling site: peri-insertion or periphery. Phospholipid fatty acids from the placenta and maternal erythrocytes were identified by gas chromatography mass spectrometry and quantified by flame ionization detection. We found elevated total DMA in the PE placenta by 18% when compared to normotensive controls (p = 0.026). Moreover, the 16:0 DMA account for more than 55% of DMA fatty acids measured in the placenta, and its level is significantly higher in PE than controls (p = 0.018). Also, we found elevated placental PUFA, 20:5(n-3), 22:5(n-3) and a low level of 20:4(n-3) in PE compared to controls. Placental DMA was highly correlated with n-6 and n-3 PUFA in both, normotensive and PE pregnancies. In sum, elevated DMA fatty acids in the PE placenta could be an indirect defensive mechanism against oxidative stress and poor placental fatty acid transfer in PE.
子痫前期(PE)被证明会影响胎盘对多不饱和脂肪酸(PUFA)的含量及向胎儿的转运。缩醛磷脂是一种在sn-1位具有乙烯基醚键的磷脂,具有抗氧化作用,并且在sn-2位特别富含PUFA。在本研究中,我们根据采样部位(插入周边或外周),对正常血压(n = 20)和PE(n = 20)妊娠胎盘组织中的缩醛磷脂衍生的二甲基缩醛(DMA)脂肪酸衍生物、16:0 DMA、18:0 DMA、9c-/11c-18:1 DMA和PUFA进行了表征。通过气相色谱-质谱联用仪鉴定胎盘和母体红细胞中的磷脂脂肪酸,并通过火焰离子化检测进行定量。我们发现,与正常血压对照组相比,PE胎盘组织中的总DMA升高了18%(p = 0.026)。此外,16:0 DMA占胎盘中测得的DMA脂肪酸的55%以上,其在PE中的水平显著高于对照组(p = 0.018)。而且,我们发现与对照组相比,PE胎盘组织中的PUFA、20:5(n-3)、22:5(n-3)升高,而20:4(n-3)水平较低。在正常血压和PE妊娠中,胎盘DMA与n-6和n-3 PUFA均高度相关。总之,PE胎盘组织中DMA脂肪酸升高可能是针对PE中氧化应激和胎盘脂肪酸转运不良的一种间接防御机制。