Xu Alex, Matushewski Brad, Nygard Karen, Hammond Robert, Frasch Martin G, Richardson Bryan S
Department of Obstetrics and Gynecology, Schulich School of Medicine and Dentistry, The University of Western Ontario, London, Ontario, Canada Department of Physiology and Pharmacology, Schulich School of Medicine and Dentistry, The University of Western Ontario, London, Ontario, Canada.
Department of Obstetrics and Gynecology, Schulich School of Medicine and Dentistry, The University of Western Ontario, London, Ontario, Canada.
Reprod Sci. 2016 Jul;23(7):858-70. doi: 10.1177/1933719115623640. Epub 2015 Dec 23.
We hypothesized that repetitive umbilical cord occlusions (UCOs) with worsening fetal acidemia will lead to an inflammatory response within the brain and thereby brain injury which will be exacerbated by chronic hypoxemia and low-grade infection. Chronically instrumented fetal sheep served as controls (N = 10) or underwent repeated UCOs for up to 4 hours or until arterial pH was <7.00. Normoxic-UCO (N = 9) and hypoxic-UCO (N = 5) fetuses had arterial O2 saturation pre-UCOs of >55% and <55%, respectively, whereas lipopolysaccharide (LPS) UCO fetuses (N = 6) received LPS intra-amniotic (2 mg/h) starting 1 hour pre-UCOs. Animals were euthanized at 48 hours of recovery with fetal brains processed for assessment of inflammation (microglia and mast cell counts) and injury (necrosis-hematoxylin and eosin-and apoptosis-cleaved caspase-3 and terminal deoxynucleotidyl transferase dUTP nick end labeling [TUNEL]). Repetitive UCOs resulted in severe acidemia in most animals with pH approaching 7.00 for all 3 UCO groups. However, there was no significant effect on measures of brain inflammation or injury, except in the LPS-UCO animals where TUNEL-positive cells were increased in the hippocampus, although small animal numbers in the hypoxic-UCO group may have limited the ability to detect significance in their TUNEL cell findings. We were therefore unable to confirm our working hypothesis since the near-term ovine fetal brain showed remarkable tolerance for these cord occlusion insults and likely involving protective metabolic mechanisms, despite the severe acidemia noted.
我们假设,随着胎儿酸血症加重,反复的脐带闭塞(UCO)会导致脑内炎症反应,进而引发脑损伤,而慢性低氧血症和低度感染会加剧这种损伤。长期植入仪器的胎羊作为对照组(N = 10),或接受长达4小时的反复UCO,或直至动脉pH值<7.00。常氧-UCO组(N = 9)和低氧-UCO组(N = 5)的胎儿在UCO前动脉血氧饱和度分别>55%和<55%,而脂多糖(LPS)-UCO组胎儿(N = 6)在UCO前1小时开始羊膜腔内注射LPS(2 mg/h)。动物在恢复48小时后实施安乐死,对胎儿大脑进行处理,以评估炎症(小胶质细胞和肥大细胞计数)和损伤(坏死 - 苏木精和伊红染色 - 以及凋亡 - 裂解的半胱天冬酶 - 3和末端脱氧核苷酸转移酶dUTP缺口末端标记法[TUNEL])。反复的UCO在大多数动物中导致严重酸血症,所有3个UCO组的pH值均接近7.00。然而,除了LPS-UCO组动物海马体中TUNEL阳性细胞增加外,对脑炎症或损伤指标没有显著影响,尽管低氧-UCO组动物数量较少可能限制了其TUNEL细胞结果的显著性检测能力。因此,我们无法证实我们的工作假设,因为尽管存在严重酸血症,但近足月绵羊胎儿大脑对这些脐带闭塞损伤表现出显著的耐受性,可能涉及保护性代谢机制。