R Alvaro, V de Almeida, S al-Alaiyan, M Robertson, B Nowaczyk, D Cates, H Rigatto
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引用次数: 0
摘要
在长期未麻醉的胎羊制备中,脐带闭合在充氧条件下诱导持续呼吸和觉醒。造成这种情况的机制尚不清楚。我们假设,如果胎盘因子是抑制胎儿呼吸的原因,那么在脐带阻断后胎儿持续呼吸时给予胎盘提取物应该可以逆转这些变化。因此,在脐带阻断诱导持续呼吸后约10分钟,我们给14只妊娠133 +/- 1天的长期仪器检测的胎羊使用了胎盘提取物和超滤分离的三个亚组分。以制备胎盘提取物的克雷布斯溶液为对照。在胎儿颈动脉输注全胎盘提取物2分钟内,所有实验中呼吸输出量(EMGdi x f积分)均减少,15/17(88%)完全消除。克雷布斯溶液对呼吸没有影响。不同分子量亚段的输注表明,抑制作用主要与3.5 ~ 10 kD亚段有关。在血气紧张、pH值、血压和心率方面,没有明显的变化与提取物的注入有关。在使用整个提取物和3.5至10 kD的亚分数的大多数实验中,ECoG从低电压切换到高电压。这些发现表明胎盘因子,可能是分子量在3.5至10kd之间的肽,在胎儿生命中抑制呼吸。
A placental extract inhibits breathing induced by umbilical cord occlusion in fetal sheep.
Umbilical cord occlusion in the presence of adequate oxygenation induces continuous breathing and arousal in the chronic unanesthetized fetal sheep preparation. The mechanism responsible for this is unknown. We hypothesized that if a placental factor is responsible for the inhibition of breathing in the fetus, the administration of a placental extract while the fetus is breathing continuously after cord occlusion should reverse these changes. Thus, at about 10 min after the induction of continuous breathing by cord occlusion, we administered a placental extract and three subfractions separated by ultrafiltration to 14 chronically instrumented fetal sheep at 133 +/- 1 day gestation. The Krebs solution in which the placental extract was prepared was used as control. Within two minutes of the infusion of the whole placental extract in the carotid artery of the fetus, breathing output (integral of EMGdi x f) diminished in all experiments and was completely abolished in 15/17 (88%). Krebs solution had no effect on breathing. The infusion of subfractions of different molecular weight showed that the inhibition was primarily related to the subfraction between 3.5 and 10 kD. There were no significant changes in blood gas tensions, pH, blood pressure, and heart rate associated with the infusions of the extracts. The ECoG switched from low to high voltage in the majority of the experiments using whole extract and the subfraction 3.5 to 10 kD. These findings suggest that a placental factor, probably a peptide with a molecular weight between 3.5 and 10 kD, inhibits breathing in fetal life.