Ohashi Yayoi, Sumikura Hiroyuki, Tateda Takeshi
Department of Anesthesiology, St. Marianna University School of Medicine Hospital, 2-16-1 Sugao, Kawasaki, Kanagawa 216-8511, Japan.
J Anesth. 2007;21(3):361-6. doi: 10.1007/s00540-007-0536-8. Epub 2007 Aug 1.
For anesthetic management of cesarean sections, regardless of the use of regional or general anesthesia, it is crucial to achieve sufficient uterine contraction immediately following the delivery of an infant in order to reduce excessive bleeding. No previous study has investigated the ability of alprostadil, a synthesized prostaglandin, to inhibit myometrial relaxation induced by volatile anesthetics. The aim of the present study was to investigate the inhibitory effects of alprostadil on sevoflurane-induced myometrial relaxation using myometrial strips isolated from pregnant rats.
Myometrial strips were isolated from Sprague-Dawley rats (300-400 g) in the late stage of gestation (19-21 days). The time course of changes in spontaneous myometrium contraction was studied in the presence and absence of sevoflurane. Additionally, alprostadil was titrated at three different concentrations during continuous introduction of sevoflurane 2%, and myometrium contraction was studied. As an index of contraction, the area under the contraction curve was used, and data were analyzed by repeated measure one-way analysis of variance.
We have shown a significant decrease in myometrium contraction as a result of the use of sevoflurane (2%). Additionally, alprostadil has been shown to inhibit myometrial relaxation induced by sevoflurane in a dose-dependent manner. The areas under the contraction curve were 87%, 87%, 129%, and 172% of the baseline value for the control and at low, medium, and high concentrations of alprostadil, respectively.
The ability of alprostadil to inhibit myometrial relaxation induced by sevoflurane suggests that the use of alprostadil during general anesthesia for cesarean section may be advantageous for the reduction of postpartum bleeding.
对于剖宫产的麻醉管理,无论采用区域麻醉还是全身麻醉,在婴儿娩出后立即实现充分的子宫收缩以减少过多出血至关重要。此前尚无研究调查合成前列腺素前列地尔抑制挥发性麻醉药引起的子宫肌层松弛的能力。本研究的目的是使用从妊娠大鼠分离的子宫肌条来研究前列地尔对七氟醚诱导的子宫肌层松弛的抑制作用。
从妊娠晚期(19 - 21天)的Sprague-Dawley大鼠(300 - 400克)分离子宫肌条。在有和没有七氟醚的情况下研究自发性子宫肌层收缩的变化时间过程。此外,在持续输注2%七氟醚期间,以三种不同浓度滴定前列地尔,并研究子宫肌层收缩。作为收缩指标,使用收缩曲线下面积,数据通过重复测量单因素方差分析进行分析。
我们已经表明使用七氟醚(2%)会导致子宫肌层收缩显著降低。此外,前列地尔已被证明以剂量依赖方式抑制七氟醚诱导的子宫肌层松弛。对照以及低、中、高浓度前列地尔的收缩曲线下面积分别为基线值的87%、87%、129%和172%。
前列地尔抑制七氟醚诱导的子宫肌层松弛的能力表明,剖宫产全身麻醉期间使用前列地尔可能有利于减少产后出血。