Department of Diving Medicine, Faculty of Naval Medicine, Changhai Hospital, Second Military Medical University, Shanghai, China.
Oxid Med Cell Longev. 2009 Jan-Mar;2(1):7-13. doi: 10.4161/oxim.2.1.7697.
Exposure to hyperbaric oxygen (HBO) can lead to seizures. Many studies have demonstrated that there exist a very close relationship between the alteration of cerebral blood flow (CBF) and the onset of seizures. Nitric oxide (NO) may play a key role in the change of CBF during exposure, and modulation of endothelial nitric oxide synthase (eNOS)-derived NO by HBO is responsible for early vasoconstriction, whereas late HBO-induced vasodilation depends upon a large amount of NO from both eNOS and neuronal nitric oxide synthase (nNOS). To investigate the effect of HBO on the activity and expression of eNOS in cerebral microvascular endothelial cells (CMEC) in vitro, primarily cultured CMEC from neonatal rats were exposed to oxygen at 500 kPa [5 atmosphere absolute (ATA)] for 10, 20, 30, 60 and 120 minutes (min), then eNOS activity, protein and mRNA contents in cells were detected. Our results showed that immediately after exposure, 30, 60 and 120 min HBO exposures did not alter NOS activity. When detected no matter immediately or six hours (h) after exposure, these exposures also did not alter eNOS protein and mRNA levels. However, when detected 24 h after exposure, 30, 60 and 120 min exposures upregulated eNOS protein content by 39%, 60% and 40% respectively. 10 and 20 min exposures upregulated eNOS mRNA content by about 15%, while 30, 60 and 120 min exposures upregulated it by about 20-30%. The increased eNOS protein and mRNA contents at 24 h after exposure may reflect new protein synthesis for eNOS. Our studies showed that with the exposing protocols we used, HBO did induce eNOS expression increase in CMEC. However, compared with the decrease of CBF in vivo, which occurred in a relative short time after rat was exposed to HBO above 4 ATA, the responses of eNOS in CMEC in vitro were a little slow. Thus we considered that for the vasodilation in the late period of HBO exposure before seizure, the effect of NO produced by eNOS was limited.
高压氧(HBO)暴露可导致癫痫发作。许多研究表明,脑血流(CBF)的改变与癫痫发作的发生之间存在非常密切的关系。一氧化氮(NO)可能在暴露过程中 CBF 的变化中起关键作用,HBO 对内皮型一氧化氮合酶(eNOS)衍生的 NO 的调节导致早期血管收缩,而晚期 HBO 诱导的血管舒张则依赖于大量来自 eNOS 和神经元型一氧化氮合酶(nNOS)的 NO。为了研究 HBO 对体外培养的新生大鼠脑微血管内皮细胞(CMEC)中 eNOS 活性和表达的影响,将原代培养的 CMEC 暴露于 500 kPa [5 个大气压绝对(ATA)]的氧气中 10、20、30、60 和 120 分钟(min),然后检测细胞中 eNOS 活性、蛋白和 mRNA 含量。结果显示,暴露后即刻,30、60 和 120 min HBO 暴露并未改变 NOS 活性。无论是暴露后即刻还是 6 小时(h)检测,这些暴露也没有改变 eNOS 蛋白和 mRNA 水平。然而,暴露后 24 小时检测时,30、60 和 120 min 暴露分别使 eNOS 蛋白含量上调 39%、60%和 40%。10 和 20 min 暴露使 eNOS mRNA 含量上调约 15%,而 30、60 和 120 min 暴露使 eNOS mRNA 含量上调约 20-30%。暴露后 24 小时 eNOS 蛋白和 mRNA 含量的增加可能反映了 eNOS 的新蛋白质合成。我们的研究表明,在我们使用的暴露方案中,HBO 确实会诱导 CMEC 中 eNOS 表达增加。然而,与大鼠暴露于 HBO 以上 4 ATA 后相对较短时间内 CBF 下降相比,CMEC 中 eNOS 的反应稍慢。因此,我们认为,在 HBO 暴露后期发生癫痫之前的血管扩张中,eNOS 产生的 NO 的作用是有限的。