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甲基强的松龙增加成年小鼠体内氧气的毒性。对表面活性剂系统的机械和生化影响。

Methylprednisolone increases the toxicity of oxygen in adult mice. Mechanical and biochemical effects on the surfactant system.

作者信息

Gross N J, Smith D M

出版信息

Am Rev Respir Dis. 1984 May;129(5):805-10. doi: 10.1164/arrd.1984.129.5.805.

Abstract

Because previous studies have suggested that some of the toxic effects of oxygen may result from impaired surfactant phospholipid metabolism, we examined the effects of methylprednisolone on the surfactant system in adult mice exposed to greater than 98% O2. Mice pretreated for 7 days with methylprednisolone, 10 mg/kg/day, had a significantly greater mortality in hyperoxia than saline-pretreated, oxygen-exposed control mice. Their bronchoalveolar lavage fluid contained significantly less desaturated phospholipid, and static pressure-volume curves with air and saline showed decreased lung compliance caused by stiffness of the surface layer. The synthesis of desaturated phospholipids by lung slices in vitro was markedly impaired by the first day of hyperoxia, although in the absence of hyperoxia, it was mildly increased. The increased inhibition of phospholipid synthesis in steroid-treated mice was present even when mice were first given steroids on the day of entry into hyperoxia. These results suggest that methylprednisolone has an unfavorable effect on the surfactant system in oxygen toxicity by accentuating the inhibition of phospholipid synthesis. The possibility that these results could have been due to infection promoted by steroid treatment was considered. No cultural, histologic, or serologic evidence in support of this possibility was found, although infection cannot be conclusively excluded.

摘要

由于先前的研究表明,氧气的某些毒性作用可能源于表面活性物质磷脂代谢受损,因此我们研究了甲基强的松龙对暴露于超过98%氧气环境中的成年小鼠表面活性物质系统的影响。用10mg/kg/天的甲基强的松龙预处理7天的小鼠,在高氧环境中的死亡率显著高于用生理盐水预处理、暴露于氧气环境的对照小鼠。它们的支气管肺泡灌洗液中不饱和磷脂含量显著降低,空气和生理盐水的静态压力-容积曲线显示,由于表层僵硬导致肺顺应性下降。高氧暴露第一天,体外肺切片中不饱和磷脂的合成就明显受损,而在无高氧环境时,其合成略有增加。即使在小鼠进入高氧环境当天首次给予类固醇,类固醇处理小鼠中磷脂合成的抑制作用仍会增强。这些结果表明,甲基强的松龙通过加剧对磷脂合成的抑制,对氧中毒时的表面活性物质系统产生不利影响。我们考虑了这些结果可能是由类固醇治疗引发感染所致的可能性。尽管不能完全排除感染,但未发现支持这一可能性的培养、组织学或血清学证据。

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