The low-dose ozone concept and its pharmacology in prevention and convalescence.

Renate Viebahn-Haensler
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Abstract

Systemically administered ozone with its mild oxidative eustress, able to upregulate antioxidative enzymes and to modulate the immune response e.g. “cytokine storm” is recommended as part of a complementary treatment concept in chronic inflammatory, long lasting processes with high oxidative stress and in diseases which are accompanied by an redox imbalance, rather than in the acute stages. To restore the glutathione equilibrium GSH/ GSSG the low-dose ozone concept offers a strategy in redox medicine as shown here in primary and secondary prevention and convalescence. To illustrate the main pharmacological effects and to follow the treatment success we focus to the following refence substances: GSH (reduced glutathione), GGT (gamma glutamyl transferase) or SOD (superoxide dismutase) as protection markers and one or two parameters of stress markers: MDA (malondialdehyde). Especially liver and kidneys are prevented from oxidative stress, regularly GSH increases, MDA decreases. In post acute inflammations (convalescence) we find the same biochemical mechanisms, summarized in virus diseases and diabetic angiopathy.
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低剂量臭氧概念及其在预防和康复中的药理学作用。
系统施用臭氧具有轻度氧化应激,能够上调抗氧化酶并调节免疫反应,例如“细胞因子风暴”,建议作为补充治疗概念的一部分,用于慢性炎症、高氧化应激的长期过程和伴随氧化还原不平衡的疾病,而不是急性阶段。为了恢复谷胱甘肽平衡GSH/ GSSG,低剂量臭氧概念为氧化还原医学提供了一种策略,如这里所示,用于一级和二级预防和康复。为了说明主要的药理作用并跟踪治疗成功,我们重点关注以下参考物质:GSH(还原性谷胱甘肽),GGT (γ谷氨酰转移酶)或SOD(超氧化物歧化酶)作为保护标志物和一两个应激标志物参数:MDA(丙二醛)。特别是肝脏和肾脏防止氧化应激,定期GSH增加,MDA减少。在急性炎症(恢复期)后,我们发现了相同的生化机制,总结在病毒性疾病和糖尿病血管病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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