Zamora Zullyt B, Borrego Aluet, López Orlay Y, Delgado René, González Ricardo, Menéndez Silvia, Hernández Frank, Schulz Siegfried
Department of Biomedicine, Ozone Research Center, National center for Scientific Research, Havana, Cuba.
Mediators Inflamm. 2005 Feb 24;2005(1):16-22. doi: 10.1155/MI.2005.16.
Ozone oxidative preconditioning is a prophylactic approach, which favors the antioxidant-prooxidant balance for preservation of cell redox state by the increase of antioxidant endogenous systems in both in vivo and in vitro experimental models. Our aim is to analyze the effect of ozone oxidative preconditioning on serum TNF-alpha levels and as a modulator of oxidative stress on hepatic tissue in entodoxic shock model (mice treated with lipopolysaccharide (LPS)). Ozone/oxygen gaseous mixture which was administered intraperitoneally (0.2, 0.4, and 1.2 mg/kg) once daily for five days before LPS (0.1 mg/kg, intraperitoneal). TNF-alpha was measured by cytotoxicity on L-929 cells. Biochemical parameters such as thiobarbituric acid reactive substances (TBARS), enzymatic activity of catalase, glutathione peroxidase, and glutathione-S transferase were measured in hepatic tissue. One hour after LPS injection there was a significant increase in TNF-alpha levels in mouse serum. Ozone/oxygen gaseous mixture reduced serum TNF-alpha levels in a dose-dependent manner. Statistically significant decreases in TNF-alpha levels after LPS injection were observed in mice pretreated with ozone intraperitoneal applications at 0.2 (78%), 0.4 (98%), and 1.2 (99%). Also a significant increase in TBARS content was observed in the hepatic tissue of LPS-treated mice, whereas enzymatic activity of glutathion-S transferase and glutathione peroxidase was decreased. However in ozone-treated animals a significant decrease in TBARS content was appreciated as well as an increase in the activity of antioxidant enzymes. These results indicate that ozone oxidative preconditioning exerts inhibitory effects on TNF-alpha production and on the other hand it exerts influence on the antioxidant-prooxidant balance for preservation of cell redox state by the increase of endogenous antioxidant systems.
臭氧氧化预处理是一种预防性方法,在体内和体外实验模型中,它通过增加内源性抗氧化系统,有利于抗氧化剂-促氧化剂平衡,以维持细胞氧化还原状态。我们的目的是分析臭氧氧化预处理对内毒素休克模型(用脂多糖(LPS)处理的小鼠)血清肿瘤坏死因子-α(TNF-α)水平的影响,以及作为氧化应激调节剂对肝组织的影响。在腹腔注射LPS(0.1mg/kg)前五天,每天一次腹腔注射臭氧/氧气混合气体(0.2、0.4和1.2mg/kg)。通过对L-929细胞的细胞毒性来测量TNF-α。在肝组织中测量生化参数,如硫代巴比妥酸反应性物质(TBARS)、过氧化氢酶、谷胱甘肽过氧化物酶和谷胱甘肽-S转移酶的酶活性。注射LPS一小时后,小鼠血清中TNF-α水平显著升高。臭氧/氧气混合气体以剂量依赖的方式降低血清TNF-α水平。在用0.2(78%)、0.4(98%)和1.2(99%)腹腔注射臭氧预处理的小鼠中,观察到LPS注射后TNF-α水平有统计学意义的降低。此外,在LPS处理的小鼠肝组织中观察到TBARS含量显著增加,而谷胱甘肽-S转移酶和谷胱甘肽过氧化物酶的酶活性降低。然而,在臭氧处理组动物中,TBARS含量显著降低,同时抗氧化酶活性增加。这些结果表明,臭氧氧化预处理对TNF-α的产生具有抑制作用,另一方面,它通过增加内源性抗氧化系统,对抗氧化剂-促氧化剂平衡产生影响,以维持细胞氧化还原状态。