Ouabain attenuates the oxidative stress induced by lipopolysaccharides in the cerebellum of rats

哇巴因 氧化应激 化学 谷胱甘肽过氧化物酶 脂质过氧化 谷胱甘肽 过氧化氢酶 超氧化物歧化酶 抗氧化剂 药理学 生物化学 内科学 谷氨酸受体 内分泌学 生物 医学 受体 有机化学
作者
Israel José Pereira Garcia,Paula Fernanda Kinoshita,Italo de Oliveira Braga,Gabriela Machado Parreira,Júlio A. Mignaco,Cristóforo Scavone,Leandro A. Barbosa,Hérica de Lima Santos
出处
期刊:Journal of Cellular Biochemistry [Wiley]
卷期号:119 (2): 2156-2167 被引量:14
标识
DOI:10.1002/jcb.26377
摘要

Abstract Our study aimed to analyze the effect of ouabain administration on lipopolysaccharide (LPS)‐induced changes in oxidative parameters, membrane lipid composition, and the activities of some important enzymes of the nervous system. The content of phospholipids, cholesterol, and gangliosides were analyzed in Wistar rats after intraperitoneal injection of ouabain (1.8 μg/kg), LPS (200 μg/kg), or saline. Oxidative parameters were also evaluated, including the activities of superoxide dismutase, catalase and glutathione peroxidase, the levels of glutathione and lipid peroxidation, as well as Na,K‐ATPase activity and the level of glutamate transporter EAAT4. Administration of LPS resulted in increased oxidative stress, as evidenced by an increase in lipid peroxidation levels, glutathione peroxidase activity, decreased catalase activity and reduced glutathione levels. All changes recorded were attenuated by pretreatment with ouabain. Administration of ouabain plus LPS enhanced the total ganglioside content and EAAT4 levels, but failed to alter the Na,K‐ATPase activity. Our data suggest a neuroprotective effect of ouabain against LPS‐induced oxidative stress by promoting membrane lipid remodeling and increasing the expression of glutamate transporter EAAT4. Our results emphasize that the observed oxidative stress is not correlated with Na,K‐ATPase, but with a possible ouabain‐mediated effect on cellular signaling. The relevance of our results extends beyond LPS‐induced changes in oxidative parameters, as nanomolar doses of ouabain might prove useful in neurodegenerative models. Further study of other cardenolides and related molecules, as well as the development of new molecules derived from ouabain, could also prove useful in the fight against the oxidative and/or general cell stress triggered by neuronal pathologies.

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