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依布硒啉(Ebs)和对氨基水杨酸(PAS)对锰(Mn)诱导的神经毒性的保护作用。

Protective effects of ebselen (Ebs) and para-aminosalicylic acid (PAS) against manganese (Mn)-induced neurotoxicity.

机构信息

I-Med.UL, Department of Toxicology and Food Sciences, Faculty of Pharmacy, University of Lisbon, Lisbon, Portugal.

出版信息

Toxicol Appl Pharmacol. 2012 Feb 1;258(3):394-402. doi: 10.1016/j.taap.2011.12.003. Epub 2011 Dec 9.

Abstract

Chronic, excessive exposure to manganese (Mn) may induce neurotoxicity and cause an irreversible brain disease, referred to as manganism. Efficacious therapies for the treatment of Mn are lacking, mandating the development of new interventions. The purpose of the present study was to investigate the efficacy of ebselen (Ebs) and para-aminosalicylic acid (PAS) in attenuating the neurotoxic effects of Mn in an in vivo rat model. Exposure biomarkers, inflammatory and oxidative stress biomarkers, as well as behavioral parameters were evaluated. Co-treatment with Mn plus Ebs or Mn plus PAS caused a significant decrease in blood and brain Mn concentrations (compared to rats treated with Mn alone), concomitant with reduced brain E₂ prostaglandin (PGE₂) and enhanced brain glutathione (GSH) levels, decreased serum prolactin (PRL) levels, and increased ambulation and rearing activities. Taken together, these results establish that both PAS and Ebs are efficacious in reducing Mn body burden, neuroinflammation, oxidative stress and locomotor activity impairments in a rat model of Mn-induced toxicity.

摘要

慢性、过量暴露于锰(Mn)可能会引起神经毒性,并导致一种不可逆的脑部疾病,称为锰中毒。目前缺乏治疗 Mn 的有效疗法,因此需要开发新的干预措施。本研究的目的是探讨依布硒啉(Ebs)和对氨基水杨酸(PAS)在减轻体内大鼠模型 Mn 神经毒性作用中的疗效。评估了暴露生物标志物、炎症和氧化应激生物标志物以及行为参数。与单独用 Mn 处理的大鼠相比,Mn 加 Ebs 或 Mn 加 PAS 共同处理导致血液和大脑 Mn 浓度显著降低,同时大脑 E₂ 前列腺素(PGE₂)降低,谷胱甘肽(GSH)水平升高,血清催乳素(PRL)水平降低,以及步行和站立活动增加。综上所述,这些结果表明,PAS 和 Ebs 均能有效降低 Mn 诱导的毒性大鼠模型中的 Mn 体内负荷、神经炎症、氧化应激和运动活动障碍。

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