Epicatechin as a promising agent against arsenic-induced neurobehavioral toxicity in NMRI mice: behavioral and biochemical alterations.

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Saeedeh Shariati, Mohammad Javad Khodayar, Reza Azadnasab, Mohammadreza Rashidi Nooshabadi, Mehrad Nikravesh, Layasadat Khorsandi, Kobra Shirani, Maryam Shirani
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Abstract

Epicatechin (Epi) is one of the most abundant flavonoids present in different fruits and tea leaves. Emerging research illuminates the promising potential of catechins to serve as a shield against the damaging effects of arsenic (As) exposure in diverse organs.This study sought to discern whether Epi exhibits a therapeutic efficacy against arsenic-induced neurotoxicity in a murine model.The Naval Medical Research Institute (NMRI) mice were randomly partitioned into six distinct groups, which included a control group receiving normal saline, a group receiving a daily oral dose of arsenic (10 mg/kg) for 5 weeks, groups receiving As (10 mg/kg/day) orally for 5 weeks along with different doses of Epi (25-100 mg/kg) orally for the last 2 weeks, and a group receiving Epi (100 mg/kg) orally for 2 weeks. To assess the potential effects of Epi, neurobehavioral tests, various parameters of oxidative stress, and inflammation were evaluated.The findings of this investigation revealed that As-induced neurobehavioral toxicity was associated with a notable surge in lipid peroxidation and nitric oxide (NO) concentration, accompanied by a reduction in the levels of antioxidant markers. As heightened pro-inflammatory cytokines including tumor necrosis factor-α (TNF-α) levels were observed alongside amplified nuclear factor kappa B (NF-κB) and nuclear factor erythroid 2-related factor 2 (Nrf2) expression. However, treatment with Epi reversed these effects.On the whole, these findings indicate that Epi may hold promise therapeutic efficacy on As-induced neurotoxicity by improving antioxidant status and mitigating oxidative stress and inflammation. Nevertheless, further research is imperative to comprehensively grasp the potential protective effects of Epi in this particular context.

Abstract Image

表儿茶素是抗砷诱导的 NMRI 小鼠神经行为毒性的有效药物:行为和生化改变。
表儿茶素(Epi)是存在于不同水果和茶叶中最丰富的类黄酮之一。新近的研究表明,儿茶素具有在不同器官中抵御砷(As)暴露的破坏性影响的潜力。海军医学研究所(NMRI)的小鼠被随机分成六个不同的组,其中包括接受正常生理盐水的对照组、连续 5 周每天口服砷(10 毫克/千克)的组、连续 5 周口服砷(10 毫克/千克/天)并在最后 2 周口服不同剂量 Epi(25-100 毫克/千克)的组,以及连续 2 周口服 Epi(100 毫克/千克)的组。研究结果表明,As 引起的神经行为毒性与脂质过氧化反应和一氧化氮(NO)浓度的显著升高有关,同时伴有抗氧化标志物水平的降低。此外,还观察到包括肿瘤坏死因子-α(TNF-α)在内的促炎细胞因子水平升高,同时核因子卡巴B(NF-κB)和核因子红细胞2相关因子2(Nrf2)的表达也增加了。总体而言,这些研究结果表明,Epi 可改善抗氧化状态,减轻氧化应激和炎症反应,从而有望对砷诱导的神经毒性产生疗效。然而,要全面了解 Epi 在这一特定情况下的潜在保护作用,进一步的研究势在必行。
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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来源期刊
CiteScore
6.20
自引率
5.60%
发文量
142
审稿时长
4-8 weeks
期刊介绍: Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.
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