The neuroprotective effect of curcumin against ATO triggered neurotoxicity through Nrf2 and NF-κB signaling pathway in the brain of ducks

Arsenic trioxide (ATO) has confirmed as a global pollutant, the toxic effect of which was not fully understood and lack effective therapies to against its associated toxicities. Curcumin (Cur) is a beneficial natural pigment for its antioxidant and anti-inflammatory properties. The purpose of this p...

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Autores principales: Shaofeng Wu, Gan Rao, Rui Wang, Qiling Pang, Xiaoyong Zhang, Riming Huang, Taotao Li, Zhaoxin Tang, Lianmei Hu
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Publicado: Elsevier 2021
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spelling oai:doaj.org-article:c863eb6c458d4fb7a0f1e94c9e852a9c2021-11-14T04:28:20ZThe neuroprotective effect of curcumin against ATO triggered neurotoxicity through Nrf2 and NF-κB signaling pathway in the brain of ducks0147-651310.1016/j.ecoenv.2021.112965https://doaj.org/article/c863eb6c458d4fb7a0f1e94c9e852a9c2021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S0147651321010770https://doaj.org/toc/0147-6513Arsenic trioxide (ATO) has confirmed as a global pollutant, the toxic effect of which was not fully understood and lack effective therapies to against its associated toxicities. Curcumin (Cur) is a beneficial natural pigment for its antioxidant and anti-inflammatory properties. The purpose of this paper was to illustrate the antagonism of Cur against ATO-induced neurotoxicity. A total of 40 ducks were divided randomly into 4 groups and conducted via bite and sup for 28 days: control group (Control); 2 mg/kg ATO group (Low ATO); 4 mg/kg ATO group (Middle ATO); 8 mg/kg ATO group (High ATO); 400 mg/kg Cur group + 8 mg/kg ATO (Cur+ATO). The results showed that ATO exposure can hinder the duck growth and arsenic element accumulation rate increased in a dose-dependent manner. We observed neuronal shrinkage and vacuolize of HE staining in the ATO-treated group. In addition, SOD activity and T-AOC level reduced while MDA content increased in the ATO-exposed group. ATO exposure can decrease the expression of anti-oxidation related mRNA and proteins (Nrf2, SOD-1, GPX-1, CAT, Trx and HO-1) and anti-inflammatory makers (IL-4, IL-10), increased the expression of Keap1, NF-κB and pro-inflammatory makers (TNF-α, IL-1β, IL-18, IL-2, IL-6, INOS and COX-2). ATO treated might cause blood-brain barrier (BBB) damage through degradation of the tight junction proteins (TJs) occludin and ZO-1. Importantly, the experimental results also showed that Cur can alleviate oxidative stress, inflammatory response and BBB injury caused by ATO exposure through Nrf2 and NF-κB signaling pathway. The results suggested Cur exerted as a food additive and provided novel potential benefits of ATO toxicology in inflammation of the brain.Shaofeng WuGan RaoRui WangQiling PangXiaoyong ZhangRiming HuangTaotao LiZhaoxin TangLianmei HuElsevierarticleArsenic trioxideCurcuminBrainOxidative stressInflammatoryNrf2Environmental pollutionTD172-193.5Environmental sciencesGE1-350ENEcotoxicology and Environmental Safety, Vol 228, Iss , Pp 112965- (2021)
institution DOAJ
collection DOAJ
language EN
topic Arsenic trioxide
Curcumin
Brain
Oxidative stress
Inflammatory
Nrf2
Environmental pollution
TD172-193.5
Environmental sciences
GE1-350
spellingShingle Arsenic trioxide
Curcumin
Brain
Oxidative stress
Inflammatory
Nrf2
Environmental pollution
TD172-193.5
Environmental sciences
GE1-350
Shaofeng Wu
Gan Rao
Rui Wang
Qiling Pang
Xiaoyong Zhang
Riming Huang
Taotao Li
Zhaoxin Tang
Lianmei Hu
The neuroprotective effect of curcumin against ATO triggered neurotoxicity through Nrf2 and NF-κB signaling pathway in the brain of ducks
description Arsenic trioxide (ATO) has confirmed as a global pollutant, the toxic effect of which was not fully understood and lack effective therapies to against its associated toxicities. Curcumin (Cur) is a beneficial natural pigment for its antioxidant and anti-inflammatory properties. The purpose of this paper was to illustrate the antagonism of Cur against ATO-induced neurotoxicity. A total of 40 ducks were divided randomly into 4 groups and conducted via bite and sup for 28 days: control group (Control); 2 mg/kg ATO group (Low ATO); 4 mg/kg ATO group (Middle ATO); 8 mg/kg ATO group (High ATO); 400 mg/kg Cur group + 8 mg/kg ATO (Cur+ATO). The results showed that ATO exposure can hinder the duck growth and arsenic element accumulation rate increased in a dose-dependent manner. We observed neuronal shrinkage and vacuolize of HE staining in the ATO-treated group. In addition, SOD activity and T-AOC level reduced while MDA content increased in the ATO-exposed group. ATO exposure can decrease the expression of anti-oxidation related mRNA and proteins (Nrf2, SOD-1, GPX-1, CAT, Trx and HO-1) and anti-inflammatory makers (IL-4, IL-10), increased the expression of Keap1, NF-κB and pro-inflammatory makers (TNF-α, IL-1β, IL-18, IL-2, IL-6, INOS and COX-2). ATO treated might cause blood-brain barrier (BBB) damage through degradation of the tight junction proteins (TJs) occludin and ZO-1. Importantly, the experimental results also showed that Cur can alleviate oxidative stress, inflammatory response and BBB injury caused by ATO exposure through Nrf2 and NF-κB signaling pathway. The results suggested Cur exerted as a food additive and provided novel potential benefits of ATO toxicology in inflammation of the brain.
format article
author Shaofeng Wu
Gan Rao
Rui Wang
Qiling Pang
Xiaoyong Zhang
Riming Huang
Taotao Li
Zhaoxin Tang
Lianmei Hu
author_facet Shaofeng Wu
Gan Rao
Rui Wang
Qiling Pang
Xiaoyong Zhang
Riming Huang
Taotao Li
Zhaoxin Tang
Lianmei Hu
author_sort Shaofeng Wu
title The neuroprotective effect of curcumin against ATO triggered neurotoxicity through Nrf2 and NF-κB signaling pathway in the brain of ducks
title_short The neuroprotective effect of curcumin against ATO triggered neurotoxicity through Nrf2 and NF-κB signaling pathway in the brain of ducks
title_full The neuroprotective effect of curcumin against ATO triggered neurotoxicity through Nrf2 and NF-κB signaling pathway in the brain of ducks
title_fullStr The neuroprotective effect of curcumin against ATO triggered neurotoxicity through Nrf2 and NF-κB signaling pathway in the brain of ducks
title_full_unstemmed The neuroprotective effect of curcumin against ATO triggered neurotoxicity through Nrf2 and NF-κB signaling pathway in the brain of ducks
title_sort neuroprotective effect of curcumin against ato triggered neurotoxicity through nrf2 and nf-κb signaling pathway in the brain of ducks
publisher Elsevier
publishDate 2021
url https://doaj.org/article/c863eb6c458d4fb7a0f1e94c9e852a9c
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