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The health risk of acetochlor metabolite CMEPA is associated with lipid accumulation induced liver injury

Liver injury may cause many diseases, such as non-alcoholic fatty liver disease (NAFLD). Acetochlor is one of the representative chloroacetamide herbicides, and its metabolite 2-chloro-N-(2-ethyl-6-methyl phenyl) acetamide (CMEPA) is the main form of exposure in the environment. It has been shown th...

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Published in:Environmental pollution (1987) 2023-08, Vol.331 (Pt 2), p.121857-121857, Article 121857
Main Authors: Wang, Wei-Guo, Li, Mu-Yao, Diao, Lin, Zhang, Cheng, Tao, Li-Ming, Zhou, Wei-Xing, Xu, Wen-Ping, Zhang, Yang
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cited_by cdi_FETCH-LOGICAL-c362t-8981898c0809880a7d81825df6a831786571e7d7a986ee7cbd477f6e508ae5a73
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container_end_page 121857
container_issue Pt 2
container_start_page 121857
container_title Environmental pollution (1987)
container_volume 331
creator Wang, Wei-Guo
Li, Mu-Yao
Diao, Lin
Zhang, Cheng
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description Liver injury may cause many diseases, such as non-alcoholic fatty liver disease (NAFLD). Acetochlor is one of the representative chloroacetamide herbicides, and its metabolite 2-chloro-N-(2-ethyl-6-methyl phenyl) acetamide (CMEPA) is the main form of exposure in the environment. It has been shown that acetochlor can cause mitochondrial damage of HepG2 cells and induce apoptosis by activating Bcl/Bax pathway (Wang et al., 2021). But there has been less research on CMEPA. we explored the possibility of CMEPA and liver injury through biological experiments. In vivo, CMEPA (0–16 mg/L) induced liver damage in zebrafish larvae, including increased lipid droplets, changes in liver morphology (>1.3-fold) and increased TC/TG content (>2.5-fold). In vitro, we selected L02 (human normal liver cells) as the model, and explored its molecular mechanism. We found that CMEPA (0–160 mg/L) induced apoptosis (similar to 40%), mitochondrial damage and oxidative stress in L02 cells. CMEPA induced intracellular lipid accumulation by inhibiting AMPK/ACC/CPT-1A signaling pathway and activating SREBP-1c/FAS signaling pathway. Our study provides evidence of a link between CMEPA and liver injury. This raises concerns regarding the health risks of pesticide metabolites to liver health. [Display omitted] •CMEPA induced steatosis and liver morphological changes in zebrafish larvae.•CMEPA induced the increase of lipid content and TC/TG content in liver of zebrafish larvae.•CMEPA induced functional impairment and apoptosis of human liver L02 cells.•CMEPA induced oxidative stress and lipid accumulation in L02 cells.•CMEPA induced lipid accumulation via AMPK/ACC/CPT-1A and SREBP-1c/FAS pathways in L02 cells.
doi_str_mv 10.1016/j.envpol.2023.121857
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Acetochlor is one of the representative chloroacetamide herbicides, and its metabolite 2-chloro-N-(2-ethyl-6-methyl phenyl) acetamide (CMEPA) is the main form of exposure in the environment. It has been shown that acetochlor can cause mitochondrial damage of HepG2 cells and induce apoptosis by activating Bcl/Bax pathway (Wang et al., 2021). But there has been less research on CMEPA. we explored the possibility of CMEPA and liver injury through biological experiments. In vivo, CMEPA (0–16 mg/L) induced liver damage in zebrafish larvae, including increased lipid droplets, changes in liver morphology (&gt;1.3-fold) and increased TC/TG content (&gt;2.5-fold). In vitro, we selected L02 (human normal liver cells) as the model, and explored its molecular mechanism. We found that CMEPA (0–160 mg/L) induced apoptosis (similar to 40%), mitochondrial damage and oxidative stress in L02 cells. CMEPA induced intracellular lipid accumulation by inhibiting AMPK/ACC/CPT-1A signaling pathway and activating SREBP-1c/FAS signaling pathway. Our study provides evidence of a link between CMEPA and liver injury. This raises concerns regarding the health risks of pesticide metabolites to liver health. [Display omitted] •CMEPA induced steatosis and liver morphological changes in zebrafish larvae.•CMEPA induced the increase of lipid content and TC/TG content in liver of zebrafish larvae.•CMEPA induced functional impairment and apoptosis of human liver L02 cells.•CMEPA induced oxidative stress and lipid accumulation in L02 cells.•CMEPA induced lipid accumulation via AMPK/ACC/CPT-1A and SREBP-1c/FAS pathways in L02 cells.</description><identifier>ISSN: 0269-7491</identifier><identifier>EISSN: 1873-6424</identifier><identifier>DOI: 10.1016/j.envpol.2023.121857</identifier><identifier>PMID: 37245791</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Acetochlor metabolite ; Animals ; Chemical and Drug Induced Liver Injury, Chronic - metabolism ; Cytotoxicity ; Humans ; Lipid accumulation ; Lipid Metabolism ; Lipids ; Liver - metabolism ; Liver injury ; Zebrafish</subject><ispartof>Environmental pollution (1987), 2023-08, Vol.331 (Pt 2), p.121857-121857, Article 121857</ispartof><rights>2023 Elsevier Ltd</rights><rights>Copyright © 2023 Elsevier Ltd. 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Acetochlor is one of the representative chloroacetamide herbicides, and its metabolite 2-chloro-N-(2-ethyl-6-methyl phenyl) acetamide (CMEPA) is the main form of exposure in the environment. It has been shown that acetochlor can cause mitochondrial damage of HepG2 cells and induce apoptosis by activating Bcl/Bax pathway (Wang et al., 2021). But there has been less research on CMEPA. we explored the possibility of CMEPA and liver injury through biological experiments. In vivo, CMEPA (0–16 mg/L) induced liver damage in zebrafish larvae, including increased lipid droplets, changes in liver morphology (&gt;1.3-fold) and increased TC/TG content (&gt;2.5-fold). In vitro, we selected L02 (human normal liver cells) as the model, and explored its molecular mechanism. We found that CMEPA (0–160 mg/L) induced apoptosis (similar to 40%), mitochondrial damage and oxidative stress in L02 cells. CMEPA induced intracellular lipid accumulation by inhibiting AMPK/ACC/CPT-1A signaling pathway and activating SREBP-1c/FAS signaling pathway. Our study provides evidence of a link between CMEPA and liver injury. This raises concerns regarding the health risks of pesticide metabolites to liver health. 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CMEPA induced intracellular lipid accumulation by inhibiting AMPK/ACC/CPT-1A signaling pathway and activating SREBP-1c/FAS signaling pathway. Our study provides evidence of a link between CMEPA and liver injury. This raises concerns regarding the health risks of pesticide metabolites to liver health. [Display omitted] •CMEPA induced steatosis and liver morphological changes in zebrafish larvae.•CMEPA induced the increase of lipid content and TC/TG content in liver of zebrafish larvae.•CMEPA induced functional impairment and apoptosis of human liver L02 cells.•CMEPA induced oxidative stress and lipid accumulation in L02 cells.•CMEPA induced lipid accumulation via AMPK/ACC/CPT-1A and SREBP-1c/FAS pathways in L02 cells.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>37245791</pmid><doi>10.1016/j.envpol.2023.121857</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-6804-1840</orcidid><orcidid>https://orcid.org/0000-0002-7763-7232</orcidid></addata></record>
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subjects Acetochlor metabolite
Animals
Chemical and Drug Induced Liver Injury, Chronic - metabolism
Cytotoxicity
Humans
Lipid accumulation
Lipid Metabolism
Lipids
Liver - metabolism
Liver injury
Zebrafish
title The health risk of acetochlor metabolite CMEPA is associated with lipid accumulation induced liver injury
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