首页> 美国卫生研究院文献>Aging (Albany NY) >Co-exposure to multi-walled carbon nanotube and lead ions aggravates hepatotoxicity of nonalcoholic fatty liver via inhibiting AMPK/PPARγ pathway
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Co-exposure to multi-walled carbon nanotube and lead ions aggravates hepatotoxicity of nonalcoholic fatty liver via inhibiting AMPK/PPARγ pathway

机译:多壁碳纳米管和铅离子的共同暴露通过抑制AMPK /PPARγ途径加剧非酒精性脂肪肝的肝毒性

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摘要

Multi-walled carbon nanotubes (MWCNTs) have been widely used in sewage disposal, water purification, and disinfection. Co-exposure to MWCNTs and heavy metal ions is common during water disposal. However, the hepatotoxicity of co-exposure to MWCNTs and lead ions for nonalcoholic fatty liver disease (NAFLD) subjects has not been investigated. NAFLD mice were fed intragastrically with MWCNTs and lead acetate (PbAc). Combined administration of MWCNTs and PbAc significantly damaged the liver function, and aggravated the nonalcoholic steatohepatitis phenotype as well as the hepatic fibrosis and steatosis in NAFLD mice. Furthermore, MWCNTs and PbAc significantly induced apoptosis in primary hepatocytes isolated from NAFLD mice. Combined administration of MWCNTs and PbAc also resulted in hepatic lipid peroxidation by inducing antioxidant defense system dysfunction, and significantly enhanced the expression levels of inflammatory cytokines in NAFLD mice livers. Meanwhile, combined administration of MWCNTs and PbAc may exert its hepatotoxicity in the NAFLD via inhibiting the adenosine 5‘-monophosphate activated protein kinase (AMPK)/peroxisome proliferator-activated receptors γ (PPARγ) pathway. Taken together, we conclude that co-exposure to MWCNTs and PbAc can remarkably aggravate the hepatotoxicity in NAFLD mice via inhibiting the AMPK/PPARγ pathway. This study may provide a biosafety evaluation for the application of nanomaterials in wastewater treatment.
机译:多壁碳纳米管(MWCNT)已广泛用于污水处理,净水和消毒。在水处理期间,对MWCNT和重金属离子的共同暴露是常见的。然而,尚未研究共同暴露于MWCNT的肝毒性和非酒精性脂肪肝病(NAFLD)受试者的铅离子。 NAFLD小鼠用MWCNT和醋酸乙酸盐(PBAC)喂养胃内喂养。 MWCNT和PBAC的组合施用显着受到肝功能,并加剧了非酒精脂肪肝炎表型以及NAFLD小鼠的肝纤维化和脂肪变性。此外,MWCNT和PBAC在从NAFLD小鼠分离的原发性肝细胞中显着诱导细胞凋亡。 MWCNT和PBAC的组合施用也导致肝脂质过氧化通过诱导抗氧化防御系统功能障碍,并显着提高了NAFLD小鼠肝脏中炎性细胞因子的表达水平。同时,MWCNT和PBAC的组合施用可以通过抑制腺苷5'-单磷酸活化蛋白激酶(AMPK)/过氧缺体增殖物激活受体γ(PPARγ)途径在NAFLD中施加其肝毒性。总之,我们得出结论,通过抑制AMPK /PPARγ途径,对MWCNT和PBAC的共同暴露可以显着加剧NAFLD小鼠中的肝毒性。该研究可以提供用于在废水处理中施加纳米材料的生物安全评估。

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