Microcystin-LR and polystyrene microplastics jointly lead to hepatic histopathological damage and antioxidant dysfunction in male zebrafish

被引:8
作者
Lin, Wang [1 ,2 ,3 ]
Hu, Fen [1 ]
Liu, Fang [1 ]
Liao, Ling [1 ]
Ling, Ling [1 ]
Li, Li [4 ]
Yang, Jifeng [5 ]
Yang, Pinhong [1 ,3 ,6 ]
机构
[1] Hunan Univ Arts & Sci, Coll Life & Environm Sci, Changde 415000, Peoples R China
[2] Yunnan Univ, Inst Ecol Res & Pollut Control Plateau Lakes, Sch Ecol & Environm Sci, Kunming 650500, Peoples R China
[3] Hunan Prov Key Lab Mol Immun Technol Aquat Anim D, Changde 415000, Peoples R China
[4] Huazhong Agr Univ, Coll Fisheries, Wuhan 430070, Peoples R China
[5] Hunan Univ Arts & Sci, Coll Chem & Mat Engn, Changde 415000, Peoples R China
[6] Hunan Univ Arts & Sci, 3150 Dongting Ave, Changde 415000, Peoples R China
基金
中国国家自然科学基金;
关键词
Microcystin-LR; Microplastics; Histopathological analysis; Oxidative damage; Zebrafish; OXIDATIVE STRESS; RESPONSES; LIVER; RESISTANCE; APOPTOSIS; EXPOSURE; FISH; NRF2;
D O I
10.1016/j.envpol.2024.123789
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The co-occurrence of cyanobacterial blooms and nano-microplastic pollution in the water is becoming an emerging risk. To assess the combined hepatotoxicity of microcystin-LR (MC-LR) and polystyrene microplastics (PSMPs) on zebrafish (Danio rerio), male adult zebrafish were exposed to single MC-LR (0, 1, 5, 25 mu g/L) and a mixture of MC-LR and PSMPs (100 mu g/L). After 60 d exposure, the results indicated that PSMPs significantly increased the MC-LR bioaccumulation in the livers in contrast to the single 25 mu g/L MC-LR treatment group. Moreover, the severity of hepatic pathological lesions was aggravated in the MC-LR + PSMPs treatment groups, which were mainly characterized by cellular vacuolar degeneration, swollen hepatocytes, and pyknotic nucleus. The ultrastructural changes also proved that PSMPs combined with MC-LR could enhance the swollen mitochondria and dilated endoplasmic reticulum. The biochemical results, including increased malondialdehyde (MDA) and decreased glutathione (GSH), indicated that PSMPs intensified the MC-LR-induced oxidative damage in the combined treatment groups. Concurrently, alterations of sod1 and keap1a mRNA levels also confirmed that PSMPs together with MC-LR jointly lead to enhanced oxidative injury. Our findings demonstrated that PSMPs enhanced the MC-LR bioavailability by acting as a vector and exacerbating the hepatic injuries and antioxidant dysfunction in zebrafish.
引用
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页数:9
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