Hexavalent chromium induces mitochondrial dynamics disorder in rat liver by inhibiting AMPK/PGC-1α signaling pathway

被引:75
作者
Yang, Qingyue [1 ,2 ]
Han, Bing [1 ]
Xue, Jiangdong [3 ]
Lv, Yueying [1 ]
Li, Siyu [1 ]
Liu, Yan [1 ]
Wu, Pengfei [1 ]
Wang, Xiaoqiao [1 ]
Zhang, Zhigang [1 ,2 ]
机构
[1] Northeast Agr Univ, Coll Vet Med, 600 Changjiang Rd, Harbin 150030, Peoples R China
[2] Heilongjiang Key Lab Lab Anim & Comparat Med, 600 Changjiang Rd, Harbin 150030, Peoples R China
[3] Inner Mongolia Univ Nationalities, Coll Anim Sci & Technol, Tongliao 028000, Peoples R China
基金
中国国家自然科学基金;
关键词
Cr(VI); Liver injury; Mitochondria dynamics disorder; AMPK/PGC-1; alpha; Division and fusion; OXIDATIVE STRESS; MERCURIC-CHLORIDE; DIETARY LUTEOLIN; CELL DEATH; APOPTOSIS; PROTECTS; INJURY; ACTIVATION; AUTOPHAGY; DISEASE;
D O I
10.1016/j.envpol.2020.114855
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Occupational exposure to hexavalent chromium (Cr(VI)) can cause cytotoxicity and carcinogenicity. In this study, we established a liver injury model in rats via intraperitoneal injection of potassium dichromate (0, 2, 4, and 6 mg/kg body weight) for 35 d to investigate the mechanism of Cr(VI)-induced liver injury. We found that Cr(VI) induced hepatic histopathological lesions, oxidative stress, and apoptosis and reduced the expression of mitochondrial-related regulatory factors such as adenosine 5'-monophosphate-activated protein kinase (AMPK) and peroxisome proliferator-activated receptor gamma coactivator 1 alpha (PGC-1 alpha) in a dose-dependent manner. Furthermore, Cr(VI) promoted mitochondrial division and inhibited fusion, leading to increased expression of caspase-3 and production of mitochondrial reactive oxygen species. Our study demonstrates that long-term exposure to Cr(VI) induces mitochondrial dynamics disorder by inhibiting AMPK/PGC-1 alpha signaling pathway in rat liver. (C) 2020 Elsevier Ltd. All rights reserved.
引用
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页数:10
相关论文
共 75 条
[1]  
Abbas A, 2020, INT J PHYTOREMEDIAT, V22, P52, DOI 10.1080/15226514.2019.1644286
[2]   Nanomaterial's based chromium speciation in environmental samples: A review [J].
Arain, Muhammad Balal ;
Ali, Imtiaz ;
Yilmaz, Erkan ;
Soylak, Mustafa .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2018, 103 :44-55
[3]   Luteolin-mediated PI3K/AKT/Nrf2 signaling pathway ameliorates inorganic mercury-induced cardiac injury [J].
Baiyun, Ruiqi ;
Li, Siyu ;
Liu, Biying ;
Lu, Jingjing ;
Lv, Yueying ;
Xu, Jianwen ;
Wu, Jiahui ;
Li, Jiayi ;
Lv, Zhanjun ;
Zhang, Zhigang .
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 2018, 161 :655-661
[4]   Effects of Polycyclic Aromatic Hydrocarbons in Northern Bobwhite Quail (Colinus virginianus) [J].
Brausch, John M. ;
Blackwell, Brett R. ;
Beall, Blake N. ;
Caudillo, Cynthia ;
Kolli, Venkata ;
Godard-Codding, Celine ;
Cox, Stephen B. ;
Cobb, George ;
Smith, Philip N. .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, 2010, 73 (08) :540-551
[5]   The emerging role of skeletal muscle oxidative metabolism as a biological target and cellular regulator of cancer-induced muscle wasting [J].
Carson, James A. ;
Hardee, Justin P. ;
VanderVeen, Brandon N. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2016, 54 :53-67
[6]   Flow cytometry based assays for the measurement of apoptosis-associated mitochondrial membrane depolarisation and cytochrome c release [J].
Christensen, Melinda E. ;
Jansen, Elisa S. ;
Sanchez, Washington ;
Waterhouse, Nigel J. .
METHODS, 2013, 61 (02) :138-145
[7]   Nicotinamide adenine dinucleotide is transported into mammalian mitochondria [J].
Davila, Antonio ;
Liu, Ling ;
Chellappa, Karthikeyani ;
Redpath, Philip ;
Nakamaru-Ogiso, Eiko ;
Paolella, Lauren M. ;
Zhang, Zhigang ;
Migaud, Marie E. ;
Rabinowitz, Joshua D. ;
Baur, Joseph A. .
ELIFE, 2018, 7
[8]   Selective optical recognition and quantification of parts per million levels of Cr6+ in aqueous and organic media by immobilized polypyridyl complexes on glass [J].
de Ruiter, Graham ;
Gupta, Tarkeshwar ;
van der Boom, Milko E. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (09) :2744-+
[9]   Mdivi-1 attenuates lipopolysaccharide-induced acute lung injury by inhibiting MAPKs, oxidative stress and apoptosis [J].
Deng, Songyun ;
Zhang, Lina ;
Mo, Yunan ;
Huang, Yan ;
Li, Wenchao ;
Peng, Qianyi ;
Huang, Li ;
Ai, Yuhang .
PULMONARY PHARMACOLOGY & THERAPEUTICS, 2020, 62
[10]   Complementation between mouse Mfn1 and Mfn2 protects mitochondrial fusion defects caused by CMT2A disease mutations [J].
Detmer, Scott A. ;
Chan, David C. .
JOURNAL OF CELL BIOLOGY, 2007, 176 (04) :405-414