Atorvastatin protected from paraquat-induced cytotoxicity in alveolar macrophages via down-regulation of TLR-4

被引:15
作者
Alizadeh-Tabrizi, Nazli [1 ]
Malekinejad, Hassan [1 ,2 ]
Varasteh, Soheil [3 ]
Cheraghi, Hadi [1 ]
机构
[1] Urmia Univ, Fac Vet Med, Dept Pharmacol & Toxicol, Orumiyeh, Iran
[2] Urmia Med Univ Sci, Fac Pharm, Dept Pharmacol & Toxicol, Orumiyeh, Iran
[3] Univ Utrecht, Inst Pharmaceut Sci, Fac Sci, Utrecht, Netherlands
关键词
Alveolar macrophages; Atorvastatin; Cytotoxicity; Paraquat; Toll like receptor-4; INDUCED LUNG INFLAMMATION; PPAR-GAMMA RECEPTORS; OXIDATIVE STRESS; PULMONARY-FIBROSIS; CIGARETTE-SMOKE; NITRIC-OXIDE; INJURY; ACID; MICE; ACTIVATION;
D O I
10.1016/j.etap.2016.11.011
中图分类号
X [环境科学、安全科学];
学科分类号
083001 [环境科学];
摘要
The current study designed to clarify the mechanism of paraquat-induced cytotoxicity and protective effects of Atorvastatin on freshly isolated alveolar macrophages (AMs). AMs were collected via bronchoalveolar lavage and exposed to various concentrations of paraquat in the presence and absence of atorvastatin for 24 h. Cell viability, myeloperoxidase activity; nitric oxide generation and total antioxidant capacity were assessed. Expression of TLR-4 at mRNA and protein levels were studied by using PCR and western blot methods Atorvastatin enhanced the paraquat-reduced cell viability and reduced the paraquat-induced myeloperoxidase activity and nitric oxide production. Moreover, atorvastatin down regulated by 60% the paraquat up-regulated expression of TLR-4 at protein and mRNA level. Our results suggest that, AMs in vitro model could be a novel cytological tool for studies on paraquat poisoning and therapy regimens. Additionally, atorvastatin cytoprotective effects on paraquat-induced cytotoxicity partly attribute to its anti-myeloperoxidase, antioxidant properties, which might be regulated via TLR-4 expression. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:8 / 13
页数:6
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