Porous Se@SiO2 nanospheres treated paraquat-induced acute lung injury by resisting oxidative stress

被引:34
|
作者
Zhu, Yong [1 ]
Deng, Guoying [2 ]
Ji, Anqi [2 ]
Yao, Jiayi [1 ]
Meng, Xiaoxiao [1 ]
Wang, Jinfeng [1 ]
Wang, Qian [2 ]
Wang, Qiugen [2 ]
Wang, Ruilan [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Gen Hosp, Dept Crit Care Med, 650 Xinsongjiang Rd, Shanghai 201620, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Shanghai Gen Hosp, Ctr Trauma, 650 Xinsongjiang Rd, Shanghai 201620, Peoples R China
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2017年 / 12卷
基金
中国国家自然科学基金;
关键词
porous Se@SiO2 nanospheres; acute lung injury; paraquat poisoning; oxidative stress; inflammatory cytokines; ROS; NF-kappa B; NF-KAPPA-B; SELENIUM NANOPARTICLES; INTOXICATED RATS; INFLAMMATION; MECHANISMS; TOXICITY; PATHWAY; DEXAMETHASONE; DAMAGE; MICE;
D O I
10.2147/IJN.S143192
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Acute paraquat (PQ) poisoning is one of the most common forms of pesticide poisoning. Oxidative stress and inflammation are thought to be important mechanisms in PQ-induced acute lung injury (ALI). Selenium (Se) can scavenge intracellular free radicals directly or indirectly. In this study, we investigated whether porous Se@SiO2 nanospheres could alleviate oxidative stress and inflammation in PQ-induced ALI. Male Sprague Dawley rats and RLE-6TN cells were used in this study. Rats were categorized into 3 groups: control (n=6), PQ (n=18), and PQ + Se@SiO2 (n=18). The PQ and PQ + Se@SiO2 groups were randomly and evenly divided into 3 sub-groups according to different time points (24, 48 and 72 h) after PQ treatment. Porous Se@SiO2 nanospheres 1 mg/kg (in the PQ + Se@SiO2 group) were administered via intraperitoneal injection every 24 h. Expression levels of reduced glutathione, malondialdehyde, superoxide dismutase, reactive oxygen species (ROS), nuclear factor-kappa B (NF-kappa B), phosphorylated NF-kappa B (p-NF-kappa B), tumor necrosis factor-alpha and interleukin-1 beta were detected, and a histological analysis of rat lung tissues was performed. The results showed that the levels of ROS, malondialdehyde, NF-kappa B, p-NF-kappa B, tumor necrosis factor-alpha and interleukin-1 beta were markedly increased after PQ treatment. Glutathione and superoxide dismutase levels were reduced. However, treatment with porous Se@SiO2 nanospheres markedly alleviated PQ-induced oxidative stress and inflammation. Additionally, the results from histological examinations and wet-to-dry weight ratios of rat lung tissues showed that lung damage was reduced after porous Se@SiO2 nanosphere treatment. These data indicate that porous Se@SiO2 nanospheres may reduce NF-kappa B, p-NF-kappa B and inflammatory cytokine levels by inhibiting ROS in PQ-induced ALI. This study demonstrates that porous Se@SiO2 nanospheres may be a therapeutic method for use in the future for PQ poisoning.
引用
收藏
页码:7143 / 7152
页数:10
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