Chronic exposure to arsenic and high fat diet additively induced cardiotoxicity in male mice

被引:30
作者
Ahangarpour, Akram [1 ]
Zeidooni, Leila [2 ,3 ]
Samimi, Azin [2 ,3 ]
Alboghobeish, Soheila [3 ,4 ]
Khorsandi, Laya Sadat [5 ]
Moradi, Mitra [1 ]
机构
[1] Ahvaz Jundishapur Univ Med Sci, Hlth Res Inst, Dept Physiol, Diabet Res Ctr, Ahvaz, Iran
[2] Ahvaz Jundishapur Univ Med Sci, Sch Pharm, Dept Toxicol, Ahvaz, Iran
[3] Ahvaz Jundishapur Univ Med Sci, Sch Pharm, Student Res Comm, Ahvaz, Iran
[4] Ahvaz Jundishapur Univ Med Sci, Sch Pharm, Dept Pharmacol, Ahvaz, Iran
[5] Ahvaz Jundishapur Univ Med Sci, Cell & Mol Res Ctr, Fac Med, Ahvaz, Iran
关键词
Heart; Arsenic; High fat diet; Chronic exposure; Cardiotoxicity;
D O I
10.4103/1735-5362.220967
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
Diet is one of the important risk factors that could potentially affect arsenic-induced cardiotoxicity. The present study was undertaken to investigate the effect of high fat diet on arsenic-induced cardiotoxicity in mice. Mice were divided into six different groups (n = 12), two control groups received either low fat diet (LFD) or high fat diet (HFD) along with deionized drinking water and four test groups given LFD + 25 ppm arsenic, LFD + 50 ppm arsenic, HFD + 25 ppm arsenic, and HFD + 50 ppm arsenic in drinking water for 5 months. The body weight, heart weight to body weight ratio, cardiac biochemical markers, lipid profile, and histological examination of heart were evaluated. The results demonstrated that arsenic exposure led to a significant decrease in heart glutathione level, catalase enzyme activity, and a significant increase in reactive oxygen species (ROS), malondialdehyde levels, and biochemical enzymes. The administration of HFD resulted in above-mentioned changes as well as an alteration in lipid profile; however, arsenic exposure alone or along with HFD caused a reduction in lipid profile factors, except HDL level. Our results revealed that HFD increased arsenic-induced heart injury in the mice. This effect may be because of reduction in antioxidant activities and/or increase in oxidative stress and ROS in mice heart tissues. These findings could be important for clinical intervention to protect against or prevent arsenic-induced cardiotoxicity in humans.
引用
收藏
页码:47 / 56
页数:10
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