Restoration and stabilization of acrylamide-induced DNA, mitochondrial damages and oxidative stress by chrysin in human lymphocyte

被引:9
|
作者
Salimi, Ahmad [1 ,2 ]
Hashemidanesh, Niloufar [1 ,3 ]
Seydi, Enayatollah [4 ,5 ]
Baghal, Elahe [1 ,3 ]
Khodaparast, Farzad [1 ,3 ]
Ghobadi, Hassan [6 ]
机构
[1] Ardabil Univ Med Sci, Sch Pharm, Dept Pharmacol & Toxicol, Ardebil, Iran
[2] Ardabil Univ Med Sci, Tradit Med & Hydrotherapy Res Ctr, Ardebil, Iran
[3] Ardabil Univ Med Sci, Fac Pharm, Students Res Comm, Ardebil, Iran
[4] Alborz Univ Med Sci, Sch Hlth, Dept Occupat Hlth & Safety Engn, Karaj, Iran
[5] Alborz Univ Med Sci, Res Ctr Hlth Safety & Environm, Karaj, Iran
[6] Ardabil Univ Med Sci, Fac Med, Internal Med Dept, Pulm Div, Ardebil, Iran
关键词
Acrylamide; chrysin; oxidative stress; mitochondria; cytotoxicity; ANTIOXIDANT; APOPTOSIS; BALANCE; CANCER; RATS;
D O I
10.1080/17425255.2021.1940951
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Acrylamide (AA) is a water-soluble toxic chemical that is considered one of the most important food contaminants. Furthermore, AA is considered a major public health risk. Methods: This study was designed to evaluate the effects of AA on cytotoxicity, oxidative damage and genotoxicity in human lymphocytes and also to evaluate the protective effects of the chrysin (CH). Lymphocytes after isolation from the blood were treated with AA (50 mu M), AA (50 mu M) plus CH (10, 25, 50 mu M) and CH (50 mu M), and parameters such as cell viability, mitochondrial and lysosomal damage, as well as oxidative damage to DNA were examined. Results: The results showed that CH was able to reduce cytotoxicity, reactive oxygen species (ROS) levels, lipid peroxidation (LPO) level, collapse in mitochondrial membrane potential (MMP) and oxidative damage of DNA caused by AA in human lymphocytes. Also, co-treatment of the AA-exposed human lymphocytes with CH increases the glutathione (GSH) levels. Conclusion: Results suggest that CH (10, 25, 50 mu M) shows a protective role in AA-induced cytotoxicity, oxidative stress, mitochondrial damage and DNA oxidative damage.
引用
收藏
页码:857 / 865
页数:9
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