Potential protective effects of alpha-pinene against cytotoxicity caused by aspirin in the IEC-6 cells

被引:69
作者
Bouzenna, Hafsia [1 ,2 ,3 ]
Hfaiedh, Najla [2 ,3 ]
Giroux-Metges, Marie-Agnes [1 ]
Elfeki, Abdelfattah [2 ]
Talarmin, Helene [1 ]
机构
[1] Univ Bretagne, Lab ORPHY EA4324, UFR Sci & Tech, Occidentale 6 Ave Le Gorgeu,CS 93837, F-29238 Brest 3, France
[2] Fac Sci Sfax, Lab Environm Physiopathol Valorizat Bioact Mol &, Rd Soukra Km 3-5 PB 1171-3000, Sfax, Tunisia
[3] Fac Sci Gafsa, Lab Anim Eco Physiol, Gafsa 2112, Tunisia
关键词
Aspirin; Oxidative stress; Alpha-pinene; MAPK pathways; IEC-6; cells; INDUCED OXIDATIVE STRESS; ESSENTIAL OIL; ISOPRENE EMISSION; APOPTOSIS; ANTIOXIDANT; ANTIBACTERIAL; ACTIVATION; L; GLUTATHIONE; FOREST;
D O I
10.1016/j.biopha.2017.06.031
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Alpha-pinene is a key compound of the essential oils extracted from many species of coniferous trees. It is known for its biological activities. The aim of the present study was to determine the preventive effect of alpha-pinene on aspirin-induced toxicity in vitro, using IEC-6 cells, and to investigate its antioxidant activities. The antioxidant activities were determined by 1,1-diphenyl-2-picrylhydrazyl (DPPH) and ferric reducing antioxidant power (FRAP). The cytotoxicity and oxidative stress were detected by cell viability, antioxidant enzyme activity, malondialdehyde (MDA) and GSH production, and the activation of MAPK pathways. The results indicated that alpha-pinene revealed an important antioxidant activity. It was evaluated by DPPH test (EC50 = 310 +/- 10 mu g/mL) and FRAP test (EC50 = 238 +/- 18.92 mu g/mL). The co-exposure of alpha-pinene with aspirin on cells significantly increased the survival of cells and the level of GSH, and decreased the levels of MDA and total SOD and the activity of Mn-SOD. In addition, the activation of p38 and JNK was blocked by alpha-pinene. Therefore, these findings suggest that alpha-pinene can protect IEC-6 cells against aspirin-induced oxidative stress. (C) 2017 Published by Elsevier Masson SAS.
引用
收藏
页码:961 / 968
页数:8
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