Convalescent action of menthol against T-2 mycotoxin-induced toxicity: An in vitro study with HaCaT cells

被引:3
|
作者
Rachitha, Puttasiddaiah [1 ]
Krupashree, K. [2 ]
Brindhadevi, Kathirvel [3 ]
Pal, Ajay [4 ]
Chinnathambi, Arunachalam [5 ]
Alahmadi, Tahani Awad [6 ,7 ]
Shanmuganathan, Rajasree [8 ]
Karuppusamy, Indira [9 ]
Raghavendra, Vinay B. [1 ]
机构
[1] Teresian Coll, PG Dept Biotechnol, Mysore 570011, India
[2] CSIR Cent Food Technol Res Inst, Dept Biochem, Mysore 570020, Karnataka, India
[3] Saveetha Univ, Saveetha Inst Med & Tech Sci, Saveetha Dent Coll, Ctr Transdisciplinary Res CFTR,Dept Pharmacol, Chennai, India
[4] Chaudhary Charan Singh Haryana Agr Univ, Hisar 125004, Haryana, India
[5] King Saud Univ, Coll Sci, Dept Bot & Microbiol, POB 2455, Riyadh 11451, Saudi Arabia
[6] King Saud Univ Med City, Coll Med, Dept Pediat, POB 2925, Riyadh 11461, Saudi Arabia
[7] King Saud Med City, King Khalid Univ Hosp, POB 2925, Riyadh 11461, Saudi Arabia
[8] Chandigarh Univ, Univ Ctr Res & Dev, Mohali, India
[9] Natl Inst Mat Sci NIMS, Res Ctr Strateg Mat, Corros Resistant Steel Grp, Tsukuba, Japan
关键词
T-2; mycotoxin; Keratinocytes; i-NOS; Menthol; Oxidative stress; Cell cycle; Toxicity; OXIDATIVE STRESS; DNA-DAMAGE; TOXIN; APOPTOSIS; CYTOTOXICITY; GROWTH;
D O I
10.1016/j.envres.2023.115690
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Only T-2 mycotoxin is emitted as an aerosol and is the most toxic fungal secondary metabolite among mycotoxins. In its clinical condition, the skin is severely irritated and painful due to lesions and alimentary toxic aleukia. Herein, we have assessed various bioactive molecules, viz. kaempferol, menthol, curcumin, and quercetin, against T-2-induced toxicity in HaCaT cells. Menthol offered exceptional protection, protecting 92% of HaCaT cells after exposure to 300 nM T-2 and reducing LDH leakage by up to 42%. Its pre-treatment provided considerable protection against T-2 toxicity, as evidenced by the assessment of mitochondrial membrane potential. Propidium iodide staining revealed a cell cycle halt at the G1, S, and M phases and a significant increase in the sub-G1 percentage in T-2-challenged cells, indicating cell death. However, pre-treatment with menthol promoted cell cycle progression in cells exposed to T-2. Immunoblotting results demonstrated that menthol resulted in a discernible down-regulation of i-NOS expression in T-2-challenged HaCaT cells.
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页数:8
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