Biocell | |
Nicotine and menthol independently exert neuroprotective effects against cisplatin- or amyloid- toxicity by upregulating Bcl-xl via JNK activation in SH-SY5Y cells | |
article | |
YIBIN RUAN1  ZHONGMING XIE2  QIONG LIU2  LIXIAO ZHANG2  XIKUI HAN2  XIAOYAN LIAO2  JIAN LIU1  FENGGUANG GAO2  | |
[1] Technology Center, Ltd.;Department of Basic Medical Sciences, School of Medicine, Xiamen University | |
关键词: Nicotine; Menthol; Apoptosis; Mitochondrial membrane potential; Tumor necrosis factor-alpha; | |
DOI : 10.32604/biocell.2021.015261 | |
学科分类:仪器 | |
来源: Biocell | |
【 摘 要 】
Nicotine and menthol, agonists of nicotinic acetylcholine receptor (nAChR) and transient receptor potential melastatin type 8 (TRPM8), serve important roles in the prevention of cell death-involved neurodegenerative diseases. However, the potential synergistic effects of nicotine and menthol on anti-apoptotic ability are still uncertain. In the present study, the potential synergistic effects of nicotine and menthol on cisplatin or amyloid β 1-42 induced cell model of the neurodegenerative diseases were explored by assessing cell viability, TNF-α expression, caspase-3 activation, and the collapse of mitochondrial membrane potential in human SH-SY5Y neuroblastoma cells. Statistical significance was tested using Student’s t -test or one-way ANOVA with post hoc Newman-Keuls test. The results showed that: Firstly, SH-SY5Y cell viability was obviously increased by the treatments with nicotine and menthol. Secondly, nicotine and menthol independently alleviated cisplatin or amyloid β 1-42 induced TNF-α up-regulation. Thirdly, nicotine and menthol abrogated the effect of cisplatin and amyloid β 25-35 on caspase-3 activation. Interestingly, the effect of cisplatin and amyloid β 1-42 on the collapse of mitochondrial membrane potential was efficiently attenuated by nicotine and menthol treatments. Most importantly, the inhibition of c-jun kinase (JNK) activation abolished the effect of cisplatin, and amyloid β 1-42 stimulated Bcl-xl expression. All these findings indicate that nicotine and menthol independently exert neuroprotective effects by upregulating Bcl-xl via JNK activation. Nicotine and menthol augmented Bcl-xl expression and JNK phosphorylation, and thus they are potential therapeutic targets for altering the progress of neurodegenerative diseases.
【 授权许可】
CC BY
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