Study on SH-SY5Y autophagy inhibition and apoptosis induced by methanol extract of Zanthoxylum armatum DC. based on mTOR signal pathway

Author:

Guo Jiafu1ORCID,Wen Jiayu1,Xiang Qiwen1,Huang Yan2,Hu Tingting1,Rao Chaolong1234

Affiliation:

1. School of Public Health, Chengdu University of Traditional Chinese Medicine , No. 1166, Liutai Avenue, Chengdu, Sichuan 611137 , China

2. Key Laboratory of Southwestern Chinese Medicine Resources, Chengdu University of Traditional Chinese Medicine , No. 1166, Liutai Avenue, Chengdu, Sichuan 611137 , China

3. R&D Center for Efficiency , Safety and Application in Chinese Materia Medica with Medical and Edible Values, , No. 1166, Liutai Avenue, Chengdu, Sichuan 611137 , China

4. Chengdu University of Traditional Chinese Medicine , Safety and Application in Chinese Materia Medica with Medical and Edible Values, , No. 1166, Liutai Avenue, Chengdu, Sichuan 611137 , China

Abstract

Abstract Background Zanthoxylum armatum DC. (ZADC) is a novel food raw material resource, offering both edible and medicinal properties. Recent research has unveiled the toxic nature of ZADC, particularly its close association with the nervous system. In a prior study, we observed that administering methanol extract of Zanthoxylum armatum DC. (MZADC) to rats via gavage at a dose of 1.038 g/kg resulted in various neurotoxicity symptoms, including excessive salivation, reduced mobility, unsteady gait, muscle twitching, and altered respiratory rates. Materials and methods We conducted cell-based research to assess the safety of ZADC and elucidate its potential toxic mechanism. In addition, we used experimental methods such as Cell Counting Kit-8, Western blot, and Flow cytometry to detect cytotoxicity in SH-SY5Y cells after intervention with MZADC. Results Following exposure of SY-SY5Y cells with MZADC, a substantial decline in cell viability was observed, accompanied by a concentration-dependent increase in intracellular reactive oxygen species (ROS) levels. Additionally, MZADC induced cellular oxidative stress, leading to elevated malonic dialdehyde (MDA) and superoxide dismutase (SOD) concentrations while decreasing glutathione (GSH) levels. Furthermore, MZADC induced apoptosis at varying doses (20, 40, and 60 μg/mL), and this effect was associated with increased Caspase-3, Bax expressions, and reduced Bcl2 and Bcl2/Bax expressions. In addition, the investigation revealed that MZADC induced autophagy inhibition in SH-SY5Y cells by activating the mTOR signaling pathway, resulting in a decrease in LC3II/LCI and Beclin-1, while increasing p-mTOR/mTOR, p62. Conclusion Consequently, this study suggests that MZADC triggers the mTOR pathway through oxidative stress in SH-SY5Y cells, ultimately leading to apoptosis. Understanding the toxicity mechanisms associated with ZADC can offer a valuable theoretical and experimental basis for its development and utilization.

Publisher

Oxford University Press (OUP)

Reference31 articles.

1. Textual research on origin of Zanthoxylum armatum and consideration of its definition;Zhu;Chin. Tradit. Herb. Drugs,2018

2. Recent research status of bioactive constituents in Zanthoxylum plants;Wang;Chin. Tradit. Herb. Drugs,2002

3. Characterization and evaluation of bioactive polyphenolic constituents from Zanthoxylum armatum DC., a traditionally used plant;Nooreen;Biomed Pharmacother,2017

4. Characterization of the potent odorants in Zanthoxylum armatum DC Prodr. pericarp oil by application of gas chromatography-mass spectrometry-olfactometry and odor activity value;Liu;Food Chem,2020

5. Ethnobotanical studies of some useful shrubs and trees of district Buner, NWFP, Pakistan;Hamayun;Ethnobot Leafl,2003

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3