Dongzhu Li ,
Xianpei Tan,
Qiang Tu,
Mingqing Xiang,
Yamei Wang,
Ming Yu,
Tao Tan
Department of Neurology, First People's Hospital of Jingzhou, Jingzhou, Hubei Province, 434000, China;
For correspondence:- Dongzhu Li
Email: dzli9053@163.com Tel:+867168110534
Accepted: 11 February 2022
Published: 31 March 2022
Citation:
Li D, Tan X, Tu Q, Xiang M, Wang Y, Yu M, et al.
Breviscapine alleviates MPP+-induced damage and apoptosis of SH-SY5Y cells by activating Nrf2 pathway. Trop J Pharm Res 2022; 21(3):465-470
doi:
10.4314/tjpr.v21i3.2
© 2022 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Abstract
Purpose: To investigate the role and mechanism of action of breviscapine (Brp) in 1-methyl-4-phenylpyridinium ion (MPP+)-induced cell injury in human neuroblastoma cell line, SH-SY5Y.
Methods: The injury on SH-SY5Y cells was induced using MPP+. Cell viability and apoptotic ability were determined by CCK8 assay and Annexin V/PI staining, respectively. Protein expressions of nuclear factor E2-related factor 2 (Nrf2) and its related downstream proteins - hemeoxygenase 1(HO-1) and NAD(P)H-quinoneoxido reductase 1(NQO1), were determined using Western blotting.
Results: Brp dose-dependently attenuated MPP+ induced reduction in the viability of SH SY5Y cells, but alleviated MPP+-induced oxidative stress (OS) and cell injury, as evidenced by the levels of reactive oxygen species (ROS), tyrosine hydroxylase (TH), lactic dehydrogenase (LDH), and dopamine transporter (DAT) (p < 0.05). Brp decreased the amount of apoptotic cells induced by MPP+, as well as the protein levels of Bax and cleaved-caspase 3, and also induced the activation of Nrf2 signaling pathway (p < 0.05).
Conclusion: Brp alleviates MPP+-induced cellular damage and cell apoptosis in SH-SY5Y cells by activating Nrf2 pathway. Thus, Brp is a potential therapeutic candidate for the treatment of PD.
Keywords: Breviscapine, Parkinson’s disease, Oxidative stress, Nrf2 pathway, SH-SY5Y cell