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Ameliorative Effects of NXP031 on MPTP-Induced Neurotoxicity

MPTP로 유도된 신경 독성에 대한 NXP031의 개선 효과

  • Lee, Joo Hee (College of Nursing Science, Kyung Hee University) ;
  • Song, Min Kyung (Robert Wood Johnson Medical School Institute for Neurological Therapeutics, Rutgers Biomedical and Health Sciences, Piscataway, NJRobert Wood Johnson Medical School Institute for Neurological Therapeutics, Rutgers Biomedical and Health Sciences) ;
  • Kim, Youn-Jung (College of Nursing Science, Kyung Hee University)
  • 이주희 (경희대학교 간호과학대학) ;
  • 송민경 (로버트 우드존슨 의과대학 신경치료 연구소) ;
  • 김연정 (경희대학교 간호과학대학)
  • Received : 2021.07.13
  • Accepted : 2021.08.27
  • Published : 2021.08.31

Abstract

Purpose: The purpose of this study was to investigate effects of NXP031, an inhibitor of oxidation by specifically binding to the complex of DNA aptamer/vitamin C, on dopaminergic neurons loss and the reaction of microglia in an animal model of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced subchronic Parkinson's disease (PD). Methods: A subchronic PD mouse model was induced via an intraperitoneal (IP) injection of MPTP 30 mg/kg per day for five days. NXP031 (vitamin C/aptamer at 200 mg/4 mg/kg) and vitamin C at 200 mg/kg were administered via IP injections at one hour after performing MPTP injection. This process was performed for five days. Motor function was then evaluated with pole and rotarod tests, after which an immunohistochemical analysis was performed. Results: NXP031 administration after MPTP injection significantly improved motor functions (via both pole and rotarod tests) compared to the control (MPTP injection only) (p<.001). NXP031 alleviated the loss of dopaminergic neurons in the substantia nigra (SN) and striatum caused by MPTP injection. It was found to have a neuroprotective effect by reducing microglia activity. Conclusion: NXP031 can improve impaired motor function, showing neuroprotective effects on dopaminergic neurons in the SN and striatum of MPTP-induced subchronic Parkinson's disease mouse model. Results of this study suggest that NXP031 has potential in future treatments for PD and interventions for nerve recovery.

Keywords

Acknowledgement

This research is supported by Nexmos (KHU-20182507U0054101S000100) and National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (NRF-2020R1A2B5B0100276611).

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