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Copyright (c) 2023 Qiongwen Rong, Chang Zhou, Yuanyuan Ma
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
The undersigned hereby assign all rights, included but not limited to copyright, for this manuscript to CMB Association upon its submission for consideration to publication on Cellular and Molecular Biology. The rights assigned include, but are not limited to, the sole and exclusive rights to license, sell, subsequently assign, derive, distribute, display and reproduce this manuscript, in whole or in part, in any format, electronic or otherwise, including those in existence at the time this agreement was signed. The authors hereby warrant that they have not granted or assigned, and shall not grant or assign, the aforementioned rights to any other person, firm, organization, or other entity. All rights are automatically restored to authors if this manuscript is not accepted for publication.Effect of 4-AP on MPP+/ MPTP-induced Parkinson's disease model
Corresponding Author(s) : Yuanyuan Ma
Cellular and Molecular Biology,
Vol. 69 No. 8: Issue 8
Abstract
To study the effect of 4-AP on Parkinson's disease (PD) cells and animal model. PD cells were pretreated with different concentrations of 4-AP for 24 hours, then PD cells were prepared by MPP+, and the cell activity was detected by CCK8 kit. PD mice were prepared by MPTP and then given 4-AP for 10 days. Finally, the behavioral changes of mice were detected by pole climbing test and open field test, and the expression of TH in the midbrain was detected by IHC and WB. 4-AP could increase the activity of PD cells induced by MPP+. In the field experiment, the total spontaneous activity distance of PD mice (1380.01 ± 151.84) cm was not different from that of 4-AP intervention (1228.65 ± 358.25) cm but was reduced than that of normal mice (2121.89 ± 235.95) (P<0.05). In the pole climbing test, the pole climbing time of PD mice was (7.95 ± 1.02) seconds, compared with that of PD mice treated with 4-AP, there was no difference between the two groups, but it was reduced than that of normal mice (P<0.05). IHC and Western blot showed that the mesencephalic TH of PD mice and drug-treated mice were reduced than that of normal mice (P<0.05), however, drug intervention could not reduce the expression of TH in mice with PD (P>0.5). 4-AP pretreatment can reduce the toxic and side effects of MPP+. 4-AP can not improve the motor function impairment of PD mice, nor can it reduce the toxic effect of MPTP on dopaminergic neurons. There are differences between pre-treatment and post-intervention in the treatment of MPP+/MPTP-induced PD. In order to better explore the drug treatment and target of PD, it is hoped that a cure for PD can be found in PD animals. The timing of intervention and cell and animal experiments should complement each other.
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