» Articles » PMID: 19429044

Neuroprotective Effects of Enriched Environment in MPTP-treated SAMP8 Mice

Overview
Journal Neurosci Lett
Specialty Neurology
Date 2009 May 12
PMID 19429044
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Neuroprotective effects of enriched environment (EE) have been well established. Recent study suggests that exposure to EE can protect dopaminergic neurons against MPTP-induced Parkinsonism. After 64 female SAMP8 mice were reared in EE and standard environment (SE) for 3 months, the effects of EE and SE were compared on behavioural change, tyrosine hydroxylase (TH) immunoreaction positive neuron and dopaminetransporter (DAT) expression in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine(MPTP)-treated SAMP8. EE mice showed decreased spontaneous activity compared with SE mice. But EE+MPTP mice showed less decreased spontaneous activity compared with SE+MPTP mice. Otherwise, EE mice showed increased percentage of entries into the open arms and percentage of time spent in the open arms. Furthermore, EE mice demonstrated reduced neurotoxicity, with less decreased TH mRNA and protein expression in Substantia Nigra (SN) after MPTP administration compared with SE mice. SE mice showed a 53.77% loss of TH-positive neurons, whereas EE mice only showed a 42.28% loss. Moreover, EE mice showed decreased DAT mRNA and protein expression compared with SE mice. These data demonstrate that EE can protect dopaminergic neurons against MPTP-induced neuronal damage, which suggest that the probability of developing Parkinson's disease (PD) may be related to life environment.

Citing Articles

Dopaminergic neuron loss in mice due to increased levels of wild-type human α-Synuclein only takes place under conditions of accelerated aging.

Perez-Villalba A, Sirerol-Piquer M, Soriano-Canton R, Folgado V, Perez-Canamas A, Kirstein M Sci Rep. 2024; 14(1):2490.

PMID: 38291230 PMC: 10828501. DOI: 10.1038/s41598-024-53093-1.


Molecular mechanisms underlying the neuroprotection of environmental enrichment in Parkinson's disease.

Alarcon T, Presti-Silva S, Simoes A, Ribeiro F, Pires R Neural Regen Res. 2022; 18(7):1450-1456.

PMID: 36571341 PMC: 10075132. DOI: 10.4103/1673-5374.360264.


The dopamine transporter gene SLC6A3: multidisease risks.

Reith M, Kortagere S, Wiers C, Sun H, Kurian M, Galli A Mol Psychiatry. 2021; 27(2):1031-1046.

PMID: 34650206 PMC: 9008071. DOI: 10.1038/s41380-021-01341-5.


Maternal Protein Malnutrition: Current and Future Perspectives of Spirulina Supplementation in Neuroprotection.

Sinha S, Patro N, Patro I Front Neurosci. 2019; 12:966.

PMID: 30618587 PMC: 6305321. DOI: 10.3389/fnins.2018.00966.


Enriched environment elevates expression of growth associated protein-43 in the substantia nigra of SAMP8 mice.

Yuan Z, Yang J, Ma X, Wang Y, Wang M Neural Regen Res. 2018; 13(11):1988-1994.

PMID: 30233074 PMC: 6183044. DOI: 10.4103/1673-5374.239447.