Effects of treadmill exercise on behavioral recovery and neural changes in the substantia nigra and striatum of the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-lesioned mouse
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Our goal was to extend our understanding of the neural changes behind motor recovery with treadmill exercise in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-lesioned mouse. We determined the extent of dopamine (DA) terminal changes using Western immunoblotting [striatal dopamine transporter (DAT) and tyrosine hydroxylase (TH)] and alterations in the mean number of DA cells/section by immunohistochemistry and Nissl staining [TH-labeled cells and thionin-stained cells in the substantia nigra pars compacta (SN-PC)]. We measured recovery of gait performance and amount of spontaneous physical activity using the parallel rod activity chamber (PRAC). We hypothesized that the decrease in TH-labeled neurons in the SN-PC due to MPTP will be partially reversed by treadmill exercise, leading to recovery of motor behavior as measured by the PRAC. Following MPTP or vehicle administration, mice ran on the treadmill for 1h/day at 18cm/s, 5days/week. Results showed that treadmill exercise improves gait performance and increases physical activity while promoting increased protein expression of striatal DAT and TH. Exercise was effective for all mice; however, effects of early treadmill-based intervention appear to have an additional and unique benefit in mice who received MPTP. We are the first to show that, even following a nearly 50% decrease in the mean number of TH-labeled neurons/section in the SN-PC following MPTP, treadmill exercise leads to an increase of neurons in the SN-PC and improved motor behavior.
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In these toxin models, neuroprotection has been principally attributed to an exercise-induced increase of neurotrophic factors such as brain-derived neurotrophic factor or glial-derived neurotrophic factor.
“In these toxin models, neuroprotection has been principally attributed to an exercise-induced increase of neurotrophic factors such as brain-derived neurotrophic factor (BDNF) or glial-derived neurotrophic factor (GDNF) 78–81.”
From Exercise-enhanced neuroplasticity targeting motor and cognitive circuitry in Parkinson's disease (2013) · cites this paper as [80]
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References 57 · Cited by 67
- Authors
- Smith, B. A., Goldberg, N. R. S., & Meshul, C. K.
- Affiliations
- Oregon Health & Science University (US)
- Corresponding author
- Smith, Beth A.
- Venue
- Brain Research
- Publisher
- Elsevier BV
- Published
- 2011-04
- Volume
- 1386
- Pages
- 70-80
- ISSN
- 0006-8993 (ISSN-L)
- PMC
- PMC3073026
- OpenAlex
- W1978047491
- Cited by
- 67
- References
- 57
- Citations by year
- 2025: 2 · 2024: 4 · 2023: 2 · 2022: 2 · 2021: 2 · 2020: 6 · 2019: 3 · 2018: 3 · 2017: 12 · 2016: 4 · 2015: 7 · 2014: 6 · 2013: 6 · 2012: 3
- FWCI
- 4.06
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Brain Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Department of Veterans Affairs Merit Review Program (NIA 2T32AG023477-06)
- Topics
- Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
- Health Sciences › Medicine › Rehabilitation › Stroke Rehabilitation and Recovery
- Health Sciences › Medicine › Neurology › Neurological disorders and treatments
- Keywords
- treadmill exercise, MPTP lesion, substantia nigra pars compacta, striatum, dopamine transporter, tyrosine hydroxylase, dopaminergic neuron loss, motor recovery, gait performance, spontaneous physical activity, Parkinson's disease model, neuroprotection
- MeSH terms
- Animals, Corpus Striatum, Exercise Test, Exercise Therapy, Male, Mice, Inbred C57BL, Neural Pathways, Physical Conditioning, Animal, Substantia Nigra, Blotting, Western, Presynaptic Terminals, Recovery of Function, MPTP Poisoning, Mice
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