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Neuroprotective effects of prior limb use in 6-hydroxydopamine-treated rats: possible role of GDNF
Abstract
Unilateral administration of 6-hydroxydopamine (6-OHDA) into the medial forebrain bundle (MFB) causes a loss of dopamine (DA) in the ipsilateral striatum and contralateral motor deficits. However, if a cast is placed on the ipsilateral limb during the first 7 days following 6-OHDA infusion, forcing the animal to use its contralateral limb, both the behavioral and neurochemical deficits are reduced. Here, we examine the effect of forced reliance on a forelimb during the 7 days prior to ipsilateral infusion of 6-OHDA on the deficits characteristic of this lesion model. Casted animals displayed no behavioral asymmetries as measured 14-28 days postlesion and a marked attenuation in the loss of striatal DA and its metabolites at 30 days. In addition, animals receiving a unilateral cast alone had an increase in glial cell-line derived neurotrophic factor (GDNF) protein in the striatum corresponding to the overused limb. GDNF increased within 1 day after the onset of casting, peaked at 3 days, and returned to baseline within 7 days. These results suggest that preinjury forced limb-use can prevent the behavioral and neurochemical deficits to the subsequent administration of 6-OHDA and that this may be due in part to neuroprotective effects of GDNF.
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“Restoration of DA-D2R, in combination with increase DA release are known to be critically important in the later phase of motor learning when automaticity is developed 83.”
From Exercise-enhanced neuroplasticity targeting motor and cognitive circuitry in Parkinson's disease (2013) · cites this paper as [83]
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Goldberg, N. R. S., Haack, A. K., & Meshul, C. K. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.09.062 · Cited by 44
RetractedGoldberg, N. R. S., Fields, V. L., Pflibsen, L. R., Salvatore, M. F., & Meshul, C. K. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.12.024 · Cited by 43
Ciucci, M. R., Ma, S. T., Kane, J. R., Ahrens, A. M., & Schallert, T. J. (2008) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2008.04.027 · Cited by 43
Wang, Z., Guo, Y., Myers, K. G., Heintz, R., & Holschneider, D. P. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.02.020 · Cited by 42
Kane, J. R., Ciucci, M. R., Jacobs, A., Tews, N., Russell, J. A., Ahrens, A. M., Ma, S. T., Britt, J. M., Cormack, L. K., & Schallert, T. J. (2011) · Journal of Communication Disorders · doi:10.1016/j.jcomdis.2011.04.005 · Cited by 42
Yang, J., Sadler, T. R., Givrad, T. K., Maarek, J.-M. I., & Holschneider, D. P. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.03.010 · Cited by 41
Metadata
- Authors
- Cohen, A. D., Tillerson, J. L., Smith, A. D., Schallert, T., & Zigmond, M. J.
- Affiliations
- University of Pittsburgh (US)
- The University of Texas at Austin (US)
- University of Michigan (US)
- Corresponding author
- Zigmond, Michael J.
- ORCID
- Cohen, Ann D.
- Venue
- Journal of Neurochemistry
- Publisher
- Wiley
- Published
- 2003-04
- Volume
- 85
- Issue
- 2
- Pages
- 299-305
- ISSN
- 0022-3042 (ISSN-L)
- 1471-4159
- OpenAlex
- W2131124574
- Cited by
- 243
- References
- 52
- Citations by year
- 2026: 3 · 2025: 1 · 2024: 5 · 2023: 2 · 2022: 4 · 2021: 4 · 2020: 12 · 2019: 7 · 2018: 11 · 2017: 13 · 2016: 10 · 2015: 11 · 2014: 17 · 2013: 19 · 2012: 5
- FWCI
- 4.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurochemistry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01ns023979-15)
- U.S. Public Health Service
- National Institute of Mental Health (MH-29670)
- National Institute of Neurological Disorders and Stroke (NS 19608, NS 23979, T32NS007433, NS 07433)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- 6-hydroxydopamine, medial forebrain bundle lesion, dopamine depletion, striatum, glial cell line-derived neurotrophic factor, neuroprotection, motor impairment, behavioral asymmetry, dopamine metabolites
- MeSH terms
- Animals, Apomorphine, Behavior, Animal, Casts, Surgical, Corpus Striatum, Disease Models, Animal, Dopamine, Forelimb, Immobilization, Functional Laterality, Male, Medial Forebrain Bundle, Motor Activity, Nerve Growth Factors, Parkinson Disease, Secondary, 3,4-Dihydroxyphenylacetic Acid, Oxidopamine, Rats, Sprague-Dawley, Rats, Long-Evans, Glial Cell Line-Derived Neurotrophic Factor, Rats
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