The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Time-course gait analysis of hemiparkinsonian rats following 6-hydroxydopamine lesion
Open accessAbstract
Gait disturbances similar to those of human Parkinson's disease (PD) can be observed in animals after administration of neurotoxin 6-hydroxydopamine (6-OHDA) to induce unilateral nigrostriatal dopamine depletion. However, the relationship between gait disturbances and dopamine depletion following 6-OHDA infusion has not been determined. The present study investigated the longitudinal changes of spatiotemporal gait patterns using a walkway system to acquire footprints and lateral limb images over a 6-week period following unilateral 6-OHDA injection into the medial forebrain bundle of rats. Our results indicated that hemiparkinsonian rats exhibited changes in gait patterns, as compared to normal controls, and pre-lesion levels, including a significantly decreased walking speed and step/stride length as well as an increased base of support and foot angle. The relative percentage of the gait cycle was also altered, showing an increase in the stance to swing ratio, which was more evident in the affected hindlimb. Time-course observations showed that these gait disturbances occurred as early as 4 days post-lesion and gradually increased up to 42 days post-injury. The extents of gait disturbances were compared with conventional apomorphine-induced turning behavior and akinesia bar tests, which were also apparent at 4 days post-lesion but remained relatively unchanged after 28 days. Our time-course gait analysis of a unilateral 6-OHDA rodent model provides insight into the compensatory changes of motor functions during the 6-week development of a nigrostriatal lesion, which might be useful for future objective assessment of novel treatments for human PD subjects.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Nieuwboer, A., Dom, R., De Weerdt, W., Desloovere, K., Fieuws, S., & Broens‐Kaucsik, E. (2001) · Movement Disorders · doi:10.1002/mds.1206 · Cited by 320 · cited 1×
“In addition, PD subjects exhibit abnormal spatial ndices of gait patterns, which typically include short steps [3], reezing gait [2,4] and decreased stride length [5].”
BackgroundSymmetric informationally complete–positive operator valued measures and the extended Clifford group
Appleby, D. M. (2005) · Journal of Mathematical Physics · doi:10.1063/1.1896384 · Cited by 304
Research works printed but not linked: 44
- Bjorklund, 2007, Dopamine neuron systems in the brain: an update, Trends Neurosci, 30, 194, 10.1016/j.tins.2007.03.006 · DOI · Paper page
- Giladi, 2001, Freezing of gait in patients with advanced Parkinson's disease, J Neural Transm, 108, 53, 10.1007/s007020170096 · DOI · Paper page
- Chee, 2009, Gait freezing in Parkinson's disease and the stride length sequence effect interaction, Brain, 132, 2151, 10.1093/brain/awp053 · DOI · Paper page
- Blin, 1990, Quantitative analysis of gait in Parkinson patients: increased variability of stride length, J Neurol Sci, 98, 91, 10.1016/0022-510X(90)90184-O · DOI · Paper page
- Truong, 2006, Developing a preclinical model of Parkinson's disease: a study of behaviour in rats with graded 6-OHDA lesions, Behav Brain Res, 169, 1, 10.1016/j.bbr.2005.11.026 · DOI
- Deumens, 2002, Modeling Parkinson's disease in rats: an evaluation of 6-OHDA lesions of the nigrostriatal pathway, Exp Neurol, 175, 303, 10.1006/exnr.2002.7891 · DOI · Paper page
- Mabrouk, 2009, The novel delta opioid receptor agonist UFP-512 dually modulates motor activity in hemiparkinsonian rats via control of the nigro-thalamic pathway, Neuroscience, 164, 360, 10.1016/j.neuroscience.2009.08.058 · DOI
- Fantin, 2008, Differential effect of NR2A and NR2B subunit selective NMDA receptor antagonists on striato-pallidal neurons: relationship to motor response in the 6-hydroxydopamine model of parkinsonism, J Neurochem, 106, 957, 10.1111/j.1471-4159.2008.05439.x · DOI
- Lindner, 1997, Rats with partial striatal dopamine depletions exhibit robust and long-lasting behavioral deficits in a simple fixed-ratio bar-pressing task, Behav Brain Res, 86, 25, 10.1016/S0166-4328(96)02240-1 · DOI
- Lindner, 1996, Validation of a rodent model of Parkinson's disease: evidence of a therapeutic window for oral Sinemet, Brain Res Bull, 39, 367, 10.1016/0361-9230(96)00027-5 · DOI
- Metz, 2005, The unilateral 6-OHDA rat model of Parkinson's disease revisited: an electromyographic and behavioural analysis, Eur J Neurosci, 22, 735, 10.1111/j.1460-9568.2005.04238.x · DOI
- Amende, 2005, Gait dynamics in mouse models of Parkinson's disease and Huntington's disease, J Neuroeng Rehabil, 2, 20, 10.1186/1743-0003-2-20 · DOI
- Chang, 2006, Neural responses in multiple basal ganglia regions following unilateral dopamine depletion in behaving rats performing a treadmill locomotion task, Exp Brain Res, 172, 193, 10.1007/s00221-005-0312-7 · DOI
- Klein, 2009, Walking pattern analysis after unilateral 6-OHDA lesion and transplantation of foetal dopaminergic progenitor cells in rats, Behav Brain Res, 199, 317, 10.1016/j.bbr.2008.12.007 · DOI
- Vlamings, 2007, High frequency stimulation of the subthalamic nucleus improves speed of locomotion but impairs forelimb movement in Parkinsonian rats, Neuroscience, 148, 815, 10.1016/j.neuroscience.2007.06.043 · DOI
- Chaniary, 2009, Quantification of gait in dystonic Gunn rats, J Neurosci Methods, 180, 273, 10.1016/j.jneumeth.2009.03.023 · DOI
- Yu, 2001, Gait analysis in rats with peripheral nerve injury, Muscle Nerve, 24, 231, 10.1002/1097-4598(200102)24:2<231::AID-MUS80>3.0.CO;2-5 · DOI
- Mabrouk, 2008, Stimulation of delta opioid receptors located in substantia nigra reticulata but not globus pallidus or striatum restores motor activity in 6-hydroxydopamine lesioned rats: new insights into the role of delta receptors in parkinsonism, J Neurochem, 107, 1647, 10.1111/j.1471-4159.2008.05727.x · DOI
- Fischer, 2002, Discrimination of morphine- and haloperidol-induced muscular rigidity and akinesia/catalepsy in simple tests in rats, Behav Brain Res, 134, 317, 10.1016/S0166-4328(02)00044-X · DOI
- Paille, 2007, Rat model of Parkinson's disease with bilateral motor abnormalities, reversible with levodopa, and dyskinesias, Mov Disord, 22, 533, 10.1002/mds.21308 · DOI
- Blandini, 2007, Time-course of nigrostriatal damage, basal ganglia metabolic changes and behavioural alterations following intrastriatal injection of 6-hydroxydopamine in the rat: new clues from an old model, Eur J Neurosci, 25, 397, 10.1111/j.1460-9568.2006.05285.x · DOI
- Yoon, 2007, Treadmill exercise suppresses nigrostriatal dopaminergic neuronal loss in 6-hydroxydopamine-induced Parkinson's rats, Neurosci Lett, 423, 12, 10.1016/j.neulet.2007.06.031 · DOI
- Fearnley, 1991, Ageing and Parkinson's disease: substantia nigra regional selectivity, Brain, 114, 2283, 10.1093/brain/114.5.2283 · DOI · Paper page
- Muir, 1999, Ground reaction forces in locomoting hemi-parkinsonian rats: a definitive test for impairments and compensations, Exp Brain Res, 126, 307, 10.1007/s002210050739 · DOI
- Olsson, 1995, Forelimb akinesia in the rat Parkinson model: differential effects of dopamine agonists and nigral transplants as assessed by a new stepping test, J Neurosci, 15, 3863, 10.1523/JNEUROSCI.15-05-03863.1995 · DOI · Paper page
- Miklyaeva, 1995, Impairments and compensatory adjustments in spontaneous movement after unilateral dopamine depletion in rats, Brain Res, 681, 23, 10.1016/0006-8993(95)00277-W · DOI
- Hausdorff, 1998, Gait variability and basal ganglia disorders: stride-to-stride variations of gait cycle timing in Parkinson's disease and Huntington's disease, Mov Disord, 13, 428, 10.1002/mds.870130310 · DOI · Paper page
- Wang, 2008, A comprehensive analysis of gait impairment after experimental stroke and the therapeutic effect of environmental enrichment in rats, J Cereb Blood Flow Metab, 28, 1936, 10.1038/jcbfm.2008.82 · DOI
- Marin, 2009, Effects of early vs. late initiation of levodopa treatment in hemiparkinsonian rats, Eur J Neurosci, 30, 823, 10.1111/j.1460-9568.2009.06877.x · DOI
- Hefti, 1980, Circling behavior in rats with partial, unilateral nigro-striatal lesions: effect of amphetamine, apomorphine, and DOPA, Pharmacol Biochem Behav, 12, 185, 10.1016/0091-3057(80)90353-6 · DOI
- Hudson, 1993, Correlation of apomorphine- and amphetamine-induced turning with nigrostriatal dopamine content in unilateral 6-hydroxydopamine lesioned rats, Brain Res, 626, 167, 10.1016/0006-8993(93)90576-9 · DOI · Paper page
- Steiner, 2001, Unilateral striatal dopamine depletion: time-dependent effects on cortical function and behavioural correlates, Eur J Neurosci, 14, 1390, 10.1046/j.0953-816x.2001.01756.x · DOI
- Schallert, 2000, CNS plasticity and assessment of forelimb sensorimotor outcome in unilateral rat models of stroke, cortical ablation, parkinsonism and spinal cord injury, Neuropharmacology, 39, 777, 10.1016/S0028-3908(00)00005-8 · DOI · Paper page
- Schneider, 1998, Differential effects of GDNF treatment on rotational asymmetry, skilled forelimb use deficits and sensory neglect in unilateral 6-OHDA-lesioned rats, Restor Neurol Neurosci, 13, 205
- Prentice, 2001, Contributions of the reticulospinal system to the postural adjustments occurring during voluntary gait modifications, J Neurophysiol, 85, 679, 10.1152/jn.2001.85.2.679 · DOI
- Ferraye, 2010, Effects of pedunculopontine nucleus area stimulation on gait disorders in Parkinson's disease, Brain, 133, 205, 10.1093/brain/awp229 · DOI · Paper page
- Rauch, 2010, Effect of deep brain stimulation in the pedunculopontine nucleus on motor function in the rat 6-hydroxydopamine Parkinson model, Behav Brain Res, 210, 46, 10.1016/j.bbr.2010.02.003 · DOI
- Nandi, 2002, Deep brain stimulation of the pedunculopontine region in the normal non-human primate, J Clin Neurosci, 9, 170, 10.1054/jocn.2001.0943 · DOI
- Stefani, 2007, Bilateral deep brain stimulation of the pedunculopontine and subthalamic nuclei in severe Parkinson's disease, Brain, 130, 1596, 10.1093/brain/awl346 · DOI · Paper page
- Breit, 2001, Unilateral lesion of the nigrostriatal pathway induces an increase of neuronal activity of the pedunculopontine nucleus, which is reversed by the lesion of the subthalamic nucleus in the rat, Eur J Neurosci, 14, 1833, 10.1046/j.0953-816x.2001.01800.x · DOI
- Florio, 2007, High-frequency stimulation of the subthalamic nucleus modulates the activity of pedunculopontine neurons through direct activation of excitatory fibres as well as through indirect activation of inhibitory pallidal fibres in the rat, Eur J Neurosci, 25, 1174, 10.1111/j.1460-9568.2007.05360.x · DOI
- Elahi, 2009, Effect of transcranial magnetic stimulation on Parkinson motor function–systematic review of controlled clinical trials, Mov. Disord., 24, 357, 10.1002/mds.22364 · DOI
- Fang, 2010, Review: repetitive transcranial magnetic stimulation over the human primary motor cortex for modulating motor control and motor learning, J. Med. Biol. Eng., 30, 193, 10.5405/jmbe.30.4.01 · DOI
- Chang, 2011, A lack of modulation of motor evoked potential in sensory-impaired individuals with spinal cord injuries, J. Med. Biol. Eng., 31, 37, 10.5405/jmbe.705 · DOI
Cited by
All about running: synaptic plasticity, growth factors and adult hippocampal neurogenesis
Vivar, C., Potter, M. C., & van Praag, H. (2012) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2012_220 · Cited by 370
Implementing Reproducible Research
Stodden, V. (2014) · doi:10.1201/b16868 · Cited by 314
Challenges in Teaching English to Young Learners: Global Perspectives and Local Realities
Copland, F., Garton, S., & Burns, A. (2014) · TESOL Quarterly · doi:10.1002/tesq.148 · Cited by 300
Hsieh, T.-H., Kuo, C.-W., Hsieh, K.-H., Shieh, M.-J., Peng, C.-W., Chen, Y.-C., Chang, Y.-L., Huang, Y.-Z., Chen, C.-C., Chang, P.-K., et al. (2020) · Brain Sciences · doi:10.3390/brainsci10040206 · Cited by 174
Hydrogel-coated microfluidic channels for cardiomyocyte culture
Annabi, N., Selimović, Š., Acevedo Cox, J. P., Ribas, J., Afshar Bakooshli, M., Heintze, D., Weiss, A. S., Cropek, D., & Khademhosseini, A. (2013) · Lab on a Chip · doi:10.1039/c3lc50252j · Cited by 129
Metadata
- Authors
- Hsieh, T.-H., Chen, J.-J. J., Chen, L.-H., Chiang, P.-T., & Lee, H.-Y.
- Venue
- Behavioural Brain Research
- Publisher
- Elsevier BV
- Published
- 2011-09
- Volume
- 222
- Issue
- 1
- Pages
- 1-9
- ISSN
- 0166-4328 (ISSN-L)
- OpenAlex
- W2171078237
- Cited by
- 684
- References
- 2
- FWCI
- 83.42
- Type
- journal article
- Language
- en
- Open access
- bronze
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- Funders
- National Science Council
- National Health Research Institutes of Taiwan
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Time-course gait analysis of hemiparkinsonian rats following 6-hydroxydopamine lesion. https://app.cochat.ai/papers/10.1016/j.bbr.2011.03.031
- The paper
- Hsieh, T.-H., Chen, J.-J. J., Chen, L.-H., Chiang, P.-T., & Lee, H.-Y. (2011). Time-course gait analysis of hemiparkinsonian rats following 6-hydroxydopamine lesion. Behavioural Brain Research. https://doi.org/10.1016/j.bbr.2011.03.031
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.