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LETTER
Published Online: 1 January 2010

Central Pattern Generator: The Main Cause of Huntington’s Disease

Publication: The Journal of Neuropsychiatry and Clinical Neurosciences
To the Editor: Huntington’s disease is an inherited progressive brain disorder that causes a variety of motor, cognitive, and psychiatric disturbances. Hyperkinetic motor disturbances such as chorea, ballism, and athetosis are seen in this disease. Although there is no definite treatment for the disease, treatments that decrease the symptoms are available. It seems necessary to introduce novel effective therapeutic methods for Huntington’s disease.
Healthy lifestyle movements include different rhythmic motions such as walking and swimming. It is hypothesized that these movements are produced by sets of coupled and synchronized neurons, and these structures are introduced as central pattern generators. 1
We suppose that the movement disorders seen in Huntington’s disease, such as gait disorder, are caused by the disordered synchronization of a number of neurons resulting in the formation of an abnormal central pattern generator. Some analyses on stride-time intervals of healthy and Huntington’s disease patients show that stride-time intervals have long-term correlation and display a chaotic behavior in healthy persons. In Huntington’s disease patients, the long-term correlation is absent and random oscillations appear. 2 The manifestations of these oscillations reinforced the hypothesis that a central pattern generator is created by the disease.
We modeled Huntington’s disease with this hypothesis in mind, and the results were in accordance with our hypothesis. We supposed that the disorder would be alleviated if the faulty synchronization of the neurons is diminished.
It seems that one of the main mechanisms of removing the abnormal synchronization of neurons is deep brain stimulation. The method has been employed to treat Parkinson’s disease and has shown good results. Some theories about the formation of synchronization in Parkinson’s disease are available. 3 We propose that deep brain stimulation may be useful in treating Huntington’s disease.
In accordance with our model, a few studies have used deep brain stimulation as an experimental way to treat Huntington’s disease. A treatment by Moro et al. 4 that used bilateral globus pallidus stimulation on Huntington’s disease patients showed hopeful results. Temel et al.’s 5 use of deep brain stimulation on a rat model of Huntington’s disease improved cognitive and motor symptoms in the model. In addition, a Fawcett et al. 6 study using deep brain stimulation on some Huntington’s disease patients showed decreased prosaccade latency, total movement time, and the number of correctly executed trials, as well as increased saccade gain.
We conclude that the central pattern generator hypothesis of Huntington’s disease may be valid, and deep brain stimulation can be a suitable method to ameliorate Huntington’s disease symptoms. More experiment results are needed to validate our study.

References

1.
Grillner S: The spinal locomotor CPG: a target after spinal cord injury. Prog Brain Res 2002; 137:97–108
2.
Hausdorff JM, Ashkenazy Y, Peng CK, et al: When human walking becomes random walking: fractal analysis and modeling of gait rhythm fluctuations. Physica 2001; 302:138–147
3.
Titcombe MS, Glass L, Guehl D: Control of parkinsonian tremor by deep brain stimulation: data and dynamics (poster). Mathematics of Information Technology and Complex Systems Annual General Meeting, Toronto, Canada, June 6–7, 2000
4.
Moro E, Lang AE, Strafella AP, et al: Bilateral globus pallidus stimulation for Huntington’s disease. Ann Neurol 2004; 56:290–294
5.
Temel Y, Cao C, Vlamings R, et al: Motor and cognitive improvement by deep brain stimulation in a transgenic rat model of Huntington’s disease. Neurosci Lett 2006; 406:138–141
6.
Fawcett AP, Moro E, Lang AE, et al: Pallidal deep brain stimulation influences both reflexive and voluntary saccades in Huntington’s disease. Mov Disord 2005; 20:371–377

Information & Authors

Information

Published In

Go to The Journal of Neuropsychiatry and Clinical Neurosciences
Go to The Journal of Neuropsychiatry and Clinical Neurosciences
The Journal of Neuropsychiatry and Clinical Neurosciences
Pages: 123.e34
PubMed: 20160241

History

Published online: 1 January 2010
Published in print: Winter, 2010

Authors

Affiliations

Masood Banaie
Biomedical Engineering Faculty, Shahed University, Tehran, Iran
Farzad Towhidkhah
Biomedical Engineering Faculty, Amirkabir University of Technology, Tehran, Iran

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