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Dopamine Alters Tactile Perception in Parkinson's Disease

Published online by Cambridge University Press:  02 December 2014

Aimee J. Nelson*
Affiliation:
Department of Kinesiology, University of Waterloo, Waterloo Division of Neurology and Krembil Neuroscience Centre, Toronto Western Research Institute, Toronto, Ontario, Canada
Azra Premji
Affiliation:
Department of Kinesiology, University of Waterloo, Waterloo
Navjot Rai
Affiliation:
Department of Kinesiology, University of Waterloo, Waterloo
Tasnuva Hoque
Affiliation:
Division of Neurology and Krembil Neuroscience Centre, Toronto Western Research Institute, Toronto, Ontario, Canada
Mark Tommerdahl
Affiliation:
Biomedical Engineering, University of North Carolina, Chapel Hill, North Carolina, USA
Robert Chen
Affiliation:
Division of Neurology and Krembil Neuroscience Centre, Toronto Western Research Institute, Toronto, Ontario, Canada
*
University of Waterloo, 200 University Ave. W., BMH 1116, Waterloo, Ontario, N2L 3G1, Canada.
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Abstract

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Background:

Abnormal somatosensory processing may contribute to motor impairments observed in Parkinson's disease (PD). Dopaminergic medications have been shown to alter somatosensory processing such that tactile perception is improved. In PD, it remains unclear whether the temporal sequencing of tactile stimuli is altered and if dopaminergic medications alter this perception.

Methods:

Somatosensory tactile perception was investigated using temporal order judgment in patients with Parkinson's disease on and off dopaminergic medications and in aged-matched healthy controls. Measures of temporal order judgment were acquired using computer controlled stimulation to digits 2 and 3 on the right hand and subjects were required to determine which stimuli occurred first. Two experimental tasks were compared, temporal order judgment without and with synchronization whereby digits 2 and 3 were vibrated synchronously in advance of the temporal order judgment sequence of stimuli.

Results:

Temporal order judgment in PD patients off and on medications were similar to controls. Temporal order judgment preceded by synchronous vibration impaired tactile acuity in controls and in PD off medications to similar degrees, but this perceptual impairment by synchronous vibration was not present in PD patients on medications.

Conclusions:

These findings suggest that dopamine in PD reduces cortico-cortical connectivity within SI and this leads to changes in tactile sensitivity.

Type
Research Article
Copyright
Copyright © The Canadian Journal of Neurological 2012

References

1Shin, HW, Kang, SY, Sohn, YH.Dopaminergic influence on disturbed spatial discrimination in Parkinson’s disease. Mov Disord. 2005; 20: 16403.Google Scholar
2Schneider, JS, Diamond, SG, Markham, CH.Deficits in orofacial sensorimotor function in Parkinson’s disease. Ann Neurol. 1986; 19: 27582.Google Scholar
3Sathian, K, Zangaladze, A, Green, J, Vitek, JL, DeLong, MR.Tactile spatial acuity and roughness discrimination: impairments due to aging and Parkinson’s disease. Neurology. 1997; 49: 16877.Google Scholar
4Nolano, M, Provitera, V, Estraneo, A, et al.Sensory deficit in Parkinson’s disease: evidence of a cutaneous denervation. Brain. 2008; 131: 190311.Google Scholar
5Purves, D, Augustine, GJ, Fitzpatrick, D, et al.Modulation of movement by the basal ganglia. Sunderland, MA: Sinauer Associates; 2008.Google Scholar
6Rossini, PM, Babiloni, F, Bernardi, G, et al.Abnormalities of shortlatency somatosensory evoked potentials in parkinsonian patients. Electroencephalogr Clin Neurophysiol. 1989; 74: 27789.Google Scholar
7Gierthmuhlen, J, Lienau, F, Maag, R, et al.Somatosensory processing in a German family with PINK1 mutations: its potential role in Parkinson disease. J Neurol Neurosurg Psychiatry. 2009; 80: 5714.Google Scholar
8Artieda, J, Pastor, MA, Lacruz, F, Obeso, JA.Temporal discrimination is abnormal in Parkinson’s disease. Brain. 1992; 115 Pt 1: 199210.CrossRefGoogle ScholarPubMed
9Lee, MS, Kim, HS, Lyoo, CH.“Off” gait freezing and temporal discrimination threshold in patients with Parkinson disease. Neurology. 2005; 64: 6704.Google Scholar
10Pastor, MA, Day, BL, Macaluso, E, Friston, KJ, Frackowiak, RS.The functional neuroanatomy of temporal discrimination. J Neurosci. 2004; 24: 258591.Google Scholar
11Lacruz, F, Artieda, J, Pastor, MA, Obeso, JA.The anatomical basis of somaesthetic temporal discrimination in humans. J Neurol Neurosurg Psychiatry. 1991; 54: 107781.Google Scholar
12Fiorio, M, Valente, EM, Gambarin, M, et al.Subclinical sensory abnormalities in unaffected PINK1 heterozygotes. J Neurol. 2008; 255: 13727.Google Scholar
13Tommerdahl, M, Tannan, V, Zachek, M, Holden, JK, Favorov, OV.Effects of stimulus-driven synchronization on sensory perception. Behav Brain Funct. 2007; 3: 61.Google Scholar
14Tommerdahl, M, Tannan, V, Holden, JK, Baranek, GT.Absence of stimulus-driven synchronization effects on sensory perception in autism: evidence for local underconnectivity? Behav Brain Funct. 2008; 4: 19.Google Scholar
15Mountcastle, VB.Perceptual neuroscience, the cerebral cortex. Cambridge, MA and London, England: Harvard University Press; 1998.Google Scholar
16Smythies, J.Section II. The dopamine system. Int Rev Neurobiol. 2005; 64: 12372.Google Scholar
17Descarries, L, Lemay, B, Doucet, G, Berger, B.Regional and laminar density of the dopamine innervation in adult rat cerebral cortex. Neuroscience. 1987; 21: 80724.Google Scholar
18Foote, SL, Morrison, JH.Extrathalamic modulation of cortical function. Annu Rev Neurosci. 1987; 10: 6795.Google Scholar
19Conte, A, Modugno, N, Lena, F, et al.Subthalamic nucleus stimulation and somatosensory temporal discrimination in Parkinson’s disease. Brain. 2010; 133: 265663.Google Scholar
20Lee, MS, Lyoo, CH, Lee, MJ, Sim, J, Cho, H, Choi, YH.Impaired finger dexterity in patients with parkinson’s disease correlates with discriminative cutaneous sensory dysfunction. Mov Disord. 2010; 25: 25315.Google Scholar
21Oldfield, RC.The assessment and analysis of handedness: the Edinburgh inventory. Neuropsychologia. 1971; 9: 97113.Google Scholar
22Tannan, V, Dennis, RG, Zhang, Z, Tommerdahl, M.A portable tactile sensory diagnostic device. J Neurosci Methods. 2007; 164: 1318.Google Scholar
23Bliem, B, Frombach, E, Ragert, P, et al.Dopaminergic influences on changes in human tactile acuity induced by tactile coactivation. Exp Brain Res. 2007; 181: 1317.Google Scholar
24Godde, B, Stauffenberg, B, Spengler, F, Dinse, HR.Tactile coactivation-induced changes in spatial discrimination performance. J Neurosci. 2000; 20: 1597604.CrossRefGoogle ScholarPubMed
25de Lafuente, V, Romo, R.Neural correlate of subjective sensory experience gradually builds up across cortical areas. Proc Natl Acad Sci USA. 2006; 103: 1426671.Google Scholar
26Rao, SM, Mayer, AR, Harrington, DL.The evolution of brain activation during temporal processing. Nat Neurosci. 2001; 4: 31723.Google Scholar
27Casanova, MF, Buxhoeveden, DP, Switala, AE, Roy, E.Minicolumnar pathology in autism. Neurology. 2002; 58: 42832.Google Scholar
28Belmonte, MK, Allen, G, Beckel-Mitchener, A, Boulanger, LM, Carper, RA, Webb, SJ.Autism and abnormal development of brain connectivity. J Neurosci. 2004; 24: 922831.Google Scholar
29Hosp, JA, Hertler, B, Atiemo, CO, Luft, AR.Dopaminergic modulation of receptive fields in rat sensorimotor cortex. Neuroimage. 2011; 54: 15460.Google Scholar
30Koch, G, Franca, M, Albrecht, UV, Caltagirone, C, Rothwell, JC.Effects of paired pulse TMS of primary somatosensory cortex on perception of a peripheral electrical stimulus. Exp Brain Res. 2006; 172: 41624.Google Scholar
31Palomar, FJ, Diaz-Corrales, F, Carrillo, F, Fernandez-Del-Olmo, M, Koch, G, Mir, P.Sensory perception changes induced by transcranial magnetic stimulation over the primary somatosensory cortex in Parkinson’s disease. Mov Disord. Epub 2011 Jun 2.Google Scholar
32Gescheider, G.Chapter 3: The classical psychophysical methods. Psychophysics: the fundamentals. Mahway, New Jersey, USA: Lawrence Erlbaum Associates; 1997.Google Scholar
33Ridding, MC, Sheean, G, Rothwell, JC, Inzelberg, R, Kujirai, T.Changes in the balance between motor cortical excitation and inhibition in focal, task specific dystonia. J Neurol Neurosurg Psychiatry. 1995; 59: 4938.Google Scholar
34MacKinnon, CD, Gilley, EA, Weis-McNulty, A, Simuni, T.Pathways mediating abnormal intracortical inhibition in Parkinson’s disease. Ann Neurol. 2005; 58: 51624.Google Scholar
35Sailer, A, Molnar, GF, Paradiso, G, Gunraj, CA, Lang, AE, Chen, R.Short and long latency afferent inhibition in Parkinson’s disease. Brain. 2003; 126: 188394.CrossRefGoogle Scholar
36Mongeon, D, Blanchet, P, Messier, J.Impact of Parkinson’s disease and dopaminergic medication on proprioceptive processing. Neuroscience. 2009; 158: 42640.Google Scholar