Skip to main content
Journal of Neurology, Neurosurgery, and Psychiatry logoLink to Journal of Neurology, Neurosurgery, and Psychiatry
. 1992 Dec;55(12):1168–1176. doi: 10.1136/jnnp.55.12.1168

The effect of withdrawal of dopaminergic medication on simple and choice reaction time and the use of advance information in Parkinson's disease.

M Jahanshahi 1, R G Brown 1, C D Marsden 1
PMCID: PMC1015334  PMID: 1362212

Abstract

Eight patients with Parkinson's disease performed simple reaction time (SRT), uncued, partially and fully cued four choice (CRT) tasks. They were tested on two occasions; on their normal dose of dopaminergic medication and following withdrawal of such medication for an average of 14.4 hours. Disability as rated on the Webster scale was greater in the drug reduced state. Although RTs were generally slower when tested in the drug reduced state than when on medication, few differences emerged. Withdrawal of dopaminergic medication had no effect on unwarned SRT and unwarned and uncued CRT performance. Both on and off medication, the patients benefited from a warning signal presented before the imperative stimulus. In both medication states, the speeding up of RT was greatest with a warning signal presented 200 ms before S2. When the imperative stimulus was unwarned, the temporal predictability of its occurrence speeded RT more when on medication than when off. Advance movement parameter information was used by patients to pre-programme responses both on and off medication. In both medication states, the fully cued CRT was the same as SRT only with the 3200 ms S1-S2 interval. Medication state had no effect on movement time or the number of errors. It is suggested that slowness in motor readiness and motor programming may not be specific to striatal dopamine deficiency but rather a nonspecific concomitant of brain damage.

Full text

PDF
1168

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Alivisatos B., Milner B. Effects of frontal or temporal lobectomy on the use of advance information in a choice reaction time task. Neuropsychologia. 1989;27(4):495–503. doi: 10.1016/0028-3932(89)90054-7. [DOI] [PubMed] [Google Scholar]
  2. BECK A. T., WARD C. H., MENDELSON M., MOCK J., ERBAUGH J. An inventory for measuring depression. Arch Gen Psychiatry. 1961 Jun;4:561–571. doi: 10.1001/archpsyc.1961.01710120031004. [DOI] [PubMed] [Google Scholar]
  3. Bloxham C. A., Dick D. J., Moore M. Reaction times and attention in Parkinson's disease. J Neurol Neurosurg Psychiatry. 1987 Sep;50(9):1178–1183. doi: 10.1136/jnnp.50.9.1178. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bloxham C. A., Mindel T. A., Frith C. D. Initiation and execution of predictable and unpredictable movements in Parkinson's disease. Brain. 1984 Jun;107(Pt 2):371–384. doi: 10.1093/brain/107.2.371. [DOI] [PubMed] [Google Scholar]
  5. Brown V. J., Robbins T. W. Simple and choice reaction time performance following unilateral striatal dopamine depletion in the rat. Impaired motor readiness but preserved response preparation. Brain. 1991 Feb;114(Pt 1B):513–525. doi: 10.1093/brain/114.1.513. [DOI] [PubMed] [Google Scholar]
  6. Bruhn P., Parsons O. A. Reaction time variability in epileptic and brain-damaged patients. Cortex. 1977 Dec;13(4):373–384. doi: 10.1016/s0010-9452(77)80018-x. [DOI] [PubMed] [Google Scholar]
  7. Folstein M. F., Folstein S. E., McHugh P. R. "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975 Nov;12(3):189–198. doi: 10.1016/0022-3956(75)90026-6. [DOI] [PubMed] [Google Scholar]
  8. Garnett E. S., Nahmias C., Firnau G. Central dopaminergic pathways in hemiparkinsonism examined by positron emission tomography. Can J Neurol Sci. 1984 Feb;11(1 Suppl):174–179. doi: 10.1017/s0317167100046369. [DOI] [PubMed] [Google Scholar]
  9. Girotti F., Carella F., Grassi M. P., Soliveri P., Marano R., Caraceni T. Motor and cognitive performances of parkinsonian patients in the on and off phases of the disease. J Neurol Neurosurg Psychiatry. 1986 Jun;49(6):657–660. doi: 10.1136/jnnp.49.6.657. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Gordon B., Carson K. The basis for choice reaction time slowing in Alzheimer's disease. Brain Cogn. 1990 Jul;13(2):148–166. doi: 10.1016/0278-2626(90)90047-r. [DOI] [PubMed] [Google Scholar]
  11. Heilman K. M., Bowers D., Watson R. T., Greer M. Reaction times in Parkinson disease. Arch Neurol. 1976 Feb;33(2):139–140. doi: 10.1001/archneur.1976.00500020067011. [DOI] [PubMed] [Google Scholar]
  12. Hoehn M. M., Yahr M. D. Parkinsonism: onset, progression and mortality. Neurology. 1967 May;17(5):427–442. doi: 10.1212/wnl.17.5.427. [DOI] [PubMed] [Google Scholar]
  13. Jahanshahi M., Brown R. G., Marsden C. D. Simple and choice reaction time and the use of advance information for motor preparation in Parkinson's disease. Brain. 1992 Apr;115(Pt 2):539–564. doi: 10.1093/brain/115.2.539. [DOI] [PubMed] [Google Scholar]
  14. Miller E. Simple and choice reaction time following severe head injury. Cortex. 1970 Mar;6(1):121–127. doi: 10.1016/s0010-9452(70)80040-5. [DOI] [PubMed] [Google Scholar]
  15. Montgomery E. B., Jr, Nuessen J. The movement speed/accuracy operator in Parkinson's disease. Neurology. 1990 Feb;40(2):269–272. doi: 10.1212/wnl.40.2.269. [DOI] [PubMed] [Google Scholar]
  16. Mullen K. T., Plant G. T. Colour and luminance vision in human optic neuritis. Brain. 1986 Feb;109(Pt 1):1–13. doi: 10.1093/brain/109.1.1. [DOI] [PubMed] [Google Scholar]
  17. Pullman S. L., Watts R. L., Juncos J. L., Chase T. N., Sanes J. N. Dopaminergic effects on simple and choice reaction time performance in Parkinson's disease. Neurology. 1988 Feb;38(2):249–254. doi: 10.1212/wnl.38.2.249. [DOI] [PubMed] [Google Scholar]
  18. Pullman S. L., Watts R. L., Juncos J. L., Sanes J. N. Movement amplitude choice reaction time performance in Parkinson's disease may be independent of dopaminergic status. J Neurol Neurosurg Psychiatry. 1990 Apr;53(4):279–283. doi: 10.1136/jnnp.53.4.279. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Rafal R. D., Posner M. I., Walker J. A., Friedrich F. J. Cognition and the basal ganglia. Separating mental and motor components of performance in Parkinson's disease. Brain. 1984 Dec;107(Pt 4):1083–1094. doi: 10.1093/brain/107.4.1083. [DOI] [PubMed] [Google Scholar]
  20. Reid W. G., Broe G. A., Hely M. A., Morris J. G., Williamson P. M., O'Sullivan D. J., Rail D., Genge S., Moss N. G. The neuropsychology of de novo patients with idiopathic Parkinson's disease: the effects of age of onset. Int J Neurosci. 1989 Oct;48(3-4):205–217. doi: 10.3109/00207458909002162. [DOI] [PubMed] [Google Scholar]
  21. Sheridan M. R., Flowers K. A., Hurrell J. Programming and execution of movement in Parkinson's disease. Brain. 1987 Oct;110(Pt 5):1247–1271. doi: 10.1093/brain/110.5.1247. [DOI] [PubMed] [Google Scholar]
  22. Starkstein S. E., Esteguy M., Berthier M. L., Garcia H., Leiguarda R. Evoked potentials, reaction time and cognitive performance in on and off phases of Parkinson's disease. J Neurol Neurosurg Psychiatry. 1989 Mar;52(3):338–340. doi: 10.1136/jnnp.52.3.338. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Van Zomeren A. H., Deelman B. G. Long-term recovery of visual reaction time after closed head injury. J Neurol Neurosurg Psychiatry. 1978 May;41(5):452–457. doi: 10.1136/jnnp.41.5.452. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Velasco F., Velasco M. A quantitative evaluation of the effects of L-dopa on Parkinson's disease. Neuropharmacology. 1973 Feb;12(2):89–99. doi: 10.1016/0028-3908(73)90079-8. [DOI] [PubMed] [Google Scholar]
  25. Verfaellie M., Heilman K. M. Response preparation and response inhibition after lesions of the medial frontal lobe. Arch Neurol. 1987 Dec;44(12):1265–1271. doi: 10.1001/archneur.1987.00520240045010. [DOI] [PubMed] [Google Scholar]
  26. Webster D. D. Critical analysis of the disability in Parkinson's disease. Mod Treat. 1968 Mar;5(2):257–282. [PubMed] [Google Scholar]
  27. Wiesendanger M., Schneider P., Villoz J. P. Electromyographic analysis of a rapid volitional movement. Am J Phys Med. 1969 Feb;48(1):17–24. [PubMed] [Google Scholar]
  28. Worringham C. J., Stelmach G. E. Practice effects on the preprogramming of discrete movements in Parkinson's disease. J Neurol Neurosurg Psychiatry. 1990 Aug;53(8):702–704. doi: 10.1136/jnnp.53.8.702. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Neurology, Neurosurgery, and Psychiatry are provided here courtesy of BMJ Publishing Group

RESOURCES