Practice-related changes in human brain functional anatomy during nonmotor learning

Marcus E. Raichle, Julie A. Fiez, Tom O. Videen, Ann mary K. Macleod, Jose V. Pardo, Peter T. Fox, Steven E. Petersen

Research output: Contribution to journalArticlepeer-review

1161 Scopus citations


Practice of a novel task leads to improved performance. The brain mechanisms associated with practice-induced improvement in performance are largely unknown. To address this question we have examined the functional anatomy of the human brain with positron emission tomography (PET) during the naive and practiced performance of a simple verbal response selection task (saying an appropriate verb for a visually presented noun). As a control state, subjects were asked to repeat the visually presented nouns. Areas of the brain most active during naive performance (anterior cingulata, left prefrontal and left posterior temporal cortices, and the right cerebellar hemisphere), compared to repeating the visually presented nouns, were all significantly less active during practiced performance. These changes were accompanied by changes in the opposite direction in sylvian-insular cortex bilaterally and left medial extras-triate cortex. In effect, brief practice made the cortical circuitry used for verbal response selection indistinguishable from simple word repetition. Introduction of a novel list of words reversed the learning-related effects. These results indicate that two distinct circuits can be used for verbal response selection and normal subjects can change the brain circuits used during task performance following less than 15 min of practice. One critical factor in determining the circuitry used appears to be the degree to which a task is learned or automatic.

Original languageEnglish (US)
Pages (from-to)8-26
Number of pages19
JournalCerebral Cortex
Issue number1
StatePublished - 1994

Bibliographical note

Funding Information:
We thank the staffs of the Washington University Medical School cyclotron and of the Radiation Sciences Division of the School's Mallinckrodt Institute of Radiology for their invaluable technical assistance. We thank Eudel Tolving for helpful comments. We also thank Anna Cook, who processed drafts of our manuscript through many revisions. This research was supported by NIH Grants HL13851, NS 06833, and AG 08377, and by The Charles A. Dana Foundation and the McDonnell Center for Studies of Higher Brain Function at Washington University.

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