Brain, Vol. 125, No. 1, 86-101,
January 1, 2002
© 2002 Oxford University Press
Olfactory learning: convergent findings from lesion and brain imaging studies in humans
1Neuropsychology and Cognitive Neuroscience Unit, Montreal Neurological Institute, Montreal, Quebec, Canada H3A 2B4 Correspondence to: Lauren A. Dade, Rotman Research Institute, Baycrest Center for Geriatric Care, 3560 Bathurst Street, Toronto, Ontario, Canada M6A 2E1 E-mail: ldade{at}rotman-baycrest.on.ca
The role of temporal lobe structures in olfactory memory was investigated by (i) the examination of odour learning and memory in patients who had undergone resection from a temporal lobe (including primary olfactory regions) for the treatment of intractable epilepsy; and (ii) the examination of brain function during odour memory tasks as assessed via PET imaging of healthy individuals. In order to study different stages of odour memory, recognition of a ‘list’ of odours was tested after a first exposure, again after four exposures and once more after a 24 h delay interval. Patients with resection from a temporal lobe performed significantly less well than control subjects on all trials, and no significant differences were noted as a function of side of resection, indicating that there is not a strong hemispheric superiority for this task. The PET data yielded different levels of activity in piriform cortex (primary olfactory cortex), in relation to the ‘no-odour’ baseline scan, depending on the type of processing: no increase in activity noted during odour encoding, a small increase bilaterally during short-term recognition and a larger increase bilaterally during long-term recognition. These findings, together with findings in animal studies, suggest that piriform cortex may have an active role in odour memory processing, not simply in odour perception. Taken together, the findings from the lesion study and functional brain imaging of healthy subjects suggest that olfactory memory requires input from left and right temporal lobe regions for optimal odour recognition, and that, unlike with verbal or non-verbal visual material, there is not a strong functional lateralization for olfactory memory.
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  J. A. GOTTFRIED What Can an Orbitofrontal Cortex-Endowed Animal Do with Smells? Ann. N.Y. Acad. Sci., December 1, 2007; 1121(1): 102 - 120. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. Jung, J. Hudry, P. Ryvlin, J.-P. Royet, O. Bertrand, and J.-P. Lachaux Functional Significance of Olfactory-induced Oscillations in the Human Amygdala Cereb Cortex, January 1, 2006; 16(1): 1 - 8. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 D. A. Levy, R. O. Hopkins, and L. R. Squire Impaired odor recognition memory in patients with hippocampal lesions Learn. Mem., November 1, 2004; 11(6): 794 - 796. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J.-P. Royet and J. Plailly Lateralization of Olfactory Processes Chem Senses, October 1, 2004; 29(8): 731 - 745. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
T. W. Buchanan, D. Tranel, and R. Adolphs A Specific Role for the Human Amygdala in Olfactory Memory Learn. Mem., September 1, 2003; 10(5): 319 - 325. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. A. Gottfried, R. Deichmann, J. S. Winston, and R. J. Dolan Functional Heterogeneity in Human Olfactory Cortex: An Event-Related Functional Magnetic Resonance Imaging Study J. Neurosci., December 15, 2002; 22(24): 10819 - 10828. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. A. Gottfried, J. O'Doherty, and R. J. Dolan Appetitive and Aversive Olfactory Learning in Humans Studied Using Event-Related Functional Magnetic Resonance Imaging J. Neurosci., December 15, 2002; 22(24): 10829 - 10837. [Abstract] [Full Text] [PDF]
|
|