Chemical Senses Vol. 30 No. suppl 1 © Oxford University
Press 2005; all rights reserved
Brain Imaging Studies of the Functional Organization of Human Olfaction
Department of Neuroscience, Division of Human Brain Mapping, Karolinska Institute, Stockholm, Sweden
Correspondence to be sent to: Ivanka Savic, e-mail ivanka.savic-berglund{at}neuro.ki.se
Key words: functional MRI, identification, memory, olfaction, perception, PET
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Introduction |
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 Top Introduction Imaging of odorant perceptionFunctional organization of...Imaging of higher olfactory...ConclusionsAcknowledgementsReferences |
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It is believed that sensory functions are organized in a hierarchical and parallel manner. The sense of smell differs in several aspects from other senses: odors can immediately elicit emotional evocations, they are remembered after long time and are difficult to label. This raises the question of whether odorous stimuli may be processed differently from the other sensory stimuli. New data from brain imaging studies suggest that this is not the case and that the specific characteristics of the sense of smell can be attributed to the engagement of limbic structures at an early stage in the signal processing. Positron emission tomography (PET) and functional magnetic resonance imaging (fMRI) are useful for studies of olfactory functions. PET is generally preferable for limbic activations (but only in group comparisons), whereas fMRI should be used for single-subject studies.
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Imaging of odorant perception |
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TopIntroductionImaging of odorant perceptionFunctional organization of...Imaging of higher olfactory...ConclusionsAcknowledgementsReferences |
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In accordance with the expectations from anatomical data both PET and fMRI studies repeatedly show an engagement of limbic structures during the passive smelling of odors. Most often, the activations cover the amygdala, piriform, orbitofrontal and insular cortex, (Zatorre et al., 1992
;
Williams et al., 1997;
Zald and Pardo, 1997;
Sobel et al., 1998, 1999)
and show a right-sided predominance. Considering that the olfactory nerve projections to
the brain are ipsilateral, we recently investigated whether the observed right-sided
lateralization may be due to a more pronounced activation trough the right nostril
(Savic and Gulyas, 2000); PET
measurements of rCBF were carried out during monorhinal and passive smelling of four
odorants which were perceived as non-trigeminal. Independently of the activated nostril,
bilateral activations were found in the amygdala and piriform cortex, anterior cingulate,
in the left agranular insular cortex and the right orbitofrontal cortex. There was no
significant difference in the pattern or degree of activation between the right versus
left nostril stimulations. The observed bilaterality of the monorhinal olfactory
processing is congruent with the reports from studies with magnetic source imaging
(Kettenmann et al., 1997;
Sakuma et al., 1997;
Ayabe-Kanamura et al., 2002)
and suggests existence of functional connections via the anterior commissure. Thus, the
monorhinally presented odorants are perceived bilaterally in the brain independently on
the side of presentation. |
Functional organization of odorant perception |
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TopIntroductionImaging of odorant perceptionFunctional organization of...Imaging of higher olfactory...ConclusionsAcknowledgementsReferences |
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Odorants are capable to immediately elicit different evocations (hedonistic judgements, familiarity judgements) during the perception of odors, which is the most elemental level of odor processing. Indeed, Zald and Pardo (1997
) found that
unpleasant odors activated left orbitofrontal cortex and left amygdala significantly more
than the pleasant odors. Royet et al. recently also observed that judgements of
emotionally valenced stimuli compared to emotionally neutral stimuli activated left
amygdala and orbitofrontal cortex. The left amygdala and orbitofrontal cortex could,
thus, represent the circuits specially recruited during an automatic judgment of odor
pleasantness, which possibly is more pronounced during presentations of unpleasant
stimuli (Royet et al., 2000).
The possibility of a parallel processing during odor perception is of particular interest
in the view of the current debate on whether odors are encoded only perceptually (as
stated by
Engen and Ross, 1973), or also
semantically. Koenig used an original olfactory priming paradigm to provide evidence for
the existence of both modes (Koenig et
al., 2000). The authors proposed that perceptual odor representations
are stored in an olfactory pattern activation subsystem, whereas semantic odor
representations are stored in an associative memory. We recently addressed this issue by
comparing the pattern of cerebral activation during passive smelling of familiar and
unfamiliar odors. Apart from the different rating on the VAS scale with respect to odor
familiarity, the odors were rated similarly for other odor characteristics. In addition
to the olfactory core regions, which were recruited during smelling of both familiar and
unfamiliar odorants, smelling of familiar compounds involved networks usually attributed
to semantic associations (Savic and Berglund,
2004). Thus, depending on the evocations elicited with the particular
odorant, perception of odorous stimuli can involve additional areas to the core regions.
This suggests that already the lowest level of conscious odor processing may be executed
by distributed parallel circuits. |
Imaging of higher olfactory functions |
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TopIntroductionImaging of odorant perceptionFunctional organization of...Imaging of higher olfactory...ConclusionsAcknowledgementsReferences |
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How the human brain processes the discrimination, recognition and identification of odors has only recently been systematically explored (Royet et al., 1999
;
Savic et al., 2000). In a
series of PET studies we investigated the pattern of cerebral activation during five
different olfactory tasks: Monorhinal smelling of odorless air (AS), monorhinal smelling
single odors (OS), discrimination of odor intensity (OD-i), discrimination of odor
quality (OD-q) and odor recognition memory (OM). Whereas activations during OS were
related to AS, activations during the three odors related tasks (OD-i, OD-q and OM) were
calculated using OS as the base-line. This approach enabled us to disentangle odor
related from task related regions.
The olfactory functions were processed by common, as well as task-specific regions.
OS activated the amygdala-piriform, orbitofrontal, insular, cingulate cortex and right
thalamus. Depending on the task, different subsets of these regions were recruited along
with other areas: OD-i and OD-q engaged left insula and right cerebellum. OD-q involved,
in addition, the thalamus, cingulate, orbitofrontal and prefrontal cortex, the frontal
operculum, the right caudate and subiculum; OM did not activate the insula, but instead,
the piriform cortex; with exception for caudate and subiculum, it shared the remaining
activations with the OD-q and engaged, in addition, the temporal and parietal cortex.
Thus, the three olfactory tasks (OD-i, OD-q and OM) recruited also areas outside the
OS-regions; some of these ‘outside OS-regions’ were shared by several tasks,
whereas others were task specific. Furthermore, with the increasing complexity of the
task, the activated task-associated areas were more and more remotely connected with the
OS regions. For example, right cerebellum was activated by all three tasks (OD-i and OD-q
and OM). The brainstem (mesencephalon) and prefrontal cortex was activated by OD-q and
OM, but not OD-i. The OD-q task specifically activated right subiculum-hippocampus and
right caudate, whereas OM, the task assumed to pose the highest cognitive load, engaged
the right temporal neocortex and parietal cortex, areas which were not activated in any
of the other tasks. When testing cerebral activation during familiarity judgements (a
function posing similar cognitive load as the odor recognition memory) in relation to
odor smelling,
Royet et al. (1999) found
activation of right orbitofrontal cortex and the anterior cingulate, but also of the left
inferior frontal and left superior frontal gyri. The two latter regions are, like the
parietal and temporal neocortex remotely connected to the olfactory core regions and
constitute an additional sign of hierarchical processing of olfactory functions.
The finding that the amygdala was activated already by OS, without an additional enhancement during OM deserves a special comment. Because the amygdala is essential for the emotional valence it is highly probable that an immediate activation of this structure already during the passive perception of odors underlies the common experience that olfactory stimuli produce immediate recall of the emotional valence related to the source of smell. The same mechanism may also explain the long duration of odor memories—the amygdala is closely connected to the hippocampus and enthorhinal cortex, which leads to an emotional enhancement of odor memories and their unique long term retention.
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Conclusions |
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TopIntroductionImaging of odorant perceptionFunctional organization of...Imaging of higher olfactory...ConclusionsAcknowledgementsReferences |
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Like the visual, auditory and somatosensory system, the olfactory stimuli seem to be processed in a parallel and hierarchical mode. The special features of odorous stimuli—the immediate association to emotion and episodic memory—are, thus, not explained by a principally different organization of olfactory networks compared to other sensory modalities. Rather, the underlying physiology seems to be that limbic structures, suggested to represent a late stage in the sensory-fugal stream of information, become involved already at the most elemental level of odor processing, odor perception.
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Acknowledgements |
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TopIntroductionImaging of odorant perceptionFunctional organization of...Imaging of higher olfactory...ConclusionsAcknowledgementsReferences |
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This study was supported by the Swedish Medical Research Council, Karolinska Institute, the Swedish Royal Academy of Sciences, The Captain Ericsson’s and the Åke Wiberg Foundations.
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References |
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TopIntroductionImaging of odorant perceptionFunctional organization of...Imaging of higher olfactory...ConclusionsAcknowledgementsReferences |
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Ayabe-Kanamura, S. Gotow, N. Kobayakawa, T. Kaneda, H. and Saito, S. (2002) Human cortical areas activated by odorants: a study by MEG and EEG. Biomagnetism, 12, 292–295.
Engen, T. and Ross, B.M. (1973) Long-term memory of odors with and without verbal descriptions. J. Exp. Psychol., 100, 221–227.[CrossRef][Web of Science][Medline]
Kettenmann, B., Hummel, C., Stefan, H. and Kobal, G. (1997) Multiple olfactory activity in the human neocortex identified by magnetic source imaging. Chem. Senses, 22, 493–502.
Koenig, O., Bourron, G. and Royet, J.P. (2000) Evidence for separate perceptive and semantic memories for odours: a priming experiment. Chem. Senses, 25, 703–708.
Royet, J.P., Koenig, O., Gregoire, M.C., Cinotti, L., Lavenne, F., Le Bars, D., Costes, N., Vigouroux, M., Farget, V., Sicard, G., Holley, A., Mauguiere, F., Comar, D. and Froment, J.C. (1999) Functional anatomy of perceptual and semantic processing for odors. J. Cogn. Neurosci., 11, 94–109.[CrossRef][Web of Science][Medline]
Royet, J.P., Zald, D., Versace, R., Costes, N., Lavenne, F., Koenig, O. and Gervais, R. (2000) Emotional responses to pleasant and unpleasant olfactory, visual and auditory stimuli: a positron emission tomography study. J. Neurosci., 20, 7752–7759.
Sakuma, K., Kakigi, R., Kaneoke, Y., Hoshiyama, M., Koyama, S., Nagata, O., Takeshima, Y., Ito, Y. and Nakashima, K. (1997) Odorant evoked magnetic fields in humans. Neurosci. Res., 27, 115–122.[CrossRef][Web of Science][Medline]
Savic, I. and Berglund, H. (2004) Passive perception of odors and semantic circuits. Hum. Brain Mapp., 21, 271–278.[CrossRef][Web of Science][Medline]
Savic, I. and Gulyas, B. (2000) PET shows that odors are processed both ipsilaterally and contralaterally to the stimulated nostril. Neuroreport, 11, 2861–2866.[Web of Science][Medline]
Savic, I., Gulyas, B., Larsson, M. and Roland, P. (2000) Olfactory functions are mediated by parallel and hierarchical processing. Neuron, 26, 735–745.[CrossRef][Web of Science][Medline]
Sobel, N., Desmond, J.E., Glover, G.H. Goode, R.L., Sullivan, E.V. and Gabrielli, J.D. (1998) Sniffing and smelling: separate subsytems in the human olfactory cortex. Nature, 392, 282–286.[CrossRef][Medline]
Sobel, N., Prabhakaran, V., Hartley, C.A., Desmond, J.E., Glover, G.H., Sullivan, E.V. and Gabrieli, J.D. (1999) Blind smell: brain activation induced by an undetected air-borne chemical. Brain, 122, 209–217.
Williams, S.C.R., et al. (1997) fMRI during ‘unpleasant’ odor stimulations: normative data. Neuroimage, 5, S197.
Zald, D. and Pardo, J. (1997) Emotion, olfaction and the human amygdala: amygdala activation during aversive olfactory stimulation. Proc. Natl Acad. Sci. USA, 94, 4119–4124.
Zatorre, R.J., Jones-Gotman, M., Evans, A.C. and Meyer, E. (1992) Functional localisation of human olfactory cortex. Nature, 360, 339–341.[CrossRef][Medline]
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