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PET-based Investigation of Cerebral Activation Following Intranasal Trigeminal Stimulation

Overview
Journal Hum Brain Mapp
Publisher Wiley
Specialty Neurology
Date 2008 Apr 17
PMID 18412096
Citations 6
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Abstract

The present study aimed to investigate cerebral activation following intranasal trigeminal chemosensory stimulation using O15-H2O-PET. A total of 12 healthy male participants underwent a PET scan presented with four scanning conditions; two left-sided intranasal CO(2)-stimuli and two matched baseline conditions consisting of odorless air. CO(2) was used as it produces burning and stinging sensations. Stimulation started 20 s before intravenous injection of the isotope and lasted for the first 60 s of the 5 min scan time. A comparison between CO(2) and baseline showed a pronounced activation of the trigeminal projection area at the base of the postcentral gyrus (primary and secondary somatosensory cortex) which was more intense for the right hemisphere, contralateral to the side of stimulation. In addition, activation was also found in the piriform cortex which is typically activated following odor presentation and thus thought of as primary olfactory cortex. In conclusion, and in line with previously published work, our data suggest that intranasal trigeminal stimulation not only activates somatosensory projection areas, but that it also leads to activation in cerebral areas associated with the processing of olfactory information. This may be interpreted in terms of the intimate relation between the intranasal chemosensory systems.

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References
1.
Hummel T, Livermore A . Intranasal chemosensory function of the trigeminal nerve and aspects of its relation to olfaction. Int Arch Occup Environ Health. 2002; 75(5):305-13. DOI: 10.1007/s00420-002-0315-7. View

2.
Hasson U, Skipper J, Nusbaum H, Small S . Abstract coding of audiovisual speech: beyond sensory representation. Neuron. 2007; 56(6):1116-26. PMC: 2175551. DOI: 10.1016/j.neuron.2007.09.037. View

3.
Stevens J, Plantinga A, Cain W . Reduction of odor and nasal pungency associated with aging. Neurobiol Aging. 1982; 3(2):125-32. DOI: 10.1016/0197-4580(82)90008-2. View

4.
Lotsch J, Nordin S, Hummel T, Murphy C, Kobal G . Chronobiology of nasal chemosensitivity: do odor or trigeminal pain thresholds follow a circadian rhythm?. Chem Senses. 1997; 22(5):593-8. DOI: 10.1093/chemse/22.5.593. View

5.
van den Hoff J, Burchert W, Muller-Schauenburg W, Meyer G, Hundeshagen H . Accurate local blood flow measurements with dynamic PET: fast determination of input function delay and dispersion by multilinear minimization. J Nucl Med. 1993; 34(10):1770-7. View