Show simple item record

dc.contributor.authorZhang, Nanyin
dc.contributor.authorZhu, Xiao-Hong
dc.contributor.authorZhang, Yi
dc.contributor.authorPark, Jae-keun
dc.contributor.authorChen, Wei
dc.date2022-08-11T08:10:28.000
dc.date.accessioned2022-08-23T17:10:06Z
dc.date.available2022-08-23T17:10:06Z
dc.date.issued2010-05-01
dc.date.submitted2012-05-24
dc.identifier.citationNeuroimage. 2010 May 1;50(4):1456-63. Epub 2010 Jan 28. <a href="http://dx.doi.org/10.1016/j.neuroimage.2010.01.053">Link to article on publisher's site</a>
dc.identifier.issn1053-8119 (Linking)
dc.identifier.doi10.1016/j.neuroimage.2010.01.053
dc.identifier.pmid20114078
dc.identifier.urihttp://hdl.handle.net/20.500.14038/45974
dc.description.abstractIn this work, we exploited the superior capability of high-resolution functional magnetic resonance imaging (fMRI) for functional mapping of ocular dominance layer (ODL) in the cat lateral geniculate nucleus (LGN). The stimulus-evoked neuronal activities in the LGN ODLs associated with contralateral- and ipsilateral-eye visual inputs were successfully differentiated and mapped using both blood-oxygenation-level dependent (BOLD)-weighted and cerebral blood volume (CBV)-weighted fMRI methods. The morphology of mapped LGN ODLs was in remarkable consistency with histology findings in terms of ODL shape, orientation, thickness and eye-dominance. Compared with the BOLD signal, the CBV signal provides higher reproducibility and better spatial resolvability for function mapping of LGN because of improved contrast-to-noise ratio and point-spread function. The capability of fMRI for non-invasively imaging the functional sub-units of ODL in a small LGN overcomes the limitation of conventional neural-recording approach, and it opens a new opportunity for studying critical roles of LGN in brain function and dysfunction at the fine scale of ocular dominance layer.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=20114078&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838974/pdf/nihms175404.pdf
dc.subjectAnimals
dc.subjectArtifacts
dc.subjectBlood Volume
dc.subjectCats
dc.subjectCerebrovascular Circulation
dc.subjectFunctional Laterality
dc.subjectGeniculate Bodies
dc.subjectMagnetic Resonance Imaging
dc.subjectOxygen
dc.subjectPhotic Stimulation
dc.subjectReproducibility of Results
dc.subject*Signal Processing, Computer-Assisted
dc.subjectVisual Perception
dc.subjectPsychiatry
dc.titleHigh-resolution fMRI mapping of ocular dominance layers in cat lateral geniculate nucleus
dc.typeJournal Article
dc.source.journaltitleNeuroImage
dc.source.volume50
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/psych_pp/499
dc.identifier.contextkey2911230
html.description.abstract<p>In this work, we exploited the superior capability of high-resolution functional magnetic resonance imaging (fMRI) for functional mapping of ocular dominance layer (ODL) in the cat lateral geniculate nucleus (LGN). The stimulus-evoked neuronal activities in the LGN ODLs associated with contralateral- and ipsilateral-eye visual inputs were successfully differentiated and mapped using both blood-oxygenation-level dependent (BOLD)-weighted and cerebral blood volume (CBV)-weighted fMRI methods. The morphology of mapped LGN ODLs was in remarkable consistency with histology findings in terms of ODL shape, orientation, thickness and eye-dominance. Compared with the BOLD signal, the CBV signal provides higher reproducibility and better spatial resolvability for function mapping of LGN because of improved contrast-to-noise ratio and point-spread function. The capability of fMRI for non-invasively imaging the functional sub-units of ODL in a small LGN overcomes the limitation of conventional neural-recording approach, and it opens a new opportunity for studying critical roles of LGN in brain function and dysfunction at the fine scale of ocular dominance layer.</p>
dc.identifier.submissionpathpsych_pp/499
dc.contributor.departmentDepartment of Psychiatry
dc.source.pages1456-63


Files in this item

Thumbnail
Name:
Publisher version

This item appears in the following Collection(s)

Show simple item record