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dc.contributor.authorSchmidt, Karl F.
dc.contributor.authorFebo, Marcelo
dc.contributor.authorShen, Qiang
dc.contributor.authorLuo, Feng
dc.contributor.authorSicard, Kenneth M.
dc.contributor.authorFerris, Craig F.
dc.contributor.authorStein, Elliot A.
dc.contributor.authorDuong, Timothy Q.
dc.date2022-08-11T08:08:47.000
dc.date.accessioned2022-08-23T16:08:41Z
dc.date.available2022-08-23T16:08:41Z
dc.date.issued2006-03-22
dc.date.submitted2008-12-09
dc.identifier.citationPsychopharmacology (Berl). 2006 May;185(4):479-86. Epub 2006 Mar 21. <a href="http://dx.doi.org/10.1007/s00213-006-0319-1">Link to article on publisher's site</a>
dc.identifier.issn0033-3158 (Print)
dc.identifier.doi10.1007/s00213-006-0319-1
dc.identifier.pmid16550388
dc.identifier.urihttp://hdl.handle.net/20.500.14038/32509
dc.description.abstractRATIONALE: Physiological changes (such as heart rate and respiration rate) associated with strong pharmacological stimuli could change the blood-oxygenation-level-dependent (BOLD) functional magnetic resonance imaging (fMRI) mapping signals, independent of neural activity. OBJECTIVES: This study investigates whether the physiological changes per se associated with systemic cocaine administration (1 mg/kg) contaminate the BOLD fMRI signals by measuring BOLD and cerebral blood flow (CBF) fMRI and estimating the cerebral metabolic rate of oxygen (CMRO(2)) changes. MATERIALS AND METHODS: BOLD and CBF fMRI was performed, and changes in CMRO(2) were estimated using the BOLD biophysical model. RESULTS: After systemic cocaine administration, blood pressure, heart rate, and respiration rate increased, fMRI signals remained elevated after physiological parameters had returned to baseline. Cocaine induced changes in the BOLD signal within regions of the reward pathway that were heterogeneous and ranged from -1.2 to 5.4%, and negative changes in BOLD were observed along the cortical surface. Changes in CBF and estimated CMRO(2) were heterogeneous and positive throughout the brain, ranging from 14 to 150% and 10 to 55%, respectively. CONCLUSIONS: This study demonstrates a valuable tool to investigate the physiological and biophysical basis of drug action on the central nervous system, offering the means to distinguish the physiological from neural sources of the BOLD fMRI signal.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=16550388&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1007/s00213-006-0319-1
dc.subjectAlgorithms; Anesthesia; Animals; Blood Volume; Brain Chemistry; Cerebrovascular Circulation; Cocaine; Data Interpretation, Statistical; Hemodynamics; Hypercapnia; Injections, Intravenous; Magnetic Resonance Imaging; Male; Metabolism; Oxygen; Rats; Rats, Sprague-Dawley; Reward
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.subjectNeuroscience and Neurobiology
dc.titleHemodynamic and metabolic changes induced by cocaine in anesthetized rat observed with multimodal functional MRI
dc.typeJournal Article
dc.source.journaltitlePsychopharmacology
dc.source.volume185
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1076
dc.identifier.contextkey678845
html.description.abstract<p>RATIONALE: Physiological changes (such as heart rate and respiration rate) associated with strong pharmacological stimuli could change the blood-oxygenation-level-dependent (BOLD) functional magnetic resonance imaging (fMRI) mapping signals, independent of neural activity.</p> <p>OBJECTIVES: This study investigates whether the physiological changes per se associated with systemic cocaine administration (1 mg/kg) contaminate the BOLD fMRI signals by measuring BOLD and cerebral blood flow (CBF) fMRI and estimating the cerebral metabolic rate of oxygen (CMRO(2)) changes.</p> <p>MATERIALS AND METHODS: BOLD and CBF fMRI was performed, and changes in CMRO(2) were estimated using the BOLD biophysical model.</p> <p>RESULTS: After systemic cocaine administration, blood pressure, heart rate, and respiration rate increased, fMRI signals remained elevated after physiological parameters had returned to baseline. Cocaine induced changes in the BOLD signal within regions of the reward pathway that were heterogeneous and ranged from -1.2 to 5.4%, and negative changes in BOLD were observed along the cortical surface. Changes in CBF and estimated CMRO(2) were heterogeneous and positive throughout the brain, ranging from 14 to 150% and 10 to 55%, respectively.</p> <p>CONCLUSIONS: This study demonstrates a valuable tool to investigate the physiological and biophysical basis of drug action on the central nervous system, offering the means to distinguish the physiological from neural sources of the BOLD fMRI signal.</p>
dc.identifier.submissionpathgsbs_sp/1076
dc.contributor.departmentDepartment of Psychiatry, Center for Comparative Neuroimaging
dc.source.pages479-86
dc.contributor.studentKarl Schmidt


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