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    Hemodynamic and metabolic changes induced by cocaine in anesthetized rat observed with multimodal functional MRI

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    Authors
    Schmidt, Karl F.
    Febo, Marcelo
    Shen, Qiang
    Luo, Feng
    Sicard, Kenneth M.
    Ferris, Craig F.
    Stein, Elliot A.
    Duong, Timothy Q.
    Student Authors
    Karl Schmidt
    UMass Chan Affiliations
    Department of Psychiatry, Center for Comparative Neuroimaging
    Document Type
    Journal Article
    Publication Date
    2006-03-22
    Keywords
    Algorithms; 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
    Life Sciences
    Medicine and Health Sciences
    Neuroscience and Neurobiology
    
    Metadata
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    Link to Full Text
    http://dx.doi.org/10.1007/s00213-006-0319-1
    Abstract
    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. 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.
    Source
    Psychopharmacology (Berl). 2006 May;185(4):479-86. Epub 2006 Mar 21. Link to article on publisher's site
    DOI
    10.1007/s00213-006-0319-1
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/32509
    PubMed ID
    16550388
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1007/s00213-006-0319-1
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