Cocaine administration decreases functional connectivity in human primary visual and motor cortex as detected by functional MRI

Citation
Sj. Li et al., Cocaine administration decreases functional connectivity in human primary visual and motor cortex as detected by functional MRI, MAGN RES M, 43(1), 2000, pp. 45-51
Citations number
27
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
Journal title
MAGNETIC RESONANCE IN MEDICINE
ISSN journal
07403194 → ACNP
Volume
43
Issue
1
Year of publication
2000
Pages
45 - 51
Database
ISI
SICI code
0740-3194(200001)43:1<45:CADFCI>2.0.ZU;2-X
Abstract
Functional magnetic resonance imaging (fMRI) was conducted to observe the e ffects of cocaine administration on the physiological fluctuations of fMRI signal in two brain regions. Seven long-term cocaine users with an average age of 32 years and 8 years of cocaine use history were recruited for the s tudy. A T-2*-weighted fast echo-planar imaging (EPI) pulse sequence was emp loyed at 1.5 T to acquire three sets of brain images for each subject under three conditions (at rest, after saline injection, and after cocaine injec tion [0.57 mg/kg]), Cross-correlation maps were constructed using the synch ronous, low frequency signal from voxel time courses after filtering respir atory, cardiac, and other physiological noise. A quantitative evaluation of the changes in functional connectivity was made using spatial correlation coefficient (SCC) analysis. A marked 50% reduction in SCC values in the reg ion of primary visual cortex and 43% reduction in SCC values in the region of primary motor cortex were observed after cocaine administration. This si gnificant reduction in SCC values in these cortical regions is a reflection of changes in neuronal activity. It is suggested that the observed changes in low frequency components after acute cocaine administration during a re sting, no-task situation may be used as a baseline reference source when as sessing the effects of cocaine on task-driven activation or on mesolimbic d opamine pathways. Magn Reson Med 43:45-51, 2000. (C) 2000 Wiley-Liss, Inc.