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Assessment of the effect of 2‐chloroadenosine in normal rat brain using spin‐labeled MRI measurement of perfusion
Author(s) -
Kochanek Patrick M.,
Hendrich Kristy S.,
Robertson Courtney L.,
Williams Donald S.,
Melick John A.,
Ho Chien,
Marion Donald W.,
Jackson Edwin K.
Publication year - 2001
Publication title -
magnetic resonance in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.696
H-Index - 225
eISSN - 1522-2594
pISSN - 0740-3194
DOI - 10.1002/mrm.1123
Subject(s) - cerebral blood flow , perfusion , saline , nuclear medicine , chemistry , distribution (mathematics) , vasodilation , nuclear magnetic resonance , medicine , anesthesia , cardiology , physics , mathematics , mathematical analysis
Adenosine analogs such as 2‐chloroadenosine are potent cerebrovasodilators. Spin‐labeled MRI was used to investigate the spatial distribution, dose‐response, and timing of the effect of 2‐chloroadenosine on cerebral blood flow (CBF) after intraparenchymal injection into rat brain. Sprague‐Dawley rats ( N = 10) were injected with 2‐chloroadenosine at doses of 0.3, 6.0, or 12 nmoles, or saline vehicle (2–4 μL). CBF was serially quantified in a slice through the injection site in a circular (3.6 mm diameter) region of interest (ROI) around the injection and in ipsilateral hemispheric ROIs at ∼90 min and ∼180 min. Marked 3.77‐ and 3.93‐fold increases in CBF (vs. vehicle) were seen in the circular ROI at ∼90 min and ∼180 min after 12‐nmol injection, respectively. Similarly, 2.92‐ and 2.78‐fold increases in hemispheric CBF were observed at ∼90 min and ∼180 min, respectively, after injection of 12 nmoles. Linear dose‐response relationships were observed at both times after injection in both ROIs (all P < 0.01). Spin‐labeling MRI assessment revealed that parenchymal injection of 2‐chloroadenosine produces potent, dose‐dependent, and sustained vasodilation over large areas of brain. This treatment and imaging paradigm should facilitate investigation of the effect of CBF promotion in models of traumatic and ischemic brain injury. Magn Reson Med 45:924–929, 2001. © 2001 Wiley‐Liss, Inc.

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