Time-course and treatment response with SNX-111, an N-type calcium channel blocker, in a rodent model of focal cerebral ischemia using diffusion-weighted MRI

被引:56
作者
Yenari, MA
Palmer, JT
Sun, GH
deCrespigny, A
Moseley, ME
Steinberg, GK
机构
[1] STANFORD UNIV, MED CTR, DEPT NEUROSURG, STANFORD, CA 94305 USA
[2] STANFORD UNIV, MED CTR, DEPT NEUROL, STANFORD, CA 94305 USA
[3] STANFORD UNIV, MED CTR, DEPT RADIOL, STANFORD, CA 94305 USA
[4] STANFORD UNIV, MED CTR, STANFORD STROKE CTR, STANFORD, CA 94305 USA
关键词
focal cerebral ischemia; calcium channel; diffusion-weighted MRI; omega-conopeptide; SNX-111; excitotoxicity rat;
D O I
10.1016/S0006-8993(96)00808-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Diffusion-weighted magnetic resonance imaging (DWI) is capable of noninvasively imaging acute cerebral ischemia. We demonstrate the utility of this technique by evaluating SNX-111, a novel N-type calcium channel blocker with potential neuroprotective properties in a rodent model of transient focal ischemia. Twenty-four Sprague-Dawley rats weighting between 310-350 g underwent occlusion of the middle cerebral artery (MCAO) for 105 min followed by 22.5 h of reperfusion. Thirty minutes following MCAO, animals were randomized to receive SNX-111 5 mg/kg intravenously over 1 h vs. placebo. DW1 and T2-weighted MRIs (T2W) were performed at 0.5, 1.5 and 24 h after the onset of ischemia. Area fractions of increased signal intensity on the DWI and T2W images were measured. DWI area fractions at 1.5 and 24 h were also normalized to the initial, pre-treatment scans. Apparent diffusion coefficients (ADC) were calculated from fitted maps. Tri-phenyl tetrazolium chloride (TTC) staining was performed on brains at 24 h and infarct area fractions were measured. SNX-111 treated animals showed significantly improved 1.5-h DWI scan ratios compared to controls (ratios of 1.06 +/- 0.25 vs. 2.98 +/- 0.78 SNX vs. controls respectively, P < 0.05). A trend toward improved DWI ratios was seen by 24 h in the SNX-111 group (2.5 +/- 0.75 vs. 4.12 +/- 1.5, N.S.) DWI, T2W and TTC area functions at 24 h also showed trends favoring a neuroprotective effect of SNX-111. Bright areas on DWI corresponded to ADC decreases of about 30% compared to the non-ischemic hemisphere. These decreases were the same in both treatment groups and at each time point. DWI, T2W and TTC area fractions at 24 h were strongly correlated (r = 0.98, DWI and TTC; r = 0.99, T2W and TTC; r = 0.97, T2W and DWI, P < 0.0001). We conclude that in this ischemic model, SNX-111 provides early neuroprotection and that serial DWI is a useful way of demonstrating this.
引用
收藏
页码:36 / 45
页数:10
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