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Dynamic Contrast-Enhanced MRI for Assessing Therapeutic Response of Choroidal Neovascularization in a Rat Model

Title
Dynamic Contrast-Enhanced MRI for Assessing Therapeutic Response of Choroidal Neovascularization in a Rat Model
Author
김선일
Keywords
BLOOD-RETINAL BARRIER; ANTIANGIOGENIC AGENT KR-31831; MACULAR DEGENERATION; PARAMETERS; ANGIOGENESIS; PERMEABILITY; BEVACIZUMAB; MACULOPATHY; TUMORS; DTPA
Issue Date
2012-11
Publisher
ASSOC RESEARCH VISION OPHTHALMOLOGY INC
Citation
Investigative Ophthalmology and Visual Science, November 2012, 53(12), P.7693-7700
Abstract
PURPOSE. We evaluated the potential of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) as a noninvasive biomarker of choroidal neovascularization (CNV) and its utility as a tool for monitoring therapeutic response in laser-induced rat CNV models.METHODS. CNV was induced in the right eyes of 14 rats using a laser. Rats (n = 7) were treated daily for 14 days with a candidate drug (KR-31831, 50 mg/kg of body weight) having antiangiogenic effects, whereas control rats (n - 7) were treated with the vehicle alone (10% cremophor, 10% absolute ethyl alcohol, and 80% saline). DCE-MRI examinations were performed on the day before surgery (D - 1), and 3, 7, and 14 days after surgery (D + 3, D + 7, and D + 14), from which pharmacokinetic parameters (K-trans, v(e), v(p)) were calculated. Angiography was performed to visualize CNV using FITC-labeled high molecular weight dextran after MRI on D + 14. The paired Wilcoxon test and Mann-Whitney U test were performed for statistical analysis.RESULTS. The K-trans and v(e) values of the CNV-induced right eyes were significantly higher than those of the intact eyes in control rats at D+14 (P < 0.05). In the CNV-induced eyes, the relative K-trans and v(e) values of the KR-31831-treated group were significantly lower than those of the nontreated group at D + 14 (P < 0.05). The angiography showed that decreased CNV was observed in rats treated with KR-31831.CONCLUSIONS. Quantitative DCE-MRI produces noninvasive biomarker of CNV, thus allowing monitoring of therapeutic response of antiangiogenic drugs in neovascular age-related macular degeneration (AMD). (Invest Ophthalmol Vis Sci. 2012;53:7693-7700) DOI:10.1167/iovs.12-9805
URI
http://iovs.arvojournals.org/article.aspx?articleid=2127410http://hdl.handle.net/20.500.11754/47117
ISSN
0146-0404; 1552-5783
DOI
10.1167/iovs.12-9805
Appears in Collections:
COLLEGE OF ENGINEERING[S](공과대학) > ELECTRICAL AND BIOMEDICAL ENGINEERING(전기·생체공학부) > Articles
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