期刊
ANGIOGENESIS
卷 16, 期 4, 页码 837-846出版社
SPRINGER
DOI: 10.1007/s10456-013-9359-4
关键词
Ga-68-NOTA-c(RGDyK); Angiogenesis; Kinetic modeling; Positron emission tomography; Forelimb ischemia
资金
- National Research Foundation [2008-2003852, R31-10089, 2011K000709, NRF-2012M2A2A7035853]
- Converging Research Center Program
- Ministry of Education, Science, and Technology
- National Research Foundation of Korea [2012M2A2A7035853] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
Gallium-68-labeled 1,4,7-triazacyclononane-1,4,7-triacetic acid (NOTA)-cyclic Arg-Gly-Asp-(D)-Tyr-Lys (c(RGDyK)) was developed for alpha(v)beta(3) targeting, and is a promising agent for imaging of cancer and disorders related to angiogenesis. In this study, we performed kinetic analysis of Ga-68-NOTA-c(RGDyK) in rats with surgically induced forelimb ischemia, and immunohistochemical analysis was also performed to assess alpha(v)beta(3) immuno-staining level. Animal models were created by excision of the left brachial vessels, and a sham operation was performed on the right brachial region under 2 % isoflurane anesthesia. Using an animal positron emission tomography/computed tomography (PET/CT) scanner, a list mode PET scan (120 min) was started with the injection of Ga-68-NOTA-c(RGDyK) via the tail vein at 3, 5 and 7 days after ischemic surgery. Volumes of interest were drawn on the left ventricle, sham operation, control, and ischemic regions. Compartmental and two graphical analyses (Logan and RE plots) were performed for kinetic parameter estimation. The immunohistochemical analysis was also performed after the last PET scan, and cell components were scored on a six point scale for quantification of immuno-staining level (0-negative to 5-very high). A 3-compartment model with reversible binding best described the tissue time-activity curves. The distribution volume of the ischemic region was significantly higher than that of the sham operation (P < 10(-6)) and control region (P < 10(-9)). Both the Logan and RE plots showed high correlation with compartmental analysis (R-2 = 0.96 and 0.95 for Logan and RE, respectively). The temporal changes in distribution volume and binding potential were not significant. The immuno-staining level of the ischemic region was significantly higher than that of sham operation (P < 10(-4)) and control region (P < 10(-8)). Kinetic modeling studies with dynamic Ga-68-NOTA-c(RGDyK) PET scan are feasible based on an image-derived input function in a rat ischemia model. The kinetic modeling analysis performed in this study will be useful for the quantitative evaluation of Ga-68-NOTA-c(RGDyK) binding to alpha(v)beta(3) in angiogenic tissues.
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