کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2153701 | 1090201 | 2013 | 10 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Analysis of [11C]methyl-candesartan kinetics in the rat kidney for the assessment of angiotensin II type 1 receptor density in vivo with PET Analysis of [11C]methyl-candesartan kinetics in the rat kidney for the assessment of angiotensin II type 1 receptor density in vivo with PET](/preview/png/2153701.png)
IntroductionAngiotensin II type 1 (AT1) receptors play a key role in the regulation of renal and cardiovascular functions and have been implicated in the pathogenesis of many diseases. The aim of this study was to assess binding of the novel radioligand [11C]methyl-candesartan to AT1 receptors in the rat kidney in vivo with PET.MethodsDynamic PET images were acquired for 60 min at baseline, with coinjection of candesartan (5 mg/kg), and after injection of PD123,319 (5 mg/kg). Volumes of distribution (RC∙ VT) were estimated with a two-compartment model, by Logan analysis, and by taking the tissue-to-plasma activity ratio at 50–60 min post-injection.ResultsThe two-compartment model did not describe the kinetics at baseline adequately and the baseline scans were too short to obtain accurate estimates of RC∙ VT with the Logan approach. Based on the tissue-to-plasma ratios, roughly one-third of VT at baseline could be attributed to AT1 receptor binding. There were no indications of AT2 receptor binding in the rat kidney.ConclusionIt may be possible to detect changes in AT1 receptor density in the rat kidney in vivo with [11C]methyl-candesartan and PET. Imaging AT1 receptors with PET may provide valuable information on the role of these receptors in the pathogenesis of diseases such as hypertension, diabetic nephropathy, ventricular remodeling, and heart failure.
Journal: Nuclear Medicine and Biology - Volume 40, Issue 2, February 2013, Pages 252–261