Potential of [11C]TMSX for the evaluation of adenosine A2A receptors in the skeletal muscle by positron emission tomography

被引:13
作者
Ishiwata, K
Mizuno, M
Kimura, Y
Kawamura, K
Oda, K
Sasaki, T
Nakamura, Y
Muraoka, I
Ishii, K
机构
[1] Tokyo Metropolitan Inst Gerontol, Positron Med Ctr, Itabashi Ku, Tokyo 1730022, Japan
[2] Waseda Univ, Grad Sch Human Sci, Tokorozawa, Saitama 3591192, Japan
[3] SHI Accelerator Serv Co Ltd, Shinagawa Ku, Tokyo 1410032, Japan
[4] Waseda Univ, Sch Sport Sci, Tokorozawa, Saitama 3591192, Japan
基金
日本学术振兴会;
关键词
adenosine A(2A) receptor; C-11]TMSX; muscle; human; positron emission tomography;
D O I
10.1016/j.nucmedbio.2004.06.003
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
We examined the potential of [7-methyl-C-11]-(E)-8-(3,4,5-trimethoxystyryl)-1,3,7-trimethylxanthine ([C-11]TMSX) for the assessment of adenosine A(2A) receptors in muscle. In rodents, specific binding of [C-11]TMSX was observed in muscle and heart by blockade with A(2A)-selective CSC and non-selective theophylline, but not with A(1)-selective DPCPX. Swimming exercise fluctuated radioligand-receptor binding in these tissues. In a PET study of two subjects, theophylline-infusion slightly deceased the distribution volume of [C-11]TMSX in the heart (20% reduction) and muscle (10% reduction), which suggested the specific binding. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:949 / 956
页数:8
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