Vanlić-Razumenić N, Petrović J
Strahlentherapie. 1983 Jan;159(1):28-31.
Subcellular distribution of chlormerodrin-203Hg in the rat kidney has been studied. Two hours after i.v. injection of the radiopharmaceutical, kidney tissue homogenate was submitted to differential centrifugation to obtain cell organelles. Radioactivity distribution in relation to total radioactivity of kidney homogenate obtained in nine repeated experiments was as it follows (+/- SD): nuclei 3.5% (+/- 0.5); mitochondria 6.7% (+/- 0.6); microsomes 9.3% (+/- 0.8) and cytosol 38% (+/- 3.9). Specific activities expressed as counts/min/mg of protein were 915 (+/- 13%), 1232 (+/- 14%) and 1097 (+/- 14%) for mitochondria, microsomes and cytosol, respectively. Specific activity of the nuclei was 1445 (+/- 16%) counts/min/mg DNA. These results demonstrate that this imaging agent penetrates into the kidney cells where it remains mostly in the cytosol. A fraction of chlormerodrin-203Hg binds to microsomes, mitochondria and nuclei.
已对大鼠肾脏中氯汞丙脲 - 203Hg的亚细胞分布进行了研究。静脉注射放射性药物两小时后,将肾脏组织匀浆进行差速离心以获得细胞器。在九次重复实验中,相对于肾脏匀浆总放射性的放射性分布如下(±标准差):细胞核3.5%(±0.5);线粒体6.7%(±0.6);微粒体9.3%(±0.8);胞质溶胶38%(±3.9)。以每分钟计数/毫克蛋白质表示的比活性,线粒体为915(±13%),微粒体为1232(±14%),胞质溶胶为1097(±14%)。细胞核的比活性为1445(±16%)计数/分钟/毫克DNA。这些结果表明,这种显像剂可穿透进入肾细胞,且大部分保留在胞质溶胶中。一部分氯汞丙脲 - 203Hg与微粒体、线粒体和细胞核结合。