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放射性标记的酶抑制剂在肾上腺中的定位。

Localization of radiolabeled enzyme inhibitors in the adrenal gland.

作者信息

Beierwaltes W H, Wieland D M, Ice R D, Seabold J E, Sarkar S D, Gill S P, Mosley S T

出版信息

J Nucl Med. 1976 Nov;17(11):998-1002.

PMID:135823
Abstract

Tissue distribution studies were performed in rats and dogs at five time intervals between 10 min and 24 hr after the intravenous injection of one of the following radiolabeled adrenocortical enzyme inhibitors: 3H-amino-glutethimide, 125I-3-iodoaminoglutethimide, 3H-SKF-12185, 125I-3-SKF-12185, 3H-metyrapone. 3H-metyrapol. 3H-amphenone B, and 3H-SU-10603. In rats, 3H-SKF-12185 showed the highest uptake in the whole adrenal (3.5% kg dose/gm at 1 hr). In dogs, 3H-metyrapol showed the highest uptake in the adrenal cortex (9% kg dose/gm at 1 hr), and the peak cortex-to-liver concentration ratio was 57 at 2 hr. These peaks uptakes were comparable to those obtained with the conventional iodocholesterols, but they were reached much earlier, with elimination of most of the adrenal radioactivity by 24 hr. These properties would permit the use of 123I as the label and a higher tracer dose, resulting in a higher photon flux. Thus, the radiolabeled enzyme inhibitors show promise as adrenal-scanning agents, with a markedly shortened scanning procedure, a lower absorbed radiation dose, and better resolution.

摘要

在大鼠和狗身上进行了组织分布研究,研究对象为静脉注射以下放射性标记的肾上腺皮质酶抑制剂之一后10分钟至24小时内的五个时间间隔:3H-氨基谷氨酰胺、125I-3-碘氨基谷氨酰胺、3H-SKF-12185、125I-3-SKF-12185、3H-美替拉酮、3H-美替拉波、3H-氨苯酮B和3H-SU-10603。在大鼠中,3H-SKF-12185在整个肾上腺中的摄取量最高(1小时时为3.5%kg剂量/克)。在狗中,3H-美替拉波在肾上腺皮质中的摄取量最高(1小时时为9%kg剂量/克),皮质与肝脏的峰值浓度比在2小时时为57。这些峰值摄取量与使用传统碘胆固醇获得的摄取量相当,但达到峰值的时间要早得多,到24小时时大部分肾上腺放射性已消除。这些特性将允许使用123I作为标记物并使用更高的示踪剂剂量,从而产生更高的光子通量。因此,放射性标记的酶抑制剂有望成为肾上腺扫描剂,扫描过程明显缩短,吸收辐射剂量更低,分辨率更高。

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