Kohri H, Morita S, Nakagawa K, Nishino H
Nihon Yakurigaku Zasshi. 1976 Apr;72(3):341-50. doi: 10.1254/fpj.72.341.
Distribution of a new beta-adrenergic blocking agent, 3H-carteolol in mice was studied by whole body autoradiography. The distribution of radioactivity was observed in all organs except the eyes and brain, with particularly high specific activities in the kidneys, liver, gall bladder and content in the intestines within a short time after either oral or intravenous administration. The radioactivity was then promptly eliminated from all tissues and organs, and excreted almost entirely in the urine and bile. Propranolol is known to be distributed at a high concentration in the brain, whereas the concentration of (3H-) carteolol detectable in the brain was slight. In the adrenal gland, the radioactivity was localized in the medulla. Radioactivity was detected also in the stomach contents after the intravenous administration. The distribution of radioactivity in the fetus through the placenta was less than that in the major organs of the mother mouse, and the elimination of the activity was more rapid in the fetus than in mother. These findings indicate that carteolol and its metabolites do to some extent pass through the blood-brain barrier and placenta.
通过全身放射自显影术研究了一种新型β-肾上腺素能阻滞剂3H-卡替洛尔在小鼠体内的分布情况。除眼睛和脑外,在所有器官中均观察到放射性分布,口服或静脉给药后短时间内,肾脏、肝脏、胆囊中的比活度特别高,肠道中的含量也很高。然后,放射性迅速从所有组织和器官中消除,几乎全部经尿液和胆汁排出。已知普萘洛尔在脑中以高浓度分布,而在脑中可检测到的(3H-)卡替洛尔浓度很低。在肾上腺中,放射性定位于髓质。静脉给药后胃内容物中也检测到放射性。通过胎盘在胎儿体内的放射性分布低于母鼠主要器官中的分布,且胎儿体内放射性的消除比母鼠更快。这些发现表明卡替洛尔及其代谢产物在一定程度上可穿过血脑屏障和胎盘。