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首页> 外文期刊>Xenobiotica: the fate of foreign compounds in biological systems >Comparative evaluation of absorption, distribution, and excretion of YM758, a novel If channel inhibitor, between albino and non-albino rats.
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Comparative evaluation of absorption, distribution, and excretion of YM758, a novel If channel inhibitor, between albino and non-albino rats.

机译:比较评估白化病大鼠和非白化病大鼠YM758(一种新型的If通道抑制剂)的吸收,分布和排泄。

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摘要

1. YM758 is a novel If channel inhibitor for the treatment of stable angina and atrial fibrillation. The absorption, distribution, and excretion of YM758 have been investigated in albino and non-albino rats after a single oral administration of (14)C-YM758 monophosphate. 2. YM758 was well absorbed from all segments of the gastrointestinal tract except for the stomach. After oral administration, the ratio of AUC(0-1 h) between the plasma concentrations of radioactivity and the unchanged drug was estimated to be 17.7%, which suggests metabolism. 3. The distribution of the radioactivity derived from (14)C-YM758 in tissues was evaluated both in albino and non-albino rats. The radioactivity concentrations in most tissues were higher than those in plasma, which indicates that the radioactivity is well distributed to tissues. Extensive accumulation and slower elimination of radioactivity were noted in the thoracic aorta of albino and non-albino rats as well as in the eyeballs of non-albino rats. The recovery rates of radioactivity in urine and bile after oral dosing to bile duct-cannulated albino rats were 17.8% and 57.3%, respectively. 4. These results suggest that YM758 was extensively absorbed, subjected to metabolism, and excreted mainly into the bile after oral administration to rats, and extensive accumulation of the unchanged drug and/or metabolites into tissues such as the thoracic aorta and eyeballs was observed.
机译:1. YM758是一种新型的If通道抑制剂,用于治疗稳定型心绞痛和心房颤动。在单次口服(14)C-YM758单磷酸盐后,已经在白化病和非白化病大鼠中研究了YM758的吸收,分布和排泄。 2. YM758除胃肠外,在胃肠道的所有部位均被良好吸收。口服给药后,血浆放射性浓度和未改变药物浓度之间的AUC(0-1 h)之比估计为17.7%,表明存在新陈代谢。 3.在白化病和非白化病大鼠中评估了源自(14)C-YM758的放射性在组织中的分布。大多数组织中的放射性浓度高于血浆中的放射性浓度,这表明放射性良好地分布在组织中。在白化病和非白化病大鼠的胸主动脉以及非白化病大鼠的眼球中发现大量积累和较慢的放射性消除。经胆管插管的白化病大鼠口服给药后,尿液和胆汁中放射性的回收率分别为17.8%和57.3%。 4.这些结果表明,YM758被大鼠口服后被广泛吸收,代谢并主要排入胆汁,并且观察到未改变的药物和/或代谢产物大量积聚到组织如胸主动脉和眼球中。

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