Vohland H W, Zufelde H
Naunyn Schmiedebergs Arch Pharmacol. 1976 Jun;293(3):277-83. doi: 10.1007/BF00507350.
It was the aim of this investigation to find out why pentetrazol (PTZ) administered orally to rats has considerably lower convulsive effectiveness than PTZ injected parenterally. It could be demonstrated that PTZ is distributed to and eliminated from all organs analyzed, without any sign of storage or of redistribution. Biological halftime was found to be about 3.5 h after subcutaneous injection. PTZ is absorbed slowly from the gastrointestinal tract because PTZ given orally is retained in the stomach for many hours. PTZ absorption is slow from the stomach while it is rapid from the small intestine. Food taken in before and after PTZ administration decreases the rate of PTZ absorption. Retention in the stomach of PTZ given orally is probably due to delayed gastric emptying since PTZ is able to reduce the basal tone and the acetylcholine-induced contractions of isolated preparations of the fundus of the stomach.
本研究的目的是找出为什么口服给予大鼠的戊四氮(PTZ)惊厥效力比经肠胃外注射的PTZ低得多。可以证明,PTZ分布到所有分析的器官并从这些器官中消除,没有任何储存或再分布的迹象。皮下注射后生物半衰期约为3.5小时。PTZ从胃肠道吸收缓慢,因为口服给予的PTZ在胃中保留数小时。PTZ从胃中吸收缓慢,而从小肠吸收迅速。PTZ给药前后摄入的食物会降低PTZ的吸收速率。口服给予的PTZ在胃中的滞留可能是由于胃排空延迟,因为PTZ能够降低胃底离体标本的基础张力和乙酰胆碱诱导的收缩。