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丙戊酸在小鼠中的时辰药理学研究:口服与直肠给药比较

Chronopharmacological study of valproic acid in mice: comparison of oral and rectal administration.

作者信息

Yoshiyama Y, Nakano S, Ohdo S, Ogawa N

机构信息

School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan.

出版信息

J Pharmacobiodyn. 1992 Aug;15(8):403-8. doi: 10.1248/bpb1978.15.403.

Abstract

This study was performed to investigate the influence of the dosing route on chronopharmacological aspect of valproic acid (VPA) in mice, comparing the oral and rectal route. ICR male mice, housed under a standardized light-dark cycle (lights on from 0700 to 1900), were orally or rectally administered 400 mg/kg VPA each at the following scheduled time: 0900, 1300, 1700, 2100, 0100 and 0500. VPA concentrations in plasma and brain were determined by gas-liquid chromatography. There was a circadian rhythm in the electroshock seizure (ES) threshold 30 min after oral VPA administration, with the highest value at the midlight (1300) and the lowest at the middark (0100) (p < 0.01). A significant circadian rhythm was also found in plasma and brain VPA concentrations 30 min after oral administration (p < 0.01). This finding is related to the rhythm in the ES threshold. In contrast to oral administration, no circadian rhythm in the ES threshold, plasma and brain VPA concentrations was observed after rectal administration. These values after rectal dosing showed higher levels in comparison to those after oral dosing. Thus, the rectal route for VPA might have merit to eliminate the time-dependent changes in VPA pharmacologic action and kinetics. The timing of drug administration is an important factor that must be carefully controlled in drug pharmacokinetic and pharmacodynamic studies and must be considered in planning dosing routes.

摘要

本研究旨在通过比较口服和直肠给药途径,探讨给药途径对小鼠丙戊酸(VPA)时辰药理学方面的影响。将ICR雄性小鼠饲养在标准化的明暗周期(07:00至19:00开灯)下,分别在以下预定时间口服或直肠给予400mg/kg VPA:09:00、13:00、17:00、21:00、01:00和05:00。采用气液色谱法测定血浆和脑组织中的VPA浓度。口服VPA 30分钟后,电休克惊厥(ES)阈值存在昼夜节律,在光照中期(13:00)最高,在黑暗中期(01:00)最低(p<0.01)。口服给药30分钟后,血浆和脑组织中的VPA浓度也存在显著的昼夜节律(p<0.01)。这一发现与ES阈值的节律有关。与口服给药相比,直肠给药后未观察到ES阈值、血浆和脑组织VPA浓度的昼夜节律。直肠给药后的这些值与口服给药后的相比更高。因此,VPA的直肠给药途径可能有助于消除VPA药理作用和动力学的时间依赖性变化。给药时间是药物药代动力学和药效学研究中必须仔细控制的一个重要因素,在规划给药途径时必须予以考虑。

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