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

Y Yoshiyama, S Nakano, S Ohdo, N Ogawa
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引用次数: 4

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.

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丙戊酸对小鼠的时间药理学研究:口服和直肠给药的比较。
本研究比较口服和直肠给药途径对小鼠丙戊酸(VPA)时间药理学的影响。ICR雄性小鼠置于标准化的光-暗周期(0700 - 1900亮灯)下,分别于0900、1300、1700、2100、0100和0500口服或直肠给予400 mg/kg VPA。采用气液色谱法测定血浆和脑组织中VPA的浓度。口服VPA后30min的电休克发作阈值具有昼夜节律性,午时最高(1300),午时最低(0100)(p < 0.01)。口服给药30 min后血浆和脑VPA浓度也有明显的昼夜节律(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ES阈值、血浆和脑VPA浓度没有昼夜节律变化。直肠给药后的这些数值比口服给药后的水平更高。因此,直肠途径的VPA可能有优点,以消除VPA的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,在计划给药路线时必须考虑到这一点。
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