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Inhibition by carbapenem antibiotic imipenem of intestinal absorption of valproic acid in rats.

机译:碳青霉烯类抗生素亚胺培南抑制大鼠丙戊酸肠道吸收。

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The concomitant use of carbapenem antibiotics with valproic acid has been prohibited because panipenem induced a decrease in plasma concentration of valproic acid in epileptic patients during valproic acid therapy. To clarify the possible mechanism of the carbapenem-valproic acid interaction, we investigated the effect of imipenem on the pharmacokinetic behaviour of valproic acid in rats. Co-administration of imipenem (30 mg kg(-1), i.v.) induced a decrease in the peak plasma concentration of valproic acid after oral administration. However, the imipenem-induced decrease in plasma concentrations of valproic acid was not observed within 60 min after intravenous injection of valproic acid. By utilizing in-situ vascular and luminal perfused small intestine, it was confirmed that absorption of valproic acid from the luminal to the vascular perfusate was decreased in the presence of imipenem (0.5 mM) in the vascular perfusate. The everted gut sac method was used to determine the effect of imipenem on active transport of valproic acid. The accumulation of valproic acid on the serosal side of the intestinal sac against the concentration gradient was reduced by lactic acid that inhibits the carrier-mediated transport of valproic acid across the intestinal brush-border membrane. However, imipenem did not affect the active transport of valproic acid. Therefore, the inhibition by imipenem of valproic acid absorption may be caused by a mechanism different from that of lactic acid. In conclusion, imipenem inhibits the intestinal absorption of valproic acid, which contributes to the decrease in plasma concentration of valproic acid after oral administration.
机译:禁止将碳青霉烯类抗生素与丙戊酸同时使用,因为帕尼培南在丙戊酸治疗期间会导致癫痫患者的丙戊酸血浆浓度降低。为了阐明碳青霉烯-丙戊酸相互作用的可能机制,我们研究了亚胺培南对丙戊酸在大鼠体内药代动力学行为的影响。亚胺培南(30 mg kg(-1),i.v.)的共同给药导致口服丙戊酸后血浆血浆峰值浓度降低。但是,静脉注射丙戊酸后60分钟内未观察到亚胺培南诱导的丙戊酸血浆浓度降低。通过利用原位血管和管腔灌注的小肠,证实了在丙胺培南(0.5 mM)存在于血管灌注液中时,丙戊酸从管腔向血管灌注液的吸收减少。外翻肠囊法用于确定亚胺培南对丙戊酸主动转运的影响。乳酸可抑制丙戊酸在肠囊浆膜侧相对于浓度梯度的积累,从而抑制了丙戊酸的载体介导的跨肠刷状边界膜的转运。但是,亚胺培南没有影响丙戊酸的主动转运。因此,亚胺培南对丙戊酸吸收的抑制可能是由不同于乳酸的机理引起的。总之,亚胺培南抑制了丙戊酸在肠道的吸收,这有助于口服后丙戊酸的血浆浓度降低。

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