Kojima S, Nadai M, Kitaichi K, Wang L, Nabeshima T, Hasegawa T
Department of Hospital Pharmacy, Nagoya University School of Medicine, Nagoya 466,, Japan.
Antimicrob Agents Chemother. 1998 Dec;42(12):3136-40. doi: 10.1128/AAC.42.12.3136.
There is evidence indicating that the carbapenem antibiotic panipenem decreases plasma concentrations of valproic acid (VPA) in epileptic patients during VPA therapy. The mechanism for panipenem-induced changes in the pharmacokinetics of VPA was investigated in rats with and without bile duct cannulation. The effect of panipenem on the pharmacokinetics of diclofenac, which undergoes extensive enterohepatic recirculation, was also examined. VPA (50 mg/kg of body weight) or diclofenac (10 mg/kg of body weight) was administered intravenously under the steady-state plasma panipenem concentration of 4 microgram/ml, which had been achieved by a constant infusion rate. Panipenem decreased the plasma VPA concentrations in rats without bile duct cannulation but did not change the volume of the initial space and protein binding of VPA. However, panipenem had no effect on the plasma VPA concentrations and the biliary excretion of VPA in rats with bile duct cannulation. The secondary increase in plasma diclofenac concentration observed in the absence of panipenem was diminished in the presence of panipenem. These findings suggest that panipenem decreases plasma VPA concentrations by suppressing its enterohepatic recirculation, probably due to a panipenem-induced decrease in the numbers of enteric bacteria.
有证据表明,碳青霉烯类抗生素帕尼培南在癫痫患者丙戊酸(VPA)治疗期间会降低其血浆浓度。在有或没有胆管插管的大鼠中研究了帕尼培南引起VPA药代动力学变化的机制。还研究了帕尼培南对双氯芬酸药代动力学的影响,双氯芬酸经历广泛的肠肝循环。在通过恒定输注速率达到的稳态血浆帕尼培南浓度为4微克/毫升的情况下,静脉注射VPA(50毫克/千克体重)或双氯芬酸(10毫克/千克体重)。帕尼培南降低了无胆管插管大鼠的血浆VPA浓度,但没有改变VPA的初始分布容积和蛋白结合率。然而,帕尼培南对有胆管插管大鼠的血浆VPA浓度和VPA的胆汁排泄没有影响。在没有帕尼培南的情况下观察到的双氯芬酸血浆浓度的二次升高在有帕尼培南的情况下减弱。这些发现表明,帕尼培南可能通过抑制其肠肝循环来降低血浆VPA浓度,这可能是由于帕尼培南导致肠道细菌数量减少所致。