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抗抑郁药维洛沙嗪对癫痫患者奥卡西平及其羟基化代谢物的影响。

Effects of the antidepressant drug viloxazine on oxcarbazepine and its hydroxylated metabolites in patients with epilepsy.

作者信息

Pisani F, Fazio A, Oteri G, Artesi C, Xiao B, Perucca E, Di Perri R

机构信息

Institute of Neurological and Neurosurgical Sciences, University of Messina, Italy.

出版信息

Acta Neurol Scand. 1994 Aug;90(2):130-2. doi: 10.1111/j.1600-0404.1994.tb02692.x.

Abstract

The effects of Viloxazine (VLX, 100 mg b.i.d. for 10 days) on the steady-state plasma concentrations of Oxcarbazepine (OXC), its active metabolite 10, 11-dihydro-10-hydroxy-carbazepine (MHD) and the corresponding diol (DHD) were studied in a randomized, double-blind cross-over placebo-controlled trial in 6 epileptic patients stabilized on a fixed dosage of OXC. Administration of VLX resulted in an 11% increase in the plasma concentration of MHD (p = 0.003) associated with a 31% fall in DHD levels (p = 0.0001). Plasma concentrations of unchanged OXC were unaffected by VLX. No changes in seizure frequency nor signs of drug toxicity were observed during the study. Although VLX may inhibit the conversion of MHD to the inactive diol, the interaction is unlikely to be of clinical significance.

摘要

在一项针对6名服用固定剂量奥卡西平(OXC)病情稳定的癫痫患者的随机、双盲、交叉、安慰剂对照试验中,研究了维洛沙嗪(VLX,每日两次,每次100 mg,共10天)对奥卡西平(OXC)、其活性代谢物10,11-二氢-10-羟基卡马西平(MHD)及相应二醇(DHD)稳态血药浓度的影响。服用VLX导致MHD血药浓度升高11%(p = 0.003),同时DHD水平下降31%(p = 0.0001)。未改变的OXC血药浓度不受VLX影响。研究期间未观察到癫痫发作频率变化及药物毒性迹象。虽然VLX可能抑制MHD向无活性二醇的转化,但这种相互作用不太可能具有临床意义。

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