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Flunitrazepam does not alter cerebral distribution of buprenorphine in the rat.

机译:氟硝西m不会改变丁丙诺啡在大鼠中的大脑分布。

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Deaths have been reported among heroin addicts related to combined buprenorphine and flunitrazepam use. The aim of this study was to determine the existence of a drug-drug interaction during the distribution phase of buprenorphine. Arterial blood gases were measured after intravenous administration of buprenorphine alone (30 mg/kg), flunitrazepam alone (40 mg/kg) or both drugs in rats. Buprenorphine kinetics was studied in plasma and in striatum using cerebral microdialysis, both alone and after rat pretreatment with flunitrazepam. In contrast to buprenorphine or flunitrazepam alone, buprenorphine in combination with flunitrazepam induced a significant, rapid and sustained respiratory depression. Arterial PCO2 was increased at 1.5 min (6.7+/-0.2 versus 5.4+/-0.3 and 5.5+/-0.3 kPa, respectively, P=0.04) (mean+/-S.E.M.), and arterial pH decreased (7.37+/-0.02 versus 7.45+/-0.02 and 7.45+/-0.01, respectively, P=0.03). Plasma buprenorphine kinetics was well described by a three-compartment linear model, with a distribution half-life of 7.4+/-2.7 min and an elimination half-life of 463.9+/-152.3 min. However, neither plasma nor striatal buprenorphine kinetics were significantly altered by pre-administration of flunitrazepam. The adverse interaction between flunitrazepam and buprenorphine cannot be explained by a pharmacokinetic drug-drug interaction during the distribution phase of buprenorphine.
机译:据报道,与丁丙诺啡和氟尼西epa合用有关的海洛因成瘾者死亡。这项研究的目的是确定丁丙诺啡的分布阶段是否存在药物相互作用。在大鼠中静脉内给予丁丙诺啡(30 mg / kg),氟尼西epa(40 mg / kg)或两种药物静脉给药后,测量动脉血气。单独和在使用氟尼西epa对大鼠进行预处理后,使用脑微透析研究了血浆和纹状体中丁丙诺啡的动力学。与单独的丁丙诺啡或氟尼西epa相反,丁丙诺啡与氟尼西epa合用会引起显着,快速和持续的呼吸抑制。动脉PCO2在1.5分钟时升高(分别为6.7 +/- 0.2和5.4 +/- 0.3和5.5 +/- 0.3 kPa,P = 0.04)(平均值+/- SEM),并且动脉pH降低(7.37 +/- 0.02)分别为7.45 +/- 0.02和7.45 +/- 0.01,P = 0.03)。三室线性模型很好地描述了血浆丁丙诺啡动力学,分布半衰期为7.4 +/- 2.7分钟,消除半衰期为463.9 +/- 152.3分钟。但是,氟尼西epa的预先给药既不会显着改变血浆和纹状体丁丙诺啡的动力学。氟硝西epa与丁丙诺啡之间的不良相互作用无法用丁丙诺啡分布阶段的药代动力学药物相互作用来解释。

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