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丙磺舒与两种脂溶性巴比妥类药物在大鼠体内的相互作用。

Interaction between probenecid and two lipid-soluble barbiturates in the rat.

作者信息

Bolander H G, Wahlström G

出版信息

Neuropharmacology. 1984 Aug;23(8):977-81. doi: 10.1016/0028-3908(84)90014-5.

Abstract

The effect of pretreatment with probenecid (200 mg/kg, i.p.) on the sensitivity of the central nervous system (CNS) to thiopental and hexobarbital was investigated with an EEG-threshold method. The threshold dose was significantly decreased by pretreatment with probenecid for thiopental but not for hexobarbital. This was due to an increased penetration of thiopental into the CNS, but for hexobarbital an increase in penetration could also be demonstrated by analysis of brain and serum concentrations after infusion of an equal dose of barbiturate. The concentrations in brain at the EEG-threshold were not influenced by pretreatment with probenecid for either of these barbiturates, which shows that there was no synergism between these barbiturates and probenecid due to the depressant effect of probenecid on the CNS.

摘要

采用脑电图阈值法研究了丙磺舒(200mg/kg,腹腔注射)预处理对中枢神经系统(CNS)对硫喷妥钠和己巴比妥敏感性的影响。丙磺舒预处理可使硫喷妥钠的阈剂量显著降低,但对己巴比妥则无此作用。这是由于硫喷妥钠进入中枢神经系统的渗透率增加,但对于己巴比妥,在输注等量巴比妥酸盐后,通过分析脑和血清浓度也可证明其渗透率增加。对于这两种巴比妥酸盐,脑电图阈值时的脑内浓度均不受丙磺舒预处理的影响,这表明由于丙磺舒对中枢神经系统的抑制作用,这些巴比妥酸盐与丙磺舒之间不存在协同作用。

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