Gray P L, Taberner P V
Neuropharmacology. 1985 May;24(5):437-44. doi: 10.1016/0028-3908(85)90029-2.
Mice were rendered tolerant and dependent to barbital by a chronic feeding schedule of barbital over 5 weeks. The behavioural effects of muscimol, imidazole-acetic acid (ImAA), and gamma-hydroxybutyric acid (GHB) were measured in control, barbital-dependent, and mice dependent on barbital 48 hr after withdrawal of the drug. The sedative effects of the GABA-mimetics imidazole-acetic acid and muscimol were increased in dependent mice, but reduced in withdrawn mice. Subanaesthetic doses of barbital, given acutely, also increased the sedative effects of imidazole-acetic acid and muscimol but not of gamma-hydroxybutyric acid. Assay of plasma barbital levels by GLC indicated that a negligible amount of barbital was present 48 hr after withdrawal compared to levels of between 60 and 120 micrograms/ml during chronic treatment with barbital. The binding of [3H]GABA to membrane preparations from brain indicated that the values of Kd and Bmax for low affinity binding were not significantly altered in mice withdrawn from chronic treatment with barbital, but that the Kd for high affinity binding was significantly increased from 4.38 to 6.06 nM in barbital-withdrawn mice. There was no difference in the enhancement of GABA binding by pentobarbital between the two groups. It is concluded that barbital-tolerant and dependent mice are cross-tolerant to GABA and that this is possibly mediated by a change in the affinity of the GABA receptor for its ligand.
通过为期5周的巴比妥慢性喂养方案,使小鼠对巴比妥产生耐受性和依赖性。在对照组、巴比妥依赖组以及停药48小时后的巴比妥依赖小鼠中,测定了蝇蕈醇、咪唑乙酸(ImAA)和γ-羟基丁酸(GHB)的行为效应。在依赖小鼠中,GABA模拟物咪唑乙酸和蝇蕈醇的镇静作用增强,但在停药小鼠中减弱。急性给予亚麻醉剂量的巴比妥,也增强了咪唑乙酸和蝇蕈醇的镇静作用,但未增强γ-羟基丁酸的镇静作用。通过气相色谱法测定血浆巴比妥水平表明,与巴比妥慢性治疗期间60至120微克/毫升的水平相比,停药48小时后巴比妥的含量可忽略不计。[3H]GABA与脑细胞膜制剂的结合表明,慢性巴比妥治疗停药小鼠中,低亲和力结合的Kd和Bmax值无显著变化,但在巴比妥停药小鼠中,高亲和力结合的Kd从4.38显著增加至6.06 nM。两组之间戊巴比妥增强GABA结合的作用无差异。得出的结论是,巴比妥耐受和依赖的小鼠对GABA具有交叉耐受性,这可能是由GABA受体对其配体的亲和力变化介导的。