Clark M, Dar M S
Department of Pharmacology, School of Medicine, East Carolina University, Greenville, North Carolina 27858-4354.
Alcohol Clin Exp Res. 1989 Jun;13(3):371-7. doi: 10.1111/j.1530-0277.1989.tb00338.x.
Many classes of CNS-acting drugs have been suggested to act at least partially via inhibition of adenosine uptake. Synaptosomal uptake of [3H]adenosine and the effect of acute ethanol on it were studied in a rat brain area known to be involved in the coordination and modulation of normal motor activity, the cerebellum. Uptake of [3H]adenosine was found to be linear with time (about 40 sec) and increasing concentrations (up to 1.5 microM) of adenosine. The uptake of [3H]adenosine was inhibited by dilazep (IC50 = 2.5 x 10(-7) M) in a dose-dependent manner. Pharmacologically and/or toxicologically relevant concentrations of ethanol (2.5 to 100 mM) significantly inhibited the uptake of [3H]adenosine between 12 and 15%. Lineweaver-Burk plots indicated that both in vitro (25 mM) and in vivo (1.5 g/kg i.p.; 30 mM blood level) ethanol lowered Km as well as Vmax values for adenosine uptake to nearly the same extent. In the case of in vivo ethanol, no ethanol was present during the assay since synaptosome preparation would wash out residual ethanol. The results of the present study indicate possible membranal alterations by in vivo ethanol. It is concluded that the uptake of [3H]adenosine is inhibited by intoxicating concentrations of ethanol in vitro and by acute ethanol (1.5 g/kg) in vivo. This may partially explain the modulatory role of endogenous adenosine in ethanol-induced motor disturbances.
许多类中枢神经系统作用药物已被认为至少部分是通过抑制腺苷摄取来发挥作用的。在大鼠大脑中一个已知参与正常运动活动协调和调节的区域——小脑中,研究了[3H]腺苷的突触体摄取以及急性乙醇对其的影响。发现[3H]腺苷的摄取与时间(约40秒)和腺苷浓度增加(高达1.5微摩尔)呈线性关系。双嘧达莫(IC50 = 2.5×10^(-7) M)以剂量依赖方式抑制[3H]腺苷的摄取。药理学和/或毒理学相关浓度的乙醇(2.5至100毫摩尔)显著抑制[3H]腺苷摄取达12%至15%。Lineweaver - Burk图表明,体外(25毫摩尔)和体内(腹腔注射1.5克/千克;血药浓度30毫摩尔)乙醇降低腺苷摄取的Km值和Vmax值的程度几乎相同。就体内乙醇而言,在测定过程中不存在乙醇,因为突触体制备会洗去残留乙醇。本研究结果表明体内乙醇可能导致膜改变。结论是,体外中毒浓度的乙醇和体内急性乙醇(1.5克/千克)均抑制[3H]腺苷的摄取。这可能部分解释了内源性腺苷在乙醇诱导的运动障碍中的调节作用。