Àrea de Psicobiologia, Universitat Jaume I, Avda Sos Baynat, 12071 Castellón, Spain.
Drug Alcohol Depend. 2012 Jul 1;124(1-2):42-9. doi: 10.1016/j.drugalcdep.2011.12.003. Epub 2012 Jan 18.
In the brain, the enzyme catalase by reacting with H(2)O(2) forms Compound I (catalase-H(2)O(2) system), which is the main system of central ethanol metabolism to acetaldehyde. Previous research has demonstrated that acetaldehyde derived from central-ethanol metabolism mediates some of the psychopharmacological effects produced by ethanol. Manipulations that modulate central catalase activity or sequester acetaldehyde after ethanol administration modify the stimulant effects induced by ethanol in mice. However, the role of H(2)O(2) in the behavioral effects caused by ethanol has not been clearly addressed. The present study investigated the effects of ebselen, an H(2)O(2) scavenger, on ethanol-induced locomotion.
Swiss RjOrl mice were pre-treated with ebselen (0-50mg/kg) intraperitoneally (IP) prior to administration of ethanol (0-3.75g/kg; IP). In another experiment, animals were pre-treated with ebselen (0 or 25mg/kg; IP) before caffeine (15mg/kg; IP), amphetamine (2mg/kg; IP) or cocaine (10mg/kg; IP) administration. Following these treatments, animals were placed in an open field to measure their locomotor activity. Additionally, we evaluated the effect of ebselen on the H(2)O(2)-mediated inactivation of brain catalase activity by 3-amino-1,2,4-triazole (AT).
Ebselen selectively prevented ethanol-induced locomotor stimulation without altering the baseline activity or the locomotor stimulating effects caused by caffeine, amphetamine and cocaine. Ebselen reduced the ability of AT to inhibit brain catalase activity.
Taken together, these data suggest that a decline in H(2)O(2) levels might result in a reduction of the ethanol locomotor-stimulating effects, indicating a possible role for H(2)O(2) in some of the psychopharmacological effects produced by ethanol.
在大脑中,过氧化氢酶通过与 H(2)O(2)反应形成化合物 I(过氧化氢酶-H(2)O(2)系统),这是中枢乙醇代谢为乙醛的主要系统。先前的研究表明,来自中枢乙醇代谢的乙醛介导了乙醇产生的一些精神药理学作用。在给予乙醇后调节中枢过氧化氢酶活性或隔离乙醛的操作修饰了乙醇在小鼠中诱导的兴奋剂作用。然而,H(2)O(2)在乙醇引起的行为作用中的作用尚未得到明确解决。本研究调查了 H(2)O(2)清除剂 ebselen 对乙醇诱导的运动的影响。
瑞士 RjOrl 小鼠在给予乙醇(0-3.75g/kg;腹腔内)之前用 ebselen(0-50mg/kg)腹腔内预先处理。在另一个实验中,动物在用 ebselen(0 或 25mg/kg;腹腔内)预处理后给予咖啡因(15mg/kg;腹腔内)、安非他命(2mg/kg;腹腔内)或可卡因(10mg/kg;腹腔内)。在这些治疗后,将动物置于开阔场中以测量其运动活动。此外,我们评估了 ebselen 对 3-氨基-1,2,4-三唑(AT)介导的脑过氧化氢酶活性失活的 H(2)O(2)的影响。
ebselen 选择性地防止了乙醇诱导的运动刺激,而不改变基线活性或咖啡因、安非他命和可卡因引起的运动刺激作用。ebselen 降低了 AT 抑制脑过氧化氢酶活性的能力。
总的来说,这些数据表明 H(2)O(2)水平的下降可能导致乙醇运动刺激作用的降低,表明 H(2)O(2)在乙醇产生的一些精神药理学作用中可能起作用。