Gonzalez L E, Parada M A, Hernandez L
Department of Pharmacology, Medical School, Los Andes University, Merida, Venezuela.
Alcohol. 1992 Nov-Dec;9(6):519-22. doi: 10.1016/0741-8329(92)90090-w.
Although for many years it has been proposed that megadoses of pyridoxine protect from ethanol toxicity, this issue remains unclear. In the present report the interaction between ethanol and pyridoxine was tested. Pyridoxine was administered intramuscularly or intracerebroventricularly to rats. Intramuscular administration of 187.2 mg/kg of pyridoxine displaced the ethanol-lethality dose curve significantly toward the right (p < 0.005) and increased the LD50 of ethanol from 4.46 to 5.19 g/kg (p < 0.005). Intracerebroventricular administration of pyridoxine (1.1 mg) completely suppressed the mortality due to a LD100 of ethanol and the effect was dose dependent. We conclude that pyridoxine is an effective treatment for ethanol intoxication. The results are discussed in terms of an interaction of ethanol and pyridoxine on the GABAergic system.
尽管多年来一直有人提出大剂量的吡哆醇可预防乙醇毒性,但这个问题仍不明确。在本报告中,对乙醇与吡哆醇之间的相互作用进行了测试。给大鼠肌肉注射或脑室内注射吡哆醇。肌肉注射187.2毫克/千克的吡哆醇可使乙醇致死剂量曲线显著右移(p < 0.005),并使乙醇的半数致死量从4.46克/千克增加到5.19克/千克(p < 0.005)。脑室内注射吡哆醇(1.1毫克)可完全抑制因乙醇的100%致死剂量导致的死亡率,且该效应呈剂量依赖性。我们得出结论,吡哆醇是治疗乙醇中毒的有效药物。根据乙醇与吡哆醇在γ-氨基丁酸能系统上的相互作用对结果进行了讨论。