Mallov S, Gilmour R F
Drug Alcohol Depend. 1977 Sep-Nov;2(5-6):397-407. doi: 10.1016/0376-8716(77)90041-2.
The oral administration of single doses (0.5-6.0 g/kg) of ethanol to rats, shortly before injecting them with a large dose (3.0 mg base/kg) of epinephrine subcutaneously, significantly reduced the severity of the myocardial damage produced by the epinephrine. The larger the dose of ethanol, the greater was the protective effect. The results were the same, regardless of the method used to determine the degree of cardiac injury. Experiments employing various agents to determine the mechanisms of ethanol action have tentatively suggested that a platelet de-aggregating or an osmotic effect of alcohol may be involved.
在给大鼠皮下注射大剂量(3.0毫克碱基/千克)肾上腺素之前不久,给其口服单剂量(0.5 - 6.0克/千克)乙醇,可显著减轻肾上腺素所致心肌损伤的严重程度。乙醇剂量越大,保护作用越强。无论采用何种方法测定心脏损伤程度,结果均相同。采用各种试剂来确定乙醇作用机制的实验初步表明,可能涉及血小板解聚或酒精的渗透作用。