O'Neill P J, Rahwan R G
Res Commun Chem Pathol Pharmacol. 1976 Jan;13(1):125-8.
The ability of several compounds to protect against acetaldehyde-induced loss of righting reflex was studied in mice and compared with previously published results in rats. L-cysteine (3 mMoles/kg), L-ascorbic acid, DL-thioctic acid, or DL-homocysteine (2 mMoles/kg each) was administered orally 30 minutes prior to an intraperitoneal ED90 of acetaldehyde (415 mg/kg). Cysteine, ascorbate, and thioctic acid caused a statistically significant reduction in acetaldehyde-induced toxicity, while homocysteine afforded only little protection. These results are qualitatively, but not quantitatively, similar to those reported for rats.
研究了几种化合物对乙醛诱导的小鼠翻正反射丧失的保护能力,并与先前发表的大鼠研究结果进行了比较。在腹腔注射乙醛ED90(415mg/kg)前30分钟,口服L-半胱氨酸(3毫摩尔/千克)、L-抗坏血酸、DL-硫辛酸或DL-同型半胱氨酸(各2毫摩尔/千克)。半胱氨酸、抗坏血酸盐和硫辛酸可使乙醛诱导的毒性在统计学上显著降低,而同型半胱氨酸仅提供很少的保护。这些结果在性质上与报道的大鼠结果相似,但在数量上不同。