Hemminki K
Toxicol Lett. 1982 Apr;11(1-2):1-6. doi: 10.1016/0378-4274(82)90096-0.
Acetaldehyde and formaldehyde react in vitro with cysteine to form a product, probably a thiazolidine derivative, which eluted as a single peak in cation exchange chromatography. The reactivity of formaldehyde was much higher than that of acetaldehyde. Rats were injected with single dose of 7.6, 6.2 and 2.5 mmol, respectively of ethanol, acetaldehyde and formaldehyde, and urine was analysed for alkali-hydrolysable thiol groups. Acetaldehyde caused a significant increase in urinary alkali-hydrolysable thiols. Ethanol and acetaldehyde treatment stimulated the ability of the urine to catalyse the iodine-azide reaction suggesting the presence of an excess of compounds containing C-S-atoms.
乙醛和甲醛在体外与半胱氨酸反应形成一种产物,可能是噻唑烷衍生物,该产物在阳离子交换色谱中作为单一峰洗脱。甲醛的反应活性远高于乙醛。分别给大鼠注射7.6、6.2和2.5毫摩尔的乙醇、乙醛和甲醛单剂量,然后分析尿液中的碱可水解硫醇基团。乙醛导致尿中碱可水解硫醇显著增加。乙醇和乙醛处理刺激了尿液催化叠氮碘反应的能力,表明存在过量含C-S原子的化合物。