Brada Z, Bulba S
Res Commun Chem Pathol Pharmacol. 1987 Apr;56(1):133-6.
The synthesis of the adenosyl-moiety of S-adenosylethionine from glycine was studied in normal rats and rats fed a diet containing 0.30% DL-ethionine for three weeks, using a L-ethionine probe. The liver of rats, pretreated by DL-ethionine feeding, incorporated--after injection of 20 mg L-ethionine/100 g body wt.--six times more C-14 from glycine-2-14C into the adenosyl-moiety of SAE than normal rats. Further increasing of doses up to 100 mg/100 g body wt. did not substantially change the incorporation in pre-exposed rats while in normal rats an almost complete inhibition of the incorporation was observed. The liver cells exposed to a chronic effect of DL-ethionine are able, after higher demands for ATP, to increase the ATP generation more effectively than normal cells. This adaptation to the toxic effect of ethionine represents one of the first alterations of the metabolic functions of liver parenchyme in the course of hepatic DL-ethionine cancerogenesis.
使用L-乙硫氨酸探针,研究了正常大鼠和喂食含0.30% DL-乙硫氨酸饮食三周的大鼠中,由甘氨酸合成S-腺苷乙硫氨酸腺苷部分的情况。经DL-乙硫氨酸喂食预处理的大鼠肝脏,在注射20mg L-乙硫氨酸/100g体重后,从甘氨酸-2-¹⁴C掺入到SAE腺苷部分的¹⁴C比正常大鼠多六倍。剂量进一步增加至100mg/100g体重时,对预先暴露的大鼠的掺入情况没有实质性改变,而在正常大鼠中观察到掺入几乎完全受到抑制。暴露于DL-乙硫氨酸慢性作用的肝细胞,在对ATP有更高需求后,能够比正常细胞更有效地增加ATP生成。这种对乙硫氨酸毒性作用的适应性代表了肝脏实质代谢功能在肝脏DL-乙硫氨酸致癌过程中的首批改变之一。