Loo G, Smith J T
Biochem Biophys Res Commun. 1985 Apr 30;128(2):965-71. doi: 10.1016/0006-291x(85)90141-x.
Rat liver cytosolic thiopurine methyltransferase and microsomal thiol methyltransferase were each found to be subject to control by the absolute molar ratio of S-adenosylmethionine to S-adenosylhomocysteine using cell-free enzyme preparations. As this ratio was lowered, inhibition of both sulfhydryl xenobiotic transmethylases occurred. On the other hand, when the ratio was decreased in vivo by the administration of D,L-homocysteine thiolactone to animals, this alteration was accompanied by an inhibition of only thiopurine methyltransferase activity. Thiol methyltransferase activity was not significantly affected after drug treatment, which would suggest that there is a compartmentalization of S-adenosylhomocysteine in the intact hepatocyte.
使用无细胞酶制剂发现,大鼠肝脏胞质硫嘌呤甲基转移酶和微粒体硫醇甲基转移酶均受S-腺苷甲硫氨酸与S-腺苷同型半胱氨酸的绝对摩尔比调控。随着该比例降低,两种巯基外源性物质转甲基酶均受到抑制。另一方面,当通过向动物给药D,L-同型半胱氨酸硫内酯在体内降低该比例时,这种改变仅伴随着硫嘌呤甲基转移酶活性的抑制。药物治疗后硫醇甲基转移酶活性未受到显著影响,这表明在完整的肝细胞中存在S-腺苷同型半胱氨酸的区室化。