Takenaka S
Fukuoka Institute of Health & Environmental Sciences, Japan.
Chemosphere. 1998 Apr;36(10):2277-82. doi: 10.1016/s0045-6535(97)10196-5.
Microcystin LR metabolism in mammals was examined. The degradation of microcystin LR by the enzymes, pepsin, trypsin and chymotrypsin, from porcine or human gastrointestinal tract was examined. Microcystin LR was digested by these proteases, but 3-amino-2, 6, 8-trimethyl-10-phenyldeca-4E, 6E-dienoic acid (DmADDA) was not formed from microcystin LR treated with pepsin and chymotrypsin. The formation of DmADDA was detected from microcystin LR treated with trypsin. Furthermore, DmADDA was detected from the male ddY mice liver orally administered microcystin LR.
对微囊藻毒素-LR在哺乳动物体内的代谢进行了研究。检测了猪或人胃肠道中的胃蛋白酶、胰蛋白酶和胰凝乳蛋白酶对微囊藻毒素-LR的降解情况。微囊藻毒素-LR可被这些蛋白酶消化,但经胃蛋白酶和胰凝乳蛋白酶处理的微囊藻毒素-LR未形成3-氨基-2,6,8-三甲基-10-苯基癸-4E,6E-二烯酸(DmADDA)。经胰蛋白酶处理的微囊藻毒素-LR中检测到了DmADDA的形成。此外,在口服微囊藻毒素-LR的雄性ddY小鼠肝脏中也检测到了DmADDA。