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人体组织中醛糖还原酶和醛还原酶对醛糖还原酶抑制剂的敏感性。

Susceptibility of aldehyde and aldose reductases of human tissues to aldose reductase inhibitors.

作者信息

Srivastava S K, Petrash J M, Sadana I J, Ansari N H, Partridge C A

出版信息

Curr Eye Res. 1982;2(6):407-10. doi: 10.3109/02713688209000786.

Abstract

The effect of aldose reductase inhibitors such as sorbinil, alrestatin, and quercitrin has been studied on the aldose reductase purified from human brain and lens, and aldehyde reductase I purified from human liver, and aldehyde reductase II purified from human brain, liver, and red cells. None of the aldose reductase inhibitors have been found to be specific for aldose reductase. Fifty micromolar sorbinil besides inhibiting aldose reductase, completely inhibits aldehyde reductase II from the brain, liver and red cells. Similarly, alrestatin and quercitrin also are potent inhibitors of aldehyde reductase I and aldehyde reductase II.

摘要

已对诸如索比尼尔、阿雷司他汀和槲皮苷等醛糖还原酶抑制剂对从人脑中纯化的醛糖还原酶、从人晶状体中纯化的醛糖还原酶、从人肝脏中纯化的醛糖还原酶I以及从人脑、肝脏和红细胞中纯化的醛糖还原酶II的作用进行了研究。尚未发现任何一种醛糖还原酶抑制剂对醛糖还原酶具有特异性。50微摩尔的索比尼尔除了抑制醛糖还原酶外,还能完全抑制来自脑、肝脏和红细胞的醛糖还原酶II。同样,阿雷司他汀和槲皮苷也是醛糖还原酶I和醛糖还原酶II的有效抑制剂。

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