Hüfner M, Grussendorf M
Clin Chim Acta. 1978 May 2;85(3):243-51. doi: 10.1016/0009-8981(78)90301-7.
Properties of an inactivating pathway of T4 to 3,3'-diiodothyronine (T2') in rat liver homogenate are described. The intermediate product (of this reaction sequence) is reverse T3 (rT3) which is very labile and cannot be measured at pH 7.5. The apparent KM of the reaction rT3 to T2' is 2 X 10(-8) M. The activities catalyzing the reactions T4 to T3, T4 to T2' and rT3 to T2' are found in the 100 000 X g pellet. Propylthiouracil inhibits all three activities to a similar degree; alpha-methyl-p-tyrosine has no effect. T3 seems to be only a minor source of T2' production. The molar ratio of the two T4 deiodination pathways T4 to T3/T4 to T2' under these conditions is about 1.7; however, by changing the pH this ratio could be significantly altered.
描述了大鼠肝脏匀浆中T4向3,3'-二碘甲状腺原氨酸(T2')的失活途径的特性。(该反应序列的)中间产物是反式T3(rT3),其非常不稳定,在pH 7.5时无法测量。rT3向T2'反应的表观KM为2×10^(-8) M。催化T4向T3、T4向T2'以及rT3向T2'反应的活性存在于100000×g沉淀中。丙硫氧嘧啶对这三种活性的抑制程度相似;α-甲基对酪氨酸没有作用。T3似乎只是T2'产生的次要来源。在这些条件下,T4脱碘的两条途径T4向T3/T4向T2'的摩尔比约为1.7;然而,通过改变pH,该比例可能会显著改变。