Eales J G, McLeese J M, Holmes J A, Youson J H
Department of Zoology, University of Manitoba, Winnipeg, Manitoba, R3T 2N2, Canada.
J Exp Zool. 2000 Feb 15;286(3):305-12. doi: 10.1002/(sici)1097-010x(20000215)286:3<305::aid-jez9>3.0.co;2-5.
We measured microsomal low-K(m) outer-ring deiodination (ORD) and inner-ring deiodination (IRD) activities for thyroxine (T(4)) and 3, 5,3'-triiodothyronine (T(3)) in intestine and liver in nonmetamorphosing (undersized) larvae, immediately premetamorphic larvae, animals in stages 1-7 of metamorphosis, and immediately postmetamorphic sea lampreys (Petromyzon marinus). For intestine: T(4)ORD activity was relatively low in nonmetamorphosing larvae, increased in premetamorphic individuals, was highest in stages 1 and 2 and was very low during stages 3-7; T(4)IRD activity was negligible until stage 3 but increased 4.7-fold through stages 3 to 7 such that T(4)IRD activity was 14 times T(4)ORD activity at stage 6; T(3)ORD activity was undetectable; T(3)IRD activity was not measured through stages 3-7 but correlated with T(4)IRD activity at other stages. For liver: deiodination was only measured up to stage 2 and in postmetamorphic animals; in contrast to intestine, T(4)ORD activity fell to low levels at stage 2 and was low during postmetamorphosis; T(4)IRD and T(3)IRD activities were very low and uninfluenced by developmental stage; T(3)ORD activity was undetectable. We conclude that (1) deiodination activity is usually much higher in intestine than in liver, (2) intestinal ORD and IRD activities change reciprocally so that ORD predominates in early metamorphosis but IRD predominates in mid and late metamorphosis, and (3) changes in intestinal deiodination may contribute to the characteristic depression of plasma T(4) and T(3) levels during spontaneous metamorphosis. J. Exp. Zool. 286:305-312, 2000.
我们测定了未变态(体型过小)的七鳃鳗幼体、即将变态的幼体、处于变态1 - 7期的动物以及变态刚结束后的海七鳃鳗(海七鳃鳗)肠道和肝脏中微粒体低K(m)外环脱碘(ORD)和内环脱碘(IRD)对甲状腺素(T(4))和3,5,3'-三碘甲状腺原氨酸(T(3))的活性。对于肠道:未变态幼体中T(4)ORD活性相对较低,即将变态的个体中升高,在1期和2期最高,在3 - 7期非常低;T(4)IRD活性在3期之前可忽略不计,但在3至7期增加了4.7倍,以至于在6期时T(4)IRD活性是T(4)ORD活性的14倍;T(3)ORD活性无法检测到;在3 - 7期未测定T(3)IRD活性,但在其他阶段与T(4)IRD活性相关。对于肝脏:仅在2期及变态后动物中测定了脱碘活性;与肠道相反,T(4)ORD活性在2期降至低水平,在变态后也较低;T(4)IRD和T(3)IRD活性非常低且不受发育阶段影响;T(3)ORD活性无法检测到。我们得出结论:(1)脱碘活性通常在肠道中比在肝脏中高得多;(2)肠道ORD和IRD活性呈相反变化,因此ORD在变态早期占主导,但IRD在变态中晚期占主导;(3)肠道脱碘的变化可能导致自发变态期间血浆T(4)和T(3)水平出现特征性下降。《实验动物学杂志》286:305 - 312, 2000年。