Kaiser C A, Goumaz M O, Burger A G
Endocrinology. 1986 Aug;119(2):762-70. doi: 10.1210/endo-119-2-762.
To study the effect of rT3 on the 5'-deiodinase type II (5'D-II) of rat brain cortex and anterior pituitary, daily infusions of rT3 at rates of 0.5, 1.5, 4.5, and 13.5 nmol/day X 100 g body weight were given to a total of 87 hypothyroid rats. rT3 inhibited the 5'D-II activity in the total homogenate and in the microsomal fraction in the brain cortex, inhibition becoming significant (28-33%) with the infusion of 4.5 nmol/day X 100 g body weight, at serum levels of 2.4 pmol rT3/ml. Infusion of 13.5 nmol/day X 100 g body weight produced 71-73% inhibition. In homogenates of the anterior pituitary, inhibition was significant with infusions of 13.5 nmol/day X 100 g body weight (30%). To examine how rT3 might inhibit 5'D-II activity, labeled rT3 (137 muCi/day) was infused into 4 hypothyroid rats, and the rT3 content in the homogenate and in the cell subfractions was measured by HPLC. No rT3 was detectable in the nuclei, and less than 1% was found in the microsomal fraction. The infused rT3 was thus no longer present in the microsome preparations and homogenates. The inhibitory effect of rT3 was also compared with that of T4. Serum T4 levels of 45 pmol/ml were required in order to inhibit 5'D-II to the same extent as with 7 pmol rT3/ml. The requirement of this high serum level of T4 excludes the potential role of T4 impurities in the infused rT3 preparation. We therefore conclude that rT3 inhibits 5'D-II in brain cortex per se independently of T4.
为研究反式三碘甲状腺原氨酸(rT3)对大鼠脑皮质和垂体前叶Ⅱ型5'-脱碘酶(5'D-II)的影响,对总共87只甲状腺功能减退大鼠,以0.5、1.5、4.5和13.5 nmol/天×100 g体重的速率每日输注rT3。rT3抑制脑皮质总匀浆和微粒体部分的5'D-II活性,当以4.5 nmol/天×100 g体重输注时,在血清rT3水平为2.4 pmol/ml时,抑制作用变得显著(28 - 33%)。以13.5 nmol/天×100 g体重输注产生71 - 73%的抑制作用。在垂体前叶匀浆中,以13.5 nmol/天×100 g体重输注时抑制作用显著(30%)。为研究rT3如何抑制5'D-II活性,将标记的rT3(137 μCi/天)输注到4只甲状腺功能减退大鼠体内,并通过高效液相色谱法测量匀浆和细胞亚组分中的rT3含量。在细胞核中未检测到rT3,在微粒体部分中发现的rT3不到1%。因此,输注的rT3不再存在于微粒体制剂和匀浆中。还将rT3的抑制作用与T4的抑制作用进行了比较。为了将5'D-II抑制到与7 pmol rT3/ml相同的程度,需要血清T4水平达到45 pmol/ml。这种高血清T4水平的需求排除了输注的rT3制剂中T4杂质的潜在作用。因此我们得出结论,rT3本身独立于T4抑制脑皮质中的5'D-II。