Lanni A, Moreno M, Cioffi M, Goglia F
Department of General and Environmental Physiology, University of Naples, Italy.
Mol Cell Endocrinol. 1992 Aug;86(3):143-8. doi: 10.1016/0303-7207(92)90138-v.
We report that 3,5,3'-triiodothyronine (T3) as well as two other iodothyronines (3,3'-diiodothyronine and 3,5-diiodothyronine (T2s)) stimulate rat liver oxidative capacity (measured as cytochrome oxidase activity (COX)). In hypothyroid rats COX activity and mitochondrial protein content are significantly lower than in normal control animals. The administration of both T3 and T2s to hypothyroid rats significantly enhances hepatic COX activity with T3 having the greatest effect (+60%); moreover, T3 restores the mitochondrial protein content whereas the T2s are ineffective. Administration of T2s results in a faster stimulation (already significant 1 h after the injection) of hepatic COX activity than T3 injection. Our results suggest that T3 acts on the protein synthesis mechanism involved in the regulation of the mitochondrial mass while T2s would act directly at the mitochondrial level.
我们报告称,3,5,3'-三碘甲状腺原氨酸(T3)以及其他两种碘甲状腺原氨酸(3,3'-二碘甲状腺原氨酸和3,5-二碘甲状腺原氨酸(T2s))可刺激大鼠肝脏的氧化能力(以细胞色素氧化酶活性(COX)衡量)。在甲状腺功能减退的大鼠中,COX活性和线粒体蛋白含量显著低于正常对照动物。给甲状腺功能减退的大鼠同时给予T3和T2s可显著提高肝脏COX活性,其中T3的作用最为显著(提高60%);此外,T3可恢复线粒体蛋白含量,而T2s则无效。与注射T3相比,注射T2s能更快地刺激肝脏COX活性(注射后1小时就已显著)。我们的结果表明,T3作用于参与线粒体质量调节的蛋白质合成机制,而T2s则直接作用于线粒体水平。