Jennings A S, Crutchfield F L, Dratman M B
Endocrinology. 1984 Mar;114(3):992-7. doi: 10.1210/endo-114-3-992.
This study was undertaken to evaluate the effect of altered thyroid states on hepatic T3 production in a functioning intact organ system, the isolated perfused liver. Thyroidectomized rats were treated for 3-4 weeks with vehicle, T4, 1.5 micrograms/100 g-1 day-1, or T4, 20 micrograms/100 g-1 day-1, to produce hypothyroidism, euthyroidism, or hyperthyroidism. Livers were perfused for 1 h with medium containing T4, 10 micrograms/dl, and T3 production was estimated by RIA. T3 production in the hypothyroid, euthyroid, and hyperthyroid groups, respectively, was 1.61 +/- (SE) 0.50, 5.18 +/- 0.55, and 15.62 +/- 1.61 ng/g-1 liver h-1. These differences in T3 production resulted entirely from changes in percent conversion of T4 to T3 which were 0.87 +/- 0.25%, 3.21 +/- 0.38%, and 12.02 +/- 1.82% in the hypothyroid, euthyroid, and hyperthyroid groups, respectively. The measured hepatic uptake of T4 decreased slightly with T4 administration from 188 +/- 13 to 162 +/- 7 and 144 +/- 10 ng/g liver in these same groups. The changes in T3 production were not accounted for by differences in biliary excretion or deiodination of T3. These studies demonstrate a stimulatory effect of T4 on the conversion of T4 to T3 which is important to altering net hepatic T3 production.
本研究旨在评估甲状腺状态改变对一个功能完整的器官系统——离体灌注肝脏中肝脏T3生成的影响。对甲状腺切除的大鼠用赋形剂、1.5微克/100克体重·天的T4或20微克/100克体重·天的T4治疗3 - 4周,以产生甲状腺功能减退、甲状腺功能正常或甲状腺功能亢进状态。肝脏用含10微克/分升T4的培养基灌注1小时,并用放射免疫分析法估计T3生成量。甲状腺功能减退、甲状腺功能正常和甲状腺功能亢进组的T3生成量分别为1.61±(标准误)0.50、5.18±0.55和15.62±1.61纳克/克肝脏·小时。T3生成量的这些差异完全是由T4向T3的转化率变化引起的,甲状腺功能减退、甲状腺功能正常和甲状腺功能亢进组的转化率分别为0.87±0.25%、3.21±0.38%和12.02±1.82%。在这些相同的组中,随着T4给药,测量到的肝脏对T4的摄取量略有下降,从188±13降至162±7和144±10纳克/克肝脏。T3生成量的变化不能用T3的胆汁排泄或脱碘差异来解释。这些研究证明了T4对T4向T3转化的刺激作用,这对改变肝脏T3的净生成量很重要。