Utiger R D
Horm Metab Res. 1984 Dec;16 Suppl 1:28-31. doi: 10.1055/s-2007-1014892.
Triiodothyronine (T3) production from thyroxine (T4) was studied in isolated rat hepatocytes. With an initial T4 concentration of 0.56 microM, hepatocyte T3 production was 0.029 +/- 0.003 (SEM) pmoles/min/mg protein. T3 production was greater in hepatocytes than in homogenates from the same liver prepared either before or after liver perfusion with collagenase. Most T3 produced remained within the cells under the conditions employed. Hepatocyte T3 production was dependent on cell number, medium bovine serum albumin concentration and temperature. It was stimulated by dithiothreitol, and inhibited by propylthiouracil, 3,3',5'-triiodothyronine and dinitrophenol; glutathione and ouabain had no effect. Alterations in medium glucose concentration and exposure to insulin or glucagon at several glucose concentrations in vitro did not alter T3 production. These results indicate that in hepatic tissue T3 production is enhanced when intact cellular organization is present and that insulin and glucagon do not acutely influence cell production of T3 in vitro.
在分离的大鼠肝细胞中研究了从甲状腺素(T4)生成三碘甲状腺原氨酸(T3)的过程。初始T4浓度为0.56微摩尔时,肝细胞T3生成量为0.029±0.003(标准误)皮摩尔/分钟/毫克蛋白。肝细胞中的T3生成量高于用胶原酶灌注肝脏之前或之后制备的同一肝脏的匀浆中的T3生成量。在所采用的条件下,生成的大部分T3仍保留在细胞内。肝细胞T3生成量取决于细胞数量、培养基中牛血清白蛋白浓度和温度。它受到二硫苏糖醇的刺激,并受到丙硫氧嘧啶、3,3',5'-三碘甲状腺原氨酸和二硝基苯酚的抑制;谷胱甘肽和哇巴因没有影响。培养基葡萄糖浓度的改变以及在体外几种葡萄糖浓度下暴露于胰岛素或胰高血糖素均未改变T3生成量。这些结果表明,在肝组织中,当存在完整的细胞组织结构时T3生成会增强,并且胰岛素和胰高血糖素在体外不会急性影响细胞的T3生成。