Lim C F, Docter R, Krenning E P, van Toor H, Bernard B, de Jong M, Hennemann G
Department of Internal Medicine III, Erasmus University Medical School, Rotterdam, The Netherlands.
Clin Endocrinol (Oxf). 1994 Jan;40(1):79-85. doi: 10.1111/j.1365-2265.1994.tb02447.x.
Inhibitors of cellular T4 transport leading to diminished plasma T3 production have been identified as 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid (CMPF) and indoxyl sulphate in uraemia and bilirubin and non-esterified fatty acids (NEFA) in critically ill patients with hyperbilirubinaemia. We question whether other factors are responsible for the altered thyroid hormone parameters observed in mild illness and during calorie restriction.
We studied (i) 18 non-uraemic patients with non-thyroidal illness (NTI) (T4 > or = 60, T3 < or = 1.1 and rT3 > or = 0.45 nmol/l) with serum molar ratios of bilirubin:albumin < or = 0.17 and NEFA:albumin < or = 2.6. These molar ratios have been shown to be the minimum ratios which inhibited T4 transport into rat hepatocytes; (ii) four obese euthyroid subjects on 600 kcal/day for 10-14 days. This diet is known to inhibit the unidirectional T4 transport into human liver in vivo.
We measured iodide production from 125I-T4 by incubating rat hepatocytes with 10% human serum. The deiodination of T4 was used as an index of cellular transport of T4 in vivo.
The mean iodide production from 125I-T4 by rat hepatocytes in the presence of 10% serum from NTI patients (98 +/- 17%, mean +/- SD) was not significantly different from the normals (100 +/- 9%). Calorie restriction in euthyroid obese subjects resulted in a small but significant reduction (-12%) of iodide production. Calorie restriction increased the total serum NEFA by 91%.
Our study demonstrates that CMPF, indoxyl sulphate, bilirubin and NEFA are not responsible for the inhibition of T4 tissue uptake in patients with mild illness. In addition, studies with calorie restricted obese subjects indicate that high concentration of NEFA during calorie restriction inhibits T4 tissue uptake. This inhibition may partly explain the lower plasma T3 during calorie restriction.
已确定尿毒症患者体内导致血浆T3生成减少的细胞T4转运抑制剂为3-羧基-4-甲基-5-丙基-2-呋喃丙酸(CMPF)和硫酸吲哚酚,而高胆红素血症危重症患者体内的抑制剂为胆红素和非酯化脂肪酸(NEFA)。我们质疑是否有其他因素导致在轻症疾病和热量限制期间观察到的甲状腺激素参数改变。
我们研究了(i)18例非尿毒症非甲状腺疾病(NTI)患者(T4≥60、T3≤1.1且反T3≥0.45 nmol/l),其血清胆红素与白蛋白的摩尔比≤0.17,NEFA与白蛋白的摩尔比≤2.6。这些摩尔比已被证明是抑制T4转运至大鼠肝细胞的最小比值;(ii)4名肥胖甲状腺功能正常的受试者,每天摄入600千卡热量,持续10 - 14天。已知这种饮食会在体内抑制T4向人肝脏的单向转运。
我们通过将大鼠肝细胞与10%的人血清孵育来测量125I - T4产生的碘化物。T4的脱碘用作体内T4细胞转运的指标。
在存在10% NTI患者血清的情况下,大鼠肝细胞从125I - T4产生的碘化物平均量(98±17%,平均值±标准差)与正常组(100±9%)无显著差异。甲状腺功能正常的肥胖受试者进行热量限制导致碘化物产生量小幅但显著降低(-12%)。热量限制使血清总NEFA增加了91%。
我们的研究表明,CMPF、硫酸吲哚酚、胆红素和NEFA并非导致轻症患者T4组织摄取受抑制的原因。此外,对热量限制的肥胖受试者的研究表明,热量限制期间高浓度的NEFA会抑制T4组织摄取。这种抑制可能部分解释了热量限制期间血浆T3较低的原因。