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镉给药对大鼠肝脏甲状腺素脱碘作用及巯基的影响。

Changes induced by cadmium administration on thyroxine deiodination and sulfhydryl groups in rat liver.

作者信息

Paier B, Hagmüller K, Noli M I, Gonzalez Pondal M, Stiegler C, Zaninovich A A

机构信息

Department of Zoology, University of Graz, Austria.

出版信息

J Endocrinol. 1993 Aug;138(2):219-24. doi: 10.1677/joe.0.1380219.

Abstract

The effects of cadmium on 5'-deiodination of thyroxine (T4) by rat liver and on the hepatic concentration of non-protein sulfhydryl groups (NPSH) were studied in Wistar rats of 200-250 g body weight. A group of ten rats was injected with cadmium chloride (300 micrograms/100 g body weight i.p.) daily for 4 days. Another group of six rats received, in addition, dithiothreitol (DTT; 1 mg/100 g body weight i.p.) daily for the same period. A group of eight normal untreated rats served as control. T4 deiodination was also determined in aliquots of liver from untreated rats, with cadmium (2 or 5 mmol/l) and with or without DTT (0, 2.5, 5 or 10 mmol/l) plus 1 microCi 125I-labelled T4. Hepatic NPSH were measured by a colorimetric method employing dithioldinitrobenzoic acid. Homogenates were incubated for 90 min at 37 degrees C and chromatographed in a tertiary amyl alcohol:hexane:ammonia (2 mol/l) (10:1:12) system. Cadmium-injected rats showed a significant (P < 0.01) decrease in T4 deiodination and in the generation of 125I (P < 0.01) and tri-iodothyronine (T3) (P < 0.02). NPSH were also decreased (P < 0.02). Administration of DTT restored T4 deiodination and NPSH to normal. In-vitro addition of cadmium or DTT to normal rat liver homogenates induced similar effects on the degradation of T4. Serum concentrations of T4 (P < 0.01) and T3 (P < 0.01) declined significantly in cadmium-injected rats, whereas DTT administration failed to normalize serum hormone levels. The data suggest that cadmium may have decreased 5'-deiodinating activity through binding to sulfhydryl groups of 5'-deiodinase as it does in other enzymes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在体重200 - 250克的Wistar大鼠中,研究了镉对大鼠肝脏甲状腺素(T4)5'-脱碘作用以及肝脏非蛋白巯基(NPSH)浓度的影响。一组十只大鼠每天腹腔注射氯化镉(300微克/100克体重),持续4天。另一组六只大鼠在此期间每天还额外腹腔注射二硫苏糖醇(DTT;1毫克/100克体重)。一组八只未处理的正常大鼠作为对照。还从未处理大鼠的肝脏匀浆中取等分试样,加入镉(2或5毫摩尔/升),并加入或不加入DTT(0、2.5、5或10毫摩尔/升)以及1微居里125I标记的T4,测定T4脱碘情况。采用二硫代二硝基苯甲酸比色法测定肝脏NPSH。匀浆在37℃孵育90分钟,然后在叔戊醇:己烷:氨(2摩尔/升)(10:1:12)体系中进行色谱分析。注射镉的大鼠T4脱碘以及125I生成(P < 0.01)和三碘甲状腺原氨酸(T3)生成(P < 0.02)均显著降低。NPSH也降低(P < 0.02)。给予DTT可使T4脱碘和NPSH恢复正常。在正常大鼠肝脏匀浆中体外添加镉或DTT对T4降解产生类似影响。注射镉的大鼠血清T4(P < 0.01)和T3(P < 0.01)浓度显著下降,而给予DTT未能使血清激素水平恢复正常。数据表明,镉可能通过与5'-脱碘酶的巯基结合降低了5'-脱碘活性,就像它对其他酶的作用一样。(摘要截短于250字)

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