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新型甲状腺激素。

Novel thyroid hormones.

机构信息

Department of Pathology, Laboratory of Biochemistry, University of Pisa, Via Roma 55, Pisa, 56126, Italy.

Scuola Superiore Sant'Anna, Pisa, Italy.

出版信息

Endocrine. 2019 Oct;66(1):95-104. doi: 10.1007/s12020-019-02018-4. Epub 2019 Jul 20.

Abstract

The field of thyroid hormone signaling has grown more complex in recent years. In particular, it has been suggested that some thyroid hormone derivatives, tentatively named "novel thyroid hormones" or "active thyroid hormone metabolites", may act as independent chemical messengers. They include 3,5-diiodothyronine (T2), 3-iodothyronamine (T1AM), and several iodothyroacetic acids, i.e., 3,5,3',5'-thyroacetic acid (TA4), 3,5,3'-thyroacetic acid (TA3), and 3-thyroacetic acid (TA1). We summarize the present knowledge on these compounds, namely their biosynthetic pathways, endogenous levels, molecular targets, and the functional effects elicited in experimental preparations or intact animals after exogenous administration. Their physiological and pathophysiological role is discussed, and potential therapeutic applications are outlined. The requirements needed to qualify these substances as chemical messengers must still be validated, although promising evidence has been collected. At present, the best candidate to the role of independent chemical messenger appears to be T1AM, and its most interesting effects concern metabolism and brain function. The responses elicited in experimental animals have suggested potential therapeutic applications. TA3 has an established role in thyroid hormone resistance syndromes, and is under investigation in Allen-Herndon-Dudley syndrome. Other potential targets are represented by obesity and dyslipidemia (for T2 and T1AM); dementia and degenerative brain disease (for T1AM and TA1); cancer (for T1AM and TA4). Another intriguing and unexplored question is the potential relevance of these metabolites in the clinical picture of hypothyroidism and in the response to replacement therapy.

摘要

近年来,甲状腺激素信号领域变得更加复杂。特别是,有人提出,一些甲状腺激素衍生物,暂名为“新型甲状腺激素”或“活性甲状腺激素代谢物”,可能作为独立的化学信使发挥作用。它们包括 3,5-二碘甲状腺原氨酸(T2)、3-碘甲状腺原氨酸胺(T1AM)和几种碘代乙酸,即 3,5,3',5'-四碘乙酸(TA4)、3,5,3'-四碘乙酸(TA3)和 3-碘代乙酸(TA1)。我们总结了这些化合物的现有知识,即它们的生物合成途径、内源性水平、分子靶标以及外源性给药后在实验制剂或完整动物中引起的功能效应。讨论了它们的生理和病理生理作用,并概述了潜在的治疗应用。虽然已经收集了有希望的证据,但这些物质作为化学信使的资格所需的要求仍需验证。目前,T1AM 似乎是独立化学信使的最佳候选者,其最有趣的作用涉及代谢和大脑功能。在实验动物中引起的反应表明了潜在的治疗应用。TA3 在甲状腺激素抵抗综合征中具有既定作用,并且正在 Allen-Herndon-Dudley 综合征中进行研究。其他潜在的靶点是肥胖和血脂异常(T2 和 T1AM);痴呆和退行性脑疾病(T1AM 和 TA1);癌症(T1AM 和 TA4)。另一个有趣且尚未探索的问题是这些代谢物在甲状腺功能减退症的临床表现和替代治疗反应中的潜在相关性。

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