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碘甲状腺原氨酸对能量代谢的调控

Control of energy metabolism by iodothyronines.

作者信息

Lanni A, Moreno M, Lombardi A, de Lange P, Goglia F

机构信息

Department of Life Sciences, Second University of Naples, Caserta, Italy.

出版信息

J Endocrinol Invest. 2001 Dec;24(11):897-913. doi: 10.1007/BF03343949.

Abstract

One of the most widely recognized effects of thyroid hormones (TH) in adult mammals is their influence over energy metabolism. In the past, this has received much attention but, possibly because of the complex mode of action of thyroid hormones, no universally accepted mechanism to explain this effect has been put forward so far. Significant advances in our understanding of the biochemical processes involved in the actions of TH have been made in the last three decades and now it seems clear that TH can act through both nuclear-mediated and extranuclear-mediated pathways. TH increase energy expenditure, partly by reducing metabolic efficiency, with control of specific genes at the transcriptional level, being is thought to be the major molecular mechanism. However, both the number and the identity of the thyroid-hormone-controlled genes remain unknown, as do their relative contributions. The recent discovery of uncoupling proteins (UCPs) (in addition to UCP1 in brown adipose tissue) in almost all tissues in animals, including humans, has opened new perspectives on the understanding of the mechanisms involved in the regulation of energy metabolism by thyroid hormones. Other approaches have included the various attempts made to attribute changes in respiratory activity to a direct influence of thyroid hormones over the mitochondrial energy-transduction apparatus. In addition, an increasing number of studies has revealed that TH active in the regulation of energy metabolism include not only T3, but also other iodothyronines present in the biological fluids, such as 3,5-diiodothyronine (3,5-T2). This, in turn, may make it possible to explain some of the effects exerted by TH on energy metabolism that cannot easily be attributed to T3.

摘要

甲状腺激素(TH)对成年哺乳动物最广为人知的作用之一是其对能量代谢的影响。过去,这一点备受关注,但可能由于甲状腺激素作用方式复杂,迄今为止尚未提出一个被普遍接受的机制来解释这种效应。在过去三十年里,我们对TH作用所涉及的生化过程的理解有了重大进展,现在似乎很清楚TH可以通过核介导和核外介导途径发挥作用。TH增加能量消耗,部分是通过降低代谢效率,在转录水平控制特定基因被认为是主要分子机制。然而,甲状腺激素控制的基因数量和身份仍然未知,它们的相对贡献也不清楚。最近在包括人类在内的动物几乎所有组织中发现了解偶联蛋白(UCPs)(除了棕色脂肪组织中的UCP1),为理解甲状腺激素调节能量代谢的机制开辟了新视角。其他方法包括各种试图将呼吸活动的变化归因于甲状腺激素对线粒体能量转导装置的直接影响。此外,越来越多的研究表明,参与能量代谢调节的TH不仅包括T3,还包括生物体液中存在的其他碘甲状腺原氨酸,如3,5 - 二碘甲状腺原氨酸(3,5 - T2)。这反过来可能有助于解释TH对能量代谢产生的一些难以轻易归因于T3的效应。

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