Duntas Leonidas H
Endocrine Unit, Evgenidion Hospital, University of Athens, Medical School, Athens, Greece.
Thyroid. 2006 May;16(5):455-60. doi: 10.1089/thy.2006.16.455.
The essential micronutrient selenium (Se) occurs in the form of the amino acid selenocysteine in selenoproteins which exert various effects, while maintaining the cell reduction-oxidation balance. The discovery that all three deiodinases that convert thyroxine (T4) into triiodothyronine (T3) contain selenocysteine illustrates how the production of the active thyroid hormone is dependent on Se status. The selenoenzyme families of glutathione peroxidases (GPx) and thioredoxin reductases (TRx) possess powerful antioxidant properties and form a complex defense system that protects thyrocytes from oxidative damage. Se supplementation in patients with autoimmune thyroiditis seems to modify the immune response, probably by enhancing plasma GPx activity and decreasing excess levels of hydrogen peroxide. However, the enhancement of immunocompetence may also be the result of the synergistic action of various selenoproteins and not exclusively of GPx. There is evidence supporting considerable oxidative stress in Graves' disease where Se supplementation, because of its free radical scavenging properties, may increase the enzymatic antioxidant activity. TRx has been found significantly elevated in GD revealing its involvement in the pathogenesis of this condition and representing a potential future target for therapeutical intervention. Low Se serum levels have also been associated with increased risk of thyroid cancer and may play a role in carcinogenesis. It is noteworthy, that the Food and Drug Administration has recently determined that there is sufficient evidence to warrant a qualified health claim for Se and cancer. Furthermore, the recent discovery that defects in the SECIS-binding protein 2 (SBP2), which is an indispensable protein for the incorporation of Se into the selenoproteins, result in thyroid dysfunction, together with the recognition of the many roles of selenoprotein P in Se distribution and storage in the human body, reveal not only the indispensability of Se and the selenoproteins as essential factors in thyroid metabolism and pathogenesis, but open up new prospects for enhanced treatment.
必需微量营养素硒(Se)以硒代半胱氨酸的形式存在于硒蛋白中,这些硒蛋白发挥着各种作用,同时维持细胞的氧化还原平衡。将甲状腺素(T4)转化为三碘甲状腺原氨酸(T3)的所有三种脱碘酶都含有硒代半胱氨酸,这一发现表明活性甲状腺激素的产生如何依赖于硒的状态。谷胱甘肽过氧化物酶(GPx)和硫氧还蛋白还原酶(TRx)的硒酶家族具有强大的抗氧化特性,并形成一个复杂的防御系统,保护甲状腺细胞免受氧化损伤。自身免疫性甲状腺炎患者补充硒似乎会改变免疫反应,可能是通过提高血浆GPx活性和降低过氧化氢的过量水平。然而,免疫能力的增强也可能是各种硒蛋白协同作用的结果,而不仅仅是GPx的作用。有证据支持格雷夫斯病中存在相当大的氧化应激,由于其自由基清除特性,补充硒可能会增加酶促抗氧化活性。已发现TRx在格雷夫斯病中显著升高,表明其参与了这种疾病的发病机制,并代表了未来治疗干预的潜在靶点。血清硒水平低也与甲状腺癌风险增加有关,可能在致癌过程中起作用。值得注意的是,美国食品药品监督管理局最近确定,有足够的证据支持对硒与癌症提出有条件的健康声明。此外,最近发现硒代半胱氨酸插入序列结合蛋白2(SBP2)存在缺陷,而SBP2是将硒纳入硒蛋白所必需的蛋白质,这会导致甲状腺功能障碍,同时认识到硒蛋白P在人体硒分布和储存中的多种作用,这不仅揭示了硒和硒蛋白作为甲状腺代谢和发病机制中必需因素的不可或缺性,还为强化治疗开辟了新的前景。