Department of Surgical, Medical and Molecular Pathology and Critical Area, University of Pisa, Pisa, Italy.
Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Front Endocrinol (Lausanne). 2022 Jun 28;13:930756. doi: 10.3389/fendo.2022.930756. eCollection 2022.
Myoinositol (Myo) is an isoform of inositol, a cyclic polyol with 6 hydroxyl groups. Myo is mainly derived from dietary intake while its endogenous production is generated from glucose by enzymatic reactions. Moreover, Myo is also synthesized by catabolism of phosphatidylinositol (PI), phosphoinositides (PIP), and inositol phosphates (IP). Myo has a determinant role in thyroid function and autoimmune diseases as it regulates iodine organification and thyroid hormone biosynthesis by the formation of hydrogen peroxide (HO) in thyrocytes. Depletion of Myo that is involved in the thyroid stimulating hormone (TSH) signaling pathway, may cause the development of thyroid diseases such as hypothyroidism. TSH levels significantly decreased in patients with subclinical hypothyroidism, with or without autoimmune thyroiditis, after treatment with Myo plus Selenium (Myo+Se). In addition to TSH, antithyroid autoantibodies are reduced. This review summarizes the role of Myo in the thyroidal physiology and its role in the management of some thyroid diseases.
肌醇(Myo)是肌醇的一种异构体,肌醇是一种具有 6 个羟基的环状多元醇。Myo 主要来源于饮食摄入,而其内源性产生则是由葡萄糖通过酶促反应生成的。此外,Myo 还可以通过磷脂酰肌醇(PI)、磷酸肌醇(PIP)和肌醇磷酸(IP)的分解代谢合成。Myo 在甲状腺功能和自身免疫性疾病中具有决定性作用,因为它通过形成甲状腺细胞中的过氧化氢(HO)来调节碘的有机化和甲状腺激素的生物合成。参与促甲状腺激素(TSH)信号通路的 Myo 耗竭可能导致甲状腺疾病的发展,如甲状腺功能减退症。在亚临床甲状腺功能减退症患者中,无论是否存在自身免疫性甲状腺炎,在用 Myo 和硒(Myo+Se)治疗后,TSH 水平显著降低。除了 TSH 之外,抗甲状腺自身抗体也减少了。这篇综述总结了 Myo 在甲状腺生理学中的作用及其在一些甲状腺疾病管理中的作用。