T3 and cardiac myocyte cell: a theoretical model.

Tsatsaris Athanasios, Baldoukas Antonios, Loumousiotis Antonios, Koukounaris Eustathios, Giota Maria, Perrea Despina
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Abstract

In the last decades, the outstanding role of Thyroid gland in regulating both physiological and pathological operation of cardiovascular system has been acknowledged worldwide. Three main domains of Thyroid function, that is to say, euthyroidism -hyperthyroidism-hypothyroidism, have a direct impact on cardiac response through a variety of mechanisms. Cellular pathways mediate in cardiac contractility, cardiac output, cardiac rhythm, arterial blood pressure and peripheral vessel resistance. Particular biochemical algorithms exist not only between Thyroid hormones' serum concentration and thyroid gland but also between the hormones' serum level and heart muscle genes. These biochemical pathways primarily regulate the appropriate secretion of levothyroxine (T4) and triiodothyronine(T3) via Thyroid- Stimulating-Hormone(TSH) pituitary system, and secondly adjust the cardiac function. In this study, a mathematic model has been developed describing significant aspects of positive or negative feedback mechanisms of THYRO-CARDIAC (THY-CAR) system along with potential applications of novel up-to-date patents in this area of research.

T3与心肌细胞:一个理论模型。
近几十年来,甲状腺在调节心血管系统的生理和病理功能方面的突出作用已为世界所公认。甲状腺功能的三个主要领域,即甲状腺功能亢进-甲亢-甲减,通过多种机制直接影响心脏反应。细胞通路介导心脏收缩力、心输出量、心律、动脉血压和外周血管阻力。不仅甲状腺激素的血清浓度与甲状腺之间存在特定的生化规律,而且甲状腺激素的血清水平与心肌基因之间也存在特定的生化规律。这些生化途径首先通过垂体促甲状腺激素(TSH)调节左甲状腺素(T4)和三碘甲状腺原氨酸(T3)的适当分泌,其次调节心功能。在本研究中,建立了一个数学模型,描述了甲状腺-心脏(THY-CAR)系统的正反馈或负反馈机制的重要方面,以及该研究领域最新专利的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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