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Bioenergetic impact of tissue-specific regulation of iodothyronine deiodinases during nutritional imbalance

机译:营养失衡过程中组织特异性调节碘甲状腺素脱碘酶的生物能影响

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摘要

The regulation of energy homeostasis by thyroid hormones is unquestionable, and iodothyronine deiodinases are enzymes involved in the metabolic activation or inactivation of these hormones at the cellular level. T3 is produced through the outer ring deiodination of the prohormone T4, which is catalyzed by types 1 and 2 iodothyronine deiodinases, D1 and D2. Conversely, type 3 iodothyronine deiodinase (D3) catalyzes the inner ring deiodination, leading to the inactivation of T4 into reverse triiodothyronine (rT3). Leptin acts as an important modulator of central and peripheral iodothyronine deiodinases, thus regulating cellular availability of T3. Decreased serum leptin during negative energy balance is involved in the down regulation of liver and kidney D1 and BAT D2 activities. Moreover, in high fat diet induced obesity, instead of increased serum T_3 and T_4 secondary to higher circulating leptin and thyrotropin levels, elevated serum rT3 is found, a mechanism that might impair the further increase in oxygen consumption.
机译:甲状腺激素对能量稳态的调节是毫无疑问的,碘甲状腺素脱碘酶是在细胞水平上参与这些激素代谢激活或失活的酶。 T3是通过激素原T4的外环去碘化而产生的,该激素由1型和2型碘甲状腺素脱碘酶D1和D2催化。相反,类型3碘甲状腺素去碘酶(D3)催化内环去碘化,导致T4失活为反向三碘甲状腺素(rT3)。瘦素是中枢和外周碘甲状腺素脱碘酶的重要调节剂,从而调节T3的细胞利用率。负能量平衡过程中血清瘦素的降低与肝脏和肾脏D1和BAT D2活性的下调有关。此外,在高脂饮食诱导的肥胖中,发现血清rT3升高,而不是由于循环中的瘦素和促甲状腺素水平升高而导致的血清T_3和T_4升高,这种机制可能会损害氧气消耗的进一步增加。

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