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Thyroid Hormone and Vascular Remodeling in Heart

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Thyroid and Heart
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Abstract

Thyroid hormones (TH) play an important role in heart vascular system, and both hyperthyroidism and hypothyroidism are associated with altered cardiovascular system. Moreover, several evidences suggest that heart diseases trigger a reduction in cardiac tissue thyroid hormone levels.

This chapter summarizes the beneficial effects of TH on vascular remodeling of heart, analyzing the most important pillars involved in this process: thyroid receptors (TRα and TRβ), angiogenesis, nitric oxide (NO), reactive oxygen species (ROS), renin angiotensin system (RAS), and hyperlipidemia. TH actions occur largely through binding to TRα and TRβ receptors and particularly TRα-reduced vascular contractility of coronary arteries. Triiodothyronine (T3), the biologically active TH, has been found to induce angiogenesis in heart of hypothyroid mice and in rat aorta after 3 days ischemia reperfusion. TH stimulates angiogenesis through transduction of the extracellular kinase ERK 1/2 and AKT signals and transcription of angiogenic genes. Hypothyroidism shows endothelial dysfunction with a reduction in NO, whereas TH therapy improves it, reducing arterial stiffness. A decrease in ROS and NADPH oxidase activity was observed in ventricles and aortic tissue of myocardial infarcted rats treated with TH. Angiotensin type 1 receptor (AT1R) that is involved in vascular remodeling has been observed downregulated in the aorta in hyperthyroidism. Finally, in hypothyroidism, intima-media thickness (IMT) of the carotid artery was significantly higher than that in control and improved after treatment with levothyroxine. In conclusion, this chapter underlines the role of TH in heart vascular remodeling.

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Balzan, S., Lubrano, V. (2020). Thyroid Hormone and Vascular Remodeling in Heart. In: Iervasi, G., Pingitore, A., Gerdes, A., Razvi, S. (eds) Thyroid and Heart . Springer, Cham. https://doi.org/10.1007/978-3-030-36871-5_10

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