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Updated: May 12, 2026

Isolation and Physiological Analysis of Mouse Cardiomyocytes
Published on: September 7, 2014
New insights into mechanisms of cardioprotection mediated by thyroid hormones
G Nicolini1, L Pitto, C Kusmic
1Institute of Clinical Physiology, CNR, 56100 Pisa, Italy ; CNR, Tuscany Region G. Monasterio Foundation, Pisa, Italy.
Insights
Thyroid hormone plays a key role in cardiovascular health. Understanding its protective effects on cardiac remodeling, particularly in heart failure, is crucial for developing new treatments.
Area of Science:
- Cardiology
- Endocrinology
- Molecular Biology
Background:
- Heart failure, a major outcome of cardiovascular diseases, has high morbidity and mortality despite advances.
- Cardiac remodeling is a key process in heart failure, necessitating early intervention for better patient prognosis.
- Thyroid hormone signaling is vital for cardiovascular homeostasis, and "low triiodothyronine" syndrome predicts mortality in heart disease.
Purpose of the Study:
- To explore the cardioprotective role of thyroid hormone in reversing adverse cardiac remodeling.
- To discuss recent findings on thyroid hormone's impact on cardiac mitochondria, interstitium, and vasculature.
- To highlight the role of specific microRNAs (miRNAs) in thyroid hormone regulation within the heart.
Main Methods:
- Review of experimental models of cardiac hypertrophy and myocardial infarction.
- Analysis of thyroid hormone signaling pathways in cardiovascular tissues.
- Investigation of miRNA involvement in thyroid hormone-mediated cardiac regulation.
Main Results:
- Alterations in thyroid hormone signaling are linked to cardiac dysfunction in experimental heart disease models.
- Thyroid hormone influences cardiac mitochondria, interstitium, and vasculature, impacting remodeling processes.
- Specific miRNAs are implicated in mediating thyroid hormone effects at mitochondrial and interstitial levels.
Conclusions:
- Thyroid hormone demonstrates cardioprotective effects by reverting regulatory networks involved in adverse cardiac remodeling.
- Further understanding of thyroid hormone and miRNA interactions is essential for novel therapeutic strategies against heart failure.
- Targeting thyroid hormone pathways offers a promising avenue for ameliorating heart failure prognosis.
Abstract:
Heart failure represents the final common outcome in cardiovascular diseases. Despite significant therapeutic advances, morbidity and mortality of heart failure remain unacceptably high. Heart failure is preceded and sustained by a process of structural remodeling of the entire cardiac tissue architecture. Prevention or limitation of cardiac remodeling in the early stages of the process is a crucial step in order to ameliorate patient prognosis. Acquisition of novel pathophysiological mechanisms of cardiac remodeling is therefore required to develop more efficacious therapeutic strategies. Among all neuroendocrine systems, thyroid hormone seems to play a major homeostatic role in cardiovascular system. In these years, accumulating evidence shows that the "low triiodothyronine" syndrome is a strong prognostic, independent predictor of death in patients affected by both acute and chronic heart disease. In experimental models of cardiac hypertrophy or myocardial infarction, alterations in the thyroid hormone signaling, concerning cardiac mitochondrion, cardiac interstitium, and vasculature, have been suggested to be related to heart dysfunction. The aim of this brief paper is to highlight new developments in understanding the cardioprotective role of thyroid hormone in reverting regulatory networks involved in adverse cardiac remodeling. Furthermore, new recent advances on the role of specific miRNAs in thyroid hormone regulation at mitochondrion and interstitial level are also discussed.
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