» Articles » PMID: 35326451

Bioenergetic Aspects of Mitochondrial Actions of Thyroid Hormones

Overview
Journal Cells
Publisher MDPI
Date 2022 Mar 25
PMID 35326451
Authors
Affiliations
Soon will be listed here.
Abstract

Much is known, but there is also much more to discover, about the actions that thyroid hormones (TH) exert on metabolism. Indeed, despite the fact that thyroid hormones are recognized as one of the most important regulators of metabolic rate, much remains to be clarified on which mechanisms control/regulate these actions. Given their actions on energy metabolism and that mitochondria are the main cellular site where metabolic transformations take place, these organelles have been the subject of extensive investigations. In relatively recent times, new knowledge concerning both thyroid hormones (such as the mechanisms of action, the existence of metabolically active TH derivatives) and the mechanisms of energy transduction such as (among others) dynamics, respiratory chain organization in supercomplexes and cristes organization, have opened new pathways of investigation in the field of the control of energy metabolism and of the mechanisms of action of TH at cellular level. In this review, we highlight the knowledge and approaches about the complex relationship between TH, including some of their derivatives, and the mitochondrial respiratory chain.

Citing Articles

Application of Human Plasma Targeted Lipidomics and Analysis of Toxic Elements to Capture the Metabolic Complexities of Hypothyroidism.

Blazewicz A, Kielbus M, Skorzynska-Dziduszko K, Grabrucker A, Jonklaas J, Sosnowski P Molecules. 2024; 29(21).

PMID: 39519809 PMC: 11547455. DOI: 10.3390/molecules29215169.


Brain Abnormalities in Young Single- and Double-Heterozygote Mice for Both Nkx2-1- and Pax8-Null Mutations.

Giacco A, Iervolino S, Cioffi F, Peluso T, Mercurio G, Roberto L Mol Neurobiol. 2024; 62(4):4023-4041.

PMID: 39375286 PMC: 11880048. DOI: 10.1007/s12035-024-04524-7.


Comparative effects of 3,5-diiodo-L-thyronine and 3,5,3'-triiodo-L-thyronine on mitochondrial damage and cGAS/STING-driven inflammation in liver of hypothyroid rats.

Giacco A, Petito G, Silvestri E, Scopigno N, Vigliotti M, Mercurio G Front Endocrinol (Lausanne). 2024; 15:1432819.

PMID: 39301315 PMC: 11410700. DOI: 10.3389/fendo.2024.1432819.


Mitochondrial function is enhanced by thyroid hormones during zebra finch development.

Oefele M, Hau M, Ruuskanen S, Casagrande S R Soc Open Sci. 2024; 11(7):240417.

PMID: 39086825 PMC: 11288688. DOI: 10.1098/rsos.240417.


Association between physical activity and thyroid function in American adults: a survey from the NHANES database.

Tian L, Lu C, Teng W BMC Public Health. 2024; 24(1):1277.

PMID: 38730302 PMC: 11084014. DOI: 10.1186/s12889-024-18768-4.


References
1.
MOWBRAY J . Evidence for the rapid direct control both in vivo and in vitro of the efficiency of oxidative phosphorylation by 3,5,3'-tri-iodo-L-thyronine in rats. Biochem J. 1979; 184(3):527-38. PMC: 1161834. DOI: 10.1042/bj1840527. View

2.
Kuhlbrandt W . Structure and Mechanisms of F-Type ATP Synthases. Annu Rev Biochem. 2019; 88:515-549. DOI: 10.1146/annurev-biochem-013118-110903. View

3.
Blaza J, Serreli R, Jones A, Mohammed K, Hirst J . Kinetic evidence against partitioning of the ubiquinone pool and the catalytic relevance of respiratory-chain supercomplexes. Proc Natl Acad Sci U S A. 2014; 111(44):15735-40. PMC: 4226120. DOI: 10.1073/pnas.1413855111. View

4.
Frezza C, Cipolat S, Martins de Brito O, Micaroni M, Beznoussenko G, Rudka T . OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion. Cell. 2006; 126(1):177-89. DOI: 10.1016/j.cell.2006.06.025. View

5.
Silvestri E, Lombardi A, Coppola M, Gentile A, Cioffi F, Senese R . Differential Effects of 3,5-Diiodo-L-Thyronine and 3,5,3'-Triiodo-L-Thyronine On Mitochondrial Respiratory Pathways in Liver from Hypothyroid Rats. Cell Physiol Biochem. 2018; 47(6):2471-2483. DOI: 10.1159/000491620. View