Overnutrition in mice impairs thyroid hormone biosynthesis and utilization, causing hypothyroidism, despite remarkable thyroidal adaptations

Thyroid hormones (THs [T3 and T4] ) are key regulators of metabolic rate and nutrient metabolism. They are controlled centrally and peripherally in a coordinated manner to elegantly match T3-mediated energy expenditure (EE) with energy availability. Hypothyroidism reduces EE and has long been blamed for obesity; however, emerging evidence suggests that, instead, obesity may drive thyroid dysfunction. Thus, we used a mouse model of diet-induced obesity to determine its direct effects on thyroid histopathology and function, deiodinase activity, and T3 action. Strikingly, overnutrition induced hypothyroidism within 3 weeks. Levels of thyroidal THs and their precursor protein thyroglobulin decreased, and ER stress was induced, indicating that thyroid function was directly impaired. We also observed pronounced histological and vascular expansion in the thyroid. Overnutrition additionally suppressed T4 activation, rendering the mice resistant to T4 and reducing EE. Our findings collectively show that overnutrition deals a double strike to TH biosynthesis and action, despite large efforts to adapt - but, fortunately, thyroid dysfunction in mice can be reversed by weight loss. In humans, BMI correlated with thyroidal vascularization, importantly demonstrating preliminary translatability. These studies lay the groundwork for obesity therapies that tackle hypothyroidism, which are much needed, as no current obesity treatment works for everyone.

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Publication Details

Journal
Journal of Clinical Investigation
Published
2026-04-14
DOI
https://doi.org/10.1172/jci194207
Citations
1
Primary Topic
Thyroid Disorders and Treatments
Type
article
Field-Weighted Citation Impact
19.16

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article

Overnutrition in mice impairs thyroid hormone biosynthesis and utilization, causing hypothyroidism, despite remarkable thyroidal adaptations

Federico Salas-Lucia, Alejandra Paola Torres-Manzo, H Wang, Nancy Carrasco et al.
1 citations
Journal of Clinical Investigation
Thyroid Disorders and Treatments
19.16
article

Overnutrition in mice impairs thyroid hormone biosynthesis and utilization, causing hypothyroidism, despite remarkable thyroidal adaptations

Federico Salas-Lucia, Alejandra Paola Torres-Manzo, H Wang, Nancy Carrasco, Jessica Rampy, Kendra Hoffsmith, Quanhu Sheng, Rafael [UNIFESP] Arrojo e Drigo, Vivian L. Weiss, Matthew A. Loberg, Antonio C. Bianco
article en
1 citations

Abstract

Thyroid hormones (THs [T3 and T4] ) are key regulators of metabolic rate and nutrient metabolism. They are controlled centrally and peripherally in a coordinated manner to elegantly match T3-mediated energy expenditure (EE) with energy availability. Hypothyroidism reduces EE and has long been blamed for obesity; however, emerging evidence suggests that, instead, obesity may drive thyroid dysfunction. Thus, we used a mouse model of diet-induced obesity to determine its direct effects on thyroid histopathology and function, deiodinase activity, and T3 action. Strikingly, overnutrition induced hypothyroidism within 3 weeks. Levels of thyroidal THs and their precursor protein thyroglobulin decreased, and ER stress was induced, indicating that thyroid function was directly impaired. We also observed pronounced histological and vascular expansion in the thyroid. Overnutrition additionally suppressed T4 activation, rendering the mice resistant to T4 and reducing EE. Our findings collectively show that overnutrition deals a double strike to TH biosynthesis and action, despite large efforts to adapt - but, fortunately, thyroid dysfunction in mice can be reversed by weight loss. In humans, BMI correlated with thyroidal vascularization, importantly demonstrating preliminary translatability. These studies lay the groundwork for obesity therapies that tackle hypothyroidism, which are much needed, as no current obesity treatment works for everyone.

Journal of Clinical InvestigationVol. 136(8)
Vanderbilt University (US), Yale University (US), University of Chicago (US), Czech Academy of Sciences, Institute of Microbiology (CZ), Bipar (FR), Vanderbilt University Medical Center (US)
American Cancer Society, American Thyroid Association, Vanderbilt Institute for Clinical and Translational Research, National Institutes of Health, Vanderbilt Diabetes Research and Training Center, Vanderbilt University Medical Center
Zero hunger
Openalex Percentile: Top 1%
Thyroid Disorders and Treatments
19.16
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