# The gut-thyroid axis: physiological regulation of barrier function, microbiota, endocrine signaling and the consequences on energy metabolism

**Authors:** Lucia Acampora, Federica Restolfer, Pierluigi De Pierro, Maria Masulli, Monica Dentice, Giovanni Sarnelli, Annunziata Gaetana Cicatiello

PMC · DOI: 10.3389/fphys.2026.1753136 · Frontiers in Physiology · 2026-03-11

## TL;DR

This review explores how the gut and thyroid interact to regulate digestion, hormone balance, and energy use, highlighting their mutual influence on health.

## Contribution

The paper provides a comprehensive overview of the physiological mechanisms of the gut–thyroid axis and its implications for metabolic health.

## Key findings

- THs regulate intestinal barrier function and immune defenses via TRα1 signaling.
- The gut modulates TH homeostasis through absorption, microbial activity, and enterohepatic recycling.
- Gut–thyroid interactions influence energy metabolism and inflammatory status.

## Abstract

The gut-thyroid axis is a bidirectional physiological network in which intestinal barrier function, microbiota composition, micronutrient absorption, and Thyroid Hormone (TH) homeostasis are closely interconnected. Growing evidence indicates that alterations in intestinal integrity and microbial metabolism can significantly influence TH bioavailability and systemic endocrine regulation, while THs themselves actively shape intestinal structure and function. In this review, we summarize current knowledge on the physiological mechanisms underlying the gut–thyroid crosstalk. We first describe the organization of the intestinal barrier, focusing on epithelial transporters, tight junction dynamics, immune–epithelial interactions, and their role in controlling permeability and nutrient absorption. We then discuss how THs, via TRα1 signaling, regulate intestinal epithelial differentiation, stem-cell activity, barrier maintenance, and innate immune defenses, including the induction of intestinal alkaline phosphatase. Conversely, we examine how the intestine contributes to TH homeostasis by modulating hormone absorption, transporter-mediated uptake, deiodinase-dependent activation and inactivation, microbial deconjugation, and enterohepatic recycling. We also review the intestinal handling of iodine and selenium, emphasizing how epithelial and microbial mechanisms influence TH synthesis and peripheral metabolism. Finally, we integrate these processes into a systemic framework linking gut–thyroid interactions to energy metabolism, inflammatory status, and metabolic flexibility. Overall, this review delineates the gut–thyroid axis as a key physiological interface coordinating endocrine and gastrointestinal function and discusses emerging perspectives for therapeutic strategies targeting intestinal health to optimize TH action.

## Linked entities

- **Proteins:** HSP90B1 (heat shock protein 90 beta family member 1)
- **Chemicals:** iodine (PubChem CID 807), selenium (PubChem CID 6326970)

## Full-text entities

- **Genes:** PLSCR4 (phospholipid scramblase 4) [NCBI Gene 57088] {aka TRA1}
- **Diseases:** inflammatory (MESH:D007249)
- **Chemicals:** iodine (MESH:D007455), selenium (MESH:D012643)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13012955/full.md

## References

89 references — full list in the complete paper: https://tomesphere.com/paper/PMC13012955/full.md

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Source: https://tomesphere.com/paper/PMC13012955