# Caloric Restriction and Dietary Taurine Regulate Taurine Homeostasis Through Distinct Tissue‐Specific Mechanisms in Mice

**Authors:** András Gregor, Arturo Auñon‐Lopez, Qendrim Zebeli, Marc Pignitter, Kalina Duszka

PMC · DOI: 10.1002/mnfr.70414 · 2026-02-12

## TL;DR

Caloric restriction and dietary taurine affect taurine levels in mice through different mechanisms in the liver and intestine.

## Contribution

The study reveals distinct tissue-specific mechanisms by which caloric restriction and dietary taurine regulate taurine homeostasis.

## Key findings

- Caloric restriction increases intestinal taurine retention and GSH conjugates independently of dietary taurine.
- Dietary taurine primarily influences hepatic taurine levels rather than intestinal pools.
- GST activity correlates with substrate availability, not gene expression, in the intestine.

## Abstract

Caloric restriction (CR) stimulates taurine‐conjugated bile acids (BA) synthesis in the liver. Upon secretion into the intestine, BAs undergo deconjugation, increasing taurine, and taurine conjugate levels, including taurine‐glutathione (GSH). This study aimed to determine whether dietary taurine and CR‐induced taurine changes operate through distinct regulatory mechanisms. Male C57Bl/6 mice were subjected to ad libitum feeding or 20% CR with low‐taurine diet (LTD) or 5% taurine in drinking water. LTD and taurine supplementation minimally affected intestinal taurine concentrations and did not disrupt CR‐induced changes in intestinal taurine levels, GSH conjugates, and GST expression, demonstrating mechanistic independence. Both interventions significantly altered hepatic and plasma taurine levels, indicating tissue‐specific regulation. While CR primarily influenced GSH‐S transferase (GST) mRNA expression in the intestine, GST activity correlated with substrate availability rather than gene expression. CR maintained enhanced intestinal taurine retention during taurine supplementation, evidenced by reduced fecal taurine excretion compared to controls. Dietary and CR‐related taurine are affected by distinct tissue‐specific mechanisms, with CR primarily impacting intestinal taurine while modulation of dietary taurine (restriction or supplementation) predominantly influences hepatic pools. The study reveals independent regulatory mechanisms governing taurine homeostasis and emphasizes differences between dietary factors and physiological responses during CR.

Caloric restriction and dietary taurine each regulate taurine homeostasis independently. The intestinal taurine pool is predominantly affected by synthesis triggered by caloric restriction, whereas hepatic taurine levels vary according to dietary intake.

## Linked entities

- **Proteins:** LOC23687505 (pyrimidodiazepine synthase), SLCO6A1 (solute carrier organic anion transporter family member 6A1)
- **Chemicals:** taurine (PubChem CID 1123)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Chemicals:** BAs (MESH:D001464), taurine-conjugated bile acids (-), GSH (MESH:D005978), BA (MESH:D001647), Taurine (MESH:D013654)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12896083/full.md

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Source: https://tomesphere.com/paper/PMC12896083