# Effects of 17,18-Epoxyeicosatetraenoic Acid and 19,20-Epoxydocosapentaenoic Acid Combined with Soluble Epoxide Hydrolase Inhibitor t-TUCB on Brown Adipogenesis and Mitochondrial Respiration

**Authors:** Yang Yang, Haoying Wu, Xinyun Xu, Christophe Morisseau, Kin Sing Stephen Lee, Bruce D. Hammock, Jiangang Chen, Ling Zhao

PMC · DOI: 10.3390/nu17060936 · Nutrients · 2025-03-07

## TL;DR

This study shows that combining specific fatty acid metabolites with an inhibitor enhances brown fat development and energy-burning activity in mice.

## Contribution

The study reveals that 17,18-EEQ and 19,20-EDP with t-TUCB promote brown adipogenesis and thermogenesis in murine cells.

## Key findings

- 17,18-EEQ and 19,20-EDP with t-TUCB increased brown adipocyte differentiation and mitochondrial respiration.
- Only 17,18-EEQ with t-TUCB significantly boosted mitochondrial uncoupling and heat production.
- PPARγ is involved in differentiation but not in thermogenic function post-differentiation.

## Abstract

Background/Objectives: 17,18-epoxyeicosatetraenoic acid (17,18-EEQ) and 19,20-epoxydocosapentaenoic acid (19,20-EDP) are bioactive metabolites produced from eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), respectively, by CYP450s. These metabolites are unstable and quickly metabolized by auto-oxidation, esterification, β-oxidation, or hydrolysis by soluble epoxide hydrolase (sEH). 17,18-EEQ or 19,20-EDP combined with a potent sEH inhibitor t-TUCB differentially activated brown adipose tissue in diet-induced obesity. In the current study, we investigated whether these n-3 epoxy fatty acids with t-TUCB directly promote brown adipocyte differentiation and their thermogenic capacities. Methods: Murine brown preadipocytes were treated with 17,18-EEQ or 19,20-EDP with t-TUCB during and post differentiation. Brown marker protein expression and mitochondrial respiration were measured. In addition, the activation of PPARγ and suppression of NFκB reporter by 17,18-EEQ or 19,20-EDP alone or with t-TUCB were assessed, and the roles of PPARγ were evaluated with PPARγ knockdown and GW9662. Results: 17,18-EEQ or 19,20-EDP with t-TUCB promoted brown adipogenesis and mitochondrial respiration and uncoupling. Moreover, with t-TUCB, both epoxides improved mitochondrial respiration, but only 17,18-EEQ with t-TUCB significantly increased mitochondrial uncoupling (and heat production) in the differentiated adipocytes. PPARγ may be required for the effects of epoxides on differentiation but not on the thermogenic function post differentiation. Conclusions: The results demonstrate that, with t-TUCB, 17,18-EEQ and 19,20-EDP promote brown adipogenesis and mitochondrial respiration and uncoupling. 17,18-EEQ also promotes thermogenesis in differentiated brown adipocytes. Together, the results suggest thermogenic potentials of tested n-3 epoxides, especially 17,18-EEQ with t-TUCB. Translational studies of these n-3 epoxides on human brown adipocyte differentiation and functions are warranted.

## Linked entities

- **Proteins:** PPARG (peroxisome proliferator activated receptor gamma), NFKB1 (nuclear factor kappa B subunit 1)
- **Chemicals:** 17,18-epoxyeicosatetraenoic acid (PubChem CID 6439311), t-TUCB (PubChem CID 16756850), eicosapentaenoic acid (PubChem CID 5282847), docosahexaenoic acid (PubChem CID 445580), GW9662 (PubChem CID 644213)
- **Diseases:** obesity (MONDO:0011122)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, EPHX2 (epoxide hydrolase 2) [NCBI Gene 2053] {aka ABHD20, CEH, SEH}
- **Diseases:** obesity (MESH:D009765)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11946110/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC11946110/full.md

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Source: https://tomesphere.com/paper/PMC11946110