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November 5, 2025European Heart Journal2 citations

From bile to vessels: linking obesity to endothelial dysfunction

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SKSimon KralerGVGemma VilahurPKPetra Kleinbongard

Key Result

Taurochenodeoxycholic acid (TCDCA) alleviates obesity-induced endothelial dysfunction across human, murine, and cellular models through farnesoid X receptor (FXR) activation.

Structured PICO

Does Taurochenodeoxycholic acid (TCDCA) alleviate obesity-induced endothelial dysfunction?

P
Population
Human, murine, and cellular models of obesity-induced endothelial dysfunction
E
Exposure
Taurochenodeoxycholic acid (TCDCA)
O
Outcome
Endothelial dysfunction (nitric oxide bioavailability and oxidative stress)surrogate

TCDCA alleviates obesity-induced endothelial dysfunction via FXR activation across multiple models, highlighting a potential therapeutic pathway.

Limitations

  • Disease heterogeneity
  • Uncertain efficacy in old and multimorbid patients of both sexes
  • Vascular-bed specific differences
  • Potential differences between CDCA and TCDCA
  • Efficacy in old and multimorbid patients of both sexes

Abstract

Taurochenodeoxycholic acid (TCDCA; the taurine-conjugated form of CDCA) alleviates obesity-induced endothelial dysfunction through farnesoid X receptor (FXR) activation and metabolic reprogramming. This TCDCA-FXR interaction restores nitric oxide bioavailability, reduces oxidative stress, and thereby alleviates endothelial dysfunction across human, murine, and cellular models. Remaining uncertainties include disease heterogeneity, its efficacy in old and multimorbid patients of both sexes, vascular-bed specific differences, and potential differences between CDCA and TCDCA.

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Cite This Study

Kraler et al. (2025) conducted a review in Obesity-induced endothelial dysfunction. Taurochenodeoxycholic acid (TCDCA) was evaluated on Endothelial dysfunction. Taurochenodeoxycholic acid (TCDCA) alleviates obesity-induced endothelial dysfunction across human, murine, and cellular models through farnesoid X receptor (FXR) activation.

synapsesocial.com/papers/6a963e8b120a22c5bc86cb8ehttps://doi.org/10.1093/eurheartj/ehaf957
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