Taurochenodeoxycholic acid (TCDCA) alleviates obesity-induced endothelial dysfunction across human, murine, and cellular models through farnesoid X receptor (FXR) activation.
Does Taurochenodeoxycholic acid (TCDCA) alleviate obesity-induced endothelial dysfunction?
TCDCA alleviates obesity-induced endothelial dysfunction via FXR activation across multiple models, highlighting a potential therapeutic pathway.
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.
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.