Tissue-specific mechanisms of bile acid homeostasis and activation of FXR-FGF19 signaling in preterm and term neonatal pigs
Caitlin E. Vonderohe, Gregory J. Guthrie, Barbara J. Stoll, Shaji K. Chacko, Harry Dale Dawson, Douglas G. Burrin
Abstract
Caitlin E. Vonderohe, Gregory J. Guthrie, Barbara J. Stoll, Shaji K. Chacko, Harry Dale Dawson, Douglas G. Burrin
Abstract
Our results show that the lower hepatic bile acid synthesis and ileum FXR-FGF19 pathway responsiveness to bile acids contribute to low-circulating FGF19 in preterm compared with term neonatal pigs. The molecular mechanism explaining immature or low-ileum FXR-FGF19 signaling may be linked to developmental patterning effects of GATA-4.
OpenAlex reports 11 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Our results show that the lower hepatic bile acid synthesis and ileum FXR-FGF19 pathway responsiveness to bile acids contribute to low-circulating FGF19 in preterm compared with term neonatal pigs. The molecular mechanism explaining immature or low-ileum FXR-FGF19 signaling may be linked to developmental patterning effects of GATA-4.
Key concepts: FGF19, Bile acid, Homeostasis, Term (time), Endocrinology, Internal medicine, Cell biology, Biology