bile salts Dotaz Zobrazit nápovědu
Gastroenterology clinics of North America, ISSN 0889-8553 Vol. 28, No. 1
VIII, 254 s. : il. ; 24 cm
Falk symposium ; 93
xv, 328 stran : ilustrace, tabulky ; 24 cm
- MeSH
- hepatobiliární exkrece MeSH
- klinické lékařství MeSH
- nemoci jater MeSH
- nemoci žlučového ústrojí MeSH
- žlučové kyseliny a soli biosyntéza fyziologie metabolismus terapeutické užití MeSH
- Publikační typ
- sborníky MeSH
- Konspekt
- Patologie. Klinická medicína
- NLK Obory
- hepatologie
BACKGROUND: Bile salts of hepatic and microbial origin mediate interorgan cross talk in the gut-liver axis. Here, we assessed whether the newly discovered class of microbial bile salt conjugates (MBSCs) activate the main host bile salt receptors (Takeda G protein-coupled receptor 5 [TGR5] and farnesoid X receptor [FXR]) and enter the human systemic and enterohepatic circulation. METHODS: N-amidates of (chenodeoxy) cholic acid and leucine, tyrosine, and phenylalanine were synthesized. Receptor activation was studied in cell-free and cell-based assays. MBSCs were quantified in mesenteric and portal blood and bile of patients undergoing pancreatic surgery. RESULTS: MBSCs were activating ligands of TGR5 as evidenced by recruitment of Gsα protein, activation of a cAMP-driven reporter, and diminution of lipopolysaccharide-induced cytokine release from macrophages. Intestine-enriched and liver-enriched FXR isoforms were both activated by MBSCs, provided that a bile salt importer was present. The affinity of MBSCs for TGR5 and FXR was not superior to host-derived bile salt conjugates. Individual MBSCs were generally not detected (ie, < 2.5 nmol/L) in human mesenteric or portal blood, but Leu-variant and Phe-variant were readily measurable in bile, where MBSCs comprised up to 213 ppm of biliary bile salts. CONCLUSIONS: MBSCs activate the cell surface receptor TGR5 and the transcription factor FXR and are substrates for intestinal (apical sodium-dependent bile acid transporter) and hepatic (Na+ taurocholate co-transporting protein) transporters. Their entry into the human circulation is, however, nonsubstantial. Given low systemic levels and a surplus of other equipotent bile salt species, the studied MBSCs are unlikely to have an impact on enterohepatic TGR5/FXR signaling in humans. The origin and function of biliary MBSCs remain to be determined.
- MeSH
- játra metabolismus MeSH
- lidé MeSH
- receptory cytoplazmatické a nukleární * metabolismus MeSH
- receptory spřažené s G-proteiny * metabolismus MeSH
- transkripční faktory MeSH
- žluč chemie MeSH
- žlučové kyseliny a soli * farmakologie metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Falk symposium series ; No. 52, 1989
xxi, 385 stran, 3 nečíslované listy obrazové přílohy : ilustrace ; 24 cm
The publication contains the proceedings of a symposium that focused on bile acids, biliary tract diseases and related gastrointestinal and liver diseases. Intended for professional public.
- MeSH
- gastrointestinální nemoci MeSH
- metabolismus MeSH
- nemoci jater MeSH
- nemoci žlučového ústrojí MeSH
- žlučové kyseliny a soli MeSH
- Publikační typ
- kongresy MeSH
- sborníky MeSH
- zprávy MeSH
- Konspekt
- Patologie. Klinická medicína
- NLK Obory
- gastroenterologie
Methods and applications ; volume 4
xix, 582 stran : grafy, tabulky ; 23 cm
- Konspekt
- Biochemie. Molekulární biologie. Biofyzika
- NLK Obory
- biochemie
- NLK Publikační typ
- kolektivní monografie