Targeting fatty acid amide hydrolase and transient receptor potential vanilloid-1 simultaneously to modulate colonic motility and visceral sensation in the mouse: A pharmacological intervention with N-arachidonoyl-serotonin (AA-5-HT)

Bashashati, M.; Fichna, J.; Piscitelli, F.; Capasso, R.; Izzo, A. A.; Sibaev, A.; Timmermans, J.-P.; Cenac, N.; Vergnolle, N.; Marzo, V. di und Storr, M. (2017): Targeting fatty acid amide hydrolase and transient receptor potential vanilloid-1 simultaneously to modulate colonic motility and visceral sensation in the mouse: A pharmacological intervention with N-arachidonoyl-serotonin (AA-5-HT). In: Neurogastroenterology and Motility, Bd. 29, Nr. 12, e13148

Abstract

BackgroundEndocannabinoid anandamide (AEA) inhibits intestinal motility and visceral pain, but it may also be proalgesic through transient receptor potential vanilloid-1 (TRPV1). AEA is degraded by fatty acid amide hydrolase (FAAH). This study explored whether dual inhibition of FAAH and TRPV1 reduces diarrhea and abdominal pain. MethodsImmunostaining was performed on myenteric plexus of the mouse colon. The effects of the dual FAAH/TRPV1 inhibitor AA-5-HT on electrically induced contractility, excitatory junction potential (EJP) and fast (f) and slow (s) inhibitory junction potentials (IJP) in the mouse colon, colonic propulsion and visceromotor response (VMR) to rectal distension were studied. The colonic levels of endocannabinoids and fatty acid amides were measured. Key ResultsCB1-positive neurons exhibited TRPV1;only some TRPV1 positive neurons did not express CB1. CB1 and FAAH did not colocalize. AA-5-HT (100nM-10M) decreased colonic contractility by similar to 60%;this effect was abolished by TRPV1 antagonist 5-IRTX, but not by CB1 antagonist, SR141716. AA-5-HT (1M-10M) inhibited EJP by similar to 30% and IJPs by similar to 50%. The effects of AA-5-HT on junction potentials were reversed by SR141716 and 5`-IRTX. AA-5-HT (20mg/kg;i.p.) inhibited colonic propulsion by similar to 30%;SR141716 but not 5`-IRTX reversed this effect. AA-5-HT decreased VMR by similar to 50%-60%;these effects were not blocked by SR141716 or 5`-IRTX. AA-5-HT increased AEA in the colon. Conclusions and InferencesThe effects of AA-5-HT on visceral sensation and colonic motility are differentially mediated by CB1, TRPV1 and non-CB1/TRPV1 mechanisms, possibly reflecting the distinct neuromodulatory roles of endocannabinoid and endovanilloid FAAH substrates in the mouse intestine.

• Dokumententyp: Zeitschriftenartikel
• Fakultät: Medizin
• Themengebiete: 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit
• ISSN: 1350-1925
• Sprache: Englisch