Referenced in: none

Automatically associated channels: TRP , TRPV , TRPV1

Title: Contribution of TRPV1 and multidrug resistance proteins in the permeation of capsaicin across different intestinal regions.

Authors: Lian Duan, Yuan Yan, YaBin Sun, Boxin Zhao, WenJun Hu, GuoFeng Li

Journal, date & volume: Int J Pharm, 2013 Mar 10 , 445, 134-40

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/23402980

Abstract
The aim of the study was to observe the characteristic of permeation of capsaicin across jejunum, ileum and colon in the rat, and to investigate the role of transient receptor potential cation channel (TRPV1). The interaction of capsaicin with P-glycoprotein (P-gp), multidrug resistance-associated protein 2 (MRP2) and breast cancer resistance protein (BCRP) was also investigated.The transport of capsaicin across three intestinal segments in rats was investigated using Ussing-chamber System.The permeability of capsaicin across the colonic ileac or jejunal membrane was significantly different in M-S direction (11.679 ± 2.001, 5.336 ± 1.248, 1.395 ± 0.673, ×10(-6)cm/s). TRPV1 non-competitive antagonist ruthenium red significantly decreased the permeability of capsaicin in M-S direction across colonic membrane. The permeability of capsaicin could also be inhibited unconventionally by the BCRP inhibitor novobiocin in M-S direction across colon. However, either the P-gp inhibitor verapamil or the MRP2 inhibitor probenecid did not affect the transport of capsaicin in all three segments.We firstly proved that the permeability of capsaicin across colon was significantly higher than that across jejunum or ileum. Furthermore, TRPV1 might mediate the transport of capsaicin across the intestinal membrane. Therefore, the colon-specific highest permeation of capsaicin could be the consequence of the colon-specific distribution of TRPV1. For another, there may be another transport pathway mediating the permeation of capsaicin in M-S direction, which could be inhibited by novobiocin.