4.6 Review

Role of TRPV1 and TRPA1 Ion Channels in Inflammatory Bowel Diseases: Potential Therapeutic Targets?

Journal

PHARMACEUTICALS
Volume 12, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/ph12020048

Keywords

IDB; Crohn's disease; ulcerative colitis; TRPV1; TRPA1; human studies; animal studies; colitis models

Funding

  1. Higher Education Institutional Excellence Program of the Ministry of Human Capacities in Hungary [20765-3/2018/FEKUTSRTAT]
  2. PEPSYS: Complexity of Peptidergic Signalization and its Role in Systemic Diseases [GINOP-2.3.2-15-2016-00050]
  3. Human Resource Development Operational Program [EFOP-3.6.2-16-2017-00006 LIVE LONGER]
  4. Economic Development and Innovation Operational Program [GINOP-2.3.2-15-2016-00048 STAY ALIVE]
  5. New National Excellence Program of the Ministry of Human Capacities [UNKP-18-3-IV-PTE-143]

Ask authors/readers for more resources

Inflammatory bowel diseases (IBD) have long been recognized to be accompanied by pain resulting in high morbidity. Transient receptor potential vanilloid 1 (TRPV1) and ankyrin 1 (TRPA1) ion channels located predominantly on the capsaicin-sensitive sensory neurons play a complex role in hyperalgesia and neurogenic inflammation. This review provides an overview of their expression and role in intestinal inflammation, in particular colitis, that appears to be virtually inconsistent based on the thorough investigations of the last twenty years. However, preclinical results with pharmacological interventions, as well as scarcely available human studies, more convincingly point out the potential therapeutic value of TRPV1 and TRPA1 antagonists in colitis and visceral hypersensitivity providing future therapeutical perspectives through a complex, unique mechanism of action for drug development in IBD.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available