Recent advances in vasoactive intestinal peptide physiology and pathophysiology: focus on the gastrointestinal system

F1000Res. 2019 Sep 12:8:F1000 Faculty Rev-1629. doi: 10.12688/f1000research.18039.1. eCollection 2019.

Abstract

Vasoactive intestinal peptide (VIP), a gut peptide hormone originally reported as a vasodilator in 1970, has multiple physiological and pathological effects on development, growth, and the control of neuronal, epithelial, and endocrine cell functions that in turn regulate ion secretion, nutrient absorption, gut motility, glycemic control, carcinogenesis, immune responses, and circadian rhythms. Genetic ablation of this peptide and its receptors in mice also provides new insights into the contribution of VIP towards physiological signaling and the pathogenesis of related diseases. Here, we discuss the impact of VIP on gastrointestinal function and diseases based on recent findings, also providing insight into its possible therapeutic application to diabetes, autoimmune diseases and cancer.

Keywords: VIP; VPAC1; VPAC2; colitis; gastrointestinal; gastrointestinal motility; gastrointestinal secretion; gastrointestinal tract; mast cells; neuropeptide; vasoactive intestinal peptide; vasodilation; ​​​​​​​functional bowel syndromes.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Animals
  • Gastrointestinal Diseases* / metabolism
  • Gastrointestinal Tract* / physiology
  • Mice
  • Receptors, Vasoactive Intestinal Peptide, Type II
  • Receptors, Vasoactive Intestinal Polypeptide, Type I
  • Signal Transduction
  • Vasoactive Intestinal Peptide* / physiology

Substances

  • Receptors, Vasoactive Intestinal Peptide, Type II
  • Receptors, Vasoactive Intestinal Polypeptide, Type I
  • Vasoactive Intestinal Peptide

Grants and funding

This work was supported by a Department of Veterans Affairs Merit Review Award.