Drugs or diet?--Developing novel therapeutic strategies targeting the free fatty acid family of GPCRs

Br J Pharmacol. 2013 Oct;170(4):696-711. doi: 10.1111/bph.12327.

Abstract

Free fatty acids (FFAs) are metabolic intermediates that may be obtained through the diet, synthesized endogenously, or produced via fermentation of carbohydrates by gut microbiota. In addition to serving as an important source of energy, FFAs are known to produce a variety of both beneficial and detrimental effects on metabolic and inflammatory processes. While historically, FFAs were believed to produce these effects only through intracellular targets such as peroxisome proliferator-activated receptors, it has now become clear that FFAs are also agonists for several GPCRs, including a family of four receptors now termed FFA1-4. Increasing evidence suggests that FFA1-4 mediate many of the beneficial properties of FFAs and not surprisingly, this has generated significant interest in the potential of these receptors as therapeutic targets for the treatment of a variety of metabolic and inflammatory disorders. In addition to the traditional strategy of developing small-molecule therapeutics targeting these receptors, there has also been some consideration given to alternate therapeutic approaches, specifically by manipulating endogenous FFA concentrations through alteration of either dietary intake, or production by gut microbiota. In this review, the current state of knowledge for FFA1-4 will be discussed, together with their potential as therapeutic targets in the treatment of metabolic and inflammatory disorders. In particular, the evidence in support of small molecule versus dietary and microbiota-based therapeutic approaches will be considered to provide insight into the development of novel multifaceted strategies targeting the FFA receptors for the treatment of metabolic and inflammatory disorders.

Keywords: diet; free fatty acid; free fatty acid receptor; glucose homeostasis; gut microbiota; inflammation; metabolism; therapeutics.

Publication types

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

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / metabolism
  • Anti-Inflammatory Agents / pharmacology
  • Dietary Fats / metabolism
  • Dietary Fats / pharmacology*
  • Drug Design*
  • Fatty Acids, Nonesterified / metabolism
  • Fatty Acids, Nonesterified / pharmacology*
  • Humans
  • Inflammation / drug therapy
  • Inflammation / metabolism
  • Ligands
  • Metabolic Diseases / drug therapy
  • Metabolic Diseases / metabolism
  • Molecular Targeted Therapy
  • Receptors, G-Protein-Coupled / agonists*
  • Receptors, G-Protein-Coupled / metabolism
  • Signal Transduction / drug effects*

Substances

  • Anti-Inflammatory Agents
  • Dietary Fats
  • Fatty Acids, Nonesterified
  • Ligands
  • Receptors, G-Protein-Coupled