Cannabinoid Receptors in Metabolic Regulation and Diabetes

Abstract

There is an urgent need for developing effective drugs to combat the obesity and Type 2 diabetes mellitus epidemics. The endocannabinoid system plays a major role in energy homeostasis. It comprises the cannabinoid receptors 1 and 2 (CB 1 and CB 2 ), endogenous ligands called endocannabinoids and their metabolizing enzymes. Because the CB 1 receptor is overactivated in metabolic alterations, pharmacological blockade of the CB 1 receptor arose as a promising candidate to treat obesity. However, because of the wide distribution of CB 1 receptors in the central nervous system, their negative central effects halted further therapeutic use. Although the CB 2 receptor is mostly peripherally expressed, its role in metabolic homeostasis remains unclear. This review discusses the potential of CB 1 and CB 2 receptors at the peripheral level to be therapeutic targets in metabolic diseases. We focus on the impact of pharmacological intervention and/or silencing on peripheral cannabinoid receptors in organs/tissues relevant for energy homeostasis. Moreover, we provide a perspective on novel therapeutic strategies modulating these receptors. Targeting CB 1 with peripherally restricted antagonists, neutral antagonists, inverse agonists, or monoclonal antibodies could represent successful strategies. CB 2 agonism has shown promising results at preclinical level. Beyond classic antagonism and agonism targeting orthosteric sites, the recently described crystal structures of CB 1 and CB 2 open new possibilities for therapeutic interventions with negative and positive allosteric modulators. The challenge of simultaneously targeting CB 1 and CB 2 might be possible by developing dual-steric ligands. The future will tell whether these promising strategies result in a renaissance of the cannabinoid receptors as therapeutic targets in metabolic diseases.

Topics & Concepts