Published April 1, 2021 | Version v.1

Functional Fine-Tuning of Metabolic Pathways by the Endocannabinoid System—Implications for Health and Disease

  • 1. Department of Biochemistry and Molecular Biomedicine, Faculty of Biology, University of Barcelona, and Institute of Biomedicine of the University of Barcelona (IBUB), 08028 Barcelona, Spain
  • 2. Department of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Pasterova 14, 11000 Belgrade, Serbia; milena.cavic@ncrc.ac.rs
  • 3. Department of Biochemistry and Molecular Biomedicine, Faculty of Biology, University of Barcelona, and Institute of Biomedicine of the University of Barcelona (IBUB), 08028 Barcelona, Spain; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), 28031 Madrid, Spain * Authors to whom correspondence should be addressed.

Description

The endocannabinoid system (ECS) employs a huge network of molecules (receptors, ligands, and enzymatic machinery molecules) whose interactions with other cellular networks have still not been fully elucidated. Endogenous cannabinoids are molecules with the primary function of control of multiple metabolic pathways. Maintenance of tissue and cellular homeostasis by functional fine-tuning of essential metabolic pathways is one of the key characteristics of the ECS. It is implicated in a variety of physiological and pathological states and an attractive pharmacological target yet to reach its full potential. This review will focus on the involvement of ECS in glucose and lipid metabolism, food intake regulation, immune homeostasis, respiratory health, inflammation, cancer and other physiological and pathological states will be substantiated using freely available data from open-access databases, experimental data and literature review. Future directions should envision capturing its diversity and exploiting pharmacological options beyond the classical ECS suspects (exogenous cannabinoids and cannabinoid receptor monomers) as signaling through cannabinoid receptor heteromers offers new possibilities for different biochemical outcomes in the cell.

Notes

This work was supported by the "Ministerio de Ciencia, Innovación y Universidades/Agencia Estatal de Investigación/Fondo Europeo de Desarrollo Regional" of the European Union (Grant No. SAF2017-87629-R) and the Ministry of Education, Science and Technological Development of the Republic of Serbia (451-03-9/2021-14/200043). MC is supported by the Science Fund of the Republic of Serbia (TRACEPIGEN PROMIS Project No. 6060876).

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