An update on PPAR activation by cannabinoids

SE O'Sullivan - British journal of pharmacology, 2016 - Wiley Online Library
Some cannabinoids activate the different isoforms of PPARs (α, β and γ), as shown through
the use of reporter gene assays, binding studies, selective antagonists and knockout …

Endocannabinoids and endocannabinoid-related mediators: Targets, metabolism and role in neurological disorders

FA Iannotti, V Di Marzo, S Petrosino - Progress in lipid research, 2016 - Elsevier
The endocannabinoid system (ECS) is composed of two G protein-coupled receptors
(GPCRs), the cannabinoid CB1 and CB2 receptors, and the two main endogenous lipid …

Antibiotic-induced microbiota perturbation causes gut endocannabinoidome changes, hippocampal neuroglial reorganization and depression in mice

F Guida, F Turco, M Iannotta, D De Gregorio… - Brain, behavior, and …, 2018 - Elsevier
The microbiota-gut-brain axis (MGBA) regulates the reciprocal interaction between chronic
inflammatory bowel and psychiatric disorders. This interaction involves multiple pathways …

Endocannabinoids—at the crossroads between the gut microbiota and host metabolism

PD Cani, H Plovier, M Van Hul, L Geurts… - Nature Reviews …, 2016 - nature.com
Various metabolic disorders are associated with changes in inflammatory tone. Among the
latest advances in the metabolism field, the discovery that gut microorganisms have a major …

The pharmacology of palmitoylethanolamide and first data on the therapeutic efficacy of some of its new formulations

S Petrosino, V Di Marzo - British journal of pharmacology, 2017 - Wiley Online Library
Palmitoylethanolamide (PEA) has emerged as a potential nutraceutical, because this
compound is naturally produced in many plant and animal food sources, as well as in cells …

Clinical endocannabinoid deficiency reconsidered: current research supports the theory in migraine, fibromyalgia, irritable bowel, and other treatment-resistant …

EB Russo - Cannabis and cannabinoid research, 2016 - liebertpub.com
Medicine continues to struggle in its approaches to numerous common subjective pain
syndromes that lack objective signs and remain treatment resistant. Foremost among these …

The basal pharmacology of palmitoylethanolamide

L Rankin, CJ Fowler - International Journal of Molecular Sciences, 2020 - mdpi.com
Palmitoylethanolamide (PEA, N-hexadecanoylethanolamide) is an endogenous compound
belonging to the family of N-acylethanolamines. PEA has anti-inflammatory and analgesic …

Plant-derived alkaloids: the promising disease-modifying agents for inflammatory bowel disease

J Peng, TT Zheng, X Li, Y Liang, LJ Wang… - Frontiers in …, 2019 - frontiersin.org
Inflammatory bowel disease (IBD) represents a group of intestinal disorders with self-
destructive and chronic inflammation in the digestive tract, requiring long-term medications …

Palmitoylethanolamide, a naturally occurring lipid, is an orally effective intestinal anti‐inflammatory agent

F Borrelli, B Romano, S Petrosino… - British journal of …, 2015 - Wiley Online Library
Background and Purpose Palmitoylethanolamide (PEA) acts via several targets, including
cannabinoid CB 1 and CB2 receptors, transient receptor potential vanilloid type‐1 (TRPV1) …

Progress in understanding mechanisms of opioid-induced gastrointestinal adverse effects and respiratory depression

MZ Imam, A Kuo, S Ghassabian, MT Smith - Neuropharmacology, 2018 - Elsevier
Opioids evoke analgesia through activation of opioid receptors (predominantly the μ opioid
receptor) in the central nervous system. Opioid receptors are abundant in multiple regions of …