Study: CBD receptors in cat gastrointestinal tract

18/08/2023

We work with researchers and universities around the world to gain valuable knowledge about how CBD products work in humans and animals and to get detailed information about how the cannabinoids react with the CB1 and CB2 receptors.

University of Bologna seal

We work with the University of Bologna and Professor Roberto Chiocchetti DVM, PhD. and his team from the Department of Veterinary Medical Science and are funding a number of research studies on CBD and animals.

Disclaimer: we supported the University of Bologna with financial funds for research. The authors declare they have no conflict of interest.

Research study: Localization of cannabinoid and cannabinoid related receptors in the cat gastrointestinal tract

The present study aimed to immunohistochemically investigate the distribution of the canonical cannabinoid receptors CB1 and CB2 and other key receptors in tissue samples of the gastrointestinal tract of the cat.

Abstract: Cannabinoid receptors showed a wide distribution in the feline gastrointestinal tract layers. Although not yet confirmed/supported by functional evidences, the present research might represent an anatomical substrate potentially useful to support, in feline species, the therapeutic use of cannabinoids during gastrointestinal inflammatory diseases.

Cannabinoid receptors regulate gastrointestinal tract (GIT) motility and secretion, sensation, emesis, satiety, and inflammation.

The primary and most studied cannabinoid receptors are two G protein-coupled receptors: cannabinoid receptors type 1 (CB1R) and type 2 (CB2R). CB1R is mostly expressed in the central and peripheral nervous system, while CB2R is mainly expressed in immune cells.

Cannabidiol (CBD) is currently one of the most studied cannabinoids and is a non-psychoactive compound.

CBD seems to act preferentially on cannabinoid-related receptors, such as GPR3 (inverse agonist), GPR6 (inverse agonist), GPR12 (inverse agonist), GPR55 (antagonist), TRPA1 (agonist), TRPV1 (agonist), and serotoninergic receptors 5-HT1a (agonist), 5-HT2a (partial agonist), and 5-HT3 (antagonist)

Read the full 18-page research study here for free.

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