Pseudocannabinoid H4CBD improves glucose response during advanced metabolic syndrome in OLETF rats independent of increase in insulin signaling proteins.

Adiponectin Ghrelin Insulin Receptor Leptin Obesity

Journal

American journal of physiology. Regulatory, integrative and comparative physiology
ISSN: 1522-1490
Titre abrégé: Am J Physiol Regul Integr Comp Physiol
Pays: United States
ID NLM: 100901230

Informations de publication

Date de publication:
30 Oct 2023
Historique:
medline: 30 10 2023
pubmed: 30 10 2023
entrez: 30 10 2023
Statut: aheadofprint

Résumé

Cannabidiol (CBD) use has grown exponentially more popular in the last two decades, particularly amongst older adults (>55 years), though very little is known about the effects of CBD use during age-associated metabolic dysfunction. Additionally, synthetic analogues of CBD have generated great interest because they can offer a chemically pure product, which is free of plant-associated contaminants. To assess the effects of a synthetic analogue of CBD (H4CBD) on advanced metabolic dysfunction, a cohort of 41-week-old Otsuka Long-Evans Tokushima Fatty (OLETF) rats were administered 200 mg H4CBD/kg by oral gavage for 4 weeks. Animals were fed ad libitum and monitored alongside vehicle-treated OLETF and Long-Evans Tokushima Otsuka (LETO) rats, the lean-strain controls. An oral glucose tolerance test (oGTT) was performed after 4 weeks of treatment. When compared to vehicle-treated OLETF rats, H4CBD decreased body mass (BM) by 15%, which was attributed to a significant loss in abdominal fat. H4CBD reduced glucose response (AUC

Identifiants

pubmed: 37899754
doi: 10.1152/ajpregu.00125.2022
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : UC | UCSD | Center for Medicinal Cannabis Research, University of California, San Diego (CMCR, UCSD)
ID : A21-0086

Auteurs

Jessica N Wilson (JN)

Molecular and Cell Biology, University of California, Merced (Merced, California, United States), Merced, CA, United States.

Dora A Mendez (DA)

MCB, University of California, Merced, Merced, CA, United States.

Francis Dhoro (F)

Department of Chemistry, University of California, Davis, Davis, CA, United States.

Nikolay Shevchenko (N)

Department of Chemistry, University of California, Davis, Davis, CA, United States.

Mark Mascal (M)

Department of Chemistry, University of California, Davis, Davis, CA, United States.

Kyle Lund (K)

Department of Pathology, University of California, San Diego, San Diego, CA, United States.

Robert Fitzgerald (R)

Department of Pathology, University of California, San Diego, San Diego, CA, United States.

Nicholas V DiPatrizio (NV)

University of California, Riverside, Riverside, CA, United States.

Rudy M Ortiz (RM)

Department of Molecular & Cell Biology, University of California, Merced, Merced, CA, United States.

Classifications MeSH