The Atypical Cannabinoid Abn-CBD Reduces Inflammation and Protects Liver, Pancreas, and Adipose Tissue in a Mouse Model of Prediabetes and Non-alcoholic Fatty Liver Disease

Background and Aims: The synthetic atypical cannabinoid Abn-CBD, a cannabidiol (CBD) derivative, has been recently shown to modulate the immune system in different organs, but its impact in obesity-related meta-inflammation remains unstudied. We investigated the effects of Abn-CBD on metabolic and i...

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Detalles Bibliográficos
Autores: Romero-Zerbo, Silvana Y., García-Fernández, María, Espinosa-Jiménez, Vanesa, Pozo-Morales, Macarena, Escamilla-Sánchez, Alejandro, Sánchez-Salido, Lourdes, Lara, Estrella, Cobo-Vuilleumier, Nadia, Rafacho, Alex, Olveira, Gabriel, Rojo-Martínez, Gemma, Gauthier, Benoit R., González-Mariscal, Isabel, Bermúdez-Silva, Francisco J.
Tipo de recurso: artículo
Fecha de publicación:2020
País:España
Institución:Instituto de Salud Carlos III (ISCIII)
Repositorio:Repisalud
Idioma:inglés
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/18014
Acceso en línea:http://hdl.handle.net/20.500.12105/18014
Access Level:acceso abierto
Palabra clave:Cannabinoids
Inflammation
Prediabetes
NAFLD
Obesity
Liver
Islets of langerhans
Adipose tissue
Cannabinoides
Inflamación
Enfermedad del hígado graso no alcohólico
Obesidad
Hígado
Islotes pancreáticos
Tejido adiposo
Adipose Tissue
Animals
Cytoprotection
Diet, High-Fat
Disease Models, Animal
Male
Mice
Mice, Inbred C57BL
Mice, Obese
Fatty Liver
Pancreas
Prediabetic State
Resorcinols
Descripción
Sumario:Background and Aims: The synthetic atypical cannabinoid Abn-CBD, a cannabidiol (CBD) derivative, has been recently shown to modulate the immune system in different organs, but its impact in obesity-related meta-inflammation remains unstudied. We investigated the effects of Abn-CBD on metabolic and inflammatory parameters utilizing a diet-induced obese (DIO) mouse model of prediabetes and non-alcoholic fatty liver disease (NAFLD). Materials and Methods: Ten-week-old C57Bl/6J mice were fed a high-fat diet for 15 weeks, following a 2-week treatment of daily intraperitoneal injections with Abn-CBD or vehicle. At week 15 mice were obese, prediabetic and developed NAFLD. Body weight and glucose homeostasis were monitored. Mice were euthanized and blood, liver, adipose tissue and pancreas were collected and processed for metabolic and inflammatory analysis. Results: Body weight and triglycerides profiles in blood and liver were comparable between vehicle- and Abn-CBD-treated DIO mice. However, treatment with Abn-CBD reduced hyperinsulinemia and markers of systemic low-grade inflammation in plasma and fat, also promoting white adipose tissue browning. Pancreatic islets from Abn-CBD-treated mice showed lower apoptosis, inflammation and oxidative stress than vehicle-treated DIO mice, and beta cell proliferation was induced. Furthermore, Abn-CBD lowered hepatic fibrosis, inflammation and macrophage infiltration in the liver when compared to vehicle-treated DIO mice. Importantly, the balance between hepatocyte proliferation and apoptosis was improved in Abn-CBD-treated compared to vehicle-treated DIO mice. Conclusions: These results suggest that Abn-CBD exerts beneficial immunomodulatory actions in the liver, pancreas and adipose tissue of DIO prediabetic mice with NAFLD, thus protecting tissues. Therefore, Abn-CBD and related compounds could represent novel pharmacological strategies for managing obesity-related metabolic disorders.