| First Author | Kim W | Year | 2011 |
| Journal | Diabetes | Volume | 60 |
| Issue | 4 | Pages | 1198-209 |
| PubMed ID | 21346174 | Mgi Jnum | J:171758 |
| Mgi Id | MGI:4999674 | Doi | 10.2337/db10-1550 |
| Citation | Kim W, et al. (2011) Cannabinoids inhibit insulin receptor signaling in pancreatic beta-cells. Diabetes 60(4):1198-209 |
| abstractText | OBJECTIVE: Optimal glucose homeostasis requires exquisitely precise adaptation of the number of insulin-secreting beta-cells in the islets of Langerhans. Insulin itself positively regulates beta-cell proliferation in an autocrine manner through the insulin receptor (IR) signaling pathway. It is now coming to light that cannabinoid 1 receptor (CB1R) agonism/antagonism influences insulin action in insulin-sensitive tissues. However, the cells on which the CB1Rs are expressed and their function in islets have not been firmly established. We undertook the current study to investigate if intraislet endogenous cannabinoids (ECs) regulate beta-cell proliferation and if they influence insulin action. RESEARCH DESIGN AND METHODS: We measured EC production in isolated human and mouse islets and beta-cell line in response to glucose and KCl. We evaluated human and mouse islets, several beta-cell lines, and CB1R-null (CB1R(-/-)) mice for the presence of a fully functioning EC system. We investigated if ECs influence beta-cell physiology through regulating insulin action and demonstrated the therapeutic potential of manipulation of the EC system in diabetic (db/db) mice. RESULTS: ECs are generated within beta-cells, which also express CB1Rs that are fully functioning when activated by ligands. Genetic and pharmacologic blockade of CB1R results in enhanced IR signaling through the insulin receptor substrate 2-AKT pathway in beta-cells and leads to increased beta-cell proliferation and mass. CB1R antagonism in db/db mice results in reduced blood glucose and increased beta-cell proliferation and mass, coupled with enhanced IR signaling in beta-cells. Furthermore, CB1R activation impedes insulin-stimulated IR autophosphorylation on beta-cells in a Galpha(i)-dependent manner. CONCLUSIONS: These findings provide direct evidence for a functional interaction between CB1R and IR signaling involved in the regulation of beta-cell proliferation and will serve as a basis for developing new therapeutic interventions to enhance beta-cell function and proliferation in diabetes. |
