Islet Beta Cell Research on Insulin Secretion
Understanding the mechanisms that regulate insulin secretion could lead to novel therapies for Type 1 and Type 2 diabetes. Two areas of interest focused on islet beta cells at Cedars-Sinai include:
- The role of anandamide, an endogenous cannabinoid receptor ligand, on insulin secretion
- The physiological relevance of islet size heterogeneity
Research is underway to elucidate the in vitro effects of anandamide on isolated pancreatic islets from lean and fat-fed animals using a canine model.
Another islet beta cell study is designed to ascertain why there are different-sized pancreatic islets and to determine whether small or large islets are primarily responsible for beta cell compensation in response to fat-diet-induced insulin resistance.
Current studies include:
- Beta cells' response to anandamide in diet-induced obesity
- Examine pancreatic islets in normal-fed and fat-fed animal models, focusing on beta cells.
- Work with islets in vitro to study effect of anandamide on beta cells.
- Explore possible mechanism of anandamide and whether it stimulates beta cells directly or through a secondary response.
- Compare response of beta cells to anandamide in normal-fed verses fat-fed models.
- Determine whether anandamide directly signals beta cells to produce insulin and, if so, how this occurs.
- Examine pancreatic islets in normal-fed and fat-fed animal models, focusing on beta cells.
- Efficiency of large and small islets in diet-induced obesity
- Examine insulin secretion in large and small islets in both normal-fed and fat-fed animal models.
- Isolate islets for measurement and classify as small or large.
- Express beta cell function as the ratio of insulin secretion induced by glucose and as insulin units normalized to islet size.
- Determine whether larger or smaller islets compensate more for fat-induced insulin resistance.
- Examine insulin secretion in large and small islets in both normal-fed and fat-fed animal models.
Research that elucidates the mechanisms of insulin secretion can lead to breakthroughs for both Type 1 and Type 2 diabetes therapies. The link between the endocannabinoid system and pancreatic islet function is a relatively new frontier of study that may hold promise for creating therapies targeted to impaired pancreatic endocrine function. Understanding the physiological relevance of islet size heterogeneity also could help scientists identify medications aimed at specific islets for improved insulin production.
- Woolcott OO, Richey JM, Kabir M, Chow RH, Iyer MS, Kirkman EL, Stefanovski D, Lottati M, Kim SP, Harrison LN, et al. High-fat diet-induced insulin resistance does not increase plasma anandamide levels or potentiate anandamide insulinotropic effect in isolated canine islets. PLOS One. 2015;10(4):e0123558. http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0123558.
- Woolcott OO, Bergman RN, Richey JM, Kirkman EL, Harrison, LN, Ionut V, Lottati M, Zheng D, Hsu IR, Stefanovski D, et al. Simplified method to isolate highly pure canine pancreatic islets. Pancreas. 2012 Jan;41(1):31-38. http://journals.lww.com/pancreasjournal/pages/articleviewer.aspx?year=2012&issue=01000&article=00005&type=abstract.
- Woolcott OO, Gustafsson AJ, Dzabic M, Pierroa C, Tedeschia P, Sandgrena J, Rizuanul Baria M, Hoab NK, Bianchia M, Rakonjacc M, et al. Arachidonic acid is a physiological activator of the ryanodine receptor in pancreatic beta cells. Cell Calcium. 2006 Jun;39(6):529-537. http://www.sciencedirect.com/science/article/pii/S0143416006000340.
- Woolcott OO, Richey JM, Chow RH, Kabir M, Iyer M, Kirkman EL, Stefanovski D, Lottati M, Harrison IN, Ionut V, et al. Physiological anandamide levels potentiate glucose-stimulated insulin secretion in isolated canine pancreatic islets. 71st Scientific Sessions 2011;1840-P. http://professional.diabetes.org/abstract/physiological-anandamide-levels-potentiate-glucose-stimulated-insulin-secretion-isolated.
- Woolcott OO, Richey JM, Stefanovski D, Ader M, Yae S, Dittman J, Chow RH, Kirkman E, Bergman, RN. Larger pancreatic islets compensate relatively more than smaller islets in response to diet-induced insulin resistance in dogs. 70th Scientific Sessions 2010: 1723-P. http://professional.diabetes.org/abstract/larger-pancreatic-islets-compensate-relatively-more-smaller-islets-response-diet-induced.
- Woolcott OO, Richey JM, Chow R, Kirkman EL, Stefanovski D, Hsu IR, Lottati M, Ionut V, Zheng D, Harrison LN, et al. Evidence of increased CB-1 receptor activity in isolated pancreatic islets from high fat-fed dogs. 69th Scientific Sessions 2009:1643-P. http://professional.diabetes.org/abstract/evidence-increased-cb-1-receptor-activity-isolated-pancreatic-islets-high-fat-fed-dogs.
- Richey JM, Woolcott OO, Stefanovski D, Harrison LN, Zheng D, Lottati M, Hsu IR, Kim SP, Kabi M, Catalano KJ, et al. Rimonabant prevents additional accumulation of visceral and subcutaneous fat during high-fat feeding in dogs. Am J Physiol Endocrinol Metab. 2009 Jun;296(6):E1311-8. http://ajpendo.physiology.org/content/296/6/E1311.
- Richey JM, Woolcott OO, Kim SP, Stefanovski D, Ionut V, Catalano K, Chiu J, Hsu I, Harrison L, Lottati M, et al. Effect of CB-1 antagonist (rimonabant) to increase insulin sensitivity, independent of weight loss. 67th Scientific Sessions 2007: 0248-OR. http://professional.diabetes.org/abstract/effect-cb-1-antagonist-rimonabant-increase-insulin-sensitivity-independent-weight-loss.
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8700 Beverly Blvd.
Thalians Health Center, Room E104
Los Angeles, CA 90048