6 November DRC Director's Report - November 2018 November 6, 2018 By The Fraternal Order of Eagles Diabetes Research Center 0 We have known for a very long time that obesity is associated with many cardiovascular and metabolic diseases. Type 2 diabetes, fatty liver disease (where liver stores fat in large lipid droplets), coronary artery disease, heart failure, and many more chronic diseases are all linked to obesity. Although there are many factors at play in an obese human that contribute to these diseases, one common theme that all have in common is something called ‘carbonyl stress.’ Carbonyl stress is a particular form of oxidative stress (i.e., ‘free radicals, hydrogen peroxide, etc). Although carbonyl stress can be a good thing in small quantities, such as with exercise, we know that with obesity, carbonyl stress coming from highly reactive lipids and sugars can cause lasting damage to proteins, DNA, and other necessary ‘building blocks’ in the cell. Fortunately, cells have many natural defense systems that work to counteract this stress, and one of these is the amino L-carnosine. L-carnosine is a naturally occurring dipeptide that humans have in high quantities in muscle, heart and brain, and it is beneficial because it neutralizes carbonyls, thus rendering them harmless. Humans actually consume carnosine with the meat that we eat- white meat such as chicken has particularly very high levels of carnosine. Unfortunately, immediately after getting absorbed into our bloodstream, our bodies have an enzyme called ‘carnosinase’ that breaks down the carnosine, making it no longer effective as a carbonyl scavenger. The work by Ethan Anderson, PhD, Associate Professor of Pharmacology and member of the FOEDRC, and collaborators which was recently published in the Journal of Clinical Investigation is the result of a collaboration between his laboratory and other labs across the United States and Italy. It is important for two main reasons. First, Anderson’s group and another group of medicinal chemists in Italy had the clever idea to create a slightly modified version of l-carnosine that is resistant to carnosinase, yet still retains the ability to scavenge the reactive lipids and sugars. Since it is essentially the same structure as the natural carnosine, this new molecule, ‘Carnosinol,’ displays almost no toxicity at all, and can be administered in drinking water because it is tasteless. Most importantly, Anderson’s group used multiple rodent models of obesity caused by high fat, high sugar diet, to show that Carnosinol substantially reversed metabolic syndrome and fatty liver disease in the obese animals. Of particular importance is that Carnosinol restored insulin sensitivity in the treated mice, meaning that it may be effective as a drug for ‘pre-diabetes’ in obese patients. Unpublished findings from this study also demonstrated that Carnosinol greatly improved the structure and metabolic capacity of the heart. Collectively, what is most exciting is that this work may represent a ‘first-in-class’ new drug therapy that could help reverse the metabolic and cardiovascular disorders known to be associated with obesity. As a recent recruit to the University of Iowa and the FOEDRC, Anderson and his group in the College of Pharmacy will continue to find new and better ways to exploit the beneficial effects of l-carnosine through medicinal chemistry, and work to bring these therapies to the clinic. Related Articles DRC Director's Report - December 2018 As we come to the end of another successful year for the FOEDRC, I want to thank the FOE and my colleagues within the Diabetes Research Center for continuing to push the research boundaries to improve the lives of many who suffer from diabetes. On a personal note, I received a number of honors for my work this year including being asked to deliver the Presidential Lecture of the University of Iowa, receiving Fraternal Order of Eagles Humanitarian Award and the 2018 History Makers Award - the African American Museum of Iowa (AAMI). My receipt of this recognition is really a recognition of what you do and I consider myself very fortunate to lead such an outstanding organization. To close out the year I thought you might be interested in reading about some ways that our researchers are turning “fun and games” into a benefit for our patients with diabetes. DRC Director's Report - December 2018 As we come to the end of another successful year for the FOEDRC, I want to thank the FOE and my colleagues within the Diabetes Research Center for continuing to push the research boundaries to improve the lives of many who suffer from diabetes. On a personal note, I received a number of honors for my work this year including being asked to deliver the Presidential Lecture of the University of Iowa, receiving Fraternal Order of Eagles Humanitarian Award and the 2018 History Makers Award - the African American Museum of Iowa (AAMI). My receipt of this recognition is really a recognition of what you do and I consider myself very fortunate to lead such an outstanding organization. To close out the year I thought you might be interested in reading about some ways that our researchers are turning “fun and games” into a benefit for our patients with diabetes. DRC Director's Report - November 2023 A critical function of the Fraternal Order of Eagles Diabetes Research Center is to train new generations of diabetes researchers. To this end, since 2017, the FOEDRC has received a “T32” grant from the NIH that funds up to six annual positions for postdoctoral fellows to receive advanced training in diabetes research. Postdoctoral fellows are scientists and/or physicians who have recently received their doctorate degree and who are in the final stages of training to become independent scientists. DRC Director's Report - November 2020 FOE Diabetes Research Center scientists from the University of Iowa have discovered a safe new way to manage blood sugar non-invasively. Exposing diabetic mice to a combination of static electric and magnetic fields for a few hours per day normalizes two major hallmarks of type 2 diabetes, namely reducing blood glucose levels and preventing insulin resistance. These new findings were published Oct. 6 in Cell Metabolism. DRC Director's Report - November 2021 In September 2021, Brian T. O’Neill, Assistant Professor in Internal Medicine and member of FOEDRC, published a paper in the Journal of Clinical Investigation that shows how insulin and the closely related insulin-like growth factor-1 (IGF-1) work in muscle to regulate energy production in mitochondria by suppressing the activation of FoxO transcription factors. Decreased muscle strength and muscle atrophy are features of long-standing or uncontrolled diabetes that can worsen with aging or bedrest after surgery. DRC Director's Report - March 2019 Brian T. O’Neill, MD, PhD, assistant professor in the Division of Endocrinology in the Department of Internal Medicine and member of the FOEDRC recently published in the journal Diabetes the discovery that FoxO proteins, which are transcription factors that regulate DNA, are the critical regulators of diabetes-related muscle atrophy. Showing 0 Comment Comments are closed.