Novel approach to accelerate metabolism could lead to new obesity treatment

(Press-News.org) BOSTON – By manipulating a biochemical process that underlies cells' energy-burning abilities, investigators at Beth Israel Deaconess Medical Center (BIDMC) have made a novel discovery that could lead to a new therapy to combat obesity and diabetes.

Published in the April 10 issue of the journal Nature, the new findings show that reducing the amount of nicotinamide N-methyltransferase (NNMT) protein in fat and liver dramatically reduces the development of obesity and diabetes in mice.

'With this discovery, we now have a means of metabolic manipulation that could help speed energy production and lead to weight loss," explains senior author Barbara Kahn, MD, Vice Chair of the Department of Medicine at BIDMC and George Richards Minot Professor of Medicine at Harvard Medical School. "Our findings are particularly exciting because the antisense oligonucleotide [ASO] technology we used to inhibit the NNMT gene in our study is already being used to treat other diseases in humans."

NNMT is an enzyme that processes vitamin B3 and has been linked to certain types of cancer, as well as Alzheimer's disease, explains co-corresponding author Qin Yang, MD, PhD, a Klarman Scholar in the Kahn laboratory at BIDMC and Assistant Professor of Medicine at Harvard Medical School. "Now we have identified an entirely new role for this enzyme in fat tissue, and that is to regulate energy metabolism," he adds.

The new findings hinge on a biochemical mechanism known as a futile cycle, in which cellular reactions are sped up, thereby generating more energy. "We all know people who can seemingly eat whatever they want and not gain weight," explains Kahn. "Part of the reason for this natural weight control owes to basal cellular metabolism – the body's inherent rate of burning energy. A futile cycle is one way to speed up energy utilization in cells."

The investigators first confirmed that levels of NNMT were increased in obese and diabetic mice.

"In a comparison of genetic profiles of fat from mice that were either prone to or protected from developing diabetes, we discovered that the animals that were prone to develop diabetes had a lot of NNMT in the fat and liver," explains Yang. Together with co-first author Daniel Kraus, MD, Kahn and Yang hypothesized that reducing NNMT levels in these tissues would accelerate a series of metabolic reactions involving molecules called polyamines, thereby leading to increased energy expenditure, increased leanness and reduced risk of diabetes and its complications.

"Polyamines are a group of biological molecules that are found throughout the body, which have fundamental functions, including regulating cell growth," explains Kraus. "What's interesting about the polyamines is that the process of building and degrading them creates a biochemical cycle in which energy is used up. This is a futile cycle." The team discovered that NNMT inhibition speeds up this futile cycle, resulting in more dietary calories being burned for energy and fewer calories being incorporated into fat.

Importantly, notes Kahn, the team used antisense oligonucleotide (ASO) technology to knock down the NNMT gene. ASOs are short molecular strings of DNA, which can be designed to prevent the synthesis of specific proteins.

"When an ASO is transferred into a cell, it can target a specific gene and suppress it, as was the case with NNMT," explains Kahn. "Because ASOs have already been approved by the U.S. Food and Drug Administration [FDA] for the treatment of genetic causes of elevated cholesterol or hyperlipidemia, as well as the treatment of a viral eye infection, it's possible that clinical trials to test an ASO anti-obesity therapy in humans could readily move forward."

More than one-third of the U.S. adult population is currently obese, according to the U.S. Centers for Disease Control and Prevention (CDC). "Obesity is a serious economic burden to our healthcare system and a major risk factor for developing insulin resistance and diabetes," says Kahn. "While diet and exercise are important in controlling weight, anti-obesity therapies could be of tremendous help, and NNMT looks to be a promising target for future therapeutic development. Furthermore, because obesity is associated with an increased incidence of Alzheimer's disease and certain cancers, disease states in which NNMT is also elevated, an NNMT ASO could potentially also be beneficial in managing these other devastating conditions."

INFORMATION: In addition to Kahn, Kraus and Yang, coauthors include Dong Kong, Alexander S. Banks, Lin Zhang, Joseph T. Rodgers, Eija Pirinen, Thomas C. Pulinilkunnil, Fengying Gong, Ya-chin Wang, Yana Cen, Anthony A. Sauve, John M. Asara, Odile D. Peroni, Brett P. Monia, Sanjay Bhanot, Leena Alhonen, and Pere Puigserver.

This work is supported, in part, by grants from the National Institutes of Health (R37 DK43051, P30 DK57521; K08 DK090149, RO1 DK100385, BNORC P30 DK046200, NORCH P30 DK040561; RO1 DK69966; P91CA120964, P30CA006516-46) as well as support from the JPB Foundation, the Klarman Foundation, Deutsche Forschungsgemeinschaft, the American Heart Association, the Ellison Medical Foundation and Academy of Finland Grant.

Beth Israel Deaconess Medical Center is a patient care, teaching and research affiliate of Harvard Medical School, and currently ranks third in National Institutes of Health funding among independent hospitals nationwide.

The BIDMC health care team includes Beth Israel Deaconess Hospital-Milton, Beth Israel Deaconess Hospital-Needham, Beth Israel Deaconess Hospital-Plymouth, Anna Jaques Hospital, Cambridge Health Alliance, Lawrence General Hospital, Signature Health Care, Commonwealth Hematology-Oncology, Beth Israel Deaconess HealthCare, Community Care Alliance, and Atrius Health. BIDMC is also clinically affiliated with the Joslin Diabetes Center and Hebrew Senior Life and is a research partner of Dana-Farber/Harvard Cancer Center. BIDMC is the official hospital of the Boston Red Sox. For more information, visit http://www.bidmc.org.