Methuselah Foundation Newsletter, July 2010
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July 23, 2010Methuselah Foundation Newsletter, July 2010
July 21, 2010New Mprize Competitors, Alan Cash & Holly Brown BorgWe are very pleased to announce the addition of two new Mprize competitors, Alan Cash & Holly Brown Borg. Here are their stories. Alan Cash Although the pain was completely gone, the experience left Alan with “the intense feeling that Aging was bad.” So he decided to do something about it. A lengthy recuperation gave him the opportunity to read about aging. He became fascinated by the work involving Calorie Restriction (CR) by such notable researchers as Leonard Guarente and David Sinclair, because CR was a proven method to slow aging. He learned that CR leads to changes in metabolism and gene expression that result in increased lifespan and the reduction of the incidence of heart disease, kidney disease, Alzheimer’s disease, type-2 diabetes and cancer. Alan realized that three molecular pathways that extend life as a result of CR had been identified: 1. Increasing the NAD+/NADH ratio in the cells, All of these could be achieved by supplementing the diet with the metabolite oxaloacetate. Oxaloacetate is a human metabolite, and is consumed in the foods we eat on a daily basis, such as apples, chicken, and potatoes, but these foods do not contain enough oxaloacetate to continually activate AMPK, the AMP-activated protein kinase that regulates metabolism. Working with scientists at UCSD and UCLA schools of medicine, Alan showed that animals given supplements of oxaloacetate have increased lifespan, just like animals under CR. And equally important, others have already shown that oxaloacetate provides many of the same health benefits as CR, including mitochondrial DNA protection, and protection of retinal, neural and pancreatic tissues. Human studies indicate a substantial reduction in fasting glucose levels and improvement in insulin resistance. With his training as a physicist, Alan strove to take the complex biology of aging and reduce it to a simple idea to slow aging and extend life--- mainly to supplement the diet with higher amounts of oxaloacetate. When Alan presented his ideas to a molecular biologist at University of California San Diego, the biologist immediately cleared space and invited him to test his theory! Together they did tests on worms, flies and mice, and the initial data was very promising, leading to journal articles in “Aging Cell”, “Open Longevity Science” and “Anti-Aging Therapeutics.” A simple solution for aging with a human metabolite had extended lifespan! To publicize the discovery, Alan saw that the Mprize might be the best route, but additional data was required. Various long-term tests of oxaloacetate are underway at UC Riverside, LSU Baton Rouge, and, through the National Institute on Aging Interventions Testing Program, at UT Austin, UM Ann Arbor and the Jackson Laboratory in Bar Harbor. Concurrently, after submitting extensive safety information, Alan received approval to market the new dietary supplement in Canada, Europe and the USA for human use, under the trade name “benaGene”. Holly Brown Borg After heading to North Dakota, where she became an Assistant Professor in Pharmacology, Physiology & Therapeutics, Holly continued to follow the progress of the mice. Their long life intrigued her. What was it that caused them to live so much longer than other mice? Holly began exploring so she could understand what it was about these mice, lacking growth hormone, which allowed them to live so long. She explains her hypothesis, “A lack of growth hormone means there is no demand to make protein and turn amino acid into muscle; this frees the mice, metabolically, to fight off internal and external stresses.” The human nutrition center on campus suggested that Holly turn her attention to methionine metabolism. This essential amino acid is critical for protein synthesis and growth, and is also integral to metabolism. To go a bit deeper, glutathione, an important antioxidant, is generated by the methionine (MET) pathway. Glutathione is made up of three amino acids, the key one in these studies is cysteine. The essential amino acids, MET and cysteine, can be easily modified in the diet. The Ames mice have highly active methionine metabolism but when they are given growth hormone, this activity goes down. This was the proof Holly needed that methionine metabolism is regulated by growth hormone. According to Holly, “The mechanisms leading to this potential ‘slower’ aging and lifespan extension are unknown. Our lab is interested in pursuing studies altering the level of essential amino acids in the diet and following modifications to key metabolic pathways involved in aging processes and lifespan. The beauty of these studies lies in their simplicity and potential therapeutic value.” Organomics: A Better SystemJust today on the radio I heard a woman talk about the agony of waiting for someone to die so she can live – she needs a transplant. Everything she said about her situation, and the hopelessness of many, many others waiting for organs, demonstrated the challenges and limitations of the current system of organ replacement. We believe it’s time for dramatic change. You already know Methuselah doesn’t accept the idea that “everyone falls apart.” (I have a harder time accepting that each year as I get closer to senior status.) Our vision is a long, healthy life for you, me and everyone on the waiting list for an organ. This year we are focusing our efforts on tissue engineering and organ replacement. We are looking ahead 10 years and projecting that, with our help, everyone who needs an organ will get an organ. To realize our vision we are advocating nothing short of a whole new system. We call it Organomics. It is the science of organ regeneration combined with the economic means to make it possible. The promise of Organomics is to provide a new organ to any patient in need, not from a donor or from the black market but from their own cells. NewOrgan Prize was created to reach this ambitious goal. Methuselah Foundation has been working for years to find causes and solutions of deteriorating health and productivity. I’m glad to be part of an organization that drives science to find solutions that will work for all of us. I challenge you to be Organomical! July 14, 2010Silverstone Solutions in the NewsSilverstone Solutions is one of the Methuselah Foundation's strategic investments made in support of the recently launched NewOrgan Prize. Silverstone's Matchmaker product was recently featured in an ABC7 article and video: Technology developed in the Bay Area could soon have a dramatic impact on kidney transplants. It is designed to help patients who need a matching donor and a new version may be able to pair up thousands of patients in a fraction of the time. Identifying and arranging these donation chains in time and space - a very challenging problem - is the benefit provided by Silverstone's work. July 12, 2010David Gobel Interviewed by ABC CanberraMethuselah Foundation co-founder and CEO David Gobel was recently featured in an interview on the Morning radio program for the Australian Broadcasting Corporation in Canberra. You can download an MP3 copy of the interview and listen at your leisure. An Organovo Photo EssayWired is running a photo essay on organ-printing startup company Organovo. Generous Methuselah Foundation donors provided the funds for the Foundation to invest in the growth of Organovo, an investment that is a part of the Foundation's long-term strategy to support and nurture important research: "Right now we’re really good at printing blood vessels," says Ben Shepherd, senior research scientist at regenerative-medicine company Organovo. "We printed 10 this week. We’re still learning how to best condition them to be good, strong blood vessels." The photos are good, but the article mistakenly suggests that hundreds of millions of dollars will be needed to develop the organ printing system. In fact, Organovo's devices are already on sale to research groups - the large expenditures of the future will be spread amongst researchers who are working on moving from printing blood vessels to printing entire complex human organs. |
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