Research examines effects of lower and higher tyrosine levels
SAN ANTONIO (Jan. 6, 2013) — Elevated levels of an amino acid, tyrosine, alter development and longevity in animals and may contribute to the development of diabetes in people, new research from the UT Health Science Center at San Antonio indicates. This line of study could potentially lead to a novel way to prevent or treat the disease. The research was reported Dec. 19 in PLOS Genetics, a journal of the Public Library of Science.
Tyrosine is increased in the blood of people who are obese or diabetic, said study senior author Alfred Fisher, M.D., Ph.D., of the Barshop Institute for Longevity and Aging Studies at the UT Health Science Center. Among people who are obese, those at the highest risk of developing diabetes tend to have higher tyrosine levels. “It was unknown whether this was simply a marker of diabetes risk or could be playing a direct role in the disease,” Dr. Fisher said. “Our work suggests that tyrosine has a direct effect.”
Dr. Fisher is a physician scientist with the Barshop Institute’s Center for Healthy Aging and the Geriatric Research, Education and Clinical Center of the South Texas Veterans Health Care System. He has studied tyrosine’s effect on insulin signaling in an animal model called C. elegans (roundworms) since 2005. The observation that tyrosine was elevated in human diabetics further spurred the research. Now he is ready to take research insights back into people.
“This will be tested in small human clinical trials,” Dr. Fisher said. “Our team will augment tyrosine levels in study participants for a short period and observe whether this changes the ability of the body to respond to insulin, which is a key hormone involved in controlling blood sugar levels. This will not be detrimental to participants, as the increase will be transient and well below the level of what is clinically relevant.”
As a postdoctoral fellow at the University of California, San Francisco, Dr. Fisher found that increasing the levels of tyrosine in roundworms promoted their longevity. Worms with mutations of certain genes lived 10 percent to 20 percent longer. One combination of genetic mutations produced an almost 60 percent increase in life span.
“In both humans and worms, the effect is due to an inhibition of insulin signaling,” Dr. Fisher said. “Interfering with this pathway produces longevity in worms, whereas in people it leads to insulin resistance and an elevated risk of developing diabetes.”
Tyrosine has been studied for decades, but few if any research groups have made the connection between tyrosine and diabetes.
“The key concept that comes out of our latest paper is, rather than amino acids being only building blocks in our bodies, they are detected and produce changes in physiology, including potentially undesirable ones such as diabetes in humans,” Dr. Fisher said.
Dr. Fisher, associate professor of medicine in the School of Medicine, joined the Health Science Center in 2013 from the University of Pittsburgh School of Medicine. He earned Ph.D. and M.D. degrees at the Weill Cornell Medical College in New York, and completed residency and a geriatrics fellowship at the University of California, San Francisco.
“It was attractive to me to move my lab here,” he said. “The number and diversity of people studying the basic biology of aging here is very impressive.”
Funding for the project is from the National Institute on Aging, the National Institute of Environmental Health Sciences, and the Geriatric Research, Education and Clinical Center of the South Texas Veterans Health Care System.
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