Anti- organ rejection medication or immunosuppressants could be used to slow down the progression of early-stage Alzheimer's disease, finds a new study. The findings of this study are published in the Journal of Science Signaling.
Alzheimer's disease, a progressive form of dementia, affects an estimated 5 million people in the U.S. - a number expected to nearly triple by 2050. Although Alzheimer's usually strikes after age 65, changes in the brain can begin years before symptoms appear, according to the Centers for Disease Control and Prevention.
The researchers studied how the connections between neurons - synapses - are lost early in the course of the disease. This loss likely causes the behavioral and memory changes that occur as the disease develops, said Dr. James Malter, Chairman of Pathology and corresponding author of the Science Signaling study. The study's first authors are Drs. Nancy Stallings and Melissa O'Neal, both Instructors of Pathology.
"We found that beta-amyloid, which is overproduced in the brains of most people with Alzheimer's, turns on a protein called calcineurin. Activated calcineurin then causes the inhibition of a second protein called Pin1, leading to loss of dendritic spines and synapses," said Dr. Malter, who holds The Senator Betty and Dr. Andy Andujar Distinguished Chairmanship of Pathology.
In experiments in neurons and in genetically engineered mice unable to produce Pin1, the researchers were able to duplicate the loss of dendritic spines and synapses even in the absence of exposure to beta-amyloid, demonstrating a critical role for Pin1 in this process.
"In additional experiments, we showed that synapses could be rescued if the neurons received extra Pin1 or were exposed to FK506 - a drug that blocks calcineurin and is currently approved by the Food and Drug Administration [FDA] for the prevention of solid organ transplant rejection. The oldest drug in this class, cyclosporin, has been used since 1983," Dr. Malter said.
Intriguingly, a recent study from UT Medical Branch at Galveston showed that patients who receive FK506 for long-term immunosuppression following transplant, developed Alzheimer's less frequently than expected.
"As an FDA-approved drug, we propose that FK506 be evaluated through clinical trials as a treatment for early-stage Alzheimer's disease," Dr. Malter said. "Anti-rejection drugs given to organ transplant recipients work by suppressing the immune system and, as a result, can increase the risk of infection. Our experiments suggest that lower doses of FK506 that are needed to block transplant rejection may be able to protect neurons from beta-amyloid without significant immunosuppression."
UTSW co-authors include Dr. Ege Kavalali, Professor of Neuroscience and Physiology; Dr. Ilya Bezprozvanny, Professor of Physiology; and Dr. Jie Hu, a research scientist in Pathology. Dr. Bezprozvanny holds the Carl J. and Hortense M. Thomsen Chair in Alzheimer's Disease Research. Dr. Kavalali, an Effie Marie Cain Scholar in Medical Research, holds the Rosewood Corporation Chair in Biomedical Science.
The study was supported by the Senator Betty and Dr. Andy Andujar Endowment and by the National Institutes of Health.