In this study, Andersen and her team dosed the genetically-engineered mice with an amount of lithium equivalent to about a quarter of what humans receive for the treatment of psychiatric diseases. Treatment began when the mice reached late middle-age, the human equivalent of about 60, which is the average age of onset of Parkinson’s in humans. “We clearly saw a prevention of the motor difficulties we would expect to see in the animals,” said Andersen. “The treatment also protected the area of the brain that is normally damaged by Parkinson’s.”

Andersen says the mechanistic action of lithium is not entirely clear. In the treated animals researchers saw a reduction of inflammation in astrocytes and microglia, cells that play “housekeeping” roles in the brain. “Our findings suggest that low dose lithium could be an anti-inflammatory,” said Andersen. “This gives us another avenue to study its effects in humans.”

There is currently no cure for Parkinson’s, which is characterized by tremor, slowness of spontaneous movement, rigidity and postural instability. As the disease progresses, patients often suffer from cognitive decline. Existing treatments can help ease symptoms, but over time the drugs themselves can cause debilitating side effects. “Developing new treatments for Parkinson’s requires extensive preclinical testing and expensive human trials,” said Andersen. “In lithium we have a medication that provides neuroprotection and is already approved for clinical use. It is an ideal candidate for therapy.”

“While it would be premature for PD patients to take lithium supplements based on these data, this study is sufficiently promising to warrant further study,” said David K. Simon, MD, PhD, Associate Professor of Neurology at Harvard Medical School in Boston. Simon chairs the Scientific Review Committee for the Parkinson’s Study Group, a not-for-profit network of Parkinson’s Centers. “While questions remain about optimal doses for human studies and we still need sufficient safety and efficacy data in PD patients, I do agree that Dr. Andersen’s work along with other data, make a strong argument for further studies, potentially even early phase clinical studies of low-dose lithium as a disease modifying agent in PD.”

Citation: Lithium prevents parkinsonian behavioral and striatal phenotype in an aged parkin mutant transgenic mouse model

This work was supported by grants from National Institutes of Health: AG025901 and T32 Fellowship AG000266.

Other Buck Institute contributors include: Christopher A. Lieu, Colleen M. Dewey, Shankar J. Chinta, Anand Rane, Subramanian Rajagopalan, Sean Batir, and Yong-Hwan Kim

About the Buck Institute for Research on Aging

The Buck Institute is the U.S.’s first independent research organization devoted to Geroscience – focused on the connection between normal aging and chronic disease. Based in Novato, CA, The Buck is dedicated to extending “Healthspan”, the healthy years of human life and does so utilizing a unique interdisciplinary approach involving laboratories studying the mechanisms of aging and those focused on specific diseases. Buck scientists strive to discover new ways of detecting, preventing and treating age-related diseases such as Alzheimer’s and Parkinson’s, cancer, cardiovascular disease, macular degeneration, osteoporosis, diabetes and stroke. In their collaborative research, they are supported by the most recent developments in genomics, proteomics, bioinformatics and stem cell technologies. For more information: