A molecule critical to the development and plasticity of nerve cells called brain-derived neurotrophic factor (BDNF) is severely lacking in brainstem neurons in mutations leading to Rett syndrome. This is the finding by Researchers at Oregon Health & Science University (http://www.ohsu.edu).
Rett syndrome is a neurological developmental disorder. The finding has implications for the treatment of neurological disorders, including Rett syndrome that affects one in 10,000 baby girls.
The new discovery is published online in Neuroscience (http://www.sciencedirect.com/science/article/pii/S0306452212000395?v=s5) and is expected in the print issue of Neuroscience in March.
According to the National Institutes of Health, Rett syndrome is estimated to affect one in every 10,000 to 15,000 live births and almost exclusively girls because it is caused by an X-linked gene mutation. In addition to severe problems with motor function, other symptoms of Rett syndrome may include breathing difficulties while awake.
"The new finding, coupled with our previously published data that show BDNF is involved in normal maturation of neuronal pathways controlling cardiorespiratory function, could play a significant role in the development of a treatment for Rett syndrome," said Agnieszka Balkowiec, M.D., Ph.D., principal investigator and associate professor of integrative biosciences in the OHSU School of Dentistry; and adjunct assistant professor of physiology and pharmacology in the OHSU School of Medicine. To conduct this research, Balkowiec partnered with John M. Bissonnette, M.D., professor of obstetrics and gynecology, and cell and developmental biology in the OHSU School of Medicine.