Frontal cortex BDNF levels correlate with working memory in an animal model of Down syndrome

• Published in: Behavioural brain research Vol. 139; no. 1; pp. 47 - 57
• Main Authors: Bimonte-Nelson, Heather A, Hunter, Christopher L, Nelson, Matthew E, Granholm, Ann-Charlotte E
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 17.02.2003
• Subjects: Animals; Behavior, Animal; Brain Chemistry - genetics; Brain-derived neurotrophic factor; Brain-Derived Neurotrophic Factor - analysis; Cerebral Cortex - chemistry; Disease Models, Animal; Down syndrome; Down Syndrome - physiopathology; Escape Reaction; Frontal Lobe - chemistry; Male; Maze Learning - physiology; Memory Disorders - genetics; Memory Disorders - physiopathology; Memory, Short-Term - physiology; Mice; Mice, Inbred Strains; Nerve Growth Factor - analysis; NGF; Radial-arm maze; Reference memory; Ts65Dn; Working memory; Reference memory; Brain-derived neurotrophic factor; Radial-arm maze; Down syndrome; Working memory; Ts65Dn; NGF
• ISSN: 0166-4328; 1872-7549
• DOI: 10.1016/S0166-4328(02)00082-7

Individuals with Down syndrome (DS) develop most neuropathological hallmarks of Alzheimer's disease early in life, including loss of cholinergic markers in the basal forebrain. Ts65Dn mice, an animal model of DS, perform poorly on tasks requiring spatial memory and also exhibit basal forebrain pathology beginning around 6 months of age. We evaluated memory as well as brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) protein levels in basal forebrain, frontal cortex, hippocampus, and striatum in Ts65Dn mice at the age when cholinergic degeneration is first observed, and compared values to normosomic controls. Six-month-old Ts65Dn mice exhibited impairments in working and reference memory as assessed on a water radial-arm maze. The working memory deficit was related to the inability of Ts65Dn mice to successfully sustain performance as the working memory load increased. Coupled with cognitive performance deficiencies, Ts65Dn mice also exhibited lower frontal cortex BDNF protein levels than controls. Further, BDNF levels were negatively correlated with working memory errors during the latter portion of testing in Ts65Dn mice, thereby suggesting that lower BDNF protein levels in the frontal cortex may be associated with the observed working memory impairment.