Combined adult neurogenesis and BDNF mimic exercise effects on cognition in an Alzheimer’s mouse model

Se Hoon Choi(Harvard University), Enjana Bylykbashi(Harvard University), Zena K. Chatila(Harvard University), Star W. Lee(Salk Institute for Biological Studies), Benjamin Pulli(Massachusetts General Hospital), Gregory D. Clemenson(Salk Institute for Biological Studies), Eunhee Kim(Harvard University), Alexander Rompala(Harvard University), Mary K. Oram(Harvard University), Caroline Asselin(Harvard University), Jenna Aronson(Harvard University), Can Zhang(Harvard University), Sean Miller(Harvard University), Andrea N. Lesinski(Harvard University), John W. Chen(Massachusetts General Hospital), Doo Yeon Kim(Harvard University), Henriette van Praag(Florida Atlantic University), Bruce M. Spiegelman(Dana-Farber Cancer Institute), Fred H. Gage(Salk Institute for Biological Studies), Rudolph E. Tanzi(Harvard University)
Science
September 6, 2018
Cited by 813Open Access
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Abstract

Adult hippocampal neurogenesis (AHN) is impaired before the onset of Alzheimer's disease (AD) pathology. We found that exercise provided cognitive benefit to 5×FAD mice, a mouse model of AD, by inducing AHN and elevating levels of brain-derived neurotrophic factor (BDNF). Neither stimulation of AHN alone, nor exercise, in the absence of increased AHN, ameliorated cognition. We successfully mimicked the beneficial effects of exercise on AD mice by genetically and pharmacologically inducing AHN in combination with elevating BDNF levels. Suppressing AHN later led to worsened cognitive performance and loss of preexisting dentate neurons. Thus, pharmacological mimetics of exercise, enhancing AHN and elevating BDNF levels, may improve cognition in AD. Furthermore, applied at early stages of AD, these mimetics may protect against subsequent neuronal cell death.


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