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Background: Over the past decades, great effort has been spending on research of Alzheimer disease (AD), many scientists
focus on the predictors of AD. Spatial memory deficits have been recognized in the early stages of AD, but have been studied
less[1]. The previous studies have shown a cloes relationship between spatial memory and postrhinal cortex (POR)[2], but
which projection from POR impacts on spatial memory is still to be found out. So with the help of optogenetics, we can do
further research.
Purpose: To find out which projection from POR impacts on spatial memory.
Methods: Using optogenetics to control neuron activity, using novel object recognition to test the spatial memory performance
of mice, using immunofluorescence of c-Fos to search the terminal cortex, choose 3-month C57BL/6 mouse.
Results: In novel object recognition testing, when inhibiting glutamatergic neurons activity of POR in both study and
recognition phase, the spatial memory level of experimental group is lower than matched group (t=2.38, P<0.05); when
inhibiting glutamatergic neurons activity of POR only in study phase, there is no significant differences in both group (t=7.68,
P>0.05); when inhibiting glutamatergic neurons activity of POR only in recognition phase, the spatial memory level of
experimental group is lower than matched group (t=3.23, P<0.05). 1.5h after optical stimulation, immunofluorescence of c-Fos
shows that c-Fos positive neurons of ventral lateral orbitofrantal cortex (OFC) in experimental group is less than matched
group (t=2.87, P<0.05).
Conclusion: The projection from POR to OFC impacts on the recognition phase of spatial memory via glutamatergic neuron.