A new study on mice has found that the lack of an enzyme that contributes to Alzheimer's disease can result in the development of a number of schizophrenia-like behaviours.
A new study on mice has found that the lack of an enzyme that contributes to Alzheimer's disease can result in the development of a number of schizophrenia-like behaviours.
Neuroscientists at Johns Hopkins say that the finding raises the possibility that this enzyme may participate in the development of schizophrenia and related psychiatric disorders and therefore may provide a new target for developing therapies.The BACE1 enzyme, for beta-site amyloid precursor protein cleaving enzyme, generates the amyloid proteins that lead to Alzheimer's disease.
The research team years ago suspected that removing BACE1 might prevent Alzheimer.
"We knew at the time that in addition to amyloid precursor protein, BACE1 interacts with other proteins but we didn't know how those interactions might affect behavior," says Alena Savonenko, M.D., Ph.D., an assistant professor in neuropathology at Hopkins.
They describe how mice lacking the BACE1 enzyme show deficits in social recognition among other behaviours classically linked to schizophrenia.
A normal mouse, when introduced to another mouse, shows a lot of interest the first time they meet. If the mice are separated then reintroduced, their interest drops because they remember having met before, a phenomenon the researchers call habituation. If they then introduce a completely different mouse, interest piques again at the newbie.
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"These mice were totally disinterested, normal mice just don't behave like this," says Savonenko.
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Because schizophrenia is a disorder likely caused by many different factors, Savonenko explains that BACE1 might contribute to an increased risk of schizophrenia in certain patients and the BACE1 mice will be a useful animal model.
"We never thought we would see one mouse that closely mimics so many of the clinical features of schizophrenia. This could be a really useful model to study and understand the molecular contributions to the disease," says Savonenko.
Source-ANI
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