Schizophrenia is a unique disorder where there are many
possible ways of looking at the pathology and circuitry of it. Both articles had unique ways of examining
the aspects of schizophrenia. I enjoyed Moore et al.’s approach to examining
schizophrenia at a developmental point, since changes in the brain could occur
before birth, even though schizophrenia can be diagnosed after puberty. I would
definitely be interested in reading more about these models that can be used
for early detection of behavioral abnormalities. I also thought that adding the analysis of
ataxia was interesting to use for behavioral testing. It would be cool to look
at ataxia models by observing cerebellar circuits in schizophrenia patients.
Kellendonk et al.
take an approach step by step observing the overexpression of D2
receptors in the striatum, which was a lot for me to understand. However, each
experiment only helped me validate the use of D2 receptors, even though there
was not a lot of significance in the experiments performed. These models were
sufficient with getting the idea that D2 overexpression does not affect
cognitive deficits as much and that even D1 receptors in the PFC are an
important factor in working memory. Perhaps looking at research with just D1
receptors could help validate more things. However, as the authors mentioned in
this paper, rodent model tend to cause some limitations when they are being
examined. Looking at a clinical view, it’s easier to examine other positive
symptoms, like hallucinations and delusions, in human models. It would be
interesting to examine research done for bipolar disorder, since both
schizophrenia and bipolar disorder to exhibit some similar circuitry with GABA
neurons.
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