Reduction of the small synaptic vesicle protein synaptophysin but not the large dense core chromogranins in the left thalamus of subjects with schizophrenia

Citation
M. Landen et al., Reduction of the small synaptic vesicle protein synaptophysin but not the large dense core chromogranins in the left thalamus of subjects with schizophrenia, BIOL PSYCHI, 46(12), 1999, pp. 1698-1702
Citations number
45
Categorie Soggetti
Neurosciences & Behavoir
Journal title
BIOLOGICAL PSYCHIATRY
ISSN journal
00063223 → ACNP
Volume
46
Issue
12
Year of publication
1999
Pages
1698 - 1702
Database
ISI
SICI code
0006-3223(199912)46:12<1698:ROTSSV>2.0.ZU;2-X
Abstract
Background: It has been hypothesized that a lesion in the neuronal circuits of thalamus might contribute to the symptoms in schizophrenia. It has also been suggested that impaired synaptic transmission is an important compone nt of the pathophysiology of schizophrenia. In the present study we assess the synaptic integrity of thalamus by means of examining the protein levels of: (I) synaptophysin, a membrane bound protein of small synaptic vesicles , and (2) chromogranins, a family of soluble secretory proteins stored and released from the secretory large dense-core vesicles. Methods: The brains of 9 patients with schizophrenia and 9 age-matched cont rol subjects were studied. The levels of synaptophysin and chromogranins we re measured by radioimmunoassays. Results: The amount of synaptophysin in the left thalamus was significantly decreased (p = .036) in the schizophrenic group (2655 +/- 605 nmol synapth ophysin/mg total protein) compared to the control group (3248 +/- 827 nmol synaptophysin/mg total protein). There were no differences between the grou ps in the levels of chromogranins, nor in the levels of synaptophysin of th e right thalamus, Conclusions: These findings indicate defect synaptic function in the left r halamrrs of patients with schizophrenia. This may be the cause of a reducti on of synaptic terminals or a defect limited to eel-rain structures of the synapse, namely the small presynaptic vesicles. Biol Psychiatry 1999;46:169 8-1702 (C) 1999 Society of Biological Psychiatry.