scholarly journals Hippocampal deep brain stimulation reverses physiological and behavioural deficits in a rodent model of schizophrenia

2013 ◽  
Vol 16 (6) ◽  
pp. 1331-1339 ◽  
Author(s):  
Stephanie M. Perez ◽  
Amiksha Shah ◽  
Amber Asher ◽  
Daniel J. Lodge

Abstract Subcortical dopamine system dysregulation has been suggested to underlie the positive symptoms of schizophrenia. Recent preclinical investigations and human imaging studies have proposed that the augmented dopamine system function observed in schizophrenia patients may be secondary to aberrant hippocampal activity. Thus, we posit that the hippocampus represents a novel therapeutic target for the treatment of schizophrenia. Here we provide evidence of the effectiveness of a unique approach aimed at decreasing hippocampal function in a rodent model of schizophrenia. Specifically, in a rodent model of schizophrenia, we demonstrate that ventral hippocampal (vHipp) deep brain stimulation (DBS) can normalize aberrant dopamine neuron activity and behaviours associated with positive symptoms. In addition, we provide evidence that this approach may also be effective in restoring deficits in cognitive function, often left unaltered by conventional antipsychotic medications. Therefore, we have provided initial preclinical evidence demonstrating the feasibility of hippocampal DBS as a potential novel approach for the treatment of schizophrenia.

2018 ◽  
Vol 33 (4) ◽  
pp. 652-654 ◽  
Author(s):  
Gian Pal ◽  
Bichun Ouyang ◽  
Leo Verhagen ◽  
Geidy Serrano ◽  
Holly A. Shill ◽  
...  

2015 ◽  
Vol 233 (11) ◽  
pp. 3073-3085 ◽  
Author(s):  
Luciano L. Furlanetti ◽  
Volker A. Coenen ◽  
Iñigo A. Aranda ◽  
Máté D. Döbrössy

2020 ◽  
Vol 9 (1) ◽  
Author(s):  
Ti-Fei Yuan ◽  
Wei-Guang Li ◽  
Chencheng Zhang ◽  
Hongjiang Wei ◽  
Suya Sun ◽  
...  

AbstractDeficits in synaptic transmission and plasticity are thought to contribute to the pathophysiology of Alzheimer’s disease (AD) and Parkinson’s disease (PD). Several brain stimulation techniques are currently available to assess or modulate human neuroplasticity, which could offer clinically useful interventions as well as quantitative diagnostic and prognostic biomarkers. In this review, we discuss several brain stimulation techniques, with a special emphasis on transcranial magnetic stimulation and deep brain stimulation (DBS), and review the results of clinical studies that applied these techniques to examine or modulate impaired neuroplasticity at the local and network levels in patients with AD or PD. The impaired neuroplasticity can be detected in patients at the earlier and later stages of both neurodegenerative diseases. However, current brain stimulation techniques, with a notable exception of DBS for PD treatment, cannot serve as adequate clinical tools to assist in the diagnosis, treatment, or prognosis of individual patients with AD or PD. Targeting the impaired neuroplasticity with improved brain stimulation techniques could offer a powerful novel approach for the treatment of AD and PD.


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