Literature DB >> 22982727

Variations in the temporal pattern of perforant pathway stimulation control the activity in the mesolimbic pathway.

Cornelia Helbing1, Grit Werner, Frank Angenstein.   

Abstract

Signal processing in the hippocampal formation and resultant signal propagation to cortical and subcortical structures during high frequency stimulation (i.e. 100 Hz) of the perforant pathway was studied in medetomidine anesthetized rats by functional magnetic resonance imaging (fMRI) and electrophysiological recordings. The perforant pathway was stimulated with bursts of 20 pulses, one burst per second, or with continuously applied pulses. The stimulation duration was adjusted to 8 s (short) or 30 s (long). In general, extending the stimulation duration only caused a local spreading of the fMRI response, but no changes in the magnitude of the fMRI response. This was in agreement with the electrophysiological responses, which also remained unchanged. In contrast, increasing the number of pulses in one stimulus train (i.e. changing from burst to continuous stimulation), caused both spreading and an increase in local fMRI responses that were accompanied by an altered neuronal response pattern. Continuous stimulation also triggered additional fMRI responses in the septum, nucleus accumbens, anterior cingulate cortex/medial prefrontal cortex, and ventral tegmental area/substantia nigra. The appearance of fMRI responses outside the hippocampal formation required at least 3 consecutive stimulation trains, characterized by region specific hemodynamic response functions. Thus, once triggered, continuous stimulation caused a sequential appearance in fMRI responses starting in the hippocampal formation, followed by signal changes in the ventral tegmental area/substantia nigra and anterior cingulate cortex/medial prefrontal cortex and eventually in the nucleus accumbens. These results indicate that high frequency stimulation of the hippocampal formation can activate the mesolimbic pathway, provided that repetitive stimulations are applied.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22982727     DOI: 10.1016/j.neuroimage.2012.09.001

Source DB:  PubMed          Journal:  Neuroimage        ISSN: 1053-8119            Impact factor:   6.556


  7 in total

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2.  Fornix deep brain stimulation circuit effect is dependent on major excitatory transmission via the nucleus accumbens.

Authors:  Erika K Ross; Joo Pyung Kim; Megan L Settell; Seong Rok Han; Charles D Blaha; Hoon-Ki Min; Kendall H Lee
Journal:  Neuroimage       Date:  2016-01-11       Impact factor: 6.556

3.  From unspecific to adjusted, how the BOLD response in the rat hippocampus develops during consecutive stimulations.

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Authors:  Andrew J Weitz; Zhongnan Fang; Hyun Joo Lee; Robert S Fisher; Wesley C Smith; ManKin Choy; Jia Liu; Peter Lin; Matthew Rosenberg; Jin Hyung Lee
Journal:  Neuroimage       Date:  2014-10-22       Impact factor: 6.556

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Review 6.  A guide to using functional magnetic resonance imaging to study Alzheimer's disease in animal models.

Authors:  Mazen Asaad; Jin Hyung Lee
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7.  Electrical Stimulation of the Lateral Entorhinal Cortex Causes a Frequency-Specific BOLD Response Pattern in the Rat Brain.

Authors:  Karla Krautwald; Liv Mahnke; Frank Angenstein
Journal:  Front Neurosci       Date:  2019-05-24       Impact factor: 4.677

  7 in total

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