Literature DB >> 23507376

Perforant pathway stimulation as a conditioned stimulus for active avoidance learning triggers BOLD responses in various target regions of the hippocampus: a combined fMRI and electrophysiological study.

Frank Angenstein1, Karla Krautwald2, Wolfram Wetzel3, Henning Scheich4.   

Abstract

Functional magnetic resonance imaging and electrophysiology were combined to monitor blood oxygen level dependent (BOLD) signals in the entire rat brain and neuronal activities in the dentate gyrus during electrical stimulation of the right perforant pathway. In naïve, medetomidine sedated animals, stimulation of the fiber bundle with 15 trains (i.e. 8 bursts of 20 pulses given with 10 ms intervals, one burst per second, pulse width 0.2 ms) generated significant BOLD responses in the right hippocampal formation and the left entorhinal cortex. The stimulation condition also caused changes in the synaptic efficacy of perforant pathway granular cell synapses that lasted for at least one day. Rerun of the same experiment one day later resulted in a significantly increased electrophysiological response in the dentate gyrus and an increase of the BOLD response in the entire hippocampal formation. Consequently, long-lasting changes in synaptic efficacy go along with changes in the generated BOLD response. Additional electrical stimulations of the perforant pathway in the awake animal between the two fMRI experiments caused in the second fMRI measurement an increased BOLD response in the hippocampal formation and an appearance of significant BOLD responses in target regions of the hippocampus, such as the septum, nucleus accumbens (NAcc), and anterior cingulate cortex/medial prefrontal cortex/motor cortex (ACC/mPFC/MC) regions. Consequently, the efficacy of signal processing in and propagation through the hippocampus can be monitored by variations of the BOLD response in target regions of the hippocampus. Using the electrical perforant pathway stimulations as conditioned stimulus for an active avoidance task (shuttle box) caused a further spreading of the BOLD response in the hippocampus formation, septum and ACC/mPFC/MC but not in the NAcc. In addition, the magnitude of the BOLD response in the trained animals was further increased in the right and left hippocampus and the ACC/mPFC/MC region but not in the septum. These results demonstrate that in addition to general stimulus parameter the behavioral relevance of the stimulus controls the quality of the generated BOLD response.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23507376     DOI: 10.1016/j.neuroimage.2013.03.007

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


  6 in total

1.  The role of the mesolimbic dopamine system in the formation of blood-oxygen-level dependent responses in the medial prefrontal/anterior cingulate cortex during high-frequency stimulation of the rat perforant pathway.

Authors:  Cornelia Helbing; Marta Brocka; Thomas Scherf; Michael T Lippert; Frank Angenstein
Journal:  J Cereb Blood Flow Metab       Date:  2015-11-05       Impact factor: 6.200

2.  Functional MRI during Hippocampal Deep Brain Stimulation in the Healthy Rat Brain.

Authors:  Nathalie Van Den Berge; Christian Vanhove; Benedicte Descamps; Ine Dauwe; Pieter van Mierlo; Kristl Vonck; Vincent Keereman; Robrecht Raedt; Paul Boon; Roel Van Holen
Journal:  PLoS One       Date:  2015-07-20       Impact factor: 3.240

3.  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

Review 4.  A circuit view of deep brain stimulation in Alzheimer's disease and the possible mechanisms.

Authors:  Danfang Yu; Huanhuan Yan; Jun Zhou; Xiaodan Yang; Youming Lu; Yunyun Han
Journal:  Mol Neurodegener       Date:  2019-08-08       Impact factor: 14.195

5.  From nociception to pain perception, possible implications of astrocytes.

Authors:  Frida Higinio-Rodríguez; Angélica Rivera-Villaseñor; Isnarhazni Calero-Vargas; Mónica López-Hidalgo
Journal:  Front Cell Neurosci       Date:  2022-09-07       Impact factor: 6.147

Review 6.  Preclinical Magnetic Resonance Imaging and Spectroscopy Studies of Memory, Aging, and Cognitive Decline.

Authors:  Marcelo Febo; Thomas C Foster
Journal:  Front Aging Neurosci       Date:  2016-06-29       Impact factor: 5.750

  6 in total

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