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Morphofunctional Correlation of Excitatory and Depressor Synaptic Processes in Hippocampus, Amygdala and Basal Meynert Nucleus Neurons in Dynamics of Development of Alzheimer's Disease Model Induced by Aand#946;25-35| Abstract
ISSN: 2161-0460

Journal of Alzheimers Disease & Parkinsonism
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  • Research Article   
  • J Alzheimers Dis Parkinsonism 2017, Vol 7(6): 391
  • DOI: 10.4172/2161-0460.1000391

Morphofunctional Correlation of Excitatory and Depressor Synaptic Processes in Hippocampus, Amygdala and Basal Meynert Nucleus Neurons in Dynamics of Development of Alzheimer's Disease Model Induced by Aβ25-35

Sarkissian JS1, Minasyan AL2, Sahakyan KT2, Danielyan MH1, Stepanyan HY1*, Poghossyan MV1 and Sarkisian VH1
1L.Orbeli Institute of Physiology, National Academy of Sciences of Armenia, , Armenia
2Yerevan State Medical University after M. Heratsi, , Yerevan, Armenia, Armenia
*Corresponding Author : Stepanyan HY, Orbeli Institute of Physiology, NAS RA, 22 Orbeli Bross St., 0028Yerevan, Armenia, Tel: +374 10273861, Fax: +374 10 272247, Email: [email protected]

Received Date: Sep 28, 2017 / Accepted Date: Oct 18, 2017 / Published Date: Oct 25, 2017

Abstract

Objective: Compensatory mechanisms are responsible for the clinical signs of suppression of neurodegeneration. Intervention into their mechanisms on an example of the ratio of excitatory and depressor synaptic responses will contribute to the development of therapeutic strategies.
Methods: After 12-28 weeks (w) of experiment on the model of Alzheimer’s disease (AD), an activity of single neurons of hippocampus (H), Amygdala (Am) and, nucleus basalis of Meynert (NBM) to high frequency stimulation (HFS) of entorhinal cortex (EC) was recorded. The high frequency stimulation of H resulted in an activity of single neurons of the Am and NBM. By means of on-line selection and special mathematical analysis, tetanic potentiation (TP) and depression (TD) with further combination into posttetanic uni and multidirectional sequences, were revealed. In morpho- and histochemical study, the method of revelation of Сa2+- dependent phosphorylation was used.
Results: After 12 weeks of experiment on the model of AD, a heavy TD of NBM and Аm neurons to HFS of H, as well as a weak (TD) in H and NBM neurons to HFS of EC were found. TP occurred by the activation of ЕС in the H (TP PTP) and in Am (TP PTD) neurons, equal to and above the norm in neurons of Am to HFS of H. In the neurons of NBM to HFS of EC, the weakest excitation to HFS of H was detected. In the neurons H to HFS of EC, Am and NBM to HFS of H, after 13-28 weeks, TD and tetanic excitation in all cases were low, which indicating on depletion of compensatory opportunities. Morpho- and histo-chemical changes of H, Am and NBM neurons on the model of AD were characterized by total tendency to structural-metabolic dysfunctions, with distortion of forms, central chromatolysis, presence of light ectopic nucleus with increased nucleolus, change reaction of neurofibrills, lack of reaction processes, accumulation of hyper phosphorylated entities and, presence of spaces with the lack of cellular reaction.
Conclusion: The absence of expressed depression, presupposed by us as a protector in the present study, makes it necessary to involve pharmacological interventions with a view to its strengthening, and therefore is the subject of the next reports. Electrophysiological data have been confirmed morphologically.

Keywords: Alzheimer’s disease; Hippocampus; Rostral amygdalopiriform area; Basal nucleus of meynert; Single spike activity; Acid phosphatase

Citation: Sarkissian JS, Minasyan AL, Sahakyan KT, Danielyan MH, Stepanyan HY, et al. (2017) Morphofunctional Correlation of Excitatory and Depressor Synaptic Processes in Hippocampus, Amygdala and Basal Meynert Nucleus Neurons in Dynamics of Development of Alzheimer’s Disease Model Induced by Aβ25-35. J Alzheimers Dis Parkinsonism 7: 391. Doi: 10.4172/2161-0460.1000391

Copyright: ©2017 Sarkissian JS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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