Effect of Chronic Morphine Consumption on Synaptic Plasticity of Rat’s Hippocampus: A Transmission Electron Microscopy Study

It is well known that the synapses undergo some changes in the brain during the course of normal life and under certain pathological or experimental circumstances. One of the main goals of numerous researchers has been to find the reasons for these structural changes. In the present study, we invest...

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Main Authors: Mohammad Hassan Heidari, Abdollah Amini, Zohreh Bahrami, Ali Shahriari, Abolfazle Movafag, Reihane Heidari
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Neurology Research International
Online Access:http://dx.doi.org/10.1155/2013/290414
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author Mohammad Hassan Heidari
Abdollah Amini
Zohreh Bahrami
Ali Shahriari
Abolfazle Movafag
Reihane Heidari
author_facet Mohammad Hassan Heidari
Abdollah Amini
Zohreh Bahrami
Ali Shahriari
Abolfazle Movafag
Reihane Heidari
author_sort Mohammad Hassan Heidari
collection DOAJ
description It is well known that the synapses undergo some changes in the brain during the course of normal life and under certain pathological or experimental circumstances. One of the main goals of numerous researchers has been to find the reasons for these structural changes. In the present study, we investigated the effects of chronic morphine consumption on synaptic plasticity, postsynaptic density thickness, and synaptic curvatures of hippocampus CA1 area of rats. So for reaching these goals, 24 N-Mary male rats were randomly divided into three groups, morphine (n=8), placebo (n=8), and control (n=8) groups. In the morphine group, complex of morphine (0.1, 0.2, 0.3, and 0.4) mg/mL and in the placebo (sucrose) group complex of sucrose (% 0.3) were used for 21 days. After the end of drug treatment the animals were scarified and perfused intracardinally and finally the CA1 hippocampal samples were taken for ultrastructural studies, and then the obtained data were analyzed by SPSS and one-way analysis of variance. Our data indicated that synaptic numbers per nm3 change significantly in morphine group compared to the other two groups (placebo and control) (P<0.001) and also statistical analysis revealed a significant difference between groups in terms of thickness of postsynaptic density (P<0.001) and synaptic curvature (P<0.007). It seems that morphine dependence in rats plays a main role in the ultrastructural changes of hippocampus.
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spelling doaj-art-fcc4281135ab40fb87cebe5d311d8c5c2025-02-03T05:58:16ZengWileyNeurology Research International2090-18522090-18602013-01-01201310.1155/2013/290414290414Effect of Chronic Morphine Consumption on Synaptic Plasticity of Rat’s Hippocampus: A Transmission Electron Microscopy StudyMohammad Hassan Heidari0Abdollah Amini1Zohreh Bahrami2Ali Shahriari3Abolfazle Movafag4Reihane Heidari5Department of Biology and Anatomical Sciences, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, IranDepartment of Biology and Anatomical Sciences, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, IranDepartment of Biology and Anatomical Sciences, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, IranDepartment of Anesthesiology, Roozbeh Hospital, Tehran University of Medical Sciences, P.O. Box 1417653761, Tehran, IranDepartment of Genetic Science, Medical Faculty, Shahid Beheshti University of Medical Sciences, Tehran, IranDepartment of Anesthesiology, Roozbeh Hospital, Tehran University of Medical Sciences, P.O. Box 1417653761, Tehran, IranIt is well known that the synapses undergo some changes in the brain during the course of normal life and under certain pathological or experimental circumstances. One of the main goals of numerous researchers has been to find the reasons for these structural changes. In the present study, we investigated the effects of chronic morphine consumption on synaptic plasticity, postsynaptic density thickness, and synaptic curvatures of hippocampus CA1 area of rats. So for reaching these goals, 24 N-Mary male rats were randomly divided into three groups, morphine (n=8), placebo (n=8), and control (n=8) groups. In the morphine group, complex of morphine (0.1, 0.2, 0.3, and 0.4) mg/mL and in the placebo (sucrose) group complex of sucrose (% 0.3) were used for 21 days. After the end of drug treatment the animals were scarified and perfused intracardinally and finally the CA1 hippocampal samples were taken for ultrastructural studies, and then the obtained data were analyzed by SPSS and one-way analysis of variance. Our data indicated that synaptic numbers per nm3 change significantly in morphine group compared to the other two groups (placebo and control) (P<0.001) and also statistical analysis revealed a significant difference between groups in terms of thickness of postsynaptic density (P<0.001) and synaptic curvature (P<0.007). It seems that morphine dependence in rats plays a main role in the ultrastructural changes of hippocampus.http://dx.doi.org/10.1155/2013/290414
spellingShingle Mohammad Hassan Heidari
Abdollah Amini
Zohreh Bahrami
Ali Shahriari
Abolfazle Movafag
Reihane Heidari
Effect of Chronic Morphine Consumption on Synaptic Plasticity of Rat’s Hippocampus: A Transmission Electron Microscopy Study
Neurology Research International
title Effect of Chronic Morphine Consumption on Synaptic Plasticity of Rat’s Hippocampus: A Transmission Electron Microscopy Study
title_full Effect of Chronic Morphine Consumption on Synaptic Plasticity of Rat’s Hippocampus: A Transmission Electron Microscopy Study
title_fullStr Effect of Chronic Morphine Consumption on Synaptic Plasticity of Rat’s Hippocampus: A Transmission Electron Microscopy Study
title_full_unstemmed Effect of Chronic Morphine Consumption on Synaptic Plasticity of Rat’s Hippocampus: A Transmission Electron Microscopy Study
title_short Effect of Chronic Morphine Consumption on Synaptic Plasticity of Rat’s Hippocampus: A Transmission Electron Microscopy Study
title_sort effect of chronic morphine consumption on synaptic plasticity of rat s hippocampus a transmission electron microscopy study
url http://dx.doi.org/10.1155/2013/290414
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