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Developmental effect of light deprivation on synaptic plasticity of rats’ hippocampus: implications for melatonin

OBJECTIVE(S): There are few reports have demonstrated the effect of a change-in-light experience on the structure and function of hippocampus. A change-in-light experience also affects the circadian pattern of melatonin secretion. This study aimed to investigate developmental effect of exogenous mel...

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Autores principales: Talaei, Sayyed Alireza, Azami, Abolfazl, Salami, Mahmoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5048127/
https://www.ncbi.nlm.nih.gov/pubmed/27746873
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author Talaei, Sayyed Alireza
Azami, Abolfazl
Salami, Mahmoud
author_facet Talaei, Sayyed Alireza
Azami, Abolfazl
Salami, Mahmoud
author_sort Talaei, Sayyed Alireza
collection PubMed
description OBJECTIVE(S): There are few reports have demonstrated the effect of a change-in-light experience on the structure and function of hippocampus. A change-in-light experience also affects the circadian pattern of melatonin secretion. This study aimed to investigate developmental effect of exogenous melatonin on synaptic plasticity of hippocampus of light deprived rats. MATERIALS AND METHODS: The effects of intracerebroventricular (ICV) injection of 2μg/5μl melatonin was evaluated on the basic and tetanized field excitatory post-synaptic potentials (fEPSPs) recorded in the hippocampal CA3-CA1 pathway of normal light-reared (LR) and dark-reared (DR) rats at 2, 4, and 6 weeks of age. Using RT-PCR and western blotting, developmental changes in the expression of melatonin receptors, MT1 and MT2, in the hippocampus were also evaluated. RESULTS: The amplitude of basic responses decreased across age in the LR rats. While light deprivation increased the amplitude of baseline fEPSPs, it decreased the degree of potentiation in post-tetanus responses. Melatonin injection also increased the amplitude of fEPSPs and suppressed the induction of long-term potentiation in both LR and DR rats. The expression of melatonin receptors increased in the hippocampus during brain development, and dark rearing reversed the expression patterns of both receptors. CONCLUSION: Although melatonin changed basic and tetanized responses of CA1 neurons across age during critical period of brain development, the pattern of its effects did not match the expression pattern of melatonin receptors in the hippocampus. Thus, the effects of melatonin on hippocampal neuronal responses may be exerted through other ways, like intercellular molecules and nuclear hormone receptors.
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spelling pubmed-50481272016-10-14 Developmental effect of light deprivation on synaptic plasticity of rats’ hippocampus: implications for melatonin Talaei, Sayyed Alireza Azami, Abolfazl Salami, Mahmoud Iran J Basic Med Sci Original Article OBJECTIVE(S): There are few reports have demonstrated the effect of a change-in-light experience on the structure and function of hippocampus. A change-in-light experience also affects the circadian pattern of melatonin secretion. This study aimed to investigate developmental effect of exogenous melatonin on synaptic plasticity of hippocampus of light deprived rats. MATERIALS AND METHODS: The effects of intracerebroventricular (ICV) injection of 2μg/5μl melatonin was evaluated on the basic and tetanized field excitatory post-synaptic potentials (fEPSPs) recorded in the hippocampal CA3-CA1 pathway of normal light-reared (LR) and dark-reared (DR) rats at 2, 4, and 6 weeks of age. Using RT-PCR and western blotting, developmental changes in the expression of melatonin receptors, MT1 and MT2, in the hippocampus were also evaluated. RESULTS: The amplitude of basic responses decreased across age in the LR rats. While light deprivation increased the amplitude of baseline fEPSPs, it decreased the degree of potentiation in post-tetanus responses. Melatonin injection also increased the amplitude of fEPSPs and suppressed the induction of long-term potentiation in both LR and DR rats. The expression of melatonin receptors increased in the hippocampus during brain development, and dark rearing reversed the expression patterns of both receptors. CONCLUSION: Although melatonin changed basic and tetanized responses of CA1 neurons across age during critical period of brain development, the pattern of its effects did not match the expression pattern of melatonin receptors in the hippocampus. Thus, the effects of melatonin on hippocampal neuronal responses may be exerted through other ways, like intercellular molecules and nuclear hormone receptors. Mashhad University of Medical Sciences 2016-08 /pmc/articles/PMC5048127/ /pubmed/27746873 Text en Copyright: © Iranian Journal of Basic Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Talaei, Sayyed Alireza
Azami, Abolfazl
Salami, Mahmoud
Developmental effect of light deprivation on synaptic plasticity of rats’ hippocampus: implications for melatonin
title Developmental effect of light deprivation on synaptic plasticity of rats’ hippocampus: implications for melatonin
title_full Developmental effect of light deprivation on synaptic plasticity of rats’ hippocampus: implications for melatonin
title_fullStr Developmental effect of light deprivation on synaptic plasticity of rats’ hippocampus: implications for melatonin
title_full_unstemmed Developmental effect of light deprivation on synaptic plasticity of rats’ hippocampus: implications for melatonin
title_short Developmental effect of light deprivation on synaptic plasticity of rats’ hippocampus: implications for melatonin
title_sort developmental effect of light deprivation on synaptic plasticity of rats’ hippocampus: implications for melatonin
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5048127/
https://www.ncbi.nlm.nih.gov/pubmed/27746873
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