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Behavioral and electrophysiological aspects of cognition in neonate rats lactated by morphine addicted mothers
OBJECTIVE(S): In addition to genetic factors, environmental phenomena during postnatal age highly affect development and, in turn, function of the brain. The present work evaluates if morphine consumption during lactation period influences the spatial performances and synaptic plasticity in rats at...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6880524/ https://www.ncbi.nlm.nih.gov/pubmed/31807250 http://dx.doi.org/10.22038/ijbms.2019.36892.8789 |
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author | Aghighi, Fatemeh Mohammadifar, Mojgan Banafsheh, Hamidreza Salami, Mahmoud Talaei, Sayyed Alireza |
author_facet | Aghighi, Fatemeh Mohammadifar, Mojgan Banafsheh, Hamidreza Salami, Mahmoud Talaei, Sayyed Alireza |
author_sort | Aghighi, Fatemeh |
collection | PubMed |
description | OBJECTIVE(S): In addition to genetic factors, environmental phenomena during postnatal age highly affect development and, in turn, function of the brain. The present work evaluates if morphine consumption during lactation period influences the spatial performances and synaptic plasticity in rats at neonatal period of age. MATERIALS AND METHODS: Three groups of mothers were subcutaneously administered by 5 (M5), 10 (M10) or 20 (M20) mg/kg morphine every 12 hours during the lactation period. At 45 days old, their offspring were introduced to Morris water maze for assessment of spatial learning and memory. Basic field excitatory post-synaptic potentials (fEPSPs) were recorded in the CA1 area of hippocampus and, then, long term potentiation (LTP) was induced by tetanic stimulation. RESULTS: We found that the M10 and M20 rats spent more time and traveled longer distance to find the hidden platform of maze when compared to the control animals (P<0.05 for all comparisons). Similarly, these two morphine-exposed groups were inferior in the memory consolidation compared to their control counterparts. Comparing control and M20 rats revealed that morphine exposure decreases the mean amplitude and slope 10-90% of fEPSPs about 30 percent (P<0.001 for both comparisons) and inhibits the LTP induction in the CA1 area circuits. CONCLUSION: The present study provides behavioral and electrophysiological proofs for negative effect of morphine on the hippocampal-related function in the neonatally morphine-exposed rats. |
format | Online Article Text |
id | pubmed-6880524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-68805242019-12-05 Behavioral and electrophysiological aspects of cognition in neonate rats lactated by morphine addicted mothers Aghighi, Fatemeh Mohammadifar, Mojgan Banafsheh, Hamidreza Salami, Mahmoud Talaei, Sayyed Alireza Iran J Basic Med Sci Original Article OBJECTIVE(S): In addition to genetic factors, environmental phenomena during postnatal age highly affect development and, in turn, function of the brain. The present work evaluates if morphine consumption during lactation period influences the spatial performances and synaptic plasticity in rats at neonatal period of age. MATERIALS AND METHODS: Three groups of mothers were subcutaneously administered by 5 (M5), 10 (M10) or 20 (M20) mg/kg morphine every 12 hours during the lactation period. At 45 days old, their offspring were introduced to Morris water maze for assessment of spatial learning and memory. Basic field excitatory post-synaptic potentials (fEPSPs) were recorded in the CA1 area of hippocampus and, then, long term potentiation (LTP) was induced by tetanic stimulation. RESULTS: We found that the M10 and M20 rats spent more time and traveled longer distance to find the hidden platform of maze when compared to the control animals (P<0.05 for all comparisons). Similarly, these two morphine-exposed groups were inferior in the memory consolidation compared to their control counterparts. Comparing control and M20 rats revealed that morphine exposure decreases the mean amplitude and slope 10-90% of fEPSPs about 30 percent (P<0.001 for both comparisons) and inhibits the LTP induction in the CA1 area circuits. CONCLUSION: The present study provides behavioral and electrophysiological proofs for negative effect of morphine on the hippocampal-related function in the neonatally morphine-exposed rats. Mashhad University of Medical Sciences 2019-09 /pmc/articles/PMC6880524/ /pubmed/31807250 http://dx.doi.org/10.22038/ijbms.2019.36892.8789 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Aghighi, Fatemeh Mohammadifar, Mojgan Banafsheh, Hamidreza Salami, Mahmoud Talaei, Sayyed Alireza Behavioral and electrophysiological aspects of cognition in neonate rats lactated by morphine addicted mothers |
title | Behavioral and electrophysiological aspects of cognition in neonate rats lactated by morphine addicted mothers |
title_full | Behavioral and electrophysiological aspects of cognition in neonate rats lactated by morphine addicted mothers |
title_fullStr | Behavioral and electrophysiological aspects of cognition in neonate rats lactated by morphine addicted mothers |
title_full_unstemmed | Behavioral and electrophysiological aspects of cognition in neonate rats lactated by morphine addicted mothers |
title_short | Behavioral and electrophysiological aspects of cognition in neonate rats lactated by morphine addicted mothers |
title_sort | behavioral and electrophysiological aspects of cognition in neonate rats lactated by morphine addicted mothers |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6880524/ https://www.ncbi.nlm.nih.gov/pubmed/31807250 http://dx.doi.org/10.22038/ijbms.2019.36892.8789 |
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