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Effect of cypermethrin on the postnatal development of the medulla oblongata and the possible protective role of melatonin in albino rats

Previous studies have shown that cypermethrin (CYP), a broad spectrum pesticide has a teratogenic effect on rat offspring born to an exposed dam with no information on its effect on the development of the brain. To the best of our knowledge, this research is the first attempt to study the postnatal...

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Autores principales: Al-Gholam, Marwa A., Issa, Noha M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Anatomists 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769100/
https://www.ncbi.nlm.nih.gov/pubmed/33361544
http://dx.doi.org/10.5115/acb.20.193
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author Al-Gholam, Marwa A.
Issa, Noha M.
author_facet Al-Gholam, Marwa A.
Issa, Noha M.
author_sort Al-Gholam, Marwa A.
collection PubMed
description Previous studies have shown that cypermethrin (CYP), a broad spectrum pesticide has a teratogenic effect on rat offspring born to an exposed dam with no information on its effect on the development of the brain. To the best of our knowledge, this research is the first attempt to study the postnatal development medulla oblongata of rat offspring exposed to CYP during the perinatal period and the possible neuroprotective role of melatonin. The offspring of treated female rats were organized into control, melatonin (1 mg/kg/day orally); CYP (12 mg/kg/day orally); and CYP/melatonin groups. The mothers received treatments from day 6 of gestation until day 21 after birth. At Postnatal days 7 and 21, the animals were sacrificed and their medulla oblongata was removed and subjected to histological, immunohistochemical, and electron microscopic studies. CYP induced neuronal degeneration by chromatolysis and pyknosis. Nuclear changes, cytoplasmic vacuolation, damage mitochondria, and breakdown of RER were also detected. Reduction of microtubule-associated protein-2 (MAP-2), myelin basic protein (MBP), and oligodendrocyte transcription factor expressions and increment of glial fibrillary acidic protein expression in the medulla oblongata of the developing rats were observed. On the other hand, melatonin led to an obvious improvement of the injured medulla oblongata tissues and ameliorating the damaging effects of CYP. In conclusion, melatonin has protected rats against CYP-induced histopathological and immunohistochemical changes. This may be due to the protection of MAP-2, conservation of MBP, an increment of oligodendrocytes, and alleviation of astrogliosis.
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spelling pubmed-77691002021-01-05 Effect of cypermethrin on the postnatal development of the medulla oblongata and the possible protective role of melatonin in albino rats Al-Gholam, Marwa A. Issa, Noha M. Anat Cell Biol Original Article Previous studies have shown that cypermethrin (CYP), a broad spectrum pesticide has a teratogenic effect on rat offspring born to an exposed dam with no information on its effect on the development of the brain. To the best of our knowledge, this research is the first attempt to study the postnatal development medulla oblongata of rat offspring exposed to CYP during the perinatal period and the possible neuroprotective role of melatonin. The offspring of treated female rats were organized into control, melatonin (1 mg/kg/day orally); CYP (12 mg/kg/day orally); and CYP/melatonin groups. The mothers received treatments from day 6 of gestation until day 21 after birth. At Postnatal days 7 and 21, the animals were sacrificed and their medulla oblongata was removed and subjected to histological, immunohistochemical, and electron microscopic studies. CYP induced neuronal degeneration by chromatolysis and pyknosis. Nuclear changes, cytoplasmic vacuolation, damage mitochondria, and breakdown of RER were also detected. Reduction of microtubule-associated protein-2 (MAP-2), myelin basic protein (MBP), and oligodendrocyte transcription factor expressions and increment of glial fibrillary acidic protein expression in the medulla oblongata of the developing rats were observed. On the other hand, melatonin led to an obvious improvement of the injured medulla oblongata tissues and ameliorating the damaging effects of CYP. In conclusion, melatonin has protected rats against CYP-induced histopathological and immunohistochemical changes. This may be due to the protection of MAP-2, conservation of MBP, an increment of oligodendrocytes, and alleviation of astrogliosis. Korean Association of Anatomists 2020-12-31 2020-12-31 /pmc/articles/PMC7769100/ /pubmed/33361544 http://dx.doi.org/10.5115/acb.20.193 Text en Copyright © 2020. Anatomy & Cell Biology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Al-Gholam, Marwa A.
Issa, Noha M.
Effect of cypermethrin on the postnatal development of the medulla oblongata and the possible protective role of melatonin in albino rats
title Effect of cypermethrin on the postnatal development of the medulla oblongata and the possible protective role of melatonin in albino rats
title_full Effect of cypermethrin on the postnatal development of the medulla oblongata and the possible protective role of melatonin in albino rats
title_fullStr Effect of cypermethrin on the postnatal development of the medulla oblongata and the possible protective role of melatonin in albino rats
title_full_unstemmed Effect of cypermethrin on the postnatal development of the medulla oblongata and the possible protective role of melatonin in albino rats
title_short Effect of cypermethrin on the postnatal development of the medulla oblongata and the possible protective role of melatonin in albino rats
title_sort effect of cypermethrin on the postnatal development of the medulla oblongata and the possible protective role of melatonin in albino rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769100/
https://www.ncbi.nlm.nih.gov/pubmed/33361544
http://dx.doi.org/10.5115/acb.20.193
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