Protective effects of: Nigella sativa L. seed extract on lead induced neurotoxicity during development and early life in mouse models

Lead (Pb), a ubiquitous heavy metal and a known neurotoxicant, produces adverse effects on the brain via increased production of reactive oxygen species (ROS) and causes oxidative stress. In this study we examined the neuroprotective effects of the ethanolic extract of Nigella sativa L. seeds on Pb...

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Published in:Toxicology Research
Main Author: Butt U.J.; Shah S.A.A.; Ahmed T.; Zahid S.
Format: Article
Language:English
Published: Royal Society of Chemistry 2018
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85040179433&doi=10.1039%2fc7tx00201g&partnerID=40&md5=a691d749f278bc9c70a93b8cfa1120cf
id 2-s2.0-85040179433
spelling 2-s2.0-85040179433
Butt U.J.; Shah S.A.A.; Ahmed T.; Zahid S.
Protective effects of: Nigella sativa L. seed extract on lead induced neurotoxicity during development and early life in mouse models
2018
Toxicology Research
7
1
10.1039/c7tx00201g
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85040179433&doi=10.1039%2fc7tx00201g&partnerID=40&md5=a691d749f278bc9c70a93b8cfa1120cf
Lead (Pb), a ubiquitous heavy metal and a known neurotoxicant, produces adverse effects on the brain via increased production of reactive oxygen species (ROS) and causes oxidative stress. In this study we examined the neuroprotective effects of the ethanolic extract of Nigella sativa L. seeds on Pb induced oxidative stress in the developing brain of mice. Mouse pups were exposed to low (0.1%) and high (0.2%) doses of Pb from the first day of pregnancy through their mothers (via drinking water) and lactation until post-natal day (PND) 21. The mRNA expression levels of superoxide dismutase (SOD1), peroxiredoxin (Prdx6), amyloid precursor protein (APP) common, APP695 and APP770 were examined in the cortex and hippocampus of the mouse brain excised on PND 21 by semi-quantitative RT-PCR. The free radical scavenging activity of ethanolic Nigella sativa L. extract was assessed by DPPH assay. The results showed that Pb exposure caused a significant decrease in the expression of SOD1, Prdx6 and APP695 and an increase in APP770 in both cortex and hippocampus in a dose dependent manner as compared to the control group. The expression of APP common remained unaltered. Histological assessment of the cortex and hippocampus demonstrated a decrease in the neuronal number and Nissl bodies. The administration of 250 and 500 mg kg-1 ethanolic Nigella sativa L. extract reversed the adverse effects by significantly increasing the expression of SOD1, Prdx6 and APP695 and decreasing the expression of APP770 in both the regions. These results strongly suggest that Nigella sativa L. supplementation greatly improves Pb-induced neurotoxicity in early life and provides neuroprotective and antioxidant potentials. © 2018 The Royal Society of Chemistry.
Royal Society of Chemistry
2045452X
English
Article
All Open Access; Green Open Access
author Butt U.J.; Shah S.A.A.; Ahmed T.; Zahid S.
spellingShingle Butt U.J.; Shah S.A.A.; Ahmed T.; Zahid S.
Protective effects of: Nigella sativa L. seed extract on lead induced neurotoxicity during development and early life in mouse models
author_facet Butt U.J.; Shah S.A.A.; Ahmed T.; Zahid S.
author_sort Butt U.J.; Shah S.A.A.; Ahmed T.; Zahid S.
title Protective effects of: Nigella sativa L. seed extract on lead induced neurotoxicity during development and early life in mouse models
title_short Protective effects of: Nigella sativa L. seed extract on lead induced neurotoxicity during development and early life in mouse models
title_full Protective effects of: Nigella sativa L. seed extract on lead induced neurotoxicity during development and early life in mouse models
title_fullStr Protective effects of: Nigella sativa L. seed extract on lead induced neurotoxicity during development and early life in mouse models
title_full_unstemmed Protective effects of: Nigella sativa L. seed extract on lead induced neurotoxicity during development and early life in mouse models
title_sort Protective effects of: Nigella sativa L. seed extract on lead induced neurotoxicity during development and early life in mouse models
publishDate 2018
container_title Toxicology Research
container_volume 7
container_issue 1
doi_str_mv 10.1039/c7tx00201g
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85040179433&doi=10.1039%2fc7tx00201g&partnerID=40&md5=a691d749f278bc9c70a93b8cfa1120cf
description Lead (Pb), a ubiquitous heavy metal and a known neurotoxicant, produces adverse effects on the brain via increased production of reactive oxygen species (ROS) and causes oxidative stress. In this study we examined the neuroprotective effects of the ethanolic extract of Nigella sativa L. seeds on Pb induced oxidative stress in the developing brain of mice. Mouse pups were exposed to low (0.1%) and high (0.2%) doses of Pb from the first day of pregnancy through their mothers (via drinking water) and lactation until post-natal day (PND) 21. The mRNA expression levels of superoxide dismutase (SOD1), peroxiredoxin (Prdx6), amyloid precursor protein (APP) common, APP695 and APP770 were examined in the cortex and hippocampus of the mouse brain excised on PND 21 by semi-quantitative RT-PCR. The free radical scavenging activity of ethanolic Nigella sativa L. extract was assessed by DPPH assay. The results showed that Pb exposure caused a significant decrease in the expression of SOD1, Prdx6 and APP695 and an increase in APP770 in both cortex and hippocampus in a dose dependent manner as compared to the control group. The expression of APP common remained unaltered. Histological assessment of the cortex and hippocampus demonstrated a decrease in the neuronal number and Nissl bodies. The administration of 250 and 500 mg kg-1 ethanolic Nigella sativa L. extract reversed the adverse effects by significantly increasing the expression of SOD1, Prdx6 and APP695 and decreasing the expression of APP770 in both the regions. These results strongly suggest that Nigella sativa L. supplementation greatly improves Pb-induced neurotoxicity in early life and provides neuroprotective and antioxidant potentials. © 2018 The Royal Society of Chemistry.
publisher Royal Society of Chemistry
issn 2045452X
language English
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accesstype All Open Access; Green Open Access
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