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Moringa oleifera Seed Extract Alleviates Scopolamine-Induced Learning and Memory Impairment in Mice

The extract of Moringa oleifera seeds has been shown to possess various pharmacological properties. In the present study, we assessed the neuropharmacological effects of 70% ethanolic M. oleifera seed extract (MSE) on cognitive impairment caused by scopolamine injection in mice using the passive avo...

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Autores principales: Zhou, Juan, Yang, Wu-shuang, Suo, Da-qin, Li, Ying, Peng, Lu, Xu, Lan-xi, Zeng, Kai-yue, Ren, Tong, Wang, Ying, Zhou, Yu, Zhao, Yun, Yang, Li-chao, Jin, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928465/
https://www.ncbi.nlm.nih.gov/pubmed/29740317
http://dx.doi.org/10.3389/fphar.2018.00389
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author Zhou, Juan
Yang, Wu-shuang
Suo, Da-qin
Li, Ying
Peng, Lu
Xu, Lan-xi
Zeng, Kai-yue
Ren, Tong
Wang, Ying
Zhou, Yu
Zhao, Yun
Yang, Li-chao
Jin, Xin
author_facet Zhou, Juan
Yang, Wu-shuang
Suo, Da-qin
Li, Ying
Peng, Lu
Xu, Lan-xi
Zeng, Kai-yue
Ren, Tong
Wang, Ying
Zhou, Yu
Zhao, Yun
Yang, Li-chao
Jin, Xin
author_sort Zhou, Juan
collection PubMed
description The extract of Moringa oleifera seeds has been shown to possess various pharmacological properties. In the present study, we assessed the neuropharmacological effects of 70% ethanolic M. oleifera seed extract (MSE) on cognitive impairment caused by scopolamine injection in mice using the passive avoidance and Morris water maze (MWM) tests. MSE (250 or 500 mg/kg) was administered to mice by oral gavage for 7 or 14 days, and cognitive impairment was induced by intraperitoneal injection of scopolamine (4 mg/kg) for 1 or 6 days. Mice that received scopolamine alone showed impaired learning and memory retention and considerably decreased cholinergic system reactivity and neurogenesis in the hippocampus. MSE pretreatment significantly ameliorated scopolamine-induced cognitive impairment and enhanced cholinergic system reactivity and neurogenesis in the hippocampus. Additionally, the protein expressions of phosphorylated Akt, ERK1/2, and CREB in the hippocampus were significantly decreased by scopolamine, but these decreases were reversed by MSE treatment. These results suggest that MSE-induced ameliorative cognitive effects are mediated by enhancement of the cholinergic neurotransmission system and neurogenesis via activation of the Akt, ERK1/2, and CREB signaling pathways. These findings suggest that MSE could be a potent neuropharmacological drug against amnesia, and its mechanism might be modulation of cholinergic activity via the Akt, ERK1/2, and CREB signaling pathways.
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spelling pubmed-59284652018-05-08 Moringa oleifera Seed Extract Alleviates Scopolamine-Induced Learning and Memory Impairment in Mice Zhou, Juan Yang, Wu-shuang Suo, Da-qin Li, Ying Peng, Lu Xu, Lan-xi Zeng, Kai-yue Ren, Tong Wang, Ying Zhou, Yu Zhao, Yun Yang, Li-chao Jin, Xin Front Pharmacol Pharmacology The extract of Moringa oleifera seeds has been shown to possess various pharmacological properties. In the present study, we assessed the neuropharmacological effects of 70% ethanolic M. oleifera seed extract (MSE) on cognitive impairment caused by scopolamine injection in mice using the passive avoidance and Morris water maze (MWM) tests. MSE (250 or 500 mg/kg) was administered to mice by oral gavage for 7 or 14 days, and cognitive impairment was induced by intraperitoneal injection of scopolamine (4 mg/kg) for 1 or 6 days. Mice that received scopolamine alone showed impaired learning and memory retention and considerably decreased cholinergic system reactivity and neurogenesis in the hippocampus. MSE pretreatment significantly ameliorated scopolamine-induced cognitive impairment and enhanced cholinergic system reactivity and neurogenesis in the hippocampus. Additionally, the protein expressions of phosphorylated Akt, ERK1/2, and CREB in the hippocampus were significantly decreased by scopolamine, but these decreases were reversed by MSE treatment. These results suggest that MSE-induced ameliorative cognitive effects are mediated by enhancement of the cholinergic neurotransmission system and neurogenesis via activation of the Akt, ERK1/2, and CREB signaling pathways. These findings suggest that MSE could be a potent neuropharmacological drug against amnesia, and its mechanism might be modulation of cholinergic activity via the Akt, ERK1/2, and CREB signaling pathways. Frontiers Media S.A. 2018-04-24 /pmc/articles/PMC5928465/ /pubmed/29740317 http://dx.doi.org/10.3389/fphar.2018.00389 Text en Copyright © 2018 Zhou, Yang, Suo, Li, Peng, Xu, Zeng, Ren, Wang, Zhou, Zhao, Yang and Jin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Zhou, Juan
Yang, Wu-shuang
Suo, Da-qin
Li, Ying
Peng, Lu
Xu, Lan-xi
Zeng, Kai-yue
Ren, Tong
Wang, Ying
Zhou, Yu
Zhao, Yun
Yang, Li-chao
Jin, Xin
Moringa oleifera Seed Extract Alleviates Scopolamine-Induced Learning and Memory Impairment in Mice
title Moringa oleifera Seed Extract Alleviates Scopolamine-Induced Learning and Memory Impairment in Mice
title_full Moringa oleifera Seed Extract Alleviates Scopolamine-Induced Learning and Memory Impairment in Mice
title_fullStr Moringa oleifera Seed Extract Alleviates Scopolamine-Induced Learning and Memory Impairment in Mice
title_full_unstemmed Moringa oleifera Seed Extract Alleviates Scopolamine-Induced Learning and Memory Impairment in Mice
title_short Moringa oleifera Seed Extract Alleviates Scopolamine-Induced Learning and Memory Impairment in Mice
title_sort moringa oleifera seed extract alleviates scopolamine-induced learning and memory impairment in mice
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928465/
https://www.ncbi.nlm.nih.gov/pubmed/29740317
http://dx.doi.org/10.3389/fphar.2018.00389
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