Effect of hydroalcoholic Echium amoenum extract on scopolamine-induced learning and memory impairment in rats

Context: Scopolamine, a muscarinic receptor antagonist, causes memory loss that resembles Alzheimer's disease (AD). Echium amoenum L. (Boraginaceae) is a famous medicinal plant of Iran that is traditionally used as a sedative and mood enhancer. Objective: This study evaluates the effect of hydr...

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Main Authors: Zahra Rabiei, Mahbubeh Setorki
Format: Article
Language:English
Published: Taylor & Francis Group 2018-01-01
Series:Pharmaceutical Biology
Subjects:
Online Access:http://dx.doi.org/10.1080/13880209.2018.1543330
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author Zahra Rabiei
Mahbubeh Setorki
author_facet Zahra Rabiei
Mahbubeh Setorki
author_sort Zahra Rabiei
collection DOAJ
description Context: Scopolamine, a muscarinic receptor antagonist, causes memory loss that resembles Alzheimer's disease (AD). Echium amoenum L. (Boraginaceae) is a famous medicinal plant of Iran that is traditionally used as a sedative and mood enhancer. Objective: This study evaluates the effect of hydroalcoholic extract of E. amoenum flowers on scopolamine-induced memory impairment in rats. Materials and methods: Fifty male Wistar rats were randomly divided into five groups. Control group received normal saline, model group received scopolamine (0.7 mg/kg, IP, daily for 21 days), and test groups received E. amoenum extract (50, 75, and 100 mg/kg, IP, daily for 21 days) 30 min before each scopolamine injection. The elevated plus maze (EPM), shuttle box, novel object and rotarod tests were performed after treatment. Brain levels of malondialdehyde (MDA) and total antioxidant capacity (TCA) were also determined. Results: Scopolamine-treated rats spent more time exploring the novel object compared to the control, and E. amoenum extract at all three doses significantly decreased the time spent exploring the novel object (p < 0.05). E. amoenum extract (75 and 100 mg/kg) significantly elongated the secondary latency in rats receiving scopolamine in the shuttle box test (p < 0.05). In addition, treatment with 75 and 100 mg/kg doses of E. amoenum extract significantly ameliorated scopolamine-induced motor in coordination in rotarod test (p < 0.05). It also significantly increased the time spent in the open arms and reduced the time spent in the closed arms of EPM (p < 0.05). Treatment of scopolamine-exposed rats with E. amoenum extract significantly increased TCA and reduced MDA level of brain (p < 0.05). Discussion and conclusions: E. amoenum extract shows protective effect against scopolamine-induced impairment and is suggested to be tested in clinical trials to evaluate the efficacy on AD.
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spelling doaj.art-7486d8ce157648f187a9e96e7bcb93212022-12-21T18:52:39ZengTaylor & Francis GroupPharmaceutical Biology1388-02091744-51162018-01-0156167267710.1080/13880209.2018.15433301543330Effect of hydroalcoholic Echium amoenum extract on scopolamine-induced learning and memory impairment in ratsZahra Rabiei0Mahbubeh Setorki1Shahrekord University of Medical SciencesIzeh Branch, Islamic Azad UniversityContext: Scopolamine, a muscarinic receptor antagonist, causes memory loss that resembles Alzheimer's disease (AD). Echium amoenum L. (Boraginaceae) is a famous medicinal plant of Iran that is traditionally used as a sedative and mood enhancer. Objective: This study evaluates the effect of hydroalcoholic extract of E. amoenum flowers on scopolamine-induced memory impairment in rats. Materials and methods: Fifty male Wistar rats were randomly divided into five groups. Control group received normal saline, model group received scopolamine (0.7 mg/kg, IP, daily for 21 days), and test groups received E. amoenum extract (50, 75, and 100 mg/kg, IP, daily for 21 days) 30 min before each scopolamine injection. The elevated plus maze (EPM), shuttle box, novel object and rotarod tests were performed after treatment. Brain levels of malondialdehyde (MDA) and total antioxidant capacity (TCA) were also determined. Results: Scopolamine-treated rats spent more time exploring the novel object compared to the control, and E. amoenum extract at all three doses significantly decreased the time spent exploring the novel object (p < 0.05). E. amoenum extract (75 and 100 mg/kg) significantly elongated the secondary latency in rats receiving scopolamine in the shuttle box test (p < 0.05). In addition, treatment with 75 and 100 mg/kg doses of E. amoenum extract significantly ameliorated scopolamine-induced motor in coordination in rotarod test (p < 0.05). It also significantly increased the time spent in the open arms and reduced the time spent in the closed arms of EPM (p < 0.05). Treatment of scopolamine-exposed rats with E. amoenum extract significantly increased TCA and reduced MDA level of brain (p < 0.05). Discussion and conclusions: E. amoenum extract shows protective effect against scopolamine-induced impairment and is suggested to be tested in clinical trials to evaluate the efficacy on AD.http://dx.doi.org/10.1080/13880209.2018.1543330cognitive performancelocomotor activityanxiety
spellingShingle Zahra Rabiei
Mahbubeh Setorki
Effect of hydroalcoholic Echium amoenum extract on scopolamine-induced learning and memory impairment in rats
Pharmaceutical Biology
cognitive performance
locomotor activity
anxiety
title Effect of hydroalcoholic Echium amoenum extract on scopolamine-induced learning and memory impairment in rats
title_full Effect of hydroalcoholic Echium amoenum extract on scopolamine-induced learning and memory impairment in rats
title_fullStr Effect of hydroalcoholic Echium amoenum extract on scopolamine-induced learning and memory impairment in rats
title_full_unstemmed Effect of hydroalcoholic Echium amoenum extract on scopolamine-induced learning and memory impairment in rats
title_short Effect of hydroalcoholic Echium amoenum extract on scopolamine-induced learning and memory impairment in rats
title_sort effect of hydroalcoholic echium amoenum extract on scopolamine induced learning and memory impairment in rats
topic cognitive performance
locomotor activity
anxiety
url http://dx.doi.org/10.1080/13880209.2018.1543330
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