Volume 6 Issue 4 • 1000245
J Alzheimers Dis Parkinsonism
ISSN:2161-0460 JADP an open access journal
Open Access Research Article
Uddin et al., J Alzheimers Dis Parkinsonism 2016, 6:4
DOI: 10.4172/2161-0460.1000245 Journal of
Alzheimer’s Disease & Parkinsonism
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ISSN: 2161-0460
Keywords: Neuroprotective; Asparagus racemosus; Cognitive
impairment; Oxidative stress; Alzheimer’s disease
Abbreviations: AD: Alzheimer’s disease; AR: Asparagus racemosus;
EEAR: Ethanolic extract of Asparagus racemosus; EPM: Elevated
plus maze; PA: Passive avoidance; MWM: Morris water maze; NOR:
Novel object recognition;TBARS: Tiobarbituric acid reactive species
(TBARS); AChE: Acetylcholinesterase; ITL: Initial transfer latency;
RTL: Retention transfer latency; EL: Escape latency; RL: Retention
latency; TSTQ: Time spent in the target quadrant; TSA: Time spent
in the annuli; DI: Discrimination index; PUFA: Polyunsaturated fatty
acids; CNS: Central nervous system; Aβ: amyloid beta; WHO: World
Health Organization; TCA: Trichloroacetic acid; TBA: Tiobarbituric
acid; ATCI: Acetyl thiocholine iodide; DTNB: 5,5-dithiobis-2-
nitrobenzoate ion; Tris-HCl: Trisfamino methane hydrochloride; BSA:
Bovine serum albumin; NIH: National Institutes of Health; OECD:
Organisation for Economic Cooperation and Development .
Introduction
Alzheimer’s disease (AD) is the most common form of dementia
that results in memory impairment and cognitive dysfunction due to
Neuroprotective Activity of Asparagus racemosus Linn. Against Ethanol-
Induced Cognitive Impairment and Oxidative Stress in Rats Brain:
Auspicious for Controlling the Risk of Alzheimer’s Disease
Md. Sahab Uddin
1†
*, Md. Asaduzzaman
1†
, Abdullah Al Mamun
1
, Mohammed Ashraful Iqbal
2
, Ferdous Wahid
3
and Ram Kamol Rony
4
1
Department of Pharmacy, Southeast University, Dhaka, Bangladesh
2
Department of Chemistry, Fareast International University, Dhaka, Bangladesh
3
Department of Pharmacy, University of Development Alternative, Dhaka, Bangladesh
4
Department of Pharmacology and Clinical Pharmacy, North South University, Dhaka, Bangladesh
Abstract
Background: Medicinal plants are superior gift of nature to human lives to support disease free healthy life.
Neurodegenerative diseases especially Alzheimer’s disease (AD) affects the central nervous system causing
progressive degeneration of neurons, which affect cognitive function. The plant Asparagus racemosus (AR) Linn.
has been used traditionally by Ayurvedic practitioners for nervous disorders. In this consequence, the intention of this
study was to evaluate the neuroprotective effects of ethanolic extract of Asparagus racemosus (EEAR) Linn. roots in
ethanol-induced cognitive impairment and oxidative stress in rats brain.
Methods: The learning and memory enhancing activity of EEAR roots extract were investigated in Swiss albino
male rats for 21 days and its effects on learning and memory were examined using various behavioral studies such as
elevated plus maze (EPM) test, passive avoidance (PA) test, morris water maze (MWM) test, novel object recognition
(NOR) test and biochemical studies such as lipid peroxidation (TBARS) contents and acetylcholinesterase (AChE)
activity.
Results: In the EPM test, administration of EEAR (i.e., 100 and 200 mg/kg b.w.) signifcantly (P<0.05, P<0.01)
decreased retention transfer latency (RTL) on 21
st
day with respect to the disease control group. EEAR at 200 mg/kg
b.w. markedly (P<0.05, P<0.01) increased the retention latency (RL) on 11
th
and 21
st
day compared to disease control
group for PA test. In the NOR test administration of EEAR (i.e., 200 mg/kg b.w.) considerably (P<0.05) increased DI
of rats on 21
st
day with respect to disease control group. Both doses of EEAR (i.e., 100 and 200 mg/kg b.w.) markedly
(P<0.05, P<0.01) decreased escape latency (EL) and highest dose of EEAR (i.e., 200 mg/kg b.w.) noticeably (P<0.05,
P<0.001) increased time spent in the target quadrant (TSTQ) on successive days for acquisition trial of MWM test. In
case of probe trial administration of EEAR (i.e., 200 mg/kg b.w.) considerably (P<0.05, P<0.01) increased TSTQ and
TSA (time spent in the annuli) of rats as compared to that of disease control group. EEAR administration (i.e., 100 and
200 mg/kg b.w.) signifcantly (P<0.01) decreased the TBARS level in the brain tissue of rats with respect to disease
control group. The lowest and highest dose of EEAR (i.e., 100 and 200 mg/kg b.w.) signifcantly (P<0.05, P<0.01)
decreases the AChE activity in the brain tissue of rats as compared to disease control group.
Conclusion: The existing study displays that EEAR roots possesses an outstanding source for natural nootropic
and confrming the traditional uses of this plant which could be industrialized for enhancing learning and memory
impairment associated with neurodegenerative disorders particularly AD.
*Corresponding author: Md. Sahab Uddin, Department of Pharmacy,
Southeast University, Dhaka, Bangladesh, Tel: +8801670760546; E-mail:
msu-neuropharma@hotmail.com, msu_neuropharma@hotmail.com
†
Equal contributors
Received February 17, 2016; Accepted June 27, 2016; Published July 04, 2016
Citation: Uddin MS, Asaduzzaman M, Mamun AA, Iqbal MA, Wahid F, et al. (2016)
Neuroprotective Activity of Asparagus racemosus Linn. Against Ethanol-Induced
Cognitive Impairment and Oxidative Stress in Rats Brain: Auspicious for Control-
ling the Risk of Alzheimer’s Disease. J Alzheimers Dis Parkinsonism 6: 245. doi:
10.4172/2161-0460.1000245
Copyright: © 2016 Uddin MS, et al. This is an open-access article distributed under
the terms of the Creative Commons Attribution License, which permits unrestricted
use, distribution, and reproduction in any medium, provided the original author and
source are credited.
progressive neurodegeneration [1]. Worldwide at present 35 million
people are afected by AD, including 5.5 million Americans and it is
projected that in 2050 more than 115 million people will have dementia
[2,3]. AD is currently ranked as the 6
th
leading cause of death in the
United States, but recent estimates indicate that the disorder may rank
3
rd
, just behind heart disease and cancer, as a cause of death for older
people [4]. Tis disease is characterized by deposition of amyloid β (Aβ)