Protective effects of Centella asiatica on cognitive deficits induced by D-gal/AlCl3 via inhibition of oxidative stress and attenuation of acetylcholinesterase level

Alzheimer's disease (AD) is a progressive neurodegenerative disorder with cholinergic dysfunctions and impaired redox homeostasis. The plant Centella asiatica (CA) is renowned for its nutritional benefits and herbal formulas for promoting health, enhancing cognition, and its neuroprotective eff...

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Main Authors: Adenan, M.I (Author), Amom, Z. (Author), Baharuldin, M.T.H (Author), Chiroma, S.M (Author), Jagadeesan, S. (Author), Mahdi, O. (Author), Moklas, M.A.M (Author), Taib, C.N.M (Author)
Format: Article
Language:English
Published: MDPI AG 2019
Subjects:
rat
Online Access:View Fulltext in Publisher
View in Scopus
LEADER 03990nam a2200661Ia 4500
001 10.3390-toxics7020019
008 220121s2019 CNT 000 0 und d
020 |a 23056304 (ISSN) 
245 1 0 |a Protective effects of Centella asiatica on cognitive deficits induced by D-gal/AlCl3 via inhibition of oxidative stress and attenuation of acetylcholinesterase level 
260 0 |b MDPI AG  |c 2019 
650 0 4 |a acetylcholinesterase 
650 0 4 |a Acetylcholinesterase 
650 0 4 |a aluminum chloride 
650 0 4 |a Alzheimer's disease 
650 0 4 |a animal experiment 
650 0 4 |a animal model 
650 0 4 |a Article 
650 0 4 |a attenuation 
650 0 4 |a brain cortex 
650 0 4 |a Centella asiatica 
650 0 4 |a Centella asiatica extract 
650 0 4 |a cognitive defect 
650 0 4 |a Cognitive deficit 
650 0 4 |a controlled study 
650 0 4 |a donepezil 
650 0 4 |a enzyme activity 
650 0 4 |a enzyme inhibition 
650 0 4 |a enzyme linked immunosorbent assay 
650 0 4 |a ethology 
650 0 4 |a galactose 
650 0 4 |a hippocampus 
650 0 4 |a male 
650 0 4 |a malonaldehyde 
650 0 4 |a mitochondrion 
650 0 4 |a Morphological aberration 
650 0 4 |a Morris water maze test 
650 0 4 |a nonhuman 
650 0 4 |a oxidative stress 
650 0 4 |a Oxidative stress 
650 0 4 |a prefrontal cortex 
650 0 4 |a protein phosphorylation 
650 0 4 |a rat 
650 0 4 |a superoxide dismutase 
650 0 4 |a tau protein 
650 0 4 |a transmission electron microscopy 
650 0 4 |a ultrastructure 
856 |z View Fulltext in Publisher  |u https://doi.org/10.3390/toxics7020019 
856 |z View in Scopus  |u https://www.scopus.com/inward/record.uri?eid=2-s2.0-85066828855&doi=10.3390%2ftoxics7020019&partnerID=40&md5=606f88bea48ca9d96eaefdcc3dee4c2a 
520 3 |a Alzheimer's disease (AD) is a progressive neurodegenerative disorder with cholinergic dysfunctions and impaired redox homeostasis. The plant Centella asiatica (CA) is renowned for its nutritional benefits and herbal formulas for promoting health, enhancing cognition, and its neuroprotective effects. The present study aims to investigate the protective role of CA on D-gal/AlCl3-induced cognitive deficits in rats. The rats were divided into six groups and administered with donepezil 1 mg/kg/day, CA (200, 400, and 800 mg/kg/day) and D-gal 60 mg/kg/day + AlCl3 200 mg/kg/day for 10 weeks. The ethology of the rats was evaluated by the Morris water maze test. The levels of acetylcholinesterase (AChE), phosphorylated tau (P-tau), malondialdehyde (MDA) and activities of superoxide dismutase (SOD), in the hippocampus and cerebral cortex were estimated by enzyme-linked immunosorbent assay (ELISA). Additionally, the ultrastructure of the prefrontal cortex of the rats' was observed using transmission electron microscopy (TEM). Rats administered with D-gal/AlCl3 exhibited cognitive deficits, decreased activities of SOD, and marked increase in AChE and MDA levels. Further, prominent alterations in the ultrastructure of the prefrontal cortex were observed. Conversely, co-administration of CA with D-gal/AlCl3 improved cognitive impairment, decreased AChE levels, attenuated the oxidative stress in hippocampus and cerebral cortex, and prevented ultrastructural alteration of neurons in the prefrontal cortex. Irrespective of the dose of CA administered, the protective effects were comparable to donepezil. In conclusion, this study suggests that CA attenuated the cognitive deficits in rats by restoring cholinergic function, attenuating oxidative stress, and preventing the morphological aberrations. © 2019 by the authors. 
700 1 0 |a Adenan, M.I.  |e author  
700 1 0 |a Amom, Z.  |e author  
700 1 0 |a Baharuldin, M.T.H.  |e author  
700 1 0 |a Chiroma, S.M.  |e author  
700 1 0 |a Jagadeesan, S.  |e author  
700 1 0 |a Mahdi, O.  |e author  
700 1 0 |a Moklas, M.A.M.  |e author  
700 1 0 |a Taib, C.N.M.  |e author  
773 |t Toxics  |x 23056304 (ISSN)  |g 7 2