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      Anti-cholinesterases and memory improving effects of Vietnamese Xylia xylocarpa

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          Abstract

          Background

          Alzheimer’s disease (AD) is the most common cause of dementia among the elderly and is characterized by loss of memory and other cognitive functions. An increase in AChE (a key enzyme in the cholinergic nervous system) levels around β-amyloid plaques and neurofibrillary tangles is a common feature of AD neuropathology. Amnesic effects of scopolamine (acetylcholine receptor antagonist) can be investigated in various behavioral tests such as Morris water maze, object recognition, Y-maze, and passive avoidance. In the scope of this paper, we report the anti-AChE, anti-BChE properties of the isolated compound and the in vivo effects of the methanolic extract of Xylia xylocarpa (MEXX) on scopolamine-induced memory deficit.

          Results

          In further phytochemistry study, a new hopan-type triterpenoid, (3 β)-hopan-3-ol-28,22-olide ( 1), together with twenty known compounds were isolated ( 221). Compound 1, 2, 4, 5, 79, and 1113 exhibited potent acetylcholinesterase (AChE) inhibitory activity in a concentration-dependent manner with IC 50 values ranging from 54.4 to 94.6 μM. Compound 13 was also shown anti-butyrylcholinesterase (BChE) activity with an IC 50 value of 42.7 μM. The Morris water Y-maze, Y-maze, and object recognition test were also carried out.

          Conclusions

          It is noteworthy that MEXX is effective when administered orally to mice, experimental results are consistent with the traditional use of this medicinal plant species.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s13065-016-0197-5) contains supplementary material, which is available to authorized users.

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          Most cited references35

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          Alzheimer's disease.

          Alzheimer's disease is the most common cause of dementia. Research advances have enabled detailed understanding of the molecular pathogenesis of the hallmarks of the disease--ie, plaques, composed of amyloid beta (Abeta), and tangles, composed of hyperphosphorylated tau. However, as our knowledge increases so does our appreciation for the pathogenic complexity of the disorder. Familial Alzheimer's disease is a very rare autosomal dominant disease with early onset, caused by mutations in the amyloid precursor protein and presenilin genes, both linked to Abeta metabolism. By contrast with familial disease, sporadic Alzheimer's disease is very common with more than 15 million people affected worldwide. The cause of the sporadic form of the disease is unknown, probably because the disease is heterogeneous, caused by ageing in concert with a complex interaction of both genetic and environmental risk factors. This seminar reviews the key aspects of the disease, including epidemiology, genetics, pathogenesis, diagnosis, and treatment, as well as recent developments and controversies.
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            Revisiting the Role of Acetylcholinesterase in Alzheimer’s Disease: Cross-Talk with P-tau and β-Amyloid

            A common feature in the Alzheimer’s disease (AD) brain is the presence of acetylcholinesterase (AChE) which is commonly associated with β-amyloid plaques and neurofibrillary tangles (NFT). Although our understanding of the relationship between AChE and the pathological features of AD is incomplete, increasing evidence suggests that both β-amyloid protein (Aβ) and abnormally hyperphosphorylated tau (P-tau) can influence AChE expression. We also review recent findings which suggest the possible role of AChE in the development of a vicious cycle of Aβ and P-tau dysregulation and discuss the limited and temporary effect of therapeutic intervention with AChE inhibitors.
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              Acetylcholinesterase inhibitors in Alzheimer's disease.

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                Author and article information

                Contributors
                ltmlinh@agu.edu.vn
                nttmai@hcmus.edu.vn
                nxhai@hcmus.edu.vn
                dhphu@hcmus.edu.vn
                ntnhan@hcmus.edu.vn
                tmhung801018@gmail.com
                nguyenthihoahvqy@gmail.com
                minhnuinguyen@gmail.com
                bsmin@cu.ac.kr
                jkim6923@knu.ac.kr
                choijs@pknu.ac.kr
                canvanmao@yahoo.com
                Journal
                Chem Cent J
                Chem Cent J
                Chemistry Central Journal
                Springer International Publishing (Cham )
                1752-153X
                3 August 2016
                3 August 2016
                2016
                : 10
                : 48
                Affiliations
                [1 ]Faculty of Chemistry, University of Science, Vietnam National University-Hochiminh City, 227 Nguyen Van Cu, District 5, Hochiminh City, Vietnam
                [2 ]Vietnam Military Medical University, Hadong District, Hanoi, Vietnam
                [3 ]College of Pharmacy, Catholic University of Daegu, Gyeongsan, Gyeongsangbuk 712-702 Republic of Korea
                [4 ]College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu, 702-701 Republic of Korea
                [5 ]Department of Food Science and Nutrition, Pukyong National University, Busan, 608-737 Republic of Korea
                [6 ]Cancer Research Laboratory, Vietnam National University-Hochiminh City, Hochiminh City, Vietnam
                Article
                197
                10.1186/s13065-016-0197-5
                4973094
                27493681
                602e164d-4968-41e2-a969-a9d808244b45
                © The Author(s) 2016

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 27 April 2016
                : 28 July 2016
                Funding
                Funded by: Vietnam's National Foundation for Science and Technology Development (NAFOSTED)
                Award ID: 106-YS.05-2013.24
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2016

                Chemistry
                xylia xylocarpa,hopan-ol-olide,acetylcholinesterase,butyrylcholinesterase,improving memory effects

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