Mini Review Volume 1 Issue 2
Department of Pharmacy, Assam down town University, India
Correspondence: Atanu Bhattacharjee, Department of Pharmacy, Assam Down Town University, India, Tel 91-8073612051
Received: March 27, 2018 | Published: April 9, 2018
Citation: Bhattacharjee A. Anticholinesterase potential of phytoextracts and their bioactive compounds: a promising therapeutic agent against Alzheimer’s disorder. MOJ Tumor Res. 2018;1(2):84-88. DOI: 10.15406/mojtr.2018.01.00018
Alzheimer's disease (AD) is a dynamic neurodegenerative pathological condition described by low level of neurotransmitter acetylcholine (ACh) in the cerebrum. It is an irreversible age-related type of dementia that gradually dissolves the mind and burglarizes the individual memory and psychological abilities and causes changes in identity and conduct. Amid a decade ago, critical development in Alzheimer's commonness has lighted the significance of more looks into in the pursuit of new medication. One of the major clinical advances in the treatment of AD have been the utilization of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitors to reduce ACh level in cerebrum albeit cholinergic mixes with nicotinic and muscarinic agonist properties additionally have pulled in some intrigue. At present, there are extremely constrained drugs accessible to treat AD and the greater part of the treatment is accessible just to postpone the progress of indications and symptomatic alleviation for a brief timeframe. Restorative plants speak to a lot of undiscovered store of characteristic prescriptions and potential wellspring of common AChE inhibitors. The basic assorted variety of their phytoconstituents makes them an important wellspring of novel lead mixes for the mission of medications to treat AD. Consequently, methodical ethnopharmacological screening of these plants may give valuable leads in the disclosure of new medications for AD treatment. With this background, a precise review is prepared to deliver up to date information in different phytoextracts and their derivatives alongside their conceivable activity on cholinergic sensory system to ease AD treatment. Electronic database were used for searching the information related to studies performed in plants during last decades.
Keywords: Alzheimer’s disease, Acetylcholine, Acetylcholinesterase, Butyrylcholinesterase, Medicinal plant.
Alzheimer’s disease (AD) is a neurodegenerative brain disorder associated with progressive dementia, a deterioration of memory and cognition.1 AD causes changes in normal physiological behaviors of elderly patients, with duration of 09 years between beginning of symptoms and demise and has been risen as one of the deadliest issue in created countries. By 2040, World Health Organization (WHO) evaluated around 71% of the dementia cases will happen in developing nations.2‒4 The role of neurotransmitter acetylcholine (ACh) with cognitive function is clinically established now.5 One of the neurotic signs of AD is loss of cholinergic cell in basalis of Meynert and hippocampus resulting reduce level of Ach in cerebrum.6 Subsequently, repletion of Ach levels in brain has been exploited therapeutically amid most recent couple of decades to accomplish symptomatic help in AD.7 In light of these etiologies a few pharmacological procedures with various conceivable targets are under scrutiny8 and the main line remedial approach includes re-foundation of ACh levels, with the hindrance of cholinesterases viz. acetylcholinesterase (AChE), butyrylcholinesterase (BChE) and also monoamine oxidase (MAO) enzymes.9,10 AChE basically acts by termination of nerve impulses at the cholinergic neural connections by quick hydrolysis of Ach to choline and acetic acid. This inhibition alleviates half-life of AChE and in this manner increasing concentration at synapses.11 In fact, tacrine was the first clinically proven AChE inhibitor acquainted with enhances Ach level at the nerve ending. Afterward, second era inhibitors are presented however coming about symptoms and cost factor made their use constrained.12 Medicinal plants and their concentrates are assuming an indispensable part in the present treatment of psychological issue either as standard or integral drug with specific reference to their ethnopharmacological perspectives.13,14 Basically, in Ayurveda (Traditional Indian medicinal system), these restorative plants were named "medharasayanas" (Sanskrit: "medha" implies intellect/cognition and "rasayana" implies revival.15 Medharasayanas incorporate a gathering of four therapeutic plants with multifold benefits, particularly to enhance memory and acumen by Prabhava (specific action) viz. Mandukaparni (Centella asiatica; Family: Umbelliferae), Yastimadhu (Glycirrhiza glabra; Family: Leguminosae), Guduchi (Tinospora cordifolia; Family: Menispermaceae) and Shankhapushpi (Convolvulus pleuricaulis; Family: Convolvulaceae).16 Traditional Indian medicinal plants like Ashwagandha (Withania somnifera; Family: Solanaceae), Brahmi (Bacopa monnieri; Family: Scophulariaceae), Jyothishmati (Celastrus panniculata; Family: Celastraceae), Kushmanda (Benincasa hispida; Family: Cucurbitaceae), Vacha (Acorus calamus; Family: Araceae) and Jatamamsi (Nardostachys jatamamsi; Family: Valerianaceae) are very much archived in Ayurveda and other traditional messages as brain tonics and memory enhancers.17 Indian turmeric (Curcuma longa; Family: Zingiberaceae) contains curcumin, a demonstrated cell reinforcement and anticholinesterase activity, is observed to be exceptionally compelling to defer the movement of AD.18 Cholinesterase inhibitors inhibit the hydrolysis of ACh by inhibitin AChE and thereby increase the availability of acetylcholine in brain specifically in cholinergic synapse.19 However, this approach is limited to patients who have intact and functionally active presynaptic neurons capable of synthesizing and releasing ACh. Therefore, AChE inhibitors are useful in the early and moderate stages of AD.20 Recent studies indicated that cholinesterase inhibitors might play a modulatory role on Ab plaque deposition via suppressing amyloid precursor protein (APP) expression.21 Medicinal plants have been the single most productive source of lead molecule for the development of drugs, and over a hundred new products are already in clinical development.22 Indeed, several pharmacological screenings showed the efficacy of these medicinal plants extracts alone or in combination along with their active constituents to encounter AD.23 The discoveries of exploratory results on different medicinal plants influencing cholinergic neurotransmission pertinent to the treatment of AD are given underneath (Table 1).
Family |
Common name |
Source |
Parts used |
Type of extract |
Method and % of cholinesterase inhibition |
Reference |
|
---|---|---|---|---|---|---|---|
|
|
|
|
|
AchE |
BchE |
|
Araceae |
Sweet Flag |
Acorus calamus |
Rhizome |
Methanol |
96 well plate; 50% (791.35μg/ml)* |
ND |
8 |
Brassicaceae |
White mustard |
Brassica alba |
Seed |
Ethanol |
UV spectroscopy; 50% (84.3±1.36μg/ml)* |
ND |
24 |
Capparidaceae |
Varuna |
Crataeva nurvala |
Stem bark |
Chloroform |
UV spectophotometry; 2.38±0.160 (µMoles/min/g of tissue) |
ND |
11 |
Caryophyllaceae |
Clove |
Eugenia caryophyllus |
Flower bud |
Essentail oil |
96 well plate; 50.45±0.003 (100µg/ml) |
96 well plate; 49.76±0.005 (100 µg/ml) |
25 |
Combretaceae |
Bohera |
Terminalia bellirica |
Fruit |
Methanol |
TLC and 96 well plate; 39.68±8.15 (0.1mg/ml) |
ND |
26 |
Haritaki |
Terminalia chebula |
Fruit |
Methanol |
96 well plate; 89.00±1.00 (5 mg/ml) |
96 well plate; 95.00±1.00 (5mg/ml) |
26 |
|
Convolvulaceae |
Shankhapushpi |
Convolvulus pluricaulis |
Whole plant |
Methanol |
TLC and 96 well plate; 2.22±1.17 (100µg/ml) |
ND |
26 |
Dioscoreaceae |
Aerial yam |
Dioscorea bulbifera |
Whole plant |
Methanol |
96 well plate; 79.00±2.00 (5mg/ml) |
96 well plate; 82.00±2.00 (5mg/ml) |
26 |
Fumariaceae |
Indian Fumitory |
Fumaria asepala |
Whole plant |
Chloroform: methanol (1:1) |
96 well plate; 91.99±0.70 (1mg/ml) |
96 well plate; 93.12±0.28 (1mg/ml) |
26 |
Ginkgoaceae |
Ginkgo |
Ginkgo biloba |
Whole plant |
Ethanol |
96 well plate; 50% (268.33µg/ml)* |
ND |
26 |
Hyperaceae |
St. Johns Wort |
Hypericum perforatum |
Aerial part |
Methanol |
UV spectophotometry; 73.5±2.40 (400µg/ml) |
UVspectophotometry; 50.5 ± 0.70 (400mg/ml) |
26 |
Lamiaceae |
Lavender |
Lavandula angustifolia |
Aerial parts |
Ethanol |
UV spectophotometry; 64.30±9.00 (1mg/ml) |
ND |
26 |
Menthe/Pudina |
Mentha spicata |
Whole plant |
Methanol |
TLC and 96 well plate; 15.00±0.00 (0.1mg/ml) |
ND |
26 |
|
Sage |
Salvia albimaculata |
Whole plant |
Petroleum ether |
96 well plate; 89.40±2.07 (1mg/ml) |
96 well plate; 73.90±0.76 (1 mg/ml) |
26 |
|
Leguminosae |
White siris |
Albizia procera |
Bark |
Methanol |
TLC and 96 well plate; 40.71±0.46 (0.1mg/ml) |
ND |
26 |
Indian Laburnum |
Cassia fistula |
Root |
Methanol |
TLC and 96 well plate; 54.13±3.90 (0.1mg/ml) |
ND |
26 |
|
Touch me not/Lajjavati |
Mimosa pudica |
Whole plant |
Water |
TLC and 96 well plate; 1.68±0.22 (100µg/ml) |
ND |
26 |
|
Licorice |
Glycyrrhiza glabra |
Root |
Methanol |
96 well plate; 50% (418±30.7µg/ml) * |
ND |
27 |
|
Fagaceae |
Menthi |
Trigonella foenum graecum |
Seeds |
Hydro alcohol |
TLC and 96 well plate; 50% (6±0.9µg/ml) |
ND |
28 |
Lythraceae |
Pomegranate |
Punica granatum |
Fruit |
Methanol |
96 well plate; 50% (77± 6.2µg/ml) * |
ND |
26 |
Nelumbonaceae |
Indian lotus |
Nelumbo nucifera |
Stamen |
Methanol |
TLC and 96 well plate; 23.77±2.83 (0.1mg/ml) |
ND |
23 |
Rubiaceae |
Indian Madder |
Rubia cordifolia |
Stem |
Methanol |
TLC and 96 well plate; 22.12±2.22 (100µg/ml) |
ND |
22 |
Scrophulariaceae |
Brahmi |
Bacopa monniera |
Whole plant |
Ethanol |
96 well plate; 42.90±1.20 (0.1mg/ml) |
ND |
18 |
Solanaceae |
Aswagandha |
Withania somnifera |
Root |
Methanol |
TLC and 96 well plate; 75.95±0.16 (100µg/ml) |
ND |
26 |
Root |
Aqueous |
TLC and 96 well plate; 24.60±0.38 (100µg/ml) |
ND |
26 |
|||
Umbelliferae |
Mandookparni |
Centella asiatica |
Whole plant |
Hydroalcohol |
96 well plate; 50% (106.55µg/ml)* |
ND |
26 |
Valerianaceae |
Indian Valerian |
Nardostachys jatamansi |
Rhizomes |
Methanol |
96 well plate; 50% (562.21µg/ml)* |
ND |
26 |
Zingiberaceae |
Galanga |
Alpinia galanga |
Rhizomes |
Methanol |
TLC and 96 well plate; 16.98±0.37 (100µg/ml) |
ND |
26 |
Zygophyllaceae |
Land-Caltrops/ Gokhru |
Tribulus terrestris |
Whole plants |
Chloroform: methanol (1:1) |
96 well plate; 37.89±0.77 (1mg/ml) |
96 well plate; 78.32±1.27 (1mg/ml) |
26 |
Table 1 Medicinal plants affecting cholinergic neurotransmission
ND, not done; *, represents IC50
Bioactive phytoconstituents resulted from isolation and characterization of natural flora and fauna have always been an important reservoir of drugs. The majority of the compounds examined till date affecting cholinergic neurotransmission and aiding protection against AD are primarily derived from plants sources.24 A list of phytoconstituents having significant AChE inhibitory activity is provided in Table 2. Natural alkaloids with AChE inhibitory activity viz. physostigmine, huperzine-A, galan- thamine, are successfully practiced to encounter progression of AD.25‒29 Stilbene oligomer viz. a-viniferin and triterpenoid viz. ursolic acid are another highly potential lead molecule with AChE inhibitory activity.30,31 The other major classes of phytoconstituents reported to have such activity are the flavonoids, glycosides and coumarins.32 Although, with enormous efforts structure activity relationship (SAR) of few isolated bioactive compounds have been established but most of them are yet to be finalized. Moreover, cellular based mechanism of action, clinical efficacy and toxicity profile of these phytoextracts and their derivatives requires further assessment, before proceeding towards clinical trials and final approval to encounter AD.
Chemical nature of phytoconstituents |
|
|
|
|||
---|---|---|---|---|---|---|
Alkaloid |
||||||
|
Class |
Source |
Family |
Activity on AchE |
References |
|
Assoanine |
Steroidal alkaloid |
Narcissus assoanus |
Amaryllidaceae |
50% inhibition at 3.87±0.24 pM |
29 |
|
Buxamine B |
Steroidal alkaloid |
Bums hyrcana |
Buxaceae |
50% inhibition at 7.56±0.008 pM |
29 |
|
Epinorgalantamine |
Steroidal alkaloid |
Narcissus confuses |
Amaryllidaceae |
50% inhibition at 9.60±0.65 pM |
29 |
|
Galantamine |
Steroidal alkaloid |
Galanthus nivalis |
Amaryllidaceae |
50% inhibition at 1.07±0.18 pM |
29 |
|
Sanguinine |
Steroidal alkaloid |
Eucharis grandeora |
Amaryllidaceae |
50% inhibition at 0.10±0.01 pM |
29 |
|
Oxoassoanine |
Steroidal alkaloid |
Narcissus assoanus |
Amaryllidaceae |
50% inhibition at 47.21±1.13 pM |
29 |
|
a-Solanine |
Glycoalkaloid |
Sarcococca saligna |
Buxaceae |
50% inhibition at 8.59±0.155 pM |
30 |
|
Vaganine |
Steroidal alkaloid |
Solanum tuberosum |
Solanaceae |
50% inhibition at 7.028±0.007 pM |
30 |
|
Physostigmine |
Indole alkaloid |
Physostigtna venenosiun |
Fabaceae |
50% inhibition at 6±1.0 pM |
31 |
|
Coronaridine |
Indole alkaloid |
Tabernaernontana austral |
Apocynaceae |
Minimum concentration of 25 pM to produce detectable spot in TLC |
28 |
|
Voacangine |
Indole alkaloid |
Tabernaentontana austral |
Apocynaceae |
Minimum concentration of 25pM to produce detectable spot in TLC |
28 |
|
Rupicoline |
Indole alkaloid |
Tabernaetnontana australis |
Apocynaceae |
Minimum concentration of 25µM to produce detectable spot in TLC |
6 |
|
Retamine |
Quinolizidine alkaloid |
Genista aucheri |
Fabaceae |
AchE and BchE inhibition (%) at 1 mg/ml at 15.0±1.08 & 66.3±0.88 respectively |
17 |
|
Corynoline |
Isoquinoline alkaloid |
Corydalis incisa |
Papaveraceae |
50% inhibition at 30.6 pM |
28 |
|
Palmatine |
Isoquinoline alkaloid |
Corydath speciosa |
Papaveraceae |
50% inhibition at 5.8 pM |
28 |
|
(-)-Huperzine A |
Quinolizidine alkaloid |
Huperzia serrate |
Lycopodiaceae |
50% inhibition at 10.1 pM |
31 |
|
Glycoside |
||||||
Cynatroside A |
Pregnant glycoside |
Cynanchum frown |
Asclepiadaceae |
50% inhibition at 6.4 pM |
31 |
|
Cynatroside B |
Pregnant glycoside |
Cynanchum stratum |
Asclepiadaceae |
50% inhibition at 3.6pM |
31 |
|
Norswertianolin |
Ggluco pyranoside |
Gentiana cambpestris |
Coniferae |
Minimum concentration of 1.20nM to produce detectable spot in TLC |
31 |
|
Swertianolin |
Bellidifolin 8-o-13 glucopyranoside |
Gentians cambpestris |
Coniferae |
Minimum concentration of 0.18nM to produce detectable spot in TLC |
31 |
|
Others |
||||||
Scopoletin |
Coumarin |
Vaccinium oldhami |
Ericaceae |
IC50 value of 79μM |
14 |
|
Murranganin |
Coumarins |
Murraya paniculata |
Rutaceae |
IC50 value of 79.1μM |
7 |
|
Viniferin |
Stilbene oligomer |
Caragana chantlague |
Leguminosae |
50% inhibition at 2.0pM |
5 |
|
Bellidin |
Xanthone |
Centime cambpestris |
Coniferae |
Minimum concentration of 0.03 nM to produce detectable spot in TLC bioassay |
14 |
|
Ursolic acid |
Triterpenoids |
Origami majorana |
Lamiaceae |
50% inhibition of AChE and BchE at 75.87±0.92 & 32.21±0.88 respectively |
18 |
|
Capsaicin |
Pungent principle |
Capsicum annum |
Solanaceae |
50% inhibition of AChE and BchE at 62.7±0.79 and 75.3±0.98 respectively |
18 |
|
Viniferin |
Polyphenol |
Caragana chamlague |
Leguminosae |
IC50 values of 2.0mM |
31 |
|
Kobophenol A |
Polyphenol |
Caragana chamlague |
Leguminosae |
IC50 value of 115.8mM |
31 |
|
Curcuminoids |
Triterpene |
Curcuma longa |
Ziniberaceae |
IC50 value of 19.67mM |
31 |
Table 2 Lead phytomolecules affecting cholinergic neurotransmission
The author is grateful to Assam Down Town University, Assam for providing necessary support for preparation of the manuscript.
There is no conflict of interest.
©2018 Bhattacharjee. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.