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Anti-Acetylcholinesterase Activities of Mono-Herbal Extracts and Exhibited Synergistic Effects of the Phytoconstituents: A Biochemical and Computational Study
被引:40
|作者:
Balkrishna, Acharya
[1
,2
]
Pokhrel, Subarna
[1
]
Tomer, Meenu
[1
]
Verma, Sudeep
[1
]
Kumar, Ajay
[1
]
Nain, Pradeep
[1
]
Gupta, Abhishek
[1
]
Varshney, Anurag
[1
,2
]
机构:
[1] Patanjali Res Fdn Trust, Patanjali Res Inst, Drug Discovery & Dev Div, Roorkee Haridwar Rd, Haridwar 249405, India
[2] Univ Patanjali, Dept Allied Sci, Roorkee Haridwar Rd, Haridwar 249405, India
来源:
关键词:
Alzheimer's disease;
anti-acetylcholinesterase activity;
herbal extracts;
HPLC;
synergistic effect;
molecular docking;
ALZHEIMERS-DISEASE;
ACETYLCHOLINESTERASE INHIBITORS;
BERBERINE;
PLANTS;
D O I:
10.3390/molecules24224175
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Alzheimer's disease (AD), a neurodegenerative disease, is the most common form of dementia. Inhibition of acetylcholinesterase (AChE) is a common strategy for the treatment of AD. In this study, aqueous, hydro-methanolic, and methanolic extracts of five potent herbal extracts were tested for their in vitro anti-AChE activity. Among all, the Tinospora cordifolia (Giloy) methanolic fraction performed better with an IC50 of 202.64 mu g/mL. Of the HPLC analyzed components of T. cordifolia (methanolic extract), palmatine and berberine performed better (IC50 0.66 and 0.94 mu g/mL, respectively) as compared to gallic acid and the tool compound "galantamine hydrobromide" (IC50 7.89 and 1.45 mu g/mL, respectively). Mode of inhibition of palmatine and berberine was non-competitive, while the mode was competitive for the tool compound. Combinations of individual alkaloids palmatine and berberine resulted in a synergistic effect for AChE inhibition. Therefore, the AChE inhibition by the methanolic extract of T. cordifolia was probably due to the synergism of the isoquinoline alkaloids. Upon molecular docking, it was observed that palmatine and berberine preferred the peripheral anionic site (PAS) of AChE, with pi -interactions to PAS residue Trp286, indicating that it may hinder the substrate binding by partially blocking the entrance of the gorge of the active site or the product release.
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页数:15
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