| Autor: |
Singh JV; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar 143005, Punjab, India., Thakur S; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar 143005, Punjab, India., Kumar N; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar 143005, Punjab, India.; Drug and Pollution Testing Laboratory, Guru Nanak Dev University, Amritsar 143005, Punjab, India., Singh H; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar 143005, Punjab, India., Mithu VS; Department of Chemistry, Guru Nanak Dev University, Amritsar 143005, Punjab, India., Singh H; Department of Chemistry, Guru Nanak Dev University, Amritsar 143005, Punjab, India., Bhagat K; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar 143005, Punjab, India., Gulati HK; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar 143005, Punjab, India., Sharma A; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar 143005, Punjab, India., Singh H; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar 143005, Punjab, India., Sharma S; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar 143005, Punjab, India., Bedi PMS; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar 143005, Punjab, India.; Drug and Pollution Testing Laboratory, Guru Nanak Dev University, Amritsar 143005, Punjab, India. |
| Abstrakt: |
In continuous efforts to develop anti-Alzheimer's agents, we rationally designed and synthesized a series of multitargeting molecules by incorporating the essential molecular features of the standard drug donepezil. Among the series, compound 4b showed multitargeting properties to act as an anti-Alzheimer's agent, which is better tolerable in vivo than donepezil. Acetylcholinesterase (AChE) inhibition data showed that compound 4b inhibits the enzyme with a half-maximal inhibitory concentration (IC 50 ) value of 0.78 μM and also showed DNA protection, which was confirmed through the DNA nicking assay, suggesting the protective effect of 4b against oxidative DNA damage. Compound 4b also showed 53.04% inhibition against Aβ 1-42 aggregations, which was found comparable to that of the standard compound curcumin. Molecular dynamics simulations were performed to check the stability of compound 4b with the enzyme AChE, which showed that the enzyme-ligand complex is stable enough to block the hydrolysis of acetylcholine in the brain. Its higher LD 50 cutoff value (50 mg/kg) in comparison to donepezil (LD 50 : 25 mg/kg) made it safer, suggesting that it can be used in further clinical experiments. To evaluate its anti-Alzheimer property, a mice model with melamine-induced cognitive dysfunction was used, and Morris water maze and Rotarod tests were performed. A significant improvement in memory was observed after the treatment with compound 4b and donepezil. The study postulated that the introduction of important structural features of donepezil (dimethoxyindanone moiety as ring-A) embarked with terminal aromatic ether (ring-B and ring-C) made 4b a multitargeting molecule that offers a way for developing alternative therapeutics in the future against Alzheimer's disease (AD). |
