Abstract
Background: A simultaneous administration of an acetylcholinesterase (AChE) inhibitor and a NSAID as a drug cocktail has been documented to exhibit significantly protective effects in AD patients. But it suffers from poor patent compliance, pharmacodynamics and pharmacokinetic issues.
Objective: The present study is aimed to design and synthesize a hybrid molecule capable of exhibiting both AChE inhibition and anti-inflammatory activities for de-accelerating the progression of AD. The synthesized molecules will be evaluated for in vitro and in vivo models.
Methods: The present study involves the coupling of ibuprofen or naproxen to varied disubstituted amines (AChE inhibitor pharmacophore) through benzimidazole to develop two series of compounds i.e. IB01-IB05 and NP01-NP05. The synthesized compounds were characterized using FTIR, 1H-NMR, 13C-NMR and MS. All compounds were evaluated for in vitro AChE inhibitory and COX inhibitory activities. The most active compound was taken for in vivo evaluation.
Results: Compounds of series IB01-IB05 are found more potent as compared to NP01-NP05. The maximally potent compound IB04 in in vitro evaluation is selected for in vivo evaluation of memory restoration activity using scopolamine-induced amnesia model in mice. It significantly reverses the scopolamine-induced changes (i.e., escape latency time, mean time spent in target quadrant, brain AChE activity and oxidative stress) in a dose-dependent manner. IB04 at 8 mg/kg is significantly effective in lowering AD manifestation in comparison to donepezil.
Conclusion: The findings indicate that Benzimidazole hybrids utilizing ibuprofen and pyrrolidine moiety may prove a useful template for the development of new chemical moieties against AD with multiple potencies.
Keywords: NsCOXi, Alzheimer’s disease, acetylcholinesterase inhibitor, hybrid, benzimidazole, ibuprofen, naproxen.
Graphical Abstract
[http://dx.doi.org/10.1111/j.1755-5949.2010.00175.x] [PMID: 20560995]
[http://dx.doi.org/10.2165/00002512-200724020-00007] [PMID: 17313203]
[http://dx.doi.org/10.1016/j.drudis.2013.01.008] [PMID: 23340113]
[http://dx.doi.org/10.3389/fnagi.2018.00083] [PMID: 29643804]
[http://dx.doi.org/10.1136/bmj.327.7407.128] [PMID: 12869452]
[http://dx.doi.org/10.3233/JAD-141506] [PMID: 25227314]
[http://dx.doi.org/10.1016/j.neurobiolaging.2006.03.013] [PMID: 16697488]
[http://dx.doi.org/10.1080/07391102.2017.1338164] [PMID: 28571516]
[http://dx.doi.org/10.1016/j.bmcl.2010.02.102] [PMID: 20347302]
[http://dx.doi.org/10.1016/j.bmc.2012.09.013] [PMID: 23031649]
[http://dx.doi.org/10.1016/0006-2952(61)90145-9] [PMID: 13726518]
[http://dx.doi.org/10.2174/1573406415666190409111459] [PMID: 30963980]
[http://dx.doi.org/10.1073/pnas.88.7.2692] [PMID: 1849272]
[http://dx.doi.org/10.1212/WNL.62.1.66] [PMID: 14718699]
[http://dx.doi.org/10.1016/0003-2697(79)90738-3] [PMID: 36810]
[PMID: 13967893]