Aryal Babita, Raut Bimal Kumar, Bhattarai Salyan, Bhandari Sobika, Tandan Parbati, Gyawali Kabita, Sharma Kabita, Ranabhat Deepa, Thapa Ranjita, Aryal Dipa, Ojha Atul, Devkota Hari Prasad, Parajuli Niranjan
Biological Chemistry Lab, Central Department of Chemistry, Tribhuvan University, Kirtipur, Kathmandu, Nepal.
Meakins-Christie Laboratories, Department of Medicine, McGill University, Montreal, Quebec, Canada.
Evid Based Complement Alternat Med. 2022 Mar 9;2022:7299778. doi: 10.1155/2022/7299778. eCollection 2022.
Alkaloids are a type of natural compound possessing different pharmacological activities. Natural products, including alkaloids, which originate from plants, have emerged as potential protective agents against neurodegenerative disorders (NDDs) and chronic inflammations. A wide array of prescription drugs are used against these conditions, however, not free of limitations of potency, side effects, and intolerability. In the context of personalized medicine, further research on alkaloids to unravel novel therapeutic approaches in reducing complications is critical. In this review, a systematic survey was executed to collect the literature on alkaloids and their health complications, from which we found that majority of alkaloids exhibit anti-inflammatory action via nuclear factor-B and cyclooxygenase-2 (COX-2), and neuroprotective interaction through acetylcholinesterase (AChE), COX, and -site amyloid precursor protein activity. ADMET and ProTox-II-related descriptors were calculated to predict the pharmacological properties of 280 alkaloids isolated from traditional medicinal plants towards drug development. Out of which, eight alkaloids such as tetrahydropalmatine, berberine, tetrandrine, aloperine, sinomenine, oxymatrine, harmine, and galantamine are found to be optimal within the categorical range when compared to nicotine. These alkaloids could be exploited as starting materials for novel drug synthesis or, to a lesser extent, manage inflammation and neurodegenerative-related complications.
生物碱是一类具有不同药理活性的天然化合物。包括生物碱在内的源自植物的天然产物已成为对抗神经退行性疾病(NDDs)和慢性炎症的潜在保护剂。针对这些病症使用了各种各样的处方药,然而,这些药物并非没有效力、副作用和耐受性方面的局限性。在个性化医疗的背景下,进一步研究生物碱以揭示减少并发症的新治疗方法至关重要。在本综述中,我们进行了系统的调查以收集有关生物碱及其健康并发症的文献,从中我们发现大多数生物碱通过核因子-κB和环氧化酶-2(COX-2)发挥抗炎作用,并通过乙酰胆碱酯酶(AChE)、COX和β-位点淀粉样前体蛋白活性产生神经保护作用。计算了与ADMET和ProTox-II相关的描述符,以预测从传统药用植物中分离出的280种生物碱对药物开发的药理特性。其中,与尼古丁相比,四氢巴马汀、小檗碱、粉防己碱、苦参碱、青藤碱、氧化苦参碱、去氢骆驼蓬碱和加兰他敏等八种生物碱在分类范围内被发现是最佳的。这些生物碱可作为新型药物合成的起始原料,或者在较小程度上用于管理炎症和神经退行性相关并发症。