Sajjad Haider Muhammad, Ashraf Waseem, Javaid Sana, Fawad Rasool Muhammad, Muhammad Abdur Rahman Hafiz, Saleem Hammad, Muhammad Muneeb Anjum Syed, Siddique Farhan, Morales-Bayuelo Alejandro, Kaya Savas, Alqahtani Faleh, Alasmari Fawaz, Imran Imran
Department of Pharmacology, Faculty of Pharmacy, Bahauddin Zakariya University, Multan 60800, Pakistan.
Department of Pharmacy, The Women University, Multan 60000, Pakistan.
Saudi J Biol Sci. 2021 Aug;28(8):4384-4398. doi: 10.1016/j.sjbs.2021.04.033. Epub 2021 Apr 21.
In the current study, we investigated the phytochemical and neuropharmacological potential of , an indigenous least characterized plant widely distributed in deserted areas of Pakistan. The crude extract of the whole plant (IS.CR) was preliminary tested for the existence of polyphenol content, antioxidant and anticholinesterase potential followed by detailed chemical characterization through UHPLC-MS. Rats administered with different doses of IS.CR (100-300 mg/kg) for the duration of 4-weeks were behaviorally tested for anxiety and cognition followed by biochemical evaluation of dissected brain. The studies were employed to predict the blood-brain barrier crossing tendencies of secondary metabolites with the elucidation of the target binding site. The assays revealed ample phenols and flavonoids content in IS.CR with adequate anti-oxidant and anticholinesterase potential. The dose-dependent anxiolytic potential of IS.CR was demonstrated in open field (OFT), light/dark (L/D) and elevated plus maze (EPM) tests as animals spent more time in open, illuminated and elevated zones (P < 0.05). In the behavioral tests for learning/memory, the IS.CR reversed the scopolamine-induced cognitive deficits, as animals showed better (P < 0.05) spontaneous alternation and discrimination index in y-maze and novel object recognition (NOR) tests. Similarly, as compared to amnesic rats, the step-through latencies were increased (P < 0.05) and escape latencies were decreased (P < 0.05) in passive avoidance (PAT) and Morris water maze (MWM) tests, respectively. Biochemical analysis of rat brains showed significant reduction in malondialdehyde and acetylcholinesterase levels, alongwith preservation of glutathione peroxidase and superoxide dismutase activity. The docking studies further portrayed a possible interaction of detected phytoconstituents with acetylcholinesterase target. The results of the study show valuable therapeutic potential of phytoconstituents present in IS.CR to correct the neurological disarrays which might be through antioxidant activity or via modulation of GABAergic and cholinergic systems by artocommunol, 1,9-dideoxyforskolin and 6E,9E-octadecadienoic acid.
在本研究中,我们调查了一种广泛分布于巴基斯坦荒漠地区、特性鲜为人知的本土植物的植物化学和神经药理学潜力。对全株植物的粗提物(IS.CR)进行了多酚含量、抗氧化和抗胆碱酯酶潜力的初步测试,随后通过超高效液相色谱-质谱联用仪(UHPLC-MS)进行详细的化学表征。给大鼠连续4周给予不同剂量的IS.CR(100 - 300毫克/千克),对其进行焦虑和认知行为测试,随后对解剖后的大脑进行生化评估。采用相关研究预测次生代谢产物穿越血脑屏障的趋势,并阐明目标结合位点。分析表明,IS.CR中含有丰富的酚类和黄酮类物质,具有足够的抗氧化和抗胆碱酯酶潜力。在旷场试验(OFT)、明暗试验(L/D)和高架十字迷宫试验(EPM)中,IS.CR呈现出剂量依赖性抗焦虑潜力,因为动物在开放、明亮和高架区域停留的时间更长(P < 0.05)。在学习/记忆行为测试中,IS.CR逆转了东莨菪碱诱导的认知缺陷,因为动物在Y迷宫和新物体识别(NOR)测试中表现出更好的(P < 0.05)自发交替和辨别指数。同样,与记忆缺失大鼠相比,在被动回避试验(PAT)和莫里斯水迷宫试验(MWM)中,穿梭潜伏期分别增加(P < 0.05),逃避潜伏期减少(P < 0.05)。大鼠大脑生化分析显示,丙二醛和乙酰胆碱酯酶水平显著降低,同时谷胱甘肽过氧化物酶和超氧化物歧化酶活性得以保留。对接研究进一步描绘了检测到的植物成分与乙酰胆碱酯酶靶点之间可能的相互作用。研究结果表明,IS.CR中存在的植物成分具有宝贵的治疗潜力,可纠正神经紊乱,这可能是通过抗氧化活性,或通过artocommunol、1,9 - 二脱氧佛司可林和6E,9E十八碳二烯酸调节γ-氨基丁酸能和胆碱能系统来实现的。