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对Linn.叶的植物药理学和计算分析揭示了其针对氧化、高血糖、疼痛和腹泻的药理特性。

Phyto-pharmacological and computational profiling of Linn. Leaves revealed pharmacological properties against oxidation, hyperglycemia, pain, and diarrhea.

作者信息

Taher Mohammad Abdullah, Hossain Md Jamal, Zahan Miss Sharmin, Hasan Mohammad Mahmudul, Ferdous Jannatul, Rahman Asheka, Khan Mala, Hosain Md Khalid, Rashid Mohammad A

机构信息

Phytochemical Research Laboratory, Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Dhaka, Dhaka 1000, Bangladesh.

Bangladesh Bangladesh Reference Institute for Chemical Measurements (BRiCM), Laboratory Road, Dhaka 1205, Bangladesh.

出版信息

Heliyon. 2024 Jul 30;10(15):e35422. doi: 10.1016/j.heliyon.2024.e35422. eCollection 2024 Aug 15.

Abstract

The present study aimed to conduct phytochemical and pharmacological profiling of methanolic crude extract of leaves of Linn. via experimental and computational approaches. Six secondary metabolites were isolated chromatographically, and the structures were elucidated by extensive analyses of high-resolution H and C NMR data. The separated compounds were characterized as β-sitosterol (), β-amyrin (), β-amyrin acetate (), β-amyrin palmitate (), β-amyrone (), and isoscopoletin (). DPPH free radical scavenging assay, tail-tipping method, writhing assay, and castor oil-induced diarrheal mice methods, respectively, were used to assess the antioxidant, hypoglycemic, analgesic, and anti-diarrheal activities of the leaf extract of plant species. The study observed significant reductions (p < 0.05) in the level of blood glucose at 30, 60, 120, and 180 min following the administration of the crude extracts (200 mg/kg body weight (bw) and 400 mg/kg bw). These reductions occurred in a time-dependent manner. Additionally, both doses of the investigated extracts exhibited significant (p < 0.05) central and peripheral analgesic effects compared to morphine (2 mg/kg bw) and diclofenac sodium (50 mg/kg bw), respectively. Furthermore, the 400 mg/kg bw extract demonstrated anti-diarrheal activity, reducing 54.17 % of diarrheal episodes in mice compared to loperamide with 70.83 % inhibition. The computational investigations yielded results consistent with existing findings. The results obtained from molecular docking showed that the isolated compounds had a better or comparable binding affinity to the active binding sites of the glutathione reductase enzyme, mu-opioid receptor, cyclooxygenase 2 (COX-2), glucose transporter 3 (GLUT 3), and kappa opioid receptor. These findings may indicate that the compounds isolated from the plant species have antioxidant, analgesic, hypoglycemic, and anti-diarrheal, properties. Consequently, it was inferred that the plant might be beneficial in dealing with oxidation, diarrhea, hyperglycemia, and pain. Nonetheless, further investigations are necessary to perform thorough phytochemical profiling and elucidate the exact mechanistic ways of the crude extract and the isolated phytoconstituents.

摘要

本研究旨在通过实验和计算方法对[植物名称] Linn. 叶片的甲醇粗提物进行植物化学和药理学分析。通过色谱法分离出六种次生代谢产物,并通过对高分辨率氢谱和碳谱数据的广泛分析阐明其结构。分离出的化合物被鉴定为β-谷甾醇()、β-香树脂醇()、β-香树脂醇乙酸酯()、β-香树脂醇棕榈酸酯()、β-香树脂酮()和异莨菪亭()。分别采用DPPH自由基清除试验、剪尾法、扭体试验和蓖麻油诱导的腹泻小鼠模型,评估该植物叶片提取物的抗氧化、降血糖、镇痛和止泻活性。研究观察到,在给予粗提物(200毫克/千克体重和400毫克/千克体重)后30、60、120和180分钟,血糖水平显著降低(p < 0.05)。这些降低呈时间依赖性。此外,与吗啡(2毫克/千克体重)和双氯芬酸钠(50毫克/千克体重)相比,两种剂量的受试提取物分别表现出显著的(p < 0.05)中枢和外周镇痛作用。此外,400毫克/千克体重的提取物表现出止泻活性,与洛哌丁胺相比,可减少小鼠54.17%的腹泻发作,洛哌丁胺的抑制率为70.83%。计算研究结果与现有发现一致。分子对接结果表明,分离出的化合物与谷胱甘肽还原酶、μ-阿片受体、环氧化酶2(COX-2)、葡萄糖转运蛋白3(GLUT 3)和κ-阿片受体的活性结合位点具有较好或相当的结合亲和力。这些发现可能表明,从该植物物种中分离出的化合物具有抗氧化、镇痛、降血糖和止泻特性。因此,可以推断该植物可能有助于应对氧化、腹泻、高血糖和疼痛。尽管如此,仍需要进一步研究以进行全面的植物化学分析,并阐明粗提物和分离出的植物成分的确切作用机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb13/11336592/51aecb124af6/gr1.jpg

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