Anti-ulcer Activity of Ethanolic Extract of Alstonia scholaris Bark: An in vivo and in silico Approach

M. Raju, R. Manisha, V. Reddy, M. Niharika
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引用次数: 1

Abstract

Aims: The present research is focused on screening in vivo anti-ulcer activity using pylorus ligation and ethanol induced ulcer model.  Study Design: Fourty eight rats, randomly divided into eight groups, were used in this study. Bark of Alstonia scholaris were air-dried, ground into fine powder and used in the preparation of an ethanolic extract. Place and Duration of Study: Department of Pharmacology, Osmania University, Hyderabad between December 2020 and September 2021. Methodology: Ethanol related ulcer was induced using 1 mL/kg b.w, p.o. Treated rats received ethanolic extract of Alstonia scholaris at various doses of 200 and 400 mg/kg b.w. Ulcer index, % ulcer protection were calculated and histological studies were conducted at 6 hr after pylorous ligation respectively. Results: Pharmacological estimations were done by means of 200 mg/kg, b.w. and 400 mg/kg, b.w. The total acidity and free acidity were decreased, pH was increased and ulcer index was decreased by Ethanolic extract of Alstonia scholaris (EEAS 200 and 400 mg/kg b.w., p.o.) in pylorus ligation model. Treatment with EEAS (200 and 400 mg/kg b.w. p.o.) has significantly decreased the ulcer index by ethanol induced ulcer model. To appreciate the ligand-binding attraction of the dynamic ingredients of the excerpt, docking trainings were accomplished for natural compounds against protein data bank (PDB) ID: 5A5N, PDB ID: 6Q2T, PDB ID: 7MBX, PDB ID: 2FV5. The results revealed that vanillic acid, venoterpine, loganetin, dibutyl phthalate, guaia-3,9- diene, 3,6-Bis[2-methylphenyl]-2,5-dihydropyrrolo[3,4-c] pyrrole-1,4- dione, 2H-1-Benzopyran- 2-one,7-acetyl-8-[acetyloxy]-4, n-hexadecanoic acid, stigmasterol, diospyrolide, D- Friedoolean-14-en-3-one, betulin, lupeol acetate, pentanoic acid and standard drug omeprazole had shown highest glide scores with all the selected proteins which indicate a stronger receptor-ligand binding affinity. Conclusion: From in vivo and in silico results it is evident that ethanolic bark extract of Alstonia scholaris possessed significant anti-ulcer activity.
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枸杞子树皮乙醇提取物抗溃疡活性的体内和体外实验研究
目的:采用幽门结扎法和乙醇诱导的溃疡模型,对其体内抗溃疡活性进行筛选。研究设计:48只大鼠随机分为8组。用风干的方法将Alstonia scholaris树皮磨成细粉,用于制备乙醇提取物。学习地点和时间:2020年12月至2021年9月,海得拉巴Osmania大学药学系。方法:以1 mL/kg b.w, p.o诱导乙醇相关性溃疡,大鼠分别以200、400 mg/kg b.w的不同剂量给药,计算幽门结扎后6小时的溃疡指数、溃疡保护率,并进行组织学观察。结果:以200 mg/kg b.w.和400 mg/kg b.w.对幽门结扎模型进行药理学评价。Alstonia scholaris乙醇提取物(EEAS 200和400 mg/kg b.w., p.o.)可降低幽门结扎模型的总酸度和游离酸度,提高pH,降低溃疡指数。EEAS(200和400 mg/kg b.w.p o)可显著降低乙醇致溃疡模型的溃疡指数。为了了解该摘录的动态成分对配体结合的吸引力,对天然化合物进行了对接训练,以蛋白质数据库(PDB) ID: 5A5N, PDB ID: 6Q2T, PDB ID: 7MBX, PDB ID: 2FV5。结果表明,香草酸、维诺特平、马尾草素、邻苯二甲酸二丁酯、愈伤草-3,9-二烯、3,6-二[2-甲基苯基]-2,5-二氢吡咯- 3,4-c]吡咯-1,4-二酮、2h -1-苯并吡喃-2 - 1,7 -乙酰基-8-[乙酰氧基]-4、正十六酸、豆甾醇、二ospyrolide、D- Friedoolean-14-en-3-one、白桦林、lupeoil acetate、戊酸和标准药物奥美拉唑与所有选择的蛋白质的滑翔得分最高,表明它们具有较强的受体-配体结合亲和力。结论:从体内和体外实验结果可以看出,石桐树皮乙醇提取物具有明显的抗溃疡活性。
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