Morphological, Biochemical and Molecular Docking Evaluation of the Anti-inflammatory Effects of Methanolic Extract of Bridelia ferruginea stem bark on Acetic acid-induced Ulcerative Colitis in Rats

Q4 Medicine
Omolaso Blessing Oluwagbamila, Adeoti Adeniran, Kayode Adeniran, Alfred Abioye, Esther Nathaniel-Ukwa
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引用次数: 0

Abstract

Ulcerative colitis (UC) is a chronic disorder that involves inflammation. This study was carried out to examine the anti-inflammatory effect of the methanol extract of Brideliaferrugineastem barkinAcetic acid-induced ulcerative colitis inmaleWistarrats. Twenty-four rats were randomly divided into 6 groups of 4 animals each, colitis was thereafter induced by intrarectal administration of4% (v/v)Aceticacidin all except group 1, which received distilled water. For post-colitis induction treatment group 2 received distilled water, groups 3, 4 and 5 were orally administeredthe extract at doses of 100mg/kg, 200mg/kg and 400mg/kg, respectively while group 6 received sulfasalazine 500mg/kg orally.Post colitis induction, treatment lasted for 7 days and at the end of the experiment, colon samples were collected for estimation of antioxidant, inflammatory and histological parameters. Molecular docking study was also carried out to gain more insights about the promising anti-inflammatory compounds earlier identified in the extract.Results revealed that the extract significantly (p<0.05) attenuated the increased MDA, nitrite,TNF-α and IL-6 levels. Activities of SOD, CAT, MPO and GSH levelswere also, significantly (p<0.05) increased. Furthermore, molecular docking study revealed that α-amyrin may have contributed significantly to the anti-inflammatory activity of the extract because of its remarkable binding affinity for IL-6, iNOS, IL1-β,TNF-α and COX-2 relative to prednisolone and celecoxib. This study suggests that the extract attenuated acetic acid-induced colitis via antioxidative and anti-inflammatory mechanisms. .
铁娘子茎皮甲醇提取物对醋酸致溃疡性结肠炎大鼠抗炎作用的形态学、生化和分子对接评价
溃疡性结肠炎(UC)是一种涉及炎症的慢性疾病。本研究旨在探讨桥柳荆叶提取物甲醇提取物对醋酸致溃疡性结肠炎雄性大鼠的抗炎作用。将24只大鼠随机分为6组,每组4只,除1组给予蒸馏水外,其余均以4% (v/v)醋酸素直肠灌胃诱导结肠炎。结肠炎诱导后治疗组2给予蒸馏水,3、4、5组分别给予100mg/kg、200mg/kg、400mg/kg的提取物口服,6组给予磺胺嘧啶500mg/kg口服。结肠炎诱导后,处理7 d,实验结束时收集结肠样本,评估抗氧化、炎症和组织学参数。分子对接研究也进行了,以获得更多的见解,有前途的抗炎化合物早期发现的提取物。结果显示,提取物显著(p < 0.05)降低了MDA、亚硝酸盐、TNF-α和IL-6水平的升高。SOD、CAT、MPO活性和GSH水平均显著升高(p < 0.05)。此外,分子对接研究显示,α-amyrin可能与强的松龙和塞来昔布相比,对IL-6、iNOS、il - 1-β、TNF-α和COX-2具有显著的结合亲和力,从而显著促进了提取物的抗炎活性。本研究提示该提取物通过抗氧化和抗炎机制减轻醋酸性结肠炎。.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nigerian Journal of Physiological Sciences
Nigerian Journal of Physiological Sciences Medicine-Physiology (medical)
CiteScore
0.80
自引率
0.00%
发文量
23
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