Johnson Titilayo Omolara, Odoh Kenneth Daniel, Nwonuma Charles Obiora, Akinsanmi Augustina Oduje, Adegboyega Abayomi Emmanuel
Department of Biochemistry, Faculty of Medical Sciences, University of Jos, Jos, Nigeria.
Department of Biochemistry, College of Pure and Applied Sciences, Landmark University, Omu-Aran, Nigeria.
Heliyon. 2020 May 12;6(5):e03893. doi: 10.1016/j.heliyon.2020.e03893. eCollection 2020 May.
Ulcerative colitis (UC) is an inflammation of the colon that can progress to colorectal cancer if left untreated. No medication completely cures UC and natural products are sources of alternative approaches. This study aimed to determine the anti-inflammatory potential of leaf extract and fractions in a rat model of ulcerative colitis and to identify the active ingredients. UC was induced in rats by intra-rectal infusion of 1ml of 4% acetic acid (AA) in normal saline. AA exposed groups of rats were treated with 100 mg/kg bodyweight of methanol extract, hexane, ethyl-acetate and butanol fractions orally for four days. Another group received the standard drug - Dexamethasone and control rats were given distilled water only. Some biochemical changes were evaluated and the active ingredients were identified using Gas Chromatography-Mass Spectrometry (GC-MS) followed by molecular docking against interleukin-1-beta converting enzyme (Caspase-1), beta-2 adrenergic receptor (ADRB2), cyclooxygenase-2 (COX-2) and tumour necrosis factor-alpha (TNF-α). Exposure of rat colon to acetic acid significantly altered (p < 0.05) serum levels of tumour necrosis factor-alpha (TNF-α), interleukin - 6 (IL-6), nitric oxide (NO), lipid peroxidation product (malondialdehyde or MDA), reduced glutathione (GSH); and activities of superoxide dismutase (SOD) and catalase (CAT). These alterations were however restored in the rats treated with leaf with the ethyl-acetate fraction displaying the highest ameliorative activity. GC-MS analysis of the ethyl acetate fraction revealed the presence of 40 compounds which when subjected to molecular docking demonstrated varying degrees of binding affinities for the protein targets. Ethyl iso-allocholate demonstrated the highest binding affinity for caspase-1, cholest-22-ene-21-ol, 3,5-dehydro-6- methoxy-, pivalate for ADRB2 and TNF-α; and alpha-cadinol for COX-2. The anti-inflammatory potential of leaf as a natural remedy and as a source of new drugs against ulcerative colitis is validated.
溃疡性结肠炎(UC)是结肠的一种炎症,如果不治疗可能会发展为结直肠癌。目前尚无药物能完全治愈UC,天然产物是替代治疗方法的来源。本研究旨在确定叶提取物及其馏分在溃疡性结肠炎大鼠模型中的抗炎潜力,并鉴定其活性成分。通过向大鼠直肠内注入1ml含4%乙酸(AA)的生理盐水诱导UC。AA暴露组大鼠口服100mg/kg体重的甲醇提取物、己烷、乙酸乙酯和丁醇馏分,持续四天。另一组接受标准药物——地塞米松,对照组大鼠仅给予蒸馏水。评估了一些生化变化,并使用气相色谱-质谱联用仪(GC-MS)鉴定活性成分,随后针对白细胞介素-1-β转化酶(半胱天冬酶-1)、β-2肾上腺素能受体(ADRB2)、环氧化酶-2(COX-2)和肿瘤坏死因子-α(TNF-α)进行分子对接。大鼠结肠暴露于乙酸后,肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、一氧化氮(NO)、脂质过氧化产物(丙二醛或MDA)、还原型谷胱甘肽(GSH)的血清水平以及超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的活性均发生了显著变化(p<0.05)。然而,用叶治疗的大鼠这些变化得以恢复,其中乙酸乙酯馏分显示出最高的改善活性。对乙酸乙酯馏分的GC-MS分析显示存在40种化合物,对这些化合物进行分子对接后发现它们对蛋白质靶点具有不同程度的结合亲和力。异乙基别胆甾醇对半胱天冬酶-1的结合亲和力最高,胆甾-22-烯-21-醇、3,5-脱氢-6-甲氧基-、新戊酸酯对ADRB2和TNF-α的结合亲和力最高;α-杜松醇对COX-2的结合亲和力最高。叶作为治疗溃疡性结肠炎的天然药物和新药来源的抗炎潜力得到了验证。