Naser Eva H, Idries Ahmed H, Elmubarak Sara A A, Dafalla Maha B, Abdelrahim Yusria E, Abdalrhman Entsar A, Ahmed Bashir M, Osman Makarim Elfadil M, Awadallah Amna K E, Ebrahim Reem M A, Abdellatif Ashraf O, Saad Haseeba A, Konozy Emadeldin H E
Biotechnology Department, Africa City of Technology, Khartoum, Sudan.
Medicinal, Aromatic Plants and Traditional Medicine Research Institute (MAPTRI), National Center for Research, Khartoum, Sudan.
Biochimie. 2024 Dec;227(Pt A):273-285. doi: 10.1016/j.biochi.2024.08.003. Epub 2024 Aug 3.
In the pursuit of safer and more effective treatments, there is a growing interest in plant-derived compounds, particularly lectins, because of their diverse pharmacological properties. This study focused on isolating, purifying, and characterizing lectin from Combretum glutinosum seeds (CGSLs) to assess its potential as an analgesic and antiulcer agent. CGSL extraction involved defatting and buffer extraction, followed by purification using ammonium sulfate fractionation and fetuin-agarose affinity column chromatography. The isolectins (iso-CGSLs), each consisting of 60 kDa and 57 kDa heterodimeric subunits, displayed glycoprotein properties with a 40 % neutral sugar content. They exhibited peak activity at 55 °C and remained stable for up to the fifth day at room temperature. The activity exhibited a pH dependence, peaking between 7.5 and 10.5, and all seemingly operated independently of metal ions. CGSL, at optimal doses ranging from 6 to 12 mg/kg, had significant analgesic effects on acetic acid-induced writhing and hot plate tests in mice. Evaluation using 0.7 % acetic acid resulted in notable pain reduction across all doses (P < 0.05). The analgesic effect of lectin was partially reversed by naloxone (a morphine antagonist), indicating partial involvement of the opioid receptor system. Furthermore, CGSL exhibited antiulcer effects in ethanol-induced gastric ulcer models in rats, highlighting its therapeutic potential as a natural alternative for analgesic and antiulcer treatments.
在追求更安全、更有效的治疗方法的过程中,由于植物来源的化合物,特别是凝集素具有多种药理特性,人们对它们的兴趣与日俱增。本研究聚焦于从多穗风车子种子(CGSLs)中分离、纯化和鉴定凝集素,以评估其作为镇痛和抗溃疡药物的潜力。CGSL的提取包括脱脂和缓冲液提取,随后使用硫酸铵分级分离和胎球蛋白 - 琼脂糖亲和柱色谱法进行纯化。这些异凝集素(iso - CGSLs),每个由60 kDa和57 kDa的异二聚体亚基组成,显示出糖蛋白特性,中性糖含量为40%。它们在55°C时表现出峰值活性,在室温下最多可保持五天稳定。其活性表现出pH依赖性,在7.5至10.5之间达到峰值,并且似乎都独立于金属离子起作用。CGSL在6至12 mg/kg的最佳剂量下,对小鼠醋酸诱导的扭体和热板试验具有显著的镇痛作用。使用0.7%醋酸进行评估,所有剂量均导致显著的疼痛减轻(P < 0.05)。凝集素的镇痛作用被纳洛酮(一种吗啡拮抗剂)部分逆转,表明阿片受体系统部分参与其中。此外,CGSL在大鼠乙醇诱导的胃溃疡模型中表现出抗溃疡作用,突出了其作为镇痛和抗溃疡治疗天然替代品的治疗潜力。