Muhammad Hafsa, Salahuddin Zari, Akhtar Tasleem, Aftab Usman, Rafi Ali, Hussain Safdar, Shahzad Muhammad
Department of Pharmacology, University of Health Sciences, Lahore, Pakistan.
Centre for Applied Molecular Biology (CAMB), University of the Punjab, Lahore, Pakistan.
J Cell Biochem. 2023 Oct;124(10):1503-1515. doi: 10.1002/jcb.30459. Epub 2023 Aug 16.
Glabridin, a polyphenolic flavonoid derived from Glycyrrhiza glabra (licorice) roots, has shown anti-inflammatory and antioxidant properties. The current study sought to investigate glabridin's immunomodulatory effect in ovalbumin induced allergic asthma. Healthy male Wistar rats were divided into five groups. Group I served as a control group. Asthma was induced in groups II- IV. Groups III and IV were treated with glabridin (40 mg/kg) and methylprednisolone (15 mg/kg), respectively. Inflammatory cells counts were determined in blood and bronchoalveolar lavage fluid (BALF). Serum IgE levels and levels of catalase, superoxide dismutase and glutathione peroxidase in lung homogenate were measured. The levels of mRNA expression of pro-inflammatory, anti-inflammatory and oxidative stress markers were analysed. Delayed type hypersensitivity (DTH) and acute toxicity of glabridin were also checked. Glabridin significantly decreased inflammatory cells in the blood and BALF. It increased the concentration of antioxidant enzymes catalase, superoxide dismutase and glutathione peroxidase. Glabridin markedly decreased serum IgE levels and DTH when compared to asthmatic rats. It significantly alleviated the expression of TNF-α, IL-4, IL-5, CXCL1, iNOS, and NF-κB. Administering 10 times the therapeutic dose of glabridin did not show any signs of acute toxicity. Findings suggest that glabridin has the potential to ameliorate allergic asthma and its effects are comparable to those of methylprednisolone. The immunomodulatory effect of glabridin might be contributed by the suppression of pro-inflammatory cytokines, oxidative stress markers, IgE antibodies, and elevation of antioxidant enzymes, suggesting future study and clinical trials to propose it as a candidate to treat allergic asthma.
光甘草定是一种从甘草根中提取的多酚类黄酮,具有抗炎和抗氧化特性。本研究旨在探讨光甘草定对卵清蛋白诱导的过敏性哮喘的免疫调节作用。将健康雄性Wistar大鼠分为五组。第一组作为对照组。第二至四组诱导哮喘。第三组和第四组分别用光甘草定(40mg/kg)和甲基强的松龙(15mg/kg)治疗。测定血液和支气管肺泡灌洗液(BALF)中的炎症细胞计数。检测血清IgE水平以及肺匀浆中过氧化氢酶、超氧化物歧化酶和谷胱甘肽过氧化物酶的水平。分析促炎、抗炎和氧化应激标志物的mRNA表达水平。还检测了光甘草定的迟发型超敏反应(DTH)和急性毒性。光甘草定显著降低了血液和BALF中的炎症细胞。它提高了抗氧化酶过氧化氢酶、超氧化物歧化酶和谷胱甘肽过氧化物酶的浓度。与哮喘大鼠相比,光甘草定显著降低了血清IgE水平和DTH。它显著减轻了TNF-α、IL-4、IL-5、CXCL1、iNOS和NF-κB的表达。给予10倍治疗剂量的光甘草定未显示任何急性毒性迹象。研究结果表明,光甘草定有改善过敏性哮喘的潜力,其效果与甲基强的松龙相当。光甘草定的免疫调节作用可能是通过抑制促炎细胞因子、氧化应激标志物、IgE抗体以及提高抗氧化酶来实现的,这表明未来需要进行研究和临床试验,以将其作为治疗过敏性哮喘的候选药物。