Alyami Mohammad H, Hamdan Dalia I, Khalil Heba M A, Orabi Mohamed A A, Aborehab Nora M, Osama Nada, Abdelhafez Mai M, Al-Mahallawi Abdulaziz Mohsen, Alyami Hamad S
Department of Pharmaceutics, College of Pharmacy, Najran University, Najran 66462, Saudi Arabia.
Department of Pharmacognosy and Natural Products, Faculty of Pharmacy, Menoufia University, Shibin Elkom 32511, Egypt.
Saudi Pharm J. 2024 Mar;32(3):101968. doi: 10.1016/j.jsps.2024.101968. Epub 2024 Feb 2.
Asthma is a chronic disease affecting people of all ages. Asthma medications are associated with adverse effects restricting their long-term usage, demanding newer alternative therapies. This study aimed to investigate the anti-asthmatic properties of extract and its prepared nano-cubosomal dispersion (Ruta-ND). Firstly, the methanolic extract exhibited higher anti-inflammatory activity on Lipopolysaccharide (LPS)-activated BEAS-2B cells. To ensure best bioavailability and hence best cellular uptake, extract was loaded in nano-cubosomal dispersion (ND). Then, the anti-asthmatic effects of extract and ND were simultaneously evaluated in rats' model with ovalbumin-induced allergic asthma. extract and Ruta-ND subsided asthma score and improved lung function by restoring FEV1/FVC ratio to the expected values in control rats. Also, it showed strong antioxidant and anti-inflammatory activities manifested by lowering levels of malondialdehyde (MDA), IL-4, IL-7, TGF-β, and Ig-E, and increasing levels of superoxide dismutase (SOD) and INF-γ in bronchoalveolar lavage fluid. Our research findings also indicate autophagy induction and apoptosis inhibition by extract and Ruta-ND. Finally, the HPLC MS/MS phytochemical profiling of extract evident production of various alkaloids, flavonoids, coumarins, and other phenolics with reported pharmacological properties corresponding to/emphasize our study findings. In conclusion, exhibited promise in managing Ova-induced allergic asthma and could be developed as an alternative anti-allergic asthma drug.
哮喘是一种影响所有年龄段人群的慢性疾病。哮喘药物存在不良反应,限制了其长期使用,因此需要更新的替代疗法。本研究旨在探究[提取物名称]提取物及其制备的纳米立方液晶分散体(Ruta-ND)的抗哮喘特性。首先,[提取物名称]甲醇提取物对脂多糖(LPS)激活的BEAS-2B细胞表现出更高的抗炎活性。为确保最佳生物利用度从而实现最佳细胞摄取,将[提取物名称]提取物载入纳米立方液晶分散体(ND)中。然后,在卵清蛋白诱导的过敏性哮喘大鼠模型中同时评估[提取物名称]提取物和ND的抗哮喘作用。[提取物名称]提取物和Ruta-ND降低了哮喘评分,并通过将FEV1/FVC比值恢复到对照大鼠的预期值改善了肺功能。此外,它还表现出强大的抗氧化和抗炎活性,表现为降低支气管肺泡灌洗液中丙二醛(MDA)、IL-4、IL-7、TGF-β和Ig-E的水平,并提高超氧化物歧化酶(SOD)和INF-γ的水平。我们的研究结果还表明,[提取物名称]提取物和Ruta-ND可诱导自噬并抑制细胞凋亡。最后,[提取物名称]提取物的HPLC MS/MS植物化学图谱显示产生了各种生物碱、黄酮类、香豆素和其他酚类物质,其已报道的药理特性与我们的研究结果相符/强调了我们的研究结果。总之,[提取物名称]在治疗卵清蛋白诱导的过敏性哮喘方面显示出前景,可开发为一种替代抗过敏哮喘药物。