Aati Hanan Y, Attia Hala A, Alanazi Arwa S, Al Tamran Luluh K, Wanner Juergen K
Department of Pharmacognosy, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.
Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.
Pharmaceuticals (Basel). 2024 Oct 31;17(11):1460. doi: 10.3390/ph17111460.
This study aimed to analyze the chemical composition and biological activities of L. essential oil, focusing on its antioxidant and enzyme inhibition (α-amylase and urease) properties. Additionally, in vitro pharmacokinetic and pharmacodynamic evaluations were conducted through in silico molecular docking and BOILED-Egg models to assess its therapeutic potential and its potency in treating oxidative-stress-related diseases. The essential oil was isolated by the hydrodistillation (HD) of fresh plant material, and volatiles released from dried plant material were sampled via headspace solid-phase microextraction (HS-SPME), followed by a phytochemical profiling analysis through the GC-MS tool. Antioxidant capacity was assessed using DPPH, ABTS, FRAP, and nitric oxide scavenging assays, while enzyme inhibition activities were tested against α-amylase and urease. Molecular docking and BOILED-Egg models were used to evaluate compound interactions with NADPH oxidase and predict pharmacokinetic behavior, respectively. HS-SPME and HD yielded 46 and 25 compounds, respectively, primarily terpenoids represented by camphor (26.4%) and cis-davanone (18.0%) in HS-SPME, while in the HD essential oil, cis-davanone (60.2%) and chamazulene (10.8%) were most prevalent. The antioxidant assays showed a strong activity, with a total antioxidant capacity of 821.8 mg ascorbic acid Eq/gm. The essential oil inhibited urease by 86.7% and α-amylase by 81.8%. Molecular docking showed strong binding affinities with NADPH oxidase, supporting the antioxidant results. EO demonstrated potent antioxidant and enzyme inhibitory activities, suggesting its therapeutic potential for treating enzyme-related disorders like diabetes mellitus and its possible use as a cure for many oxidative-stress-related diseases, thus validating the folkloric use of this plant.
本研究旨在分析某植物精油的化学成分和生物活性,重点关注其抗氧化和酶抑制(α-淀粉酶和脲酶)特性。此外,通过计算机模拟分子对接和“水煮蛋”模型进行了体外药代动力学和药效学评估,以评估其治疗潜力以及治疗氧化应激相关疾病的效力。通过对新鲜植物材料进行水蒸馏(HD)分离出精油,并通过顶空固相微萃取(HS-SPME)对干燥植物材料释放的挥发物进行采样,随后通过气相色谱-质谱联用(GC-MS)工具进行植物化学剖析分析。使用1,1-二苯基-2-苦基肼(DPPH)、2,2'-联氮-双-3-乙基苯并噻唑啉-6-磺酸(ABTS)、铁离子还原抗氧化能力(FRAP)和一氧化氮清除试验评估抗氧化能力,同时针对α-淀粉酶和脲酶测试酶抑制活性。分子对接和“水煮蛋”模型分别用于评估化合物与烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶的相互作用并预测药代动力学行为。HS-SPME和HD分别产生了46种和25种化合物,主要是萜类化合物,在HS-SPME中以樟脑(26.4%)和顺式达瓦酮(18.0%)为代表,而在HD精油中,顺式达瓦酮(60.2%)和天蓝烃(10.8%)最为普遍。抗氧化试验显示出较强的活性,总抗氧化能力为821.8毫克抗坏血酸当量/克。该精油对脲酶的抑制率为86.7%,对α-淀粉酶的抑制率为81.8%。分子对接显示与NADPH氧化酶具有很强的结合亲和力,支持了抗氧化结果。该精油表现出强大的抗氧化和酶抑制活性,表明其在治疗糖尿病等酶相关疾病方面的治疗潜力,以及其作为许多氧化应激相关疾病治疗方法的可能性,从而验证了该植物的民间药用价值。