Alsaleh Asma N, Aziz Ibrahim M, Aljowaie Reem M, Alshalan Rawan M, Alkubaisi Noorah A, Aboul-Soud Mourad A M
Department of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, P.O. Box 10219, Riyadh 11433, Saudi Arabia.
Pharmaceuticals (Basel). 2024 Dec 7;17(12):1646. doi: 10.3390/ph17121646.
L., is a plant with established pharmacological properties, but the root extract (AARE) remains unexplored. The aim of this study was to examine the chemical composition of AARE and assess its biological activity, which included antidiabetic, antibacterial, anticancer, and antioxidant properties. GC-MS was used to analyze the chemical components. The antioxidant activity of the total phenolic and flavonoid content was evaluated. Antibacterial activity and cytotoxic effects were identified. Enzyme inhibition experiments were performed to determine its antidiabetic potential. Molecular docking was utilized to evaluate the potential antioxidant, antibacterial, and anticancer activities of the compounds from AARE using Maestro 11.5 from the Schrödinger suite. AARE exhibited moderate antioxidant activity in DPPH (IC: 172.41 ± 3.15 μg/mL) and ABTS (IC: 378.94 ± 2.18 μg/mL) assays. Cytotoxicity tests on MCF-7 and HepG2 cancer cells demonstrated significant anticancer effects, with IC values of 150.12 ± 0.74 μg/mL and 137.11 ± 1.33 μg/mL, respectively. Apoptotic studies indicated an upregulation of pro-apoptotic genes (-, , , ) and a downregulation of anti-apoptotic markers ( and ). AARE also inhibited α-amylase and α-glucosidase, suggesting potential antidiabetic effects, with IC values of 224.12 ± 1.17 μg/mL and 243.35 ± 1.51 μg/mL. Antibacterial assays revealed strong activity against Gram-positive bacteria. Molecular docking and pharmacokinetic analysis identified promising inhibitory effects of key AARE compounds on NADPH oxidase, Gyrase B, and Topoisomerase IIα, with favorable drug-like properties. These findings suggest AARE's potential in treating cancer, diabetes, and bacterial infections, warranting further in vivo and clinical studies.
L.是一种具有既定药理特性的植物,但其根提取物(AARE)尚未得到充分研究。本研究的目的是研究AARE的化学成分并评估其生物活性,包括抗糖尿病、抗菌、抗癌和抗氧化特性。采用气相色谱-质谱联用(GC-MS)分析化学成分。评估了总酚和黄酮含量的抗氧化活性。确定了抗菌活性和细胞毒性作用。进行酶抑制实验以确定其抗糖尿病潜力。利用分子对接,使用薛定谔软件包中的Maestro 11.5评估AARE中化合物的潜在抗氧化、抗菌和抗癌活性。在二苯基苦味酰基自由基(DPPH,IC₅₀:172.41±3.15μg/mL)和2,2'-联氮-二(3-乙基苯并噻唑啉-6-磺酸)二铵盐(ABTS,IC₅₀:378.94±2.18μg/mL)实验中,AARE表现出中等程度的抗氧化活性。对MCF-7和HepG2癌细胞的细胞毒性测试显示出显著的抗癌效果,IC₅₀值分别为150.12±0.74μg/mL和137.11±1.33μg/mL。凋亡研究表明促凋亡基因(-、-、-、-)上调,抗凋亡标志物(-和-)下调。AARE还抑制α-淀粉酶和α-葡萄糖苷酶,表明具有潜在的抗糖尿病作用,IC₅₀值分别为224.12±1.17μg/mL和243.35±1.51μg/mL。抗菌实验显示对革兰氏阳性菌有较强活性。分子对接和药代动力学分析确定AARE关键化合物对NADPH氧化酶、促旋酶B和拓扑异构酶IIα有良好的抑制作用,且具有良好的类药性质。这些发现表明AARE在治疗癌症、糖尿病和细菌感染方面具有潜力,值得进一步开展体内和临床研究。