Wang Siyu, Yang Jianzhan, Cai Lei, Li Haoxiang, Han Xiaodong, Liu Bo, Wu Jianwei
School of Traditional Chinese Medicine and Health, Nanfang College Guangzhou, Guangzhou 510970, China.
Chinese Medicine Guangdong Laboratory, Zhuhai 519060, China.
Antioxidants (Basel). 2025 May 5;14(5):551. doi: 10.3390/antiox14050551.
L. is well known for its use in medicinal and edible homologous application. Various diseases, including those related to oxidation, are commonly treated with it. However, its antioxidant effect is still lacking systematical study. We aimed to screen the most potential antioxidant fraction of the crude ethanolic extract from (KG) and evaluate its antioxidant activity and potential mechanism. The ethyl acetate fraction of ethanolic extract from (KGEA) was chosen as the most potent antioxidant activity from all the fractions tested. UPLC-Q-TOF-MS/MS was used to determine 43 compounds in KGEA, and 25 potential bioactive compounds were identified by pharmacokinetic analysis. Network pharmacology revealed 174 overlapping targets of chemical and antioxidant targets, and the key targets were identified. Molecular docking and MD simulation revealed a strong binding affinity between the core compounds and their targets. In tests against DPPH and ABTS, KGEA exhibited potent radical scavenging activity. In HO-induced cells, KGEA could decrease reactive oxygen species (ROS) production; alleviate mitochondrial damage; promote the increase in antioxidant enzymes SOD, CAT, GSH-Px; and reduce the levels of MDA. Mechanistically, KGEA regulated PI3K/Akt and MAPK signaling pathways against oxidative damage. Moreover, in HO-induced zebrafish, KGEA attenuated ROS generation, cell death, lipid peroxidation, and increased SOD, CAT, GSH-Px activities; it also decreased MDA levels. The antioxidant properties of KGEA were demonstrated in vitro and in vivo, and it should be considered as an antioxidant agent for further profound study.
L因其在药食同源应用中的使用而闻名。包括与氧化相关的各种疾病通常用它来治疗。然而,其抗氧化作用仍缺乏系统研究。我们旨在筛选[KG]粗乙醇提取物中最具潜力的抗氧化部分,并评估其抗氧化活性和潜在机制。从所有测试部分中选择[KG]乙醇提取物的乙酸乙酯部分作为最具抗氧化活性的部分。采用超高效液相色谱-四极杆飞行时间串联质谱(UPLC-Q-TOF-MS/MS)测定KGEA中的43种化合物,并通过药代动力学分析鉴定出25种潜在的生物活性化合物。网络药理学揭示了化学和抗氧化靶点的174个重叠靶点,并确定了关键靶点。分子对接和分子动力学模拟揭示了核心化合物与其靶点之间有很强的结合亲和力。在针对二苯基苦味酰基自由基(DPPH)和2,2'-联氮-二(3-乙基苯并噻唑啉-6-磺酸)二铵盐(ABTS)的测试中,KGEA表现出强大的自由基清除活性。在过氧化氢(HO)诱导的细胞中,KGEA可减少活性氧(ROS)的产生;减轻线粒体损伤;促进抗氧化酶超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GSH-Px)的增加;并降低丙二醛(MDA)水平。机制上,KGEA通过调节磷脂酰肌醇-3激酶(PI3K)/蛋白激酶B(Akt)和丝裂原活化蛋白激酶(MAPK)信号通路来抵抗氧化损伤。此外,在HO诱导的斑马鱼中,KGEA减弱了ROS的产生、细胞死亡、脂质过氧化,并增加了SOD、CAT、GSH-Px的活性;它还降低了MDA水平。KGEA的抗氧化特性在体外和体内都得到了证明,应将其作为一种抗氧化剂进行进一步深入研究。