Goel Narender, Gajbhiye Rahul L, Saha Moumita, Nagendra Chennuru, Reddy Araveeti Madhusudhana, Ravichandiran V, Das Saha Krishna, Jaisankar Parasuraman
Department of Natural Products, National Institute of Pharmaceutical Education and Research (NIPER-Kolkata) Chunilal Bhawan, 168, Maniktala Main Road 700054 Kolkata India.
Laboratory of Catalysis and Chemical Biology, Department of Organic and Medicinal Chemistry, CSIR-Indian Institute of Chemical Biology 4 Raja S. C. Mullick Road Kolkata-700032 India
RSC Adv. 2021 Nov 8;11(57):35918-35936. doi: 10.1039/d1ra07496b. eCollection 2021 Nov 4.
(Burm. f.) Nees and J.L.Ellis have traditionally been used to treat various ailments such as mouth ulcers, intermittent fever, inflammation, snake bite. This study compares the comparative cytotoxic activity, and phytochemical profiling of methanol extract of (ANM) and (APM). UPLC-ESI-QTOF-MS/MS analysis has been performed. The cytotoxic activity of crude methanol extracts were evaluated against three different cancer cell lines (HCT 116, HepG2, and A549 cell line). Both plants' extract exhibited significant cytotoxic activity against tested cell lines in a dose-dependent manner. IC of ANM and APM in HCT 116 cell was 11.71 ± 2.48 μg ml and 45.32 ± 0.86 μg ml and in HepG2 cell line was 15.65 ± 2.25 μg ml and 60.32 ± 1.05 μg ml respectively. Cytotoxicity of these two extracts was comparatively similar in A549 cells. ANM induced cytotoxicity involved programmed cell death, externalisation of phosphatidylserine, ROS generation, up-regulation and down-regulation of major apoptotic markers. HRMS analysis of ANM and APM resulted in the identification of 59 and 42 compounds, respectively. Further, using the MS/MS fragmentation approach, 20 compounds, of which 18 compounds were identified for the first time from ANM, which belongs to phenolic acids, flavonoids, and their glycosides. Three known compounds, echioidinin, skullcapflavone I and 5,2',6'-trihydroxy-7-methoxyflavone 2'--β-d-glucopyranoside, were isolated from and their crystal structures were reported for the first time. Subsequently, seven major compounds were identified in by direct comparison (retention time and UV-spectra) with authentic commercial standards and isolated compounds using HPLC-UV analysis. The cytotoxicity of phytochemicals from both the plants using tools also justify their cytotoxic activity. It is the first report on the comparative characterisation of phytochemicals present in the methanolic extract of both the species of , along with the cytotoxic activity of .
(缅甸文名称)Nees和J.L. Ellis传统上被用于治疗各种疾病,如口腔溃疡、间歇热、炎症、蛇咬伤。本研究比较了(ANM)和(APM)甲醇提取物的细胞毒性活性及植物化学图谱。已进行了超高效液相色谱-电喷雾电离-四极杆飞行时间串联质谱(UPLC-ESI-QTOF-MS/MS)分析。对粗甲醇提取物针对三种不同癌细胞系(HCT 116、HepG2和A549细胞系)的细胞毒性活性进行了评估。两种植物的提取物均以剂量依赖方式对受试细胞系表现出显著的细胞毒性活性。ANM和APM在HCT 116细胞中的半数抑制浓度(IC)分别为11.71±2.48μg/ml和45.32±0.86μg/ml,在HepG2细胞系中分别为15.65±2.25μg/ml和60.32±1.05μg/ml。这两种提取物在A549细胞中的细胞毒性相对相似。ANM诱导的细胞毒性涉及程序性细胞死亡、磷脂酰丝氨酸外化、活性氧生成以及主要凋亡标志物的上调和下调。对ANM和APM的高分辨质谱(HRMS)分析分别鉴定出59种和42种化合物。此外,使用串联质谱碎裂方法,从ANM中鉴定出20种化合物,其中18种化合物为首次鉴定,它们属于酚酸、黄酮类及其糖苷。从(该植物)中分离出三种已知化合物,即紫花前胡宁、灯盏花黄酮I和5,2',6'-三羟基-7-甲氧基黄酮2'-β-D-葡萄糖苷,并首次报道了它们的晶体结构。随后,通过与正品商业标准品和使用高效液相色谱-紫外(HPLC-UV)分析分离得到的化合物进行直接比较(保留时间和紫外光谱),在(该植物)中鉴定出七种主要化合物。使用(相关)工具对两种植物的植物化学物质的细胞毒性分析也证实了它们的细胞毒性活性。这是关于两种(该植物)甲醇提取物中植物化学物质的比较特征以及(该植物提取物)细胞毒性活性的首次报道。