Phoopha Sathianpong, Sangkaew Surat, Wattanapiromsakul Chatchai, Nuankaew Wanlapa, Kang Tong Ho, Dej-Adisai Sukanya
Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai 90112, Songkhla, Thailand.
Traditional Thai Medical Research and Innovation Center, Faculty of Traditional Thai Medicine, Prince of Songkla University, Hat Yai 90112, Songkhla, Thailand.
Pharmaceuticals (Basel). 2023 Aug 10;16(8):1132. doi: 10.3390/ph16081132.
This study presents a phytochemical investigation of leaf extracts and their anti-diabetic activities. Traditionally, leaves were used as vegetables and food in local recipes, but the root extracts of the plant can also be used in body tonic and erectile dysfunction treatments. Following a preliminary anti-diabetic activity screening test, the 80% ethanolic leaf extract exhibited potent anti-alpha glucosidase activity. So, the leaves' active components were selected for further investigation. Firstly, the plant was extracted via maceration using lower to higher polarity solvents such as hexane, ethyl acetate, ethanol, and water, respectively, to obtain the four crude extracts. Then, the phytochemicals contained in this plant were investigated via classical column chromatography and spectroscopy techniques. Anti-diabetic activity was evaluated via anti-alpha glucosidase and insulin secretagogue assays. The results showed that five compounds were isolated from the fractionated ethanolic leaf extract: interruptin A; interruptin C; ergosterol; diglycerol; and 15-16-epoxy-neo-cleoda-3,7(20),13(16),14-tetraene-12,17:18,19-diolide, a new diterpene derivative which is herein referred to as lepionurodiolide. Interruptin A and the new diterpene derivative exhibited the greatest effect on anti-alpha glucosidase activity, showing IC values of 293.05 and 203.71 μg/mL, respectively. Then, molecular docking was used to study the sites of action of these compounds. The results showed that interruptin A and the new compound interacted through H-bonds with the GLN279 residue, with a binding energy of -9.8 kcal/mol, whereas interruptin A and C interacted with HIS280 and ARG315 a with binding energy of -10.2 kcal/mol. Moreover, the extracts were investigated for their toxicity toward human cancer cells, and a zebrafish embryonic toxicity model was used to determine herbal drug safety. The results indicated that ethyl acetate and hexane extracts showed cytotoxicity to both Hela cells and human breast adenocarcinomas (MCF-7), which was related to the results derived from using the zebrafish embryonic toxicity model. The hexane and ethyl acetate presented LC values of 33.25 and 36.55 μg/mL, respectively, whereas the ethanol and water extracts did not show embryonic toxicity. This study is the first of its kind to report on the chemical constituents and anti-diabetic activity of , the leaf extract of which has been traditionally used in southern Thailand as a herbal medicine and food ingredient.
本研究对叶提取物进行了植物化学研究及其抗糖尿病活性。传统上,叶子在当地食谱中用作蔬菜和食物,但该植物的根提取物也可用于滋补身体和治疗勃起功能障碍。经过初步的抗糖尿病活性筛选试验,80%乙醇叶提取物表现出强大的抗α-葡萄糖苷酶活性。因此,选择叶子的活性成分进行进一步研究。首先,分别使用己烷、乙酸乙酯、乙醇和水等极性由低到高的溶剂通过浸渍法提取该植物,以获得四种粗提物。然后,通过经典柱色谱和光谱技术对该植物中含有的植物化学物质进行研究。通过抗α-葡萄糖苷酶和胰岛素促分泌剂试验评估抗糖尿病活性。结果表明,从分级乙醇叶提取物中分离出五种化合物:interruptin A;interruptin C;麦角甾醇;甘油二酯;以及15-16-环氧-新克罗达-3,7(20),13(16),14-四烯-12,17:18,19-二内酯,一种新的二萜衍生物,本文中称为lepionurodiolide。interruptin A和新的二萜衍生物对抗α-葡萄糖苷酶活性表现出最大的影响,IC值分别为293.05和203.71μg/mL。然后,使用分子对接研究这些化合物的作用位点。结果表明,interruptin A和新化合物通过氢键与GLN279残基相互作用,结合能为-9.8 kcal/mol,而interruptin A和C与HIS280和ARG315 a相互作用,结合能为-10.2 kcal/mol。此外,研究了提取物对人癌细胞的毒性,并使用斑马鱼胚胎毒性模型来确定草药的安全性。结果表明,乙酸乙酯和己烷提取物对Hela细胞和人乳腺腺癌(MCF-7)均表现出细胞毒性,这与使用斑马鱼胚胎毒性模型得出的结果相关。己烷和乙酸乙酯的LC值分别为33.25和36.55μg/mL,而乙醇和水提取物未表现出胚胎毒性。本研究首次报道了[植物名称]叶提取物的化学成分和抗糖尿病活性,该叶提取物在泰国南部传统上用作草药和食品成分。