Taviano Maria Fernanda, Miceli Natalizia, Acquaviva Rosaria, Malfa Giuseppe Antonio, Ragusa Salvatore, Giordano Deborah, Cásedas Guillermo, Les Francisco, López Víctor
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, Polo Annunziata, University of Messina, 98168 Messina, Italy.
Department of Drug Science, Biochemistry Section, University of Catania, 95123 Catania, Italy.
Biology (Basel). 2020 Jul 13;9(7):163. doi: 10.3390/biology9070163.
(L.) R. Br. (Brassicaceae) is widely cultivated for ornamental purposes and utilized as a medicinal plant. In the present work, the hydroalcoholic extract from the aerial parts of this species has been evaluated in different bioassays in order to detect potential pharmacological applications. The cytotoxic capacity against the human colorectal adenocarcinoma (CaCo-2) and breast cancer (MCF-7) cell lines was tested using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. The extract was investigated as a neuroprotective inhibitor of central nervous system (CNS) enzymes such as monoamine oxidase A, tyrosinase, acetylcholinesterase, and as a natural enzyme inhibitor of α-glucosidase and lipase involved in some metabolic disorders such as obesity or type 2 diabetes. The antioxidant ability was also evaluated in an enzymatic system (xanthine/xanthine oxidase assay). Results showed that the extract displayed moderate to low cytotoxicity vs. CaCo-2 cells. The extract acted as a superoxide radical scavenger and enzymatic inhibitor of monoamine oxidase A, tyrosinase, α-glucosidase, and lipase. The best results were found in the α-glucosidase assay, as hydroalcoholic extract was able to inhibit the enzyme α-glucosidase up to 100% without significant differences, compared to the antidiabetic drug acarbose. has been demonstrated to exert different biological properties. These are important in order to consider this species as a source of bioactive compounds.
十字花科的芸苔(L.)R. Br. 因其观赏价值被广泛种植,并被用作药用植物。在本研究中,对该物种地上部分的水醇提取物进行了不同的生物测定,以检测其潜在的药理应用。使用MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐)法测试了对人结肠腺癌(CaCo-2)和乳腺癌(MCF-7)细胞系的细胞毒性。该提取物被研究作为中枢神经系统(CNS)酶如单胺氧化酶A、酪氨酸酶、乙酰胆碱酯酶的神经保护抑制剂,以及作为参与肥胖或2型糖尿病等一些代谢紊乱的α-葡萄糖苷酶和脂肪酶的天然酶抑制剂。还在酶系统(黄嘌呤/黄嘌呤氧化酶测定)中评估了抗氧化能力。结果表明,该提取物对CaCo-2细胞显示出中度至低度的细胞毒性。该提取物作为超氧自由基清除剂以及单胺氧化酶A、酪氨酸酶、α-葡萄糖苷酶和脂肪酶的酶抑制剂发挥作用。在α-葡萄糖苷酶测定中发现了最佳结果,与抗糖尿病药物阿卡波糖相比,水醇提取物能够抑制α-葡萄糖苷酶达100%,且无显著差异。已证明其具有不同的生物学特性。为了将该物种视为生物活性化合物的来源,这些特性很重要。