Ndjoubi Kadidiatou O, Omoruyi Sylvester I, Luckay Robert C, Hussein Ahmed A
Chemistry Department, Cape Peninsula University of Technology, Symphony Rd. Bellville, Cape Town 7535, South Africa.
School of Anatomical Sciences, Faculty of Health Sciences, University of the Witwatersrand, Parktown, Johannesburg 2193, South Africa.
Plants (Basel). 2024 Nov 1;13(21):3076. doi: 10.3390/plants13213076.
(synonym ) is an important South African medicinal plant used traditionally to treat different human pathologies and is considered an adaptogenic plant. This study sought to isolate compounds from the plant and determine their protective potentials using SH-SY5Y cells and MPP (1-methyl-4-phenylpyridinium) to mimic Parkinson's disease. The phytochemical analysis of a 70% aqueous methanolic extract of leaves resulted in the isolation and identification of 11 pure compounds (-), among which compounds and were identified as new metabolites. The new compounds were characterised using IR, UV, NMR, and HRESIMS and were given the trivial names lessertiosides A () and B (). Additionally, the flavonoids 8-methoxyvestitol () and mucronulatol () were isolated for the first time from the plant. The biological actions show that the isolated compounds had negligible toxicity on SH-SY5Y cells and improved cell viability in the cells exposed to MPP. Furthermore, as a mechanism of action, the compounds could sustain cellular ATP generation and prevent MPP-induced apoptotic cell death. Our findings provide evidence for the neuroprotective properties of compounds isolated from in MPP-induced neuronal damage for the first time and create an avenue for these compounds to be further investigated to elucidate their molecular targets.
(同义词)是一种重要的南非药用植物,传统上用于治疗各种人类疾病,被认为是一种适应原性植物。本研究旨在从该植物中分离化合物,并使用SH-SY5Y细胞和MPP(1-甲基-4-苯基吡啶鎓)模拟帕金森病来确定它们的保护潜力。对该植物70%甲醇水溶液提取物进行植物化学分析,分离并鉴定出11种纯化合物(-),其中化合物和被鉴定为新的代谢产物。使用红外光谱、紫外光谱、核磁共振和高分辨电喷雾电离质谱对新化合物进行了表征,并分别赋予其俗名lessertiosides A()和B()。此外,黄酮类化合物8-甲氧基vestitol()和mucronulatol()首次从该植物中分离得到。生物学作用表明,分离得到的化合物对SH-SY5Y细胞的毒性可忽略不计,并提高了暴露于MPP的细胞的活力。此外,作为作用机制,这些化合物可以维持细胞内ATP的生成并防止MPP诱导的凋亡性细胞死亡。我们的研究结果首次为从该植物中分离得到的化合物在MPP诱导的神经元损伤中的神经保护特性提供了证据,并为进一步研究这些化合物以阐明其分子靶点开辟了一条途径。