Department of Biochemistry, School of Life Sciences, University of KwaZulu-Natal (Westville Campus), Durban 4000, South Africa; Nutrition and Toxicology Division, Federal Institute of Industrial Research, Lagos, Nigeria.
Department of Biochemistry, School of Life Sciences, University of KwaZulu-Natal (Westville Campus), Durban 4000, South Africa.
Biomed Pharmacother. 2017 Dec;96:37-47. doi: 10.1016/j.biopha.2017.09.106. Epub 2017 Nov 24.
The leaves of Dacryodes edulis were investigated for their anti-oxidative and anti-diabetic potentials in vitro. Extracts from sequential extraction with solvents of increasing polarity (n-hexane, ethyl acetate, ethanol and aqueous) of the leaves were subjected to in vitro antioxidant assays using the 2,2'-diphenyl-1-picrylhydrazyl (DPPH) scavenging and Ferric reducing antioxidant power (FRAP) protocols respectively. Their inhibitory effects were investigated on α-glucosidase, pancreatic lipases, pancreatic ATPase and glucose-6-phospatase activities. Their antioxidant and anti-apoptotic effects on Fe - induced oxidative injuries in pancreatic and hepatic tissues were also investigated ex vivo. The ethanol extract was subjected to Gas chromatography mass spectroscopy (GC-MS) and Fourier transform infrared (FTIR) spectroscopic analysis to identify its bioactive chemical constituents. The extracts showed potent free radical scavenging activity and significantly (p<0.05) inhibited all studied enzymes, with the ethanol extract showing greater activities. Superoxide Dismutase (SOD) and Catalase (CAT) activities were significantly (p<0.05) increased in both pancreatic and hepatic tissues with concomitant elevation of reduced glutathione (GSH) levels as well as reduced levels of malondialdehyde (MDA). The extracts significantly inhibited DNA fragmentation. These activities were dose - dependent. Amongst compounds identified, only Kaur-15-ene, Urs-12-ene-3-ol acetate and 2,3,23-trihydroxyolean-12-en-28-oic acid methyl ester showed strong binding affinities when docked with α-glucosidase (PDB ID:3TON). These results indicate the anti-oxidative, anti-diabetic and anti-obesogenic potentials of D. edulis leaves, which gives credence to its antidiabetic folkloric claims.
对灯台树叶片的抗氧化和抗糖尿病潜力进行了体外研究。采用不同极性溶剂(正己烷、乙酸乙酯、乙醇和水)依次提取叶片,分别用 2,2'-二苯基-1-苦基肼(DPPH)清除和铁还原抗氧化能力(FRAP)测定法进行体外抗氧化测定。研究了它们对α-葡萄糖苷酶、胰腺脂肪酶、胰腺三磷酸腺苷酶和葡萄糖-6-磷酸酶活性的抑制作用。还研究了它们在 Fe 诱导的胰腺和肝脏组织氧化损伤中的抗氧化和抗凋亡作用。将乙醇提取物进行气相色谱质谱联用(GC-MS)和傅里叶变换红外(FTIR)光谱分析,以鉴定其生物活性化学成分。提取物显示出很强的自由基清除活性,显著(p<0.05)抑制了所有研究的酶,其中乙醇提取物活性更强。超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性在胰腺和肝脏组织中均显著增加(p<0.05),同时还原型谷胱甘肽(GSH)水平升高,丙二醛(MDA)水平降低。提取物显著抑制 DNA 片段化。这些活性是剂量依赖性的。在所鉴定的化合物中,只有 Kaur-15-ene、Urs-12-ene-3-ol acetate 和 2,3,23-trihydroxyolean-12-en-28-oic acid methyl ester 与α-葡萄糖苷酶(PDB ID:3TON)结合时显示出很强的结合亲和力。这些结果表明灯台树叶片具有抗氧化、抗糖尿病和抗肥胖潜力,这为其抗糖尿病的民间说法提供了依据。