Benrahou Kaoutar, Guourrami Otman El, Mrabti Hanae Naceiri, Cherrah Yahia, Faouzi My El Abbes
Laboratory of Pharmacology and Toxicology, Bio Pharmaceutical and Toxicological Analyzes Research Team, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, Morocco.
Laboratory of Analytical Chemistry and Bromatology, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, Morocco.
J Pharmacopuncture. 2022 Sep 30;25(3):242-249. doi: 10.3831/KPI.2022.25.3.242.
The aim of this work is to evaluate the in vitro antioxidant, hypoglycemic, and antiobesity effects of Euphorbia resinifera extracts and investigate the phenolic constituents and the toxicity of these extracts.
Phytochemical screening was performed to detect polyphenols and flavonoids. Antioxidant activity was evaluated by four methods (DPPH, ABTS, HO, and xanthine oxidase inhibition). The hypoglycemic effect was determined by the inhibition of α-amylase and α-glucosidase enzymes in vitro and via a starch tolerance study in normal rats. The antiobesity effect was estimated by in vitro inhibition of lipase.
Phytochemical screening revealed that the ethanolic extract was rich in polyphenols (99 ± 0.56 mg GEA/g extract) and tannins (55.22 ± 0.17 mg RE/g extract). Moreover, this extract showed higher antioxidant activity in different tests the DPPH assay (IC = 53.81 ± 1.83 µg/mL), ABTS assay (111.4 ± 2.64 mg TE/g extract), HO (IC = 98.15 ± 0.68 µg/mL), and xanthine oxidase (IC = 10.26 ± 0.6 µg/mL). With respect to hypoglycemic effect, the aqueous and ethanolic extracts showed IC values of 119.7 ± 2.15 µg/mL and 102 ± 3.63 µg/mL for α-amylase and 121.4 ± 1.88 and 56.6 ± 1.12 µg/mL for α-glucosidase, respectively, and the extracts lowered blood glucose levels in normal starch-loaded rats. Additionally, lipase inhibition was observed with aqueous (IC = 25.3 ± 1.53 µg/mL) and ethanolic (IC = 13.7 ± 3.03 µg/mL) extracts.
These findings show the antioxidant, hypoglycemic, and hyperlipidemic effects of E. resinifera extracts, which should be investigated further to validate their medicinal uses and their pharmaceutical applications.
本研究旨在评估树脂大戟提取物的体外抗氧化、降血糖和抗肥胖作用,并研究这些提取物的酚类成分及其毒性。
进行植物化学筛选以检测多酚和黄酮类化合物。通过四种方法(DPPH、ABTS、HO和黄嘌呤氧化酶抑制)评估抗氧化活性。通过体外抑制α-淀粉酶和α-葡萄糖苷酶以及在正常大鼠中进行淀粉耐受性研究来确定降血糖作用。通过体外抑制脂肪酶来评估抗肥胖作用。
植物化学筛选显示乙醇提取物富含多酚(99±0.56mg GEA/g提取物)和单宁(55.22±0.17mg RE/g提取物)。此外,该提取物在不同测试中表现出较高的抗氧化活性,DPPH测定(IC = 53.81±1.83μg/mL)、ABTS测定(111.4±2.64mg TE/g提取物)、HO(IC = 98.15±0.68μg/mL)和黄嘌呤氧化酶(IC = 10.26±0.6μg/mL)。关于降血糖作用,水提取物和乙醇提取物对α-淀粉酶的IC值分别为119.7±2.15μg/mL和102±3.63μg/mL以及对α-葡萄糖苷酶的IC值分别为121.4±1.88和56.6±1.12μg/mL,并且这些提取物降低了正常淀粉负荷大鼠的血糖水平。此外,水提取物(IC = 25.3±1.53μg/mL)和乙醇提取物(IC = 13.7±3.03μg/mL)观察到脂肪酶抑制作用。
这些发现表明树脂大戟提取物具有抗氧化、降血糖和降血脂作用,应进一步研究以验证其药用价值及其药物应用。