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从南非一种海藻中分离出的粗制和纯化硫酸化多糖的抗糖尿病潜力。

Antidiabetic potentials of crude and purified sulphated polysaccharides isolated from , a seaweed from South Africa.

作者信息

Pillay Leah R, Olasehinde Tosin A, Olofinsan Kolawole A, Erukainure Ochuko L, Islam Md Shahidul, Olaniran Ademola O

机构信息

Department of Microbiology, School of Life Sciences, University of KwaZulu-Natal, Westville Campus, Durban, 4000, South Africa.

Nutrition and Toxicology Division, Food Technology Department, Federal Institute of Industrial Research Oshodi, Nigeria.

出版信息

Heliyon. 2024 Aug 2;10(15):e35729. doi: 10.1016/j.heliyon.2024.e35729. eCollection 2024 Aug 15.

Abstract

Over 90 % of all cases of diabetes that have been diagnosed are type 2 diabetes (T2D), a disease exacerbated by an increase in sedentary behaviour, bad eating habits, and obesity. This study investigated the antidiabetic properties of , using and experimental models. The sulphated polysaccharides (SPs) from crude extracts of the seaweed powder was prepared via hot (100°C) and cold (25°C) aqueous extraction procedures before purification via an anion exchange chromatographic technique. Both the crude and purified extracts were characterised by Fourier-transform infrared spectroscopy (FT-IR), LC-MS analysis, and Nuclear Magnetic Resonance (NMR) spectroscopy. The crude cold-aqueous and purified hot-aqueous SPs from had the strongest α-glucosidase inhibitory effect with IC value of 0.15 and 0.07 mg/ml, respectively. The purified cold-aqueous SP was the most potent inhibitor of α-glucosidase with an IC value of 0.17 mg/ml. The crude and purified SP-rich extracts inhibited pancreatic lipase (hot aqueous SP = 0.03 mg/ml) activity and effectively stimulated glucose uptake in yeast cells. Moreover, they showed significantly ( < 0.05) better intestinal glucose absorption inhibitory properties at the highest concentration (1 mg/ml) and displayed significantly ( < 0.05) better muscle glucose uptake compared to the commercial antidiabetic drug, metformin, at the same concentration. Overall, the current findings indicate that SPs may inhibit carbohydrate-hydrolysing enzymes, limit the release of simple sugars from the gut whilst effectively stimulating the use of glucose by peripheral tissue thus may be suitable to develop antidiabetic food supplements after further animal and clinical trials.

摘要

所有已确诊的糖尿病病例中,超过90%为2型糖尿病(T2D),这种疾病会因久坐行为增加、不良饮食习惯和肥胖而加剧。本研究使用[具体模型1]和[具体模型2]实验模型,研究了[海藻名称]的抗糖尿病特性。通过热(100°C)水提取和冷(25°C)水提取程序制备海藻粉粗提物中的硫酸化多糖(SPs),然后通过阴离子交换色谱技术进行纯化。粗提物和纯化提取物均通过傅里叶变换红外光谱(FT-IR)、液相色谱-质谱联用(LC-MS)分析和核磁共振(NMR)光谱进行表征。来自[海藻名称]的粗冷水性和纯化热水性SPs对α-葡萄糖苷酶的抑制作用最强,IC50值分别为0.15和0.07 mg/ml。纯化的冷水性SP是最有效的α-葡萄糖苷酶抑制剂,IC50值为0.17 mg/ml。粗提和纯化的富含SP的提取物抑制胰脂肪酶(热水性SP = 0.03 mg/ml)活性,并有效刺激酵母细胞对葡萄糖的摄取。此外,在最高浓度(1 mg/ml)下,它们表现出显著(P < 0.05)更好的肠道葡萄糖吸收抑制特性,并且在相同浓度下,与商用抗糖尿病药物二甲双胍相比,它们表现出显著(P < 0.05)更好的肌肉葡萄糖摄取。总体而言,目前的研究结果表明,[海藻名称]的SPs可能抑制碳水化合物水解酶,限制肠道中单糖的释放,同时有效刺激外周组织对葡萄糖的利用,因此在进一步的动物和临床试验后可能适合开发抗糖尿病食品补充剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd88/11336833/4c1a1f0b5cbc/gr1.jpg

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