阿尔及利亚撒哈拉沙棘多糖对链脲佐菌素诱导的糖尿病大鼠的降糖作用。

Turkish journal of biology = Turk biyoloji dergisi Pub Date : 2025-01-13 eCollection Date: 2025-01-01 DOI:10.55730/1300-0152.2724
Houria Medjdoub, Waffa Bouali, Arezki Azzi, Nacéra Belkacem, Nabila Benariba, Nawel Meliani
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引用次数: 0

摘要

背景/目的:阿尔及利亚特有的一种刺槐(Zygophyllum geslini)具有许多特性,特别是作为一种抗糖尿病药物。在阿尔及利亚,这种草药被用作撒哈拉菜肴的调味品和动物饲料(绵羊、山羊和骆驼)。然而,很少有科学研究报道这种撒哈拉物种的药用特性。本研究的目的是研究1)从该植物中提取的多糖的化学成分,2)对胰腺α-淀粉酶的体外抑制作用,以及3)对链脲霉素诱导的糖尿病大鼠的体内降糖作用。材料与方法:首先,在热水条件下,从江蓠中提取多糖,用乙醇沉淀得到乙醇多糖,用丙酮沉淀得到丙酮多糖。采用傅里叶红外光谱(FTIR)对提取物进行了表征。采用胰α-淀粉酶(一种与糖尿病相关的酶)进行体外抗糖尿病评价。此外,我们还对链脲佐菌素诱导的糖尿病大鼠进行了4周的体内乙醇多糖测定。大鼠注射100 mg/kg ZGAP乙醇多糖。结果:FTIR光谱显示,ZGAP多糖成分呈非均质性,提取率分别为14.07±2.61和4.48±1.01 g/100 g,乙醇多糖和丙酮多糖的pH值分别为7.03和7.2。ZGAP多糖具有α-淀粉酶抑制剂的潜力,对乙醇多糖的IC50为3.53±0.09 μg/mL,对丙酮多糖的IC50为7.31±0.42 μg/mL。乙醇多糖对链脲佐菌素损伤引起的高血糖有一定的纠正作用。观察到乙醇多糖显著降低血糖水平和改善口服葡萄糖耐量。乙醇多糖提取物对糖尿病大鼠体重进化有促进作用。结论:ZGAP多糖具有良好的体内和体外抗糖尿病活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antidiabetic potential of polysaccharides from Algerian Saharan Zygophyllum geslini in streptozotocin-induced diabetic rats.

Background/aim: Zygophyllum geslini, an endemic Algerian species, has numerous properties, especially as an antidiabetic drug. In Algeria, this herb serves as condiment in Saharan dishes and as animal feed (Sheep, Goat and Camel). However, few scientific studies have reported on the medicinal properties of this Saharan species. The aims of the present work were to study 1) the chemical aspects of polysaccharides extracted from this plant, 2) their inhibitory effect on pancreatic α-amylase in vitro, and 3) their antihyperglycemic effect in streptozotocin-induced diabetic rats in vivo.

Materials and methods: First, polysaccharides were extracted from Z. geslini aerial part (ZGAP) in hot water and precipitated with ethanol to obtain ethanolic polysaccharides and with acetone to obtain acetonic polysaccharides. The extracts were characterized using Fourier-transform infrared (FTIR) spectroscopy. In vitro antidiabetic evaluation was performed using pancreatic α-amylase, an enzyme related to diabetes. In addition, ethanolic polysaccharides were tested in vivo in streptozotocin-induced diabetic rats for 4 weeks. The rats received 100 mg/kg ZGAP ethanolic polysaccharides.

Results: FTIR spectra showed that ZGAP polysaccharides were heterogeneous in composition, with extraction yield of 14.07 ± 2.61 and 4.48 ± 1.01 g/100 g of dry ZGAP and had a neutral pH (7.03 and 7.2) for ethanolic and acetonic polysaccharides, respectively. Furthermore, ZGAP polysaccharides showed potential as an α-amylase inhibitor, with IC50 = 3.53 ± 0.09 μg/mL for ethanolic and 7.31 ± 0.42 μg/mL for acetonic polysaccharides. Ethanolic polysaccharides were able to correct hyperglycemia caused by streptozotocin damage. A significant decrease in blood glucose levels and improvement in oral glucose tolerance were observed with ethanolic polysaccharides. Ethanolic polysaccharides extract enhanced the body weight evolution in diabetic rats.

Conclusion: Based on these findings, we conclude that ZGAP polysaccharides have interesting in vivo and in vitro antidiabetic activities.

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