Department of Pharmacy, Practice & Clinical Pharmacy, Faculty of Pharmacy, Future University, Egypt.
Department of Biochemistry, Faculty of Applied Medical Sciences, October 6th University, October 6th City, Egypt.
Curr Pharm Biotechnol. 2023;24(14):1812-1826. doi: 10.2174/1389201024666230313105049.
Nanoparticles can be employed to improve the therapeutic activity of natural products. Type 2 diabetes mellitus is a serious health condition that has spread like a "modern pandemic" worldwide. In the present study, we developed silver nanoparticles, Ag-NPs, with an aqueous extract from to investigate their antioxidant and anti-inflammatory activity in STZ-induced diabetic rats.
Aqueous extracts of seeds (BAAE) were used in the synthesis of BAAE-AgNPs, which were characterized using FTIR and TEM. Different doses of BAAE-AgNP (1/50 LD; 29.4 mg/kg b.w. and 1/20 LD: 73.5 mg/kg b.w.) were administered to STZ-induced diabetic rats to evaluate their potential antidiabetic activity.
FTIR spectral data indicated the presence of flavonoids and polyphenols in BAAEAgNPs. The size of the BAAE-AgNPs, determined by TEM examination, was 49.33 ± 7.59 nm, with a zeta potential of +25.37. BAAE-AgNPs were characterized by an LD value of 1470 mg/kg b.w. In diabetic rats, the daily oral administration of both doses of BAAE-AgNPs (29.4 and 73.5 mg/kg b.w.) for 12 weeks resulted in a significant improvement in body weight, insulin homeostasis, HbA1c, HDL-C, MDA, and pancreatic SOD, CAT, and GSH. They reduced plasma glucose, cholesterol, and triglycerides. This treatment also resulted in a significant decrease in pancreatic IL-6, p53, and TNF-α in diabetic rats. Furthermore, BAAE-AgNPs down-regulated pancreatic TGF-β1 and Akt gene expression in diabetic rats and resulted in a significant decrease in the regulation of hepatic GLUT-2, as well as an increase in the regulation of hepatic GK and pancreatic B-cl2 gene expression. The histopathological results obtained indicated that BAAEAgNPs improved pancreatic tissue metabolism by enhancing antioxidant enzymes, suppressing inflammatory cytokines, and scavenging free radicals.
The findings implied that similar to the glibenclamide-treated groups, in the BAAEAgNPs treated group, the compromised antioxidant status normalized in STZ-induced diabetes. By scavenging free radicals, BAAE-Ag-NPs protected against lipid peroxidation while reducing the risk of complications from diabetes. Compared to the daily dose of 29.4 mg, the impact was more prominent at 73.5 mg.
纳米粒子可用于提高天然产物的治疗活性。2 型糖尿病是一种严重的健康状况,已在全球范围内像“现代流行病”一样蔓延。本研究中,我们制备了银纳米粒子(Ag-NPs),并用其水提物(BAAE-AgNPs)来研究其对 STZ 诱导的糖尿病大鼠的抗氧化和抗炎活性。
用 种子的水提取物(BAAE)合成 BAAE-AgNPs,用傅里叶变换红外光谱(FTIR)和透射电子显微镜(TEM)进行表征。将不同剂量的 BAAE-AgNP(1/50LD:29.4mg/kg.b.w.和 1/20LD:73.5mg/kg.b.w.)给予 STZ 诱导的糖尿病大鼠,以评估其潜在的抗糖尿病活性。
FTIR 光谱数据表明 BAAE-AgNPs 中存在类黄酮和多酚。TEM 检查确定 BAAE-AgNPs 的粒径为 49.33±7.59nm,zeta 电位为+25.37。BAAE-AgNPs 的 LD 值为 1470mg/kg.b.w.。在糖尿病大鼠中,每天口服给予两种剂量的 BAAE-AgNPs(29.4 和 73.5mg/kg.b.w.)12 周,可显著改善体重、胰岛素稳态、HbA1c、HDL-C、MDA 和胰腺 SOD、CAT 和 GSH。它们降低了血浆葡萄糖、胆固醇和甘油三酯。这种治疗还导致糖尿病大鼠胰腺中 IL-6、p53 和 TNF-α 的显著减少。此外,BAAE-AgNPs 下调了糖尿病大鼠胰腺 TGF-β1 和 Akt 基因的表达,并导致肝 GLUT-2 的调节显著降低,同时增加了胰腺 B-cl2 基因的表达。获得的组织病理学结果表明,BAAE-AgNPs 通过增强抗氧化酶、抑制炎症细胞因子和清除自由基来改善胰腺组织代谢。
研究结果表明,与格列本脲治疗组相似,在 BAAE-AgNPs 治疗组中,STZ 诱导的糖尿病导致的抗氧化状态受损得到了纠正。BAAE-Ag-NPs 通过清除自由基来防止脂质过氧化,从而降低糖尿病并发症的风险。与 29.4mg 的日剂量相比,73.5mg 的效果更为显著。