Wahab Maryam, Bhatti Attya, John Peter
Department of Healthcare Biotechnology, Atta-ur-Rahman School of Applied Biosciences (ASAB), National University of Sciences and Technology (NUST), Islamabad 44000, Pakistan.
Department of Dairy and Food Science, South Dakota State University, Brookings, SD 57007, USA.
Polymers (Basel). 2022 Aug 1;14(15):3138. doi: 10.3390/polym14153138.
Type 2 Diabetes Mellitus is one of the most common metabolic disorders, and is characterized by abnormal blood sugar level due to impaired insulin secretion or impaired insulin action-or both. Metformin is the most commonly used drug for the treatment of Type 2 Diabetes Mellitus, but due to its slow mode of action and various side effects it shows poor and slow therapeutic response in patients. Currently, scientists are trying to tackle these limitations by developing nanomedicine. This research reports novel synthesis of silver nanoparticles using aqueous extract of and aims to elucidate its therapeutic potential as an antidiabetic agent on streptozotocin induced diabetic BALB/c mice. mediated silver nanoparticles were characterized through UV, SEM, XRD, and FTIR. The alpha amylase inhibition and antioxidant activity were checked through α amylase and DPPH radical scavenging assay, respectively. To check the effect of silver nanoparticles on blood glucose levels FBG, IPGTT, ITT tests were employed on STZ induced BALB/c mice. To assess the morphological changes in the anatomy of liver, pancreas, and kidney of BALB/c mice due to silver nanoparticles, histological analysis was done through H&E staining system. Finally, AMPK and IRS1 genes expression analysis was carried out via real time PCR. Silver nanoparticles were found to be spherical in shape with an average size of 42 nm. They showed an IC50 of 8 μg/mL and 10 μg/mL for α amylase and DPPH assay, respectively. Our study suggests that silver nanoparticles-specifically 10 mg/kg-cause a significant increase in the expression of AMPK and IRS1, which ultimately increase the glucose uptake in cells. mediated silver nanoparticles possess strong antioxidant and antidiabetic potential and can further be explored as an effective and cheaper alternative option for treatment of Type 2 Diabetes Mellitus.
2型糖尿病是最常见的代谢紊乱疾病之一,其特征是由于胰岛素分泌受损或胰岛素作用受损(或两者皆有)导致血糖水平异常。二甲双胍是治疗2型糖尿病最常用的药物,但由于其作用方式缓慢且有各种副作用,在患者中显示出较差且缓慢的治疗反应。目前,科学家们正试图通过开发纳米药物来解决这些局限性。本研究报告了使用[具体植物名称]水提取物合成新型银纳米颗粒,并旨在阐明其作为抗糖尿病药物对链脲佐菌素诱导的糖尿病BALB/c小鼠的治疗潜力。通过紫外可见光谱(UV)、扫描电子显微镜(SEM)、X射线衍射(XRD)和傅里叶变换红外光谱(FTIR)对[具体植物名称]介导的银纳米颗粒进行了表征。分别通过α淀粉酶和二苯基苦味酰基自由基(DPPH)清除试验检测了α淀粉酶抑制活性和抗氧化活性。为了检测银纳米颗粒对血糖水平的影响,对链脲佐菌素诱导的BALB/c小鼠进行了空腹血糖(FBG)、腹腔注射葡萄糖耐量试验(IPGTT)和胰岛素耐量试验(ITT)。为了评估银纳米颗粒对BALB/c小鼠肝脏、胰腺和肾脏解剖结构的形态学变化,通过苏木精-伊红(H&E)染色系统进行了组织学分析。最后,通过实时聚合酶链反应(PCR)进行了腺苷酸活化蛋白激酶(AMPK)和胰岛素受体底物1(IRS1)基因表达分析。发现银纳米颗粒呈球形,平均尺寸为42纳米。它们对α淀粉酶和DPPH试验的半数抑制浓度(IC50)分别为8微克/毫升和10微克/毫升。我们的研究表明,银纳米颗粒——特别是10毫克/千克——会导致AMPK和IRS1的表达显著增加,最终增加细胞对葡萄糖的摄取。[具体植物名称]介导的银纳米颗粒具有很强的抗氧化和抗糖尿病潜力,可以进一步探索作为治疗2型糖尿病的一种有效且廉价的替代选择。