Evaluation of the Effect of an Advance Diabetes Support Product Targeting the Improved β-Cell Functions and β-Cell Regeneration for the Management of Diabetes Mellitus

D. Nagore, S. Pandya, Chetan Savaliya, Kamlesh Thummar, V. Undale
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Abstract

Aim: Diabetes support product (ADSP) with phytocompounds was proposed to improve insulin secretion, avoid pancreatic beta cell apoptosis, and moderate beta cell differentiation and proliferation. In this research work, beta cell regenerative potential of ADSP was evaluated with STZ induced diabetes in rodents. Method: Single dose of Streptozotocin (STZ) (70mpk; i.p.) was used to induce diabetes in the Wistar rats. The treatment of vehicle or test or GLB was continued for the next 28 days to assess sub-acute anti-diabetic potential. Fasting blood glucose levels (BGL) was monitored weekly once throughout the experiment. Bodyweight, Feed-water consumption was calculated on every day till end of the experiment. Interleukin-6, Interleukin-1β and Interferon-γ was also analysis from blood serum after 28 days of treatment in rats. Further, animal was humanely sacrifice and organs such as liver, kidney(s) and pancreas were isolated for histopathology analysis. Result: Research showed that Insulin is Increased by 3 times in comparison with the diabetic group by ADSP after 28 days. After 28 days treatment of ADSP to rodents, Interleukin-6 decreased by 52%, Interleukin-1β decreased by 73% and Interferon-γ decreased by 28% in comparison with the diabetic control group. It is also observed in histopathology studies that there was a rise in the quantity of islets after 28 days treatment of ADSP in Streptozotocin carried diabetic rats. Conclusion: Hence in conclusion, advance diabetes support product supposed to be appreciated as synergistic product of encouraging the β-cell regeneration in vivo.
针对改善β细胞功能和β细胞再生的先进糖尿病支持产品对糖尿病管理的效果评估
目的:提出植物性糖尿病支持产品(ADSP)可改善胰岛素分泌,避免胰腺β细胞凋亡,调节β细胞分化和增殖。本研究以STZ诱导的啮齿动物糖尿病为实验对象,对ADSP的β细胞再生潜能进行了评价。方法:单剂量链脲佐菌素(STZ) 70mpk;)诱导Wistar大鼠糖尿病。在接下来的28天里,继续进行载体或试验或GLB的治疗,以评估亚急性抗糖尿病的潜力。在整个实验过程中,每周监测一次空腹血糖水平(BGL)。每天计算体重、饲水量,直至试验结束。对治疗28天后的大鼠血清中白细胞介素-6、白细胞介素-1β和干扰素-γ进行分析。人道宰杀动物,分离肝脏、肾脏、胰腺等脏器进行组织病理学分析。结果:研究表明,与糖尿病组相比,ADSP治疗28天后胰岛素水平升高3倍。ADSP治疗28天后,与糖尿病对照组相比,白介素-6降低52%,白介素-1β降低73%,干扰素-γ降低28%。在组织病理学研究中也观察到,携带链脲佐菌素的糖尿病大鼠经ADSP治疗28天后,胰岛数量增加。结论:advance糖尿病支持产品在体内可作为促进β细胞再生的协同产物。
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