Effect of Glutathione Enriched Polyherbal Formulation on Streptozotocin Induced Diabetic Model by Regulating Oxidative Stress and PKC Pathway

IF 0.7 Q4 PHARMACOLOGY & PHARMACY Pharmacognosy Research Pub Date : 2023-02-22 DOI:10.5530/pres.15.2.037
Sheethal S, R. M, Svenia P. Jose, S. S
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Abstract

Background: Increasing evidence shows that oxidative stress is one of the root causes of metabolic disorders like diabetes. Glucose oxidation and activation of various metabolic pathways lead to a disproportionate generation of free radicals. This will significantly reduce the antioxidant status in the body. Objectives: In the present study, we aimed to evaluate the effect of a novel glutathione enriched polyherbal formulation on a streptozotocin induced diabetic model. Materials and Methods: Diabetes was induced by a single intraperitoneal injection of streptozotocin. After 3 days of injection, Glibenclamide (5mg/kg), and glutathione enriched polyherbal formulation were given orally for 28 days. Fasting blood glucose and body weight changes were measured at specific intervals. For the study, antioxidant enzymes, lipid peroxidation products, nitrite, liver enzyme markers, gene expression of GLUT–2, and PKC levels were evaluated. Histopathological analysis was also done. Results: The result shows that glutathione enriched polyherbal formulation treated rats significantly reduced their blood glucose and maintained their body weight. As a result, the GLUT–2 expression was reduced, which prevented the activation of PKC. Moreover, oxidative stress was reduced by improving antioxidants like SOD, CAT, GPx, and GSH by inhibiting the lipid peroxidation process. In addition, hepatic damage was also prevented by protecting the liver cells, and thereby shielding the excessive leakage of SGOT, SGPT, and ALP enzymes. The histopathological analysis of the liver gives more support to other data. Conclusion: Findings show that glutathione–enriched polyherbal formulations have a powerful anti-diabetic effect by inhibiting oxidative stress and thus blocking PKC activation.
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谷胱甘肽复方通过调节氧化应激和PKC通路对链脲佐菌素诱导的糖尿病模型的影响
背景:越来越多的证据表明,氧化应激是糖尿病等代谢紊乱的根本原因之一。葡萄糖的氧化和各种代谢途径的激活导致自由基的过度产生。这将显著降低体内的抗氧化状态。目的:在本研究中,我们旨在评估一种新型富含谷胱甘肽的多羟基制剂对链脲佐菌素诱导的糖尿病模型的影响。材料与方法:单次腹腔注射链脲佐菌素诱发糖尿病。注射3天后,口服格列本脲(5mg/kg)和富含谷胱甘肽的多羟基制剂28天。在特定的时间间隔测量空腹血糖和体重的变化。在这项研究中,评估了抗氧化酶、脂质过氧化产物、亚硝酸盐、肝酶标记物、GLUT-2基因表达和PKC水平。还进行了组织病理学分析。结果:结果表明,富含谷胱甘肽的多羟基制剂治疗大鼠可显著降低血糖并保持体重。结果,GLUT–2的表达减少,从而阻止了PKC的激活。此外,通过抑制脂质过氧化过程来改善抗氧化剂如SOD、CAT、GPx和GSH,从而降低氧化应激。此外,还通过保护肝细胞来防止肝损伤,从而屏蔽SGOT、SGPT和ALP酶的过度泄漏。肝脏的组织病理学分析为其他数据提供了更多的支持。结论:研究结果表明,富含谷胱甘肽的多醇制剂通过抑制氧化应激从而阻断PKC的激活,具有强大的抗糖尿病作用。
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来源期刊
Pharmacognosy Research
Pharmacognosy Research PHARMACOLOGY & PHARMACY-
自引率
14.30%
发文量
61
期刊介绍: Pharmacognosy Research [ISSN: Print -0976-4836, Online - 0974-8490] [http://www.phcogres.com], Quarterly a publication of Phcog.Net is published by Wolters Kluwer - Medknow Publications. It provides peer-reviewed original research articles from the field of Natural Products. The journal serves an international audience of scientists and researchers in a variety of research and academia by quickly disseminating research findings related to Medicinal Plants and Natural Products. It is a peer reviewed journal aiming to publish high quality original research articles, methods, techniques and evaluation reports, critical reviews, short communications, commentaries and editorials of all aspects of medicinal plant research. The journal is aimed at a broad readership, publishing articles on all aspects of pharmacognosy, and related fields. The journal aims to increase understanding of pharmacognosy as well as to direct and foster further research through the dissemination of scientific information by the publication of manuscripts. The submissions of original contributions in all areas of pharmacognosy are welcome.
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