黄芩苷:一种潜在的糖尿病和肾保护治疗剂

Leena Rajathy Port Louis, Prithiviraj Nagarajan, Pavithra Muthiah, Ravikumar Sambandam
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引用次数: 0

摘要

背景:糖尿病是一种复杂的代谢性疾病,表现为血液中葡萄糖水平升高和胰岛素功能受损,导致各种器官并发症,包括糖尿病肾病。黄芩苷是黄芩中提取的一种黄酮类化合物,因其具有抗炎、抗过敏、抗细胞凋亡等多种有益作用而受到广泛关注。有趣的是,在大鼠体内的研究进一步揭示了黄芩苷直接调节胰腺β细胞的潜力,这表明黄芩苷作为一种抗糖尿病药物具有很好的作用。目的:通过对链脲佐菌素诱导的糖尿病大鼠血浆胰岛素水平、血糖水平、血红蛋白水平、糖化血红蛋白水平等关键指标的研究,全面探讨黄芩苷的抗糖尿病作用。此外,我们试图通过评估血清肾脏标志物来探索黄芩苷提供肾脏保护的能力。方法:本研究共涉及30只Wistar白化雄性大鼠。通过单次腹腔注射链脲佐菌素(40 mg/kg),大鼠产生糖尿病。72h后,将糖尿病大鼠分为4个治疗组(II组至V组),每组6只。第一组为6只正常对照大鼠(无糖尿病)。各组分别给予生理盐水、DMSO、黄芩苷(50 mg/kg/d)、格列本脲(6 mg/kg/d)治疗45 d。在整个研究过程中,对动物的总体外观、体重、行为和静脉血中的空腹血糖水平进行了细致的观察。结果:与格列苯脲治疗的2型糖尿病大鼠相比,以50 mg/kg体重的速率口服黄芩苷可显著增强胰岛素分泌和血红蛋白水平,同时显著降低血糖和糖化血红蛋白水平。此外,黄芩苷对肾组织有保护作用,如降低血清肌酐、尿酸和尿素水平。结论:黄芩苷作为一种具有抗糖尿病作用的药物,具有保护肾组织的作用。观察到的各种生理参数的改善为黄芩苷的治疗机制和临床应用的进一步探索提供了依据,表明黄芩苷是糖尿病治疗和糖尿病肾病预防的有力候选者。关键词:黄芩苷,血糖,糖尿病,雄性wistar大鼠,链脲佐菌素
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Baicalin: A potential therapeutic agent for diabetes and renal protection
Background: Diabetes is a complex metabolic disease manifested by raised glucose levels in the blood and impaired insulin function leading to various organ complications, including diabetic nephropathy. Baicalin, a flavonoid derived from Scutellaria baicalensis Georgi, has garnered substantial attention for its diverse beneficial effects, including anti-inflammatory, anti-allergic, anti- apoptotic properties, etc. Intriguingly, in vivo studies in rats have further unveiled baicalin’s potential to directly modulate pancreatic beta cells, suggesting a promising role as an anti-diabetic agent.Objective: The purpose of this study is to comprehensively explore the anti-diabetic effect of baicalin, focusing on key parameters such as plasma insulin levels, glucose levels, hemoglobin, and glycated hemoglobin levels in streptozotocin-induced diabetic rats. Additionally, we sought to explore Baicalin’s ability to provide renal protection by evaluating serum renal markers. Methodology: This study involved a total of 30 Wistar albino male rats. Diabetes was created in rats by a single intraperitoneal streptozotocin injection (40 mg/kg). After 72 hours, the rats with diabetes were segregated into four treatment groups (Group II to Group V) comprising 6 animals each. Group I consists of six normal control rats (without diabetes). The groups received different treatment protocols, including normal saline, DMSO, Baicalin (50 mg/kg/day), and glibenclamide (6 mg/kg/day) for 45 days. Throughout the study, meticulous observations were made regarding the animals’ general appearance, body weight, behavior, and their fasting glucose levels in venous blood.Results: Oral dosing with Baicalin at the rate of 50 mg/kg body weight revealed notable enhancements in insulin secretion and hemoglobin levels, alongside notable reductions in blood levels of glucose and glycated hemoglobin compared to the glibenclamide-treated type 2 diabetic rats. Additionally, Baicalin displayed a protective action on renal tissue, as shown by reduced serum creatinine, uric acid, and urea levels.Conclusion: Our investigation unveils Baicalin’s potential as a promising anti-diabetic agent with the added benefit of renal tissue protection. The observed improvements in various physiological parameters warrant further exploration of Baicalin’s therapeutic mechanisms and clinical applications, presenting it as a compelling candidate for diabetes management and diabetic nephropathy prevention. IAEC Approval No: AVMC/IAEC/2019/07/25/08 Keywords: Baicalin, Blood glucose, Diabetes, Male wistar rats, Streptozotocin
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