Chirata、胡芦巴和芝麻联合提取物对糖尿病大鼠TNF-α、TGF-β和氧化应激的调节作用及毒理学评价。

Shivam, Asheesh Kumar Gupta
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引用次数: 0

摘要

背景:獐牙菜、胡芦和芝麻是治疗糖尿病的传统药物。一系列被称为糖尿病(DM)的代谢性疾病涉及由胰岛素分泌、功能缺陷或两者兼有引起的慢性高血糖。先天免疫和炎症在糖尿病相关微血管问题的病因中都起着重要作用。目的:研究香菜、胡芦巴和芝麻联合提取物(1:1:1)的抗糖尿病作用和急性毒性。为了满足对更高有效性和安全性的需求,目前的努力旨在构建含有草药甲醇提取物的抗糖尿病制剂。方法:采用OECD 423法对大鼠急性毒性进行研究。大鼠被用作试验对象,并且给予大鼠35mg/kg BW注射链脲佐菌素以发展为糖尿病。糖尿病对照组给予25 mg/kg体重的格列本脲,而实验组的糖尿病大鼠给予125 mg/kg体重和250 mg/kg体重的所有植物的联合甲醇提取物。所观察的测量包括急性口服毒性、行为变化、体重、血糖水平、脂质状况、氧化应激、肾功能测试和炎症介质。比较了所有大鼠组的肾脏、肝脏和胃的组织病理学。使用方差分析对数据进行评估,然后进行事后检验。结果:复方提取物的中致死剂量(LD50)均大于2000mg/kg,表明其在可观察到的条件下无毒。链脲佐菌素诱导的糖尿病大鼠的血糖升高在治疗组大鼠中显著降低(p 0.01)。在治疗组大鼠中,发现链脲佐菌素诱导的DM的典型细胞损伤和混乱已经修复。治疗组大鼠的血脂、高血糖、血清蛋白和肝糖原降低、肝功能和肾功能标志物恢复到DM对照组大鼠中的正常水平。结论:经评价的复方甲醇提取物在大鼠体内使用是安全的。将所有选定药用植物(香菜、胡芦巴和芝麻)的甲醇提取物相结合,具有潜在的抗糖尿病作用,可以安全地作为替代药物开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Toxicological Assessment and Anti-diabetic Effects of Combined Extract of Chirata, Fenugreek and Sesame on Regulating TNF-α, TGF-β and Oxidative Stress in Streptozotocin Induced Diabetic Rats.

Background: Swertia chirayita, Trigonella foenum-gracum and Sesamum indicum are used as traditional medicines to treat diabetes mellitus. A collection of metabolic illnesses known as diabetes mellitus (DM) involves chronic hyperglycemia caused by flaws in insulin secretion, function, or both. Innate immunity and inflammation both play important roles in the etiology of diabetes- related microvascular problems.

Objective: This study aims to examine the anti-diabetic effects and the acute toxicity of combined extract (1:1:1) of Swertia chirayita, Trigonella foenum-gracum and Sesamum indicum. To address the demand for higher effectiveness and safety, the current effort aims to construct anti-diabetic preparations containing methanolic extract from herbal medications.

Methods: The OECD 423 method was used to investigate acute toxicity in rats. Rats were used as test subjects, and rats were given a 35 mg/kg BW injection of streptozotocin to develop diabetes. The diabetic control group was given Glibenclamide 0.25 mg/kg BW, while the experimental group's diabetic rats received 125 mg/kg BW and 250 mg/kg BW of a combined methanolic extract of all plants. Among the measurements looked at were acute oral toxicity, behavioral changes, body weight, serum glucose levels, lipid profiles, oxidative stress, renal function tests, and inflammatory mediators. All the rat groups' histopathologies of the kidney, liver, and stomach were compared. The data were evaluated using analysis of variance, and a post hoc test was then carried out.

Results: The combined extracts' medium lethal doses (LD50) were higher than 2000 mg/kg, indicating that they are not poisonous under the conditions that can be observed. Streptozotocin-induced diabetic rats' elevated blood glucose was found to be considerably lower (p 0.01) in the treated group of rats. In the treated group of rats, it was discovered that the damage and disarray in the cells typical of Streptozotocin-induced DM had been repaired. The treated group of rats returned to normal levels of the lipid profile, hyperglycemia, decreased serum protein and liver glycogen, increased liver function, and kidney function markers seen in the rats of the DM control group.

Conclusion: The evaluated combined methanolic extract can be considered safe for use in rats. Combining methanolic extract from all selected medicinal plants (Swertia chirayita, Trigonella foenum-gracum and Sesamum indicum) has a potential anti-diabetic effect and can be safely developed as an alternative medicine.

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