Oleander Stem and Root Standardized Extracts Mitigate Acute Hyperglycaemia by Limiting Systemic Oxidative Stress Response in Diabetic Mice.

Q1 Pharmacology, Toxicology and Pharmaceutics
Advances in Pharmacological Sciences Pub Date : 2019-01-08 eCollection Date: 2019-01-01 DOI:10.1155/2019/7865359
Priyankar Dey, Manas Ranjan Saha, Sumedha Roy Choudhuri, Indrani Sarkar, Biswajit Halder, Mousumi Poddar-Sarkar, Arnab Sen, Tapas Kumar Chaudhuri
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引用次数: 12

Abstract

The extracts of different parts of Nerium oleander L. are used as antidiabetic remedy in the traditional medicinal systems of different parts of the world. Despite these uses in ethnomedicinal system, the antihyperglycemic potentials of oleander stem (NOSE) and root (NORE) extracts have not been pharmacologically evaluated. Therefore, we aimed at evaluating the antidiabetic ethnomedicinal claims of NOSE and NORE, primarily focusing on glucose homeostasis and associated metabolic implications. Alloxan-treated mice with hyperglycaemia (blood glucose >200 mg/dL) were treated with oleander 70% hydromethanolic extracts (200 mg/kg) for 20 consecutive days, and the results were compared with positive control glibenclamide. Blood glucose level was 52-65% lowered (P < 0.001) in oleander treated groups, which was otherwise 4.62 times higher in diabetic mice, compared to control. Insulin resistance was lowered 51-36% irrespective of any significant (P > 0.05) changes in insulin sensitivity throughout the treatments. Improved serum insulin remained associated with lowered glucose level (r P = -0.847 and -0.772; P < 0.01). Markers of hyperglycaemia-related hepatic glycogen, glycated haemoglobin (HbA1c), hyperlipidaemia, hepatic injury, and diabetic nephropathy were normalized as well. Improvement of systemic intrinsic antioxidant enzymes (catalase and peroxidase) were correlated (r P = -0.952 to -0.773; P < 0.01) with lower lipid peroxidation by-product malondialdehyde (MDA) in the circulation. Principal component analysis coupled with hierarchical cluster analysis represented shift in metabolic homeostasis in diabetic mice, which was further normalized by oleander and glibenclamide treatment. Additionally, molecular docking studies of the phenolic acids measured by HPLC with intracellular cytoprotective transcription factor nuclear factor erythroid 2-related factor 2 (Nrf2) revealed strong molecular interactions. The results collectively support the ethnomedicine antidiabetic claims of oleander stem and root and suggest that the oleander mediated elevation of systemic antioxidant status is likely responsible for the improved glycaemic control.

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夹竹桃茎和根标准化提取物通过限制糖尿病小鼠的全身氧化应激反应来减轻急性高血糖。
夹竹桃不同部位的提取物在世界各地的传统医药体系中被用作抗糖尿病药物。尽管在民族医学系统中有这些用途,夹竹桃茎(NOSE)和根(NORE)提取物的降糖潜能尚未得到药理学评价。因此,我们旨在评估NOSE和NORE的抗糖尿病民族医学功效,主要关注葡萄糖稳态和相关代谢影响。采用夹竹桃70%氢甲醇提取物(200 mg/kg)连续20 d治疗四氧嗪治疗的高血糖小鼠(血糖>200 mg/dL),并与阳性对照格列本脲进行比较。与对照组相比,夹竹桃组的血糖水平降低了52-65% (P < 0.001),而糖尿病小鼠的血糖水平则高出4.62倍。胰岛素抵抗降低了51-36%,在整个治疗过程中,胰岛素敏感性没有显著变化(P > 0.05)。改善的血清胰岛素仍与降低的血糖水平相关(r P = -0.847和-0.772;P < 0.01)。高血糖相关的肝糖原、糖化血红蛋白(HbA1c)、高脂血症、肝损伤和糖尿病肾病的标志物也恢复正常。改善全身固有抗氧化酶(过氧化氢酶和过氧化物酶)相关(r P = -0.952 ~ -0.773;P < 0.01),循环中脂质过氧化副产物丙二醛(MDA)降低。主成分分析结合层次聚类分析表明,糖尿病小鼠代谢稳态发生了改变,夹竹桃和格列本脲治疗进一步正常化了这一变化。此外,HPLC测定的酚酸与细胞内细胞保护转录因子核因子红系2相关因子2 (Nrf2)的分子对接研究显示出强的分子相互作用。这些结果共同支持了夹竹桃茎和根的民族医学抗糖尿病主张,并表明夹竹桃介导的全身抗氧化状态的升高可能是改善血糖控制的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advances in Pharmacological Sciences
Advances in Pharmacological Sciences PHARMACOLOGY & PHARMACY-
CiteScore
6.40
自引率
0.00%
发文量
0
审稿时长
14 weeks
期刊介绍: Advances in Pharmacological and Pharmaceutical Sciences is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of experimental and clinical pharmacology, pharmaceutics, medicinal chemistry and drug delivery. Topics covered by the journal include, but are not limited to: -Biochemical pharmacology, drug mechanism of action, pharmacodynamics, pharmacogenetics, pharmacokinetics, and toxicology. -The design and preparation of new drugs, and their safety and efficacy in humans, including descriptions of drug dosage forms. -All areas of medicinal chemistry, such as drug discovery, design and synthesis. -Basic biology of drug and gene delivery through to application and development of these principles, through therapeutic delivery and targeting. Areas covered include bioavailability, controlled release, microcapsules, novel drug delivery systems, personalized drug delivery, and techniques for passing biological barriers.
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