Polyherbal extract improves glycometabolic control in alloxan-induced diabetic rats via down-regulating the MAPK/JNK pathway, modulating Nrf-2/Keap-1 expression, and stimulating insulin signaling.

IF 2.1 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Bilal Aslam, Asif Hussain, Muhammad Naeem Faisal, Shaneel Kousar, Alishbah Roobi, Muhammad Rehan Sajid, Aneela Gul
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引用次数: 0

Abstract

Objectives: This study focused on the evaluation of antioxidant and antidiabetic activities of polyherbal extract (PHE), containing Cassia absus (L.), Gymnema sylvestre (R. Br.), Nigella sativa (L.), and Piper nigrum (L.), in alloxan-induced diabetes model.

Materials and methods: In vitro, HPLC characterization, DPPH scavenging assay, and α-amylase inhibition test were conducted. In vivo, acute oral toxicity of PHE was assessed. Alloxan-induced diabetic Wistar rats (n=6) were orally treated with PHE (200, 400, and 600 mg/kg/day) and glibenclamide (GLB; 10 mg/kg/day) for six consecutive weeks. Then, biochemical biomarkers, oxidative stress parameters, histopathological examination, and mRNA expression levels (RT-qPCR) were determined.

Results: The presence of polyphenols in PHE was confirmed in correlation to marked DPPH scavenging (IC50: 1.60 mg/ml) and α-amylase inhibition (IC50: 0.82 mg/ml). PHE demonstrated no toxicity in rats up to a dose of 2000 mg/kg. In diabetic rats, PHE dose-dependently ameliorated the serum levels of glucose, insulin, glycated hemoglobin A1c (HbA1c), leptin, and glucokinase (GCK). Also, PHE substantially alleviated serum inflammatory markers (TNF-α and CRP) and oxidative stress indicators (MDA, SOD, and CAT) in pancreatic tissues. PHE, particularly at 600 mg/kg, attenuated cellular oxidative stress via modulating the mRNA expression levels of genes regulating MAPK/JNK (Mapk-8, Traf-4, and Traf-6) and Nrf-2/Keap-1 pathways and promoted insulin signaling through up-regulating insulin signaling cascade (Pdx-1, Ins-1, and Ins-2), as compared to GLB. Furthermore, histopathological findings supported the aforementioned results.

Conclusion: Our study suggests that polyherbal extract has promising antioxidant and antidiabetic activities by modulating the MAPK/JNK, Nrf-2/Keap-1, and insulin signaling pathways.

多草本植物提取物通过下调 MAPK/JNK 通路、调节 Nrf-2/Keap-1 的表达和刺激胰岛素信号传导,改善阿脲诱导的糖尿病大鼠的糖代谢控制。
研究目的本研究的重点是评价含有决明子、裸冠菊、黑千层和胡椒的多草本提取物(PHE)在阿脲诱导的糖尿病模型中的抗氧化和抗糖尿病活性:在体外,进行了高效液相色谱表征、DPPH 清除试验和 α 淀粉酶抑制试验。在体内,评估了 PHE 的急性口服毒性。阿脲诱导的糖尿病 Wistar 大鼠(n=6)连续六周口服 PHE(200、400 和 600 毫克/千克/天)和格列本脲(GLB;10 毫克/千克/天)。然后测定生化生物标志物、氧化应激参数、组织病理学检查和 mRNA 表达水平(RT-qPCR):结果:PHE 中的多酚类物质被证实具有明显的 DPPH 清除作用(IC50:1.60 毫克/毫升)和α-淀粉酶抑制作用(IC50:0.82 毫克/毫升)。PHE 对大鼠无毒性,最高剂量为 2000 毫克/千克。在糖尿病大鼠体内,PHE 可剂量依赖性地改善血糖、胰岛素、糖化血红蛋白 A1c(HbA1c)、瘦素和葡萄糖激酶(GCK)的血清水平。此外,PHE 还大大减轻了胰腺组织中的血清炎症指标(TNF-α 和 CRP)和氧化应激指标(MDA、SOD 和 CAT)。与 GLB 相比,PHE(尤其是 600 mg/kg)通过调节 MAPK/JNK(Mapk-8、Traf-4 和 Traf-6)和 Nrf-2/Keap-1 通路调控基因的 mRNA 表达水平减轻了细胞氧化应激,并通过上调胰岛素信号级联(Pdx-1、Ins-1 和 Ins-2)促进了胰岛素信号转导。此外,组织病理学结果也支持上述结果:我们的研究表明,多草药提取物通过调节 MAPK/JNK、Nrf-2/Keap-1 和胰岛素信号通路,具有良好的抗氧化和抗糖尿病活性。
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来源期刊
Iranian Journal of Basic Medical Sciences
Iranian Journal of Basic Medical Sciences MEDICINE, RESEARCH & EXPERIMENTAL-PHARMACOLOGY & PHARMACY
CiteScore
4.00
自引率
4.50%
发文量
142
审稿时长
6-12 weeks
期刊介绍: The Iranian Journal of Basic Medical Sciences (IJBMS) is a peer-reviewed, monthly publication by Mashhad University of Medical Sciences (MUMS), Mashhad, Iran . The Journal of "IJBMS” is a modern forum for scientific communication. Data and information, useful to investigators in any discipline in basic medical sciences mainly including Anatomical Sciences, Biochemistry, Genetics, Immunology, Microbiology, Pathology, Pharmacology, Pharmaceutical Sciences, and Physiology, will be published after they have been peer reviewed. This will also include reviews and multidisciplinary research.
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