通过靶向 miRNA-146a、miRNA-223、TLR4/TRAF6/NLRP3 炎性体通路和 HIF-1α ,6-姜酚和二甲双胍的新型组合对高脂饮食/链脲佐菌素诱导的大鼠糖尿病肾病具有肾保护作用

IF 4.3 2区 生物学 Q1 BIOLOGY
Merna G Aboismaiel, Mohamed N Amin, Laila A Eissa
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引用次数: 0

摘要

背景:miRNA-146a和miRNA-223是toll样受体4(TLR4)/肿瘤坏死因子受体相关因子6(TRAF6)/NOD样受体家族含吡啶域3(NLRP3)炎性小体通路的关键表观遗传调节因子,而该通路参与了糖尿病肾病(DN)的发病机制。目前可用的口服抗糖尿病疗法不足以阻止 DN 的发生和发展。因此,本研究旨在评估天然化合物 6-姜酚(GR)单独或与二甲双胍(MET)联用对高脂饮食/链脲佐菌素诱导的大鼠 DN 的肾保护作用。此外,还对拟议的分子机制进行了研究:方法:每天给大鼠灌胃 6-姜酚(100 毫克/千克)和二甲双胍(300 毫克/千克),连续八周。采用实时 PCR 法检测 MiRNA-146a、miRNA-223、TLR4、TRAF6、核因子-kappa B(NF-κB)(p65)、NLRP3、caspase-1 和缺氧诱导因子-1 α(HIF-1α)mRNA 的表达。用酶联免疫吸附法测定 TLR4、TRAF6、NLRP3、caspase-1、肿瘤坏死因子-α(TNF-α)和白细胞介素-1-β(IL-1β)的肾组织水平。对肾组织进行组织病理学检查,并对纤维连接蛋白和 NF-κB (p65) 进行免疫组化检查:结果:6-姜酚治疗能明显减轻肾组织损伤和纤维化。6-姜酚上调了 miRNA-146a 和 miRNA-223,降低了 TLR4、TRAF6、NF-κB (p65)、NLRP3、caspase-1、TNF-α、IL-1β、HIF-1α 和纤维连接蛋白的肾脏表达。6 姜酚改善了血脂状况和肾功能,减轻了肾肥大,增加了还原型谷胱甘肽,降低了血糖和丙二醛水平。结论:6-姜酚通过诱导 miRNA-146a 和 miRNA-223 的表达以及抑制 TLR4/TRAF6/NLRP3 炎性体信号转导,对 DN 起着关键的保护作用。6-姜酚是一种安全、经济、丰富的天然化合物,有望与二甲双胍一起作为糖尿病患者的辅助疗法,以减轻肾损伤并阻止 DN 的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Renoprotective effect of a novel combination of 6-gingerol and metformin in high-fat diet/streptozotocin-induced diabetic nephropathy in rats via targeting miRNA-146a, miRNA-223, TLR4/TRAF6/NLRP3 inflammasome pathway and HIF-1α.

Background: MiRNA-146a and miRNA-223 are key epigenetic regulators of toll-like receptor 4 (TLR4)/tumor necrosis factor-receptor-associated factor 6 (TRAF6)/NOD-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome pathway, which is involved in diabetic nephropathy (DN) pathogenesis. The currently available oral anti-diabetic treatments have been insufficient to halt DN development and progression. Therefore, this work aimed to assess the renoprotective effect of the natural compound 6-gingerol (GR) either alone or in combination with metformin (MET) in high-fat diet/streptozotocin-induced DN in rats. The proposed molecular mechanisms were also investigated.

Methods: Oral gavage of 6-gingerol (100 mg/kg) and metformin (300 mg/kg) were administered to rats daily for eight weeks. MiRNA-146a, miRNA-223, TLR4, TRAF6, nuclear factor-kappa B (NF-κB) (p65), NLRP3, caspase-1, and hypoxia-inducible factor-1 alpha (HIF-1α) mRNA expressions were measured using real-time PCR. ELISA was used to measure TLR4, TRAF6, NLRP3, caspase-1, tumor necrosis factor-alpha (TNF-α), and interleukin-1-beta (IL-1β) renal tissue levels. Renal tissue histopathology and immunohistochemical examination of fibronectin and NF-κB (p65) were performed.

Results: 6-Gingerol treatment significantly reduced kidney tissue damage and fibrosis. 6-Gingerol up-regulated miRNA-146a and miRNA-223 and reduced TLR4, TRAF6, NF-κB (p65), NLRP3, caspase-1, TNF-α, IL-1β, HIF-1α and fibronectin renal expressions. 6-Gingerol improved lipid profile and renal functions, attenuated renal hypertrophy, increased reduced glutathione, and decreased blood glucose and malondialdehyde levels. 6-Gingerol and metformin combination showed superior renoprotective effects than either alone.

Conclusion: 6-Gingerol demonstrated a key protective role in DN by induction of miRNA-146a and miRNA-223 expression and inhibition of TLR4/TRAF6/NLRP3 inflammasome signaling. 6-Gingerol, a safe, affordable, and abundant natural compound, holds promise for use as an adjuvant therapy with metformin in diabetic patients to attenuate renal damage and stop the progression of DN.

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来源期刊
Biological Research
Biological Research 生物-生物学
CiteScore
10.10
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: Biological Research is an open access, peer-reviewed journal that encompasses diverse fields of experimental biology, such as biochemistry, bioinformatics, biotechnology, cell biology, cancer, chemical biology, developmental biology, evolutionary biology, genetics, genomics, immunology, marine biology, microbiology, molecular biology, neuroscience, plant biology, physiology, stem cell research, structural biology and systems biology.
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