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Ameliorative effects of resveratrol against cadmium-induced nephrotoxicity via modulating nuclear xenobiotic receptor response and PINK1/Parkin-mediated Mitophagy

机译:白藜芦醇对镉诱导的肾毒性的改善作用通过调节核异源性受体反应和PINK1 / Parkin介导的乳化剂

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摘要

Cadmium (Cd) is a toxic pollutant with high nephrotoxicity in the agricultural environment. Resveratrol has been found to have a renoprotective effect but the underlying mechanisms of this have not yet been fully elucidated. The aim of this study is to illustrate the antagonism of resveratrol against Cd-induced nephrotoxicity. A total of 80 birds were divided randomly into 4 groups and treated via diet for 90 days as follows: control group (Con); 400 mg kg(-1) resveratrol group (Resv); 140 mg kg(-1) Cd group (Cd 140); and 140 mg kg(-1) Cd + 400 mg kg(-1) resveratrol group (Cd + Resv). It was observed that resveratrol treatment dramatically alleviated Cd-induced histopathological lesions of the kidney. Simultaneously, resveratrol mitigated Cd-induced oxidative stress by reducing MDA and H2O2 production, alleviating GSH depletion and restoring the activity of antioxidant enzymes (T-SOD, Cu-Zn SOD, CAT, GST and GSH-Px). Resveratrol activated NXRs (CAR/PXR/AHR/Nrf2) signaling pathways and exerted antidotal roles by enhancing the phase I and II detoxification systems to relieve oxidative damage. Moreover, resveratrol ameliorated Cd-induced ultrastructural abnormality and mitochondria dysfunction by recovering mitochondrial function-related factors VDAC1, Cyt C and Sirt3 upregulation and Sirt1, PGC-1 alpha, Nrf1 and TFAM transcription restrictions. Resveratrol attenuated Cd-induced excessive mitochondrial fission and promoted mitochondrial fusion, which reversed PINK1/Parkin-mediated mitophagy initiation. Collectively, our findings explicate the potential protection against Cd-induced nephrotoxicity and mitochondria damage.
机译:镉(CD)是农业环境中具有高肾毒性的有毒污染物。已发现白藜芦醇具有一次防御性效果,但尚未完全阐明的潜在机制。本研究的目的是说明白藜芦醇对CD诱导的肾毒性的拮抗作用。将80只鸟类随机分为4组,并通过饮食治疗90天,如下:对照组(CON); 400 mg kg(-1)白藜芦醇组(RESV); 140 mg kg(-1)CD组(CD 140);和140 mg kg(-1)Cd + 400 mg kg(-1)白藜芦醇组(CD + Resv)。观察到,白藜芦醇治疗显着缓解了肾脏的CD诱导的CD诱导的组织病理学病变。同时,通过还原MDA和H 2 O 2的产生,减轻GSH耗尽并恢复抗氧化酶活性(T-SOD,Cu-Zn SOD,CAT,GST和GSH-PX),通过降低CD诱导的氧化应激。白藜芦醇活性NXRS(CAR / PXR / AHR / NRF2)信号传导途径,并通过增强相I和II解毒系统来缓解氧化损伤来发挥对抗作用。此外,通过回收线粒体功能相关因素Vdac1,Cyt C和Sirt3上调和SIRT1,PGC-1α,NRF1和TFAM转录限制,将CD诱导的CD诱导的CD诱导的超微结构异常和线粒体功能障碍。白藜芦醇衰减CD诱导的过量线粒体裂变和促进的线粒体融合,其逆转粉红色的粉红色1 / parkin介导的乳化剂引发。集体,我们的研究结果促使潜在的免受CD诱导的肾毒性和线粒体损伤的保护。

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  • 来源
    《Food & Function》 |2020年第2期|共13页
  • 作者单位

    Northeast Agr Univ Coll Vet Med Harbin 150030 Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin 150030 Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin 150030 Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin 150030 Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin 150030 Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin 150030 Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin 150030 Peoples R China;

    Northeast Agr Univ Coll Vet Med Harbin 150030 Peoples R China;

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  • 正文语种 eng
  • 中图分类 食品工业;
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