首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Polysulfide and Hydrogen Sulfide Ameliorate Cisplatin-Induced Nephrotoxicity and Renal Inflammation through Persulfidating STAT3 and IKKβ
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Polysulfide and Hydrogen Sulfide Ameliorate Cisplatin-Induced Nephrotoxicity and Renal Inflammation through Persulfidating STAT3 and IKKβ

机译:通过脱硫化STAT3和IKKβ多硫化物和硫化氢改善顺铂诱导的肾毒性和肾炎

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摘要

Cisplatin, a widely used chemotherapy for the treatment of various tumors, is clinically limited due to its extensive nephrotoxicity. Inflammatory response in tubular cells is a driving force for cisplatin-induced nephrotoxicity. The plant-derived agents are widely used to relieve cisplatin-induced renal dysfunction in preclinical studies. Polysulfide and hydrogen sulfide (H2S) are ubiquitously expressed in garlic, and both of them are documented as potential agents for preventing and treating inflammatory disorders. This study was designed to determine whether polysulfide and H2S could attenuate cisplatin nephrotoxicity through suppression of inflammatory factors. In renal proximal tubular cells, we found that sodium tetrasulfide (Na2S4), a polysulfide donor, and sodium hydrosulfide (NaHS) and GYY4137, two H2S donors, ameliorated cisplatin-caused renal toxicity through suppression of the massive production of inflammatory cytokines, including tumor necrosis factor α (TNF-α), interleukin-1β (IL-1β), interleukin-6 (IL-6), and cyclooxygenase-2 (COX-2). Mechanistically, the anti-inflammatory actions of Na2S4 and H2S may be mediated by persulfidation of signal transducer and activator of transcription 3 (STAT3) and inhibitor kappa B kinase β (IKKβ), followed by decreased phosphorylation of STAT3 and IKKβ. Moreover, the nuclear translocation of nuclear transcription factor kappa B (NF-κB), and phosphorylation and degradation of nuclear factor kappa B inhibitor protein alpha (IκBα) induced by cisplatin, were also mitigated by both polysulfide and H2S. In mice, after treatment with polysulfide and H2S donors, cisplatin-associated renal dysfunction was strikingly ameliorated, as evidenced by measurement of serum blood urea nitrogen (BUN) and creatinine levels, renal morphology, and the expression of renal inflammatory factors. Our present work suggests that polysulfide and H2S could afford protection against cisplatin nephrotoxicity, possibly via persulfidating STAT3 and IKKβ and inhibiting NF-κB-mediated inflammatory cascade. Our results might shed light on the potential benefits of garlic-derived polysulfide and H2S in chemotherapy-induced renal damage.
机译:Cisplatin,一种用于治疗各种肿瘤的广泛使用的化疗,由于其广泛的肾毒性,临床限制。管状电池中的炎症反应是顺铂诱导的肾毒性的驱动力。植物衍生的药剂广泛用于缓解顺铂诱导的临床前研究肾功能障碍。多硫化物和硫化氢(H 2 S)在大蒜中普遍地表达,它们两者被记录为用于预防和治疗炎症疾病的潜在剂。本研究旨在通过抑制炎症因素来确定多硫化物和H 2是否可以衰减顺铂肾毒性。在肾近侧管状细胞中,我们发现硫酰胺钠(Na2S4),多硫化物供体和氢硫化钠(NaHS)和Gyy4137,两种H2S供体,通过抑制巨大产生炎性细胞因子,包括肿瘤而改善的顺铂导致肾毒性。坏死因子α(TNF-α),白细胞介素-1β(IL-1β),白细胞介素-6(IL-6)和环氧氧酶-2(COX-2)。机械地,Na 2 S 4和H 2 S的抗炎作用可以通过脱硫化信号传感器和转录3(STAT3)和抑制剂Kappa B激酶β(Ikkβ)的激活,然后降低STAT3和IKKβ的磷酸化。此外,二硫铂和H2S还减轻了二氯铂核转录因子κB(NF-κB)和核因子Kappa抑制剂蛋白α(IκBα)的核转化和核因子Kappa B抑制剂蛋白α(IκBα)的磷酸化和降解。在小鼠中,在用多硫化物和H 2 S供体处理后,激烈的相关肾功能障碍被令人惊讶,如血清血尿尿素氮(BUN)和肌酐水平,肾形态和肾炎症因子的表达所证明的。我们目前的作品表明,多硫化物和H2S可以提供​​对顺铂肾毒性的保护,可能通过过硫化STAT3和IKKβ和抑制NF-κB介导的炎症级联。我们的结果可能阐明了大蒜衍生的多硫化物和H2S在化疗诱导的肾损伤中的潜在益处。

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