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Aerosol inhalation of a hydrogen-rich solution restored septic renal function

机译:气溶胶吸入富氢溶液可恢复化脓性肾功能

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摘要

Sepsis-related acute kidney injury (AKI) is known to be caused by inflammation. We explored the renal protective effects of aerosol inhalation of a hydrogen-rich solution (HRS; hydrogen gas dissolved to saturation in saline) in a mouse model of septic AKI. Septic AKI was induced through 18 hours of cecal ligation and puncture. AKI occurred during the early stage of sepsis, as evidenced by increased blood urea nitrogen and serum creatinine levels, pathological changes, renal fibrosis and renal tubular epithelial cell apoptosis, accompanied by macrophage infiltration and M1 macrophage-associated pro-inflammatory cytokine ( and ) generation in renal tissues. Aerosol inhalation of the HRS increased anti-inflammatory cytokine ( and ) mRNA levels in renal tissues and promoted macrophage polarization to the M2 type, which generated additional anti-inflammatory cytokines ( and ). Ultimately, aerosol inhalation of HRS protected the kidneys and increased survival among septic mice. HRS was confirmed to promote M2 macrophage polarization in lipopolysaccharide-stimulated RAW 264.7 cells. The TGF-β1 receptor inhibitor SB-431542 partly reversed the effects of HRS on renal function, fibrosis, tubular epithelial cell apoptosis and senescence in mice. Thus, HRS aerosol inhalation appears highly useful for renal protection and inflammation reduction in septic AKI.
机译:脓毒症相关的急性肾损伤(AKI)已知是由炎症引起的。我们探讨了在化脓性AKI小鼠模型中气雾吸入富氢溶液(HRS;氢气溶解至饱和盐水)的肾脏保护作用。通过盲肠结扎和穿刺18小时诱导败血性AKI。 AKI发生在败血症的早期,其表现为血液尿素氮和血清肌酐水平升高,病理变化,肾纤维化和肾小管上皮细胞凋亡,并伴有巨噬细胞浸润和M1巨噬细胞相关的促炎性细胞因子(和)生成在肾组织中。气溶胶吸入HRS可增加肾组织中抗炎细胞因子(和)mRNA的水平,并促进巨噬细胞极化至M2型,从而产生其他抗炎细胞因子(和)。最终,吸入HRS的气雾剂可保护肾脏,并增加败血症小鼠的存活率。证实HRS可以促进脂多糖刺激的RAW 264.7细胞中的M2巨噬细胞极化。 TGF-β1受体抑制剂SB-431542部分逆转了HRS对小鼠肾功能,纤维化,肾小管上皮细胞凋亡和衰老的影响。因此,HRS气雾剂吸入对于脓毒症AKI的肾脏保护和减轻炎症反应非常有用。

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