2018
DOI: 10.1016/j.biopha.2018.08.087
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Erythropoietin attenuates LPS-induced microvascular damage in a murine model of septic acute kidney injury

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Cited by 43 publications
(35 citation statements)
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“…Renoprotective effects of EPO in mice with septic acute kidney injury has been observed and has been linked to attenuation of microvascular damage, reducing renal inflammatory response and improvement of renal tissue oxygenation through the decrease of hypoxia‐inducible factor‐1 alpha, inducible nitric oxide synthase, and NF‐κB and also enhancement of erythropoietin receptor (EPO‐R), PeCAM‐1, vascular endothelial growth factor, and VEGFR‐2 expression 8 …”
Section: Discussionmentioning
confidence: 99%
“…Renoprotective effects of EPO in mice with septic acute kidney injury has been observed and has been linked to attenuation of microvascular damage, reducing renal inflammatory response and improvement of renal tissue oxygenation through the decrease of hypoxia‐inducible factor‐1 alpha, inducible nitric oxide synthase, and NF‐κB and also enhancement of erythropoietin receptor (EPO‐R), PeCAM‐1, vascular endothelial growth factor, and VEGFR‐2 expression 8 …”
Section: Discussionmentioning
confidence: 99%
“…EPO has shown protective effects in several experimental AKI models, through various mechanisms including the regulation of microvascular injury [7], the reduction in tubulointerstitial injury (independent of its hemopoietic effects) [16], anti-inflammatory and anti-apoptotic effects [17], decreased fibrocyte accumulation [18], and the modulation of macrophage polarization [19,20]. Notably, EPO has shown efficacy in animal models of IR-AKI [21], as well as in an in vitro hypoxia-reoxygenation study [22], via the regulation of PI3K/Akt signaling.…”
Section: Discussionmentioning
confidence: 99%
“…Treatment with erythropoiesis-stimulating agents has led to significant improvements in patients' quality of life [5,6]. Furthermore, the anti-inflammatory and antioxidant effects of EPO in AKI have been demonstrated in renal cell and animal models [7]. Here, we investigated the renoprotective mechanisms of EPO in IR-AKI mice, as well as the role of the inflammasome in mediating these effects.…”
Section: Introductionmentioning
confidence: 99%
“…Menos receptores ECA2 explicarían la disminución de la COVID-19 en poblaciones de altura, así como el decremento de mortalidad, pues al haber menos receptores ECA2 la carga viral que reciben los afectados será menor y de ella depende su evolución 9 . La hipoxia hipobárica incrementa la eritropoyetina (EPO), hormona citoprotectora multifuncional, que disminuye la inflamación por shock séptico y mejora la lesión microvascular endotoxémica 10 , lo que también podría explicar por qué los pacientes COVID-19 fallecen menos en la altura. En Francia se halló que los malos resultados clínicos y virológicos en pacientes COVID-19 tratados con hidroxicloroquina-azitromicina se asociaron al uso de bloqueadores de AT1 11 .…”
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