2000
DOI: 10.1016/s0272-6386(00)70309-x
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In vivo exposure to bicarbonate/lactate- and bicarbonate-buffered peritoneal dialysis fluids improves ex vivo peritoneal macrophage function

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Cited by 69 publications
(95 citation statements)
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“…In humans, the data available from in vivo effects of solution components are mainly derived from ex vivo measurements of cell function in different effluent drained with varying of dwell times. [17][18][19] Over the past decade, there was increased interest for the possible identification of any measurable potential marker in PD effluent, which can be informative for the overall in vivo peritoneum status. [20,21] These markers also might represent candidate biocompatibility markers, while the changes in their concentration may indicate the host's long-term response to different dialysis solutions.…”
Section: Discussionmentioning
confidence: 99%
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“…In humans, the data available from in vivo effects of solution components are mainly derived from ex vivo measurements of cell function in different effluent drained with varying of dwell times. [17][18][19] Over the past decade, there was increased interest for the possible identification of any measurable potential marker in PD effluent, which can be informative for the overall in vivo peritoneum status. [20,21] These markers also might represent candidate biocompatibility markers, while the changes in their concentration may indicate the host's long-term response to different dialysis solutions.…”
Section: Discussionmentioning
confidence: 99%
“…[17][18][19] Over the past decade, there was increased interest for the possible identification of any measurable potential marker in PD effluent, which can be informative for the overall in vivo peritoneum status. [20,21] These markers also might represent candidate biocompatibility markers, while the changes in their concentration may indicate the host's long-term response to different dialysis solutions. To date, several candidate markers have been identified based on their relationship to changes in inflammatory status, mesothelial cell integrity, and the processes of wound healing and fibrosis.…”
Section: Discussionmentioning
confidence: 99%
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“…Cumulative evidences indicated that those GDPs directly cause cellular injury in cells such as fibroblasts, mesothelial cells, and mononuclear cells in vitro and ex vivo [2, 3, 4, 5]. In addition to this direct action, some GDPs with dicarbonyl residues may indirectly exert their pathological actions on the peritoneum by facilitating the generation of advanced glycation endproducts (AGEs) [6, 7, 8], which play a pathological role for the high-transport membrane, causing an ultrafiltration failure [9, 10, 11].…”
Section: Introductionmentioning
confidence: 99%
“…, en la medida en que se va observando un aumento de la quimiotasis y de la capacidad bactericida de los macrófagos [39][40][41][42][43][44][45] .…”
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