Cargando…
Na/K-ATPase assay in the intact mice lung subjected to perfusion
BACKGROUND: Among the characteristics of acute respiratory distress syndrome (ARDS) is edema formation and its resolution depends on pneumocyte Na/K-ATPase activity. Increased concentration of oleic acid (OA) in plasma induces lung injury by targeting Na/K-ATPase and, thus, interfering in sodium tra...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4242599/ https://www.ncbi.nlm.nih.gov/pubmed/25399325 http://dx.doi.org/10.1186/1756-0500-7-798 |
_version_ | 1782345971429015552 |
---|---|
author | Gonçalves-de-Albuquerque, Cassiano Felippe Burth, Patrícia Silva, Adriana Ribeiro de Moraes, Isabel Matos Medeiros de Oliveira, Flora Magno Jesus Santelli, Ricardo Erthal Freire, Aline Soares Younes-Ibrahim, Mauricio de Castro-Faria-Neto, Hugo Caire de Castro-Faria, Mauro Velho |
author_facet | Gonçalves-de-Albuquerque, Cassiano Felippe Burth, Patrícia Silva, Adriana Ribeiro de Moraes, Isabel Matos Medeiros de Oliveira, Flora Magno Jesus Santelli, Ricardo Erthal Freire, Aline Soares Younes-Ibrahim, Mauricio de Castro-Faria-Neto, Hugo Caire de Castro-Faria, Mauro Velho |
author_sort | Gonçalves-de-Albuquerque, Cassiano Felippe |
collection | PubMed |
description | BACKGROUND: Among the characteristics of acute respiratory distress syndrome (ARDS) is edema formation and its resolution depends on pneumocyte Na/K-ATPase activity. Increased concentration of oleic acid (OA) in plasma induces lung injury by targeting Na/K-ATPase and, thus, interfering in sodium transport. FINDINGS: Presently, we adapted a radioactivity-free assay to detect Na/K-ATPase activity in perfused lung mice, comparing the inhibitory effect of ouabain and OA. We managed to perfuse only the lung, avoiding the systemic loss of rubidium. Rb(+) incorporation into lung was measured by inductively coupled plasma optical emission spectrometry (ICP OES) technique, after lung tissue digestion. Na/K-ATPase activity was the difference between Rb(+) incorporation with or without ouabain. Lung Na/K-ATPase was completely inhibited by perfusion with ouabain. However, OA caused a partial inhibition. CONCLUSIONS: In the present work the amount of incorporated Rb(+) was greater than seen in our previous report, showing that the present technique is trustworthy. This new proposed assay may allow researchers to study the importance of Na/K-ATPase activity in lung pathophysiology. |
format | Online Article Text |
id | pubmed-4242599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42425992014-11-25 Na/K-ATPase assay in the intact mice lung subjected to perfusion Gonçalves-de-Albuquerque, Cassiano Felippe Burth, Patrícia Silva, Adriana Ribeiro de Moraes, Isabel Matos Medeiros de Oliveira, Flora Magno Jesus Santelli, Ricardo Erthal Freire, Aline Soares Younes-Ibrahim, Mauricio de Castro-Faria-Neto, Hugo Caire de Castro-Faria, Mauro Velho BMC Res Notes Short Report BACKGROUND: Among the characteristics of acute respiratory distress syndrome (ARDS) is edema formation and its resolution depends on pneumocyte Na/K-ATPase activity. Increased concentration of oleic acid (OA) in plasma induces lung injury by targeting Na/K-ATPase and, thus, interfering in sodium transport. FINDINGS: Presently, we adapted a radioactivity-free assay to detect Na/K-ATPase activity in perfused lung mice, comparing the inhibitory effect of ouabain and OA. We managed to perfuse only the lung, avoiding the systemic loss of rubidium. Rb(+) incorporation into lung was measured by inductively coupled plasma optical emission spectrometry (ICP OES) technique, after lung tissue digestion. Na/K-ATPase activity was the difference between Rb(+) incorporation with or without ouabain. Lung Na/K-ATPase was completely inhibited by perfusion with ouabain. However, OA caused a partial inhibition. CONCLUSIONS: In the present work the amount of incorporated Rb(+) was greater than seen in our previous report, showing that the present technique is trustworthy. This new proposed assay may allow researchers to study the importance of Na/K-ATPase activity in lung pathophysiology. BioMed Central 2014-11-15 /pmc/articles/PMC4242599/ /pubmed/25399325 http://dx.doi.org/10.1186/1756-0500-7-798 Text en © Gonçalves-de-Albuquerque et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Gonçalves-de-Albuquerque, Cassiano Felippe Burth, Patrícia Silva, Adriana Ribeiro de Moraes, Isabel Matos Medeiros de Oliveira, Flora Magno Jesus Santelli, Ricardo Erthal Freire, Aline Soares Younes-Ibrahim, Mauricio de Castro-Faria-Neto, Hugo Caire de Castro-Faria, Mauro Velho Na/K-ATPase assay in the intact mice lung subjected to perfusion |
title | Na/K-ATPase assay in the intact mice lung subjected to perfusion |
title_full | Na/K-ATPase assay in the intact mice lung subjected to perfusion |
title_fullStr | Na/K-ATPase assay in the intact mice lung subjected to perfusion |
title_full_unstemmed | Na/K-ATPase assay in the intact mice lung subjected to perfusion |
title_short | Na/K-ATPase assay in the intact mice lung subjected to perfusion |
title_sort | na/k-atpase assay in the intact mice lung subjected to perfusion |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4242599/ https://www.ncbi.nlm.nih.gov/pubmed/25399325 http://dx.doi.org/10.1186/1756-0500-7-798 |
work_keys_str_mv | AT goncalvesdealbuquerquecassianofelippe nakatpaseassayintheintactmicelungsubjectedtoperfusion AT burthpatricia nakatpaseassayintheintactmicelungsubjectedtoperfusion AT silvaadrianaribeiro nakatpaseassayintheintactmicelungsubjectedtoperfusion AT demoraesisabelmatosmedeiros nakatpaseassayintheintactmicelungsubjectedtoperfusion AT deoliveirafloramagnojesus nakatpaseassayintheintactmicelungsubjectedtoperfusion AT santelliricardoerthal nakatpaseassayintheintactmicelungsubjectedtoperfusion AT freirealinesoares nakatpaseassayintheintactmicelungsubjectedtoperfusion AT younesibrahimmauricio nakatpaseassayintheintactmicelungsubjectedtoperfusion AT decastrofarianetohugocaire nakatpaseassayintheintactmicelungsubjectedtoperfusion AT decastrofariamaurovelho nakatpaseassayintheintactmicelungsubjectedtoperfusion |