Adipose-derived stem cells attenuate pulmonary microvascular hyperpermeability after smoke inhalation.

Pulmonary edema is a hallmark of acute respiratory distress syndrome (ARDS). Smoke inhalation causes ARDS, thus significantly increasing the mortality of burn patients. Adipose-derived stem cells (ASCs) exert potent anti-inflammatory properties. The goal of the present study was to test the safety a...

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Main Authors: Koji Ihara, Satoshi Fukuda, Baigalmaa Enkhtaivan, Raul Trujillo, Dannelys Perez-Bello, Christina Nelson, Anita Randolph, Suzan Alharbi, Hira Hanif, David Herndon, Donald Prough, Perenlei Enkhbaatar
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5628899?pdf=render
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author Koji Ihara
Satoshi Fukuda
Baigalmaa Enkhtaivan
Raul Trujillo
Dannelys Perez-Bello
Christina Nelson
Anita Randolph
Suzan Alharbi
Hira Hanif
David Herndon
Donald Prough
Perenlei Enkhbaatar
author_facet Koji Ihara
Satoshi Fukuda
Baigalmaa Enkhtaivan
Raul Trujillo
Dannelys Perez-Bello
Christina Nelson
Anita Randolph
Suzan Alharbi
Hira Hanif
David Herndon
Donald Prough
Perenlei Enkhbaatar
author_sort Koji Ihara
collection DOAJ
description Pulmonary edema is a hallmark of acute respiratory distress syndrome (ARDS). Smoke inhalation causes ARDS, thus significantly increasing the mortality of burn patients. Adipose-derived stem cells (ASCs) exert potent anti-inflammatory properties. The goal of the present study was to test the safety and ecfficacy of ASCs, in a well-characterized clinically relevant ovine model of ARDS.Female sheep were surgically prepared. ARDS was induced by cooled cotton smoke inhalation. Following injury, sheep were ventilated, resuscitated with lactated Ringer's solution, and cardiopulmonary hemodynamics were monitored for 48 hours in a conscious state. Pulmonary microvascular hyper-permeability was assessed by measuring lung lymph flow, extravascular lung water content, protein content in plasma and lung lymph fluid. Sheep were randomly allocated to two groups: 1) ASCs: infused with 200 million of ASCs in 200mL of PlasmaLyteA starting 1 hours post-injury, n = 5; 2) control, treated with 200mL of PlasmaLyteA in a similar pattern, n = 5.Lung lymph flow increased 9-fold in control sheep as compared to baseline. Protein in the plasma was significantly decreased, while it was increased in the lung lymph. The treatment with ASCs significantly attenuated these changes. Treatment with ASCs almost led to the reversal of increased pulmonary vascular permeability and lung water content. Pulmonary gas exchange was significantly improved by ASCs. Infusion of the ASCs did not negatively affect pulmonary artery pressure and other hemodynamic variables.ASCs infusion was well tolerated. The results suggest that intravenous ASCs modulate pulmonary microvascular hyper-permeability and prevent the onset of ARDS in our experimental model.
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spelling doaj.art-3ce67387b954413d96739d2ba62f610e2022-12-21T20:11:17ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-011210e018593710.1371/journal.pone.0185937Adipose-derived stem cells attenuate pulmonary microvascular hyperpermeability after smoke inhalation.Koji IharaSatoshi FukudaBaigalmaa EnkhtaivanRaul TrujilloDannelys Perez-BelloChristina NelsonAnita RandolphSuzan AlharbiHira HanifDavid HerndonDonald ProughPerenlei EnkhbaatarPulmonary edema is a hallmark of acute respiratory distress syndrome (ARDS). Smoke inhalation causes ARDS, thus significantly increasing the mortality of burn patients. Adipose-derived stem cells (ASCs) exert potent anti-inflammatory properties. The goal of the present study was to test the safety and ecfficacy of ASCs, in a well-characterized clinically relevant ovine model of ARDS.Female sheep were surgically prepared. ARDS was induced by cooled cotton smoke inhalation. Following injury, sheep were ventilated, resuscitated with lactated Ringer's solution, and cardiopulmonary hemodynamics were monitored for 48 hours in a conscious state. Pulmonary microvascular hyper-permeability was assessed by measuring lung lymph flow, extravascular lung water content, protein content in plasma and lung lymph fluid. Sheep were randomly allocated to two groups: 1) ASCs: infused with 200 million of ASCs in 200mL of PlasmaLyteA starting 1 hours post-injury, n = 5; 2) control, treated with 200mL of PlasmaLyteA in a similar pattern, n = 5.Lung lymph flow increased 9-fold in control sheep as compared to baseline. Protein in the plasma was significantly decreased, while it was increased in the lung lymph. The treatment with ASCs significantly attenuated these changes. Treatment with ASCs almost led to the reversal of increased pulmonary vascular permeability and lung water content. Pulmonary gas exchange was significantly improved by ASCs. Infusion of the ASCs did not negatively affect pulmonary artery pressure and other hemodynamic variables.ASCs infusion was well tolerated. The results suggest that intravenous ASCs modulate pulmonary microvascular hyper-permeability and prevent the onset of ARDS in our experimental model.http://europepmc.org/articles/PMC5628899?pdf=render
spellingShingle Koji Ihara
Satoshi Fukuda
Baigalmaa Enkhtaivan
Raul Trujillo
Dannelys Perez-Bello
Christina Nelson
Anita Randolph
Suzan Alharbi
Hira Hanif
David Herndon
Donald Prough
Perenlei Enkhbaatar
Adipose-derived stem cells attenuate pulmonary microvascular hyperpermeability after smoke inhalation.
PLoS ONE
title Adipose-derived stem cells attenuate pulmonary microvascular hyperpermeability after smoke inhalation.
title_full Adipose-derived stem cells attenuate pulmonary microvascular hyperpermeability after smoke inhalation.
title_fullStr Adipose-derived stem cells attenuate pulmonary microvascular hyperpermeability after smoke inhalation.
title_full_unstemmed Adipose-derived stem cells attenuate pulmonary microvascular hyperpermeability after smoke inhalation.
title_short Adipose-derived stem cells attenuate pulmonary microvascular hyperpermeability after smoke inhalation.
title_sort adipose derived stem cells attenuate pulmonary microvascular hyperpermeability after smoke inhalation
url http://europepmc.org/articles/PMC5628899?pdf=render
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