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      Effect of Low Versus High Tidal-Volume Total Liquid Ventilation on Pulmonary Inflammation

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          Abstract

          Animal experiments suggest that total liquid ventilation (TLV) induces less ventilator-induced lung injury (VILI) than conventional mechanical gas ventilation. However, TLV parameters that optimally minimize VILI in newborns remain unknown. Our objective was to compare lung inflammation between low (L-V T) and high (H-V T) liquid tidal volume and evaluate impacts on the weaning process. Sixteen anesthetized and paralyzed newborn lambs were randomized in an L-V T group (initial tidal volume of 10 mL/kg at 10/min) and an H-V T group (initial tidal volume of 20 mL/kg at 5/min). Five unventilated newborn lambs served as controls. After 4 h of TLV in the supine position, the lambs were weaned in the prone position for another 4 h. The levels of respiratory support needed during the 4 h post-TLV were compared. The anterior and posterior lung regions were assessed by a histological score and real-time quantitative PCR for IL1B, IL6, and TNF plus 12 other exploratory VILI-associated genes. All but one lamb were successfully extubated within 2 h post-TLV (72 ± 26 min vs. 63 ± 25 min, p = 0.5) with similar FiO 2 at 4 h post-TLV (27 ± 6% vs. 33 ± 7%, p = 0.3) between the L-V T and H-V T lambs. No significant differences were measured in histological inflammation scores between L-V T and H-V T lambs, although lambs in both groups exhibited slightly higher scores than the control lambs. The L-V T group displayed higher IL1B mRNA expression than the H-V T group in both anterior (2.8 ± 1.5-fold increase vs. 1.3 ± 0.4-fold increase, p = 0.02) and posterior lung regions (3.0 ± 1.0-fold change increase vs. 1.1 ± 0.3-fold increase, p = 0.002), respectively. No significant differences were found in IL6 and TNF expression levels. Gene expression changes overall indicated that L-V T was associated with a qualitatively distinct inflammatory gene expression profiles compared to H-V T, which may indicate different clinical effects. In light of these findings, further mechanistic studies are warranted. In conclusion, we found no advantage of lower tidal volume use, which was in fact associated with a slightly unfavorable pattern of inflammatory gene expression.

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          Most cited references36

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          High-throughput quantification of splicing isoforms.

          Most human messenger RNAs (mRNAs) are alternatively spliced and many exhibit disease-specific splicing patterns. However, the contribution of most splicing events to the development and maintenance of human diseases remains unclear. As the contribution of alternative splicing events to diagnosis and prognosis is becoming increasingly recognized, it becomes important to develop precise methods to quantify the abundance of these isoforms in clinical samples. Here we present a pipeline for real-time PCR annotation of splicing events (RASE) that allows accurate identification of a large number of splicing isoforms in human tissues. The RASE automatically designed specific primer pairs for 81% of all alternative splicing events in the NCBI build 36 database. Experimentally, the majority of the RASE designed primers resulted in isoform-specific amplification suitable for quantification in human cell lines or in formalin-fixed, paraffin-embedded (FFPE) RNA extract. Using this pipeline it is now possible to rapidly identify splicing isoform signatures in different types of human tissues or to validate complete sets of data generated by microarray expression profiling and deep sequencing techniques.
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            Airway injury from initiating ventilation in preterm sheep.

            Premature infants exposed to ventilation are at risk of developing bronchopulmonary dysplasia and persistent lung disease in childhood. We report where injury occurred within the lung after brief ventilation at birth. Preterm sheep (129 d gestation) were ventilated with an escalating tidal volume to 15 mL/kg by 15 min to injure the lungs, with the placental circulation intact (fetal) or after delivery (newborn). Fetal lambs were returned to the uterus for 2 h 45 min, whereas newborn lambs were maintained with gentle ventilatory support for the same period. The control group was not ventilated. Bronchoalveolar lavage fluid (BALF) and lung tissue were analyzed. In both fetal and newborn lambs, ventilation caused bronchial epithelial disruption in medium-sized airways. Early growth response protein 1 (Egr-1), monocyte chemotactic protein 1 (MCP-1), IL-6, and IL-1beta mRNA increased in the lung tissue from fetal and newborn lambs. Egr-1, MCP-1, and IL-6 mRNA were induced in mesenchymal cells surrounding small airways, whereas IL-1beta mRNA localized to the epithelium of medium/small airways. Ventilation caused loss of heat shock protein 70 (HSP70) mRNA from the bronchial epithelium, but induced mRNA in the smooth muscle surrounding large airways. HSP70 protein decreased in the lung tissue and increased in BALF with ventilation. Initiation of ventilation induced a stress response and inflammatory cytokines in small and medium-sized airways.
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              Effects of respiratory rate on ventilator-induced lung injury at a constant PaCO2 in a mouse model of normal lung.

              The aim of this study was to evaluate the effects of respiratory rate (RR) at a constant PaCO2 and conventional tidal volume (VT) on the development of ventilator-induced lung injury in normal lungs. Prospective, randomized, experimental study. University research laboratory. Adult male C57BL/6 mice. Four groups of anesthetized mice were exposed to mechanical ventilation with different RRs and VTs. Three groups were assigned to one of three RRs (80, 120, and 160 breaths/min), and VT was set to 12, 10, and 8 mL/kg, respectively (RR80 VT12, RR120 VT10, and RR160 VT8), to achieve normal PaCO2. A fourth group was ventilated at 160 breaths/min and VT of 10 mL/kg (RR160 VT10) with adjustment of dead space. All animals were ventilated for 120 mins with a positive end-expiratory pressure of 1.5 cm H2O and FiO2 of 1. Nonventilated animals were also studied. Arterial blood gases and static pressure-volume curves were not different among groups at the end of the experiment. Independent of ventilator settings, mechanical ventilation was associated with increased bronchoalveolar lavage protein and increased bronchoalveolar lavage and serum interleukin-6. Total bronchoalveolar lavage protein and interleukin-6 were significantly lower in RR80 VT12 and RR160 VT8 compared with RR120 VT10 and RR160 VT10. In all experimental conditions, mechanical ventilation was associated with activation of AKT and ERK1/2 kinases, known to be activated on stretch. Phosphorylation both of AKT and ERK1/2 was lower in RR80 VT12 compared with other groups of ventilated animals. Histologic injury did not differ among nonventilated, RR80 VT12, and RR160 VT8 animals; however, it increased significantly and progressively in RR120 VT10 and RR160 VT10 animals. Mechanical ventilation with conventional VT induces lung injury in normal lungs, even without alteration in lung mechanics. Reduction of RR and VT ameliorates lung inflammation and injury.
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                Author and article information

                Contributors
                Journal
                Front Physiol
                Front Physiol
                Front. Physiol.
                Frontiers in Physiology
                Frontiers Media S.A.
                1664-042X
                18 June 2020
                2020
                : 11
                : 603
                Affiliations
                [1] 1Department of Pharmacology-Physiology, Université de Sherbrooke , Sherbrooke, QC, Canada
                [2] 2BC Children’s Hospital Research Institute, The University of British Columbia , Vancouver, BC, Canada
                [3] 3Department of Experimental Medicine, The University of British Columbia , Vancouver, BC, Canada
                [4] 4Department of Microbiology and Infectiology, Université de Sherbrooke , Sherbrooke, QC, Canada
                [5] 5Department of Pathology, Université de Sherbrooke , Sherbrooke, QC, Canada
                [6] 6Department of Pediatrics, The University of British Columbia , Vancouver, BC, Canada
                [7] 7Department of Mechanical Engineering, Université de Sherbrooke , Sherbrooke, QC, Canada
                [8] 8Department of Pediatrics, Université de Sherbrooke , Sherbrooke, QC, Canada
                Author notes

                Edited by: Yu Ru Kou, National Yang-Ming University, Taiwan

                Reviewed by: Noah H. Hillman, Saint Louis University, United States; Beth J. Allison, Hudson Institute of Medical Research, Australia

                *Correspondence: Étienne Fortin-Pellerin, etienne.fortin-pellerin@ 123456usherbrooke.ca

                This article was submitted to Respiratory Physiology, a section of the journal Frontiers in Physiology

                Article
                10.3389/fphys.2020.00603
                7315809
                648cdd9c-aba7-4c95-bbf4-f6ec5e5b0d3c
                Copyright © 2020 Sage, See, Nault, Morin, Michalski, Chabot, Marouan, Lavoie, Micheau, Praud and Fortin-Pellerin.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 06 March 2020
                : 14 May 2020
                Page count
                Figures: 4, Tables: 2, Equations: 0, References: 41, Pages: 11, Words: 0
                Funding
                Funded by: Fonds de Recherche du Québec - Santé 10.13039/501100000156
                Award ID: 0000
                Categories
                Physiology
                Original Research

                Anatomy & Physiology
                liquid ventilation,ventilator-induced lung injury,tidal volume,newborn lamb,transcriptome

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