<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(8)</volume><submitter>Bruells CS</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>Mechanical ventilation (MV) is a life saving intervention for patients with respiratory failure. Even after 6 hours of MV, diaphragm atrophy and dysfunction (collectively referred to as ventilator-induced diaphragmatic dysfunction, VIDD) occurs in concert with a blunted blood flow and oxygen delivery. The regulation of hypoxia sensitive factors (i.e. hypoxia inducible factor 1α, 2α (HIF-1α,-2α), vascular endothelial growth factor (VEGF)) and angio-neogenetic factors (angiopoietin 1-3, Ang) might contribute to reactive and compensatory alterations in diaphragm muscle.&lt;h4>Methods&lt;/h4>Male Wistar rats (n = 8) were ventilated for 24 hours or directly sacrificed (n = 8), diaphragm and mixed gastrocnemius muscle tissue was removed. Quantitative real time PCR and western blot analyses were performed to detect changes in angio-neogenetic factors and inflammatory markers. Tissues were stained using Isolectin (IB 4) to determine capillarity and calculate the capillary/fiber ratio.&lt;h4>Results&lt;/h4>MV resulted in up-regulation of Ang 2 and HIF-1α mRNA in both diaphragm and gastrocnemius, while VEGF mRNA was down-regulated in both tissues. HIF-2α mRNA was reduced in both tissues, while GLUT 4 mRNA was increased in gastrocnemius and reduced in diaphragm samples. Protein levels of VEGF, HIF-1α, -2α and 4 did not change significantly. Additionally, inflammatory cytokine mRNA (Interleukin (IL)-6, IL-1β and TNF α) were elevated in diaphragm tissue.&lt;h4>Conclusion&lt;/h4>The results demonstrate that 24 hrs of MV and the associated limb disuse induce an up-regulation of angio-neogenetic factors that are connected to HIF-1α. Changes in HIF-1α expression may be due to several interactions occurring during MV.</pubmed_abstract><journal>PloS one</journal><pagination>e70524</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3738548</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Prolonged mechanical ventilation alters the expression pattern of angio-neogenetic factors in a pre-clinical rat model.</pubmed_title><pmcid>PMC3738548</pmcid><pubmed_authors>Loetscher U</pubmed_authors><pubmed_authors>Cielen N</pubmed_authors><pubmed_authors>Bruells CS</pubmed_authors><pubmed_authors>Weis J</pubmed_authors><pubmed_authors>Gayan-Ramirez G</pubmed_authors><pubmed_authors>Maes K</pubmed_authors><pubmed_authors>Dreier A</pubmed_authors><pubmed_authors>Bleilevens C</pubmed_authors><pubmed_authors>Rossaint R</pubmed_authors><pubmed_authors>Thomas D</pubmed_authors><pubmed_authors>Bergs I</pubmed_authors><pubmed_authors>Behnke BJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prolonged mechanical ventilation alters the expression pattern of angio-neogenetic factors in a pre-clinical rat model.</name><description>&lt;h4>Objective&lt;/h4>Mechanical ventilation (MV) is a life saving intervention for patients with respiratory failure. Even after 6 hours of MV, diaphragm atrophy and dysfunction (collectively referred to as ventilator-induced diaphragmatic dysfunction, VIDD) occurs in concert with a blunted blood flow and oxygen delivery. The regulation of hypoxia sensitive factors (i.e. hypoxia inducible factor 1α, 2α (HIF-1α,-2α), vascular endothelial growth factor (VEGF)) and angio-neogenetic factors (angiopoietin 1-3, Ang) might contribute to reactive and compensatory alterations in diaphragm muscle.&lt;h4>Methods&lt;/h4>Male Wistar rats (n = 8) were ventilated for 24 hours or directly sacrificed (n = 8), diaphragm and mixed gastrocnemius muscle tissue was removed. Quantitative real time PCR and western blot analyses were performed to detect changes in angio-neogenetic factors and inflammatory markers. Tissues were stained using Isolectin (IB 4) to determine capillarity and calculate the capillary/fiber ratio.&lt;h4>Results&lt;/h4>MV resulted in up-regulation of Ang 2 and HIF-1α mRNA in both diaphragm and gastrocnemius, while VEGF mRNA was down-regulated in both tissues. HIF-2α mRNA was reduced in both tissues, while GLUT 4 mRNA was increased in gastrocnemius and reduced in diaphragm samples. Protein levels of VEGF, HIF-1α, -2α and 4 did not change significantly. Additionally, inflammatory cytokine mRNA (Interleukin (IL)-6, IL-1β and TNF α) were elevated in diaphragm tissue.&lt;h4>Conclusion&lt;/h4>The results demonstrate that 24 hrs of MV and the associated limb disuse induce an up-regulation of angio-neogenetic factors that are connected to HIF-1α. Changes in HIF-1α expression may be due to several interactions occurring during MV.</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013</publication><modification>2025-04-18T18:27:00.72Z</modification><creation>2019-03-26T23:15:14Z</creation></dates><accession>S-EPMC3738548</accession><cross_references><pubmed>23950950</pubmed><doi>10.1371/journal.pone.0070524</doi></cross_references></HashMap>