<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(2)</volume><submitter>Yan T</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Systemic leukocyte activation and disseminated leukocyte adhesion will impair the microcirculation and cause severe decrements in tissue perfusion and organ function in the process of severe sepsis. Gu-4, a lactosyl derivative, could selectively target CD11b to exert therapeutic effect in a rat model of severe burn shock. Here, we addressed whether Gu-4 could render protective effects on septic animals.&lt;h4>Methodology/principal findings&lt;/h4>On a murine model of endotoxemia induced by lipopolysaccharide (LPS), we found that the median effective dose (ED50) of Gu-4 was 0.929 mg/kg. In vivo treatment of Gu-4 after LPS challenge prominently attenuated LPS-induced lung injury and decreased lactic acid level in lung tissue. Using the ED50 of Gu-4, we also demonstrated that Gu-</pubmed_abstract><journal>PloS one</journal><pagination>e30110</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3271073</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Gu-4 suppresses affinity and avidity modulation of CD11b and improves the outcome of mice with endotoxemia and sepsis.</pubmed_title><pmcid>PMC3271073</pmcid><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Yu S</pubmed_authors><pubmed_authors>Yan T</pubmed_authors><pubmed_authors>Li Q</pubmed_authors><pubmed_authors>Zhou H</pubmed_authors><pubmed_authors>Xu G</pubmed_authors><pubmed_authors>Zhao Z</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Yin Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Gu-4 suppresses affinity and avidity modulation of CD11b and improves the outcome of mice with endotoxemia and sepsis.</name><description>&lt;h4>Background&lt;/h4>Systemic leukocyte activation and disseminated leukocyte adhesion will impair the microcirculation and cause severe decrements in tissue perfusion and organ function in the process of severe sepsis. Gu-4, a lactosyl derivative, could selectively target CD11b to exert therapeutic effect in a rat model of severe burn shock. Here, we addressed whether Gu-4 could render protective effects on septic animals.&lt;h4>Methodology/principal findings&lt;/h4>On a murine model of endotoxemia induced by lipopolysaccharide (LPS), we found that the median effective dose (ED50) of Gu-4 was 0.929 mg/kg. In vivo treatment of Gu-4 after LPS challenge prominently attenuated LPS-induced lung injury and decreased lactic acid level in lung tissue. Using the ED50 of Gu-4, we also demonstrated that Gu-</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012</publication><modification>2025-05-29T20:31:17.896Z</modification><creation>2019-06-05T17:02:16Z</creation></dates><accession>S-EPMC3271073</accession><cross_references><pubmed>22319560</pubmed><doi>10.1371/journal.pone.0030110</doi></cross_references></HashMap>