<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ito T</submitter><funding>Japan Society for the Promotion of Science</funding><pagination>17413</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7566838</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(1)</volume><pubmed_abstract>Recombinant thrombomodulin (rTM) has been used for treatment of sepsis-associated disseminated intravascular coagulation. Recent studies have suggested that anticoagulant therapy might dampen the protective role of immunothrombosis. We examined if rTM might worsen infectious diseases. Male Sprague-Dawley rats with jugular-vein catheterization were divided into three groups: no anticoagulation; rTM pretreatment; rTM treatment at 6 h. Live methicillin-resistant Staphylococcus aureus (MRSA) was inoculated into the tail vein of rats. rTM was administered into the jugular-vein catheter before or 6 h after MRSA inoculation, while an equal volume of saline was administered in the no-anticoagulation group. Blood samples were collected from the jugular-vein catheter before, 6 h and 12 h after MRSA </pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Recombinant thrombomodulin alleviates oxidative stress without compromising host resistance to infection in rats infected with methicillin-resistant Staphylococcus aureus.</pubmed_title><pmcid>PMC7566838</pmcid><funding_grant_id>Grants-in-Aid 15H05684 and 18K16543</funding_grant_id><pubmed_authors>Ito T</pubmed_authors><pubmed_authors>Maruyama I</pubmed_authors><pubmed_authors>Kakihana Y</pubmed_authors><pubmed_authors>Shrestha B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Recombinant thrombomodulin alleviates oxidative stress without compromising host resistance to infection in rats infected with methicillin-resistant Staphylococcus aureus.</name><description>Recombinant thrombomodulin (rTM) has been used for treatment of sepsis-associated disseminated intravascular coagulation. Recent studies have suggested that anticoagulant therapy might dampen the protective role of immunothrombosis. We examined if rTM might worsen infectious diseases. Male Sprague-Dawley rats with jugular-vein catheterization were divided into three groups: no anticoagulation; rTM pretreatment; rTM treatment at 6 h. Live methicillin-resistant Staphylococcus aureus (MRSA) was inoculated into the tail vein of rats. rTM was administered into the jugular-vein catheter before or 6 h after MRSA inoculation, while an equal volume of saline was administered in the no-anticoagulation group. Blood samples were collected from the jugular-vein catheter before, 6 h and 12 h after MRSA </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Oct</publication><modification>2025-04-19T00:43:58.713Z</modification><creation>2020-10-29T12:37:44Z</creation></dates><accession>S-EPMC7566838</accession><cross_references><pubmed>33060764</pubmed><doi>10.1038/s41598-020-74529-4</doi></cross_references></HashMap>