<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li RC</submitter><funding>NHLBI NIH HHS</funding><pagination>124-31</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3172891</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>184(1)</volume><pubmed_abstract>&lt;h4>Rationale&lt;/h4>Obstructive sleep apnea, which is characterized by intermittent hypoxia (IH) during sleep, has emerged as an independent risk factor for cardiovascular disease, including atherosclerosis. Leukotriene B4 (LTB4) production is increased in patients with obstructive sleep apnea and negatively correlates to hypoxic levels during sleep, with continuous positive airway pressure therapy decreasing LTB4 production.&lt;h4>Objectives&lt;/h4>Determine the potential role of LTB4 in IH-induced atherosclerosis in a monocyte cellular model and a murine model.&lt;h4>Methods&lt;/h4>THP-1 cells were exposed to IH for 3, 6, 24, and 48 hours. Macrophage transformation and foam cell formation were assessed after IH exposures. Apolipopotein E (ApoE)(-/-) or BLT1(-/-)/ApoE(-/-) mice were fed an atherogenic </pubmed_abstract><journal>American journal of respiratory and critical care medicine</journal><pubmed_title>Leukotriene B4 receptor-1 mediates intermittent hypoxia-induced atherogenesis.</pubmed_title><pmcid>PMC3172891</pmcid><funding_grant_id>R01 HL065270</funding_grant_id><funding_grant_id>HL-086662</funding_grant_id><funding_grant_id>HL-65270</funding_grant_id><funding_grant_id>R01 HL086662</funding_grant_id><pubmed_authors>Mathis SP</pubmed_authors><pubmed_authors>Gozal D</pubmed_authors><pubmed_authors>Li RC</pubmed_authors><pubmed_authors>Kim J</pubmed_authors><pubmed_authors>Haribabu B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Leukotriene B4 receptor-1 mediates intermittent hypoxia-induced atherogenesis.</name><description>&lt;h4>Rationale&lt;/h4>Obstructive sleep apnea, which is characterized by intermittent hypoxia (IH) during sleep, has emerged as an independent risk factor for cardiovascular disease, including atherosclerosis. Leukotriene B4 (LTB4) production is increased in patients with obstructive sleep apnea and negatively correlates to hypoxic levels during sleep, with continuous positive airway pressure therapy decreasing LTB4 production.&lt;h4>Objectives&lt;/h4>Determine the potential role of LTB4 in IH-induced atherosclerosis in a monocyte cellular model and a murine model.&lt;h4>Methods&lt;/h4>THP-1 cells were exposed to IH for 3, 6, 24, and 48 hours. Macrophage transformation and foam cell formation were assessed after IH exposures. Apolipopotein E (ApoE)(-/-) or BLT1(-/-)/ApoE(-/-) mice were fed an atherogenic </description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Jul</publication><modification>2025-04-18T13:21:50.923Z</modification><creation>2019-03-27T00:43:55Z</creation></dates><accession>S-EPMC3172891</accession><cross_references><pubmed>21493735</pubmed><doi>10.1164/rccm.201012-2039OC</doi><doi>10.1164/rccm.201012-2039oc</doi></cross_references></HashMap>