1 Ludwig Boltzmann Institute for Experimental and Clinical Traumatology in the AUVA Research Center, Vienna, Austria.
2 Department of General-, Visceral-, Thoracic- and Vascular Surgery, Helios Hanseklinikum Stralsund, Germany.
Innate Immun. 2018 May;24(4):262-273. doi: 10.1177/1753425918771748. Epub 2018 Apr 26.
Activation of peroxisome proliferator-activated receptor (PPAR)-β/δ reduces tissue injury in murine endotoxemia. We hypothesized that the PPAR-β/δ-agonist GW0742 improves long-term outcome after sepsis caused by cecal ligation and puncture (CLP). Fifty-one CD-1 female mice underwent CLP and received either vehicle (control), GW0742 (0.03 mg/kg/injection; five post-CLP i.v. injections), GSK0660 (PPAR-β/δ-antagonist) or both and were monitored for 28 d. Another 20 CLP mice treated with GW0742 and vehicle were sacrificed 24 h post-CLP to assess coagulopathy. Compared to vehicle, survival of CLP-mice treated with GW0742 was higher by 35% at d 7 and by 50% at d 28. CLP mice treated with GW0742 had 60% higher IFN-γ but circulating monocyte chemoattractant protein-1 and chemokine ligand were lower at 48 h post-CLP. Compared to vehicle, CLP mice treated with GW0742 exhibited a 50% reduction in the circulating plasminogen activator inhibitor-1 associated with an increase in platelet number at 24 h post-CLP (but no changes occurred in anti-thrombin-III, plasminogen, fibrinogen and clotting-times). CLP mice treated with GW0742 exhibited a similar increase in most of the biochemical markers of organ injury/dysfunction (lactate dehydrogenase, alanine aminotransferase, creatine kinase, creatinine, blood urea nitrogen, and triglycerides) measured. Treatment with GW0742 consistently improved long-term survival in septic CD-1 mice by partially modulating the post-CLP systemic cytokine response and coagulation systems.
过氧化物酶体增殖物激活受体 (PPAR)-β/δ 的激活可减轻内毒素血症小鼠的组织损伤。我们假设 PPAR-β/δ-激动剂 GW0742 可改善盲肠结扎穿刺 (CLP) 引起的败血症的长期预后。51 只 CD-1 雌性小鼠接受 CLP 并接受载体(对照)、GW0742(0.03mg/kg/注射;CLP 后 5 次静脉注射)、GSK0660(PPAR-β/δ 拮抗剂)或两者的治疗,并监测 28 天。另外 20 只接受 GW0742 和载体治疗的 CLP 小鼠在 CLP 后 24 小时处死,以评估凝血功能障碍。与载体相比,GW0742 治疗的 CLP 小鼠在第 7 天的存活率提高了 35%,在第 28 天的存活率提高了 50%。GW0742 治疗的 CLP 小鼠在 CLP 后 48 小时 IFN-γ 增加 60%,但循环单核细胞趋化蛋白-1 和趋化因子配体降低。与载体相比,GW0742 治疗的 CLP 小鼠在 CLP 后 24 小时循环纤溶酶原激活物抑制剂-1 降低 50%,血小板数量增加(但抗凝血酶-III、纤溶酶原、纤维蛋白原和凝血时间没有变化)。GW0742 治疗的 CLP 小鼠大多数器官损伤/功能障碍的生化标志物(乳酸脱氢酶、丙氨酸氨基转移酶、肌酸激酶、肌酐、血尿素氮和甘油三酯)也有类似的增加。GW0742 的治疗一致改善了败血症 CD-1 小鼠的长期存活率,部分调节了 CLP 后的全身细胞因子反应和凝血系统。