Journal
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
Volume 1867, Issue 1, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.bbagen.2022.130264
Keywords
Roxadustat; Septic shock; Cardiac dysfunction; Mitochondrial oxidative stress; Energy metabolism
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The new anti-anemia drug Roxadustat (FG-4592) has shown potential in protecting against mortality and shock in septic animals by antagonizing mitochondrial oxidative stress and metabolic disorders, providing a novel treatment approach for septic shock.
Background: Septic shock is a serious clinical syndrome leading to high mortality. A new anti-anemia drug Roxadustat (FG-4592) protected against cardiac injury and hypertension. However, its effect and mechanism on shock and cardiac dysfunction induced by sepsis require to be investigated.Methods: C57BL/6j mice received FG-4592 (10 mg/kg/day) by i.p injection, followed by lipopolysaccharide (LPS) or cecal ligation and puncture (CLP) treatment. Mortality and shock status were monitored during the experiment. Cardiac function was assessed using echocardiography and serum lactate dehydrogenase (LDH) and creatine kinase-MB (CK-MB) assay. TEM, COX-SDH staining and ATP production were used to evaluate mito-chondrial function. A non-targeted metabolomic analysis was performed to evaluate the metabolic disorders.Results: Both pre-and post-treatment of FG-4592 could improve the survival rate in LPS-and CLP-induced sepsis mice with a better effect in pre-treated animals. Meanwhile, FG-4592 improved systolic blood pressure and body temperature drop in septic mice along with alleviated cardiac dysfunction (as shown by the restoration of decreased LVEF and LVFS and increased LDH and CK-MB) and inflammation. Interestingly, we observed that FG-4592 improved mitochondrial oxidative stress possibly by upregulating the anti-oxidative enzymes of SOD2 and HO-1. Furthermore, FG-4592 improved the energy supply and glycerophospholipid metabolism in car-diomyocytes, possibly through upregulating the HIF-1 alpha-targeted genes of LDHA and PDK1 in glycolysis and CHK-alpha, respectively.Conclusions: FG-4592 protected against mortality and shock in septic animals possibly by antagonizing mito-chondrial oxidative stress and metabolic disorders. General significance: This study provides a potential of FG-4592 as a novel drug for treating septic shock.
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