<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(8)</volume><submitter>Su Y</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>This study sought to investigate the protective effects of Astragaloside IV (AS-IV) on ischemia-reperfusion (I/R) renal injury based on the keap1-Nrf2/ARE signaling pathway.&lt;h4>Methods&lt;/h4>A total of 36 male Sprague-Dawley rats (aged: 8 weeks; weighing: 200-220 g) were randomly divided into the following 6 groups (n=6 per group): (I) the control group; (II) the sham operation group; (III) the kidney I/R injury group (the I/R group); (IV) the kidney I/R injury group treated with 2 mg/kg of AS-IV (the low-dose group); (V) the kidney I/R injury group treated with 5 mg/kg of AS-IV (the mid-dose group); and (VI) the kidney I/R injury group treated with 10 mg/kg of AS-IV (the high-dose group). Serum creatinine (CRE), serum urea, malondialdehyde (MDA), and superoxide dismutase </pubmed_abstract><journal>Translational andrology and urology</journal><pagination>1177-1188</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9459544</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Astragaloside IV protects against ischemia/reperfusion (I/R)-induced kidney injury based on the Keap1-Nrf2/ARE signaling pathway.</pubmed_title><pmcid>PMC9459544</pmcid><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Feng J</pubmed_authors><pubmed_authors>Lei Z</pubmed_authors><pubmed_authors>Su Y</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Xu J</pubmed_authors><pubmed_authors>Zeng D</pubmed_authors><pubmed_authors>Qiao L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Astragaloside IV protects against ischemia/reperfusion (I/R)-induced kidney injury based on the Keap1-Nrf2/ARE signaling pathway.</name><description>&lt;h4>Background&lt;/h4>This study sought to investigate the protective effects of Astragaloside IV (AS-IV) on ischemia-reperfusion (I/R) renal injury based on the keap1-Nrf2/ARE signaling pathway.&lt;h4>Methods&lt;/h4>A total of 36 male Sprague-Dawley rats (aged: 8 weeks; weighing: 200-220 g) were randomly divided into the following 6 groups (n=6 per group): (I) the control group; (II) the sham operation group; (III) the kidney I/R injury group (the I/R group); (IV) the kidney I/R injury group treated with 2 mg/kg of AS-IV (the low-dose group); (V) the kidney I/R injury group treated with 5 mg/kg of AS-IV (the mid-dose group); and (VI) the kidney I/R injury group treated with 10 mg/kg of AS-IV (the high-dose group). Serum creatinine (CRE), serum urea, malondialdehyde (MDA), and superoxide dismutase </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-18T22:40:38.721Z</modification><creation>2025-04-07T10:25:08.353Z</creation></dates><accession>S-EPMC9459544</accession><cross_references><pubmed>36092836</pubmed><doi>10.21037/tau-22-505</doi></cross_references></HashMap>