<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Balhorn R</submitter><funding>Deutsche Forschungsgemeinschaft</funding><pagination>E4679</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7370281</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(13)</volume><pubmed_abstract>Hypertensive patients have an increased risk of developing chronic kidney disease (CKD). Many of these patients have increased levels of the blood pressure regulating mineralocorticoid aldosterone. As a protection against aldosterone-induced damage, kidney cells can upregulate key regulators of the antioxidant defense, such as nuclear factor-erythroid-2-related factor 2 (Nrf2). In the present study aldosterone-induced kidney damage and Nrf2 activation in kidney cells of mice treated with three different concentrations of aldosterone for 4 weeks was localized. Increased albumin and neutrophil gelatinase-associated lipocalin (NGAL) in urine revealed an impaired kidney function of the aldosterone-infused mice. Localization of aldosterone-induced oxidative damage (in the form of DNA lesions) i</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Aldosterone Induces DNA Damage and Activation of Nrf2 Mainly in Tubuli of Mouse Kidneys.</pubmed_title><pmcid>PMC7370281</pmcid><funding_grant_id>Schu 2367/5-4</funding_grant_id><pubmed_authors>Balhorn R</pubmed_authors><pubmed_authors>Hartmann C</pubmed_authors><pubmed_authors>Schupp N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aldosterone Induces DNA Damage and Activation of Nrf2 Mainly in Tubuli of Mouse Kidneys.</name><description>Hypertensive patients have an increased risk of developing chronic kidney disease (CKD). Many of these patients have increased levels of the blood pressure regulating mineralocorticoid aldosterone. As a protection against aldosterone-induced damage, kidney cells can upregulate key regulators of the antioxidant defense, such as nuclear factor-erythroid-2-related factor 2 (Nrf2). In the present study aldosterone-induced kidney damage and Nrf2 activation in kidney cells of mice treated with three different concentrations of aldosterone for 4 weeks was localized. Increased albumin and neutrophil gelatinase-associated lipocalin (NGAL) in urine revealed an impaired kidney function of the aldosterone-infused mice. Localization of aldosterone-induced oxidative damage (in the form of DNA lesions) i</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jun</publication><modification>2025-04-05T08:45:13.777Z</modification><creation>2025-04-05T08:45:13.777Z</creation></dates><accession>S-EPMC7370281</accession><cross_references><pubmed>32630085</pubmed><doi>10.3390/ijms21134679</doi></cross_references></HashMap>