<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>397(8)</volume><submitter>Mahmoud SA</submitter><funding>Helwan University</funding><pubmed_abstract>Gastric ulcer is a disturbing disease that impacts many people worldwide. Pioglitazone (Piog), a thiazolidinedione, and ligustrazine (Ligu), a natural component of Ligusticum chuanxiong possess gastroprotective properties. However, the underlying mechanism is not well elucidated. The present study aimed to investigate the gastroprotective effects of Piog (15 mg/kg, p.o.), Ligu (15 mg/kg, p.o.), and their combination against ethanol-induced gastric ulcer in rats. Omeprazole (10 mg/kg) was used as a standard. Pre-treatment for 7 days with Piog, Ligu, and (Piog+Ligu) effectively alleviated ethanol-predisposed oxidative stress and inflammation through restoring HO-1, GSH, and SOD tissue levels and decreasing elevated MDA, TNF-α, ICAM, I-NOS, and IL-1β contents. Moreover, Piog, Ligu, and (Piog+</pubmed_abstract><journal>Naunyn-Schmiedeberg's archives of pharmacology</journal><pagination>6177-6195</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11329587</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Enhanced upregulation of SIRT1 via pioglitazone and ligustrazine confers protection against ethanol-induced gastric ulcer in rats.</pubmed_title><pmcid>PMC11329587</pmcid><pubmed_authors>Ahmed AAE</pubmed_authors><pubmed_authors>Elkhoely A</pubmed_authors><pubmed_authors>Mahmoud SA</pubmed_authors><pubmed_authors>El-Sayed EK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Enhanced upregulation of SIRT1 via pioglitazone and ligustrazine confers protection against ethanol-induced gastric ulcer in rats.</name><description>Gastric ulcer is a disturbing disease that impacts many people worldwide. Pioglitazone (Piog), a thiazolidinedione, and ligustrazine (Ligu), a natural component of Ligusticum chuanxiong possess gastroprotective properties. However, the underlying mechanism is not well elucidated. The present study aimed to investigate the gastroprotective effects of Piog (15 mg/kg, p.o.), Ligu (15 mg/kg, p.o.), and their combination against ethanol-induced gastric ulcer in rats. Omeprazole (10 mg/kg) was used as a standard. Pre-treatment for 7 days with Piog, Ligu, and (Piog+Ligu) effectively alleviated ethanol-predisposed oxidative stress and inflammation through restoring HO-1, GSH, and SOD tissue levels and decreasing elevated MDA, TNF-α, ICAM, I-NOS, and IL-1β contents. Moreover, Piog, Ligu, and (Piog+</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2025-04-21T22:06:13.485Z</modification><creation>2025-04-05T18:37:01.399Z</creation></dates><accession>S-EPMC11329587</accession><cross_references><pubmed>38441571</pubmed><doi>10.1007/s00210-024-03026-6</doi></cross_references></HashMap>