Canagliflozin Improves Liver Function in Rats by Upregulating Asparagine Synthetase

التفاصيل البيبلوغرافية
العنوان: Canagliflozin Improves Liver Function in Rats by Upregulating Asparagine Synthetase
المؤلفون: Dong Ruoyao, Yasong Ding, Meng Shengnan, Shiqi Wang, Hongyun Wang, Lingdi Yin
المصدر: Pharmacology. 106:606-615
بيانات النشر: S. Karger AG, 2021.
سنة النشر: 2021
مصطلحات موضوعية: medicine.medical_specialty, NF-E2-Related Factor 2, Asparagine synthetase, Rats, Sprague-Dawley, chemistry.chemical_compound, Liver Function Tests, AMP-activated protein kinase, Internal medicine, Lactate dehydrogenase, Diabetes mellitus, medicine, Animals, Canagliflozin, Carbon Tetrachloride, Sodium-Glucose Transporter 2 Inhibitors, Pharmacology, Liver injury, biology, business.industry, Adenylate Kinase, AMPK, Aspartate-Ammonia Ligase, General Medicine, medicine.disease, Activating Transcription Factor 4, Rats, Disease Models, Animal, Endocrinology, Liver, chemistry, Carbon tetrachloride, biology.protein, Liver function, Chemical and Drug Induced Liver Injury, business
الوصف: Introduction: Canagliflozin (CANA) is a sodium-glucose cotransporter 2 inhibitor that was recently approved for treating diabetes. However, its effects on liver function are not well understood. The function of asparagine synthetase (ASNS) has been studied in several cancers but not in liver injury. Therefore, we investigated the connection between CANA and ASNS in alleviating damage (i.e., their hepatoprotective effect) in a rat liver injury model. Methods: The rat model of liver injury was established using carbon tetrachloride treatment. Rats with liver injury were administered CANA orally for 8 weeks daily. After week 8, peripheral blood was collected to measure serum alanine aminotransferase, aspartate aminotransferase, and lactate dehydrogenase levels. Liver histopathology was examined using hematoxylin and eosin staining to determine the degree of liver injury. Protein expression in the rat livers was examined using Western blotting. Results: CANA treatment decreased serum alanine aminotransferase, aspartate aminotransferase, and lactate dehydrogenase levels compared with those of the untreated group, demonstrating diminished liver injury. Mechanistically, CANA treatment activated AMP-activated protein kinase (AMPK), leading to increased nuclear translocation of nuclear factor erythroid 2-related factor 2 (Nrf2) and activating transcription factor 4 (ATF4), which upregulated ASNS expression in liver-injured rats. Conclusion: CANA significantly alleviated liver injury by activating the AMPK/Nrf2/ATF4 axis and upregulating ASNS expression, indicating its potential for treating patients with type 2 diabetes mellitus with impaired liver function.
تدمد: 1423-0313
0031-7012
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80026caec34e989580809335f6671343Test
https://doi.org/10.1159/000518492Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....80026caec34e989580809335f6671343
قاعدة البيانات: OpenAIRE