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Evaluating the potential impact of sodium-glucose cotransporter-2 inhibitor "canagliflozin" on the hepatic damage triggered by hypertension in rats.
Hassan, Fatma E; El-Mosallamy, Aliaa E M K; Khalifa, Mohamed Mansour; Aljuaydi, Samira H; Ali, Merhan E; Hosny, Sara Adel; Bastawy, Nermeen.
Afiliación
  • Hassan FE; Medical Physiology Department, Kasr Alainy, Faculty of Medicine, Cairo University, Giza, Egypt.
  • El-Mosallamy AEMK; General Medicine Practice Program, Department of Physiology, Batterjee Medical College, Jeddah, Saudi Arabia.
  • Khalifa MM; Department of Pharmacology, Medical Research and Clinical Studies Institute, National Research Center, Giza, Egypt.
  • Aljuaydi SH; Medical Physiology Department, Kasr Alainy, Faculty of Medicine, Cairo University, Giza, Egypt.
  • Ali ME; Department of Human Physiology, College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia.
  • Hosny SA; Department of Biochemistry and Molecular Biology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
  • Bastawy N; Department of Pathology, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.
Microsc Res Tech ; 2024 Jul 25.
Article en En | MEDLINE | ID: mdl-39051105
ABSTRACT
Hypertension (HTN) is a prevalent chronic disease. HTN and liver disease association is extensively noted. Thus, finding a medication that can alleviate HTN and its accompanying liver insult would be promising. This study investigated the potential impacts of canagliflozin "sodium-glucose cotransporter-2 inhibitor" on the liver of the Nω-nitro-L-arginine methyl ester (L-NAME)-induced HTN rat model. Twenty-four adult male rats were divided into four groups; negative control group, canagliflozin group, L-NAME group 50 mg/kg of L-NAME was injected daily for 5 weeks and L-NAME + canagliflozin group 1 week after L-NAME injection both L-NAME + canagliflozin (40 mg/kg) were given concomitantly daily for further 4 weeks. Liver functions, serum lipid profile, hepatic oxidative/nitrative stress biomarkers, gene expression of lipogenic enzymes, B-cell lymphoma 2 (Bcl2), and DNA fragmentation, were measured. Besides, hepatic histology and immunohistochemistry of nuclear factor kappa B (NF-κB) and endothelial nitric oxide synthase (eNOS) were assessed. Canagliflozin improved hepatic lipogenesis via the downregulation of fatty acid synthase (FAS) and transcriptional regulatory element binding protein 1c (SREBP1c) genes leading to an improved serum lipid profile. Further, canagliflozin modified the eNOS/inducible nitric oxide synthase (iNOS) pathway and decreased the NF-κB immunoreactivity besides restoring the oxidants-antioxidants balance; increased reduced glutathione concomitant with declined malondialdehyde. This improvement of the liver was mirrored by the significant restoration of liver architecture and confirmed by the preserved liver DNA content and upregulation of the antiapoptotic Bcl2 mRNA level and attenuation of the alanine transaminase, aspartate aminotransferase. In conclusion, canagliflozin is a promising anti-hypertensive and hepatic-supportive medication. RESEARCH HIGHLIGHTS Canagliflozin's antioxidant, anti-inflammatory, anti-lipogenic, and antiapoptotic characteristics mitigate remote liver compromise caused by hypertension. Canagliflozin can be exploited as a hepatoprotective and antihypertensive medication.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Microsc Res Tech Asunto de la revista: DIAGNOSTICO POR IMAGEM Año: 2024 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Microsc Res Tech Asunto de la revista: DIAGNOSTICO POR IMAGEM Año: 2024 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Estados Unidos