Your browser doesn't support javascript.
loading
Transcriptomic changes in glomeruli in response to a high salt challenge in the Dahl SS rat.
Semenikhina, Marharyta; Lysikova, Daria V; Spires, Denisha R; Domondon, Mark; Stadler, Krisztian; Palygin, Oleg; Ilatovskaya, Daria V.
Afiliação
  • Semenikhina M; Division of Nephrology, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, United States.
  • Lysikova DV; Department of Physiology, Augusta University, Augusta, Georgia, United States.
  • Spires DR; Department of Physiology, Augusta University, Augusta, Georgia, United States.
  • Domondon M; Division of Nephrology, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, United States.
  • Stadler K; Pennington Biomedical Research Center, Baton Rouge, Louisiana, United States.
  • Palygin O; Division of Nephrology, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, United States.
  • Ilatovskaya DV; Department of Physiology, Augusta University, Augusta, Georgia, United States.
Physiol Genomics ; 56(1): 98-111, 2024 Jan 01.
Article em En | MEDLINE | ID: mdl-37955135
ABSTRACT
Salt sensitivity impacts a significant portion of the population and is an important contributor to the development of chronic kidney disease. One of the significant early predictors of salt-induced damage is albuminuria, which reflects the deterioration of the renal filtration barrier the glomerulus. Despite significant research efforts, there is still a gap in knowledge regarding the molecular mechanisms and signaling networks contributing to instigating and/or perpetuating salt-induced glomerular injury. To address this gap, we used 8-wk-old male Dahl salt-sensitive rats fed a normal-salt diet (0.4% NaCl) or challenged with a high-salt diet (4% NaCl) for 3 wk. At the end of the protocol, a pure fraction of renal glomeruli obtained by differential sieving was used for next-generation RNA sequencing and comprehensive semi-automatic transcriptomic data analyses, which revealed 149 differentially expressed genes (107 and 42 genes were downregulated and upregulated, respectively). Furthermore, a combination of predictive gene correlation networks and computational bioinformatic analyses revealed pathways impacted by a high salt dietary challenge, including renal metabolism, mitochondrial function, apoptotic signaling and fibrosis, cell cycle, inflammatory and immune responses, circadian clock, cytoskeletal organization, G protein-coupled receptor signaling, and calcium transport. In conclusion, we report here novel transcriptomic interactions and corresponding predicted pathways affecting glomeruli under salt-induced stress.NEW & NOTEWORTHY Our study demonstrated novel pathways affecting glomeruli under stress induced by dietary salt. Predictive gene correlation networks and bioinformatic semi-automatic analysis revealed changes in the pathways relevant to mitochondrial function, inflammatory, apoptotic/fibrotic processes, and cell calcium transport.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cloreto de Sódio na Dieta / Hipertensão Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cloreto de Sódio na Dieta / Hipertensão Idioma: En Ano de publicação: 2024 Tipo de documento: Article