Kidney Week

Abstract: SA-PO367

Salt-Induced Phosphoproteomic Changes in the Hypothalamic Paraventricular Nucleus in Rats with Chronic Renal Failure

Session Information

• CKD: Risk Factors for Incidence and Progression - III
  November 04, 2017 | Location: Hall H, Morial Convention Center
  Abstract Time: 10:00 AM - 10:00 AM

Category: Chronic Kidney Disease (Non-Dialysis)

• 301 CKD: Risk Factors for Incidence and Progression

Authors

• Li, Aiqing, Nanfang Hospital, Southern Medical University, Guangzhou, China

Aiqing Li,

• Li, Lanying, Nanfang Hospital, Southern Medical University, Guangzhou, China

Lanying Li,

• Li, Jiawen, Nanfang Hospital, Southern Medical University, Guangzhou, China

Jiawen Li,

• Tan, Lishan, Nanfang Hospital, Southern Medical University, Guangzhou, China

Lishan Tan,

• Qiu, Minzi, Nanfang Hospital, Southern Medical University, Guangzhou, China

Minzi Qiu,

Background

Hypothalamic paraventricular nucleus (PVN) is a cardiovascular regulating center within the brain，which plays a critical role in high salt-induced progression of chronic renal failure (CRF). However, the phosphoproteomic changes in the PVN caused by CRF remain unclear. This study aimed to perform large-scale phosphoproteomic analysis of PVN induced by CRF and high salt intake.

Methods

Eight weeks post 5/6 nephrectomy (CRF model) or sham operation, Sprague–Dawley rats were fed a high-salt (4%) or normal-salt (0.4%) diet for 3 weeks. TiO₂ enrichment, iTRAQ labeling, and liquid chromatography tandem mass spectrometry were applied for phosphoproteomic profiling of PVN.

Results

A total of 3723 unique phosphopeptides corresponding to 1530 phosphoproteins were identified. Compared with sham group, 133 upregulated and 141 downregulated phosphopeptides were identified in CRF group during normal-salt feeding. However, with a high-salt diet, 160 phosphopeptides were upregulated and 142 downregulated in the CRF group. Gene Ontology analysis revealed that these phosphoproteins were involved in binding, catalytic, transporter, and other molecular functions. Search Tool for the Retrieval of Interacting Genes protein–protein analysis showed direct or indirect functional links among 25 differentially expressed phosphoproteins in CRF rats compared with sham group. However, 24 differentially phosphorylated proteins induced by high salt intake were functionally linked in CRF animals.The altered phosphorylation levels of dynamin 1 and TPPP were validated.

Conclusion

Phosphoproteomic changes of PVN triggered by CRF and high salt-load have been investigated. It will provide new insight into pathogenetic mechanisms of development of chronic kidney disease and salt sensitivity.