Activation of renal epithelial Na+ channels (ENaC) in infants with congenital heart disease

被引:0
作者
Ortmann, Laura A. [1 ]
Nandi, Shyam [2 ]
Li, Yu-long [3 ]
Zheng, Hong [4 ]
Patel, Kaushik P. [2 ]
机构
[1] Univ Nebraska Med Ctr, Dept Pediat, Omaha, NE 68198 USA
[2] Univ Nebraska Med Ctr, Dept Integrat Cellular Physiol, Omaha, NE USA
[3] Univ Nebraska Med Ctr, Dept Emergency Med, Omaha, NE USA
[4] Univ South Dakota, Sanford Sch Med, Basic Biomed Sci, Vermillion, SD USA
关键词
ENaC; sodium retention; proteases; congenital heart disease; pediatric; ACUTE KIDNEY INJURY; FLUID OVERLOAD; SODIUM-CHANNELS; POOR OUTCOMES; MORBIDITY;
D O I
10.3389/fped.2024.1338672
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Introduction: This study was designed to measure the concentration and activity of urinary proteases that activate renal epithelial sodium channel (ENaC) mediated Na+ transport in infants with congenital heart disease, a potential mechanism for fluid retention. Methods: Urine samples from infants undergoing cardiac surgery were collected at three time points: T1) pre-operatively, T2) 6-8 h after surgery, and T3) 24 h after diuretics. Urine was collected from five heathy infant controls. The urine was tested for four proteases and whole-cell patch-clamp testing was conducted in renal collecting duct M-1 cells to test whether patient urine increased Na+ currents consistent with ENaC activation. Results: Heavy chain of plasminogen, furin, and prostasin were significantly higher in cardiac patients prior to surgery compared to controls. There was no difference in most proteases before and after surgery. Urine from cardiac patients produced a significantly greater increase in Na+ inward currents compared to healthy controls. Conclusion: Urine from infants with congenital heart disease is richer in proteases and has the potential to increase activation of ENaC in the nephron to enhance Na+ reabsorption, which may lead to fluid retention in this population.
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页数:9
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共 34 条
[1]   Fluid Accumulation After Neonatal Congenital Cardiac Operation: Clinical Implications and Outcomes [J].
Bailly, David K. ;
Alten, Jeffrey A. ;
Gist, Katja M. ;
Mah, Kenneth E. ;
Kwiatkowski, David M. ;
Valentine, Kevin M. ;
Diddle, J. Wesley ;
Tadphale, Sachin ;
Clarke, Shanelle ;
Selewski, David T. ;
Banerjee, Mousumi ;
Reichle, Garrett ;
Lin, Paul ;
Gaies, Michael ;
Blinder, Joshua J. .
ANNALS OF THORACIC SURGERY, 2022, 114 (06) :2288-2294
[2]   Experimental nephrotic syndrome leads to proteolytic activation of the epithelial Na+ channel in the mouse kidney [J].
Bohnert, Bernhard N. ;
Essigke, Daniel ;
Janessa, Andrea ;
Schneider, Jonas C. ;
Woern, Matthias ;
Kalo, M. Zaher ;
Xiao, Mengyun ;
Kong, Lingsi ;
Omage, Kingsley ;
Hennenlotter, Joerg ;
Amend, Bastian ;
Birkenfeld, Andreas L. ;
Artunc, Ferruh .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2021, 321 (04) :F480-F493
[3]   Urokinase-type plasminogen activator (uPA) is not essential for epithelial sodium channel (ENaC)-mediated sodium retention in experimental nephrotic syndrome [J].
Bohnert, Bernhard N. ;
Daiminger, Sophie ;
Woern, Matthias ;
Sure, Florian ;
Staudner, Tobias ;
Ilyaskin, Alexandr V. ;
Batbouta, Firas ;
Janessa, Andrea ;
Schneider, Jonas C. ;
Essigke, Daniel ;
Kanse, Sandip ;
Haerteis, Silke ;
Korbmacher, Christoph ;
Artunc, Ferruh .
ACTA PHYSIOLOGICA, 2019, 227 (04)
[4]   Aprotinin prevents proteolytic epithelial sodium channel (ENaC) activation and volume retention in nephrotic syndrome [J].
Bohnert, Bernhard N. ;
Menacher, Martina ;
Janessa, Andrea ;
Woern, Matthias ;
Schork, Anja ;
Daiminger, Sophie ;
Kalbacher, Hubert ;
Haering, Hans-Ulrich ;
Daniel, Christoph ;
Amann, Kerstin ;
Sure, Florian ;
Bertog, Marko ;
Haerteis, Silke ;
Korbmacher, Christoph ;
Artunc, Ferruh .
KIDNEY INTERNATIONAL, 2018, 93 (01) :159-172
[5]   Early postoperative weight-based fluid overload is associated with worse outcomes after neonatal cardiac surgery [J].
Brandewie, Katie M. ;
Selewski, David ;
Bailly, David ;
Bhat, Priya ;
Diddle, John ;
Ghbeis, Muhammad ;
Krawczeski, Catherine R. ;
Mah, Kenneth ;
Neumayr, Tara ;
Raymond, Tia ;
Reichle, Garrett ;
Zang, Huaiyu ;
Alten, Jeffrey .
PEDIATRIC NEPHROLOGY, 2023, 38 (09) :3129-3137
[6]   Regulation of epithelial Na+ channels from M-1 cortical collecting duct cells [J].
Chalfant, ML ;
PetersonYantorno, K ;
OBrien, TG ;
Civan, MM .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1996, 271 (04) :F861-F870
[7]   Zymogen-locked mutant prostasin (Prss8) leads to incomplete proteolytic activation of the epithelial sodium channel (ENaC) and severely compromises triamterene tolerance in mice [J].
Essigke, Daniel ;
Ilyaskin, Alexandr, V ;
Woern, Matthias ;
Bohnert, Bernhard N. ;
Xiao, Mengyun ;
Daniel, Christoph ;
Amann, Kerstin ;
Birkenfeld, Andreas L. ;
Szabo, Roman ;
Bugge, Thomas H. ;
Korbmacher, Christoph ;
Artunc, Ferruh .
ACTA PHYSIOLOGICA, 2021, 232 (01)
[8]   Early Postoperative Fluid Overload Precedes Acute Kidney Injury and Is Associated With Higher Morbidity in Pediatric Cardiac Surgery Patients [J].
Hassinger, Amanda B. ;
Wald, Eric L. ;
Goodman, Denise M. .
PEDIATRIC CRITICAL CARE MEDICINE, 2014, 15 (02) :131-138
[9]   Fluid Overload in Infants Following Congenital Heart Surgery [J].
Hazle, Matthew A. ;
Gajarski, Robert J. ;
Yu, Sunkyung ;
Donohue, Janet ;
Blatt, Neal B. .
PEDIATRIC CRITICAL CARE MEDICINE, 2013, 14 (01) :44-49
[10]   Prevalence and associated factors of renal dysfunction and proteinuria in cyanotic congenital heart disease [J].
Hongsawong, Nattaphorn ;
Khamdee, Prapimdaw ;
Silvilairat, Suchaya ;
Chartapisak, Wattana .
PEDIATRIC NEPHROLOGY, 2018, 33 (03) :493-501