Development of a fluorescence-based assay for screening of urate transporter 1 inhibitors using 6-carboxyfluorescein

2021 ◽  
pp. 114246
Author(s):  
Haiyan Zhou ◽  
Guorui Zhong ◽  
Jing Bai ◽  
Xiaolei Li ◽  
Wen Peng ◽  
...  
Keyword(s):  
Critical Care ◽  
2021 ◽  
Vol 25 (1) ◽  
Author(s):  
Inès Dufour ◽  
Alexis Werion ◽  
Leila Belkhir ◽  
Anastazja Wisniewska ◽  
Marie Perrot ◽  
...  

Abstract Background The severity of coronavirus disease 2019 (COVID-19) is highly variable between individuals, ranging from asymptomatic infection to critical disease with acute respiratory distress syndrome requiring mechanical ventilation. Such variability stresses the need for novel biomarkers associated with disease outcome. As SARS-CoV-2 infection causes a kidney proximal tubule dysfunction with urinary loss of uric acid, we hypothesized that low serum levels of uric acid (hypouricemia) may be associated with severity and outcome of COVID-19. Methods In a retrospective study using two independent cohorts, we investigated and validated the prevalence, kinetics and clinical correlates of hypouricemia among patients hospitalized with COVID-19 to a large academic hospital in Brussels, Belgium. Survival analyses using Cox regression and a competing risk approach assessed the time to mechanical ventilation and/or death. Confocal microscopy assessed the expression of urate transporter URAT1 in kidney proximal tubule cells from patients who died from COVID-19. Results The discovery and validation cohorts included 192 and 325 patients hospitalized with COVID-19, respectively. Out of the 517 patients, 274 (53%) had severe and 92 (18%) critical COVID-19. In both cohorts, the prevalence of hypouricemia increased from 6% upon admission to 20% within the first days of hospitalization for COVID-19, contrasting with a very rare occurrence (< 1%) before hospitalization for COVID-19. During a median (interquartile range) follow-up of 148 days (50–168), 61 (12%) patients required mechanical ventilation and 93 (18%) died. In both cohorts considered separately and in pooled analyses, low serum levels of uric acid were strongly associated with disease severity (linear trend, P < 0.001) and with progression to death and respiratory failure requiring mechanical ventilation in Cox (adjusted hazard ratio 5.3, 95% confidence interval 3.6–7.8, P < 0.001) or competing risks (adjusted hazard ratio 20.8, 95% confidence interval 10.4–41.4, P < 0.001) models. At the structural level, kidneys from patients with COVID-19 showed a major reduction in urate transporter URAT1 expression in the brush border of proximal tubules. Conclusions Among patients with COVID-19 requiring hospitalization, low serum levels of uric acid are common and associate with disease severity and with progression to respiratory failure requiring invasive mechanical ventilation.


2009 ◽  
Vol 106 (25) ◽  
pp. 10338-10342 ◽  
Author(s):  
O. M. Woodward ◽  
A. Kottgen ◽  
J. Coresh ◽  
E. Boerwinkle ◽  
W. B. Guggino ◽  
...  

2010 ◽  
Vol 49 (2) ◽  
pp. 89-94 ◽  
Author(s):  
Daijiro Uetake ◽  
Iwao Ohno ◽  
Kimiyoshi Ichida ◽  
Yuichiro Yamaguchi ◽  
Hajime Saikawa ◽  
...  

1997 ◽  
Vol 272 (1) ◽  
pp. 617-625 ◽  
Author(s):  
Edgar Leal-Pinto ◽  
Wenjing Tao ◽  
Jay Rappaport ◽  
Max Richardson ◽  
Barbara A. Knorr ◽  
...  

2002 ◽  
Vol 283 (1) ◽  
pp. F150-F163 ◽  
Author(s):  
Edgar Leal-Pinto ◽  
B. Eleazar Cohen ◽  
Michael S. Lipkowitz ◽  
Ruth G. Abramson

Recombinant protein, designated hUAT, the human homologue of the rat urate transporter/channel (UAT), functions as a highly selective urate channel in lipid bilayers. Functional analysis indicates that hUAT activity, like UAT, is selectively blocked by oxonate from its cytosolic side, whereas pyrazinoate and adenosine selectively block from the channel's extracellular face. Importantly, hUAT is a galectin, a protein with two β-galactoside binding domains that bind lactose. Lactose significantly increased hUAT open probability but only when added to the channel's extracellular side. This effect on open probability was mimicked by glucose, but not ribose, suggesting a role for extracellular glucose in regulating hUAT channel activity. These functional observations support a four-transmembrane-domain structural model of hUAT, as previously predicted from the primary structure of UAT. hUAT and UAT, however, are not functionally identical: hUAT has a significantly lower single-channel conductance and open probability is voltage independent. These differences suggest that evolutionary changes in specific amino acids in these highly homologous proteins are functionally relevant in defining these biophysical properties.


2019 ◽  
Vol 47 (11) ◽  
pp. 1343-1351 ◽  
Author(s):  
Gentao Li ◽  
Lifeng Han ◽  
Ruicong Ma ◽  
Khawar Saeed ◽  
Hui Xiong ◽  
...  

2020 ◽  
Vol 63 (19) ◽  
pp. 10829-10854 ◽  
Author(s):  
Tong Zhao ◽  
Qing Meng ◽  
Zhuosen Sun ◽  
Yanyu Chen ◽  
Wei Ai ◽  
...  

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