Aquaporin-2 and NKCC2 expression pattern in patients with hepatosplenic schistosomiasis.
Autor: | Duarte DB; Post-Graduation Program in Medical Sciences, Department of Internal Medicine, Federal University of Ceará, Fortaleza, Brazil.; School of Medicine, Federal University of Alagoas, Maceió, Brazil.; School of Medicine, Tiradentes University Center, Maceió, Brazil.; School of Medicine, CESMAC University Center, Maceió, Brazil., Meneses GC; Post-Graduation Program in Medical Sciences, Department of Internal Medicine, Federal University of Ceará, Fortaleza, Brazil., Lima DB; Department of Clinical and Toxicological Analysis, School of Pharmacy, Federal University of Ceará, Fortaleza, Brazil., Martins AMC; Department of Clinical and Toxicological Analysis, School of Pharmacy, Federal University of Ceará, Fortaleza, Brazil., da Silva Júnior GB; School of Medicine, University of Fortaleza, Fortaleza, Brazil., Daher EF; Post-Graduation Program in Medical Sciences, Department of Internal Medicine, Federal University of Ceará, Fortaleza, Brazil. |
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Jazyk: | angličtina |
Zdroj: | Tropical medicine & international health : TM & IH [Trop Med Int Health] 2020 Sep; Vol. 25 (9), pp. 1140-1144. Date of Electronic Publication: 2020 Jul 30. |
DOI: | 10.1111/tmi.13461 |
Abstrakt: | Objective: Schistosoma mansoni infection is considered a public health problem. Glomerular involvement in schistosomiasis is a well-documented complication, especially in hepatosplenic schistosomiasis (HSS). However, renal tubular function is poorly understood. The aim of this study was to investigate, through urinary exosomes, tubular transporters functionally in HSS patients. Methods: Cross-sectional study of 20 HSS patients who had isolated exosomes from urine samples. Protease inhibitor was added in the urine samples who were immediately frozen at -80 °C for further exosomes isolation. After urine had thawed, urinary exosomes were obtained using extensive vortexing, centrifugation and ultracentrifugation steps of urine. Urinary transporters expression from exosomes was evaluated by western blot, including NHE3, AQP2 and NKCC2. Charge amounts for gel electrophoresis were adjusted by urinary creatinine concentration of each patient to avoid urinary concentration bias. All protein expression of HSS patients was relative to healthy controls. Results: The expression of aquaporin-2 (AQP2) was lower in HSS patients than in controls (46.8 ± 40.7 vs. 100 ± 70.2%, P = 0.03) and the expression of the NKCC2 co-transporter was higher (191.7 ± 248.6 vs. 100 ± 43.6%, P = 0.02). Conclusions: The decrease of AQP2 and the increase of NKCC2 expression in HSS patients seem to be involved with the inability of urinary concentration in these patients. These data show renal tubular abnormalities in HSS patients without manifest clinical disease. (© 2020 John Wiley & Sons Ltd.) |
Databáze: | MEDLINE |
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