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Iran J Kidney Dis ; 16(4): 252-258, 2022 07.
Artículo en Inglés | MEDLINE | ID: mdl-35962640

RESUMEN

INTRODUCTION: The aim of this study was to investigate the expression of aquaporin 1 (AQP-1), AQP-3 and vascular endothelial growth factor A (VEGF-A) in peritoneal tissues of patients without kidney disease, chronic kidney disease at stages 5 (CKD 5) and patients on prolonged peritoneal dialysis with ultrafiltration failure (PDUFF), and elucidate the possible mechanism of peritoneal dialysis ultrafiltration failure. METHODS: Peritoneal specimens were collected from the following patient groups at Xianju People's hospital: CKD 5, PD-UFF and normal control groups. Routine staining and immunohistochemical analyses were performed on samples obtained from the three groups. RESULTS: The expression of AQP-1 and AQP-3 on peritoneal mesothelial cells, peritoneal vessels and in the interstitium was significantly lower in the PD-UFF group than the CKD 5 and control groups (P < .01), while no statistically significant difference was found between the CKD 5 and control groups (P > .05). In contrast, VEGF-A expression was significantly higher in peritoneal mesothelial cells, peritoneal vessels and the interstitium in the PD-UFF group than the CKD 5 and control groups (P < .01). No statistically significant difference was found between the CKD 5 and control groups (P > .05). CONCLUSION: AQP-1 and AQP-3 expression levels decrease in peritoneal mesothelial cells and the vascular interstitium of patients with a prolonged peritoneal dialysis course, while VEGF-A expression gradually increases. The formation of peritoneal neovascularization and the decrease in AQP expression may be primarily associated with peritoneal dialysis ultrafiltration failure.  DOI: 10.52547/ijkd.6928.


Asunto(s)
Fallo Renal Crónico , Diálisis Peritoneal , Acuaporina 1/metabolismo , Acuaporina 3/metabolismo , Humanos , Fallo Renal Crónico/metabolismo , Fallo Renal Crónico/terapia , Diálisis Peritoneal/efectos adversos , Peritoneo/irrigación sanguínea , Peritoneo/metabolismo , Ultrafiltración , Factor A de Crecimiento Endotelial Vascular
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