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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Chronic exposure to hypoxia attenuates renal injury and innate immunity activation in the remnant kidney model

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Author(s):
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Tono Rempel, Lisienny Campoli [1] ; Faustino, Viviane Dias [1] ; Foresto-Neto, Orestes [1] ; Fanelli, Camilla [1] ; Alarcon Arias, Simone Costa [1] ; da Silva Moreira, Gizely Cristina [1] ; Nascimento, Thalita Fabiana [1] ; Avila, Victor Ferreira [1] ; Costa Malheiros, Denise Maria Avancini [1] ; Saraiva Camara, Niels Olsen [1, 2] ; Fujihara, Clarice Kazue [1] ; Zatz, Roberto [1]
Total Authors: 12
Affiliation:
[1] Univ Sao Paulo, Fac Med, Dept Clin Med, Renal Div, Sao Paulo, SP - Brazil
[2] Univ Sao Paulo, Inst Biomed Sci, Lab Transplantat Immunobiol, Sao Paulo, SP - Brazil
Total Affiliations: 2
Document type: Journal article
Source: AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY; v. 317, n. 5, p. F1285-F1292, NOV 2019.
Web of Science Citations: 0
Abstract

Hypoxia is thought to influence the pathogenesis of chronic kidney disease, but direct evidence that prolonged exposure to tissue hypoxia initiates or aggravates chronic kidney disease is lacking. We tested this hypothesis by chronically exposing normal rats and rats with 5/6 nephrectomy (Nx) to hypoxia. In addition, we investigated whether such effect of hypoxia would involve activation of innate immunity. Adult male Munich-Wistar rats underwent Nx (n = 54) or sham surgery (sham; n = 52). Twenty-six sham rats and 26 Nx rats remained in normoxia, whereas 26 sham rats and 28 Nx rats were kept in a normobaric hypoxia chamber (12% O-2) for 8 wk. Hypoxia was confirmed by immunohistochemistry for pimonidazole. Hypoxia was confined to the medullary area in sham + normoxia rats and spread to the cortical area in sham + hypoxia rats, without changing the peritubular capillary density. Exposure to hypoxia promoted no renal injury or elevation of the content of IL-1 beta or Toll-like receptor 4 in sham rats. In Nx, hypoxia also extended to the cortical area without ameliorating the peritubular capillary rarefaction but, unexpectedly, attenuated hypertension, inflammation, innate immunity activation, renal injury, and oxidative stress. The present study, in disagreement with current concepts. shows evidence that hypoxia exerts a renoprotective effect in the Nx model instead of acting as a factor of renal injury. The mechanisms for this unexpected beneficial effect are unclear and may involve NF-kappa B inhibition, amelioration of oxidative stress, and limitation of angiotensin II production by the renal tissue. (AU)

FAPESP's process: 12/10926-5 - Pathogenesis and treatment of chronic kidney disease: role of innate immunity in glomerular, tubular and interstitial injury
Grantee:Roberto Zatz
Support type: Research Projects - Thematic Grants
FAPESP's process: 13/26726-8 - Role of hypoxia in the activation of innate immunity in the progression of chronic kidney disease associated with ablation 5/6 renal model
Grantee:Lisienny Campoli Tono Rempel
Support type: Scholarships in Brazil - Doctorate