Gender Differences in the Acute Kidney Injury to Chronic Kidney Disease Transition

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作者
Ixchel Lima-Posada
Cinthya Portas-Cortés
Rosalba Pérez-Villalva
Francesco Fontana
Roxana Rodríguez-Romo
Rodrigo Prieto
Andrea Sánchez-Navarro
Guadalupe L. Rodríguez-González
Gerardo Gamba
Elena Zambrano
Norma A. Bobadilla
机构
[1] Universidad Nacional Autónoma de México,Molecular Physiology Unit, Instituto de Investigaciones Biomédicas
[2] Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán,Departament of Nephrology
[3] Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán,Departament of Reproductive Biology
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This study evaluated if there is a sexual dimorphism in the acute kidney injury (AKI) to chronic kidney disease (CKD) transition and the time-course of the potential mechanisms involved in the dimorphic response. Female and male rats were divided into sham-operated or underwent 45-min renal ischemia (F + IR, and M + IR). All groups were studied at 24-h and 1, 2, 3, or 4-months post-ischemia. Additionally, oophorectomized rats were divided into sham or IR groups. After 24-h, AKI extent was simllar in females and males, but female rats exhibited less oxidative stress and increased renal GSH content. After 4-months and despite similar AKI, the M + IR group developed CKD characterized by proteinuria, tubulointerstitial fibrosis, glomerular hypertrophy, increased oxidative stress and a reduction in HIF1α and VEGF from the 1st-month and persisting throughout the time-course studied. Interestingly, the F + IR group did not develop CKD due to lesser oxidative stress and increased eNOS, TGFβ and HIF1α mRNA levels from the 1st-month after IR. Whereas, oophorectomized rats did develop CKD. We found a sexual dimorphic response in the AKI to CKD transition. Early antioxidant defense and higher TGFβ, HIF1α and eNOS were among the renoprotective mechanisms that the F + IR group demonstrated.
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