Gender Differences in the Acute Kidney Injury to Chronic Kidney Disease Transition.
Ixchel Lima-PosadaCinthya Portas-CortésRosalba Pérez-VillalvaFrancesco FontanaRoxana Rodríguez-RomoRodrigo PrietoAndrea Sánchez-NavarroGuadalupe L Rodríguez-GonzálezGerardo GambaElena ZambranoNorma A BobadillaPublished in: Scientific reports (2017)
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.
Keyphrases
- chronic kidney disease
- acute kidney injury
- oxidative stress
- end stage renal disease
- cardiac surgery
- endothelial cells
- dna damage
- ischemia reperfusion injury
- mental health
- transforming growth factor
- diabetic rats
- diabetic nephropathy
- nitric oxide synthase
- nitric oxide
- double blind
- clinical trial
- anti inflammatory
- risk assessment
- human health
- cell proliferation
- vascular endothelial growth factor
- liver fibrosis
- high glucose
- heat stress
- heat shock protein