Login / Signup

Paraoxonase-1 Regulation of Renal Inflammation and Fibrosis in Chronic Kidney Disease.

Fatimah K KhalafChrysan J MohammedPrabhatchandra DubeJacob A ConnollyApurva LadUsman M AshrafJoshua D BreidenbachRobin C SuAndrew L KleinhenzDeepak MalhotraAmira F GoharaSteven T HallerDavid J Kennedy
Published in: Antioxidants (Basel, Switzerland) (2022)
Papraoxonase-1 (PON1) is a hydrolytic lactonase enzyme that is synthesized in the liver and circulates attached to high-density lipoproteins (HDL). Clinical studies have demonstrated an association between diminished PON-1 and the progression of chronic kidney disease (CKD). However, whether decreased PON-1 is mechanistically linked to renal injury is unknown. We tested the hypothesis that the absence of PON-1 is mechanistically linked to the progression of renal inflammation and injury in CKD. Experiments were performed on control Dahl salt-sensitive rats (SS Mcwi , hereafter designated SS rats) and Pon1 knock-out rats (designated SS-Pon1 em1Mcwi , hereafter designated SS-PON-1 KO rats) generated by injecting a CRISPR targeting the sequence into SS Mcwi rat embryos. The resulting mutation is a 7 bp frameshift insertion in exon 4 of the PON-1 gene. First, to examine the renal protective role of PON-1 in settings of CKD, ten-week-old, age-matched male rats were maintained on a high-salt diet (8% NaCl) for up to 5 weeks to initiate the salt-sensitive hypertensive renal disease characteristic of this model. We found that SS-PON-1 KO rats demonstrated several hallmarks of increased renal injury vs. SS rats including increased renal fibrosis, sclerosis, and tubular injury. SS-PON-1 KO also demonstrated increased recruitment of immune cells in the renal interstitium, as well as increased expression of inflammatory genes compared to SS rats (all p < 0.05). SS-PON-1 KO rats also showed a significant ( p < 0.05) decline in renal function and increased renal oxidative stress compared to SS rats, despite no differences in blood pressure between the two groups. These findings suggest a new role for PON-1 in regulating renal inflammation and fibrosis in the setting of chronic renal disease independent of blood pressure.
Keyphrases
  • oxidative stress
  • chronic kidney disease
  • blood pressure
  • genome wide
  • poor prognosis
  • transcription factor
  • metabolic syndrome
  • weight loss
  • heart rate
  • binding protein
  • gestational age