AI Article Synopsis

  • Osteopontin (OPN) levels are elevated in the kidneys of rats with hyperoxaluria and calcium oxalate kidney stones, prompting research on the impact of reducing OPN.
  • The study involved four groups of rats, including a control group and groups treated with ethylene glycol (EG) and OPN siRNA to observe the effects on calcium oxalate crystal formation.
  • Results showed that reducing OPN expression through siRNA led to lower crystal deposition, indicating that targeting OPN could be a potential strategy to decrease kidney stone formation.

Article Abstract

Osteopontin (OPN) expression is increased in kidneys of rats with ethylene glycol (EG) induced hyperoxaluria and calcium oxalate (CaOx) nephrolithiasis. The aim of this study is to clarify the effect of OPN knockdown by in vivo transfection of OPN siRNA on deposition of CaOx crystals in the kidneys. Hyperoxaluria was induced in 6-week-old male Sprague-Dawley rats by administering 1.5% EG in drinking water for 2 weeks. Four groups of six rats each were studied: Group A, untreated animals (tap water); Group B, administering 1.5% EG; Group C, 1.5% EG with in vivo transfection of OPN siRNA; Group D, 1.5% EG with in vivo transfection of negative control siRNA. OPN siRNA transfections were performed on day 1 and 8 by renal sub-capsular injection. Rats were killed at day 15 and kidneys were removed. Extent of crystal deposition was determined by measuring renal calcium concentrations and counting renal crystal deposits. OPN siRNA transfection resulted in significant reduction in expression of OPN mRNA as well as protein in group C compared to group B. Reduction in OPN expression was associated with significant decrease in crystal deposition in group C compared to group B. Specific suppression of OPN mRNA expression in kidneys of hyperoxaluric rats leads to a decrease in OPN production and simultaneously inhibits renal crystal deposition.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979578PMC
http://dx.doi.org/10.1007/s00240-014-0649-0DOI Listing

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