The unsolved cyclosporine-induced kidney injury: is paricalcitol a feasible new renoprotective option?
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 20508662.
- Also identified by DOI 10.1038/ki.2010.93.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
The management of cyclosporine A (CsA)-induced nephrotoxicity remains one of the main challenges in kidney transplantation. The animal study by Park et al. proposes that paricalcitol, a vitamin D analog with renoprotective actions reported in other conditions, attenuates CsA-induced kidney injury via the suppression of inflammatory, fibrotic, and apoptotic factors. Before paricalcitol can be considered a feasible new therapeutic option for post-transplantation nephropathy, these interesting data require further studies assessing other mechanisms of CsA-induced nephrotoxicity.
Medical subject headings
- Cyclosporine
- Ergocalciferols
- Kidney Diseases