2002
DOI: 10.1097/00007890-200209270-00016
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Prevention of chronic rejection by pravastatin in a rat kidney transplant model.

Abstract: This study demonstrates the ability of pravastatin to inhibit chronic rejection in rat renal allografts. Pravastatin's pleiotropic effects of reducing intragraft inflammatory cytokines, inhibiting immune cell infiltration, and causing up-regulation of the antiapoptotic gene Bag-1 suggest that its ability to prevent transplant chronic rejection may be multifactorial.

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Cited by 22 publications
(11 citation statements)
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“…Anti-inflammatory effects may be greater with statin therapy as demonstrated in a recent comparison of C-reactive protein reductions versus eztimibe (20). Lastly, statins may reduce chronic allograft nephropathy (21) and due to mild immunosuppression provided by statin agents, acute rejection rates maybe lowered (22). No adverse events were reported by the patients nor discerned on laboratory measurements (liver functions, serum creatinine).…”
Section: Discussionmentioning
confidence: 91%
“…Anti-inflammatory effects may be greater with statin therapy as demonstrated in a recent comparison of C-reactive protein reductions versus eztimibe (20). Lastly, statins may reduce chronic allograft nephropathy (21) and due to mild immunosuppression provided by statin agents, acute rejection rates maybe lowered (22). No adverse events were reported by the patients nor discerned on laboratory measurements (liver functions, serum creatinine).…”
Section: Discussionmentioning
confidence: 91%
“…Moreover, the functions of statins also extend to immunomodulation, as shown by their inhibition of the expression of class II major histocompatibility antigens and of natural killer cell activity (44). Indeed, experimental and clinical studies in cardiac and renal-transplant recipients demonstrate that administration of statins successfully decreases acute or chronic rejection episodes and improves graft survival (45)(46)(47). Thus, combined treatment of LSRT plus PRVT may provide additional renoprotection not only for chronic CsA-induced nephropathy but also for rejection episodes in transplant recipients receiving CsA.…”
Section: Discussionmentioning
confidence: 99%
“…These actions lead to tubule-interstitial fibrosis and arteriolopathy [5][6][7]. It has been demonstrated by several groups in different experimental models that blocking some pathways of this cascade can actually limit CsA nephrotoxicity [8][9][10][11][12].…”
Section: Introductionmentioning
confidence: 99%