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Cyclosporine A suppresses cyclooxygenase-2 expression in the rat kidney
Klaus Höcherl1, Franziska Dreher, Helga Vitzthum
1Institut für Pharmakologie, University of Regensburg, Regensburg, Germany. klaus.hoecherl@chemie.uni-regensburg.de
Abstract:
On the basis of recent evidence that the cyclooxygenase-2 (COX-2) gene promoter contains functional binding sites for the nuclear factor of activated T cells (NFAT) and that COX-2 is expressed in a regulated fashion in the kidney, this study aimed to assess the effect of immunosuppressants on COX-2 expression in the kidney. Therefore, Wistar-Kyoto rats were treated with cyclosporine A (CsA; 15 mg/kg per day) or tacrolimus (5 mg/kg per day) for 7 d each. Both drugs markedly lowered COX-2 expression while COX-1 expression remained unaltered. Furthermore, CsA blunted the increase of renocortical COX-2 expression in response to low salt intake or a combination of low-salt diet with the ACE inhibitor ramipril (10 mg/kg per day), which strongly stimulates renocortical COX-2 expression. At the same time, calcineurin inhibitors moderately enhanced basal as well as stimulated renin secretion and renin gene expression. These findings suggest that inhibition of calcineurin could be a crucial determinant for the regulated expression of COX-2 in the kidney. Inhibition of COX-2 expression may therefore at least in part account for the well-known adverse effects of immunosuppressants in the kidney. Moreover, our data suggest that the stimulation of the renin system by low salt and by ACE inhibitors is not essentially mediated by COX-2 activity.
Insights
Immunosuppressants like cyclosporine A and tacrolimus reduce kidney cyclooxygenase-2 (COX-2) expression. This inhibition may contribute to the adverse effects of these drugs on kidney function.
Area of Science:
- Nephrology
- Immunology
- Molecular Biology
Background:
- Cyclooxygenase-2 (COX-2) is regulated in the kidney.
- Nuclear factor of activated T cells (NFAT) binds to the COX-2 gene promoter.
- Immunosuppressants are known to cause kidney-related adverse effects.
Purpose of the Study:
- To investigate the impact of immunosuppressants on kidney COX-2 expression.
- To determine if calcineurin inhibitors affect COX-2 regulation in the kidney.
Main Methods:
- Wistar-Kyoto rats were treated with cyclosporine A (CsA) or tacrolimus.
- COX-2 and COX-1 expression levels were measured.
- Renocortical COX-2 expression was assessed under conditions of low salt intake and ACE inhibitor treatment.
- Renin secretion and gene expression were evaluated.
Main Results:
- Both CsA and tacrolimus significantly decreased kidney COX-2 expression, while COX-1 remained unchanged.
- CsA inhibited the increase in renocortical COX-2 expression induced by low salt diet and ACE inhibitor (ramipril).
- Calcineurin inhibitors enhanced basal and stimulated renin secretion and renin gene expression.
Conclusions:
- Calcineurin inhibition is a key factor in regulating kidney COX-2 expression.
- Reduced COX-2 expression by immunosuppressants may contribute to their nephrotoxicity.
- The renin system's stimulation by low salt and ACE inhibitors is not solely mediated by COX-2.