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Journal of Renin-Angiotensin-Aldosterone System
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Review: Potential protective effects of telmisartan on renal function deterioration

Andrea Remuzzi

Mario Negri Institute for Pharmacological Research, Via Gavazzeni, 11 24125 Bergamo, Italy, aremuzzi{at}marionegri.it

Giuseppe Remuzzi

Mario Negri Institute for Pharmacological Research, Via Gavazzeni, 11 24125 Bergamo, Italy, Unit of Nephrology and Dialysis, Azienda Ospedaliera, Ospedali Riuniti di Bergamo, Largo Barozzi, 1 24128 Bergamo, Italy

Experimental and clinical evidence is now available that antagonism of angiotensin II (Ang II) with both angiotensin-converting enzyme inhibitors and Ang II receptor antagonists (AIIAs) is effective in slowing the rate of renal functional loss in patients affected by proteinuric kidney diseases.Among AIIAs, telmisartan has been shown to be characterised by a potent and long lasting antihypertensive effect that may be associated with another specific effect of this molecule, the partial agonism of the peroxisome-activated receptor-gamma.Although this action has also been observed with other AIIAs, telmisartan seems to exert a more effective and specific action as in such a way to influence beneficially adipocyte metabolism, diabetes onset and insulin resistance. Recently, we have demonstrated, at the experimental and clinical level, that sustained blockade of Ang II biological activity with this class of compounds can potentially reduce the progression of renal dysfunction and in some circumstances induce the regression of renal functional and structural changes. In this review we analyse available experimental and clinical data that suggest that blocking Ang II with telmisartan may effectively ameliorate renal dysfunction in patients affected by the now frequently observed condition termed metabolic syndrome.

Key Words: angiotensin II peroxisome-activated receptor-gamma • angiotensin receptor antagonists • angiotensin-converting enzyme inhibitors • metabolic syndrome • insulin resistance renal diseases • renoprotection

Journal of Renin-Angiotensin-Aldosterone System, Vol. 7, No. 4, 185-191 (2006)
DOI: 10.3317/jraas.2006.036


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