Carboplatin elicits minor side effects with respect to its first generation analogue cisplatin. Nevertheless, a dose-dependent nephrotoxicity of the drug has been reported to occur both in patients and in rats and a possible pathogenic role have been attributed to oxidative stress. We have studied the effect of carboplatin administration on the thiol/disulfide balance, on other biomarkers of oxidative stress and on antioxidant enzymes in the isolated perfused rat kidney. A 5-500 μM carboplatin dose range did not alter renal function but significantly decreased levels of cysteine, glutathione and exposed protein sulfhydryl groups. Only a minimal increment in disulfides was observed, whereas malonyldialdehyde and protein carbonyls did not increase significantly. Among the antioxidant enzymes studied, only thioltransferase was inhibited by the treatment. Our data suggest that a minimal oxidative stress is present under our experimental conditions, thus indicating that platinum-based drugs do not produce significant amount of reactive oxygen species.

Giustarini, D., Dalle Donne, I., Paccagnini, E., Milzani, A., Rossi, R. (2009). Carboplatin-induced alteration of the thiol homeostasis in the isolated perfused rat kidney. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 488(1), 83-89 [10.1016/j.abb.2009.06.007].

Carboplatin-induced alteration of the thiol homeostasis in the isolated perfused rat kidney

Giustarini, D.
;
Paccagnini, E.;Rossi, Ranieri
2009-01-01

Abstract

Carboplatin elicits minor side effects with respect to its first generation analogue cisplatin. Nevertheless, a dose-dependent nephrotoxicity of the drug has been reported to occur both in patients and in rats and a possible pathogenic role have been attributed to oxidative stress. We have studied the effect of carboplatin administration on the thiol/disulfide balance, on other biomarkers of oxidative stress and on antioxidant enzymes in the isolated perfused rat kidney. A 5-500 μM carboplatin dose range did not alter renal function but significantly decreased levels of cysteine, glutathione and exposed protein sulfhydryl groups. Only a minimal increment in disulfides was observed, whereas malonyldialdehyde and protein carbonyls did not increase significantly. Among the antioxidant enzymes studied, only thioltransferase was inhibited by the treatment. Our data suggest that a minimal oxidative stress is present under our experimental conditions, thus indicating that platinum-based drugs do not produce significant amount of reactive oxygen species.
2009
Giustarini, D., Dalle Donne, I., Paccagnini, E., Milzani, A., Rossi, R. (2009). Carboplatin-induced alteration of the thiol homeostasis in the isolated perfused rat kidney. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 488(1), 83-89 [10.1016/j.abb.2009.06.007].
File in questo prodotto:
File Dimensione Formato  
2009 Giustarini ABB.pdf

non disponibili

Descrizione: Author's copy
Tipologia: Post-print
Licenza: NON PUBBLICO - Accesso privato/ristretto
Dimensione 469.33 kB
Formato Adobe PDF
469.33 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
Carboplatin-induced alteration of the thiol homeostasis in the isolated perfused rat kidney.pdf

non disponibili

Descrizione: articolo definitivo
Tipologia: PDF editoriale
Licenza: NON PUBBLICO - Accesso privato/ristretto
Dimensione 297.94 kB
Formato Adobe PDF
297.94 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/411682