Na+/K+-ATPase is in charge ofmaintaining the ionic and osmotic intracellular balance by using ATP as an energy source to drive excessNa+ions out of the cell in exchange for K+ions.We exploredwhether three representative cytotoxic gold(III) compoundsmight interferewithNa+/K+-ATPase and cause its inhibition at pharmacologically relevant concentrations. The tested complexes were [Au(bipy)(OH)2][PF6] (bipy= 2,2′-bipyridine), [Au(pydmb- H)(CH3COO)2] (pydmb-H = deprotonated 6-(1,1-dimethylbenzyl)-pyridine), and [Au(bipydmb-H)(OH)][PF6] (bipydmb-H = deprotonated 6-(1,1-dimethylbenzyl)-2,2′-bipyridine). We found that all of them caused a pronounced and similar inhibition of Na+/K+-ATPase activity. Inhibition was found to be non-competitive and reversible. Remarkably, treatment with cysteine resulted in reversal or prevention of Na+/K+-ATPase inhibition. It is very likely that the described effects may contribute to the overall cytotoxic profile of these gold complexes
Inhibition of Na+/K+-ATPase and cytotoxicity of a few selected gold(III) complexes / Voin Petrovic; Sandra Petrovic; Gordana Joksic; Jasmina Savic; Mirjana Colovic; Maria A Cinellu; Lara Massai; Luigi Messori; Vesna Vasic. - In: JOURNAL OF INORGANIC BIOCHEMISTRY. - ISSN 0162-0134. - STAMPA. - 140:(2014), pp. 228-235. [10.1016/j.jinorgbio.2014.07.015]
Inhibition of Na+/K+-ATPase and cytotoxicity of a few selected gold(III) complexes
MASSAI, LARA;MESSORI, LUIGI;
2014
Abstract
Na+/K+-ATPase is in charge ofmaintaining the ionic and osmotic intracellular balance by using ATP as an energy source to drive excessNa+ions out of the cell in exchange for K+ions.We exploredwhether three representative cytotoxic gold(III) compoundsmight interferewithNa+/K+-ATPase and cause its inhibition at pharmacologically relevant concentrations. The tested complexes were [Au(bipy)(OH)2][PF6] (bipy= 2,2′-bipyridine), [Au(pydmb- H)(CH3COO)2] (pydmb-H = deprotonated 6-(1,1-dimethylbenzyl)-pyridine), and [Au(bipydmb-H)(OH)][PF6] (bipydmb-H = deprotonated 6-(1,1-dimethylbenzyl)-2,2′-bipyridine). We found that all of them caused a pronounced and similar inhibition of Na+/K+-ATPase activity. Inhibition was found to be non-competitive and reversible. Remarkably, treatment with cysteine resulted in reversal or prevention of Na+/K+-ATPase inhibition. It is very likely that the described effects may contribute to the overall cytotoxic profile of these gold complexesI documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.