Probenecid, a gout remedy, inhibits pannexin 1 channels
Author(s) -
William R. Silverman,
Silviu Locovei,
Gerhard Dahl
Publication year - 2008
Publication title -
ajp cell physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.432
H-Index - 181
eISSN - 1522-1563
pISSN - 0363-6143
DOI - 10.1152/ajpcell.00227.2008
Subject(s) - probenecid , pannexin , chemistry , transporter , sulfinpyrazone , gout , organic anion transporter 1 , pharmacology , uric acid , biochemistry , connexin , gap junction , intracellular , medicine , aspirin , gene
Probenecid is a well-established drug for the treatment of gout and is thought to act on an organic anion transporter, thereby affecting uric acid excretion in the kidney by blocking urate reuptake. Probenecid also has been shown to affect ATP release, leading to the suggestion that ATP release involves an organic anion transporter. Other pharmacological evidence and the observation of dye uptake, however, suggest that the nonvesicular release of ATP is mediated by large membrane channels, with pannexin 1 being a prominent candidate. In the present study we show that probenecid inhibited currents mediated by pannexin 1 channels in the same concentration range as observed for inhibition of transport processes. Probenecid did not affect channels formed by connexins. Thus probenecid allows for discrimination between channels formed by connexins and pannexins.
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