Abstract

The effect of 2,3,5-trimethyl-6-(12-hydroxy-5,10-dodecadiynyl)-1,4-benzoquinone (AA-861), a 5-lipoxygenase inhibitor, on Ca2+ mobilization in Madin Darby canine kidney (MDCK) cells has been examined by fluorimetry using fura-2 as a Ca2+ indicator. AA-861 at 10–200 μM increased [Ca2+]i concentration dependently. The signal comprised an initial rise and a sustained phase. Ca2+ removal inhibited the Ca2+ signals by reducing both the initial rise and the sustained phase. In Ca2+-free medium, pretreatment with 50 μM AA-861 abolished the Ca2+ release induced by thapsigargin (1 μM), an endoplasmic reticulum Ca2+ pump inhibitor, and carbonylcyanide m-chlorophenylhydrazone (CCCP; 2 μM), a mitochondrial uncoupler. Pretreatment with CCCP, thapsigargin and gly-phe-β-naphthylamide to deplete the Ca2+ stores in mitochondria, the endoplasmic reticulum, and lysosomes, respectively, only partly inhibited AA-861-induced Ca2+ release. This suggests AA-861 released Ca2+ from multiple internal pools. Addition of 3 mM Ca2+ induced a [Ca2+]i rise after pretreatment with 50 μM AA-861 in Ca2+-free medium. AA-861 (50 μM)-induced internal Ca2+ release was not altered by inhibition of phospholipase C with U73122 (2 μM) but was inhibited by 40% by inhibition of phospholipase A2 with aristolochic acid (40 μM). Collectively, we found that AA-861 increased [Ca2+]i in MDCK cells by releasing Ca2+ from multiple internal stores in a manner independent of the formation of inositol-1,4,5-trisphosphate, followed by Ca2+ entry from external medium.

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