The mechanisms involved in 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid
(DIDS)- and 4,4'-dibenzamidostilbene-2,2'-disulfonic acid (DBDS)-modificat
ion of sheep cardiac ryanodine receptor (RyR) channel function have been in
vestigated. DIDS (50-500 mu M) exerts at least three effects on single chan
nel function. With Ca2+ as the permeant ion, DIDS increases both channel op
en probability (P-o) and single channel conductance in a similar manner to
the effects observed with suramin. Both effects occur immediately and are f
ully reversible. Similar effects were observed with DBDS (10 mu M-2 mM), a
compound with the 4,4'-NCS groups of DIDS replaced with NHCOC6H5. DIDS (500
mu M) also caused irreversible modification to the fully open channel leve
l in 74% of the channels. This effect was not observed with suramin or DBDS
(10 mu M-1 mM). Competition studies with DBDS and suramin coupled with the
close similarities in the effects of DIDS, DBDS and suramin on gating and
conduction suggest that these ligands may all bind to the same sites on RyR
. The DIDS-induced irreversible modification to the fully open state may re
sult from the binding of the isothiocyanate groups to positively charged am
ino acids at or near the suramin binding sites although it is possible that
this modification is unrelated to its other effects on channel function.