Introduction: To investigate whether in the ciliary epithelium of isolated
porcine ciliary body cyclic 3 ' ,5 ' adenosine monophosphate (cAMP) activat
es transmembrane anionic currents.
Methods: Changes in membrane potential induced either by the adenylcyclase
activator forskolin (10 muM; n = 4) or the stable membrane permeable cAMP a
nalog 8-bromo-adenosine 3 ' ,5 ' -cyclic monophosphothioate (8-br-cAMP; 30
muM; n = 4) were measured with intracellular microelectrodes. The effect of
the drugs were assessed in the absence or in the presence of the non-selec
tive anionic channel/transporter inhibitor diisothiocyanatostilbene-2.2 ' d
isulfonic acid (DIDS; 1 mM; n = 4).
Results: Significant (p<0.001) membrane potential depolarization were induc
ed by both forskolin (11 <plus/minus> 0.3 mV) or 8-br-cAMP (9.3 +/- 0.4mV).
In the presence of DIDS, a significant (p<0.001) inhibition of the depolar
ization evoked by forskolin (0.3 <plus/minus> 1.1 mV) and 8-bromo-cAMP (0.7
+/- 0.2 mV) was observed.
Conclusions: In the ciliary epithelium of isolated porcine ciliary body cAM
P induces membrane potential depolarization through a process that could in
volve anionic channels.