1. Zinc-protoporphyrin-IX (ZnPP-IX) is an inhibitor of the enzyme heme
-oxygenase-2 (HO-2) and consequently has been used to examine the role
of carbon monoxide production in neural tissues. We have measured vol
tage-gated Ca current in AtT-20 pituitary cells using the whole-cell p
atch-clamp technique and have assessed the effects of extracellularly
applied ZnPP-IX and related compounds. 2. Ca currents evoked by depola
rizing steps from a holding potential of -90 mV were of the high-thres
hold, slowly inactivating type. Fifty-six percent of this current was
blocked by 10 muM nifedipine and 16% by 3 muM omega-conotoxin with the
remainder resistant to both drugs in combination, suggesting that the
total Ca current was a mixture of L, N, and possibly P-type conductan
ces. 3. Bath application of ZnPP-IX resulted in an irreversible, dose-
dependent attenuation of Ca current. Five micromolar ZnPP-IX produced
a 62% reduction of peak current amplitude with no shift in the current
-voltage relation, 0.5 muM produced a 19% reduction, and 0.05 muM prod
uced a variable response, either a small transient attenuation or pote
ntiation. 4. The attenuation of Ca current by 5 muM ZnPP-IX could be n
early completely blocked by co-application of superoxide dismutase in
the bath (90 U/ml) but not by addition of an inhibitor of cGMP-depende
nt protein kinase to the internal saline (KT5823, 1 muM). 5. Other inh
ibitors of heme-oxygenase with similar potency such as tin-protoporphy
rin-IX (Sn-PP-IX) and Zn-deuteroporphyrin-bis-glycol (ZnBG) did not at
tenuate Ca current when applied at 5 muM. Rather, these compounds prod
uced a small, transient and variable potentiation. A similar effect wa
s also seen with 5 muM copper-protoporphyrin-IX (CuPP-IX), a compound
which may not inhibit heme oxygenase. KT-5823 did not block the small,
transient potentiation produced by 5 muM CuPP-IX. 6. Protoporphyrin-I
X (PP-IX) is known to activate soluble guanylyl cyclase. Application o
f 5 muM PP-IX produced a large (55%) transient potentiation of Ca curr
ent with no shift in the current-voltage relation. This potentiation w
as nearly completely blocked by KT-5823. 7. These results indicate tha
t ZnPP-IX attenuates voltage-gated Ca current, and suggest that it doe
s so through a mechanism other than inhibition of HO-2 or soluble guan
ylyl cyclase, possibly one related to the production of free radicals.
Furthermore, PP-IX potentiates voltage-gated Ca current through a mec
hanism that is likely to involve activation of soluble guanylyl cyclas
e and the consequent activation of cyclic guanosine 3,5'-monophosphate
(cGMP)-dependent protein kinase.