TY - JOUR
T1 - Hippocampal CA1 pyramidal cells of rats have four voltage-dependent calcium conductances
AU - Takahashi, K.
AU - Wakamori, M.
AU - Akaike, N.
N1 - Funding Information:
We thank M. Ohara for helpful comments. This research was supported by Grants-in-Aid to N.A. from The Ministry of Education, Sciencea nd Culture Japan (63480107a nd 63641526)a,n d from the Epilepsy ResearchF oundation.
PY - 1989/9/25
Y1 - 1989/9/25
N2 - In isolated rat hippocampal neurons, we observed 4 voltage- and extracellular Ca2+-dependent conductances; i.e. the T-, N- and L-type Ca2+ currents and tetrodotoxin-sensitive transient Ca2+ current. Intracellular perfusion with F- suppressed irreversibly the L-type Ca2+ current and partially the N-type one. ω-Conotoxin inhibited selectively the L-type Ca2+ current. Amiloride reduced strongly the T-type Ca2+ current without affecting the L-type one. Gd3+, nicardipine, phenytoin and octanol had no specific inhibition on the T-, N- and L-type Ca2+ currents. Thereby, the pharmacological property of mammalian CNS neurons for Ca2+ channel blockers considerably differs from that in the peripheral and cultured cells.
AB - In isolated rat hippocampal neurons, we observed 4 voltage- and extracellular Ca2+-dependent conductances; i.e. the T-, N- and L-type Ca2+ currents and tetrodotoxin-sensitive transient Ca2+ current. Intracellular perfusion with F- suppressed irreversibly the L-type Ca2+ current and partially the N-type one. ω-Conotoxin inhibited selectively the L-type Ca2+ current. Amiloride reduced strongly the T-type Ca2+ current without affecting the L-type one. Gd3+, nicardipine, phenytoin and octanol had no specific inhibition on the T-, N- and L-type Ca2+ currents. Thereby, the pharmacological property of mammalian CNS neurons for Ca2+ channel blockers considerably differs from that in the peripheral and cultured cells.
KW - CA1 pyramidal cell
KW - Calcium channel blocker
KW - Calcium-sensitive current
KW - Concentration-clamp
KW - Intracellular perfusion
KW - Rat hippocampal cell
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U2 - 10.1016/0304-3940(89)90359-5
DO - 10.1016/0304-3940(89)90359-5
M3 - Article
C2 - 2554221
AN - SCOPUS:0024325834
SN - 0304-3940
VL - 104
SP - 229
EP - 234
JO - Neuroscience Letters
JF - Neuroscience Letters
IS - 1-2
ER -