Voltage-gated Ca2+ channels participate in dendritic integration, yet funct
ional properties of Ca2+ channels and mechanisms of their modulation by neu
rotransmitters in dendrites are unknown. Here we report how pharmacological
ly identified Ca2+ channels behave in different neural compartments. Whole-
cell and cell-attached patch-clamp recordings were made on both cell bodies
and electrically isolated dendrites of sympathetic neurons. We found not o
nly that Ca2+ channel populations differentially contribute to somatic and
dendritic currents but also that families of Ca2+ channels display gating p
roperties and neurotransmitter modulation that depend on channel compartmen
talization. By comparison with their somatic counterparts,; dendritic N-typ
e Ca2+ currents were hypersensitive to neurotransmitters and C proteins. Si
ngle-channel analysis showed that dendrites express a unique N-type channel
that has enhanced interaction with G beta gamma. Thus Ca2+ channels in den
drites seem to be specialized elements with unique regulatory mechanisms.