I. Niespodziany et al., Properties of T-type calcium current in enkephalinergic neurones in guinea-pig hypothalamic slices, PFLUG ARCH, 437(6), 1999, pp. 871-880
The guinea-pig hypothalamic magnocellular dorsal nucleus (mdn) exclusively
contains enkephalinergic neurones providing inputs to the septum. This nucl
eus is believed to play a role in hippocampo-septo-hypothalamic relationshi
ps. mdn neurones display prominent low-threshold Ca2+ spikes, which differ
in their propensity to trigger either a burst of Na+ spikes or a single spi
ke. In the present study, whole-cell voltage-clamp experiments were carried
out on thick slices at 34 degrees C to characterize the pharmacological an
d physical properties of the transient Ca2+ current (I-T) underlying the lo
w-threshold spikes. Recorded cells were dye-labelled and identified as belo
nging to the mdn. In bursting and nonbursting neurones, I,was reduced by am
iloride (1 mu M) and octanol (1 mM), and during replacement of Ca2+ by Ba2. The Ca2+ channel blocker mibefradil (10 mu M) had only a slight blocking
action. Nifedipine (100 mu M) and flunarizine (1 mu M) had no effect. I-T a
ctivated between -80 mV and -50 mV and the mean peak current was 1050 pA. S
teady-state activation and inactivation curves were fitted by a Boltzmann e
quation. The half-activation voltage was -70 mV, slope factor=3.6, and half
-inactivation voltage was about -80 mV, slope factor=4.5. Time-to-peak and
time constant of inactivation were voltage dependent. Recovery from activat
ion occurred within 500 ms. When compared with results on other I-T, the pr
esent data show that the current possesses distinct pharmacological and phy
sical properties. Nevertheless, all investigated cells displayed a homogeno
us profile of I-T, suggesting that the differences in spike pattern between
mdn neurones are not due to different populations of Ca2+ channels.