Jp. Winpenny et al., SOME EFFECTS OF SHORT-CHAIN PHOSPHOLIPIDS AND N-ALKANES ON A TRANSIENT POTASSIUM CURRENT (I-A) IN IDENTIFIED HELIX NEURONS, The Journal of membrane biology, 137(1), 1994, pp. 79-90
Many effects of short-chain phospholipids and n-alkanes on the squid a
xon sodium current (I-Na) are consistent with mechanisms involving cha
nges in membrane thickness. Here, we suggest that the actions of short
-chain phospholipids on an A-type potassium current (I-A) in two-micro
electrode voltage clamped Helix D1 and F77 neurons are incompatible wi
th such simple mechanisms. Diheptanoyl phosphatidylcholine (diC(7)PC,
0.2 and 0.3 mM) caused substantial (58 and 79%), and in some cases par
tially reversible, increases in I-A amplitude. These were correlated w
ith hyperpolarizing shifts of up to -7 mV in the voltage dependence of
current activation. The voltage dependence of steady-state inactivati
on was also moved in the hyperpolarizing direction. These effects are
the opposite of those described for squid I-Na 0.5 Saturated n-pentane
and saturated n-hexane caused significant (-3 and -6 mV) hyperpolariz
ing shifts in the voltage dependence of I-A inactivation, qualitativel
y consistent with their effects on squid I-Na, while the voltage depen
dence of activation was moved slightly to the left or unchanged. Hydro
carbons had variable effects on peak current amplitude, although satur
ated n-pentane produced a clear suppression. DiC(7)PC caused a 25% inc
rease in the time constant of macroscopic I-A inactivation (tau(b)) bu
t 0.5 saturated n-pentane and saturated n-hexane reduced tau(b) by 40%
. The effects of these agents on current-clamped cells were broadly co
nsistent with their opposing actions on tau(b)-phospholipids tended to
reduce excitability and n-alkanes tended to increase it. Possible mec
hanisms of I-A perturbation are discussed.