摘要

Some of the excitatory effects of norepinephrine on central neurons are mediated by alpha-1 (alpha 1) adrenoceptors. These receptors are coupled to the Gq family of G proteins, and hence stimulate hydrolysis of the membrane phospholipid phosphatidylinositol-4,5-bisphosphate. Other receptors of this type can excite neurons by inhibiting the subthreshold voltage-gated potassium M-current. We tested this possibility using rat sympathetic neurons transformed to express alpha 1a receptors. The alpha 1 agonist phenylephrine strongly inhibited the M-current recorded under voltage-clamp by 72 +/- A 11 % (n = 4) and in an unclamped neuron dramatically increased the number of action potentials produced by a 2 s depolarizing current step from 2 to 40, without effect on control neurons devoid of alpha 1 receptors. We suggest that this might be a potential cause of the increased excitability produced by norepinephrine in some central neurons.

  • 出版日期2013-1