Maurice N, Tkatch T, Meisler M, Sprunger L K, Surmeier D J
Department of Physiology/Institute for Neuroscience, Northwestern University Medical School, Chicago, Illinois 60611, USA.
J Neurosci. 2001 Apr 1;21(7):2268-77. doi: 10.1523/JNEUROSCI.21-07-02268.2001.
Dopamine (DA) is a well established modulator of prefrontal cortex (PFC) function, yet the cellular mechanisms by which DA exerts its effects in this region are controversial. A major point of contention is the consequence of D(1) DA receptor activation. Several studies have argued that D(1) receptors enhance the excitability of PFC pyramidal neurons by augmenting voltage-dependent Na(+) currents, particularly persistent Na(+) currents. However, this conjecture is based on indirect evidence. To provide a direct test of this hypothesis, we combined voltage-clamp studies of acutely isolated layer V-VI prefrontal pyramidal neurons with single-cell RT-PCR profiling. Contrary to prediction, the activation of D(1) or D(5) DA receptors consistently suppressed rapidly inactivating Na(+) currents in identified corticostriatal pyramidal neurons. This modulation was attenuated by a D(1)/D(5) receptor antagonist, mimicked by a cAMP analog, and blocked by a protein kinase A (PKA) inhibitor. In the same cells the persistent component of the Na(+) current was unaffected by D(1)/D(5) receptor activation-suggesting that rapidly inactivating and persistent Na(+) currents arise in part from different channels. Single-cell RT-PCR profiling showed that pyramidal neurons coexpressed three alpha-subunit mRNAs (Nav1.1, 1.2, and 1.6) that code for the Na(+) channel pore. In neurons from Nav1.6 null mice the persistent Na(+) currents were significantly smaller than in wild-type neurons. Moreover, the residual persistent currents in these mutant neurons-which are attributable to Nav1.1/1.2 channels-were reduced significantly by PKA activation. These results argue that D(1)/D(5) DA receptor activation reduces the rapidly inactivating component of Na(+) current in PFC pyramidal neurons arising from Nav1.1/1.2 Na(+) channels but does not modulate effectively the persistent component of the Na(+) current that is attributable to Nav1.6 Na(+) channels.
多巴胺(DA)是一种已被充分证实的前额叶皮质(PFC)功能调节剂,然而DA在该区域发挥作用的细胞机制仍存在争议。一个主要的争议点是D(1) DA受体激活的后果。多项研究认为,D(1)受体通过增强电压依赖性Na(+)电流,特别是持续性Na(+)电流,来提高PFC锥体神经元的兴奋性。然而,这一推测是基于间接证据。为了直接验证这一假设,我们将急性分离的V-VI层前额叶锥体神经元的电压钳研究与单细胞RT-PCR分析相结合。与预测相反,D(1)或D(5) DA受体的激活持续快速抑制已鉴定的皮质纹状体锥体神经元中快速失活的Na(+)电流。这种调节作用被D(1)/D(5)受体拮抗剂减弱,被cAMP类似物模拟,并被蛋白激酶A(PKA)抑制剂阻断。在同一细胞中,Na(+)电流的持续性成分不受D(1)/D(5)受体激活的影响,这表明快速失活和持续性Na(+)电流部分源自不同的通道。单细胞RT-PCR分析表明,锥体神经元共表达三种编码Na(+)通道孔的α亚基mRNA(Nav1.1、1.2和1.6)。在来自Nav1.6基因敲除小鼠的神经元中,持续性Na(+)电流明显小于野生型神经元。此外,这些突变神经元中归因于Nav1.1/1.2通道的残余持续性电流被PKA激活显著降低。这些结果表明,D(1)/D(5) DA受体激活减少了PFC锥体神经元中由Nav1.1/1.2 Na(+)通道产生的Na(+)电流的快速失活成分,但没有有效调节归因于Nav1.6 Na(+)通道的Na(+)电流的持续性成分。