Activity-dependent serotonergic excitation of callosal projection neurons in the mouse prefrontal cortex

被引:24
|
作者
Stephens, Emily K. [1 ,2 ]
Avesar, Daniel [1 ,2 ]
Gulledge, Allan T. [1 ,2 ]
机构
[1] Geisel Sch Med Dartmouth, Dept Physiol & Neurobiol, Lebanon, NH USA
[2] Dartmouth Coll, Program Expt & Mol Med, Hanover, NH 03755 USA
关键词
serotonin; 5-HT2A receptor; 5-HT1A receptor; prefrontal cortex; executive function; pyramidal neuron; mouse; REACTION-TIME-TASK; 5-HT2C RECEPTOR ANTAGONISTS; DORSAL RAPHE NUCLEUS; PYRAMIDAL NEURONS; IN-VIVO; HETEROLOGOUS DESENSITIZATION; SEROTONIN(2A) RECEPTORS; GABAERGIC NEURONS; CHANNELS MEDIATE; 2A RECEPTORS;
D O I
10.3389/fncir.2014.00097
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Layer 5 pyramidal neurons (L5PNs) in the mouse prefrontal cortex respond to serotonin (5-HT) according to their long-distance axonal projections; 5-HT1A (1A) receptors mediate inhibitory responses in corticopontine (CPn) L5PNs, while 5-HT2A (2A) receptors can enhance action potential (AP) output in callosal/commissural (COM) L5PNs, either directly (in "COM-excited" neurons), or following brief 1A-mediated inhibition (in "COM-biphasic" neurons). Here we compare the impact of 5-HT on the excitability of CPn and COM L5PNs experiencing variable excitatory drive produced by current injection (DC current or simulated synaptic current) or with exogenous glutamate. 5-HT delivered at resting membrane potentials, or paired with subthreshold depolarizing input, hyperpolarized CPn and COM-biphasic L5PNs and failed to promote AP generation in COM-excited L5PNs. Conversely, when paired with suprathreshold excitatory drive generating multiple APs, 5-HT suppressed AP output in CPn L5PNs, enhanced AP generation in COM-excited L5PNs, and generated variable responses in COM-biphasic L5PNs. While COM-excited neurons failed to respond to 5-HT in the presence of a 2A receptor antagonist, 32% of CPn neurons exhibited 2A-dependent excitation following blockade of 1A receptors. The presence of pharmacologically revealed 2A receptors in CPn L5PNs was correlated with the duration of 1A-mediated inhibition, yet biphasic excitatory responses to 5-HT were never observed, even when 5-HT was paired with strong excitatory drive. Our results suggest that 2A receptors selectively amplify the output of COM L5PNs experiencing suprathreshold excitatory drive, while shaping the duration of 1A-mediated inhibition in a subset of CPn L5PNs. Activity-dependent serotonergic excitation of COM L5PNs, combined with 1A-mediated inhibition of CPn and COM-biphasic L5PNs, may facilitate executive function by focusing network activity within cortical circuits subserving the most appropriate behavioral output.
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页数:17
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