Modulation of distal calcium electrogenesis by neuropeptide Y1 receptors inhibits neocortical long-term depression
Faculty Advisor
Date
2013
Keywords
neuropeptide Y, hyperpolarization, long-term depression (neuronal)
Abstract (summary)
In layer 5 neocortical pyramidal neurons, backpropagating action potentials (bAPs) firing at rates above a critical frequency (CF) induce supralinear Ca2+ influx and regenerative potentials in apical dendrites. Paired temporally with an EPSP, this Ca2+ influx can result in synaptic plasticity. We studied the actions of neuropeptide Y (NPY), an abundant neocortical neuropeptide, on Ca2+ influx in layer 5 pyramidal neurons of somatosensory neocortex in Sprague Dawley and Wistar rats, using a combination of somatic and dendritic intracellular recordings and simultaneous Ca2+ imaging. Ca2+ influx induced by trains of bAPs above a neuron's CF was inhibited by NPY, acting only at the distal dendrite, via Y1 receptors. NPY does not affect evoked synaptic glutamate release, paired synaptic facilitation, or synaptic rundown in longer trains. Extracellular Cs+ did not prevent NPY's postsynaptic effects, suggesting it does not act via either G-protein-activated inwardly rectifying K+ conductance (GIRK) or hyperpolarization-activated, cyclic nucleotide-gated channels. NPY application suppresses the induction of the long-term depression (LTD) normally caused by pairing 100 EPSPs with bursts of 2 bAPs evoked at a supracritical frequency. These findings suggest that distal dendritic Ca2+ influx is necessary for LTD induction, and selective inhibition of this distal dendritic Ca2+ influx by NPY can thus regulate synaptic plasticity in layer 5 pyramidal neurons.
Publication Information
Hamilton, T., Xiapelli, S., Larkum, M., & Colmers, W. (2013). Modulation of distal calcium electrogenesis by neuropeptide Y1 receptors inhibits neocortical long-term depression. Journal of Neuroscience, 33(27): 11184-11193; doi: 10.1523/JNEUROSCI.5595-12.2013
Notes
Item Type
Article
Language
English
Rights
Attribution (CC BY)
