Prolonged deficits in parvalbumin neuron stimulation-evoked network activity despite recovery of dendritic structure and excitability in the somatosensory cortex following global ischemia in mice

• Published in: The Journal of neuroscience Vol. 34; no. 45; pp. 14890 - 14900
• Main Authors: Xie, Yicheng, Chen, Shangbin, Wu, Yujin, Murphy, Timothy H
• Format: Journal Article
• Language: English
• Published: United States Society for Neuroscience 05.11.2014
• Subjects: Action Potentials; Animals; Cerebral Infarction - physiopathology; Channelrhodopsins; Dendrites - pathology; Dendrites - physiology; GABAergic Neurons - metabolism; GABAergic Neurons - pathology; GABAergic Neurons - physiology; Inhibitory Postsynaptic Potentials; Interneurons - metabolism; Interneurons - pathology; Interneurons - physiology; Mice; Mice, Inbred C57BL; Optogenetics; Parvalbumins - genetics; Parvalbumins - metabolism; Somatosensory Cortex - pathology; Somatosensory Cortex - physiopathology; two-photon imaging; parvalbumin neuron; reperfusion; stroke; inhibitory synaptic transmission; optogenetics
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/jneurosci.1775-14.2014

Relatively few studies have examined plasticity of inhibitory neuronal networks following stroke in vivo, primarily due to the inability to selectively monitor inhibition. We assessed the structure of parvalbumin (PV) interneurons during a 5 min period of global ischemia and reperfusion in mice, which mimicked cerebral ischemia during cardiac arrest or forms of transient ischemic attack. The dendritic structure of PV-neurons in cortical superficial layers was rapidly swollen and beaded during global ischemia, but recovered within 5-10 min following reperfusion. Using optogenetics and a multichannel optrode, we investigated the function of PV-neurons in mouse forelimb somatosensory cortex. We demonstrated pharmacologically that PV-channelrhodopsin-2 (ChR2) stimulation evoked activation in layer IV/V, which resulted in rapid current sinks mediated by photocurrent and action potentials (a measure of PV-neuron excitability), which was then followed by current sources mediated by network GABAergic synaptic activity. During ischemic depolarization, the PV-ChR2-evoked current sinks (excitability) were suppressed, but recovered rapidly following reperfusion concurrent with repolarization of the DC-EEG. In contrast, the current sources reflecting GABAergic synaptic network activity recovered slowly and incompletely, and was coincident with the partial recovery of the forepaw stimulation-evoked current sinks in layer IV/V 30 min post reperfusion. Our in vivo data suggest that the excitability of PV inhibitory neurons was suppressed during global ischemia and rapidly recovered during reperfusion. In contrast, PV-ChR2 stimulation-evoked GABAergic synaptic network activity exhibited a prolonged suppression even ∼1 h after reperfusion, which could contribute to the dysfunction of sensation and cognition following transient global ischemia.