Chronic in vivo optogenetic stimulation modulates neuronal excitability, spine morphology, and Hebbian plasticity in the mouse hippocampus
Autor: | Lyvia Lintzmaier Petiz, Olavo B. Amaral, Jessica Winne, Thiago C. Moulin, Rafael V. Lima da Cruz, Richardson N. Leão, Danielle Rayêe, Roberto G. Maia |
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Rok vydání: | 2018 |
Předmět: |
Dendritic spine
Cognitive Neuroscience Dendritic Spines Hippocampus Action Potentials Stimulation AMPA receptor Optogenetics 050105 experimental psychology 03 medical and health sciences Mice 0302 clinical medicine synaptic scaling Animals long-term depression 0501 psychology and cognitive sciences optogenetics Long-term depression long-term potentiation Neurons synaptic plasticity Synaptic scaling Neuronal Plasticity Chemistry musculoskeletal neural and ocular physiology 05 social sciences Long-term potentiation Hebbian theory nervous system Synaptic plasticity Synapses NMDA receptor Neuroscience 030217 neurology & neurosurgery |
Zdroj: | Repositório Institucional da UFRN Universidade Federal do Rio Grande do Norte (UFRN) instacron:UFRN |
ISSN: | 1098-1063 |
Popis: | Prolonged increases in excitation can trigger cell-wide homeostatic responses in neurons, altering membrane channels, promoting morphological changes and ultimately reducing synaptic weights. However, how synaptic downscaling interacts with classical forms of Hebbian plasticity is still unclear. In this study, we investigated whether chronic optogenetic stimulation of hippocampus CA1 pyramidal neurons in freely-moving mice could (a) cause morphological changes reminiscent of homeostatic scaling, (b) modulate synaptic currents that might compensate for chronic excitation, and (c) lead to alterations in Hebbian plasticity. After 24 h of stimulation with 15-ms blue light pulses every 90 s, dendritic spine density and area were reduced in the CA1 region of mice expressing channelrhodopsin-2 (ChR2) when compared to controls. This protocol also reduced the amplitude of mEPSCs for both the AMPA and NMDA components in ex vivo slices obtained from ChR2-expressing mice immediately after the end of stimulation. Lastly, chronic stimulation impaired the induction of LTP and facilitated that of LTD in these slices. Our results indicate that neuronal responses to prolonged network excitation can modulate subsequent Hebbian plasticity in the hippocampus. |
Databáze: | OpenAIRE |
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