4.7 Article

Inspiratory Off-Switch Mediated by Optogenetic Activation of Inhibitory Neurons in the preBotzinger Complex In Vivo

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出版社

MDPI
DOI: 10.3390/ijms22042019

关键词

neuronal control of breathing; glycine; GABA; respiratory network

资金

  1. VolkswagenStiftung [ZN3153]
  2. Deutsche Forschungsgemeinschaft [HU 797/12-1]

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The role of inhibitory neurons in the respiratory network remains controversial, with recent studies indicating that their activation in vivo can significantly impact respiratory rate by potentially inhibiting excitatory rhythmogenic neurons within the preBotzinger complex. This suggests that inhibitory neurons may play a crucial role in mediating phase-switching in the respiratory rhythm.
The role of inhibitory neurons in the respiratory network is a matter of ongoing debate. Conflicting and contradicting results are manifold and the question whether inhibitory neurons are essential for the generation of the respiratory rhythm as such is controversial. Inhibitory neurons are required in pulmonary reflexes for adapting the activity of the central respiratory network to the status of the lung and it is hypothesized that glycinergic neurons mediate the inspiratory off-switch. Over the years, optogenetic tools have been developed that allow for cell-specific activation of subsets of neurons in vitro and in vivo. In this study, we aimed to identify the effect of activation of inhibitory neurons in vivo. Here, we used a conditional transgenic mouse line that expresses Channelrhodopsin 2 in inhibitory neurons. A 200 mu m multimode optical fiber ferrule was implanted in adult mice using stereotaxic surgery, allowing us to stimulate inhibitory, respiratory neurons within the core excitatory network in the preBotzinger complex of the ventrolateral medulla. We show that, in anesthetized mice, activation of inhibitory neurons by blue light (470 nm) continuously or with stimulation frequencies above 10 Hz results in a significant reduction of the respiratory rate, in some cases leading to complete cessation of breathing. However, a lower stimulation frequency (4-5 Hz) could induce a significant increase in the respiratory rate. This phenomenon can be explained by the resetting of the respiratory cycle, since stimulation during inspiration shortened the associated breath and thereby increased the respiratory rate, while stimulation during the expiratory interval reduced the respiratory rate. Taken together, these results support the concept that activation of inhibitory neurons mediates phase-switching by inhibiting excitatory rhythmogenic neurons in the preBotzinger complex.

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