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de Sousa Abreu, R. P.

Publications and source records attributed to de Sousa Abreu, R. P..

2 recordsLinked to original sources

Episodic slow breathing in mice markedly reduces fear responses

We sought to delineate neural mechanisms underlying the effects of controlled breathing in humans, such as in meditation or breathwork, which can reduce depression, anxiety, stress, and pain. Thus, we developed a murine model, where breathing frequency in awake mice can be substantially slowed. When done for 30 min/day for 4 weeks, these mice had significant reductions in stress-related changes in behavior compared to control mice. We conclude that slow breathing effects on emotional state are present in mice, and which cannot be attributed directly to top-down influences such as volitional or emotional control or placebo effects. Our study paves the way for investigations of the neural mechanisms underlying body-brain interactions related to the effects of controlled breathing as well as a platform for optimization of its therapeutic use for amelioration of ordinary and pathological stress and anxiety in humans.

neuroscience↗

Phase- and State-Dependent Modulation of Breathing Pattern by preBötzinger Complex Somatostatin Expressing Neurons

As neuronal subtypes are increasingly categorized, delineating their functional role is paramount. The preBotzinger Complex (preBotC) subpopulation expressing the neuropeptide somatostatin (SST) is classified as mostly excitatory, inspiratory-modulated and not rhythmogenic. We further characterized their phenotypic identity; 87% were glutamatergic and the balance were glycinergic and/or GABAergic. We then used optogenetics to investigate their modulatory role in both anesthetized and freely moving mice. In anesthetized mice, short photostimulation (100 ms) of preBotC SST+ neurons modulated breathing-related variables in a combinatory phase- and state-dependent manner; changes in inspiratory duration, inspiratory peak amplitude (Amp), and phase were different at higher ([&ge;]2.5 Hz) vs. lower (<2.5 Hz) breathing frequency. Moreover, we observed a biphasic effect of photostimulation during expiration that is probabilistic, i.e., photostimulation given at the same phase in consecutive cycles can evoke opposite responses (lengthening vs. shortening of the phase). This unexpected probabilistic state- and phase-dependent responses to photostimulation exposed properties of the preBotC that were not predicted and cannot be readily accounted for in current models of preBotC pattern generation. In freely moving mice, prolonged photostimulation decreased f in normoxia, hypoxia, or hypercapnia, and increased Amp and produced a phase advance, which was similar to the results in anesthetized mice when f[&ge;]2.5 Hz. We conclude that preBotC SST+ neurons are a key mediator of the extraordinary and essential lability of breathing pattern. Key points summaryO_LIWe transfected preBotzinger Complex (preBotC) somatostatin-expressing (SST+) neurons, which modulate respiratory pattern, but are not rhythmogenic, with channelrhodopsin to investigate phase- and state-dependent modulation of breathing pattern in anesthetized and freely behaving mice in normoxia, hypoxia, and hypercapnia. C_LIO_LIIn anesthetized mice, photostimulation of preBotC SST+ neurons during inspiration increased inspiratory duration and amplitude regardless of baseline breathing frequency, f. C_LIO_LIIn anesthetized mice with low f (<2.5 Hz), photostimulation of preBotC SST+ neurons during expiration evoked either phase advance or phase delay, whereas in anesthetized mice with high f ([&ge;]2.5 Hz) and in freely behaving mice in normoxia, hypoxia, or hypercapnia, photostimulation always evoked phase advance. C_LIO_LIPhase- and state-dependency is a function of overall breathing network excitability. C_LIO_LIThe f-dependent probabilistic modulation of breathing pattern by preBotC SST+ neurons was unexpected, requiring reconsideration of current models of preBotC function, which neither predict nor can readily account for such responses. C_LI

neuroscience↗