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Biology subjects

Sartori, M. R.

Publications and source records attributed to Sartori, M. R..

3 recordsLinked to original sources

Drowning a frog respiratory rhythm generator in a wash of excitation: State-dependent architecture of a ventilatory oscillator

Breathing begins at birth and continues to death, providing a unique system to understand the architecture of rhythm-generating circuits in vertebrates. In mammals and frogs, three discrete rhythmogenic brainstem nuclei appear essential for generating different phases of breathing, with individual neurons intrinsically tuned to each phase. This discrete multi-oscillator architecture differs fundamentally from the distributed spinal locomotor networks, where rhythmogenesis spans multiple segments and the active phase of individual neurons depends on network state. However, whether these discrete respiratory oscillators are strictly essential and whether the phase of their neurons remains constant across states is coming under increasing scrutiny. Here, we focus on the frog buccal oscillator, which shares anatomical and functional similarities with the mammalian preBotzinger Complex. We developed a technique to silence motor neurons in frogs and mapped premotor unit activity within and surrounding the putative buccal oscillator under standard conditions and during heightened network excitability. We found that increasing network excitation caused the rhythmically active area to expand, in part by converting premotor lung units into buccal units. Next, we located the buccal area using excitatory and inhibitory microinjections and established the minimum number of inhibitory injections required to suppress buccal bursts. We then increased network excitability and again tested whether inhibitory microinjections could suppress the rhythm. While inhibitory microinjections could reverse local excitatory effects, they were unable to abolish the buccal rhythm under elevated excitation. Our data shows that not only does the region containing rhythmic premotor buccal units enlarge as network excitation increases, but the essential requirement for a discrete, rudimentary buccal oscillator is also lost. Thus, although rostral-caudal segments of the frog brainstem generally contribute to discrete phases of ventilatory motor patterns, our findings suggest that oscillator identity should be refined: oscillators should be viewed as promiscuous flexible functional entities that expand or contract to occupy different extents of the brainstem, rather than as fixed anatomical nuclei. Key points summaryO_LIThe respiratory rhythm is hypothesized to be generated by specialized brainstem circuits comprised of individual non-redundant, discrete, and intrinsically rhythmic oscillators. C_LIO_LIThese oscillators are essential in the impoverished network, often generating rhythmic output in isolation. The inspiratory preBotzinger Complex (preBotC) is the most important of these oscillators in mammals. C_LIO_LIIsolated brainstem preparations in frogs have revealed a ventilatory rhythm-generating circuit closely resembling that of mammals. Particularly, the Buccal Area shares anatomical and functional similarities to the preBotC. C_LIO_LIWe demonstrate that the discrete Buccal Area is rearranged with mild increases in network excitation to a diffuse network that appears to generate the buccal rhythm instead. C_LIO_LIThese findings support the broader hypothesis that respiratory rhythm-generating circuits can switch to being diffuse and redundant, with discrete oscillators quickly drowning in a sea of excitation. C_LI

neuroscience↗

CETP expression in females increases body metabolism under both cold exposure and thermoneutrality contributing to a leaner phenotype

Susceptibility to obesity differs depending on the genetic background and housing temperatures. We have recently reported that CETP expressing female mice are leaner due to increased lipolysis, brown adipose tissue (BAT) activity and body energy expenditure compared to non-transgenic (NTg) littermates under standard housing temperature (22{degrees}C). The aim of this study is to evaluate how CETP expression affect body temperature, composition and metabolism during cold exposure (4{degrees}C) and thermoneutrality (30{degrees}C). When submitted to cold, CETP mice maintained rectal temperature, body weight and food intake similarly to NTg mice along acute or chronic exposure to 4{o}C. The body oxygen consumption in response to an isoproterenol challenge was 21% higher at 22{o}C, and 41% higher after 7 days of cold exposure in CETP than in NTg mice. In addition, BAT biopsies from CETP mice showed reduced lipid content and increased basal oxygen consumption rates. Under thermoneutrality (30{o}C), when BAT activity is inhibited, CETP mice showed higher rectal and tail temperatures, increased food intake and increased energy expenditure. Lean mass was elevated and fat mass reduced in CETP mice kept at 30{o}C. In this thermoneutrality condition, soleus muscle, but not gastrocnemius or liver of CETP mice showed increased mitochondrial respiration rates. These data indicate that CETP expression confers a greater capacity of elevating body metabolic rates at both cold exposure, through BAT activity, and at thermoneutrality, through increased muscle metabolism. Thus, the CETP expression levels in females should be considered as a new influence in the contexts of obesity and metabolic disorders propensity. NEW & NOTEWORTHYWe demonstrate here that CETP expression in females increases body metabolism under cold (4{o}C) and thermoneutrality (30{o}C). Since this has also been shown at 22{o}C, it seems a constitutive feature of CETP expression. Brown adipose tissue and red fiber muscle contribute to the overall high metabolism and leaner phenotype of CETP mice. Elevated mitochondrial respiration rates were demonstrated in these tissues. Thus, CETP is a new relevant variable in the context of obesity and metabolic disorders. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=114 SRC="FIGDIR/small/623058v1_ufig1.gif" ALT="Figure 1"> View larger version (28K): org.highwire.dtl.DTLVardef@19ed73org.highwire.dtl.DTLVardef@3458acorg.highwire.dtl.DTLVardef@a9896forg.highwire.dtl.DTLVardef@7e1138_HPS_FORMAT_FIGEXP M_FIG C_FIG

physiology↗

Feeding effects on liver mitochondrial bioenergetics of Boa constrictor (Serpentes: Boidae)

Snakes are interesting examples of overcoming energy metabolism challenges as many species can endure long periods without feeding, and their eventual meals are of reasonably large sizes, thus exhibiting dual extreme adaptations. Consequently, metabolic rate increases considerably to attend to the energetic demand of digestion, absorption and, protein synthesis. These animals should be adapted to transition from these two opposite states of energy fairly quickly, and therefore we investigated mitochondrial function plasticity in these states. Herein we compared liver mitochondrial bioenergetics of the boid snake Boa constrictor during fasting and after meal intake. We fasted the snakes for 60 days, then we fed a subgroup with 30% of their body size and evaluated their maximum postprandial response. We measured liver respiration rates from permeabilized tissue and isolated mitochondria, and from isolated mitochondria, we also measured Ca2+ retention capacity, the release of H2O2, and NAD(P) redox state. Mitochondrial respiration rates were maximized after feeding, reaching until 60% increase from fasting levels when energized with complex I-linked substrates. Interestingly, fasting and fed snakes exhibited similar respiratory control ratios and citrate synthase activity. Furthermore, we found no differences in Ca2+ retention capacity, indicating no increase in susceptibility to mitochondrial permeability transition pore (PTP), or redox state of NAD(P), although fed animals exhibited increases in the release of H2O2. Thus, we conclude that liver mitochondria from B. constrictor snakes increase the maintenance costs during the postprandial period and quickly improve the mitochondrial bioenergetics capacity without compromising the redox balance.

biochemistry↗