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1.
J Neurosci ; 37(7): 1807-1819, 2017 02 15.
Article in English | MEDLINE | ID: mdl-28073937

ABSTRACT

Homeostatic control of breathing, heart rate, and body temperature relies on circuits within the brainstem modulated by the neurotransmitter serotonin (5-HT). Mounting evidence points to specialized neuronal subtypes within the serotonergic neuronal system, borne out in functional studies, for the modulation of distinct facets of homeostasis. Such functional differences, read out at the organismal level, are likely subserved by differences among 5-HT neuron subtypes at the cellular and molecular levels, including differences in the capacity to coexpress other neurotransmitters such as glutamate, GABA, thyrotropin releasing hormone, and substance P encoded by the Tachykinin-1 (Tac1) gene. Here, we characterize in mice a 5-HT neuron subtype identified by expression of Tac1 and the serotonergic transcription factor gene Pet1, referred to as the Tac1-Pet1 neuron subtype. Transgenic cell labeling showed Tac1-Pet1 soma resident largely in the caudal medulla. Chemogenetic [clozapine-N-oxide (CNO)-hM4Di] perturbation of Tac1-Pet1 neuron activity blunted the ventilatory response of the respiratory CO2 chemoreflex, which normally augments ventilation in response to hypercapnic acidosis to restore normal pH and PCO2Tac1-Pet1 axonal boutons were found localized to brainstem areas implicated in respiratory modulation, with highest density in motor regions. These findings demonstrate that the activity of a Pet1 neuron subtype with the potential to release both 5-HT and substance P is necessary for normal respiratory dynamics, perhaps via motor outputs that engage muscles of respiration and maintain airway patency. These Tac1-Pet1 neurons may act downstream of Egr2-Pet1 serotonergic neurons, which were previously established in respiratory chemoreception, but do not innervate respiratory motor nuclei.SIGNIFICANCE STATEMENT Serotonin (5-HT) neurons modulate physiological processes and behaviors as diverse as body temperature, respiration, aggression, and mood. Using genetic tools, we characterize a 5-HT neuron subtype defined by expression of Tachykinin1 and Pet1 (Tac1-Pet1 neurons), mapping soma localization to the caudal medulla primarily and axonal projections to brainstem motor nuclei most prominently, and, when silenced, observed blunting of the ventilatory response to inhaled CO2Tac1-Pet1 neurons thus appear distinct from and contrast previously described Egr2-Pet1 neurons, which project primarily to chemosensory integration centers and are themselves chemosensitive.


Subject(s)
Lectins/metabolism , Neurons/physiology , Raphe Nuclei/cytology , Respiration , Transcription Factors/metabolism , Action Potentials/drug effects , Animals , Carbon Dioxide/pharmacology , Choline O-Acetyltransferase/metabolism , Clozapine/analogs & derivatives , Clozapine/pharmacology , Early Growth Response Protein 2/genetics , Early Growth Response Protein 2/metabolism , Female , Green Fluorescent Proteins/genetics , Green Fluorescent Proteins/metabolism , Homeodomain Proteins/metabolism , Lectins/genetics , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic , Neurons/drug effects , Raphe Nuclei/metabolism , Respiration/drug effects , Serotonin/metabolism , Transcription Factors/genetics , Tyrosine 3-Monooxygenase/metabolism
2.
J Neurophysiol ; 114(1): 381-9, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25878157

ABSTRACT

Serotonin (5-HT)-synthesizing neurons of the medullary raphe are putative central chemoreceptors, proposed to be one of potentially multiple brain stem chemosensitive cell types and loci interacting to produce the respiratory chemoreflex. Hypocretin-synthesizing neurons of the lateral hypothalamus are important contributors to arousal state, thermoregulation, and feeding behavior and are also reportedly involved in the hypercapnic ventilatory response. Recently, a functional interaction was found between the hypocretin system and 5-HT neurons of the dorsal raphe. The validity and potential significance of hypocretin modulation of medullary raphe 5-HT neurons, however, is unknown. As such, the purpose of this study was to explore functional interactions between the hypocretin system and 5-HT system of the medullary raphe on baseline respiratory output and central chemosensitivity. To explore such interactions, we used the neonatal in vitro medullary slice preparation derived from wild-type (WT) mice (normal 5-HT function) and a knockout strain lacking all central 5-HT neurons (Lmx1b(f/f/p) mice). We examined effects of acidosis, hypocretin-1, a hypocretin receptor antagonist (SB-408124), and the effect of the antagonist on the response to acidosis. We confirmed the critical role of 5-HT neurons in central chemosensitivity given that the increased hypoglossal burst frequency with acidosis, characteristic of WT mice, was absent in preparations derived from Lmx1b(f/f/p) mice. We also found that hypocretin facilitated baseline neural ventilatory output in part through 5-HT neurons. Although the impact of hypocretin on 5-HT neuronal sensitivity to acidosis is still unclear, hypocretins did appear to mediate the burst duration response to acidosis via serotonergic mechanisms.


Subject(s)
Acidosis/physiopathology , Medulla Oblongata/physiology , Orexins/metabolism , Respiration , Serotonin/metabolism , Action Potentials/drug effects , Action Potentials/physiology , Animals , Hydrogen-Ion Concentration , Hypoglossal Nerve/drug effects , Hypoglossal Nerve/physiology , Hypoglossal Nerve/physiopathology , LIM-Homeodomain Proteins/genetics , LIM-Homeodomain Proteins/metabolism , Medulla Oblongata/drug effects , Mice, Knockout , Orexin Receptor Antagonists/pharmacology , Orexin Receptors/metabolism , Phenylurea Compounds/pharmacology , Respiration/drug effects , Serotonergic Neurons/drug effects , Serotonergic Neurons/physiology , Tissue Culture Techniques , Transcription Factors/genetics , Transcription Factors/metabolism
3.
Cell Rep ; 9(6): 2152-65, 2014 Dec 24.
Article in English | MEDLINE | ID: mdl-25497093

ABSTRACT

Serotonergic neurons modulate behavioral and physiological responses from aggression and anxiety to breathing and thermoregulation. Disorders involving serotonin (5HT) dysregulation are commensurately heterogeneous and numerous. We hypothesized that this breadth in functionality derives in part from a developmentally determined substructure of distinct subtypes of 5HT neurons each specialized to modulate specific behaviors. By manipulating developmentally defined subgroups one by one chemogenetically, we find that the Egr2-Pet1 subgroup is specialized to drive increased ventilation in response to carbon dioxide elevation and acidosis. Furthermore, this subtype exhibits intrinsic chemosensitivity and modality-specific projections-increasing firing during hypercapnic acidosis and selectively projecting to respiratory chemosensory but not motor centers, respectively. These findings show that serotonergic regulation of the respiratory chemoreflex is mediated by a specialized molecular subtype of 5HT neuron harboring unique physiological, biophysical, and hodological properties specified developmentally and demonstrate that the serotonergic system contains specialized modules contributing to its collective functional breadth.


Subject(s)
Brain Stem/cytology , Respiration , Serotonergic Neurons/classification , Acidosis/metabolism , Action Potentials , Animals , Brain Stem/growth & development , Brain Stem/physiology , Carbon Dioxide/metabolism , Chemoreceptor Cells/metabolism , Chemoreceptor Cells/physiology , Early Growth Response Protein 2/genetics , Early Growth Response Protein 2/metabolism , Hypercapnia/metabolism , Mice , Motor Neurons/metabolism , Motor Neurons/physiology , Reflex , Serotonergic Neurons/metabolism , Serotonergic Neurons/physiology , Serotonin/metabolism , Transcription Factors/genetics , Transcription Factors/metabolism
4.
Respir Physiol Neurobiol ; 203: 28-34, 2014 Nov 01.
Article in English | MEDLINE | ID: mdl-25087734

ABSTRACT

Previous studies have reported subsets of medullary raphé neurons that are either stimulated or inhibited by CO2/pH in vitro, in situ, and in vivo. We tested the hypothesis that medullary raphé CO2-inhibited neurons are GABAergic. Extracellular recordings in unanesthetized juvenile in situ rat preparations showed reversible hypercapnia-induced suppression of 19% (63/323) of medullary raphé neurons, and this suppression persisted after antagonism of NMDA, AMPA/kainate, and GABAA receptors. We stained a subset of CO2-inhibited cells and found that most (11/12) had glutamic acid decarboxylase 67 immunoreactivity (GAD67-ir). These data indicate that the majority of acidosis-inhibited medullary raphé neurons are GABAergic, and that their chemosensitivity is independent of major fast synaptic inputs. Thus, CO2-sensitive GABAergic neurons may play a role in central CO2/pH chemoreception.


Subject(s)
Carbon Dioxide/pharmacology , GABAergic Neurons/drug effects , Midbrain Raphe Nuclei/cytology , gamma-Aminobutyric Acid/metabolism , 6-Cyano-7-nitroquinoxaline-2,3-dione/pharmacology , Action Potentials/drug effects , Animals , Animals, Newborn , Bicuculline/pharmacology , Biotin/analogs & derivatives , Biotin/metabolism , Dose-Response Relationship, Drug , Excitatory Amino Acid Antagonists/pharmacology , GABA Antagonists/pharmacology , Glutamate Decarboxylase/metabolism , In Vitro Techniques , Male , Patch-Clamp Techniques , Piperazines/pharmacology , Rats , Rats, Sprague-Dawley , Tryptophan Hydroxylase/metabolism
5.
J Neurosci ; 34(1): 51-9, 2014 Jan 01.
Article in English | MEDLINE | ID: mdl-24381267

ABSTRACT

Inhibitory 5-HT(1a) receptors are located on serotonin (5-HT) neurons (autoreceptors) as well as neurons of the respiratory network (heteroreceptors). Thus, effects on breathing of 5-HT(1a) agonists, such as (R)-(+)-8-hydroxy-2-(di-N-propylamino) tetralin (8-OH-DPAT), could either be due to decreased firing of 5-HT neurons or direct effects on the respiratory network. Mice in which the transcription factor LMX1B is genetically deleted selectively in Pet1-1-expressing cells (Lmx1b(f/f/p)) essentially have complete absence of central 5-HT neurons, providing a unique opportunity to separate the effect of activation of downstream 5-HT(1a) heteroreceptors from that of autoreceptors. We used rhythmically active medullary slices from wild-type (WT) and Lmx1b(f/f/p) neonatal mice to differentiate autoreceptor versus heteroreceptor effects of 8-OH-DPAT on hypoglossal nerve respiratory output. 8-OH-DPAT transiently increased respiratory burst frequency in Lmx1b(f/f/p) preparations, but not in WT slices. This excitation was abolished when synaptic inhibition was blocked by GABAergic/glycinergic receptor antagonists. Conversely, after 10 min of application, frequency in Lmx1b(f/f/p) slices was not different from baseline, whereas it was significantly depressed in WT slices. In WT mice in vivo, subcutaneous injection of 8-OH-DPAT produced similar biphasic respiratory effects as in Lmx1b(f/f/p) mice. We conclude that 5-HT1a receptor agonists have two competing effects: rapid stimulation of breathing due to excitation of the respiratory network, and delayed inhibition of breathing due to autoreceptor inhibition of 5-HT neurons. The former effect is presumably due to inhibition of inhibitory interneurons embedded in the respiratory network.


Subject(s)
Receptor, Serotonin, 5-HT1A/metabolism , Respiratory Mechanics/physiology , Serotonin 5-HT1 Receptor Agonists/pharmacology , Animals , Animals, Newborn , Female , Male , Mice , Mice, Knockout , Organ Culture Techniques , Protein Binding/physiology , Respiration/drug effects , Respiratory Center/drug effects , Respiratory Center/physiology , Respiratory Mechanics/drug effects , Serotonergic Neurons/drug effects , Serotonergic Neurons/physiology
6.
J Neurochem ; 126(6): 749-57, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23692315

ABSTRACT

The sudden infant death syndrome is associated with a reduction in brainstem serotonin 5-hydroxytryptamine (5-HT) and 5-HT(1A) receptor binding, yet it is unknown if and how these findings are linked. In this study, we used quantitative tissue autoradiography to determine if post-natal development of brainstem 5-HT(1A) receptors is altered in two mouse models where the development of 5-HT neurons is defective, the Lmx1b(f/f/p) , and the Pet-1⁻/⁻ mouse. 5-HT(1A) receptor agonist-binding sites were examined in both 5-HT-source nuclei (autoreceptors) and in sites that receive 5-HT innervation (heteroreceptors). In control mice between post-natal day (P) 3 and 10, 5-HT(1A) receptor binding increased in several brainstem sites; by P25, there were region-specific increases and decreases, refining the overall binding pattern. In the Lmx1b(f/f/p) and Pet-1⁻/⁻ mice, 5-HT(1A)-autoreceptor binding was significantly lower than in control mice at P3, and remained low at P10 and P25. In contrast, 5-HT(1A) heteroreceptor levels were comparable between control and 5-HT-deficient mice. These data define the post-natal development of 5-HT(1A)-receptor binding in the mouse brainstem. Furthermore, the data suggest that 5-HT(1A)-heteroreceptor deficits detected in sudden infant death syndrome are not a direct consequence of a 5-HT neuron dysfunction nor reduced brain 5-HT levels. To elucidate the developmental relationship between serotonin (5-HT) levels and 5-HT(1A) receptors in the brainstem, we examined 5-HT(1A) binding in two 5-HT-deficient mouse models. In nuclei containing 5-HT neurons, 5-HT(1A) binding was decreased (autoreceptors), while binding was maintained in projection sites (heteroreceptors). Thus, brainstem 5-HT(1A)-heteroreceptor-binding sites do not appear developmentally sensitive to reduced brain 5-HT levels.


Subject(s)
Brain Stem/growth & development , Brain Stem/metabolism , Receptor, Serotonin, 5-HT1A/metabolism , Serotonin/deficiency , Aging/metabolism , Animals , Autoradiography , Binding Sites , Data Interpretation, Statistical , Genotype , LIM-Homeodomain Proteins/genetics , Mice , Mice, Knockout , Raphe Nuclei/metabolism , Transcription Factors/genetics
7.
Respir Physiol Neurobiol ; 186(2): 214-20, 2013 Apr 01.
Article in English | MEDLINE | ID: mdl-23454177

ABSTRACT

Evidence from in vivo and in vitro experiments conclude that serotonin (5-HT) neurons are involved in and play an important role in central respiratory CO2/H(+) chemosensitivity. This study was designed to assess the importance of 5-HT neurons and 5-HT receptor activation in the frequency and amplitude components of the hypercapnic response of the respiratory network in the unanesthetized perfused in situ juvenile rat brainstem preparation that exhibits patterns of phrenic nerve discharge similar to breathing in vivo. Exposure to a hypercapnic perfusate increased phrenic burst frequency and/or amplitude, the neural correlates of breathing frequency and tidal volume in vivo. Hypercapnic responses were also assessed during exposure to ketanserin (5-HT2 receptor antagonist), and 8-OH-DPAT (inhibiting 5-HT neurons via 5-HT1A autoreceptors). Neither of these drugs substantially altered baseline activity, however, both abolished hypercapnic responses of the respiratory network. These data illustrate that 5-HT neurons and 5-HT receptor activation are not required for respiratory rhythm generation per se, but are critical for CO2 responses in situ, supporting the hypothesis that 5-HT neurons play an important role in central ventilatory chemosensitivity in vivo.


Subject(s)
Brain Stem/metabolism , Hypercapnia/metabolism , Receptors, Serotonin/metabolism , Respiratory Mechanics/physiology , Serotonergic Neurons/metabolism , 8-Hydroxy-2-(di-n-propylamino)tetralin/pharmacology , Animals , Ketanserin/pharmacology , Phrenic Nerve/metabolism , Rats , Rats, Sprague-Dawley , Serotonin 5-HT2 Receptor Antagonists/pharmacology , Serotonin Receptor Agonists/pharmacology
8.
Brain Res ; 1511: 115-25, 2013 May 20.
Article in English | MEDLINE | ID: mdl-23261662

ABSTRACT

`The early growth response 2 transcription factor, Egr2, establishes a population of brainstem neurons essential for normal breathing at birth. Egr2-null mice die perinatally of respiratory insufficiency characterized by subnormal respiratory rate and severe apneas. Here we bypass this lethality using a noninvasive pharmacogenetic approach to inducibly perturb neuron activity postnatally, and ask if Egr2-neurons control respiration in adult mice. We found that the normal ventilatory increase in response to elevated tissue CO2 was impaired, blunted by 63.1 ± 8.7% after neuron perturbation due to deficits in both respiratory amplitude and frequency. By contrast, room-air breathing was unaffected, suggesting that the drive for baseline breathing may not require those Egr2-neurons manipulated here. Of the multiple brainstem sites proposed to affect ventilation in response to hypercapnia, only the retrotrapezoid nucleus, a portion of the serotonergic raphé, and a portion of the A5 nucleus have a history of Egr2 expression. We recently showed that acute inhibition of serotonergic neurons en masse blunts the CO2 chemoreflex in adults, causing a difference in hypercapnic response of ∼50% after neuron perturbation through effects on respiratory amplitude only. The suppressed respiratory frequency upon perturbation of Egr2-neurons thus may stem from non-serotonergic neurons within the Egr2 domain. Perturbation of Egr2-neurons did not affect body temperature, even on exposure to ambient 4°C. These findings support a model in which Egr2-neurons are a critical component of the respiratory chemoreflex into adulthood. Methodologically, these results highlight how pharmacogenetic approaches allow neuron function to be queried in unanesthetized adult animals, reaching beyond the roadblocks of developmental lethality and compensation as well as the anatomical disturbances associated with invasive methods. This article is part of a Special Issue entitled Optogenetics (7th BRES).


Subject(s)
Brain Stem/pathology , Early Growth Response Protein 2/metabolism , Hypercapnia/pathology , Neurons/metabolism , Respiration/genetics , Action Potentials/genetics , Action Potentials/physiology , Animals , Carbon Dioxide/pharmacology , Cold Temperature , Early Growth Response Protein 2/genetics , Mice , Neurons/drug effects , Respiration/drug effects , Thermogenesis/genetics
9.
Respir Physiol Neurobiol ; 181(3): 249-58, 2012 May 31.
Article in English | MEDLINE | ID: mdl-22450012

ABSTRACT

In adult mammals, severe hypothermia leads to respiratory and cardiac arrest, followed by death. Neonatal rats and hamsters can survive much lower body temperatures and, upon artificial rewarming, spontaneously recover from respiratory arrest (autoresuscitate), typically suffering no long-term effects. To determine developmental and species differences in cold tolerance (defined here as the temperature of respiratory arrest) and its relation to the ability to autoresuscitate, we cooled neonatal and juvenile Sprague-Dawley rats and Syrian hamsters until respiration ceased, followed by rewarming. Ventilation and heartbeat were continuously monitored. In rats, cold tolerance did not change throughout development, however the ability to autoresuscitate from hypothermic respiratory arrest did (lost between postnatal days, P, 14 and 20), suggesting that the mechanisms for maintaining breathing at low temperatures was retained throughout development while those initiating breathing on rewarming were altered. Hamsters, however, showed increased cold tolerance until P26-28 and were able to autoresuscitate into adulthood (provided the heart kept beating throughout respiratory arrest). Also, hamsters were more cold tolerant than rats. We saw no evidence of gasping to initiate breathing following respiratory arrest, contributing to the hypothesis that hypothermic respiratory arrest does not lead to anoxia.


Subject(s)
Aging/physiology , Body Temperature Regulation/physiology , Hypothermia/physiopathology , Respiratory Insufficiency/physiopathology , Respiratory Physiological Phenomena , Animals , Animals, Newborn , Cold Temperature/adverse effects , Cricetinae , Hypothermia/complications , Mesocricetus , Rats , Rats, Sprague-Dawley , Remission, Spontaneous , Respiratory Insufficiency/complications , Resuscitation , Species Specificity
10.
Science ; 333(6042): 637-42, 2011 Jul 29.
Article in English | MEDLINE | ID: mdl-21798952

ABSTRACT

Physiological homeostasis is essential for organism survival. Highly responsive neuronal networks are involved, but their constituent neurons are just beginning to be resolved. To query brain serotonergic neurons in homeostasis, we used a neuronal silencing tool, mouse RC::FPDi (based on the synthetic G protein-coupled receptor Di), designed for cell type-specific, ligand-inducible, and reversible suppression of action potential firing. In mice harboring Di-expressing serotonergic neurons, administration of the ligand clozapine-N-oxide (CNO) by systemic injection attenuated the chemoreflex that normally increases respiration in response to tissue carbon dioxide (CO(2)) elevation and acidosis. At the cellular level, CNO suppressed firing rate increases evoked by CO(2) acidosis. Body thermoregulation at room temperature was also disrupted after CNO triggering of Di; core temperatures plummeted, then recovered. This work establishes that serotonergic neurons regulate life-sustaining respiratory and thermoregulatory networks, and demonstrates a noninvasive tool for mapping neuron function.


Subject(s)
Body Temperature Regulation , Chemoreceptor Cells/physiology , Clozapine/analogs & derivatives , Neural Inhibition , Neurons/physiology , Respiration , Serotonin/physiology , Acidosis/physiopathology , Action Potentials/drug effects , Animals , Brain Stem/cytology , Carbon Dioxide/blood , Clozapine/metabolism , Clozapine/pharmacology , G Protein-Coupled Inwardly-Rectifying Potassium Channels/metabolism , Homeostasis , Hydrogen-Ion Concentration , Ligands , Mice , Mice, Transgenic , Models, Neurological , Receptors, G-Protein-Coupled/genetics , Receptors, G-Protein-Coupled/metabolism
11.
Respir Physiol Neurobiol ; 168(1-2): 49-58, 2009 Aug 31.
Article in English | MEDLINE | ID: mdl-19394450

ABSTRACT

Serotonergic (5-HT) neurons are putative central respiratory chemoreceptors, aiding in the brain's ability to detect arterial changes in PCO2 and implement appropriate ventilatory responses to maintain blood homeostasis. These neurons are in close proximity to large medullary arteries and are intrinsically chemosensitive in vitro, characteristics expected for chemoreceptors. 5-HT neurons of the medullary raphé are stimulated by hypercapnia in vivo, and their disruption results in a blunted hypercapnic ventilatory response. More recently, data collected from transgenic and knockout mice have provided further insight into the role of 5-HT in chemosensitivity. This review summarizes current evidence in support of the hypothesis that 5-HT neurons are central chemoreceptors, and addresses arguments made against this role. We also briefly explore the relationship between the medullary raphé and another chemoreceptive site, the retrotrapezoid nucleus, and discuss how they may interact during hypercapnia to produce a robust ventilatory response.


Subject(s)
Carbon Dioxide/metabolism , Chemoreceptor Cells/physiology , Raphe Nuclei/cytology , Serotonin/metabolism
12.
Respir Physiol Neurobiol ; 165(2-3): 195-201, 2009 Feb 28.
Article in English | MEDLINE | ID: mdl-19110076

ABSTRACT

We examined developmental changes in alpha-adrenoceptor influences and descending pontine inputs on the medullary respiratory network in the neonatal rat in vitro brainstem-spinal cord preparation. Using a split bath preparation to isolate the pons from the medulla, antagonists for alpha1 and alpha2 adrenoreceptors were applied to only the medulla at postnatal days 0, 2 and 4, before and after transection of the pons. Blocking alpha1 and alpha2 receptors in the medulla in the absence of a pons reduced burst frequency at all ages with a more pronounced effect in younger animals. At all ages the presence of a pons diminished the effect of blocking alpha2 receptors in the medulla and eliminated the effect of blocking alpha1 receptors. These results indicate that there is a tonic release of catecholamines within the medulla that is under influence from the pons. Additionally, transection experiments indicated that during development, the net influence of the pons changed from one of excitation to one of inhibition.


Subject(s)
Medulla Oblongata/growth & development , Medulla Oblongata/physiology , Pons/growth & development , Pons/physiology , Receptors, Adrenergic, alpha-1/physiology , Receptors, Adrenergic, alpha-2/physiology , Adrenergic alpha-1 Receptor Antagonists , Adrenergic alpha-2 Receptor Antagonists , Adrenergic alpha-Antagonists/pharmacology , Age Factors , Animals , Animals, Newborn , Catecholamines/metabolism , In Vitro Techniques , Medulla Oblongata/cytology , Pons/cytology , Prazosin/pharmacology , Rats , Rats, Sprague-Dawley , Respiratory Center/cytology , Respiratory Center/growth & development , Respiratory Center/physiology , Respiratory Mechanics/physiology , Yohimbine/pharmacology
13.
Respir Physiol Neurobiol ; 164(3): 429-40, 2008 Dec 31.
Article in English | MEDLINE | ID: mdl-18948229

ABSTRACT

We examined the effect of age, mass and the presence of the pons on the longevity (length of time spontaneous respiratory-related activity is produced) of brainstem-spinal cord preparations of neonatal rodents (rats and hamsters) and the level of oxygenation in the medulla respiratory network in these preparations. We found the longevity of the preparations from both species decreased with increasing postnatal age. Physical removal of the pons increased respiratory frequency and the longevity of the preparation. However, tissue oxygenation at the level of the medullary respiratory network was not affected by removal of the pons or increasing postnatal age (up to postnatal day 4). Taken together, these data suggest that the effect of removing the pons on respiratory frequency and the longevity of brainstem-spinal cord preparations with increasing postnatal age are primarily due to postnatal development and appear to be unrelated to mass or changes in levels of tissue oxygenation.


Subject(s)
Aging , Brain Stem/physiology , Hyperbaric Oxygenation , Respiration , Spinal Cord/physiology , Action Potentials/drug effects , Action Potentials/physiology , Age Factors , Anesthetics, Local/pharmacology , Animals , Animals, Newborn , Brain Stem/drug effects , Brain Stem/growth & development , Cricetinae , In Vitro Techniques , Longevity , Neural Pathways/physiology , Periodicity , Rats , Rats, Sprague-Dawley , Respiration/drug effects , Spinal Cord/drug effects , Spinal Cord/growth & development , Tetrodotoxin/pharmacology
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