When exposed to a hypoxic environment the body's first response is a reflex increase in ventilation, termed the hypoxic ventilatory response (HVR). With chronic sustained hypoxia (CSH), such as during acclimatization to high altitude, an additional time-dependent increase in ventilation occurs, which increases the HVR. This secondary increase persists after exposure to CSH and involves plasticity within the circuits in the central nervous system that control breathing.
View Article and Find Full Text PDFThis study addressed the hypotheses that exposure to chronic hypoxia (CH) and chronic hypercapnia (CHC) would modify the acute hypercapnic ventilatory response in the cane toad (Rhinella marina; formerly Bufo marinus or Chaunus marinus) and its regulation by NMDA-mediated processes. Cane toads were exposed to 10 days of CH (10% O(2)) or CHC (3.5% CO(2)) followed by acute in vivo hypercapnic breathing trials, conducted before and after an injection of the NMDA-receptor channel blocker, MK801 into the dorsal lymph sac.
View Article and Find Full Text PDFRespir Physiol Neurobiol
February 2008
Previous studies have shown that exposure to chronic hypoxia (CH) and chronic hypercapnia (CHC) alone have opposite effects on central respiratory-related pH/CO(2) chemosensitivity in the cane toad (Bufo marinus). This study examined the effects of chronic hypoxic hypercapnia (CHH) on central pH/CO(2) chemosensitivity. Cane toads were maintained at 10% O(2) and 3.
View Article and Find Full Text PDFAerobic organisms maintain O(2) homeostasis by responding to changes in O(2) supply and demand in both short and long time domains. In this review, we introduce several specific examples of respiratory plasticity induced by chronic changes in O(2) supply (environmental hypoxia or hyperoxia) and demand (exercise-induced and temperature-induced changes in aerobic metabolism). These studies reveal that plasticity occurs throughout the respiratory system, including modifications to the gas exchanger, respiratory pigments, respiratory muscles, and the neural control systems responsible for ventilating the gas exchanger.
View Article and Find Full Text PDFThe goal of this study was to examine the role of respiratory-related afferent input on the chronic hypercapnia (CHC)-induced increase in central respiratory-related pH/CO2 chemosensitivity in cane toads (Bufo marinus). Toads were exposed to CHC (3.5% CO2) for 10 days, following which in vitro brainstem-spinal cord preparations were used to assess central respiratory-related pH/CO2 chemosensitivity.
View Article and Find Full Text PDFRespir Physiol Neurobiol
June 2007
This study examined the effects of chronic hypoxia (CH) and mid-brain transection on central respiratory-related pH/CO(2) chemosensitivity in cane toads (Bufo marinus). Toads were exposed to 10 days of CH (10% O(2)) following which in vitro brainstem-spinal cord preparations, with the mid-brain attached, were used to examine central pH/CO(2) chemosensitivity. A reduction in artificial cerebral spinal fluid (aCSF) pH increased fictive breathing frequency (fR) and total fictive ventilation.
View Article and Find Full Text PDFAm J Physiol Regul Integr Comp Physiol
November 2006
This study investigated whether changes in GABA-mediated neurotransmission within the nucleus of the solitary tract (NTS) contribute to the changes in breathing (resting ventilation and the acute HVR) that occur following exposure to chronic hypoxia (CH). Rats were exposed to 9 days of hypobaric hypoxia (0.5 atm) and then subjected to acute hypoxic breathing trials before and after bilateral microinjections of GABA, bicuculline (a GABAA-receptor antagonist), or bicuculline plus CGP-35348 (a GABAB receptor antagonist) into the caudal regions of the NTS.
View Article and Find Full Text PDFThe present study examined the role of branchial and orobranchial O(2) chemoreceptors in the cardiorespiratory responses, aquatic surface respiration (ASR), and the development of inferior lip swelling in tambaqui during prolonged (6 h) exposure to hypoxia. Intact fish (control) and three groups of denervated fish (bilateral denervation of cranial nerves IX+X (to the gills), of cranial nerves V+VII (to the orobranchial cavity) or of cranial nerves V alone), were exposed to severe hypoxia (Pw(O)2=10 mmHg) for 360 min. Respiratory frequency (fr) and heart rate (fh) were recorded simultaneously with ASR.
View Article and Find Full Text PDFAnuran amphibians have multiple populations of pH/CO2-sensitive respiratory-related chemoreceptors. This study examined in cane toads (Bufo marinus) whether chronic hypercapnia (CHC) altered the pH/CO2 sensitivity of central respiratory-related chemoreceptors in vitro and whether CHC altered the acute hypercapnic ventilatory response (HCVR; 5% CO2) in vivo. Toads were exposed to CHC (3.
View Article and Find Full Text PDFRespir Physiol Neurobiol
November 2006
The hypercapnic drive to breathe in amphibians is generally greater than hypoxic ventilatory drive and a variety of interdependent control systems function to regulate both the hypoxic and hypercapnic ventilatory responses. During exposure to hypercapnic conditions, breathing increases in response to input from central chemoreceptors (sensitive to CSF pH/CO(2) levels) and peripheral chemoreceptors (sensitive to arterial blood O(2) and CO(2)). On the other hand, olfactory CO(2) receptors in the nasal epithelium inhibit breathing during exposure to acute hypercapnia.
View Article and Find Full Text PDFThis study examined whether a hypoxia-tolerant amphibian, the Cane toad, undergoes mammalian-like ventilatory acclimatisation to hypoxia (VAH) and whether chronic hypoxia (CH) alters NMDA-mediated regulation of the acute hypoxic ventilatory response (HVR). Toads were exposed to 10 days of CH (10% O2) followed by acute hypoxic breathing trials or an intra-arterial injection of NaCN. Trials were conducted before and after i.
View Article and Find Full Text PDFJ Appl Physiol (1985)
December 2005
Chronic hypoxia increases the sensitivity of the central nervous system to afferent input from carotid body chemoreceptors. We hypothesized that this process involves N-methyl-D-aspartate (NMDA) receptor-mediated mechanisms and predicted that chronic hypoxia would change the effect of the NMDA receptor blocker dizocilpine (MK-801) on the poikilocapnic hypoxic ventilatory response (HVR). Male Sprague-Dawley rats were studied before and after acclimatization to hypoxia (70 Torr inspiratory Po(2) for 9 days).
View Article and Find Full Text PDFRespir Physiol Neurobiol
April 2005
This study examined the effect of acute hypoxic and hypercapnic cardiorespiratory stimuli, superimposed on existing cardiorespiratory disturbances in tambaqui. In their natural habitat, these fish often encounter periods of hypoxic hypercapnia that can be acutely exacerbated by water turnover. Tambaqui were exposed to periods of normoxia, hypoxia, hyperoxia and hypercapnia during which, externally oriented O2 and CO2 chemoreceptors were further stimulated, by administration into the inspired water of sodium cyanide and CO2-equilibrated water, respectively.
View Article and Find Full Text PDFRespir Physiol Neurobiol
September 2004
This study examined the role of phasic pulmonary stretch receptor (PSR) feedback in ventilatory control, breath clustering and breath timing in decerebrate, paralysed and artificially-ventilated cane toads (Bufo marinus) under conditions designed to minimise tonic PSR feedback. Fictive breathing was recorded as trigeminal motor output to the buccal musculature. Artificial tidal ventilation, with hypercarbic gas mixtures, was either continuous or activated by the fictive breaths and was manipulated to provide differing amounts/patterns of phasic PSR feedback.
View Article and Find Full Text PDFWe examined the cardiorespiratory responses to 6 h of acute hypercarbia (1, 2.5, and 5% CO(2)) in intact and gill-denervated (bilateral denervation of branchial branches of cranial nerves IX and X) tambaqui, Colossoma macropomum. Intact fish exposed to 1 and 2.
View Article and Find Full Text PDFThis study used a decerebrate and artificially-ventilated preparation to examine the roles of various afferent inputs in breathing pattern formation in the tambaqui (Colossoma macropomum). Three general breathing patterns were observed: (1) regular breathing; (2) frequency cycling and (3) episodic breathing. Under normoxic, normocapnic conditions, 50% of control fish exhibited regular continuous breathing and 50% exhibited frequency cycling.
View Article and Find Full Text PDFAm J Physiol Regul Integr Comp Physiol
April 2003
This study addressed the hypothesis that the secretion of catecholamines from trout (Oncorhynchus mykiss) chromaffin cells, during hypoxia, is triggered by stimulation of O(2) chemoreceptors located within the gills. Sodium cyanide was administered into the inspired water (external cyanide) or injected into the gill circulation (internal cyanide) to pharmacologically stimulate external (water sensing) or internal (blood sensing) O(2) chemoreceptors, respectively. Both of these treatments caused an elevation of circulating catecholamine levels.
View Article and Find Full Text PDFExperiments were performed to test the hypothesis that the marked ventilatory and cardiovascular responses to hypercarbia in rainbow trout Oncorhynchus mykiss arise from specific stimulation of chemoreceptors localised to the first gill arch. This was accomplished by measuring cardiorespiratory variables during acute hypercarbia (20 min at P(CO(2))=8 mmHg; 1 mmHg=0.133 kPa) in fish subjected to selective bilateral extirpation of the first gill arch.
View Article and Find Full Text PDFIn a previous study, complete denervation of the gills in the tambaqui Colossoma macropomum did not eliminate the increase in breathing amplitude seen during exposure of this species to hypoxia. The present study was designed to examine other sites of putative O(2)-sensitive receptors that could be involved in this reflex action. Superfusion of the exposed brain of decerebrate, spinalectomized fish did not reveal the presence of central chemoreceptors responsive to hyperoxic, hypoxic, hypercarbic, acidic or alkaline solutions.
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