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1.
Thorax ; 65(10): 908-14, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20861295

ABSTRACT

BACKGROUND: Obstructive sleep apnoea (OSA) is a common disease that leads to daytime sleepiness and cognitive impairment. Attempts to investigate changes in brain morphology that may underlie these impairments have led to conflicting conclusions. This study was undertaken to aim to resolve this confusion, and determine whether OSA is associated with changes in brain morphology in a large group of patients with OSA, using improved voxel-based morphometry analysis, an automated unbiased method of detecting local changes in brain structure. METHODS: 60 patients with OSA (mean apnoea hypopnoea index 55 (95% CI 48 to 62) events/h, 3 women) and 60 non-apnoeic controls (mean apnoea hypopnoea index 4 (95% CI 3 to 5) events/h, 5 women) were studied. Subjects were imaged using T1-weighted 3-D structural MRI (69 subjects at 1.5 T, 51 subjects at 3 T). Differences in grey matter were investigated in the two groups, controlling for age, sex, site and intracranial volume. Dedicated cerebellar analysis was performed on a subset of 108 scans using a spatially unbiased infratentorial template. RESULTS: Patients with OSA had a reduction in grey matter volume in the right middle temporal gyrus compared with non-apnoeic controls (p<0.05, corrected for topological false discovery rate across the entire brain). A reduction in grey matter was also seen within the cerebellum, maximal in the left lobe VIIIb close to XI, extending across the midline into the right lobe. CONCLUSION: These data show that OSA is associated with focal loss of grey matter that could contribute to cognitive decline. Specifically, lesions in the cerebellum may result in both motor dysfunction and working memory deficits, with downstream negative consequences on tasks such as driving.


Subject(s)
Brain/pathology , Sleep Apnea, Obstructive/pathology , Adult , Brain Mapping/methods , Case-Control Studies , Cerebellum/pathology , Female , Humans , Image Interpretation, Computer-Assisted/methods , Magnetic Resonance Imaging/methods , Male , Middle Aged , Temporal Lobe/pathology
2.
Adv Exp Med Biol ; 669: 341-5, 2010.
Article in English | MEDLINE | ID: mdl-20217379

ABSTRACT

Dyspnoea, usually defined as an uncomfortable awareness of breathing, is one of the most frequent and distressing symptoms experienced by patients with lung disease. Idiopathic hyperventilation (IHV) has unknown aetiology and little is known about the mechanisms that cause the characteristic sustained hypocapnia and chronic dyspnoea. We have shown in IHV and other chronic respiratory disorders that air hunger is the dominant sensation during exercise, while resting breathlessness is characterised by an affective component. The increased drive to breathe in IHV, and indeed dyspnoea in all chronic respiratory disorders, might be better understood if the central mechanisms of dyspnoea were known. The aim of the present study was to characterise the cortical processing of respiratory-related sensory inputs in patients with IHV. Four patients with IHV were studied with ethical approval. Respiratory stimulation was produced using transient occlusion of inspiration (TIO) during spontaneous breathing (delivered in early inspiration with duration c. 300 ms; this is well tolerated) while BOLD fMRI was performed on a 3 Tesla Siemens Trio. TIO was associated with significant activation in sensorimotor and pre-motor cortical areas and the cerebellum, notably the anterior insula, an area previously associated with breathlessness in healthy volunteers. These preliminary observations on the pattern of brain activity in response to respiratory stimulation support the hypothesis that breathlessness in IHV may reflect inappropriate cortical processing of respiratory-related sensory inputs.


Subject(s)
Brain/physiology , Hyperventilation/physiopathology , Respiration , Humans , Inhalation/physiology , Magnetic Resonance Imaging
3.
Neurology ; 62(1): 134-7, 2004 Jan 13.
Article in English | MEDLINE | ID: mdl-14718717

ABSTRACT

The diaphragm is the main inspiratory muscle during REM sleep. It was hypothesized that patients with isolated bilateral diaphragm paralysis (BDP) might not be able to sustain REM sleep. Polysomnography with EMG recordings was undertaken from accessory respiratory muscles in patients with BDP and normal subjects. Patients with BDP had a normal quantity of REM sleep (mean +/- SD, 18.6 +/- 7.5% of total sleep time) achieved by inspiratory recruitment of extradiaphragmatic muscles in both tonic and phasic REM, suggesting brainstem reorganization.


Subject(s)
Respiratory Muscles/physiopathology , Respiratory Paralysis/physiopathology , Sleep, REM , Adult , Aged , Body Mass Index , Electromyography , Forced Expiratory Volume , Humans , Middle Aged , Polysomnography , Reference Values , Respiratory Muscles/physiology , Sleep, REM/physiology , Vital Capacity , Wakefulness
4.
J Appl Physiol (1985) ; 95(3): 1170-8, 2003 Sep.
Article in English | MEDLINE | ID: mdl-12754178

ABSTRACT

To investigate the functional neuroanatomy of voluntary respiratory control, blood O2 level-dependent functional magnetic resonance imaging was performed in six healthy right-handed individuals during voluntary hyperpnea. Functional images of the whole brain were acquired during 30-s periods of spontaneous breathing alternated with 30-s periods of isocapnic hyperpnea [spontaneous vs. voluntary: tidal volume = 0.5 +/- 0.01 vs. 1.3 +/- 0.1 (SE) liters and breath duration = 4.0 +/- 0.4 vs. 3.2 +/- 0.4 (SE) s]. For the group, voluntary hyperpnea was associated with significant (P < 0.05, corrected for multiple comparisons) neural activity bilaterally in the primary sensory and motor cortices, supplementary motor area, cerebellum, thalamus, caudate nucleus, and globus pallidum. Significant increases in activity were also identified in the medulla (corrected for multiple comparisons on the basis of a small volume correction for a priori region of interest) in a superior dorsal position (P = 0.012). Activity within the medulla suggests that the brain stem respiratory centers may have a role in mediating the voluntary control of breathing in humans.


Subject(s)
Nervous System Physiological Phenomena , Respiration , Respiratory Mechanics/physiology , Adult , Behavior/physiology , Brain/physiology , Brain Chemistry/physiology , Brain Stem/physiology , Carbon Dioxide/blood , Female , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Male , Medulla Oblongata/physiology , Oxygen Consumption/physiology , Tomography, Emission-Computed
5.
Neuroimage ; 15(1): 120-35, 2002 Jan.
Article in English | MEDLINE | ID: mdl-11771980

ABSTRACT

Gradient-echo echo-planar imaging is a standard technique in functional magnetic resonance imaging (fMRI) experiments based on the blood oxygenation level-dependent (BOLD) effect. A major problem is the occurrence of susceptibility gradients near air/tissue interfaces. As a consequence, the detection of neuronal activation may be greatly compromised in certain brain areas, especially in the temporal lobes and in the orbitofrontal cortex. Common approaches to overcome this problem, such as z-shimming or the use of tailored radio frequency pulses, usually compensate only for susceptibility gradients in the slice selection direction. In the present study, the influence of susceptibility gradients in the phase encoding direction is investigated both theoretically and experimentally. It is shown that these gradients influence the effective echo time TE and may reduce considerably the local BOLD sensitivity, even in the case of acceptable image intensities. A compensation method is proposed and tested in an fMRI experiment based on a hypercapnic challenge. The results suggest that the compensation method allows for the detection of activation in brain areas which are usually unavailable for BOLD studies.


Subject(s)
Brain/blood supply , Echo-Planar Imaging , Image Enhancement , Magnetic Resonance Imaging , Oxygen/blood , Brain Mapping , Frontal Lobe/blood supply , Homeostasis/physiology , Humans , Image Processing, Computer-Assisted , Prefrontal Cortex/blood supply , Regional Blood Flow/physiology , Sensitivity and Specificity , Temporal Lobe/blood supply
6.
Neuroimage ; 13(6 Pt 1): 1207-11, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11352626

ABSTRACT

Increases in cerebral blood flow produced by vasoactive agents will increase blood oxygen level-dependent (BOLD) MRI signal intensity. The effects of such vasodilation on activation-related signal changes are incompletely characterized. The two signal changes may be simply additive or there may be more a complex interaction. To investigate this, BOLD MRI was performed in four normal male subjects using T2*-weighted echo planar imaging; brain volumes were acquired every 6.2 s, using a Siemens VISION scanner operating at 2 Tesla; each volume consisted of 64 sequential transverse slices (64 x 64 pixels per slice, 3 x 3 x 3 mm). Sixteen periods of visual stimulation were produced using a flickering checkerboard (8 Hz, 31 s On/31 s Off); this was coupled with five periods of hypercapnia (4% inspired CO(2), 62 s On/124 s Off). Data were analyzed using SPM96. Mean signal intensity, calculated globally for the whole brain, closely mirrored changes in the partial pressure of end-tidal CO(2) (PCO(2)), and hypercapnia was associated with widespread significant signal increases (P < 0.001), predominantly within grey matter. As expected, the visual stimulation produced significant signal changes within the occipital cortex (P < 0.001). Within the occipital cortex, no significant interactions (P > 0.001) between the effects of the visual stimulation and PCO(2) were present. The increases in PCO(2) imposed dynamically in the present study would increase cerebral blood flow by between 25 and 40%, an increase within the physiological range and comparable to that induced by neural activation. With this flow change the effects of vasodilation, on an activation-related signal change, are simply additive.


Subject(s)
Arousal/physiology , Brain/blood supply , Carbon Dioxide/blood , Hemodynamics/physiology , Magnetic Resonance Imaging , Vasodilation/physiology , Adult , Echo-Planar Imaging , Humans , Image Enhancement , Image Processing, Computer-Assisted , Male , Occipital Lobe/blood supply , Oxygen Consumption/physiology , Photic Stimulation , Regional Blood Flow/physiology
7.
J Physiol ; 523 Pt 1: 259-70, 2000 Feb 15.
Article in English | MEDLINE | ID: mdl-10673560

ABSTRACT

1. States of peripheral autonomic arousal accompany emotional behaviour, physical exercise and cognitive effort, and their central representation may influence decision making and the regulation of social and emotional behaviours. However, the cerebral functional neuroanatomy representing and mediating peripheral autonomic responses in humans is poorly understood. 2. Six healthy volunteer subjects underwent H215O positron emission tomography (PET) scanning while performing isometric exercise and mental arithmetic stressor tasks, and during corresponding control tasks. Mean arterial blood pressure (MAP) and heart rate (HR) were monitored during scanning. 3. Data were analysed using statistical parametric mapping (SPM99). Conjunction analyses were used to determine significant changes in regional cerebral blood flow (rCBF) during states of cardiovascular arousal common to both exercise and mental stressor tasks. 4. Exercise and mental stressor tasks, relative to their control tasks, were associated with significantly (P < 0.001) increased MAP and HR. Significant common activations (increased rCBF) were observed in cerebellar vermis, brainstem and right anterior cingulate. In both exercise and mental stress tasks, increased rCBF in cerebellar vermis, right anterior cingulate and right insula covaried with MAP; rCBF in pons, cerebellum and right insula covaried with HR. Cardiovascular arousal in both categorical and covariance analyses was associated with decreased rCBF in prefrontal and medial temporal regions. 5. Neural responses in discrete brain regions accompany peripheral cardiovascular arousal. We provide evidence for the involvement of areas previously implicated in cognitive and emotional behaviours in the representation of peripheral autonomic states, consistent with a functional organization that produces integrated cardiovascular response patterns in the service of volitional and emotional behaviours.


Subject(s)
Arousal/physiology , Autonomic Nervous System/physiology , Brain/physiology , Cardiovascular Physiological Phenomena , Adult , Blood Pressure/physiology , Brain/diagnostic imaging , Cerebrovascular Circulation/physiology , Exercise , Heart Rate/physiology , Humans , Male , Stress, Psychological/psychology , Tomography, Emission-Computed
8.
J Appl Physiol (1985) ; 87(5): 1923-30, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10562638

ABSTRACT

We have determined whether changes in PCO(2) above and below eucapnia modulate the precision of the voluntary control of breathing. Twelve trained subjects performed a compensatory tracking task in which they had to maintain the position of a cursor (perturbed by a variable triangular forcing function) on a fixed target by breathing in and out of a spirometer (ventilatory tracking; at 10 l/min). Before each task, subjects hyperventilated for 5 min, and the end-tidal PCO(2) (PET(CO(2))) was controlled; tracking was then performed separately at hypocapnia, eucapnia, and hypercapnia (PET(CO(2)) approximately 25, 37, and 43 Torr, respectively). Ventilatory tracking error was unchanged during hypocapnia (P > 0.05) but was significantly worse during hypercapnia (P < 0.003), compared with eucapnia; arm tracking error, performed as a control, was not significantly affected by PET(CO(2)) (P > 0. 05). In conclusion, ventilatory tracking performance is unaffected by the eucapnic PCO(2). From this, we suggest that resting breathing in awake humans may be independent of chemical drives and of the prevailing PCO(2).


Subject(s)
Cerebral Cortex/physiology , Reflex/physiology , Respiratory Mechanics/physiology , Spinal Cord/physiology , Adult , Carbon Dioxide/blood , Female , Humans , Hypercapnia/blood , Male , Oxygen/blood , Psychomotor Performance/physiology , Respiratory Function Tests , Spirometry
9.
Respir Physiol ; 117(2-3): 109-20, 1999 Sep 15.
Article in English | MEDLINE | ID: mdl-10563439

ABSTRACT

The ventilatory responses to hypercapnia and hypoxia are reduced during sleep compared to wakefulness. However, sleep-related increases in upper airways' resistance could reduce these ventilatory responses independently of any change in the neural output to the respiratory pump muscles. It is therefore possible that respiratory chemosensitivity, per se, is unchanged by sleep. To investigate this, four healthy male subjects were mechanically ventilated to abolish spontaneous respiratory muscle activity. The response to transient isocapnic hypoxia was quantified from the magnitude of the electromyographic activity induced in the diaphragm and from the associated reduction in peak inspiratory pressure; these indicies of respiratory motor output will not be affected by any sleep-related changes in upper airways' resistance. In all individuals, the responses to hypoxia were markedly attenuated during sleep compared to wakefulness. These observations, assessing the 'neuromuscular' ventilatory response, are consistent with a sleep-related reduction in respiratory chemosensitivity that is independent of any changes that may be due to increases in upper airways' resistance.


Subject(s)
Hypoxia/physiopathology , Pulmonary Ventilation/physiology , Sleep/physiology , Adult , Airway Resistance , Brain/physiology , Carbon Dioxide , Chemoreceptor Cells , Diaphragm/physiology , Electroencephalography , Electromyography , Humans , Hypercapnia/physiopathology , Male , Regional Blood Flow , Respiration, Artificial , Sleep Deprivation/physiopathology , Sleep, REM , Wakefulness
10.
J Appl Physiol (1985) ; 86(5): 1468-77, 1999 May.
Article in English | MEDLINE | ID: mdl-10233106

ABSTRACT

We have used voluntary tongue contraction to test whether we can image activation of the hypoglossal nuclei within the human brain stem by using functional magnetic resonance imaging (fMRI). Functional images of the whole brain were acquired in eight subjects by using T2-weighted echo planar imaging (blood oxygen level development) every 6.2 s. Sequences of images were acquired during 12 periods of 31-s "isometric" rhythmic tongue contraction alternated with 12 periods of 31-s tongue relaxation. Noise arising from cardiac- and respiratory-related movement was removed either by filtration (high pass; cutoff 120 s) or by inclusion in the statistical analysis as confounding effects of no interest. For the group, tongue contraction was associated with significant signal increases (P < 0.05 corrected for multiple comparisons) in the sensorimotor cortex, supplementary motor area, operculum, insula, thalamus, and cerebellum. For the group and for six of eight individuals, significant signal increases were also seen within the medulla (P < 0.001, predefined region of interest with no correction for multiple comparisons); this signal is most likely to reflect neuronal activation associated with the hypoglossal motor nuclei. The data demonstrate that fMRI can be used to detect, simultaneously, the cerebral and brain stem control of tongue movement.


Subject(s)
Brain/physiology , Motor Cortex/physiology , Movement/physiology , Tongue/physiology , Adult , Brain Mapping , Female , Heart Rate/physiology , Hemodynamics/physiology , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Male , Middle Aged , Muscle Contraction/physiology , Respiratory Mechanics/physiology , Tongue/innervation
11.
J Appl Physiol (1985) ; 86(4): 1142-50, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10194195

ABSTRACT

Multiple factors may contribute to the dyspnea associated with restrictive ventilatory disease (RVD). Simple models that examine specific features of this problem are likely to provide insight into the mechanisms. Previous models of RVD utilizing elastic loads may not represent completely the impact on pulmonary and chest wall receptors derived from breathing at low thoracic volumes. The purpose of this study was to investigate the sensory consequences of breathing at low lung volumes induced by external thoracic restriction in an attempt to further elucidate the etiology of dyspnea in this setting. Ten men were studied, with and without an inelastic corset applied at residual volume (restriction resulted in mean reductions in vital capacity, functional residual capacity, residual volume, and forced expired volume in 1 s of 44, 31, 12.5, and 42%, respectively). During 10-min steady-state exercise tests (at a workload set to achieve approximately 65% maximum heart rate), restriction resulted in significant increases, compared with control, in minute ventilation (61 vs. 49 l/min), respiratory frequency (43 vs. 23 breaths/min), and visual analog scale measurements of respiratory discomfort (65 vs. 20 mm). Alveolar hyperventilation (end-tidal PCO2 = 39 vs. 44 Torr for control) and mild O2 desaturation (arterial blood O2 saturation = 93 vs. 95% for control) occurred. Hypoxemia, atelectasis, increased work and effort of breathing, or a decrease in the volume-related feedback from chest wall and/or lungs could be responsible for the increased dyspnea reported. External thoracic restriction provides a useful model to study mechanisms of dyspnea in RVD.


Subject(s)
Exercise/physiology , Lung/physiology , Respiratory Mechanics/physiology , Adult , Carbon Dioxide/blood , Elasticity , Humans , Lung Volume Measurements , Male , Models, Biological , Oxygen/blood , Partial Pressure , Physical Exertion/physiology , Respiratory Function Tests , Sensation , Thorax , Time Factors
12.
Respir Physiol ; 114(2): 109-17, 1998 Nov.
Article in English | MEDLINE | ID: mdl-9865585

ABSTRACT

In humans, cortico-motor excitation of the diaphragm may act directly on the phrenic motor nucleus via the cortico-spinal tract 'bypassing' brain stem respiratory centres (RC); alternatively, or in addition, this control may be indirect via the RC and bulbo-spinal paths. To investigate this, we stimulated the motor cortex using transcranial magnetic stimulation (TMS) in six subjects at end-expiration (diaphragm relaxed) and during voluntary inspiration. The sizes of the evoked compound action potentials in the diaphragm and also, as a control, in the thumb were no different whether TMS was delivered during normocapnia or during hypocapnia (PET(CO2) = 25 mmHg) when, presumably, the respiratory 'oscillator' was silent. In a further six subjects, TMS was performed during relaxed spontaneous breathing at three different points in the respiratory cycle. No perturbations in respiratory pattern (either tidal volume or respiratory timing) were seen. Thus we have been unable to demonstrate that the cortico-motor excitation of the diaphragm acts via the brain stem RC.


Subject(s)
Brain Stem/physiology , Diaphragm/physiology , Motor Cortex/physiology , Respiratory Physiological Phenomena , Adult , Evoked Potentials/physiology , Female , Humans , Hypercapnia/physiopathology , Magnetics , Male , Muscle, Skeletal/physiopathology , Physical Stimulation , Reference Values , Thumb
13.
J Appl Physiol (1985) ; 83(5): 1438-47, 1997 Nov.
Article in English | MEDLINE | ID: mdl-9375303

ABSTRACT

We have defined areas in the brain activated during speaking, utilizing positron emission tomography. Six normal subjects continuously repeated the phrase "Buy Bobby a poppy" (requiring minimal language processing) in four ways: A) spoken aloud, B) mouthed silently, C) without articulation, and D) thought silently. Statistical comparison of images from conditions A with C and B with D highlighted areas associated with articulation alone, because control of breathing for speech was controlled for; we found bilateral activations in sensorimotor cortex and cerebellum with right-sided activation in the thalamus/caudate nucleus. Contrasting images from conditions A with B and C with D highlighted areas associated with the control of breathing for speech, vocalization, and hearing, because articulation was controlled for; we found bilateral activations in sensorimotor and motor cortex, close to but distinct from the activations in the preceding contrast, together with activations in thalamus, cerebellum, and supplementary motor area. In neither subtraction was there activation in Broca's area. These results emphasize the bilaterality of the cerebral control of "speaking" without language processing.


Subject(s)
Brain/physiology , Speech/physiology , Adult , Brain/diagnostic imaging , Cerebrovascular Circulation/physiology , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Male , Middle Aged , Psychomotor Performance/physiology , Respiratory Mechanics/physiology , Tomography, Emission-Computed
14.
Respir Physiol ; 106(1): 13-20, 1996 Oct.
Article in English | MEDLINE | ID: mdl-8946573

ABSTRACT

Control of breathing was studied in a patient with a lesion in the ventral pons; no volitional behaviour, including voluntary breathing acts, was possible (locked-in syndrome, LIS). Spontaneous breathing via a tracheostomy maintained a normal PETCO2 of 39-40 mmHg. Variability of ventilatory parameters awake was similar to that seen in five tracheostomized control subjects during stage IV sleep but much smaller than during resting wakefulness. Emotion associated with laughter caused disturbances of breathing. The ventilatory response to CO2 was normal and was associated with 'hunger for air' when the PETCO2 was 49-50 mmHg. Mechanical ventilation to reduce PETCO2 by as little as 1 mmHg resulted in apnoea when the ventilator was disconnected; breathing resumed when PETCO2 crossed the threshold of 39-40 mmHg. These results demonstrate the functional dependence of the human medullary respiratory oscillator on a threshold level of PCO2 in the absence of cortico-bulbar input, even during wakefulness. The absence of such input may explain the regularity of breathing.


Subject(s)
Quadriplegia/physiopathology , Respiration/physiology , Adult , Aged , Apnea/physiopathology , Carbon Dioxide/pharmacology , Female , Humans , Male , Middle Aged , Pulmonary Ventilation , Respiration/drug effects , Rheology , Sleep/physiology , Tracheostomy , Wakefulness/physiology
15.
J Appl Physiol (1985) ; 81(3): 1295-305, 1996 Sep.
Article in English | MEDLINE | ID: mdl-8889766

ABSTRACT

Human cerebral activity with increasing inspiratory force: a study using positron emission tomography. J. Appl. Physiol. 81(3): 1295-1305, 1996.--The major aim of this study was to use positron emission tomography (PET) to assess dose-dependent effects of inspiratory loads on relative regional cerebral blood flow as an indication of neuronal activation and recruitment. Six normal men underwent H2 15O-PET scanning during unloaded breathing and with external inspiratory loads (generating mouth pressures of -5, -10, and -15 cmH2O); positive-pressure ventilation against relaxed respiratory muscles acted as control. During unloaded breathing, the supplementary motor area was significantly activated. With the addition of the smallest load, activations also occurred in the right premotor area and bilaterally in the superolateral motor cortex (MI) in areas previously shown to be activated with deeper breathing. There was little further change in these areas with greater loads. Additional force-related activations occurred in the inferolateral sensorimotor cortex, parietal cortex, and midbrain/hypothalamus. The results suggest that volitionally induced increases in inspiratory muscle force are achieved via a complex integration of neuronal activations in cortical and subcortical regions associated with motor control.


Subject(s)
Cerebral Cortex/diagnostic imaging , Cerebral Cortex/physiology , Respiration/physiology , Adult , Cerebrovascular Circulation/physiology , Electromyography , Humans , Male , Tomography, Emission-Computed
16.
Respir Physiol ; 102(2-3): 149-61, 1995 Dec.
Article in English | MEDLINE | ID: mdl-8904007

ABSTRACT

We describe a method to assess the effects of PCO2, around and below eucapnia, on the neuromuscular ventilatory response to a standard peripheral chemoreceptor stimulus. Subjects were "passively" hyperventilated (without respiratory muscle activity), at a constant level of ventilation. Stimuli (3-7 breaths N2) were delivered over a range of steady-state PETCO2 (25-43 mmHg). Stimuli during hypocapnia were coupled with a transient increase in FICO2 so that the stimulus to the peripheral chemoreceptors was always "hypoxia at eucapnia". Responses to the stimuli (quantified from the reduction in peak inflation pressure and the magnitude of the evoked diaphragm electromyographic activity) decreased in a graded manner as steady-state PETCO2 fell, disappearing at 7.5 mmHg below eucapnia. Carotid body chemoreceptor recordings from two anaesthetised cats, indicated that the peak firing rate during such stimuli was independent of steady-state PETCO2. The results suggest that the central sensitivity to a peripheral chemoreceptor input may be modulated by changes in steady-state PCO2 around eucapnia and during mild hypocapnia.


Subject(s)
Carbon Dioxide/pharmacology , Carotid Body/metabolism , Partial Pressure , Adult , Animals , Carbon Dioxide/metabolism , Cats , Chemoreceptor Cells/metabolism , Electromyography , Female , Humans , Hypocapnia/metabolism , Hypoxia/metabolism , Male , Oxygen/metabolism , Respiration/physiology , Ventilators, Mechanical
17.
J Physiol ; 489 ( Pt 3): 663-75, 1995 Dec 15.
Article in English | MEDLINE | ID: mdl-8788932

ABSTRACT

1. The neurophysiological basis for the increase in breathing associated with exercise remains obscure. The present study uses positron emission tomography (PET) to measure relative regional cerebral blood flow (rCBF) in order to identify sites of increased neuronal activation during and immediately following exercise. 2. Male volunteers underwent H2(15)O PET scanning during two complementary studies. Firstly, six subjects performed right leg exercise, adequate to increase oxygen uptake 2.5-fold. Secondly, five different subjects were scanned immediately following bicycle exercise (adequate to increase oxygen uptake 5-fold) while breathing was still increased. In each study, as a control, scanning was also performed during matched passive isocapnic positive pressure ventilation; additionally, in the first study, passive right leg movement was performed. 3. Increases in relative rCBF were obtained in each individual and co-registered with their magnetic resonance image of the brain defining individual gyral morphology. 4. During exercise, individual and group analysis revealed significant relative rCBF increases in the left and right superomedial primary motor cortex (the motor cortical 'leg' areas) and also in the left and right superolateral primary motor cortex in areas previously shown to be associated with volitional breathing. After exercise, there was no significant increase in relative rCBF in the superomedial areas but such increases were still present bilaterally in the superolateral areas which had been activated during the exercise. Other relative rCBF increases were also found, both during and after exercise, in cortical and subcortical areas known to be involved in motor control. 5. The results from PET scans during and after exercise, taken together, provide evidence for motor cortical involvement in the exercise-related hyperpnoea in man.


Subject(s)
Cerebrovascular Circulation/physiology , Exercise/physiology , Motor Cortex/physiology , Respiratory Mechanics/physiology , Adult , Electromyography , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Male , Motor Cortex/metabolism , Oxygen Consumption/physiology , Physical Education and Training , Pulmonary Gas Exchange/physiology , Respiratory Muscles/metabolism , Respiratory Muscles/physiology , Tomography, Emission-Computed
18.
J Physiol ; 488 ( Pt 1): 77-84, 1995 Oct 01.
Article in English | MEDLINE | ID: mdl-8568667

ABSTRACT

1. The role of supra-brainstem structures in the ventilatory response to inhaled CO2 is unknown. The present study uses positron emission tomography (PET), with infusion of H2(15)O, to measure changes in relative regional cerebral blood flow (rCBF) in order to identify sites of increased neuronal activation during CO2-stimulated breathing (CO2-SB) in awake man. 2. Five male volunteers were scanned during CO2-SB (mean +/- S.E.M.; end-tidal PCO2, 50.3 +/- 1.7 mmHg; respiratory frequency, 16.4 +/- 2.7 min-1; tidal volume, 1.8 +/- 0.2 l). As control, scans were performed during 'passive' isocapnic (elevated fraction of inspired CO2) positive pressure ventilation (end-tidal PCO2, 38.4 +/- 1.0 mmHg; respiratory frequency, 15.5 +/- 2.2 min-1; tidal volume, 1.6 +/- 0.2 l). With CO2-SB, all subjects reported dyspnoea. 3. The anatomical locations of the increases in relative rCBF (CO2-SB versus control) were obtained using magnetic resonance imaging. 4. Group analysis identified neuronal activation within the upper brainstem, midbrain and hypothalamus, thalamus, hippocampus and parahippocampus, fusiform gyrus, cingulate area, insula, frontal cortex, temporo-occipital cortex and parietal cortex. No neuronal activation was seen within the primary motor cortex (at sites previously shown to be associated with volitional breathing). 5. These results suggest neuronal activation within the limbic system; this activation may be important in the sensory and/or motor respiratory responses to hypercapnia in awake man.


Subject(s)
Carbon Dioxide/physiology , Limbic System/physiology , Respiration/physiology , Adult , Cerebrovascular Circulation/physiology , Humans , Limbic System/blood supply , Male , Middle Aged , Tomography, Emission-Computed
19.
Respir Physiol ; 101(2): 145-59, 1995 Aug.
Article in English | MEDLINE | ID: mdl-8570917

ABSTRACT

We have studied post-hyperventilation breathing pattern in eight, awake, healthy, naive volunteers after 5 min voluntary or mechanical hyperventilation during normocapnia (PETCO2 = 38 mmHg) and 'hypocapnia (24 mmHg). Breathing was monitored for 10 min post-hyperventilation, 'non-invasively', using calibrated respiratory inductance plethysmography; wakefulness was confirmed with electroencephalography. Comparison of breathing following hypocapnic voluntary hyperventilation with that following hypocapnic mechanical hyperventilation indicated that ventilation was elevated following voluntary hyperventilation; this would suggest that 'after-discharge' exists in man following active hyperventilation, even during hypocapnia. In the absence of 'after-discharge' (i.e. following mechanical hyperventilation), hypocapnia was clearly associated with hypoventilation. Apnoeas (increased TE) were present during hypocapnia; but neither the duration nor the occurrence of apnoea was related to the absolute level of PETCO2. Most notable, was the marked increase in breath-by-breath variability of TI, TE and VT during hypocapnia. The increased variability of breathing during hypocapnia may reflect fluctuations in behavioural drives associated with wakefulness.


Subject(s)
Hypocapnia/physiopathology , Respiration/physiology , Adult , Apnea/physiopathology , Carbon Dioxide , Electroencephalography , Female , Humans , Hyperventilation , Male , Partial Pressure , Plethysmography , Sleep Stages/physiology , Surveys and Questionnaires , Wakefulness/physiology
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