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1.
Neuroimage ; 158: 126-135, 2017 09.
Article in English | MEDLINE | ID: mdl-28669909

ABSTRACT

Recent evidence suggests that the function of the core system for face perception might extend beyond visual face-perception to a broader role in person perception. To critically test the broader role of core face-system in person perception, we examined the role of the core system during the perception of others in 7 congenitally blind individuals and 15 sighted subjects by measuring their neural responses using fMRI while they listened to voices and performed identity and emotion recognition tasks. We hypothesised that in people who have had no visual experience of faces, core face-system areas may assume a role in the perception of others via voices. Results showed that emotions conveyed by voices can be decoded in homologues of the core face system only in the blind. Moreover, there was a specific enhancement of response to verbal as compared to non-verbal stimuli in bilateral fusiform face areas and the right posterior superior temporal sulcus showing that the core system also assumes some language-related functions in the blind. These results indicate that, in individuals with no history of visual experience, areas of the core system for face perception may assume a role in aspects of voice perception that are relevant to social cognition and perception of others' emotions.


Subject(s)
Auditory Perception/physiology , Blindness/physiopathology , Neuronal Plasticity/physiology , Temporal Lobe/physiopathology , Acoustic Stimulation , Adult , Brain Mapping , Female , Humans , Magnetic Resonance Imaging , Male , Visual Perception/physiology
2.
Clin Toxicol (Phila) ; 51(4): 216-24, 2013 May.
Article in English | MEDLINE | ID: mdl-23547745

ABSTRACT

CONTEXT: Sulfur mustard is a blister agent that can cause death by pulmonary damage. There is currently no effective treatment. N-acetyl-L-cysteine (NAC) has mucolytic and antioxidant actions and is an important pre-cursor of cellular glutathione synthesis. These actions may have potential to reduce mustard-induced lung injury. OBJECTIVE: Evaluate the effect of nebulised NAC as a post-exposure treatment for inhaled sulfur mustard in a large animal model. MATERIALS AND METHODS: Fourteen anesthetized, surgically prepared pigs were exposed to sulfur mustard vapor (100 µg.kg⁻¹), 10 min) and monitored, spontaneously breathing, to 12 h. Control animals had no further intervention (n = 6). Animals in the treatment group were administered multiple inhaled doses of NAC (1 ml of 200 mg.ml⁻¹ Mucomyst™ at + 30 min, 2, 4, 6, 8, and 10 h post-exposure, n = 8). Cardiovascular and respiratory parameters were recorded. Arterial blood was collected for blood gas analysis while blood and bronchoalveolar lavage fluid were collected for hematology and inflammatory cell analysis. Urine was collected to detect a sulfur mustard breakdown product. Lung tissue samples were taken for histopathological and post-experimental analyses. RESULTS: Five of six sulfur mustard-exposed animals survived to 12 h. Arterial blood oxygenation (PaO2) and saturation levels were significantly decreased at 12 h. Arterial blood carbon dioxide (PaCO2) significantly increased, and arterial blood pH and bicarbonate (HCO3⁻) significantly decreased at 12 h. Shunt fraction was significantly increased at 12 h. In the NAC-treated group all animals survived to 12 h (n = 8). There was significantly improved arterial blood oxygen saturation, HCO3⁻ levels, and shunt fraction compared to those of the sulfur mustard controls. There were significantly fewer neutrophils and lower concentrations of protein in lavage compared to sulfur mustard controls. DISCUSSION: NAC's mucolytic and antioxidant properties may be responsible for the beneficial effects seen, improving clinically relevant physiological indices affected by sulfur mustard exposure. CONCLUSION: Beneficial effects of nebulized NAC were apparent following inhaled sulfur mustard exposure. Further therapeutic benefit may result from a combination therapy approach.


Subject(s)
Acetylcysteine/therapeutic use , Antioxidants/therapeutic use , Chemical Warfare Agents/toxicity , Disease Models, Animal , Gas Poisoning/drug therapy , Lung/drug effects , Mustard Gas/toxicity , Acetylcysteine/administration & dosage , Acetylcysteine/adverse effects , Administration, Inhalation , Aerosols , Animals , Antidotes/administration & dosage , Antidotes/adverse effects , Antidotes/therapeutic use , Antioxidants/administration & dosage , Antioxidants/adverse effects , Bronchoalveolar Lavage Fluid/chemistry , Bronchoalveolar Lavage Fluid/immunology , Chemical Warfare Agents/analysis , Chemical Warfare Agents/pharmacokinetics , Expectorants/administration & dosage , Expectorants/adverse effects , Expectorants/therapeutic use , Female , Gas Poisoning/immunology , Gas Poisoning/pathology , Gas Poisoning/physiopathology , Lung/immunology , Lung/pathology , Lung/physiopathology , Lung Diseases/etiology , Lung Diseases/prevention & control , Mustard Gas/administration & dosage , Mustard Gas/analysis , Mustard Gas/pharmacokinetics , Neutrophil Infiltration/drug effects , Random Allocation , Respiratory Insufficiency/etiology , Respiratory Insufficiency/prevention & control , Survival Analysis , Sus scrofa
3.
Inhal Toxicol ; 22(14): 1135-43, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21083508

ABSTRACT

CONTEXT: Inhalation of sulfur mustard (HD) vapor can cause life-threatening lung injury for which there is no specific treatment. A reproducible, characterized in vivo model is required to investigate novel therapies targeting HD-induced lung injury. MATERIALS AND METHODS: Anesthetized, spontaneously breathing large white pigs (~50 kg) were exposed directly to the lung to HD vapor at 60, 100, or 150 µg/kg, or to air, for ~10 min, and monitored for 6 h. Cardiovascular and respiratory parameters were recorded. Blood and bronchoalveolar lavage fluid (BALF) were collected to allow blood gas analysis, hematology, and to assay for lung inflammatory cells and mediators. Urine was collected and analyzed for HD metabolites. Histopathology samples were taken postmortem (PM). RESULTS: Air-exposed animals maintained normal lung physiology whilst lying supine and spontaneously breathing. There was a statistically significant increase in shunt fraction across all three HD-exposed groups when compared with air controls at 3-6 h post-exposure. Animals were increasingly hypoxemic with respiratory acidosis. The monosulfoxide ß-lyase metabolite of HD (1-methylsulfinyl-2-[2(methylthio)ethylsulfonyl)ethane], MSMTESE), was detected in urine from 2 h post-exposure. Pathological examination revealed necrosis and erosion of the tracheal epithelium in medium and high HD-exposed groups. CONCLUSION: These findings are consistent with those seen in the early stages of acute lung injury (ALI).


Subject(s)
Disease Models, Animal , Inhalation Exposure/adverse effects , Mustard Gas/administration & dosage , Mustard Gas/toxicity , Acute Lung Injury/chemically induced , Acute Lung Injury/pathology , Age Factors , Animals , Dose-Response Relationship, Drug , Female , Mustard Gas/metabolism , Oxyhemoglobins/metabolism , Respiratory Mucosa/drug effects , Respiratory Mucosa/pathology , Swine , Time Factors
4.
J R Army Med Corps ; 156(4): 245-50, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21275359

ABSTRACT

METHOD: Using previously validated methods, 16 anaesthetised large white pigs were exposed to phosgene (target inhaled dose 0.3 mg kg(-1)), established on mechanical ventilation and randomised to treatment with either nebulised furosemide (4 ml of 10 mg x ml(-1) solution) or saline control. Treatments were given at 1, 3, 5, 7, 9, 12, 16 and 20 hours post phosgene exposure; the animals were monitored to 24 hours following phosgene exposure. RESULTS: Furosemide treatment had no effect on survival, and had a deleterious effect on PaO2: FiO2 ratio between 19 and 24 hours. All other measures investigated were unaffected by treatment. CONCLUSION: Nebulised furosemide treatment following phosgene induced acute lung injury does not improve survival and worsens PaO2: FiO2 ratio. Nebulised furosemide should be avoided following phosgene exposure.


Subject(s)
Acute Lung Injury/drug therapy , Furosemide/therapeutic use , Phosgene , Sodium Potassium Chloride Symporter Inhibitors/therapeutic use , Acute Lung Injury/chemically induced , Acute Lung Injury/metabolism , Administration, Inhalation , Animals , Disease Models, Animal , Female , Furosemide/pharmacology , Nebulizers and Vaporizers , Oxidation-Reduction/drug effects , Swine
5.
Cereb Cortex ; 19(12): 2946-58, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19395524

ABSTRACT

We used functional magnetic resonance imaging (fMRI) to investigate the brain basis of overt and covert forms of attention during search, while employing stringent control of both eye movements and attentional shifts. A factorial design compared overt and covert forms of goal-directed serial search versus stimulus-driven tracking. To match ocular changes and the number and magnitude of attention shifts across cells in the design, stimulus-driven tracking involved trial-specific "replay" of previous goal-directed eye movements. We found that, in terms of cortical activations, engagement of the dorsal fronto-parietal network by goal-directed attention did not depend on oculomotor requirements, being found similarly for covert attention, in accord with other work. However, analyses of effective connectivity (or "functional coupling") revealed that information flow within this network changed significantly as a function of both the task (goal-directed or stimulus-driven) and the overt versus covert form of attention. Additionally, we observed a distinct set of subcortical regions (pulvinar and caudate nucleus) engaged primarily during the covert form of goal-directed search. We conclude that dynamics within the dorsal fronto-parietal attentional system flexibly reorganize to integrate task demands and oculomotor requirements.


Subject(s)
Brain/physiology , Eye Movements/physiology , Magnetic Resonance Imaging/methods , Nerve Net/physiology , Orientation/physiology , Pattern Recognition, Visual/physiology , Space Perception/physiology , Adolescent , Adult , Female , Humans , Male , Young Adult
6.
Eur J Neurosci ; 29(6): 1247-57, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19302160

ABSTRACT

The role of attention in multisensory integration (MI) is presently uncertain, with some studies supporting an automatic, pre-attentive process and others suggesting possible modulation through selective attention. The goal of this functional magnetic resonance imaging study was to investigate the role of spatial attention on the processing of congruent audiovisual speech stimuli (here indexing MI). Subjects were presented with two simultaneous visual streams (speaking lips in the left and right visual hemifields) plus a single central audio stream (spoken words). In the selective attention conditions, the auditory stream was congruent with one of the two visual streams. Subjects attended to either the congruent or the incongruent visual stream, allowing the comparison of brain activity for attended vs. unattended MI while the amount of multisensory information in the environment and the overall attentional requirements were held constant. Meridian mapping and a lateralized 'speaking-lips' localizer were used to identify early visual areas and to localize regions responding to contralateral visual stimulations. Results showed that attention to the congruent audiovisual stimulus resulted in increased activation in the superior temporal sulcus, striate and extrastriate retinotopic visual cortex, and superior colliculus. These findings demonstrate that audiovisual integration and spatial attention jointly interact to influence activity in an extensive network of brain areas, including associative regions, early sensory-specific visual cortex and subcortical structures that together contribute to the perception of a fused audiovisual percept.


Subject(s)
Attention/physiology , Brain Mapping , Brain/anatomy & histology , Brain/physiology , Space Perception/physiology , Visual Pathways/physiology , Acoustic Stimulation/methods , Adult , Brain/blood supply , Female , Functional Laterality/physiology , Humans , Image Processing, Computer-Assisted , Lipreading , Magnetic Resonance Imaging/methods , Male , Oxygen/blood , Photic Stimulation/methods , Psychophysics , Visual Pathways/blood supply , Young Adult
7.
Toxicol Mech Methods ; 18(4): 355-62, 2008.
Article in English | MEDLINE | ID: mdl-20020902

ABSTRACT

ABSTRACT Although normally regarded as a vesicant, inhalation of sulphur mustard (HD) vapor can cause life-threatening lung injury for which there is no specific treatment. Novel therapies for HD-induced lung injury are best investigated in an in vivo model that allows monitoring of a range of physiological variables. HD vapor was generated using two customized thermostatically controlled glass flasks in parallel. The vapor was passed into a carrier flow of air (81 L. min(-1)) and down a length of glass exposure tube (1.75 m). A pig was connected to the midpoint of the exposure tube via a polytetrafluoroethylene-lined endotracheal tube, Fleisch pneumotachograph, and sample port. HD vapor concentrations (40-122.8 mg. m(-3)) up-and downstream of the point of exposure were obtained by sampling onto Porapak absorption tubes with subsequent analysis by gas chromatography-flame photometric detection. Real-time estimates of vapor concentration were determined using a photo-ionization detector. Lung function indices (respiratory volumes, lung compliance, and airway resistance) were measured online throughout. Trial runs with methylsalicylate (MS) and animal exposures with HD demonstrated that the exposure system rapidly reached the desired concentration within 1 min and maintained stable output throughout exposure, and that the MS/HD concentration decayed rapidly to zero when switched off. A system is described that allows reproducible exposure of HD vapor to the lung of anesthetized white pigs. The system has proved to be robust and reliable and will be a valuable tool in assessing potential future therapies against HD-induced lung injury in the pig. Crown Copyright (c) 2007 Dstl.

8.
Rheumatology (Oxford) ; 47(1): 50-3, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18037687

ABSTRACT

OBJECTIVES: Anatomical MRI brain scans may not reflect neurological dysfunction in patients with NPSLE. We used blood-oxygen-level-dependent functional MRI (BOLD-fMRI) to investigate working memory function in NPSLE patients. METHODS: Twenty-seven females took part: nine NPSLE patients (mean age 40 yrs; SLEDAI 10.9); nine RA patients and nine healthy controls. Subjects were tested using the n-back paradigm for working memory, where patients indicate when a stimulus matches one presented n trials previously. Functional scans used 3 mm slices x 30, repetition time 2570 ms, echo time 50 ms. Echo planar images were superimposed onto T1w anatomical images (Siemens 1.5 T). Data analysis used Brain Voyager QX Version 1.7. RESULTS: During the memory task, there was activation in areas serving working memory, executive function and attention in all groups. Nine regions of interest were selected for activation during working memory (N-back task vs fixation, P < or = 0.005). In six out of nine regions, there was greater activation in the NPSLE group. This reached significance in three regions: the posterior inferior parietal lobules of both hemispheres [Brodmann area (BA) 7] separately and combined (P = 0.014, 0.016 and 0.004, respectively), and the supplementary motor area (mid-line frontal lobe) (BA32/6; P = 0.032). CONCLUSIONS: NPSLE patients showed greater frontoparietal activation than the other groups during the memory task, suggesting a greater need to recruit extra cortical pathways, possibly to supplement impaired function of standard pathways.


Subject(s)
Frontal Lobe/physiopathology , Lupus Vasculitis, Central Nervous System/psychology , Magnetic Resonance Imaging/methods , Memory Disorders/psychology , Memory, Short-Term , Parietal Lobe/physiopathology , Adult , Brain Mapping/methods , Female , Frontal Lobe/metabolism , Humans , Lupus Vasculitis, Central Nervous System/blood , Lupus Vasculitis, Central Nervous System/physiopathology , Memory Disorders/physiopathology , Oxygen/blood , Parietal Lobe/metabolism
9.
Neuropharmacology ; 44(7): 911-25, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12726823

ABSTRACT

The aim of this study was to determine whether electroconvulsive shock (ECS, an established antidepressant treatment), like acute and chronic antidepressant drug treatments, produces similar differential effects on the behavioural profile of resident rats expressed during social encounters with unfamiliar intruder conspecifics (resident-intruder paradigm). Thirty minute pretreatment with a single ECS suppressed both investigation and aggression directed at intruders concomitant with increased flight behaviour and marked sedation. Behavioural disruption subsided over the following 24 h. In contrast, resident rats subjected to bi-daily ECS treatment expressed elevated aggression at days 7 (four shocks) and 14 (eight shocks). Eight days after the last ECS treatment the behaviour of the resident rats had returned to pretreatment values. Additional studies showed that bi-daily ECS treatment nearly abolished 5-HT(2C) receptor-mediated hypolocomotion induced by acute m-chlorophenylpiperazine (mCPP, 2.5 mg/kg sc) challenge 24 h following 2 ECSs, while 4 ECSs only enhanced 5-HT(2A) receptor-mediated head shakes induced by 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI, 2.0 mg/kg sc). These studies demonstrate that repeated ECS treatment increases the aggressive behaviour of resident rats which may be associated with adaptive changes in 5-HT(2C) and 5-HT(2A) receptor-mediated function. It remains to be seen whether adaptive changes in 5-HT(2C) receptor function represent a common mechanism of clinical antidepressant efficacy.


Subject(s)
Agonistic Behavior/physiology , Electroshock , Social Behavior , Amphetamines/pharmacology , Animals , Male , Motor Activity/drug effects , Piperazines/pharmacology , Rats , Rats, Wistar , Receptor, Serotonin, 5-HT2A , Receptor, Serotonin, 5-HT2C , Receptors, Serotonin/drug effects
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