ABSTRACT
Pain is a multi-dimensional emotional experience, and pain sensation and pain emotion are the two main components. As for pain, previous studies only focused on a certain link of the pain transmission pathway or a certain key brain region, and there is a lack of evidence that connectivity of brain regions is involved in pain or pain regulation in the overall state. The establishment of new experimental tools and techniques has brought light to the study of neural pathways of pain sensation and pain emotion. In this paper, the structure and functional basis of the neural pathways involved in the formation of pain sensation and the regulation of pain emotion in the nervous system above the spinal cord level, including thalamus, amygdala, midbrain periaqueductal gray (PAG), parabrachial nucleus (PB) and medial prefrontal cortex (mPFC), are reviewed in recent years, providing clues for the in-depth study of pain.
Subject(s)
Humans , Pain , Neural Pathways/physiology , Periaqueductal Gray/physiology , Brain , Spinal Cord/physiology , Magnetic Resonance ImagingABSTRACT
We used biotinylated dextran amine (BDA) to anterogradely label individual axons projecting from primary somatosensory cortex (S1) to four different cortical areas in rats. A major goal was to determine whether axon terminals in these target areas shared morphometric similarities based on the shape of individual terminal arbors and the density of two bouton types: en passant (Bp) and terminaux (Bt). Evidence from tridimensional reconstructions of isolated axon terminal fragments (n=111) did support a degree of morphological heterogeneity establishing two broad groups of axon terminals. Morphological parameters associated with the complexity of terminal arbors and the proportion of beaded Bp vs stalked Bt were found to differ significantly in these two groups following a discriminant function statistical analysis across axon fragments. Interestingly, both groups occurred in all four target areas, possibly consistent with a commonality of presynaptic processing of tactile information. These findings lay the ground for additional work aiming to investigate synaptic function at the single bouton level and see how this might be associated with emerging properties in postsynaptic targets.
Subject(s)
Animals , Male , Nerve Net/anatomy & histology , Presynaptic Terminals , Somatosensory Cortex/anatomy & histology , Anatomy, Cross-Sectional , Biotin/analogs & derivatives , Dextrans , Fluorescent Dyes , Nerve Net/physiology , Neural Pathways/anatomy & histology , Neural Pathways/physiology , Photomicrography , Presynaptic Terminals/physiology , Rats, Wistar , Reference Values , Somatosensory Cortex/physiologyABSTRACT
Several forebrain and brainstem neurochemical circuitries interact with peripheral neural and humoral signals to collaboratively maintain both the volume and osmolality of extracellular fluids. Although much progress has been made over the past decades in the understanding of complex mechanisms underlying neuroendocrine control of hydromineral homeostasis, several issues still remain to be clarified. The use of techniques such as molecular biology, neuronal tracing, electrophysiology, immunohistochemistry, and microinfusions has significantly improved our ability to identify neuronal phenotypes and their signals, including those related to neuron-glia interactions. Accordingly, neurons have been shown to produce and release a large number of chemical mediators (neurotransmitters, neurohormones and neuromodulators) into the interstitial space, which include not only classic neurotransmitters, such as acetylcholine, amines (noradrenaline, serotonin) and amino acids (glutamate, GABA), but also gaseous (nitric oxide, carbon monoxide and hydrogen sulfide) and lipid-derived (endocannabinoids) mediators. This efferent response, initiated within the neuronal environment, recruits several peripheral effectors, such as hormones (glucocorticoids, angiotensin II, estrogen), which in turn modulate central nervous system responsiveness to systemic challenges. Therefore, in this review, we shall evaluate in an integrated manner the physiological control of body fluid homeostasis from the molecular aspects to the systemic and integrated responses.
Subject(s)
Animals , Humans , Body Fluids/physiology , Homeostasis/physiology , Neural Pathways/physiology , Neurosecretion/physiology , Neurotransmitter Agents/physiology , Signal Transduction/physiology , Brain Mapping , Osmolar ConcentrationABSTRACT
The cortical layer 1 contains mainly small interneurons, which have traditionally been classified according to their axonal morphology. The dendritic morphology of these cells, however, has received little attention and remains ill defined. Very little is known about how the dendritic morphology and spatial distribution of these cells may relate to functional neuronal properties. We used biocytin labeling and whole cell patch clamp recordings, associated with digital reconstruction and quantitative morphological analysis, to assess correlations between dendritic morphology, spatial distribution and membrane properties of rat layer 1 neurons. A total of 106 cells were recorded, labeled and subjected to morphological analysis. Based on the quantitative patterns of their dendritic arbor, cells were divided into four major morphotypes: horizontal, radial, ascendant, and descendant cells. Descendant cells exhibited a highly distinct spatial distribution in relation to other morphotypes, suggesting that they may have a distinct function in these cortical circuits. A significant difference was also found in the distribution of firing patterns between each morphotype and between the neuronal populations of each sublayer. Passive membrane properties were, however, statistically homogeneous among all subgroups. We speculate that the differences observed in active membrane properties might be related to differences in the synaptic input of specific types of afferent fibers and to differences in the computational roles of each morphotype in layer 1 circuits. Our findings provide new insights into dendritic morphology and neuronal spatial distribution in layer 1 circuits, indicating that variations in these properties may be correlated with distinct physiological functions.
Subject(s)
Animals , Rats , Action Potentials/physiology , Cell Size , Interneurons/cytology , Neurons/cytology , Neurons/physiology , Synaptic Transmission/physiology , Dendrites/physiology , Neural Pathways/cytology , Neural Pathways/physiology , Synapses/physiologyABSTRACT
Classical Pavlovian fear conditioning to painful stimuli has provided the generally accepted view of a core system centered in the central amygdala to organize fear responses. Ethologically based models using other sources of threat likely to be expected in a natural environment, such as predators or aggressive dominant conspecifics, have challenged this concept of a unitary core circuit for fear processing. We discuss here what the ethologically based models have told us about the neural systems organizing fear responses. We explored the concept that parallel paths process different classes of threats, and that these different paths influence distinct regions in the periaqueductal gray - a critical element for the organization of all kinds of fear responses. Despite this parallel processing of different kinds of threats, we have discussed an interesting emerging view that common cortical-hippocampal-amygdalar paths seem to be engaged in fear conditioning to painful stimuli, to predators and, perhaps, to aggressive dominant conspecifics as well. Overall, the aim of this review is to bring into focus a more global and comprehensive view of the systems organizing fear responses.
Subject(s)
Animals , Amygdala/physiology , Anxiety/physiopathology , Conditioning, Psychological/physiology , Fear/physiology , Periaqueductal Gray/physiology , Anxiety/psychology , Disease Models, Animal , Fear/psychology , Models, Neurological , Neural Pathways/physiologyABSTRACT
OBJECTIVE: Resting-state networks (RSNs), including the default mode network (DMN), have been considered as markers of brain status such as consciousness, developmental change, and treatment effects. The consistency of functional connectivity among RSNs has not been fully explored, especially among resting-state-related independent components (RSICs). MATERIALS AND METHODS: This resting-state fMRI study addressed the consistency of functional connectivity among RSICs as well as their spatial consistency between 'at day 1' and 'after 4 weeks' in 13 healthy volunteers. RESULTS: We found that most RSICs, especially the DMN, are reproducible across time, whereas some RSICs were variable in either their spatial characteristics or their functional connectivity. Relatively low spatial consistency was found in the basal ganglia, a parietal region of left frontoparietal network, and the supplementary motor area. The functional connectivity between two independent components, the bilateral angular/supramarginal gyri/intraparietal lobule and bilateral middle temporal/occipital gyri, was decreased across time regardless of the correlation analysis method employed, (Pearson's or partial correlation). CONCLUSION: RSICs showing variable consistency are different between spatial characteristics and functional connectivity. To understand the brain as a dynamic network, we recommend further investigation of both changes in the activation of specific regions and the modulation of functional connectivity in the brain network.
Subject(s)
Humans , Male , Young Adult , Brain/physiology , Brain Mapping , Image Processing, Computer-Assisted , Magnetic Resonance Imaging/methods , Neural Pathways/physiology , Regression Analysis , Rest/physiologyABSTRACT
Water deprivation and hypernatremia are major challenges for water and sodium homeostasis. Cellular integrity requires maintenance of water and sodium concentration within narrow limits. This regulation is obtained through engagement of multiple mechanisms and neural pathways that regulate the volume and composition of the extracellular fluid. The purpose of this short review is to summarize the literature on central neural mechanisms underlying cardiovascular, hormonal and autonomic responses to circulating volume changes, and some of the findings obtained in the last 12 years by our laboratory. We review data on neural pathways that start with afferents in the carotid body that project to medullary relays in the nucleus tractus solitarii and caudal ventrolateral medulla, which in turn project to the median preoptic nucleus in the forebrain. We also review data suggesting that noradrenergic A1 cells in the caudal ventrolateral medulla represent an essential link in neural pathways controlling extracellular fluid volume and renal sodium excretion. Finally, recent data from our laboratory suggest that these structures may also be involved in the beneficial effects of intravenous infusion of hypertonic saline on recovery from hemorrhagic shock.
Subject(s)
Humans , Blood Volume/physiology , Catecholamines/physiology , Extracellular Fluid/physiology , Medulla Oblongata/physiology , Water-Electrolyte Balance/physiology , Afferent Pathways/physiology , Aorta/innervation , Cardiovascular Physiological Phenomena , Carotid Arteries/innervation , Kidney/metabolism , Neural Pathways/physiology , Neurons/physiology , Sodium/metabolismABSTRACT
As an experimental model system, the fruit fly Drosophila melanogaster has been seminal in shaping our understanding of the circadian clockwork. The wealth of genetic tools at our disposal over the past four decades has enabled discovery of the genetic and molecular bases of circadian rhythmicity. More recently, detailed investigation leading to the anatomical, neurochemical and electrophysiological characterization of the various neuronal subgroups that comprise the circadian machinery has revealed pathways through which these neurons come together to act as a neuronal circuit. Thus the D. melanogaster circadian pacemaker circuit presents a relatively simple and attractive model for the study of neuronal circuits and their functions.
Subject(s)
Animals , Biological Clocks/physiology , Circadian Rhythm/physiology , Drosophila melanogaster/physiology , Models, Biological , Neural Pathways/physiology , Neurotransmitter Agents/pharmacologyABSTRACT
There is no consensus about the definition of self however it is traditionally associated to identity. Many researchers are searching the neural regions that process self related information. Some studies have observed an activation of midline structures during the processing of information related to self. Self perturbations are not a part of diagnostic criteria for schizophrenia, nevertheless they are implicitly considered as part of the clinical picture. Some studies have tried to determine its perturbation using psychometric tests, but there are no studies that assess the association between brain activity and the performance of schizophrenics in tasks that require self-referential evaluations. The attempt to find a neural substrate for self is polemical. However, this model could be evaluated studying if, in schizophrenic patients, the tasks related to self processing are different from normal subjects at the psychophysiological and behavioral levels. This line of research could provide new diagnostic tools for early diagnosis and prevention inpsychiatry.
Subject(s)
Humans , Ego , Neural Pathways/physiology , Personality , Schizophrenia/diagnosis , Schizophrenic Psychology , Concept Formation , Prefrontal Cortex/physiology , Schizophrenia/physiopathologyABSTRACT
The aim of the present study was to evaluate coherence measures at Theta through qEEG during the accomplishment of a specific motor task. The sample consisted of 23 healthy individuals, both sexes, with ages varying between 25 and 40 years old. All subjects were submmitted to a specific motor task of cacthing sequences of falling balls. A three-way ANOVA was employed for the statistical analysis, which demonstrated main effects for the following factors: time, block and position. However, there was no interection between the factors. A significant and generalized coherence reduction was observed during the task execution time. Coherence was also diminished at the left frontal cortex and contralateral hemisphere of the utilizing limb (comparing to the right frontal cortex). In conclusion, these findings suggest a certain specialization of the neural circuit, also according to previous investigations. The inter-coherence reduction suggests a spatial inter-electrode dependence during the task, rather than a neuronal specialization.
O objetivo do presente experimento foi avaliar medidas de coerência na banda Teta através do EEGq durante a realização de uma atividade motora. A amostra constituiu-se de 23 sujeitos saudáveis, ambos os sexos, faixa etária entre 25 e 40 anos. Os sujeitos foram submetidos à tarefa motora de apreensão seqüencial de bolas em queda livre. Para análise estatística foi realizada uma ANOVA (Three-Way) que demonstrou efeito principal para os fatores: momento, tempo e posição. Porém não houve interação entre os fatores. Uma diminuição generalizada significativa da coerência ocorreu ao longo do tempo de execução da tarefa que também se apresentou reduzida no córtex frontal esquerdo, hemisfério contralateral ao membro utilizado (em comparação com o córtex frontal direito). Em conclusão, estes achados sugerem especialização do circuito neural que estão em consonância com experimentos prévios. A diminuição da coerência inter-hemisférica sugere uma dependência espacial inter-eletrodos durante a tarefa e não uma especialização neuronal.
Subject(s)
Adult , Female , Humans , Male , Cerebral Cortex/physiology , Functional Laterality/physiology , Orientation/physiology , Psychomotor Performance/physiology , Space Perception/physiology , Electroencephalography , Neural Pathways/physiologyABSTRACT
Findings by our group have shown that the dorsolateral telencephalon of Gymnotus carapo sends efferents to the mesencephalic torus semicircularis dorsalis (TSd) and that presumably this connection is involved in the changes in electric organ discharge (EOD) and in skeletomotor responses observed following microinjections of GABA A antagonist bicuculline into this telencephalic region. Other studies have implicated the TSd or its mammalian homologue, the inferior colliculus, in defensive responses. In the present study, we explore the possible involvement of the TSd and of the GABA-ergic system in the modulation of the electric and skeletomotor displays. For this purpose, different doses of bicuculline (0.98, 0.49, 0.245, and 0.015 mM) and muscimol (15.35 mM) were microinjected (0.1 æL) in the TSd of the awake G. carapo. Microinjection of bicuculline induced dose-dependent interruptions of EOD and increased skeletomotor activity resembling defense displays. The effects of the two highest doses showed maximum values at 5 min (4.3 ± 2.7 and 3.8 ± 2.0 Hz, P < 0.05) and persisted until 10 min (11 ± 5.7 and 8.7 ± 5.2 Hz, P < 0.05). Microinjections of muscimol were ineffective. During the interruptions of EOD, the novelty response (increased frequency in response to sensory novelties) induced by an electric stimulus delivered by a pair of electrodes placed in the water of the experimental cuvette was reduced or abolished. These data suggest that the GABA-ergic mechanisms of the TSd inhibit the neural substrate of the defense reaction at this midbrain level.
Subject(s)
Animals , Behavior, Animal/physiology , Bicuculline/pharmacology , Gymnotiformes/physiology , Mesencephalon/physiology , Muscimol/pharmacology , Behavior, Animal/drug effects , Bicuculline/administration & dosage , Defense Mechanisms , Drug Interactions/physiology , Electric Stimulation , Electric Organ/drug effects , Electric Organ/physiology , GABA Agonists/pharmacology , GABA Antagonists/pharmacology , Microinjections , Mesencephalon/drug effects , Movement/drug effects , Movement/physiology , Muscimol/administration & dosage , Neural Pathways/drug effects , Neural Pathways/physiologyABSTRACT
According to the concepts of cognitive neuropsychology, there are two principal routes of reading processing: a lexical route, in which global reading of words occurs and a phonological route, responsible for the conversion of the graphemes into their respective phonemes. In the present study, functional magnetic resonance imaging (fMRI) was used to investigate the patterns of cerebral activation in lexical and phonological reading by 13 healthy women with a formal educational level greater than 11 years. Participants were submitted to a silent reading task containing three types of stimuli: real words (irregular and foreign words), nonwords and illegitimate graphic stimuli. An increased number of activated voxels were identified by fMRI in the word reading (lexical processing) than in the nonword reading (phonological processing) task. In word reading, activation was greater than for nonwords in the following areas: superior, middle and inferior frontal gyri, and bilateral superior temporal gyrus, right cerebellum and the left precentral gyrus, as indicated by fMRI. In the reading of nonwords, the activation was predominant in the right cerebellum and in the left superior temporal gyrus. The results of the present study suggest the existence of differences in the patterns of cerebral activation during lexical and phonological reading, with greater involvement of the right hemisphere in reading words than nonwords.
Subject(s)
Humans , Female , Adolescent , Adult , Brain Mapping , Language , Reading , Neural Pathways/physiology , Magnetic Resonance Imaging/methods , Brain Mapping/methodsABSTRACT
The projections of vagal brainstem neurons to the duodenal segment of the gastrointestinal tract were studied in the ferret using the WGA-HRP neurohistochemical technique. Fourteen adult ferrets with weights ranging from 800 gm to 1500 gm were used for the study. The muscular wall of the duodenum of six ferrets was injected with 0.1 ml of 5 WGA-HRP in 0.5 M sodium chloride. The eight remaining ferrets were used as controls. Two of these had injections of 0.1 ml normal saline into the muscular wall of the duodenum. The second set of two ferrets was injected with 0.1 ml of 5 WGA-HRP in buffer after bilateral truncal vagotomy. The third set of two ferrets received intraperitoneal injection of 0.1 ml of 5 WGA-HRP while, in the last set, the tracer was injected into the hepatic portal vein. Following the injections, the ferrets were allowed to survive for 48-72 hours after which each ferret was perfused transcardially first with normal saline followed by a fixative containing 1 paraformaldehyde and 1.25 glutaraldehyde in 0.1 M phosphate buffer, pH 7.4 at room temperature and finally with 10 buffered sucrose at 4 degrees C. Transverse serial frozen sections of the brainstem were then taken and processed for WGA-HRP neurohistochemistry and were analyzed under light and dark-field illuminations. The analyses of the sections taken from the six ferrets injected with WGA-HRP revealed neurons labelled with the tracer in the dorsal motor nucleus of the vagus nerve (DMNV). Sections taken from the control ferrets did not reveal any WGA-HRP labelled neurons in the brainstem
Subject(s)
Animals , Male , Female , Duodenum/drug effects , Duodenum/innervation , Autonomic Fibers, Preganglionic/drug effects , Autonomic Fibers, Preganglionic/physiology , Neurons/drug effects , Neurons/physiology , Parasympathetic Nervous System/drug effects , Parasympathetic Nervous System/physiology , Molecular Probes/pharmacology , Models, Animal , Wheat Germ Agglutinin-Horseradish Peroxidase Conjugate , Vagus Nerve/drug effects , Vagus Nerve/physiology , Molecular Probes/pharmacokinetics , Biological Transport/physiology , Neural Pathways/physiologyABSTRACT
Analysis of corpus callosum fiber composition reveals that inter-hemispheric transmission time may put constraints on the development of inter-hemispheric synchronic ensembles, especially in species with large brains like humans. In order to overcome this limitation, a subset of large-diameter callosal fibers are specialized for fast inter-hemispheric transmission, particularly in large-brained species. Nevertheless, the constraints on fast inter-hemispheric communication in large-brained species can somehow contribute to the development of ipsilateral, intrahemispheric networks, which might promote the development of brain lateralization.
Subject(s)
Humans , Visual Fields/physiology , Brain/anatomy & histology , Brain/physiology , Functional Laterality/physiology , Visual Pathways/physiology , Axons/physiology , Corpus Callosum/anatomy & histology , Corpus Callosum/physiology , Neural Pathways/physiologySubject(s)
Brain/physiology , Color Perception , Color Perception Tests , Consciousness , Female , Humans , Language , Male , Neural Pathways/physiology , Perception/physiology , Sensation/physiology , Visual PerceptionSubject(s)
Humans , Pain , Bolivia , Central Nervous System/physiology , Neurons, Afferent/physiology , Neural Pathways/physiologyABSTRACT
1. The caudal pressor area (CPA) is a recently identified site within the ventrolateral medulla which is involved in cardiovascular regulation. CPA chemical stimulation by L-glutamate produces an increase in arterial blood pressure (ABP) while its inhibition by GABA or glycine evokes marked hypotension. In the present study, we sought to determine the potential neural pathways underlyng these responses. 2. In urethane-anesthetized, paralyzed, artificially ventilated rats, CPA inhibition by bilateral microinjection of the inhibitory amino acid glycine (Gly, 100 nmol 200 nl-1 site-1) produced an average decrease of -38 + or - 4.3 mmHg in ABP (n = 6). Ten min after bilateral microinjection of the broad-spectrum glutamate antagonist kynurenic acid (KYN, 2 nmol 200 nl-1 site-1) into the cauldal ventrolateral medulla (CVLM) depressor responses to CPA inhibition were virtually abolished (-3 + or - 1.7 mmHg, P<0.05). Similar microinjection of KYN into the rostral ventrolateral medulla (RVLM) or into the CPA itself did not modify depressor responses to CPA inhibiton by glycine. 3. CPA stimulation by bilateral microinjection of the excitatory amino acid L-glutamate (L-glu, 50 nmol 200 nl-1 site-1) produced an increase in ABP (+43 + or - 5.4 mmHg, N= 6). Bilateral microinjection of the GABA A antagonist bicuculline methiodide (BIC, 200 pmol 200 nl-1 site-1) into the CVLM markedly reduced pressor responses to CPA stimulation (+6 + or - 2.7 mmHg, P<0.05). Similar application of BIC into the RVLM or CPA did not modify pressor responses to CPA stimulation by glutamic acid