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Analysis. --- Brain. --- Cortex. --- Frontal cortex. --- Frontal-cortex. --- Frontal. --- Limbic system. --- Neuropsychology. --- Prelimbic. --- Rat. --- System.
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Brain. --- Dog. --- Dogs. --- Frontal cortex. --- Functional imaging. --- Receptor. --- Receptors. --- Serotonin.
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This eBook is a collection of articles from a Frontiers Research Topic. Frontiers Research Topics are very popular trademarks of the Frontiers Journals Series: they are collections of at least ten articles, all centered on a particular subject. With their unique mix of varied contributions from Original Research to Review Articles, Frontiers Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author by contacting the Frontiers Editorial Office: frontiersin.org/about/contact
Cognition --- stress --- Motivation --- Behavior --- decision-making --- pre-frontal cortex
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Accumbens. --- Cortex. --- Expression. --- Fear. --- Frontal cortex. --- Frontal-cortex. --- Frontal. --- Memory. --- Nucleus accumbens. --- Nucleus-accumbens. --- Nucleus. --- Rat. --- Zif268.
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This eBook is a collection of articles from a Frontiers Research Topic. Frontiers Research Topics are very popular trademarks of the Frontiers Journals Series: they are collections of at least ten articles, all centered on a particular subject. With their unique mix of varied contributions from Original Research to Review Articles, Frontiers Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author by contacting the Frontiers Editorial Office: frontiersin.org/about/contact
Science: general issues --- Neurosciences --- Cognition --- stress --- Motivation --- Behavior --- decision-making --- pre-frontal cortex --- Cognition --- stress --- Motivation --- Behavior --- decision-making --- pre-frontal cortex
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This eBook is a collection of articles from a Frontiers Research Topic. Frontiers Research Topics are very popular trademarks of the Frontiers Journals Series: they are collections of at least ten articles, all centered on a particular subject. With their unique mix of varied contributions from Original Research to Review Articles, Frontiers Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author by contacting the Frontiers Editorial Office: frontiersin.org/about/contact
Science: general issues --- Neurosciences --- Cognition --- stress --- Motivation --- Behavior --- decision-making --- pre-frontal cortex
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Studies of the brain inform us about the cognitive abilities of animals and hence affect the extent to which animals of that species are respected However, they can also tell us how an individual is likely to be perceiving, attending to, evaluating, coping with, enjoying, or disturbed by its environment, and so can give direct information about welfare. In studies of welfare, we are especially interested in how an individual feels. Since this depends upon high-level brain processing, we have to investigate brain function. Brain correlates of preferred social, sexual and parental situations include elevated oxytocin in the para-ventricular nucleus of the hypothalamus. Abnormal behaviour may have brain correlates, for example, high frequencies of stereotypy are associated with down-regulated P and kappa receptors and dopamine depletion in the frontal cortex. Such results help in evaluating the effects of treatment on welfare. Some brain changes, such as increased glucocorticoid receptors in the frontal lobes or increased activity in the amygdala, may be a sensitive indicator of perceived emergency. Active immunological defences lead to cytokine production in the brain, vagal nerve activity and sickness effects. Some aspects of brain function can be temporarily suppressed, for example, by opioids when there is severe pain, or permanently impaired, for example, in severely impoverished environments or during depression. Coping attempts or environmental impact can lead to injury to the brain, damage to hippocampal neurons, remodelling of dendrites in the hippocampus, or to other brain disorganisation. Brain measures can explain the nature and magnitude of many effects on welfare
Ability. --- Abnormal behaviour,adrenal,animal welfare,brain measures,coping,opioids. --- Abnormal behaviour. --- Activity. --- Amygdala. --- Animal welfare. --- Animal-welfare. --- Animal. --- Animals. --- Behavior. --- Behaviour. --- Brain. --- Cognitive-ability. --- Coping. --- Cortex. --- Damage. --- Depression. --- Dopamine. --- Emergency. --- Environment. --- Environments. --- Frequency. --- Frontal cortex. --- Frontal lobes. --- Frontal-cortex. --- Frontal. --- Function. --- Glucocorticoid receptors. --- Glucocorticoid. --- Hippocampal-neurons. --- Hippocampal. --- Hippocampus. --- Hypothalamus. --- Impoverished. --- Injuries. --- Injury. --- Neurons. --- Nucleus. --- Opioid. --- Opioids. --- Oxytocin. --- Pain. --- Paraventricular nucleus. --- Production. --- Receptor. --- Receptors. --- Responses. --- Sexual. --- Sheep. --- Situations. --- Social. --- Sows. --- Stereotypies. --- Stereotypy. --- Stress. --- Systems. --- Treatment. --- Us. --- Welfare.
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The present study evaluated whether environmental enrichment-related effects on the development of stereotyped behavior in deer mice were associated with alterations in neurotrophin levels. Deer mice were reared in enriched or standard cage conditions for 60 days. The mice were then tested in automated photocell detectors and classified as either stereotypic or nonstereotypic. This testing paradigm yielded four behaviorally distinct groups: enriched stereotypic, enriched nonstereotypic, standard cage stereotypic, and standard cage nonstereotypic. The motor cortex, striatum, and hippocampus were dissected, and the levels of brain-derived neurotrophin factor (BDNF) and nerve growth factor (NGF) in each brain region were analyzed using Promega ELISA kits. There were no differences in either NGF or BDNF in either the motor cortex or the hippocampus. In the striatum, the enriched nonstereotypic mice exhibited significantly more BDNF than the enriched stereotypic, the standard cage nonstereotypic, or the standard cage stereotypic mice. There were no differences in NGF in the striatum. These results provide evidence that the enrichment-related prevention of stereotyped behavior in deer mice is associated with increased BDNF in the striatum. (C) 2003 Elsevier Inc. All rights reserved
Bank voles. --- Behavior. --- Brain. --- Cage. --- Complex environment. --- Cortex. --- Deer mice,stereotypy,enriched,ngf,bdnf,elisa. --- Deer mice. --- Deer. --- Development. --- Elisa. --- Enriched. --- Enrichment. --- Environmental enrichment. --- Frontal-cortex. --- Group. --- Growth. --- Hippocampus. --- Induced jumping stereotypy. --- Laboratory mice. --- Level. --- Mental-retardation. --- Messenger-rna. --- Mice. --- Ngf. --- Prevention. --- Rat-brain. --- Sex-differences. --- Stereotyped behavior. --- Stereotypic. --- Striatum.
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We evaluated whether environmental enrichment-related effects on the development of stereotyped behavior in deer mice were associated with alterations in dendritic morphology. Deer mice were reared under enriched or standard housing conditions and then tested in automated photocell detectors and classified as stereotypic or nonstereotypic. Dendritic morphology was assessed in layer V pyramidal neurons of the motor cortex, medium spiny neurons of the dorsolateral striatum, and granule cells of the dentate gyrus using Golgi-Cox histochemistry. Enriched nonstereotypic mice exhibited significantly higher dendritic spine densities in the motor cortex and the striatum than enriched stereotypic or standard-cage mice. Significant increases in dendritic arborization following environmental enrichment also were observed. These results suggest that the enrichment-related prevention of stereotyped behavior is associated with increased dendritic spine density. (C) 2003 Wiley Periodicals, Inc
Amphetamine. --- Bank voles. --- Behavior. --- Complex environments. --- Cortex. --- Deer mice. --- Deer. --- Density. --- Dentate gyrus. --- Development. --- Differential experience. --- Enriched. --- Enrichment. --- Environmental enrichment. --- Frontal-cortex. --- Golgi-cox,repetitive behavior,deer mice,brain. --- Housing conditions. --- Housing. --- Increase. --- Increases. --- Mice. --- Morphology. --- Neurons. --- Plasticity. --- Prevention. --- Rat-brain. --- Sex-differences. --- Stereotyped behavior. --- Stereotypic. --- Striatum.
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The present study aimed to determine whether the medial prefrontal cortex (mPFC) (prelimbic and infralimbic regions) is implicated in the integration of a stress response. Sprague-Dawely rats were implanted with telemetry probes and guide cannulae so that either muscimol or vehicle could be administered locally within the mPFC or dorsomedial hypothalamus (DMH). The heart rate and blood pressure of rats was continuously recorded as either muscimol or vehicle was administered centrally and rats were either exposed to restraint stress or left alone in their home cages. After the stress challenge, or equivalent period, rats that had received intra-mPFC injections were processed for immunohistochemical detection of Fos throughout the neuraxis. Bilateral microinjection of muscimol into the mPFC had no effect upon either baseline cardiovascular parameters or restraint stress-induced tachycardia or pressor responses whereas, in the DMH, pretreatment with muscimol attenuated the cardiovascular stress response. Analysis of Fos expression throughout the CNS of nonstressed rats showed no effect of muscimol injections into the mPFC on baseline expression in the nuclei examined. In contrast, rats that had received muscimol injections into their mPFC and were subsequently restrained exhibited an increase in the number of Fos-positive cells in the DMH, medial amygdala, and medial nucleus tractus solitarius as compared to vehicle-injected rats that experienced restraint stress. These results indicate that, during acute psychological stress, the mPFC does not modulate the cardiovascular system in rats but does inhibit specific subcortical nuclei to exert control over aspects of an integrated response to a stressor
Amygdala. --- Analysis. --- Blood pressure. --- Blood-pressure. --- Blood. --- C-fos expression. --- Cage. --- Cages. --- Cardiovascular system. --- Cardiovascular-system. --- Cardiovascular. --- Cingulate cortex. --- Control. --- Cortex. --- Dorsomedial hypothalamus. --- Excitotoxic lesions. --- Expression. --- Fos. --- Frontal-cortex. --- Heart rate. --- Heart-rate. --- Hypothalamus. --- Increase. --- Infralimbic cortex. --- Infralimbic. --- Injections. --- Medial amygdala. --- Medial prefrontal cortex. --- Microinjection. --- Norepinephrine release. --- Nucleus tractus solitarius. --- Nucleus-accumbens. --- Nucleus. --- Parameters. --- Prefrontal cortex. --- Prelimbic. --- Psychological stress. --- Rat. --- Rats. --- Response. --- Responses. --- Restraint stress. --- Restraint. --- Stress response. --- Stress-response. --- Stress. --- Stressor. --- System. --- Tachycardia. --- Telemetry. --- Time.
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