25 research outputs found

    The first forum on the neurobiology of stress

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    Involvement of GABAergic mechanisms of the dorsal periaqueductal gray and inferior colliculus on unconditioned fear

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    The fact that the dorsal periaqueductal gray (dPAG) and inferior colliculus (IC), together with superior colliculus, medial hypothalamus and amygdala, constitute the brain aversion system has been well-established. Stepwise increases in the intensity of electrical stimulation of dPAG or IC cause freezing and escape responses, which are followed by a freezing behavior that lasts after the interruption of the stimulation. Freezing and escape are unconditioned defensive behaviors derived from the stimulation of the output centers for the defense reaction, whereas the post-stimulation freezing is the behavioral counterpart of the processing of aversive information. Although GABA-A mechanisms of the midbrain tectum exert a tonic inhibitory influence on the neural substrates of unconditioned fear, their influence on the processing of aversive information is not completely understood. Thus, the present study examines the effects of injections of the GABA-A receptor agonist muscimol (1 and 2 nmol/0.2 µL) or the glutamic acid decarboxylase blocker semicarbazide (5 and 7.5 µg/0.2 µL) into dPAG or IC of Wistar rats on freezing and escape thresholds determined by electrical stimulation of these same structures and on post-stimulation freezing. Intra-dPAG injections of muscimol increased and semicarbazide decreased the freezing and escape thresholds of electrical stimulation of the dPAG. Only semicarbazide enhanced the dPAG post-stimulation freezing. Intra-IC injections of muscimol significantly increased aversive thresholds, while having no effect on IC post-stimulation freezing. Intra-IC injections of semicarbazide had no significant effects. These findings suggest that GABAergic mechanisms are important regulators of the expression of unconditioned fear in dPAG and IC, whereas only in dPAG GABA appears to play a role on the sensory gating towards aversive information during post-stimulation freezing.FAPESPCNP

    Dual role of dopamine D2-like receptors in the mediation of conditioned and unconditioned fear

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    AbstractA reduction of dopamine release or D2 receptor blockade in the terminal fields of the mesolimbic system, particularly the amygdala, clearly reduces conditioned fear. Similar D2 receptor antagonism in the neural substrates of fear in the midbrain tectum attenuates the processing of unconditioned aversive information. However, the implications of the interplay between opposing actions of dopamine in the rostral and caudal segments of the dopaminergic system are still unclear. Previous studies from this laboratory have reported the effects of dopaminergic drugs on behavior in rats in the elevated plus maze, auditory-evoked potentials (AEPs) recorded from the midbrain tectum, fear-potentiated startle, and conditioned freezing. These findings led to an interesting framework on the functional roles of dopamine in both anxiety and fear states. Dopamine D2 receptor inhibition in the terminal fields of the mesolimbic dopamine system generally causes anxiolytic-like effects, whereas the activity of midbrain substrates of unconditioned fear are enhanced by D2 receptor antagonists, suggesting that D2 receptor-mediated mechanisms play opposing roles in fear/anxiety processes, depending on the brain region under study. Dopamine appears to mediate conditioned fear by acting at rostral levels of the brain and regulate unconditioned fear at the midbrain level, likely by reducing the sensorimotor gating of aversive events

    Padrões de respostas defensivas de congelamento associados a diferentes transtornos de ansiedade

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    Bien que les troubles anxieux soient propres aux humains, il est possible d'établir un parallèle entre ces troubles et les réponses défensives que les animaux présentent lorsqu'ils sont confrontés à des situations dangereuses. Dans cet article, une série d'arguments est présentée indiquant que différents patterns d'immobilisation défensive sont associés avec des troubles anxieux spécifiques. En particulier, il y a un excellent isomorphisme entre la réponse d'immobilisation aux stimuli contextuels aversives et le trouble d'anxiété généralisée. De plus, le comportement d'immobilisation déclenché directement par la stimulation de la substance grise périaqueducale dorsale (dPAG) est un excellent modèle animal d'attaque de panique. D'autre part, la réponse d'immobilisation observée après interruption de la stimulation électrique du dPAG semble associée avec le trouble panique. Finalement, l'hypothèse est proposée que l'immobilisation déclenchée par les stimuli contextuels précédemment associés avec la stimulation électrique du dPAG pourrait être mise en parallèle avec le trouble panique avec agoraphobie.Although anxiety disorders are exclusive to humans, it is possible to find correlation between these disorders and defensive responses that animals present when facing dangerous situations. The present article presents a series of evidence that indicate that different freezing defensive patterns might be associated with specific anxiety disorders. Particularly, there is an excellent isomorphism between freeing response to contextual stimuli associated with electrical shocks and generalized anxiety disorder. Much evidence also shows that freezing response triggered directly through the electrical stimulation of the dorsal periaqueductal gray matter (dPAG) is an excellent animal model of panic attack. Moreover, freezing response observed after the interruption of the electrical stimulation of the dPAG which triggers an escape response seems to be associated with panic disorder. Finally, it is hypothesized that freezing to contextual stimuli previously associated with intense electrical stimulation of the dPAG might be related to panic disorder with agoraphobia.Embora os transtornos de ansiedade sejam tipicamente humanos, eles apresentam correlações com determinadas reações de defesa de animais em situações de perigo. Este trabalho apresenta algumas relações entre determinados padrões da resposta defensiva de congelamento e diferentes formas de transtornos de ansiedade. Em particular, destaca-se o isomorfismo entre a resposta de congelamento a estímulos contextuais associados a um estímulo aversivo e o transtorno de ansiedade generalizado. Evidências indicam também que a resposta de congelamento induzida pela estimulação elétrica da matéria cinzenta periaqueductal dorsal (MCPD) constitui um excelente modelo animal de ataque de pânico. A resposta de congelamento que surge imediatamente após estimulação da MCPD, capaz de produzir uma resposta de fuga, parece estar associada ao transtorno de pânico. Finalmente, é possível que a resposta de congelamento a estímulos previamente associados à estimulação elétrica da MCPD seja um modelo animal para o transtorno de pânico com agorafobia

    High-Throughput Analysis of Synthetic Peptides for the Immunodiagnosis of Canine Visceral Leishmaniasis

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    Globally, the number of new human cases of visceral leishmaniasis (VL) is estimated to be approximately 500,000 per year. This is the most severe of all forms of leishmaniasis, and the zoonotic form of VL, caused by Leishmania infantum (also known as Leishmania chagasi), represents 20% of human visceral leishmaniasis worldwide; additionally, its prevalence is increasing in urban and peri-urban areas of the tropics. In Brazil, the identification and elimination of infected dogs, which act as a reservoir for Leishmania parasites, is a control measure employed in addition to the use of insecticides against the vectors and the identification and treatment of infected humans. Currently, the diagnostic methods employed to identify infected animals are not able to detect all of these dogs, which compromises the effectiveness of control measures. Moreover, one of the most important issues in controlling VL is the difficulty of diagnosing asymptomatic dogs, which act as parasite reservoirs. Therefore, to contribute to the improvement of the diagnostic methods for CVL, we aimed to identify and characterize new antigens that were more sensitive and specific and could be applied in epidemiologic surveys

    Introduction to III Forum on the Neurobiology of Stress, Araraquara, SP, Brazil, September 8-10, 2011

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    The First Forum on the Neurobiology of Stress.

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