RÉSUMÉ
The escape response to electrical or chemical stimulation of the dorsal periaqueductal gray matter (DPAG) has been associated with panic attacks. In order to explore the validity of the DPAG stimulation model for the study of panic disorder, we determined if the aversive consequences of the electrical or chemical stimulation of this midbrain area can be detected subsequently in the elevated T-maze. This animal model, derived from the elevated plus-maze, permits the measurement in the same rat of a generalized anxiety- and a panic-related defensive response, i.e., inhibitory avoidance and escape, respectively. Facilitation of inhibitory avoidance, suggesting an anxiogenic effect, was detected in male Wistar rats (200-220 g) tested in the elevated T-maze 30 min after DPAG electrical stimulation (current generated by a sine-wave stimulator, frequency at 60 Hz) or after local microinjection of the GABA A receptor antagonist bicuculline (5 pmol). Previous electrical (5, 15, 30 min, or 24 h before testing) or chemical stimulation of this midbrain area did not affect escape performance in the elevated T-maze or locomotion in an open-field. No change in the two behavioral tasks measured by the elevated T-maze was observed after repetitive (3 trials) electrical stimulation of the DPAG. The results indicate that activation of the DPAG caused a short-lived, but selective, increase in defensive behaviors associated with generalized anxiety.
Sujet(s)
Animaux , Mâle , Rats , Anxiété/physiopathologie , Comportement animal/effets des médicaments et des substances chimiques , Réaction de fuite/effets des médicaments et des substances chimiques , Trouble panique/physiopathologie , Substance grise centrale du mésencéphale/effets des médicaments et des substances chimiques , Comportement animal/physiologie , Bicuculline/pharmacologie , Électrodes implantées , Réaction de fuite/physiologie , Apprentissage du labyrinthe/effets des médicaments et des substances chimiques , Apprentissage du labyrinthe/physiologie , Substance grise centrale du mésencéphale/physiologie , Rat WistarRÉSUMÉ
Electrical stimulation of midbrain tectum structures, particularly the dorsal periaqueductal gray (dPAG) and inferior colliculus (IC), produces defensive responses, such as freezing and escape behavior. Freezing also ensues after termination of dPAG stimulation (post-stimulation freezing). These defensive reaction responses are critically mediated by γ-aminobutyric acid and 5-hydroxytryptamine mechanisms in the midbrain tectum. Neurokinins (NKs) also play a role in the mediation of dPAG stimulation-evoked fear, but how NK receptors are involved in the global processing and expression of fear at the level of the midbrain tectum is yet unclear. The present study investigated the role of NK-1 receptors in unconditioned defensive behavior induced by electrical stimulation of the dPAG and IC of male Wistar rats. Spantide (100 pmol/0.2 μL), a selective NK-1 antagonist, injected into these midbrain structures had anti-aversive effects on defensive responses and distress ultrasonic vocalizations induced by stimulation of the dPAG but not of the IC. Moreover, intra-dPAG injections of spantide did not influence post-stimulation freezing or alter exploratory behavior in rats subjected to the elevated plus maze. These results suggest that NK-1 receptors are mainly involved in the mediation of defensive behavior organized in the dPAG. Dorsal periaqueductal gray-evoked post-stimulation freezing was not affected by intra-dPAG injections of spantide, suggesting that NK-1-mediated mechanisms are only involved in the output mechanisms of defensive behavior and not involved in the processing of ascending aversive information from the dPAG.
Sujet(s)
Animaux , Mâle , Rats , Anxiété/physiopathologie , Réaction de fuite/physiologie , Peur/physiologie , Colliculus inférieurs/effets des médicaments et des substances chimiques , Neurokinine A/pharmacologie , Substance grise centrale du mésencéphale/effets des médicaments et des substances chimiques , Récepteur de la neurokinine 1/antagonistes et inhibiteurs , Substance P/analogues et dérivés , Apprentissage par évitement , Stimulation électrique , Colliculus inférieurs/physiologie , Substance grise centrale du mésencéphale/physiologie , Rat Wistar , Substance P/pharmacologie , Vocalisation animaleRÉSUMÉ
The hypothalamus is a forebrain structure critically involved in the organization of defensive responses to aversive stimuli. Gamma-aminobutyric acid (GABA)ergic dysfunction in dorsomedial and posterior hypothalamic nuclei is implicated in the origin of panic-like defensive behavior, as well as in pain modulation. The present study was conducted to test the difference between these two hypothalamic nuclei regarding defensive and antinociceptive mechanisms. Thus, the GABA A antagonist bicuculline (40 ng/0.2 µL) or saline (0.9% NaCl) was microinjected into the dorsomedial or posterior hypothalamus in independent groups. Innate fear-induced responses characterized by defensive attention, defensive immobility and elaborate escape behavior were evoked by hypothalamic blockade of GABA A receptors. Fear-induced defensive behavior organized by the posterior hypothalamus was more intense than that organized by dorsomedial hypothalamic nuclei. Escape behavior elicited by GABA A receptor blockade in both the dorsomedial and posterior hypothalamus was followed by an increase in nociceptive threshold. Interestingly, there was no difference in the intensity or in the duration of fear-induced antinociception shown by each hypothalamic division presently investigated. The present study showed that GABAergic dysfunction in nuclei of both the dorsomedial and posterior hypothalamus elicit panic attack-like defensive responses followed by fear-induced antinociception, although the innate fear-induced behavior originates differently in the posterior hypothalamus in comparison to the activity of medial hypothalamic subdivisions.
Sujet(s)
Animaux , Mâle , Rats , Noyau hypothalamique dorsomédial/physiologie , Réaction de fuite/physiologie , Hypothalamus postérieur/physiologie , Trouble panique/métabolisme , Bicuculline/pharmacologie , Noyau hypothalamique dorsomédial/effets des médicaments et des substances chimiques , Antagonistes du récepteur GABA-A/pharmacologie , Hypothalamus postérieur/effets des médicaments et des substances chimiques , Apprentissage du labyrinthe , Seuil nociceptif/effets des médicaments et des substances chimiques , Trouble panique/étiologieRÉSUMÉ
This paper presents an up-to-date review of the evidence indicating that atypical neurotransmitters such as nitric oxide (NO) and endocannabinoids (eCBs) play an important role in the regulation of aversive responses in the periaqueductal gray (PAG). Among the results supporting this role, several studies have shown that inhibitors of neuronal NO synthase or cannabinoid receptor type 1 (CB1) receptor agonists cause clear anxiolytic responses when injected into this region. The nitrergic and eCB systems can regulate the activity of classical neurotransmitters such as glutamate and γ-aminobutyric acid (GABA) that control PAG activity. We propose that they exert a ‘fine-tuning’ regulatory control of defensive responses in this area. This control, however, is probably complex, which may explain the usually bell-shaped dose-response curves observed with drugs that act on NO- or CB1-mediated neurotransmission. Even if the mechanisms responsible for this complex interaction are still poorly understood, they are beginning to be recognized. For example, activation of transient receptor potential vanilloid type-1 channel (TRPV1) receptors by anandamide seems to counteract the anxiolytic effects induced by CB1 receptor activation caused by this compound. Further studies, however, are needed to identify other mechanisms responsible for this fine-tuning effect.
Sujet(s)
Animaux , Souris , Rats , Anxiété/physiopathologie , Réaction de fuite/physiologie , Agents neuromédiateurs/physiologie , Substance grise centrale du mésencéphale/physiologie , Transmission synaptique/physiologie , Anxiété/métabolisme , Acides arachidoniques/pharmacologie , Agonistes des récepteurs de cannabinoïdes/pharmacologie , Endocannabinoïdes/pharmacologie , Endocannabinoïdes/physiologie , Monoxyde d'azote/physiologie , Substance grise centrale du mésencéphale/métabolisme , Amides gras polyinsaturés N-alkylés/pharmacologie , Canaux cationiques TRPV/physiologieRÉSUMÉ
The mammalian stress response is an integrated physiological and psychological reaction to real or perceived adversity. Glucocorticoids are an important component of this response, acting to redistribute energy resources to both optimize survival in the face of challenge and to restore homeostasis after the immediate challenge has subsided. Release of glucocorticoids is mediated by the hypothalamo-pituitary-adrenal (HPA) axis, driven by a neural signal originating in the paraventricular nucleus (PVN). Stress levels of glucocorticoids bind to glucocorticoid receptors in multiple body compartments, including the brain, and consequently have wide-reaching actions. For this reason, glucocorticoids serve a vital function in negative feedback inhibition of their own secretion. Negative feedback inhibition is mediated by a diverse collection of mechanisms, including fast, non-genomic feedback at the level of the PVN, stress-shut-off at the level of the limbic system, and attenuation of ascending excitatory input through destabilization of mRNAs encoding neuropeptide drivers of the HPA axis. In addition, there is evidence that glucocorticoids participate in stress activation via feed-forward mechanisms at the level of the amygdala. Feedback deficits are associated with numerous disease states, underscoring the necessity for adequate control of glucocorticoid homeostasis. Thus, rather than having a single, defined feedback ‘switch’, control of the stress response requires a wide-reaching feedback ‘network’ that coordinates HPA activity to suit the overall needs of multiple body systems.
Sujet(s)
Animaux , Humains , Souris , Rats , Rétrocontrôle physiologique/physiologie , Glucocorticoïdes/physiologie , Axe hypothalamohypophysaire/métabolisme , Noyau paraventriculaire de l'hypothalamus/métabolisme , Axe hypophyso-surrénalien/métabolisme , Stress physiologique/physiologie , Réaction de fuite/physiologie , Axe hypothalamohypophysaire/physiologie , Noyau paraventriculaire de l'hypothalamus/physiologie , Axe hypophyso-surrénalien/physiologieRÉSUMÉ
Escape by Anolis lizards is influenced by microhabitats and fight initiation distance increases with predation risk. Differences in microhabitat use among ecomorphs affect escape behavior, but only two studies have reported ecomorphological differences in flight initiation distance among Greater Antillean species. I studied effects of predation risk and microhabitats on escape behavior by conducting field experiments using two species of anoles, Anolis lineatopus and A. grahami, on the campus of the University of the West Indies at Mona, Jamaica. Because ecomorphological variation of anoles has evolved independently within each island of the Greater Antilles, but relationships between ecomorphs and escape behaviors are poorly known, I characterized microhabitat use and escape tactics, and determined relationships between flight initiation distance and two risk factors, habituation to human presence and perch height, in Anolis lineatopus, a trunk-ground anole and A. grahami, a trunk-crown anole. Sample sizes for A. lineatopus and A. grahami were 214 and 93, for microhabitat use and escape destinations, 74 and 34 for human presence and 125 and 34 for perch height. The two species occurred in similar microhabitats and exhibited similar escape tactics, but exhibited key differences expected for their ecomorphs. Both species were sighted frequently on the ground and on trees, but A. lineatopus were more frequently on ground and were perched lower than A. grahami. Both species escaped from ground to trees and when on trees hid on far sides and escaped without changing climbing direction with equal frequency. The frequency of fleeing upward was greater for A. grahami than A. lineatopus. Both species exhibited habituation by having shorter flight initiation distances in areas with more frequent exposure to people. In both species flight initiation distance increased as perch height decreased because, lizards had to climb farther to be out of reach when perched lower. The relationship between flight initiation distance and perch height may apply to other anole ecomorphs that flee upward when low perched on trees. Rev. Biol. Trop. 58 (4): 1199-1209. Epub 2010 December 01.
El escape de las largarijas Anolis está influenciado por el microhábitat y la distancia de iniciación de escape incrementa el riesgo de depredación. Las diferencias en el uso de microhábitats entre ecomorfos afecta el comportamiento de escape, pero sólo dos estudios han reportado diferencias ecomorfológicas en la distancia de iniciación de escape entre las especies de las Antillas Mayores. Se estudió el efecto de riesgo de depredación y la influencia del microhábitat en el comportamiento de escape, mediante la realización de experimentos de campo con Anolis lineatopus y A. grahami, en el campus de la Universidad West Indies en Mona, Jamaica. Debido a que las variaciones ecomorfológicas de Anolis han evolucionado independientemente en cada isla de las Antillas Mayores, la relación entre ecomorfos y el comportamiento de escape son pobremente conocidos. Se caracteriza el uso del microhábitat y las tácticas de escape, se determinan las relaciones entre la distancia de iniciación de escape y los dos factores de riesgo (habituación a presencia humana y altura a la que se posan) de Anolis lineatopus, una lagartija que habita en troncos-tierra y A. grahami, una lagartija de troncos-partes más altas. Los tamaños de muestra para A. lineatopus y A. grahami fueron: 214 y 93, para uso del microhábitat y destinos de escape 74, para presencia humana 34 y para perchas altas 125 y 34. Las dos especies se presentan en microhábitats similares y mostraron tácticas de escape parecidas, pero exhibieron diferencias claves esperadas para sus ecomorfos. Ambas especies fueron vistas con frecuencia en el suelo y en los árboles, pero A. lineatopus fue encontrada más frecuentemente en el suelo y debajo de A. grahami. Ambas especies escaparon del suelo a esconderse en los árboles y huían con igual frecuencia sin cambiar de dirección. La frecuencia de huir hacia arriba fue mayor para A grahami. Ambas especies mostraron habituación al tener distancias más cortas de iniciación de escape en zonas con exposición frecuente a la gente y la distancia de iniciación de escape incrementa cuando la altura de la percha disminuye, porque las lagartijas tienden a subir más al estar fuera de nuestro alcance cuando se posan en la parte baja. La relación entre la distancia de iniciación de escape y altura de la percha puede aplicar a otros ecomorfos de Anolis que huyen hacia arriba cuando están posados en las partes bajas de los árboles.
Sujet(s)
Animaux , Humains , Écosystème , Réaction de fuite/physiologie , Lézards/physiologie , Jamaïque , Comportement prédateur , Spécificité d'espèceRÉSUMÉ
A former study with scenarios conducted in Hawaii has suggested that humans share with non-human mammals the same basic defensive strategies - risk assessment, freezing, defensive threat, defensive attack, and flight. The selection of the most adaptive strategy is strongly influenced by features of the threat stimulus - magnitude, escapability, distance, ambiguity, and availability of a hiding place. Aiming at verifying if these strategies would be consistent in a different culture, 12 defensive scenarios were translated into Portuguese and adapted to the Brazilian culture. The sample consisted of male and female undergraduate students divided into two groups: 76 students, who evaluated the five dimensions of each scenario and 248 medical students, who chose the most likely response for each scenario. In agreement with the findings from studies of non-human mammal species, the scenarios were able to elicit different defensive behavioral responses, depending on features of the threat. "Flight" was chosen as the most likely response in scenarios evaluated as an unambiguous and intense threat, but with an available route of escape, whereas "attack" was chosen in an unambiguous, intense and close dangerous situation without an escape route. Less urgent behaviors, such as "check out", were chosen in scenarios evaluated as less intense, more distant and more ambiguous. Moreover, the results from the Brazilian sample were similar to the results obtained in the original study with Hawaiian students. These data suggest that a basic repertoire of defensive strategies is conserved along the mammalian evolution because they share similar functional benefits in maintaining fitness.
Sujet(s)
Adolescent , Adulte , Femelle , Humains , Mâle , Anxiété/psychologie , Évolution biologique , Mécanismes de défense , Peur/psychologie , Étudiants/psychologie , Agressivité , Analyse de variance , Brésil , Réaction de fuite/physiologie , Hawaï , Réaction d'immobilité tonique/physiologie , Appréciation des risques , Enquêtes et questionnaires , Traduction , Population urbaineRÉSUMÉ
The learned helplessness (LH) paradigm is characterized by learning deficits resulting from inescapable events. The aims of the present study were to determine if protein-calorie malnutrition (PCM) alters learning deficits induced by LH and if the neurochemical changes induced by malnutrition alter the reactivity to treatment with GABA-ergic and serotonergic drugs during LH. Well-nourished (W) and PCM Wistar rats (61 days old) were exposed or not to inescapable shocks (IS) and treated with gepirone (GEP, 0.0-7.5 mg/kg, intraperitoneally, N = 128) or chlordiazepoxide (0.0-7.5 mg/kg, intraperitoneally, N = 128) 72 h later, 30 min before the test session (30 trials of escape learning). The results showed that rats exposed to IS had higher escape latency than non-exposed rats (12.6 ± 2.2 vs 4.4 ± 0.8 s) and that malnutrition increased learning impairment produced by LH. GEP increased the escape latency of W animals exposed or non-exposed to IS, but did not affect the response of PCM animals, while chlordiazepoxide reduced the escape deficit of both W and PCM rats. The data suggest that PCM animals were more sensitive to the impairment produced by LH and that PCM led to neurochemical changes in the serotonergic system, resulting in hyporeactivity to the anxiogenic effects of GEP in the LH paradigm.
Sujet(s)
Animaux , Mâle , Rats , Apprentissage par évitement/effets des médicaments et des substances chimiques , Modulateurs GABA/pharmacologie , Impuissance apprise , Malnutrition protéinocalorique/traitement médicamenteux , Pyrimidines/pharmacologie , Agonistes des récepteurs de la sérotonine/pharmacologie , Analyse de variance , Poids , Comportement animal/effets des médicaments et des substances chimiques , Comportement animal/physiologie , Chlordiazépoxyde/pharmacologie , Chlordiazépoxyde/usage thérapeutique , Modèles animaux de maladie humaine , Réaction de fuite/effets des médicaments et des substances chimiques , Réaction de fuite/physiologie , Modulateurs GABA/usage thérapeutique , Incapacités d'apprentissage/étiologie , Malnutrition protéinocalorique/physiopathologie , Malnutrition protéinocalorique/psychologie , Pyrimidines/usage thérapeutique , Rat Wistar , Agonistes des récepteurs de la sérotonine/usage thérapeutiqueRÉSUMÉ
We studied the defensive strike of one species of each of five recognized lineages within the genus Bothrops, namely, B. alternatus, B. jararaca, B. jararacussu, B. moojeni and B. pauloensis. The defensive strike of the studied species was in general similar to that of Crotalus viridis and C. atrox, but some important differences were observed. Bothrops alternatus and B. pauloensis struck preferentially from a tight body posture, whereas B. jararaca and B. moojeni from a loose body posture. Defensive strikes were either true or false (during the latter, the mouth remains closed or partially open). Almost all strikes were successful; only on a few occasions snakes missed their target (flawed strikes). Strike variables were very conservative among the five species, especially strike distance and height, and one possible explanation may be related to constraints imposed on strike variables as a way of increasing strike accuracy.
Estudamos o bote defensivo de uma espécie de cada uma de cinco reconhecidas linhagens do gênero Bothrops, a saber: B. alternatus, B. jararaca, B. jararacussu, B. moojeni e B. pauloensis. O bote defensivo das espécies estudadas foi, em geral, semelhante ao de Crotalus viridis e C. atrox, porém algumas diferenças foram observadas. Bothrops alternatus e B. pauloensis desferiram botes preferencialmente a partir de postura corpórea enrodilhada, ao passo que B. jararaca e B. moojeni desferiram a maioria dos botes a partir de postura corpórea frouxa. Os botes defensivos foram verdadeiros ou falsos (nestes, a boca da serpente permaneceu fechada ou parcialmente aberta). Quase todos os botes foram bem-sucedidos; apenas em alguns casos a serpente errou o alvo (botes falhos). As variáveis relativas aos botes foram bastante conservativas entre as cinco espécies, principalmente distância e altura do bote, e uma possível explicação pode estar relacionada a restrições impostas às variáveis relativas aos botes como forma de aumentar sua acurácia.
Sujet(s)
Animaux , Bothrops/physiologie , Réaction de fuite/physiologie , Bothrops/classification , Réaction de fuite/classificationRÉSUMÉ
This article reviews reported results about the effects of drugs that act upon the serotonergic neurotransmission measured in three elevated mazes that are animal models of anxiety. A bibliographic search has been performed in MEDLINE using different combinations of the key words X-maze, plus-maze, T-maze, serotonin and 5-HT, present in the title and/or the abstract, with no time limit. From the obtained abstracts, several publications were excluded on the basis of the following criteria: review articles that did not report original results, species other than the rat, intracerebral drug administration alone, genetically manipulated rats, and animals having any kind of experimental pathology. The reported results indicate that the effect of drugs on the inhibitory avoidance task performed in the elevated T-maze and on the spatio temporal indexes of anxiety measured in the X and plus mazes correlate with their effect in patients diagnosed with generalized anxiety disorder. In contrast, the drug effects on the one-way escape task in the elevated T-maze predict the drug response of panic disorder patients. Overall, the drug effects assessed with the avoidance task in the T-maze are more consistent than those measured through the anxiety indexes of the X and plus mazes. Therefore, the elevated T-maze is a promising animal model of generalized anxiety and panic disorder.
No presente artigo, revisamos resultados publicados relatando efeitos de drogas que atuam na neurotransmissão serotonérgica medidos em três labirintos elevados, que são modelos animais de ansiedade. Realizamos uma busca bibliográfica no MEDLINE, usando diferentes combinações das palavras-chave: X-maze, plus-maze, T-maze, serotonin e 5-HT, presentes no título ou no resumo, sem limite de tempo. Dos resumos obtidos, vários foram excluídos com base nos seguintes critérios: artigos de revisão que não continham resultados originais, espécies diferentes do rato, apenas injeções intracerebrais, ratos geneticamente manipulados, animais com algum tipo de patologia experimental. Os resultados relatados indicam que o efeito de drogas na tarefa de esquiva inibitória desempenhada no labirinto em T elevado, bem como nos índices espaciais de ansiedade nos labirintos em X ou em forma de cruz se correlacionam com os efeitos em pacientes diagnosticados com o transtorno de ansiedade generalizada. Por outro lado, os efeitos de drogas na tarefa de fuga unidirecional do labirinto em T predizem a resposta a drogas dos pacientes com o transtorno de pânico. De modo geral, os efeitos de drogas sobre a tarefa de esquiva no labirinto em T são mais consistentes que os medidos pelos índices de ansiedade calculados nos labirintos em X e em forma de cruz. Portanto, o labirinto em T-elevado é um modelo promissor dos transtornos de ansiedade generalizada e de pânico.
Sujet(s)
Animaux , Souris , Rats , Anxiété/physiopathologie , Réaction de fuite/physiologie , Agents sérotoninergiques/pharmacologie , Sérotonine/physiologie , Anxiété/traitement médicamenteux , Modèles animaux de maladie humaine , Réaction de fuite/effets des médicaments et des substances chimiquesRÉSUMÉ
Pharmacological evidence indicates that the basolateral nucleus of the amygdala (BLA) is involved in the mediation of inhibitory avoidance but not of escape behavior in the elevated T-maze test. These defensive responses have been associated with generalized anxiety disorder (GAD) and panic disorder, respectively. In the present study, we determined whether the BLA plays a differential role in the control of inhibitory avoidance and escape responses in the elevated T-maze. Male Wistar rats (250-280 g, N = 9-10 in each treatment group) were pre-exposed to one of the open arms of the maze for 30 min and 24 h later tested in the model after inactivation of the BLA by a local injection of the GABA A receptor agonist muscimol (8 nmol in 0.2 æL). It has been shown that a prior forced exposure to one of the open arms of the maze, by shortening latencies to withdrawal from the open arm during the test, improves the escape task as a behavioral index of panic. The effects of muscimol in the elevated T-maze were compared to those caused by this GABA agonist in the avoidance reaction generated in the light/dark transition test. This defensive behavior has also been associated with GAD. In the elevated T-maze, intra-BLA injection of muscimol impaired inhibitory avoidance (control: 187.70 ± 14.90 s, muscimol: 37.10 ± 2.63 s), indicating an anxiolytic effect, without interfering with escape performance. The drug also showed an anxiolytic effect in the light/dark transition test as indicated by the increase in the time spent in the lighted compartment (control: 23.50 ± 2.45 s, muscimol: 47.30 ± 4.48 s). The present findings point to involvement of the BLA in the modulation of defensive responses that have been associated with GAD.
Sujet(s)
Animaux , Mâle , Rats , Troubles anxieux , Agonistes GABA/pharmacologie , Amygdale (système limbique)/effets des médicaments et des substances chimiques , Apprentissage par évitement/physiologie , Muscimol/pharmacologie , Réaction de fuite/physiologie , Troubles anxieux , Agonistes GABA/administration et posologie , Amygdale (système limbique)/physiologie , Apprentissage par évitement/effets des médicaments et des substances chimiques , Obscurité , Lumière , Apprentissage du labyrinthe , Microinjections , Muscimol/administration et posologie , Rat Wistar , Réaction de fuite/effets des médicaments et des substances chimiquesRÉSUMÉ
A locomoção de animais ectotérmicos é restringida por temperaturas baixas, e muitas espécies, como alguns insetos, precisam atingir certas temperaturas antes de voar. O tamanho corpóreo influencia as trocas de calor entre um organismo e o ambiente, dessa forma, animais maiores, por apresentarem maior inércia térmica, passam mais tempo aquecendo-se antes do vôo, período em que ficam mais expostos à predação. Assim, seria esperado que, ao longo de sua história evolutiva, animais maiores desenvolvessem repertório de comportamentos defensivos mais diversificado que os menores. As mariposas são um grupo interessante para testar essa hipótese por apresentarem grande variação de tamanho e aquecerem-se com tremor muscular antes do vôo, uma evidência da restrição térmica à locomoção. Registrei o comportamento de 76 mariposas imediatamente após uma simulação de ataque de um predador, associando a resposta observada ao tamanho corpóreo. Conduzi os experimentos a 20 e 25ºC para averiguar eventuais restrições térmicas sobre o comportamento defensivo e identifiquei os animais até o nível de família para verificar os efeitos de história filogenética comum. Quando perturbadas a 25ºC, mariposas menores tenderam a voar, enquanto as maiores correram. A 20ºC, quase todos os animais correram, incluindo os menores, evidenciando possível restrição térmica ao vôo. As mariposas maiores apresentam repertório de comportamentos defensivos mais diversificado, corroborando a hipótese proposta. Uma interpretação alternativa seria a de que respostas comportamentais similares poderiam ser explicadas por uma história filogenética comum. Entretanto, duas evidências apóiam a hipótese de restrições fisiológicas à locomoção: (1) a análise com Sphinghidae e Geometridae (famílias distantes filogeneticamente) apresentou o mesmo resultado que a análise geral e (2) foi detectada associação entre maior repertório de comportamentos defensivos e temperatura experimental mais baixa e, portanto, mais restritiva à locomoção.
Sujet(s)
Animaux , Mensurations corporelles , Température du corps/physiologie , Réaction de fuite/physiologie , Papillons de nuit/anatomie et histologie , Vol animal/physiologie , Papillons de nuit/physiologie , TempératureRÉSUMÉ
The possibility of the presence of inter-individual emotional differences and the memory performance of rats was examined in the elevated T-maze. Two kinds of aversively motivated behaviors, inhibitory avoidance and escape learning, were measured. Based on the number of trials to achieve a learning criterion, rats were divided into two subgroups with either low or high avoidance reactivity (LAR or HAR, respectively). Retention test avoidance latencies showed that HAR animals had better avoidance memory (Mann-Whitney rank sum test, P = 0.0035). No such differences were found for the escape component of this test. These data suggest that individual emotional differences affect inhibitory avoidance performance, which may help to explain the dispersion of the data observed in other studies using this paradigm
Sujet(s)
Rats , Animaux , Mâle , Anxiété/psychologie , Apprentissage par évitement/physiologie , Réaction de fuite/physiologie , Apprentissage du labyrinthe/physiologie , Mémoire/physiologie , Conditionnement physique d'animal , Rat WistarRÉSUMÉ
1. There is suggestive evidence that the septo-hippocampal system and the amygdala are involved in risk assessment behavior, a response to potential threat possibly related to anxiety. In addition, experimental results have been reported implicating the medial hypothalamus in coordinated escape, while the periaqueductal gray matter (PAG) and the median raphe nucleus serotonergic projection to the hippocampus seem to mediate freezing. The latter defensive behaviors are evoked by distal danger stimuli and may be viewed as manifestations of fear. Finally, there is a sound body of evidence indicating that the PAG commands primitive fight or flight reactions elicited by proximal threat, acute pain or asphyxia. These defense reactions may be related to rage and panic, respectively. In contrast, the lateral septal area and the bed nucleus of the stria terminalis have been shown to exert tonic inhibitory influence on defense. 2. Experimental evidence indicates that gamma-aminobutyric acid (GABA) tonically inhibits defensive behavior in the amygdala, hypothalamus and the PAG, an effect opposed by excitatory amino acids. Among monoamines, serotonin (5-HT) has been suggested to facilitate anxiety in the amygdala while inhibiting panic in the PAG. The role of noradrenaline in defense is less clear, although hypotheses implicating the locus coeruleus in anxiety and panic have been suggested. Among peptides, corticotropin-releasing factor (CRF) acting as a central neurotransmitter is thought to mediate behavioral and physiological effects of acute stress, while opioid peptides have been shown to inhibit defense in the amygdala and in the dorsal PAG. Finally, acetylcholine seems to facilitate defensive behavior in the hypothalamus and the PAG.
Sujet(s)
Animaux , Mécanismes de défense , Émotions/effets des médicaments et des substances chimiques , Agents neuromédiateurs , Acétylcholine , Acide gamma-amino-butyrique/physiologie , Anxiété , Apprentissage par évitement , Chats , Cerveau , Émotions/physiologie , Endorphines , Peur , Fureur/physiologie , Corticolibérine/physiologie , Norépinéphrine , Panique/physiologie , Rats , Réaction de fuite/physiologie , SérotonineRÉSUMÉ
The mean blood pressure and heart rate of freely moving rats were directly recorded over a 1-min period of electrical stimulation of the periaqueductal gray with intensities that induced freezing behavior, intense flight or no behavioral changes. Blood pressure and heart rate increased only when flight was induced and only during the first 15 s of stimulation. These cardiovascular changes suggest that homeostatic mechanisms act during the defense reaction and are markedly inhibited only at the beginning of the stimuli that induce the flight response, this inhibition quickly undergoing attenuation. Thes data do not suggest that activation of defense area, per se, contributes to the development of primary hypertension
Sujet(s)
Rats , Animaux , Mâle , Réaction de fuite/physiologie , Rythme cardiaque , Substance grise centrale du mésencéphale/physiologie , Pression veineuse , Stimulation électrique , Lignées consanguines de ratsRÉSUMÉ
1. The effects of undernutrition during suckling and of post-training ß-endorphin administration on avoidance task were invstigated in adult rats. 2. young rats were undernourished from delivery until weaning (21 days) by feeding their mothers a diet conatining 8% protein (w/w). Mothers of well-nourished rats were fed a 20% protein diet. After weaning, both groups of rats were fed a 20% protein diet until 90-120 days if age, when they were subjected to behavioral sessions. 3. Acquistion was measured in training sessions and retention in test sessions 24 h after training. Beta-endorphin or salina (control) was injected ip immdiately after training. Rats were subjected to shuttle and step-down inhibitory avoidance sessions using footshock of 0.2 or 0.8 mA intensity. 4. Undernutrition during suckling caused hyperreactivity to 0.2 mA footshocks. Beta-endorphin caused amnesia to shuttle avoidance task only in normal rats trained with 0.8 mA. Foor-shocks. In the step-down inhibitory avoidance task, ß-endorphin was amnesic only for normal rats and only for 0.2-mA footshocks. Beta-endorphin was not amnesic in undernourished rats
Sujet(s)
Rats , Animaux , Mâle , Femelle , bêta-Endorphine/administration et posologie , Malnutrition protéinocalorique/complications , Réaction de fuite/physiologie , 12571 , bêta-Endorphine/métabolisme , Électrochoc , Hypothalamus/métabolisme , Mémoire/effets des médicaments et des substances chimiques , Lignées consanguines de rats , Réaction de fuiteRÉSUMÉ
The present study describes, for the first time, the autonomic changes concomitant to the defense reaction in the opossum. Electrical stimulation of 2305 sites in the hypothalamus and brain stem evoked from 7% of them patterns of response including 40-240% muscle vasodilatation, characteristic of the defense reaction in anaesthetized animals. These responses also included a rise in arterial blood pressure, tachy- or bradycardia, and variable changes in ventilation ranging from apneusis to polypnea. It is suggested that the defense areas of the opossum are similar to those described for other species, but the defense responses resemble those of the rabbit
Sujet(s)
Animaux , Mâle , Femelle , Pression artérielle , Opossum/physiologie , Rythme cardiaque , Réaction de fuite/physiologie , Respiration , Cerveau/physiologie , Stimulation électrique , Monitorage physiologiqueRÉSUMÉ
Control, hippocampal and Sham control male albino rats weighing 150-200 gms were trained for acquisition of conditioned avoidance behavioural response using escape avoidance apparatus. Parameters like rate of performance, error scores, conditioned stimulus latency and unconditioned stimulus latency were studied. It was observed that there was a facilitation in the behavioural response with less error scores in hippocampal animals as compared to Sham control and control groups. Our observations are similar to those of Douglas and Pribram and Douglas and it is concluded that the hippocampus acts as a gate restricting the range of stimuli to which an intact animal attends.