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Neuroscience ; 131(3): 635-45, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-15730869

RESUMO

Recently, there has been a growing interest in long-term consequences of neonatal pain because modern neonatal intensive care units routinely employ procedures that cause considerable pain and may be followed by local inflammation and hyperalgesia lasting for several hours or even days. To address this question, we developed a rat model of short lasting (<2 days) early local inflammatory insult produced by a single injection of 0.25% carrageenan (CAR) into the plantar surface of a hindpaw. Previously, we demonstrated that rats receiving this treatment within the first week after birth grow into adults with a global reduction in responsiveness to acute pain. Here, we report that these animals also manifest a low anxiety trait associated with reduced emotional responsiveness to stress. This conclusion is based in the following observations: (a) rats in our model display reduced anxiety on an elevated plus-maze; (b) in the forced swim test, these rats exhibit behavioral characteristics associated with stronger ability for stress coping; and (c) these animals have reduced basal and stress-induced plasma levels of such stress-related neuroendocrine markers as corticotropin-releasing factor, vasopressin, and adrenocorticotrophic hormone. In addition, we used DNA microarray and real-time reverse-transcriptase polymerase chain reaction to profile long-term changes in gene expression in the midbrain periaqueductal gray (PAG; a region involved in both stress and pain modulation) in our animal model. Among the affected genes, serotonergic receptors were particularly well represented. Specifically, we detected increase in the expression of 5-HT1A, 5-HT1D, 5-HT2A, 5-HT2C and 5-HT4 receptors. Several of these receptors are known to be involved in the anxiolytic and analgesic activity of the PAG. Finally, to determine whether neonatal inflammatory insult induces elevation in maternal care, which may play a role in generating long-term behavioral alterations seen in our model, we examined maternal behavior for 3 days following CAR injection. Indeed, we observed a substantial increase in maternal attention to the pups at the time of inflammation, but this increase was not without its cost: a period of significant maternal neglect afterward.


Assuntos
Comportamento Animal/fisiologia , Química Encefálica/fisiologia , Inflamação/complicações , Estresse Psicológico/fisiopatologia , Hormônio Adrenocorticotrópico/sangue , Análise de Variância , Animais , Animais Recém-Nascidos , Carragenina , Proteínas de Transporte , Hormônio Liberador da Corticotropina/sangue , Modelos Animais de Doenças , Edema/induzido quimicamente , Edema/fisiopatologia , Ensaio de Imunoadsorção Enzimática/métodos , Feminino , Inflamação/sangue , Inflamação/induzido quimicamente , Masculino , Comportamento Materno/efeitos dos fármacos , Comportamento Materno/fisiologia , Aprendizagem em Labirinto/fisiologia , Análise de Sequência com Séries de Oligonucleotídeos/métodos , Dor/etiologia , Medição da Dor , Substância Cinzenta Periaquedutal/metabolismo , Fosfoproteínas/genética , Fosfoproteínas/metabolismo , RNA Mensageiro/biossíntese , Ratos , Receptores de Serotonina/efeitos dos fármacos , Receptores de Serotonina/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa/métodos , Natação , Fatores de Tempo , Vasopressinas/sangue
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