Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/196645
Type: Artigo de periódico
Title: Nociception- And Anxiety-like Behavior In Rats Submitted To Different Periods Of Restraint Stress.
Author: Gameiro, Gustavo Hauber
Gameiro, Paula Hauber
Andrade, Annicele da Silva
Pereira, Lígia Ferrinho
Arthuri, Mariana Trevisani
Marcondes, Fernanda Klein
Veiga, Maria Cecília Ferraz de Arruda
Abstract: The aim of this study was to evaluate the effect of acute, sub-chronic and chronic stress on nociception induced by formalin injection in rats' temporomandibular joint (TMJ). It was evaluated the relation between blood levels of adrenocorticotropin, corticosterone, the levels of anxiety and nociceptive responses recorded after different stress protocols. Animals were initially submitted to acute restraint stress (15; 30 min and 1 h), or exposed to sub-chronic (3 days-1 h/day) or chronic stress (40 days-1 h/day). Then, animals were (1) killed immediately to collect blood for hormonal determinations; or (2) submitted to the elevated plus-maze to evaluate anxiety; or (3) submitted to the TMJ formalin test to evaluate nociception. It was also evaluated the role of serotoninergic and opioid systems in nociceptive changes induced by stress. For this, the serotonin-selective reuptake inhibitor (fluoxetine 10 mg/kg) and the opioid agonist (morphine 1-5 mg/kg) were administered before the nociception test. All stress protocols significantly raised the levels of ACTH or corticosterone, as well as the anxiety behavior. In relation to nociception, the chronic stressed animals showed an increase in nociceptive responses (hyperalgesia). In this group, there was a reduction in the morphine analgesic effects, suggesting dysfunction in the endogenous opioid system. Fluoxetine had an analgesic effect in both stressed and control groups, although this effect was more evident in the stressed group. It was concluded that stress-induced hyperalgesia may result from changes in the serotoninergic and opioid systems, which can explain, at least in part, the important link between stress and orofacial pain.
Subject: Acute Disease
Adrenocorticotropic Hormone
Analgesics, Opioid
Animals
Anxiety
Chronic Disease
Cortisone
Disease Models, Animal
Emotions
Exploratory Behavior
Fluoxetine
Male
Morphine
Pain
Pain Threshold
Rats
Rats, Wistar
Receptors, Opioid
Restraint, Physical
Serotonin Uptake Inhibitors
Stress, Psychological
Time Factors
Rights: fechado
Identifier DOI: 10.1016/j.physbeh.2005.12.007
Address: http://www.ncbi.nlm.nih.gov/pubmed/16488452
Date Issue: 2006
Appears in Collections:Unicamp - Artigos e Outros Documentos

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