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Thermal escape box: A cost-benefit evaluation paradigm for investigating thermosensation and thermal pain.
Dayton, Jacquelyn R; Marquez, Jose; Romo, Alejandra K; Chen, Yi-Je; Contreras, Jorge E; Griffith, Theanne N.
Afiliação
  • Dayton JR; University of California, Davis. Department of Physiology & Membrane Biology, 1275 Med Science Drive, Davis, CA 95616, United States.
  • Marquez J; University of California, Davis. Department of Physiology & Membrane Biology, 1275 Med Science Drive, Davis, CA 95616, United States.
  • Romo AK; University of California, Davis. Department of Physiology & Membrane Biology, 1275 Med Science Drive, Davis, CA 95616, United States.
  • Chen YJ; University of California, Davis. Department of Pharmacology, 1275 Med Science Drive, Davis, CA 95616, United States.
  • Contreras JE; University of California, Davis. Department of Physiology & Membrane Biology, 1275 Med Science Drive, Davis, CA 95616, United States.
  • Griffith TN; University of California, Davis. Department of Physiology & Membrane Biology, 1275 Med Science Drive, Davis, CA 95616, United States.
Neurobiol Pain ; 15: 100155, 2024.
Article em En | MEDLINE | ID: mdl-38617105
ABSTRACT
Thermosensation, the ability to detect and estimate temperature, is an evolutionarily conserved process that is essential for survival. Thermosensing is impaired in various pain syndromes, resulting in thermal allodynia, the perception of an innocuous temperature as painful, or thermal hyperalgesia, an exacerbated perception of a painful thermal stimulus. Several behavioral assays exist to study thermosensation and thermal pain in rodents, however, most rely on reflexive withdrawal responses or the subjective quantification of spontaneous nocifensive behaviors. Here, we created a new apparatus, the thermal escape box, which can be attached to temperature-controlled plates and used to assess temperature-dependent effort-based decision-making. The apparatus consists of a light chamber with an opening that fits around temperature-controlled plates, and a small entryway into a dark chamber. A mouse must choose to stay in a brightly lit aversive area or traverse the plates to escape to the enclosed dark chamber. We quantified escape latencies of adult C57Bl/6 mice at different plate temperatures from video recordings and found they were significantly longer at 5 °C, 18 °C, and 52 °C, compared to 30 °C, a mouse's preferred ambient temperature. Differences in escape latencies were abolished in male Trpm8-/- mice and in male Trpv1-/- animals. Finally, we show that chronic constriction injury procedures or oxaliplatin treatement significantly increased escape latencies at cold temperatures compared to controls, the later of which was prevented by the analgesic meloxicam. This demonstrates the utility of this assay in detecting cold pain. Collectively, our study has identified a new and effective tool that uses cost-benefit valuations to study thermosensation and thermal pain.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article