Abstract |
Opioid-induced hyperalgesia and tolerance severely impact the clinical efficacy of opiates as pain relievers in animals and humans. The molecular mechanisms underlying both phenomena are not well understood and their elucidation should benefit from the study of animal models and from the design of appropriate experimental protocols. We describe here a methodological approach for inducing, recording and quantifying morphine-induced hyperalgesia as well as for evidencing analgesic tolerance, using the tail-immersion and tail pressure tests in wild-type mice. As shown in the video, the protocol is divided into five sequential steps. Handling and habituation phases allow a safe determination of the basal nociceptive response of the animals. Chronic morphine administration induces significant hyperalgesia as shown by an increase in both thermal and mechanical sensitivity, whereas the comparison of analgesia time-courses after acute or repeated morphine treatment clearly indicates the development of tolerance manifested by a decline in analgesic response amplitude. This protocol may be similarly adapted to genetically modified mice in order to evaluate the role of individual genes in the modulation of nociception and morphine analgesia. It also provides a model system to investigate the effectiveness of potential therapeutic agents to improve opiate analgesic efficacy.
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Authors | Khadija Elhabazi, Safia Ayachi, Brigitte Ilien, Frédéric Simonin |
Journal | Journal of visualized experiments : JoVE
(J Vis Exp)
Issue 89
Pg. e51264
(Jul 29 2014)
ISSN: 1940-087X [Electronic] United States |
PMID | 25145878
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Video-Audio Media)
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Chemical References |
- Analgesics, Opioid
- Morphine
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Topics |
- Analgesics, Opioid
(pharmacology)
- Animals
- Drug Tolerance
- Female
- Hot Temperature
- Hyperalgesia
(chemically induced, diagnosis)
- Male
- Mice
- Mice, Inbred C57BL
- Morphine
(pharmacology)
- Nociception
(drug effects)
- Pain Measurement
(methods)
- Pressure
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