Buprenorphine Prevents Remifentanil-Enhanced Mechanical Allodynia in a Rat Inflammatory Pain Model

Shimane journal of medical science Volume 29 Issue 1 Page 23-30 published_at 2012-12-01
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Title
Buprenorphine Prevents Remifentanil-Enhanced Mechanical Allodynia in a Rat Inflammatory Pain Model
Creator
Deng Liqin
Nikai Tetsuro
Ishida Ryosuke
Saito Yoji
Source Title
Shimane journal of medical science
Volume 29
Issue 1
Start Page 23
End Page 30
Journal Identifire
ISSN 03865959
EISSN 24332410
Descriptions
Purpose Remifentanil is a μ-receptor agonist known to cause pain hypersensitivity. Buprenorphine targets multiple opioid receptors and exhibits good anti-hyperalgesic characteristics. We investigated whether pre-treatment with buprenorphine could prevent13;13;
remifentanil-enhanced mechanical allodynia in an inflammatory pain model.13;13;
Methods Inflammatory pain was induced by subcutaneous carrageenan injection into the hind paw of rats. In experiment 1, rats were randomized to receive intravenous remifentanil(10 μg・kg^(-1)・min^(-1) or 30 μg・kg^(-1)・min^(-1))or saline for 30 min. In experiment 2, buprenorphine(25 μg/kg)or saline was injected intravenously 10 min before remifentanil administration. Mechanical thresholds of hind paws were evaluated using von Frey filaments at 1 and 3h after carrageenan injection and daily thereafter for 7 days.13;13;
Results Intravenous infusion of remifentanil significantly enhanced bilateral mechanical allodynia induced by carrageenan. Pre-treatment with buprenorphine prevented remifentanil-enhanced bilateral mechanical allodynia significantly.13;13;
Conclusion Pre-treatment with buprenorphine effectively prevents remifentanil-enhanced mechanical allodynia in an inflammatory pain model.13;13;
13;
Subjects
Buprenorphine ( Other)
Remifentanil ( Other)
allodynia ( Other)
inflammatory pain ( Other)
Language
eng
Resource Type departmental bulletin paper
Publisher
Shimane University Faculty of Medicine
Date of Issued 2012-12-01
Publish Type Version of Record
Access Rights open access
Relation
[NCID] AA00841586