Source:http://linkedlifedata.com/resource/pubmed/id/11417852
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2001-6-21
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pubmed:abstractText |
Carrageenin causes a reproducible inflammatory reaction and remains the standard irritant for examining acute inflammation and anti-inflammatory drugs. High doses of diazepam (10.0-20.0 mg/Kg) were shown to reduce the volume of acute inflammatory paw edema in rats as a response to carrageenin administration. The present experiment was undertaken to investigate the possible roles of peripheral-type benzodiazepine receptors (PBRs) and corticosterone on the anti-inflammatory effects of diazepam. Five experiments were conducted to assess the effects of a single dose (10.0 mg/Kg) of diazepam on carrageenin-induced paw edema (CIPE), pleurisy and increase in vascular permeability in rats. Results showed that: 1. diazepam or Ro5-4864 (a PBR agonist) treatment reduced CIPE values; 2. prior treatment with PK11195 (a non-benzodiazepine PBR antagonist) suppressed the effects of either diazepam or Ro5-4864 on CIPE; 3. diazepam reduced the volume of the pleural exudate in carrageenin-injected rats, as well as its leukocyte count; 4. diazepam treatment reduced the magnitude of the increase in vascular permeability caused by carrageenin; 5. adrenalectomy suppressed the effects of diazepam on CIPE; and 6. diazepam treatment increased the serum concentration of corticosterone. These results suggest a relevant role of PBR and corticosterone on diazepam-induced changes in inflammation. They are discussed in the light of a possible activation of mitochondrial PBRs within the adrenal gland cells by diazepam, thereby increasing the serum levels of corticosterone and thus reducing CIPE.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/4'-chlorodiazepam,
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Inflammatory Agents...,
http://linkedlifedata.com/resource/pubmed/chemical/Benzodiazepinones,
http://linkedlifedata.com/resource/pubmed/chemical/Carrageenan,
http://linkedlifedata.com/resource/pubmed/chemical/Corticosterone,
http://linkedlifedata.com/resource/pubmed/chemical/Diazepam,
http://linkedlifedata.com/resource/pubmed/chemical/GABA-A Receptor Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Irritants,
http://linkedlifedata.com/resource/pubmed/chemical/Isoquinolines,
http://linkedlifedata.com/resource/pubmed/chemical/PK 11195,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, GABA-A
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0892-3973
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
23
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
253-65
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:11417852-Acute Disease,
pubmed-meshheading:11417852-Adrenalectomy,
pubmed-meshheading:11417852-Animals,
pubmed-meshheading:11417852-Anti-Inflammatory Agents, Non-Steroidal,
pubmed-meshheading:11417852-Benzodiazepinones,
pubmed-meshheading:11417852-Capillary Permeability,
pubmed-meshheading:11417852-Carrageenan,
pubmed-meshheading:11417852-Corticosterone,
pubmed-meshheading:11417852-Diazepam,
pubmed-meshheading:11417852-GABA-A Receptor Agonists,
pubmed-meshheading:11417852-Inflammation,
pubmed-meshheading:11417852-Irritants,
pubmed-meshheading:11417852-Isoquinolines,
pubmed-meshheading:11417852-Male,
pubmed-meshheading:11417852-Rats,
pubmed-meshheading:11417852-Rats, Wistar,
pubmed-meshheading:11417852-Receptors, GABA-A
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pubmed:year |
2001
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pubmed:articleTitle |
Reduction of acute inflammation in rats by diazepam: role of peripheral benzodiazepine receptors and corticosterone.
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pubmed:affiliation |
Laboratory of Applied Pharmacology and Toxicology, School of Veterinary Medicine, University of São Paulo, Brazil.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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