rdf:type |
|
lifeskim:mentions |
umls-concept:C0014298,
umls-concept:C0026549,
umls-concept:C0030685,
umls-concept:C0038587,
umls-concept:C0205227,
umls-concept:C0301630,
umls-concept:C0391871,
umls-concept:C0392747,
umls-concept:C0443172,
umls-concept:C0680255,
umls-concept:C1280500,
umls-concept:C1283071,
umls-concept:C1963578
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pubmed:issue |
9
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pubmed:dateCreated |
2001-5-21
|
pubmed:abstractText |
Recent studies have suggested that cannabinoids might initiate the consumption of other highly addictive substances, such as opiates. In this work, we show that acute administration of Delta9-tetrahydrocannabinol in mice facilitates the antinociceptive and antidepressant-like responses elicited by the endogenous enkephalins protected from their degradation by RB 101, a complete inhibitor of enkephalin catabolism. This emphasizes the existence of a physiological interaction between endogenous opioid and cannabinoid systems. Accordingly, Delta9-tetrahydrocannabinol increased the release of Met-enkephalin-like material in the nucleus accumbens of awake and freely moving rats measured by microdialysis. In addition, this cannabinoid agonist displaced the in vivo [3H]diprenorphine binding to opioid receptors in total mouse brain. The repetitive pretreatment during 3 weeks of Delta9-tetrahydrocannabinol in mice treated chronically with morphine significantly reduces the naloxone-induced withdrawal syndrome. However, this repetitive administration of Delta9-tetrahydrocannabinol did not modify or even decrease the rewarding responses produced by morphine in the place preference paradigm. Taken together, these behavioural and biochemical results demonstrate the existence of a direct link between endogenous opioid and cannabinoid systems. However, chronic use of high doses of cannabinoids does not seem to potentiate the psychic dependence to opioids.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Analgesics,
http://linkedlifedata.com/resource/pubmed/chemical/Diprenorphine,
http://linkedlifedata.com/resource/pubmed/chemical/Disulfides,
http://linkedlifedata.com/resource/pubmed/chemical/Enkephalin, Methionine,
http://linkedlifedata.com/resource/pubmed/chemical/Morphine,
http://linkedlifedata.com/resource/pubmed/chemical/Narcotic Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Narcotics,
http://linkedlifedata.com/resource/pubmed/chemical/Phenylalanine,
http://linkedlifedata.com/resource/pubmed/chemical/Psychotropic Drugs,
http://linkedlifedata.com/resource/pubmed/chemical/RB 101,
http://linkedlifedata.com/resource/pubmed/chemical/Tetrahydrocannabinol,
http://linkedlifedata.com/resource/pubmed/chemical/Tritium
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0953-816X
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:volume |
13
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
1816-24
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11359533-Analgesics,
pubmed-meshheading:11359533-Animals,
pubmed-meshheading:11359533-Binding, Competitive,
pubmed-meshheading:11359533-Conditioning (Psychology),
pubmed-meshheading:11359533-Diprenorphine,
pubmed-meshheading:11359533-Disulfides,
pubmed-meshheading:11359533-Drug Interactions,
pubmed-meshheading:11359533-Enkephalin, Methionine,
pubmed-meshheading:11359533-Extracellular Space,
pubmed-meshheading:11359533-Male,
pubmed-meshheading:11359533-Mice,
pubmed-meshheading:11359533-Morphine,
pubmed-meshheading:11359533-Motor Activity,
pubmed-meshheading:11359533-Narcotic Antagonists,
pubmed-meshheading:11359533-Narcotics,
pubmed-meshheading:11359533-Neurons,
pubmed-meshheading:11359533-Nociceptors,
pubmed-meshheading:11359533-Nucleus Accumbens,
pubmed-meshheading:11359533-Phenylalanine,
pubmed-meshheading:11359533-Psychotropic Drugs,
pubmed-meshheading:11359533-Reward,
pubmed-meshheading:11359533-Substance Withdrawal Syndrome,
pubmed-meshheading:11359533-Tetrahydrocannabinol,
pubmed-meshheading:11359533-Tritium
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pubmed:year |
2001
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pubmed:articleTitle |
Delta9-tetrahydrocannabinol releases and facilitates the effects of endogenous enkephalins: reduction in morphine withdrawal syndrome without change in rewarding effect.
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pubmed:affiliation |
Département de Pharmacochimie Moléculaire et Structurale, U266 INSERM, UMR 8600 CNRS, UFR des Sciences Pharmaceutiques et Biologiques, 4, Avenue de l'Observatoire, 75270 Paris Cedex 06, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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