Source:http://linkedlifedata.com/resource/pubmed/id/17227682
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2007-2-19
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pubmed:abstractText |
We observed that intrathecal (i.t.) bovine adrenal medulla 22, an endogenous opioid peptide, partially reverses morphine tolerance. However, its mechanism remains unclear. The present study determined the effects of BAM8-22, a derivative of BAM22 and selective sensory neuron-specific receptor (SNSR) agonist, on the development and maintenance of tolerance to spinal morphine. Intrathecal administration of BAM8-22 at various doses (0.1, 1 and 10nmol) did not alter withdraw latencies assessed in both paw withdraw and tail flick tests. Co-administration of BAM8-22 (0.1nmol) every other day, but not daily, with morphine remarkably attenuated the development of morphine tolerance. Pretreatment and co-treatment with BAM8-22 (0.1nmol) significantly reversed established morphine tolerance. Furthermore, intermittent administration of BAM8-22 with morphine consistently resumed morphine-induced antinociception. However, i.t. BAM8-22 did not alter morphine-induced hyperalgesia. These results suggested that SNSR may be able to modulate the sensitivity of opioid receptor serving as a most probable underlying mechanism for the effects of BAM8-22 on morphine tolerance. This study also demonstrated that intermittent combination of SNSR agonist BAM8-22 with morphine might be better regimen for long-term use of opioids to treat chronic pain.
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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/Analgesics,
http://linkedlifedata.com/resource/pubmed/chemical/BAM 22P,
http://linkedlifedata.com/resource/pubmed/chemical/Enkephalin, Methionine,
http://linkedlifedata.com/resource/pubmed/chemical/Morphine,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Precursors,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, G-Protein-Coupled
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0166-4328
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
12
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pubmed:volume |
178
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
154-9
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pubmed:meshHeading |
pubmed-meshheading:17227682-Analgesics,
pubmed-meshheading:17227682-Animals,
pubmed-meshheading:17227682-Dose-Response Relationship, Drug,
pubmed-meshheading:17227682-Drug Tolerance,
pubmed-meshheading:17227682-Enkephalin, Methionine,
pubmed-meshheading:17227682-Injections, Spinal,
pubmed-meshheading:17227682-Male,
pubmed-meshheading:17227682-Morphine,
pubmed-meshheading:17227682-Neurons, Afferent,
pubmed-meshheading:17227682-Pain Threshold,
pubmed-meshheading:17227682-Peptide Fragments,
pubmed-meshheading:17227682-Protein Precursors,
pubmed-meshheading:17227682-Rats,
pubmed-meshheading:17227682-Receptors, G-Protein-Coupled
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pubmed:year |
2007
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pubmed:articleTitle |
Sensory neuron-specific receptor agonist BAM8-22 inhibits the development and expression of tolerance to morphine in rats.
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pubmed:affiliation |
College of Life Sciences, Fujian Normal University, People's Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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