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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1989-6-7
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pubmed:abstractText |
Histamine (HA) is synthesized from L-histidine by histidine decarboxylase (HDC), and HA released from neurons is predominantly methylated to tele-methylhistamine (t-MH), which is further metabolized by MAO. Therefore, the HA turnover rate is determined by either a exponential decrease in HA level after treatment with alpha-fluoromethylhistidine (alpha-FMH), a specific HDC inhibitor, or a linear accumulation of t-MH after pargyline treatment. Brain HA and t-MH can be simultaneously assayed using HPLC with fluorometric detection. Care should be given to avoid the contamination by extraencephalic mast-cell HA after microwave irradiation or immersion in liquid nitrogen, and to a marked circadian variation of t-MH level. The HA turnover is the highest in the hypothalamus, low in the pons-medulla oblongata and cerebellum, and nil in the spinal cord in rats, mice and guinea pigs. The half-life of neuronal HA is 8-87 min in various brain regions of these animals. Barbiturates, enflurane, benzodiazepines, GABA-mimetic drugs, ethanol and delta 9-tetrahydrocannabinol significantly decrease the HA turnover, whereas mu-opioid agonists such as morphine and [D-Ala2, MePhe4, Gly(ol)5] enkephalin enhance it. Foot-shock and phencyclidine also enhance it at least partly via mu-opioid receptors. Chlorpromazine, haloperidol, imipramine, methamphetamine or halothane have no influence on the HA turnover.
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pubmed:language |
jpn
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anesthetics,
http://linkedlifedata.com/resource/pubmed/chemical/Ethanol,
http://linkedlifedata.com/resource/pubmed/chemical/Histamine,
http://linkedlifedata.com/resource/pubmed/chemical/Methylhistamines,
http://linkedlifedata.com/resource/pubmed/chemical/Piperidines,
http://linkedlifedata.com/resource/pubmed/chemical/Psychotropic Drugs,
http://linkedlifedata.com/resource/pubmed/chemical/Tetrahydrocannabinol,
http://linkedlifedata.com/resource/pubmed/chemical/tele-methylhistamine,
http://linkedlifedata.com/resource/pubmed/chemical/thioperamide
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0015-5691
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
92
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
271-81
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pubmed:dateRevised |
2011-7-27
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pubmed:meshHeading |
pubmed-meshheading:2854108-Anesthetics,
pubmed-meshheading:2854108-Animals,
pubmed-meshheading:2854108-Brain,
pubmed-meshheading:2854108-Circadian Rhythm,
pubmed-meshheading:2854108-Ethanol,
pubmed-meshheading:2854108-Half-Life,
pubmed-meshheading:2854108-Histamine,
pubmed-meshheading:2854108-Methylhistamines,
pubmed-meshheading:2854108-Piperidines,
pubmed-meshheading:2854108-Psychotropic Drugs,
pubmed-meshheading:2854108-Tetrahydrocannabinol
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pubmed:year |
1988
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pubmed:articleTitle |
[Turnover of brain histamine and its changes by various drugs].
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pubmed:affiliation |
Department of Pharmacology, Okayama University Medical School, Japan.
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pubmed:publicationType |
Journal Article,
English Abstract,
Review
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