Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1998-5-18
pubmed:abstractText
In [3H]myristic acid-prelabeled Chinese hamster ovary cells stably expressing the rat NK1 tachykinin receptor, the selective NK1 agonist [Pro9]substance P ([Pro9]SP) time and concentration dependently stimulated the formation of [3H]phosphatidylethanol in the presence of ethanol. This [Pro9]SP-induced activation of phospholipase D (PLD) was blocked by NK1 receptor antagonists and poorly or not mimicked by NK2 and NK3 agonists, respectively. In confirmation of previous observations, [Pro9]SP also stimulated the hydrolysis of phosphoinositides, the release of arachidonic acid, and the formation of cyclic AMP (cAMP). All these [Pro9]SP-evoked responses could be mimicked by aluminum fluoride, but they remained unaffected in cells pretreated with pertussis toxin, suggesting that a Gi/Go protein is not involved in these different signaling pathways. The activation of PLD by [Pro9]SP was sensitive to external calcium and required an active protein kinase C because the inhibition of this kinase (Ro 31-8220) or its down-regulation (long-term treatment with a phorbol ester) abolished the response. In contrast, a cAMP-dependent process was not involved in the activation of PLD because the [Pro9]SP-evoked response was neither affected by Rp-8-bromoadenosine 3',5'-cyclic monophosphorothioate nor mimicked by cAMP-generating compounds (cholera toxin or forskolin) or by 8-bromo-cyclic AMP. A functional coupling of NK1 receptors to PLD was also demonstrated in the human astrocytoma cell line U 373 MG stimulated by SP or [Pro9]SP. These results suggest that PLD activation could be an additional signaling pathway involved in the mechanism of action of SP in target cells expressing NK1 receptors.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Calcium, http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP, http://linkedlifedata.com/resource/pubmed/chemical/GTP-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Glycerophospholipids, http://linkedlifedata.com/resource/pubmed/chemical/Myristic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidic Acids, http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylcholines, http://linkedlifedata.com/resource/pubmed/chemical/Phospholipase D, http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Neurokinin-1, http://linkedlifedata.com/resource/pubmed/chemical/Substance P, http://linkedlifedata.com/resource/pubmed/chemical/Tachykinins, http://linkedlifedata.com/resource/pubmed/chemical/phosphatidylethanol, http://linkedlifedata.com/resource/pubmed/chemical/substance P, Pro(9)-
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0022-3042
pubmed:author
pubmed:issnType
Print
pubmed:volume
70
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2091-8
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:9572295-Animals, pubmed-meshheading:9572295-Astrocytoma, pubmed-meshheading:9572295-CHO Cells, pubmed-meshheading:9572295-Calcium, pubmed-meshheading:9572295-Cricetinae, pubmed-meshheading:9572295-Cyclic AMP, pubmed-meshheading:9572295-Enzyme Activation, pubmed-meshheading:9572295-GTP-Binding Proteins, pubmed-meshheading:9572295-Glycerophospholipids, pubmed-meshheading:9572295-Humans, pubmed-meshheading:9572295-Myristic Acid, pubmed-meshheading:9572295-Phosphatidic Acids, pubmed-meshheading:9572295-Phosphatidylcholines, pubmed-meshheading:9572295-Phospholipase D, pubmed-meshheading:9572295-Protein Kinase C, pubmed-meshheading:9572295-Rats, pubmed-meshheading:9572295-Receptors, Neurokinin-1, pubmed-meshheading:9572295-Substance P, pubmed-meshheading:9572295-Tachykinins, pubmed-meshheading:9572295-Tumor Cells, Cultured
pubmed:year
1998
pubmed:articleTitle
Functional coupling of the NK1 tachykinin receptor to phospholipase D in chinese hamster ovary cells and astrocytoma cells.
pubmed:affiliation
Neuropharmacologie, INSERM U114, Collège de France, Paris.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't