rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
2
|
pubmed:dateCreated |
1996-11-25
|
pubmed:abstractText |
Intracellular techniques were used to study the actions of dopaminergic D1 agonists on the afterhyperpolarization (AHP) that follows action potentials in rat neostriatal neurones. Dopamine or Cl-APB (10 microM), or 1-10 microM 6-Cl-PB all increased AHP amplitude. This effect was blocked by 1 microM SCH-23390, a D1 antagonist, but not by 1 microM sulpiride, a D2 antagonist. Both 500 microM dibutyryl cAMP and 5 microM BayK 8644 induced a similar AHP increase. BayK 8644 occluded the effect of agonists. The results suggest that the action of dopamine is mediated via the recently described protein kinase A enhancement of L-type Ca2+ channels. The results partially explain the decrease in firing frequency induced by dopamine and a possible site of antagonism with cholinergic modulation.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0959-4965
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
31
|
pubmed:volume |
7
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
454-6
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:8730804-3-Pyridinecarboxylic acid...,
pubmed-meshheading:8730804-Action Potentials,
pubmed-meshheading:8730804-Animals,
pubmed-meshheading:8730804-Bucladesine,
pubmed-meshheading:8730804-Calcium Channel Agonists,
pubmed-meshheading:8730804-Dopamine,
pubmed-meshheading:8730804-Neostriatum,
pubmed-meshheading:8730804-Neurons,
pubmed-meshheading:8730804-Rats,
pubmed-meshheading:8730804-Receptors, Dopamine D1,
pubmed-meshheading:8730804-Receptors, Dopamine D2
|
pubmed:year |
1996
|
pubmed:articleTitle |
Dopamine modulates the afterhyperpolarization in neostriatal neurones.
|
pubmed:affiliation |
Departamento de Neurociencias, UNAM, México City, DF, México.
|
pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
|