rdf:type |
|
lifeskim:mentions |
umls-concept:C0021467,
umls-concept:C0021469,
umls-concept:C0025914,
umls-concept:C0026809,
umls-concept:C0027882,
umls-concept:C0031959,
umls-concept:C0032821,
umls-concept:C0074504,
umls-concept:C0205409,
umls-concept:C0230189,
umls-concept:C0521116,
umls-concept:C1258666,
umls-concept:C1621296
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pubmed:issue |
3
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pubmed:dateCreated |
1990-9-11
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pubmed:abstractText |
The actions of (+)-3-(3-hydroxyphenyl)-N-(1-propyl)piperidine [(+)3-PPP] on sympathetic neurons of the mouse isolated hypogastric ganglion were studied using the current clamp and single electrode voltage clamp techniques. In neurons studied under current clamp (+)3-PPP (10(-5) to 3 x 10(-4) M) evoked a concentration-dependent depolarization, which was fully reversible on washout of the drug. The depolarization was associated with an increase in membrane input resistance. At membrane potentials between -43 and -65 mV the amplitude of the depolarization was inversely related to the membrane potential. (+)3-PPP had no effect on membrane potential at potentials negative to -65 mV. The effect of (+)3-PPP on the M-current was studied in cells voltage clamped at -40 mV and stepped to -60 mV for 300-500 ms. The slow current relaxations seen during and after the voltage step are largely due to the M-current. (+)3-PPP (3 x 10(-5) to 3 x 10(-4) M) inhibited the M-current and produced an inward current in a concentration-dependent manner. (-)3-PPP (3 x 10(-5) M) had similar effects, but was less potent than (+)3-PPP. (+)3-PPP (3 x 10(-5) M) also inhibited the A-current and a calcium-dependent potassium current, but to a lesser degree than the M-current.(ABSTRACT TRUNCATED AT 250 WORDS)
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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/Atropine,
http://linkedlifedata.com/resource/pubmed/chemical/Carbazoles,
http://linkedlifedata.com/resource/pubmed/chemical/Dopamine Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Piperidines,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Opioid,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, sigma,
http://linkedlifedata.com/resource/pubmed/chemical/Sulpiride,
http://linkedlifedata.com/resource/pubmed/chemical/Tetraethylammonium,
http://linkedlifedata.com/resource/pubmed/chemical/Tetraethylammonium Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Tetrodotoxin,
http://linkedlifedata.com/resource/pubmed/chemical/n-N-propyl-3-(3-hydroxyphenyl)piperi...,
http://linkedlifedata.com/resource/pubmed/chemical/rimcazole
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pubmed:status |
MEDLINE
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pubmed:issn |
0306-4522
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:volume |
35
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
725-33
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1974331-Animals,
pubmed-meshheading:1974331-Atropine,
pubmed-meshheading:1974331-Carbazoles,
pubmed-meshheading:1974331-Dopamine Agents,
pubmed-meshheading:1974331-Evoked Potentials,
pubmed-meshheading:1974331-Ganglia, Sympathetic,
pubmed-meshheading:1974331-Male,
pubmed-meshheading:1974331-Membrane Potentials,
pubmed-meshheading:1974331-Mice,
pubmed-meshheading:1974331-Mice, Inbred DBA,
pubmed-meshheading:1974331-Neurons,
pubmed-meshheading:1974331-Piperidines,
pubmed-meshheading:1974331-Potassium Channels,
pubmed-meshheading:1974331-Receptors, Opioid,
pubmed-meshheading:1974331-Receptors, sigma,
pubmed-meshheading:1974331-Sulpiride,
pubmed-meshheading:1974331-Tetraethylammonium,
pubmed-meshheading:1974331-Tetraethylammonium Compounds,
pubmed-meshheading:1974331-Tetrodotoxin
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pubmed:year |
1990
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pubmed:articleTitle |
Inhibition of potassium currents by the sigma receptor ligand (+)-3-(3-hydroxyphenyl)-N-(1-propyl)piperidine in sympathetic neurons of the mouse isolated hypogastric ganglion.
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pubmed:affiliation |
Department of Pharmacology, University of Cambridge, U.K.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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