Dual effect of lobeline on α4β2 rat neuronal nicotinic receptors
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21371469
DOI
10.1016/j.ejphar.2011.02.012
PII: S0014-2999(11)00197-X
Knihovny.cz E-zdroje
- MeSH
- acetylcholin farmakologie MeSH
- Cercopithecus aethiops MeSH
- COS buňky MeSH
- krysa rodu Rattus MeSH
- lobelin farmakologie MeSH
- neurony metabolismus MeSH
- nikotinové receptory metabolismus MeSH
- nikotinoví agonisté farmakologie MeSH
- nikotinoví antagonisté farmakologie MeSH
- synergismus léků MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- acetylcholin MeSH
- lobelin MeSH
- nicotinic receptor alpha4beta2 MeSH Prohlížeč
- nikotinové receptory MeSH
- nikotinoví agonisté MeSH
- nikotinoví antagonisté MeSH
The effect of lobeline on rat α4β2 nicotinic receptors expressed in COS cells was studied using the patch-clamp technique. Currents were recorded in whole-cell mode 2-4 days after cell transfection by plasmids coding the α4β2 combination of receptor subunits. In cells sensitive to acetylcholine, the application of lobeline evoked minor responses (up to 2% of maximal acetylcholine response). When acetylcholine was applied to the background of an already running application of lobeline, acetylcholine responses were inhibited in a concentration- and time dependent manner. However, when lobeline was applied simultaneously with acetylcholine without any prepulse or during an already running application of acetylcholine, the acetylcholine responses were potentiated up to 300-600% of that of the control. The site of lobeline action overlaps with the cholinergic site, as was proven by the partially protective effect of (+)-tubocurarine. Thus, lobeline can apparently desensitize receptors when applied alone (inhibition) whereas its binding to a second agonist site with the first one already occupied by acetylcholine leads to channel opening (potentiation).
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