Day-night variations in zinc sensitivity of GABAA receptor-channels in rat suprachiasmatic nucleus
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
14667576
DOI
10.1016/j.molbrainres.2003.09.017
PII: S0169328X03004443
Knihovny.cz E-zdroje
- MeSH
- bikukulin farmakologie MeSH
- cirkadiánní rytmus * MeSH
- GABA antagonisté farmakologie MeSH
- GABA farmakologie MeSH
- krysa rodu Rattus MeSH
- lékové interakce MeSH
- membránové potenciály účinky léků MeSH
- metoda terčíkového zámku MeSH
- nervové vedení účinky léků MeSH
- nervový útlum účinky léků fyziologie MeSH
- neurony účinky léků metabolismus MeSH
- novorozená zvířata MeSH
- nucleus suprachiasmaticus cytologie účinky léků metabolismus MeSH
- potkani Wistar MeSH
- receptory GABA-A účinky léků metabolismus MeSH
- techniky in vitro MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- zinek farmakologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- bikukulin MeSH
- GABA antagonisté MeSH
- GABA MeSH
- receptory GABA-A MeSH
- zinek MeSH
In the suprachiasmatic nucleus (SCN), electrical activity, secretion, and other cellular functions undergo profound rhythm during day-night cycle due to oscillatory expression of clock gene constituents. Although SCN is enriched with gamma-aminobutyric acid (GABA)-ergic neurons, it is unknown whether there are circadian changes in the GABAA receptor expression and/or function. Here we investigated the possible daily variations in zinc sensitivity of GABAA channels in rat SCN neurons maintained in brain slices. Extracellular zinc inhibited GABA-induced currents in all ventrolateral (VL) and dorsomedial (DM) SCN neurons studied, as well as in neurons of non-SCN regions. In SCN neurons, the currents evoked by 30 microM GABA were inhibited by Zn2+ with an IC50 of 50.3+/-3.2 microM, whereas currents evoked by 100 microM GABA were inhibited with an IC50 of 181.6+/-32.0 microM. The antagonist action of zinc saturated at 97.4+/-0.7% for 30 microM GABA and 91.6+/-2.7% for 100 microM GABA. These observations indicate that Zn2+ inhibits SCN GABAA receptor competitively and in part non-competitively. In SCN neurons, but not in other neurons, the zinc sensitivity varied with daily time. During the day, the calculated IC50 for zinc was significantly lower than during the night (43.9+/-4.7 microM vs. 58.6+/-3.8, respectively). These results indicate that native GABAA receptors in SCN neurons display pharmacological properties of receptors having and not having gamma subunit and that the proportionality of these receptors could change during the day and night.
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