Day-night variations in zinc sensitivity of GABAA receptor-channels in rat suprachiasmatic nucleus
Language English Country Netherlands Media print
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
14667576
DOI
10.1016/j.molbrainres.2003.09.017
PII: S0169328X03004443
Knihovny.cz E-resources
- MeSH
- Bicuculline pharmacology MeSH
- Circadian Rhythm * MeSH
- GABA Antagonists pharmacology MeSH
- gamma-Aminobutyric Acid pharmacology MeSH
- Rats MeSH
- Drug Interactions MeSH
- Membrane Potentials drug effects MeSH
- Patch-Clamp Techniques MeSH
- Neural Conduction drug effects MeSH
- Neural Inhibition drug effects physiology MeSH
- Neurons drug effects metabolism MeSH
- Animals, Newborn MeSH
- Suprachiasmatic Nucleus cytology drug effects metabolism MeSH
- Rats, Wistar MeSH
- Receptors, GABA-A drug effects metabolism MeSH
- In Vitro Techniques MeSH
- Dose-Response Relationship, Drug MeSH
- Zinc pharmacology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Bicuculline MeSH
- GABA Antagonists MeSH
- gamma-Aminobutyric Acid MeSH
- Receptors, GABA-A MeSH
- Zinc 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.
References provided by Crossref.org
Potentiation of inhibitory synaptic transmission by extracellular ATP in rat suprachiasmatic nuclei