γ-Aminobutyric acidB autoreceptors in substantia nigra and neostriatum of the weaver mutant mouse

The weaver mutation causes cell loss in the center of the substantia nigra, pars compacta. We compared the depression of γ-aminobutyric acid (GABA)A synaptic currents by the GABAB agonist R-baclofen in pars compacta neurons of weaver mice which were largely spared from cell degeneration and of wild-...

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Hauptverfasser: Radnikow, Gabriele (VerfasserIn) , Titz, Stefan (VerfasserIn) , Mades, Sandra Hedwig (VerfasserIn) , Bäurle, Jörg (VerfasserIn) , Misgeld, Ulrich (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 6 February 2001
In: Neuroscience letters
Year: 2001, Jahrgang: 299, Heft: 1, Pages: 81-84
ISSN:1872-7972
DOI:10.1016/S0304-3940(01)01496-3
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/S0304-3940(01)01496-3
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S0304394001014963
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Verfasserangaben:Gabriele Radnikow, Stefan Titz, Sandra Mades, Jörg Bäurle, Ulrich Misgeld

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520 |a The weaver mutation causes cell loss in the center of the substantia nigra, pars compacta. We compared the depression of γ-aminobutyric acid (GABA)A synaptic currents by the GABAB agonist R-baclofen in pars compacta neurons of weaver mice which were largely spared from cell degeneration and of wild-type mice. In weaver neurons the suppression of GABAA synaptic currents by R-baclofen was reduced compared to wild-type neurons. The EC50 of R-baclofen was 6.3 times higher in weaver than in wild-type mice. In the neostriatum, which is not a target of the mutation, such a difference did not exist. We conclude that in the pars compacta the weaver mutation leads to a reduced presynaptic autoinhibition through GABAB receptors which may promote survival of a subset of weaver neurons in the pars compacta. 
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