author_facet Ye, Jiang-Hong
Wang, Fushun
Krnjević, Kresimir
Wang, Weizhen
Xiong, Zhi-Gang
Zhang, Jingli
Ye, Jiang-Hong
Wang, Fushun
Krnjević, Kresimir
Wang, Weizhen
Xiong, Zhi-Gang
Zhang, Jingli
author Ye, Jiang-Hong
Wang, Fushun
Krnjević, Kresimir
Wang, Weizhen
Xiong, Zhi-Gang
Zhang, Jingli
spellingShingle Ye, Jiang-Hong
Wang, Fushun
Krnjević, Kresimir
Wang, Weizhen
Xiong, Zhi-Gang
Zhang, Jingli
The Journal of Neuroscience
Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
General Neuroscience
author_sort ye, jiang-hong
spelling Ye, Jiang-Hong Wang, Fushun Krnjević, Kresimir Wang, Weizhen Xiong, Zhi-Gang Zhang, Jingli 0270-6474 1529-2401 Society for Neuroscience General Neuroscience http://dx.doi.org/10.1523/jneurosci.2016-04.2004 <jats:p>GABA-mediated postsynaptic currents (IPSCs) were recorded from dopaminergic (DA) neurons of the ventral tegmental area (VTA) of rats, in acute brain slices, and from enzymatically or mechanically dissociated neurons. In young rats (3-10 d of age), where GABA is excitatory, glycine (1-3 μ<jats:sc>m</jats:sc>) and taurine (10-30 μ<jats:sc>m</jats:sc>) increased the amplitude of evoked IPSCs (eIPSCs) and the frequency of spontaneous IPSCs (sIPSCs) but had minimal postsynaptic effects. Strychnine (1 μ<jats:sc>m</jats:sc>) blocked the action of glycine; when applied alone, it reduced the amplitude of eIPSCs and the frequency of sIPSCs, indicating a tonic facilitation of GABAergic excitation by some endogenous glycine agonist(s). In medium containing no Ca<jats:sup>2+</jats:sup>, or with Cd<jats:sup>2+</jats:sup>or tetrodotoxin added, the amplitude and especially the frequency of sIPSCs greatly diminished. In many cells, glycine had no effect on remaining miniature IPSCs, suggesting a preterminal site of glycine receptors (GlyRs). Fura-2 fluorescent imaging showed a glycine-induced increase of [Ca<jats:sup>2+</jats:sup>] in nerve terminals (on DA neurons), which was suppressed by strychnine or 3 μ<jats:sc>m</jats:sc>ω-conotoxin MVIIA. Therefore, the presynaptic GlyR-mediated facilitation of GABAergic transmission seems to be mediated by N- and/or P/Q-type Ca<jats:sup>2+</jats:sup>channels. In older rats (22-30 d of age), where GABA causes inhibition, the effect of strychnine on GABAergic IPSCs was reversed to facilitation, indicating a tonic glycinergic inhibition of GABA release. Furthermore, glycine (1-3 μ<jats:sc>m</jats:sc>) reduced the amplitude of eIPSCs and the frequency of sIPSCs. Hence, the overall effect of the presynaptic action of glycine is to enhance the firing of DA cells, both in very young and older rats.</jats:p> Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area The Journal of Neuroscience
doi_str_mv 10.1523/jneurosci.2016-04.2004
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recordtype ai
record_format ai
series The Journal of Neuroscience
source_id 49
title Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
title_unstemmed Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
title_full Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
title_fullStr Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
title_full_unstemmed Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
title_short Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
title_sort presynaptic glycine receptors on gabaergic terminals facilitate discharge of dopaminergic neurons in ventral tegmental area
topic General Neuroscience
url http://dx.doi.org/10.1523/jneurosci.2016-04.2004
publishDate 2004
physical 8961-8974
description <jats:p>GABA-mediated postsynaptic currents (IPSCs) were recorded from dopaminergic (DA) neurons of the ventral tegmental area (VTA) of rats, in acute brain slices, and from enzymatically or mechanically dissociated neurons. In young rats (3-10 d of age), where GABA is excitatory, glycine (1-3 μ<jats:sc>m</jats:sc>) and taurine (10-30 μ<jats:sc>m</jats:sc>) increased the amplitude of evoked IPSCs (eIPSCs) and the frequency of spontaneous IPSCs (sIPSCs) but had minimal postsynaptic effects. Strychnine (1 μ<jats:sc>m</jats:sc>) blocked the action of glycine; when applied alone, it reduced the amplitude of eIPSCs and the frequency of sIPSCs, indicating a tonic facilitation of GABAergic excitation by some endogenous glycine agonist(s). In medium containing no Ca<jats:sup>2+</jats:sup>, or with Cd<jats:sup>2+</jats:sup>or tetrodotoxin added, the amplitude and especially the frequency of sIPSCs greatly diminished. In many cells, glycine had no effect on remaining miniature IPSCs, suggesting a preterminal site of glycine receptors (GlyRs). Fura-2 fluorescent imaging showed a glycine-induced increase of [Ca<jats:sup>2+</jats:sup>] in nerve terminals (on DA neurons), which was suppressed by strychnine or 3 μ<jats:sc>m</jats:sc>ω-conotoxin MVIIA. Therefore, the presynaptic GlyR-mediated facilitation of GABAergic transmission seems to be mediated by N- and/or P/Q-type Ca<jats:sup>2+</jats:sup>channels. In older rats (22-30 d of age), where GABA causes inhibition, the effect of strychnine on GABAergic IPSCs was reversed to facilitation, indicating a tonic glycinergic inhibition of GABA release. Furthermore, glycine (1-3 μ<jats:sc>m</jats:sc>) reduced the amplitude of eIPSCs and the frequency of sIPSCs. Hence, the overall effect of the presynaptic action of glycine is to enhance the firing of DA cells, both in very young and older rats.</jats:p>
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author Ye, Jiang-Hong, Wang, Fushun, Krnjević, Kresimir, Wang, Weizhen, Xiong, Zhi-Gang, Zhang, Jingli
author_facet Ye, Jiang-Hong, Wang, Fushun, Krnjević, Kresimir, Wang, Weizhen, Xiong, Zhi-Gang, Zhang, Jingli, Ye, Jiang-Hong, Wang, Fushun, Krnjević, Kresimir, Wang, Weizhen, Xiong, Zhi-Gang, Zhang, Jingli
author_sort ye, jiang-hong
container_issue 41
container_start_page 8961
container_title The Journal of Neuroscience
container_volume 24
description <jats:p>GABA-mediated postsynaptic currents (IPSCs) were recorded from dopaminergic (DA) neurons of the ventral tegmental area (VTA) of rats, in acute brain slices, and from enzymatically or mechanically dissociated neurons. In young rats (3-10 d of age), where GABA is excitatory, glycine (1-3 μ<jats:sc>m</jats:sc>) and taurine (10-30 μ<jats:sc>m</jats:sc>) increased the amplitude of evoked IPSCs (eIPSCs) and the frequency of spontaneous IPSCs (sIPSCs) but had minimal postsynaptic effects. Strychnine (1 μ<jats:sc>m</jats:sc>) blocked the action of glycine; when applied alone, it reduced the amplitude of eIPSCs and the frequency of sIPSCs, indicating a tonic facilitation of GABAergic excitation by some endogenous glycine agonist(s). In medium containing no Ca<jats:sup>2+</jats:sup>, or with Cd<jats:sup>2+</jats:sup>or tetrodotoxin added, the amplitude and especially the frequency of sIPSCs greatly diminished. In many cells, glycine had no effect on remaining miniature IPSCs, suggesting a preterminal site of glycine receptors (GlyRs). Fura-2 fluorescent imaging showed a glycine-induced increase of [Ca<jats:sup>2+</jats:sup>] in nerve terminals (on DA neurons), which was suppressed by strychnine or 3 μ<jats:sc>m</jats:sc>ω-conotoxin MVIIA. Therefore, the presynaptic GlyR-mediated facilitation of GABAergic transmission seems to be mediated by N- and/or P/Q-type Ca<jats:sup>2+</jats:sup>channels. In older rats (22-30 d of age), where GABA causes inhibition, the effect of strychnine on GABAergic IPSCs was reversed to facilitation, indicating a tonic glycinergic inhibition of GABA release. Furthermore, glycine (1-3 μ<jats:sc>m</jats:sc>) reduced the amplitude of eIPSCs and the frequency of sIPSCs. Hence, the overall effect of the presynaptic action of glycine is to enhance the firing of DA cells, both in very young and older rats.</jats:p>
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spelling Ye, Jiang-Hong Wang, Fushun Krnjević, Kresimir Wang, Weizhen Xiong, Zhi-Gang Zhang, Jingli 0270-6474 1529-2401 Society for Neuroscience General Neuroscience http://dx.doi.org/10.1523/jneurosci.2016-04.2004 <jats:p>GABA-mediated postsynaptic currents (IPSCs) were recorded from dopaminergic (DA) neurons of the ventral tegmental area (VTA) of rats, in acute brain slices, and from enzymatically or mechanically dissociated neurons. In young rats (3-10 d of age), where GABA is excitatory, glycine (1-3 μ<jats:sc>m</jats:sc>) and taurine (10-30 μ<jats:sc>m</jats:sc>) increased the amplitude of evoked IPSCs (eIPSCs) and the frequency of spontaneous IPSCs (sIPSCs) but had minimal postsynaptic effects. Strychnine (1 μ<jats:sc>m</jats:sc>) blocked the action of glycine; when applied alone, it reduced the amplitude of eIPSCs and the frequency of sIPSCs, indicating a tonic facilitation of GABAergic excitation by some endogenous glycine agonist(s). In medium containing no Ca<jats:sup>2+</jats:sup>, or with Cd<jats:sup>2+</jats:sup>or tetrodotoxin added, the amplitude and especially the frequency of sIPSCs greatly diminished. In many cells, glycine had no effect on remaining miniature IPSCs, suggesting a preterminal site of glycine receptors (GlyRs). Fura-2 fluorescent imaging showed a glycine-induced increase of [Ca<jats:sup>2+</jats:sup>] in nerve terminals (on DA neurons), which was suppressed by strychnine or 3 μ<jats:sc>m</jats:sc>ω-conotoxin MVIIA. Therefore, the presynaptic GlyR-mediated facilitation of GABAergic transmission seems to be mediated by N- and/or P/Q-type Ca<jats:sup>2+</jats:sup>channels. In older rats (22-30 d of age), where GABA causes inhibition, the effect of strychnine on GABAergic IPSCs was reversed to facilitation, indicating a tonic glycinergic inhibition of GABA release. Furthermore, glycine (1-3 μ<jats:sc>m</jats:sc>) reduced the amplitude of eIPSCs and the frequency of sIPSCs. Hence, the overall effect of the presynaptic action of glycine is to enhance the firing of DA cells, both in very young and older rats.</jats:p> Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area The Journal of Neuroscience
spellingShingle Ye, Jiang-Hong, Wang, Fushun, Krnjević, Kresimir, Wang, Weizhen, Xiong, Zhi-Gang, Zhang, Jingli, The Journal of Neuroscience, Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area, General Neuroscience
title Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
title_full Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
title_fullStr Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
title_full_unstemmed Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
title_short Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
title_sort presynaptic glycine receptors on gabaergic terminals facilitate discharge of dopaminergic neurons in ventral tegmental area
title_unstemmed Presynaptic Glycine Receptors on GABAergic Terminals Facilitate Discharge of Dopaminergic Neurons in Ventral Tegmental Area
topic General Neuroscience
url http://dx.doi.org/10.1523/jneurosci.2016-04.2004