Presynaptic D2 dopaminergic receptors mediate inhibition of excitatory synaptic transmission in rat neostriatum

Kuei-Sen Hsu, Chiung Chun Huang, Cheng Hsun Yang, Po-Wu Gean

Research output: Contribution to journalArticle

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Abstract

The effect of dopamine (DA) on excitatory synaptic transmission was studied in rat neostriatal neurons using intracellular- and whole-cell voltage clamp-recording methods. Depolarizing excitatory postsynaptic potentials (EPSPs) were evoked by cortical stimulation. Superfusion of DA (0.01-10 μM) reversibly decreases EPSP in a concentration-dependent manner and with a estimated IC5 of 0.3 μM. In addition, the inhibitory effect induced by DA at a low concentratiion (0.1 μM) was antagonized by sulpiride (1-10 nM), a selective D2 dopaminergic receptor antagonist. However, D1 dopaminergic receptor antagonist SKF-83566 (1-5 μM) did not affect the blocking effect by DA 0.1 μM. Based on these findings, we conclude that DA at a low concentration (≤ 0.1 μM) reduced the excitatory response of neostriatal neurons following cortical stimulation via the activation of D2, but not D1 dopaminergic receptors, located on the terminals of corticostriatal neurons.

Original languageEnglish
Pages (from-to)264-268
Number of pages5
JournalBrain Research
Volume690
Issue number2
DOIs
Publication statusPublished - 1995 Sep 4

Fingerprint

Neostriatum
Synaptic Transmission
Dopamine
Dopamine Antagonists
Excitatory Postsynaptic Potentials
Neurons
Sulpiride

All Science Journal Classification (ASJC) codes

  • Neuroscience(all)
  • Molecular Biology
  • Clinical Neurology
  • Developmental Biology

Cite this

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abstract = "The effect of dopamine (DA) on excitatory synaptic transmission was studied in rat neostriatal neurons using intracellular- and whole-cell voltage clamp-recording methods. Depolarizing excitatory postsynaptic potentials (EPSPs) were evoked by cortical stimulation. Superfusion of DA (0.01-10 μM) reversibly decreases EPSP in a concentration-dependent manner and with a estimated IC5 of 0.3 μM. In addition, the inhibitory effect induced by DA at a low concentratiion (0.1 μM) was antagonized by sulpiride (1-10 nM), a selective D2 dopaminergic receptor antagonist. However, D1 dopaminergic receptor antagonist SKF-83566 (1-5 μM) did not affect the blocking effect by DA 0.1 μM. Based on these findings, we conclude that DA at a low concentration (≤ 0.1 μM) reduced the excitatory response of neostriatal neurons following cortical stimulation via the activation of D2, but not D1 dopaminergic receptors, located on the terminals of corticostriatal neurons.",
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Presynaptic D2 dopaminergic receptors mediate inhibition of excitatory synaptic transmission in rat neostriatum. / Hsu, Kuei-Sen; Huang, Chiung Chun; Yang, Cheng Hsun; Gean, Po-Wu.

In: Brain Research, Vol. 690, No. 2, 04.09.1995, p. 264-268.

Research output: Contribution to journalArticle

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