Dopaminergic Modulation of Excitatory Transmission in the Anterior Cingulate Cortex of Adult Mice

Autor: Soroush Darvish-Ghane, Min Zhuo, Manabu Yamanaka
Rok vydání: 2016
Předmět:
0301 basic medicine
Male
Aging
evoked excitatory postsynaptic currents
Dopamine
AMPA/KA receptors
Synaptic Transmission
Receptors
G-Protein-Coupled

0302 clinical medicine
Receptors
Kainic Acid

Postsynaptic potential
spontaneous excitatory postsynaptic currents
Chemistry
musculoskeletal
neural
and ocular physiology

Pyramidal Cells
Glutamate receptor
Long-term potentiation
Excitatory postsynaptic potential
Molecular Medicine
medicine.drug
Signal Transduction
Research Article
medicine.medical_specialty
AMPA receptor
Tetrodotoxin
Inhibitory postsynaptic potential
Gyrus Cinguli
Models
Biological

Anterior cingulate cortex
03 medical and health sciences
Cellular and Molecular Neuroscience
Internal medicine
medicine
Animals
alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid
D2 receptors
Post-tetanic potentiation
Receptors
Dopamine D2

miniature excitatory postsynaptic currents
Excitatory Postsynaptic Potentials
Neural Inhibition
Benzazepines
Mice
Inbred C57BL

030104 developmental biology
Anesthesiology and Pain Medicine
Endocrinology
nervous system
Sulpiride
Neuroscience
030217 neurology & neurosurgery
Zdroj: Molecular Pain
ISSN: 1744-8069
Popis: Dopamine (DA) possesses potent neuromodulatory properties in the central nervous system. In the anterior cingulate cortex, α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors (AMPAR) are key ion channels in mediating nerve injury induced long-term potentiation (LTP) and chronic pain phenotype. In the present study, we reported the effects of DA on glutamate mediated excitatory post-synaptic currents (EPSCs) in pyramidal neurons of layer II/III of the ACC in adult mice. Bath application of DA (50 μM) caused a significant, rapid and reversible inhibition of evoked EPSCs (eEPSC). This inhibitory effect is dose-related and was absent in lower concentration of DA (5 μM). Furthermore, selective postsynaptic application of GDP-β-S (1.6 mM) in the internal solution completely abolished the inhibitory effects of DA (50 μM). We also investigated modulation of spontaneous EPSCs (sEPSCs) and TTX sensitive, miniature EPSCs (mEPSCs) by DA. Our results indicated mixed effects of potentiation and inhibition of frequency and amplitude for sEPSCs and mEPSCs. Furthermore, high doses of SCH23390 (100 μM) and sulpiride (100 μM) revealed that, inhibition of eEPSCs is mediated by postsynaptic D2-receptors (D2R). Our finding posits a pre- and postsynaptic mode of pyramidal neuron EPSC modulation in mice ACC by DA.
Databáze: OpenAIRE