Transient Activation of GABAB Receptors Suppresses SK Channel Currents in Substantia Nigra Pars Compacta Dopaminergic Neurons

Autor: D. James Surmeier, Paul Greengard, Joshua A. Goldberg, Lars Brichta, Chad M Estep, Daniel J. Galtieri, Enrico Zampese
Rok vydání: 2016
Předmět:
0301 basic medicine
Male
Patch-Clamp Techniques
Potassium Channels
Small-Conductance Calcium-Activated Potassium Channels
Physiology
lcsh:Medicine
Action Potentials
Stimulation
Biochemistry
Ion Channels
Adenylyl Cyclase Signaling Cascade
Intracellular Receptors
Mice
0302 clinical medicine
Cell Signaling
Postsynaptic potential
Animal Cells
Medicine and Health Sciences
GABAergic Neurons
lcsh:Science
gamma-Aminobutyric Acid
Neurons
Multidisciplinary
Chemistry
GABAA receptor
Physics
Neurochemistry
Neurotransmitters
Signaling Cascades
Electrophysiology
Physical Sciences
GABAergic
Female
Cellular Types
Neurochemicals
Ion Channel Gating
Adenylyl Cyclases
Research Article
Signal Transduction
Signal Inhibition
Biophysics
Neurophysiology
Substantia nigra
GABAB receptor
Membrane Potential
SK channel
03 medical and health sciences
Animals
Pars Compacta
Pars compacta
Dopaminergic Neurons
lcsh:R
Biology and Life Sciences
Proteins
Cell Biology
Receptors
GABA-A

Cyclic AMP-Dependent Protein Kinases
Mice
Inbred C57BL

030104 developmental biology
nervous system
Receptors
GABA-B

Cellular Neuroscience
lcsh:Q
Neuroscience
Dopaminergics
030217 neurology & neurosurgery
Zdroj: PLoS ONE
PLoS ONE, Vol 11, Iss 12, p e0169044 (2016)
ISSN: 1932-6203
Popis: Dopaminergic (DA) neurons in the substantia nigra pars compacta (SNc) are richly innervated by GABAergic neurons. The postsynaptic effects of GABA on SNc DA neurons are mediated by a mixture of GABAA and GABAB receptors. Although activation of GABAA receptors inhibits spike generation, the consequences of GABAB receptor activation are less well characterized. To help fill this gap, perforated patch recordings were made from young adult mouse SNc DA neurons. Sustained stimulation of GABAB receptors hyperpolarized SNc DA neurons, as previously described. However, transient stimulation of GABAB receptors by optical uncaging of GABA did not; rather, it reduced the opening of small-conductance, calcium-activated K+ (SK) channels and increased the irregularity of spiking. This modulation was attributable to inhibition of adenylyl cyclase and protein kinase A. Thus, because suppression of SK channel activity increases the probability of burst spiking, transient co-activation of GABAA and GABAB receptors could promote a pause-burst pattern of spiking.
Databáze: OpenAIRE