Evaluation of alpha7 nicotinic receptor agonist on gabaergic synaptic activity
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Transcript of Evaluation of alpha7 nicotinic receptor agonist on gabaergic synaptic activity
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Evaluation of an 7 nicotinic receptor
agonist on GABAergic spontaneous
synaptic transmission in the
hippocampus
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SUMMARY
Objectives
Materials & Methods Preparation of acute rats hippocampal slices
Slice perfusion and neurons visualization
Patch-clamp recordings and analysis
Results
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OBJECTIVES
To document the pharmacological activity of a selective a7 nAChR agonist in an acute hippocampal slice
To illustrate the pre-synaptic modulation of a7 nAChRs on spontaneous GABAergic synpatic transmission
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MATERIALS & METHODS
Preparation of acute rats hippocampal slices Experiments are carried out with Sprague-Dawley between 3 and 4 week of age
Acute horizontal brain slices (400 µm thickness) are cut with a Leica VT1200S in a ice-cold oxygenated sucrose solution (in mM: sucrose 249, KCl 2.5, MgSO4 2, NaH2PO4 1.2, NaHCO3 26, D-glucose 11 and kynurenic acid 1).
Then 4-5 slices containing the hippocampus are incubated at room temperature for at least 1h into an incubation chamber containing ACSF (in mM: NaCl 119, KCl 2.5, CaCl2 2.5, MgCl2 1.3, NaHCO3 25, NaH2PO4 1.2, D-glucose 11). All solutions are continuously bubbled with carbogen gas (95% CO2, 5% O2).
Slice perfusion and neurons visualization For experiments, the slices are transferred into a recording chamber containing about 1 ml of the above ACSF and continuously perfused with ACSF at 1.5 ml/min. Neurons are visualized using infrared differential interference contrast (IR-DIC) microscopy and a 60x objective. Pyramidal neurons of the CA1 region are visually identified for recordings.
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Patch-clamp recordings and analysis
Whole-cell patch clamp experiments are performed in voltage-clamp mode using a software-controlled MultiClamp 700B amplifier in combination with a Digidata 1440A digitizer. Data were low-pass filtered at 2 kHz before being sampled at 10 kHz using Clampex 10 (all from Molecular Devices). The pipette solution contains (in mM): KCl 110, Kgluconate 5, NaCl 5, CaCl2 1, MgCl2 2, EGTA 10, HEPES 10, Na2ATP 2, Na3GTP 0.3, pH 7.2. Cells are held at -60 mV. In order to block postsynaptic spiking activities, 5 mM QX-314(-Cl) are added to the pipette solution. With a holding potential of -60 mV, the GABA-A-evoked currents are inward. Spontaneous inhibitory postsynaptic currents (sIPSCs) are pharmacologically isolated by adding 30 µM of the NMDA receptor antagonist D-AP5 and 10 µM of the AMPA/kainate receptor antagonist CNQX to the bath solution.
GABAergic spontaneous IPSCs (sIPSCs) are recorded from pyramidal cells of the CA1 area of hippocampus for 10 minutes (control) after observing a stable activity for a 5 minute period. The compound (PNU282987) is then wash-in for 20 minutes and, an additional 10 minutes slot is recorded under the compound. To further verify if the sIPSCs are GABAA-mediated currents, 10 µM bicuculline are perfused at the end of each experiment into the bath solution to block all the spontaneous events.
The frequency of the sIPSCs are analyzed with a proprietary script developed by NEUROSERVICE: automatic sIPSCs detection is performed with margin of errors less than 5% in detection of the overall events.
MATERIALS & METHODS
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RESULTS
Representative traces of recording cells under different conditions:
Freq=4,5 Hz
Freq=7,2 Hz (57% increase relative to control)
400pA 2s
400pA 2s
400pA 2s
Addition of Bicuculline at 10µM block all activity, confirming that synaptic events where GABAergic spontaneous IPSCs
ACSF
ACSF + PNU282987 300nM
Control
VS
PNU282987
ACSF + PNU282987 300nM + Bicuculline 10µM
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RESULTS
Statistical analysis of the effect of PNU282987 on the frequency of sIPSCs
Cumulative plot of inter-event interval showing that PNU282987 at 300nM increase the frequency of sIPSCs (n=6)
Change in the frequency of spontaneous activity relative to baseline and PNU282987 at 30, 300 and 1000 nM (n=6 per concentration).
PNU282987 (nM)
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CONCLUSIONS
The frequency of the GABAergic sIPSCs recorded from pyramidal cells in the CA1 area of the hippocampus changes in the presence of PNU282987 (30, 300, 1000nM) indicating an 7 nAChRs-mediated modulation of GABAergic minis’ sIPSCs.
As previously shown (Hajos M et al., 2004), concentrations of 30 and 300 nM increase the frequency of sIPSCs whereas 1000 nM decreases it, possibly reflecting the desensitization of 7 nAChRs.
Bath application of bicuculline block all the sIPSC in pyramidal cells, confirming the GABAergic nature of spontaneous IPSCs.
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