Effects of Propofol on Glutamate-Induced Calcium Mobilization in Presynaptic Boutons of Rat Hippocampal Neurons

Shinichi Ito, Noriko Karube, Hitomi Sugiyama, Jun Hirokawa, Seiko Kitahara, Takeshi Yokoyama

Department of Dental Anesthesiology, Faculty of Dental Science, Kyushu University, Fukuoka, Japan.

DOI: 10.4236/ojanes.2016.63005                

Abstract

Recent reports have suggested that various general anesthetics affect presynaptic processes in the central nervous system. However, characterizations of the influence of intravenous anesthetics on neurotransmitter release from presynaptic nerve terminals (boutons) are insufficient. Because the presynaptic calcium concentration ([Ca²⁺]_pre) regulates neurotransmitter release, we investigate the effects of the intravenous anesthetic propofol on neurotransmitter release by measuring [Ca²⁺]_pre in the presynaptic boutons of individual dissociated hippocampal neurons. Brain slices were prepared from Sprague–Dawley rats (10 - 14 days of age). The hippocampal CA1 area was isolated with a fire-polished glass pipette, which vibrated horizontally to dissociate hippocampal CA1 neurons along with their attached presynaptic boutons. Presynaptic boutons were visualized under a confocal laser scanning microscope after staining with FM1-43 dye, and [Ca²⁺]_pre was measured using fluo-3 AM dye. Glutamate (3 – 100 μM) administration increased [Ca2+]_pre in Ca^2+- containing external solution in a concentration-dependent manner. Propofol (3 – 30 μM) dose-dependently suppressed this glutamate (30 μM)-induced increase in [Ca²⁺]_pre in boutons attached to dendrites, but not to the soma or base of the dendritic tree. The large majority of excitatory synapses on CA1 neurons are located on dendritic spines; therefore, propofol may affect glutamate-induced Ca²⁺ mobilization in excitatory, but not inhibitory, presynaptic boutons. Propofol may possibly have some effect on glutamate-regulated neurotransmitter release from excitatory presynaptic nerve terminals through inhibiting the increase in [Ca²⁺]_pre induced by glutamate.

Keywords

Propofol, Calcium Signaling, Presynaptic Terminals, Hippocampus, Glutamic Acid

Received 19 February 2016; accepted 14 March 2016; published 17 March 2016

1. Introduction

The intravenous anesthetic propofol is frequently used in general anesthesia and intravenous sedation. It is typically thought that propofol mainly affects γ-aminobutyric acid type A (GABA_A) receptors on the postsynaptic membrane of neurons in the central nervous system [1] - [7] . Recently, however, there has been great interest in the effects of propofol on presynaptic events, as several reports have suggested that propofol regulates neurotransmitter release from presynaptic nerve terminals (boutons) [8] -[11] . However, knowledge of the effects of propofol on presynaptic processes remains limited.

Glutamate acts postsynaptically as the main excitatory neurotransmitter in the brain, but is also a regulator of many presynaptic processes [12] - [14] . Presynaptic glutamate ionotropic receptors, e.g. α-Amino-3-hydroxy-5- methyl-4-isoxazolepropionic acid (AMPA)-, kainite- and N-methyl-D-aspartate (NMDA)-type receptors, are a key component of the neurotransmitter release machinery [12] [14] . In addition, metabotropic glutamate receptors mediate presynaptic processes [15] [16] . However, it is unclear if and how general anesthetics, including propofol, affect glutamate-regulated neurotransmitter release from presynaptic boutons.

The release of neurotransmitters is regulated by the presynaptic Ca²⁺ concentration ([Ca²⁺]_pre) [17] [18] . To understand the influence of general anesthetics on presynaptic events, it is therefore necessary to characterize changes in presynaptic Ca²⁺ dynamics after anesthesia administration. In this study, we investigated the effects of the intravenous anesthetic propofol on glutamate-regulated neurotransmitter release by measuring [Ca²⁺]_pre in the presynaptic boutons of hippocampal neurons.

2. Materials and Methods

2.1. Mechanical Dissociation of Hippocampal CA1 Neurons

All experiments were performed under the Guidance for Animal Experiments at the Faculty of Dental Science, Kyushu University. Ethical approval for this study (Approval Number A20-125-0) was obtained from Animal Care and Use Committee, Kyushu University, Fukuoka, Japan.

Hippocampal CA1 pyramidal neurons were dissociated from 10 - 14 day-old Sprague-Dawley rats as previously described [8] . Briefly, the brain was quickly cut into slices of 400-µm thickness using a microslicer (DTK-3000W; Dosaka EM, Kyoto, Japan). The slices were then placed in an incubation solution for 1 h, and saturated with 95% O₂ and 5% CO₂ at room temperature (23˚C - 27˚C). For disassociation, the slices were placed in a chamber containing standard external solution (500 µl, see description below), and the hippocampal CA1 region was contacted with a fire-polished glass pipette. The pipette was mechanically vibrated horizontally for 1 min using a custom-made device, which caused dissociation of pyramidal neurons along with the attached presynaptic boutons [8] [19] .

2.2. Presynaptic Calcium Measurement and Staining with FM 1-43

The dissociated neurons were incubated in standard external solution containing the acetoxymethyl ester of fluo- 3 (fluo-3 AM; 10 µM) and Pluronic F-127 (0.01%) for 30 min at room temperature. The fluo-3AM-loaded presynaptic boutons that were attached to the rat hippocampal CA1 pyramidal neurons were exposed to the standard external solution containing various concentrations (3, 10, 30 and 100 µM) of glutamate for 10 s at room temperature. Images of fluo-3-labeled neurons and their adherent presynaptic boutons were obtained using a confocal laser scanning microscope (IX70; Olympus, Tokyo, Japan). The dye-labeled neurons were excited at 488 nm by passing an argon laser beam through an objective lens (UPlanApo 40X; Olympus, Tokyo, Japan), and fluo-3 fluorescent green signals were recorded through a 505-525-nm bandpass filter using a scan unit (FVX-SU; Olympus, Tokyo, Japan) at 0.42 s intervals.

After measuring the changes in fluo-3 fluorescence intensity, individual presynaptic boutons were visualized by high K⁺ depolarization in the presence of FM1-43, as follows. A dissociated neuron was exposed to a 60 mM K⁺-containing standard external solution (prepared by replacing 55 mM NaCl with equimolar KCl) for 30 s in the presence of 10 µM FM1-43 and then washed with a standard external solution for 10 min. The FM1-43 dye was excited with an argon laser, and the emitted green fluorescence signal was recorded using a 560-nm longpass filter. The FM1-43-labeled boutons expressed a pseudo red color that distinguished them from the fluo-3 green signals. The morphology of the hippocampal neurons was clearly visualized in the fluo-3 images, and the cellular regions to which the presynaptic boutons attached were thereby readily distinguished in fluorescent images after measurement of fluo-3 and FM1-43 fluorescence, as previously described [8] . In order to estimate [Ca²⁺]_pre, the mean intensity (F) of the boutons was calculated, and the data were expressed as the ratio of fluorescence intensity change (ΔF = F − F₀) relative to the control values before stimulation (F₀), i.e. ΔF/F₀. In order to smooth the noise, the peak values of the changes in [Ca²⁺]_pre were calculated as the average of 6 - 12 points of the maximum response in each bouton.

In order to elucidate the effects of propofol on the glutamate-induced increase in [Ca²⁺]_pre in presynaptic boutons, propofol (3 - 30 µM) was pretreated for 3 min in the standard external solution and was present during the application of 30 µM glutamate.

2.3. Solutions

The incubation solution was saturated with 95% O₂ + 5% CO₂ and contained (in mM): NaCl (125), KCl (2.5), CaCl₂ (2), MgCl₂ (2), NaH₂PO₄ (1.5), NaHCO₃ (26), and glucose (20). The standard external solution (pH 7.4) contained (in mM): NaCl (150), KCl (5), CaCl₂ (2), MgCl₂ (1), HEPES (5), and glucose (10). The concentration of K⁺ was modified isosmotically by replacing NaCl with KCl.

2.4. Drugs

The drugs used were L-glutamic acid, dimethyl sulfoxide (DMSO), HEPES, Pluronic F-127 (Sigma-Aldrich, Inc, St. Louis MO, USA), fluo-3 AM (Dojindo Laboratories, Kumamoto, Japan), FM1-43 (Molecular Probes, Inc, Eugene OR, USA), and 2, 6-diisopropylphenol (propofol; Tokyo Chemical Industry Co, Ltd, Tokyo, Japan).

2.5. Statistics

Data are presented as mean ± standard error of mean (SEM). The results were tested with analysis of variance (ANOVA) followed by Dunnett’s test. Differences between control and test values were considered significant when P < 0.05. Analyses were carried out using the Japanese version of KaleidaGraph software (Version 4.5.0; Synergy Software, Reading PA, USA).

3. Results

3.1. Identification of Presynaptic Boutons

Single presynaptic boutons on a hippocampal CA1 pyramidal neuron were stained with FM1-43 after Ca²⁺ measurement so that the green fluorescence emitted by FM1-43 would not affect the measurement of fluo-3 fluorescence intensity changes. The FM1-43-labelled presynaptic boutons expressed a pseudo red color that distinguished them from the fluo-3 green fluorescence (Figure 1). To confirm that these FM1-43 labelling spots represented single boutons, a 60 mM K⁺-containing external solution was applied to the neurons. A red spot that disappeared after high K⁺ stimulation was considered a presynaptic bouton (data not shown) [19] . In order to estimate [Ca²⁺]_pre in a presynaptic bouton, the mean fluo-3 fluorescence intensity of a red spot was calculated.

3.2. Glutamate-Induced Increases in [Ca²⁺]_pre in Presynaptic Boutons

An external solution containing 2 mM Ca²⁺ and various concentrations of glutamate (3 - 100 µM) was applied to the presynaptic boutons attached to the rat hippocampal CA1 pyramidal neurons for 10 s at room temperature (23˚C - 27˚C). First, we found that the application of 30 µM glutamate produced a rapid increase in [Ca²⁺]_pre in the Ca²⁺-containing external solution (Figure 2(a)). Then, we tested the dose response of presynaptic boutons to glutamate (3 - 100 µM) and observed a concentration-dependent increase in [Ca²⁺]_pre (Figure 2(b)). Glutamate (3 - 100 µM) produced an increase in [Ca²⁺]_pre in 72.8% of the presynaptic boutons attached to the soma and the base of the dendritic tree, while 51.1% of the boutons attached to dendrites responded to glutamate (Table 1).

3.3. Effects of Propofol on the Glutamate-Induced Increase in [Ca²⁺]_pre

We investigated the effects of propofol on glutamate (30 µM)-induced presynaptic Ca²⁺ mobilization in the rat hippocampal CA1 pyramidal neuron. A large majority of excitatory synapses are located on dendritic spines [20] [21] . On the other hand, inhibitory boutons mainly attach to the soma or the base of the dendritic tree [19] .

Figure 1. Fluorescence image of a hippocampal CA1 pyramidal neuron. After measurement of changes in fluo-3 fluorescence intensity, a dissociated hippocampal neuron along with the attached presynaptic boutons was exposed to 10 µM FM1-43 in a 60 mM K+-containing standard external solution for 30 s. Subsequently, the neuron was washed with the standard solution. The FM1-43-labelled presynaptic boutons expressed a pseudo red color that distinguished them from the fluo-3 green fluorescence.

Figure 2. Glutamate induced an increase in [Ca²⁺] pre in the presence of external Ca²⁺. (a) Representative trace of 20 experiments indicating that 30 µM glutamate produced an increase in [Ca²⁺]_pre in rat hippocampal neurons in an external solution containing 2 mM Ca²⁺. (b) A concentration-response curve indicating a dose dependent glutamate-induced [Ca²⁺]_pre increase in Ca²⁺-containing solution. The ordinate shows the peak [Ca²⁺]_pre of the response after subtracting the baseline value. The data points indicate mean ± SEM of 11 - 20 boutons from 8 - 12 neurons. [Ca²⁺]_pre: presynaptic Ca²⁺ concentration.

Table 1. The number and the proportion of boutons that responded to glutamate (3 - 100 µM).

Therefore, the effects of propofol on Ca²⁺ dynamics in presynaptic boutons vary across different attachment sites.

The glutamate (30 µM)-induced changes in [Ca²⁺]_pre in the Ca²⁺-containing external solution were used as controls. Figure 3(a) and Figure 4(a) show the representative traces of controls in the bouton attached to dendrite and soma, respectively. Pretreatment with propofol (10 µM) for 3 min inhibited the 30 µM glutamate-indu- ced increase in [Ca²⁺]_pre in presynaptic boutons attached to dendrites (Figure 3(b)). However, no inhibitory effect of propofol (10 µM) was observed in presynaptic boutons attached to the soma (Figure 4(b)). Moreover, pretreatment with propofol (3 - 30 µM) dose-dependently inhibited the 30 µM glutamate-induced increase in [Ca²⁺]_pre in presynaptic boutons attached to dendrites (Figure 5(a)), but not to the soma or base of the dendritic tree (Figure 5(b)).

4. Discussion

In this study, we investigated the effects of propofol on the glutamate-induced increase in [Ca²⁺]_pre in the presynaptic boutons of hippocampal CA1 pyramidal neurons. Glutamate (3 - 100 µM) concentration-dependently in

Figure 3. Propofol inhibited the glutamate-induced increase in [Ca²⁺]_pre in boutons attached to dendrites. Glutamate (30 µM) was applied for 10 s in an external solution containing 2 mM Ca²⁺ and boutons at dendrites were analyzed in (a) control and (b) pretreatment for 3 min with 10 µM propofol. The results illustrate [Ca²⁺]_pre in boutons from different dendrites in either condition (a) or (b).

Figure 4. Propofol did not affect glutamate-induced increases in [Ca²⁺]_pre in boutons attached to the soma. Glutamate (30 µM) was applied for 10 s in an external solution containing 2 mM Ca²⁺ in (a) control and (b) pretreatment for 3 min with 10 µM propofol. The results illustrate [Ca²⁺]_pre in boutons from the different soma in either condition (a) or (b).

Figure 5. Dose dependent effects of propofol on the 30 µM glutamate-induced increase in [Ca²⁺]_pre in dendrites. Each column indicates the average of the peak value of the 30 µM glutamate-induced increase in [Ca²⁺]_pre in boutons on either the dendrite or the soma/base of the dendrite. (a) The boutons attached to dendrites were pretreated with propofol at a range of concentrations (3 µM; 6 boutons from 4 neurons, 10 µM; 8 boutons from 5 neurons, 30 µM; 6 boutons from 5 neurons). Pretreatment with propofol (10 - 30 µM) inhibited the 30 µM glutamate-induced increase in [Ca²⁺]_pre (control; 8 boutons, 6 neurons) in a concentration-dependent manner. (b) In the boutons attached to the soma or base of dendrite, there was no significant difference between the control (11 boutons from 7 neurons) and pretreatment with propofol groups (3 µM; 6 boutons from 5 neurons, 10 µM; 6 boutons from 4 neurons, 30 µM; 6 boutons from 5 neurons). Data are presented as mean ± SEM. *P < 0.05 and **P < 0.01 represent significant difference from each control, respectively.

creased [Ca²⁺]_pre in neurons/boutons bathed in a Ca²⁺-containing external solution. Furthermore, propofol (10 - 30 µM) suppressed the glutamate (30 µM)-induced increase in [Ca²⁺]_pre in the boutons attached to dendrites, but not the boutons attached to the soma or the base of the dendritic tree; this finding is consistent with an effect primarily on excitatory synapses.

Many reports have indicated that increases in [Ca²⁺]_pre are caused by Ca²⁺ influx via voltage-gated Ca²⁺ channels, and that a rise in presynaptic Ca²⁺ triggers the release of neurotransmitters from boutons [17] [18] [22] -[24] . In the present experiments, glutamate (3 - 100 µM) did not increase [Ca²⁺]_pre from all presynaptic boutons. In the boutons attached to dendrites in particular, only about half of them responded to glutamate (Table 1). These findings are likely due to the complex effects of glutamate on the modulation of neurotransmitter release from presynaptic boutons in the hippocampal CA1 region. Glutamate ionotropic receptors on presynaptic boutons participate in neurotransmitter release [12] -[14] [25] -[30] , especially in the case of presynaptic kainate receptors that modulate glutamate and GABA release. In the CA1 area, the activation of presynaptic kainate receptors depresses glutamatergic synaptic transmission [25] [27] -[29] . In addition, presynaptic kainate receptors in the hippocampus evidently evoke a metabotropic response that suppresses GABA release at interneuron-CA1 pyramidal cell synapses [30] .

AMPA receptor activation tonically facilitates spontaneous GABA release in cultured rat hippocampal neurons [31] . However, there is not sufficient evidence supporting presynaptic AMPA receptor-mediated regulation of [Ca²⁺]_pre mobilization in CA1 pyramidal cells. In the rat hippocampal CA1 area, presynaptic NMDA receptors positively modulate excitatory postsynaptic potentials [32] [33] . Furthermore, presynaptic NMDA autoreceptors were shown to facilitate glutamate release in the rat hippocampus [34] . In this study, however, the external solution did not contained glycine, which is an essential component of NMDA receptor activation [35] [36] ; therefore, presynaptic NMDA receptors might not have participated in the glutamate-induced increase in [Ca²⁺]_pre observed in this experiment.

Metabotropic glutamate receptor activation reduces excitatory [15] [37] - [39] and inhibitory synaptic transmission [15] in the hippocampal CA1 region. By contrast, it has been reported that the activation of presynaptic metabotropic glutamate receptors increases glutamate release in CA1 pyramidal cells [16] [40] [41] . It is likely that the opposing mechanisms of glutamate-receptor based regulation of neurotransmitter release described above explain why only a fraction of boutons displayed increases in [Ca²⁺]_pre. In this study, the glutamate-induced changes in fluorescence images were different between presynaptic boutons and postsynaptic neurons (soma and dendrites; data not shown). The glutamate-induced increase in [Ca²⁺]_pre observed in this experiment was the specific response of the boutons via presynaptic glutamate receptors. However, a limitation of this study is that the receptors affected by glutamate and the neurotransmitters released from boutons were not identified. Furthermore, the detailed mechanisms underlying the glutamate-induced increase in [Ca²⁺]_pre were not determined experimentally.

Many reports have suggested that [Ca²⁺]_pre increases are caused by influx of Ca²⁺ through voltage-gated Ca²⁺ channels in presynaptic boutons [17] [18] [22] -[24] . We found that the N-type voltage-gated Ca²⁺ channel blockers 500 nM GVIA and 1 µM MVIIA inhibited the glutamate (30 µM)-induced increase in [Ca²⁺]_pre in Ca²⁺-containing solution; furthermore, 30 - 100 µM glutamate did not increase [Ca²⁺]_pre in Ca²⁺-free solution (both data not shown). These findings suggest that the glutamate-induced increase in [Ca²⁺]_pre observed in the Ca²⁺-containing solution was mainly due to Ca²⁺ entry through voltage-gated Ca²⁺ channels.

Presynaptic GABA_A receptors reduce Ca²⁺ influx by affecting voltage-gated Ca²⁺ channels, thereby reducing the release of neurotransmitters [42] . Kitayama et al. have reported that intravenous anesthetics, including propofol, significantly inhibit K⁺-evoked glutamate release from rat cerebrocortical slices and this inhibition of release is probably due mainly to depression of P/Q-type voltage-gated Ca²⁺ channels and partly due to activation of GABA_A receptors [43] . Buggy et al. have reported that propofol inhibits K⁺-evoked glutamate release from rat cerebrocortical slices, and propofol inhibition of glutamate release is reversed by the GABA_A antagonist bicuculline [44] . Furthermore, Wakita et al. have demonstrated that propofol activates both presynaptic and postsynaptic GABA_A receptors within GABA ergic synapses in rat CA3 neurons [11] . Therefore, propofol may have inhibitory effects on Ca²⁺ mobilization via presynaptic GABA_A receptors even in the CA1 area.

In this study, the effects of propofol were established in a concentration of 3 - 30 µM. This concentration range of propofol is similar to those of many reports relating to the effects of propofol on neurotransmission [4] - [7] [11] [44] [45] . The propofol concentration of 3 - 30 µM is equal to 0.534 - 5.34 µg/ml and seems to correspond with the propofol effect-site concentration in clinical anesthesia. However, propofol is extensively bound to the plasma protein [46] , and hence propofol concentration of 10 µM or more is considered to be much higher than clinically relevant concentrations of propofol [11] [47] . On the other hand, propofol in a concentration of 2 - 100 µM potentiates GABA-activated currents and increases the frequency of opening of GABA channels, while 10 - 1000 µM propofol directly activates GABA_A channels [1] . In the preparation absent of endogenous GABA, therefore, inhibitory effects of propofol (≥10 µM) observed in this study probably due to direct activation of presynaptic GABA_A receptors.

The finding in this study that propofol inhibited glutamate-induced increases in [Ca²⁺]_pre in boutons attached to the dendrite and not in boutons attached to the soma or the base of dendrite provides insight into the mechanism of propofol action. Almost every excitatory bouton attaches to dendritic spines [20] [21] , while most inhibitory boutons are located on the soma or the base of the dendritic tree [19] . Therefore, propofol may have an inhibitory effect on glutamate-induced Ca²⁺ mobilization in excitatory presynaptic boutons, but not in inhibitory boutons. We have previously reported that propofol and pentobarbital inhibit the high K⁺-induced increase in [Ca²⁺]_pre in the presynaptic boutons attached to dendrite, that is, excitatory synaptic transmission by depolarization [8] . Presynaptic kainate receptors in the rat hippocampal CA3 area directly modulate [Ca²⁺]_pre and induce the exocytotic release of glutamate, contributing to the generation of a positive feedback mechanism responsible for glutamate-induced glutamate release [48] . In excitatory presynaptic boutons in the CA1 area, glutamate-in- duced increase in [Ca²⁺]_pre via some kind of presynaptic glutamate receptors is similarly considered to provide the positive feedback mechanisms on glutamate-induced neurotransmitter release. Therefore, the significance of this study is the finding of inhibitory effects of propofol on the positive feedback mechanisms by glutamate.

5. Conclusion

In conclusion, propofol may possibly have some effect on glutamate-regulated neurotransmitter release from excitatory presynaptic nerve terminals through inhibiting the increase in [Ca²⁺]_pre induced by glutamate.

Acknowledgements

This work was supported by Japan Society for the Promotion of Science (JSPS) Grant-in-Aid for Scientific Research (21592578, 24593058).

Competing Interest

The authors have no conflict of interest to declare.

Authors’ Contributions

SI participated in the study design, performed the animal experiments, and drafted the manuscript; NK, TY participated in the study design and facilitated drafting of the manuscript; HS, SK participated in the animal experiments and facilitated drafting of the manuscript; JH performed statistical analysis and facilitated drafting of the manuscript. All of the authors have read and approved the final manuscript.

List of Abbreviations

[Ca²⁺]_pre: presynaptic calcium concentration; fluo-3 AM: acetoxymethyl ester of fluo-3; GABA: γ-aminobutyric acid; AMPA: α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid; NMDA: N-methyl-D-aspartate.

Conflicts of Interest

The authors declare no conflicts of interest.

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