Effects of BD1047, a σ1 receptor antagonist, on the expression of mTOR, Camk2γ and GSK‑3β in fluvoxamine‑treated N2a cells

Introduction

Fluvoxamine, a common and widely used antidepressant agent, is intended to exert its therapeutic effects in patients with depression by inhibiting the reuptake of serotonin in synaptic clefts (1). Certain studies have supported the theory that fluvoxamine exerts therapeutic effects not only on depression but also on schizophrenia and bipolar depression (2,3). Consequently, the conventional serotonin hypothesis is not able to not fully elucidate the pharmacological mechanisms of action of fluvoxamine.

σ receptors are recognized as non-opioid, intracellular receptors that modulate a variety of types of signal transduction in cells (4). A number of studies have demonstrated the existence of at least two subtypes of the σ receptor, σ1 and σ2, and σ1 receptors are expressed in numerous organs such as the brain, liver, pancreas, spleen and adrenal glands (5–7). The wide distribution of σ1 receptors in a variety of tissues suggests a critical role in living systems (6). A previous study by Niitsu et al(8) suggested that a σ1 receptor agonist caused a significant therapeutic effect in the treatment of schizophrenia. Additionally, SA4503, a σ1 receptor agonist, alleviated schizophrenia symptoms in an animal model (9). A study using fluvoxamine for the treatment of a patient with schizophrenia suggested that σ1 receptors are probably associated with the mechanism of action of fluvoxamine (10).

Mammalian target of rapamycin (mTOR), Ca2+/calmodulin-dependent protein kinase 2γ (Camk2γ) and glycogen synthase kinase-3β (GSK-3β) are three fundamental biomarkers implicated in the underlying mechanisms of depression, schizophrenia, mania and certain neuropsychiatric diseases (11–13). The present study aimed to investigate the effects of fluvoxamine on the expression of these biomarkers by studying fluvoxamine-treated N2a cells and attempted to elucidate whether σ1 receptors mediate the pharmacological effects of fluvoxamine. Thus, BD1047, a σ1 receptor antagonist, was applied to fluvoxamine-treated N2a cells in order to observe its effects on the fluvoxamine-elicited pharmacological action.

Materials and methods

Reagents

Fluvoxamine and BD1047 were purchased from Tocris Bioscience (Minneapolis, MN, USA). Primary antibodies against mTOR, Camk2γ and GSK-3β were purchased from Cell Signalling Technology, Inc. (Danvers, MA, USA). The mouse N2a neuroblastoma cells were obtained from the Medical College, Soochow University (Suzhou, China).

Cell culture

N2a cell culture was performed as described previously (14,15). The N2a cells were cultured in DMEM (Gibco, Grand Island, NY, USA) solution supplemented with 10% fetal bovine serum (FBS; Gibco), 0.3 mM L-glutamine and 50 U/ml penicillin/streptomycin. The N2a cells were randomly divided into three groups (six duplicates per group): DMEM group (D group), 0.5 μmol/l fluvoxamine group (F group) and 0.2 μmol/l BD1047 (σ1 receptor antagonist) + 0.5 μmol/l fluvoxamine group (BF group). Each culture well contained 2×105 N2a cells. The N2a cells were prepared for analysis 48 h after the initiation of incubation,.

Western blotting

The N2a cells were washed with phosphate-buffered saline (PBS). Protein levels were determined using the bicinchoninic acid method, according to the manufacturer’s instructions (Nanjing Kaiji Biochemistry Company, Nanjing, China). Briefly, bovine serum albumin (BSA) was applied as a standard protein. Prior to electrophoresis, a mixture of bromophenol blue and dithiothreitol (DTT; final concentration, 10 mM) was added to the samples. For western blotting, 50 μg of the total protein from each sample was separated by SDS-PAGE under reducing conditions. The proteins were then transferred onto polyvinylidene fluoride membranes (Nanjing Jiancheng Bioengineering Institute, Nanjing, China). The membranes were blocked for 2 h at room temperature using non-fat dried milk blotting-grade blocker and incubated overnight with primary antibodies. The primary antibodies used were goat anti-mTOR (1:1,000), rabbit anti-Camk2γ (1:1,000) and rabbit anti-GSK-3β (1:1,000). The primary antibodies were diluted in Tris-buffered saline (Thermo Fisher Scientific Inc., Rockford, IL, USA) containing 0.1% Tween-20 (TBS-T) and 2% BSA. Following extensive washing (three times for 15 min each in TBS-T), the mTOR, Camk2γ and GSK-3β protein levels were measured with horseradish peroxidase-conjugated rabbit anti-goat IgG (1:100,000 dilution) using enhanced chemiluminescence reagents (Beyotime, Nantong, China). Equal protein loading and transfer were assessed by subjecting each sample to western blotting for GAPDH with rabbit anti-GAPDH IgG (1:2,000 dilution).

Statistical analysis

Data are expressed as the mean ± standard deviation and were analyzed using one-way analysis of variance, and post hoc analyses were performed using the least significant difference test. Statistical analysis was conducted using SPSS Software, version 17.0 (IBM, Chicago, IL, USA). P<0.05 was considered to indicate a statistically significant difference for all the data analyzed.

Results

Effects of fluvoxamine on the expression of mTOR, Camk2γ and GSK-3β in cultured N2a cells

The administration of fluvoxamine significantly increased the levels of mTOR and Camk2γ expression compared with those of the D group in the cultured N2a cells (P<0.01; Figs. 1 and 2). Fluvoxamine significantly decreased the levels of GSK-3β expression compared with those of the D group in the cultured N2a cells (P<0.01; Fig. 3).

Figure 1 Expression of mTOR following fluvoxamine and/or BD1047 treatment in N2a cells. *P<0.01 compared with D group; #P<0.01 compared with F group. mTOR, mammalian target of rapamycin; D group, DMEM group; F group, fluvoxamine group; BF group, BD1047 + fluvoxamine group.

Figure 2 Expression of Camk2γ following fluvoxamine and/or BD1047 treatment in N2a cells. *P<0.01 compared with D group; #P<0.01 compared with F group. Camk2γ, Ca2+/calmodulin-dependent protein kinase 2γ; D group, DMEM group; F group, fluvoxamine group; BF group, BD1047 + fluvoxamine group.

Figure 3 Expression of GSK-3β following fluvoxamine and/or BD1047 treatment in N2a cells. *P<0.01 compared with D group; #P<0.01 compared with F group. GSK-3β glycogen synthase kinase-3β; D group, DMEM group; F group, fluvoxamine group; BF group, BD1047 + fluvoxamine group.

Effects of BD1047 on the fluvoxamine-elicited changes in the expression levels of mTOR, Camk2γ and GSK-3β in cultured N2a cells

The administration of BD1047 significantly decreased the levels of mTOR and Camk2γ expression compared with those of the F group in the cultured N2a cells (P<0.01; Figs. 1 and 2). Moreover, BD1047 significantly increased the levels of GSK-3β expression compared with those of the F group in the cultured N2a cells (P<0.01; Fig. 3).

Discussion

Fluvoxamine is a widely used clinical antidepressant agent. Its primary pharmacological action is inhibition of the reuptake of serotonin, which ultimately increases the levels of serotonin in synaptic clefts and exerts therapeutic effects in patients with depression (1). N2a cells are a semi-adherent, fast growing, mouse neuroblastoma cell line. In the present study, N2a cells were used to investigate the pharmacological properties of fluvoxamine, and the results demonstrated that fluvoxamine significantly increased the mTOR and Camk2γ expression levels and decreased the GSK-3β expression levels.

It is generally acknowledged that fluvoxamine acts as an antidepressant agent with therapeutic effects that alleviate the symptoms of schizophrenia, obsession, bipolar depression and certain neuropsychiatric diseases (16–18). Increasing evidence has suggested that σ1 receptors may be pivotal in the mechanism of action of fluvoxamine in the treatment of schizophrenia and other psychiatric diseases (2). Notably, the results of the present study also demonstrated that BD1047, a σ1 receptor agonist, abolished the fluvoxamine-elicited pharmacological effects. This result was consistent with the expectations of the study.

mTOR is a type of protein that promotes the activity of neurons (11). The results of present study indicate that fluvoxamine increased the expression levels of mTOR in cultured N2a cells. mTOR stimulates the growth of neurons via increasing the expression levels of neurotropic factors and supplying nutrients (17). It has been demonstrated that upregulated mTOR expression levels in the prefrontal cortex are likely to be associated with the mechanisms of antidepressant effects, which facilitate the return of the depression-induced atrophic neurons to normal morphology and function (18). Additionally, a postmortem study has demonstrated downregulated mTOR expression levels in the brain tissues of depressed patients (19). Therefore, in the present study it was suggested that increased mTOR expression levels are probably involved in the mechanisms by which fluvoxamine exerts antidepressant effects. Furthermore, it was observed that BD1047 attenuated the Camk2γ-elicited increased in mTOR expression levels, which indicates that σ1 receptors are likely to be involved in the mechanism of action of fluvoxamine.

Camk2γ is a Ca2+-dependent protein kinase (13). However, there is little literature reporting whether its expression is associated with the mechanisms of psychiatric diseases. In the present study, it was observed that Camk2γ expression levels were significantly increased following treatment with fluvoxamine in cultured N2a cells. It is widely accepted that this antidepressant agent has neuroprotective effects. The results of the present study indicate that increased Camk2γ expression levels are probably associated with the neuroprotective and antidepressant effect of fluvoxamine. In addition, the results suggest that σ1 receptors are probably involved in the pharmacological effect of fluvoxamine on the expression of Camk2γ.

GSK-3β is serine/threonine kinase, which has been acknowledged as a pivotal target for the treatment of depression and mania (12). In the present study, it was observed that that fluvoxamine has the potential to inhibit GSK-3β and that σ1 receptors probably mediate this process, which suggests that fluvoxamine exerts its pharmacological effects via the serotonin pathway and also by stimulating σ1 receptors.

In conclusion, the results of this study demonstrate that fluvoxamine has an effect on the expression levels of mTOR, Camk2γ and GSK-3β, and that this process is likely to be associated with the activation of σ1 receptors. However, an in vivo study was not conducted to investigate whether σ1 receptor antagonists are able to attenuate the therapeutic effects of fluvoxamine. Future large-scale studies are required to elucidate the pharmacological properties of fluvoxamine.

References