Rapamycin provides anti-epileptogenic effect in a rat model of post-traumatic epilepsy via deactivation of mTOR signaling pathway.

The mammalian target of rapamycin (mTOR) signaling pathway has attracted much attention in recent years. However, the contribution of mTOR activation to the development of post-traumatic epilepsy (PTE) remains largely unknown. The purpose of the present study was to investigate the activation of mTOR signaling in a rat model of FeCl2-induced PTE, and to explore the potential effect of its specific inhibitor rapamycin. The results indicated that the expression levels of p-mTOR and p-P70S6K, the overactivation biomarkers of mTOR signaling, increased significantly in hippocampal and perilesional cortex following PTE induction. Notably, they were significantly decreased in the aformementioned brain regions following rapamycin treatment. Furthermore, the frequency and number of behavioral seizures and epileptic brain injury were also greatly reduced. These results suggest that hyperactivation of the mTOR signaling pathway is a crucial mechanism of PTE development, and it may be considered a novel therapeutic target for PTE treatment.

Introduction

Post-traumatic epilepsy (PTE) is a common type of acquired epilepsies secondary to traumatic brain injury (TBI), accounting for approximately 10–25% of patients with moderate to severe injuries (1). After TBI, the brain carries out a series of pathological processes, including neuronal loss, gliosis, axonal sprouting, neurogenesis, inflammatory response, neurotransmitter release, and mitochondrial dysfunction, all of which have been connected to the epileptogenesis (2,3). Evidence indicate that the risk of PTE increases obviously 10 years after TBI and it usually develops refractory to medical management (4). At present, there are still many difficulties in PTE treatment partially because of the pathological mechanism has not been fully illustrated.

The mammalian target of rapamycin (mTOR) signaling pathway has been investigated extensively in recent decades. Experimental data suggest that mTOR pathway is involved in a number of physiological processes including cell proliferation, protein synthesis and cortical development (5–8). However, in recent years, it has also been reported to implicate in several neurological diseases, such as epilepsy (9). Evidences indicate that the mTOR pathway is activated in multiple type of epilepsies. For instance, epileptogenesis of cortical dysplasia, a common type of pediatric epilepsies, has been attributed to the over activation of mTOR signaling (9), which is also proven to involve in the development of temporal lobe epilepsy, the most common epilepsy in adults (10). The activation of mTOR protein kinase is regulated by multiple signaling pathways including PI3K/AKT, Ras/MAPK and AMPK. Phosphorylation level of downstream protein, such as p70 ribosomal S6 kinase (P70S6K), increased notably when the mTOR signaling is triggered (11). Up to now, only few research concentrates on the relationship between the development of PTE and the activation of mTOR. Although previous study demonstrated that mTOR-mediated epileptogenesis was activated via PI3K-Akt signaling in vitro model of PTE (12). However, they did not further explore the activation status of mTOR in animal model of PTE, nor did others.

Anti-epileptic drugs (AEDs) is the predominant therapy for epilepsy patients, however, about 30% of them are not sensitive to the treatment. Similarly, therapeutic effects of AEDs on patients with PTE is close to 35% (13). Additionally, some patients even suffer from side effects caused by AEDs such as nausea, dizziness, lethargy and weight gain. Therefore, it is essential to find a novel therapeutic target for epilepsy patients. Fortunately, rapamycin, a macrolide antibiotic drug, has been demonstrated effectively via deactivation of mTOR signaling and then provides neuroprotective effect against epileptic injury in previous studies (9,14,15). Furthermore, a published study also confirmed that administration of rapamycin also reduced epileptic activity, cell death and axon sprouting in organotypic hippocampal culture model of PTE (12).

Therefore, we performed this study to explore whether there is a abnormal activation of mTOR signaling in a rat model of PTE, and to determine the potential effect of rapamycin on mTOR-mediated epilepsic injury, aiming to find a novel therapeutic target for PTE management.

Materials and methods

Animals

Male Sprague-Dawley rats weighing between 180–220 g were purchased from the SLAC Laboratory Animal Co., Ltd. (Shanghai, China). The rats were housed in a 12 h of light and dark cycle, and were allowed free access to water and food. All the procedures performed were approved by the Animal Care and Use Committee of Fujian Medical University and in accordance with the guidelines of National Institutes of Health.

Establishment and assessment of PTE model

Procedures to induce the rat model of PTE has been described detailedly in previous studies (16,17). Briefly, rats were anaesthetized with an intraperitoneal injection of chloral hydrate (350 mg/kg) and placed in a stereotaxic frame. Animals were injected with a 10 µl of 100 mM FeCl2 or an equal volume of normal saline (NS) at a rate of 1 µl per minute through a small burr hole with the following coordinates: 2.0 mm anterior, 3 mm lateral to bregma, 2 mm depth. The sham-operated group was inserted a neddle without receiving any solution. After the operation, the rats were kept in single cage. An experienced observer who was blinded to the experimental protocols graded the scale of seizures using modified Racine criteria, in which seizure stages were identified technically according to animal behaviors (18). Grade evaluation began at 1–2 h after the surgery.

Experimental design and pharmacological administration

In experiment 1, 129 rats were divided into three groups: Sham group (n=10), NS group (n=52), and PTE group (n=67). Brain tissues were collected at baseline, 1, 24 h, 1, 2 and 4 weeks, respectively. Each time point contained 10 rats. The expression levels of p-mTOR and p-P70S6K were determined using western blotting and immunohistochemistry. In experiment 2, 127 rats were randomly assigned to two groups: the PTE + vehicle group (n=62) and the PTE + rapamycin group (n=65). For drug administration, rapamycin was dissolved in solution containing 5% Tween 80, 5% PEG 400 and 4% ethanol, and then administered intraperitoneally at a dose of 6 mg/kg subsequently after induction of PTE. The time and dose of rapamycin injection was based on previous studis with slight modifications (19). The vehicle group received an equal volume of solution. The potential role of rapamycin was estimated also by western blotting and immunohistochemistry. In addition, the frequency and number of behavioral seizures were also evaluated.

Western blot analysis

Rats were decapitated separately at each time point after operation. Perilesional cortex and ipsilateral hippocampus were collected and processed for western blot assays as previously described (20). Protein concentrations were measured with a BCA kit (Beyotime, China). Equal amounts of protein were run on 10% SDS-PAGE and then transferred to polyvinylidene fluoride membranes at 100 V for 70 min. After blocking with 5% nonfat dry milk in PBS for 2 h at room temperature, the membranes were incubated overnight at 4°C with primary antibodies for rabbit anti-p-mTOR (1:200; Wuhan Boster Biological Technology, Ltd., Wuhan, China) and mouse anti-p-P70S6K (1:100; Wuhan Boster Biological Technology, Ltd.). The membranes were washed with PBST and further incubated with horseradish peroxidase (HRP) conjugated secondary antibodies at room temperature for 1 h. Enhanced chemiluminescence reagent kit was used to detected the band' reactivitiy according to the manufacturer' protocol (Beyotime Institute of Biotechnology, Haimen, China). Band densities were quantified with ImageJ software (http://rsb.info.nih.gov/ij/). The results are presented as the relative densities to β-actin.

Immunohistochemistry

Immunohistochemistry was carried out as previously described (21). Briefly, rats were anaesthetized with chloral hydrate and perfused transcardially with saline followed by 4% paraformaldehyde in phosphate-buffered saline (PBS; 0.l M, pH 7.4). After postfixation and dehydration, the brains were embedded in paraffin and cut into 4 µm slices. The sections were deparaffinized and rehydrated in graded concentrations of ethanol to distilled water. and were further received antigen retrieval. Sections were incubated with 3% H2O2 in PBS for 10 min to block the endogenous peroxidase activity. After blocking with 5% fetal bovine serum in PBS, the sections were incubated with primary antibodies overnight at 4°C. Next day, the sections were incubated with HRP-conjugated second antibodies at room temperature for 1 h. After that, diaminobenzidine and hematoxylin were used to stain successively. Sections were observed under an Olympus microscope and five non-overlapping fields (magnification, ×400) per section were selected. Three sections per rat were used for quantification. Immunoreactivity densities were analyzed with ImageJ software by an investigator blinded to the treatment groups.

Statistical analysis

Data are presented as means ± SD. The statistical analyses were performed using SPSS 13.0 (SPSS, Inc., Chicago, IL, USA). Student's t-test was used for comparison between groups. For behavioral data, Kruskal-Wallis test was applied. P<0.05 was considered to indicate a statistically significant difference.

Results

General condition and epilepsy evaluation

A total of 194 rats received intracortical injection of FeCl2, and 150 of 176 (85.2%) developed spontaneous behavioral seizures, including mouth and facial movement, head nodding, stiff tail, forelimb contraction and full motor seizures. In general, the frequency and number of behavioral seizures increased beginning at 1 h and peaked at 3–4 h. About 24 h later, generalized seizures almost dispeared, however, focal seizures could still be seen in most of the FeCl2-injected rats. Over the next four weeks, epileptic duration and frequency decreased continuously, in which rats primarily performed shivering, head nodding, facial movements and few limb clonus (Fig. 1). Additionally, 18 rats subjected to FeCl2 injection died during the observation, of which 10 rats died for status epilepticus, 8 rats for high seizures frequency. The remaining 26 rats failed to develop behavioral seizures and were excluded from final analyses. For animals injected with NS, only three rats developed focal seizures including head nodding and facial movements, but none of these rats died (data not shown). As expected, none of rats died or showed abnormal performance in the sham group.

Figure 1.

The number of behavioral seizures in rats subjected to FeCl2 injection. The frequency and number of behavioral seizures increased beginning at 1 h and sustained at least four weeks after the development of post-traumatic epilepsy.

Cortical and hippocampal injury in rats subjected to FeCl2 injection

As shown in Fig. 2A, granule cells, molecular and polymorphic layer of the dentate gyrus in the sham group showed normal arrangements and distributions. Moreover, there was also no neuronal degeneration or cell loss in frontal cortex (Fig. 2D). Slight cellular changes in frontal lobe and hippocampus were found in the NS-injected rats including neuronal degeneration, nuclear pyknosis and granule cells proliferation (Fig. 2B and E). However, more obvious cellular changes in perilesional cortex and hippocampus were confirmed in the FeCl2-injected rats than that in the NS-injected rats, such as plenty of neuronal loss, swelling, degeneration and death, as well as inflammatory cell infiltration and glial cell proliferation (Fig. 2C and F).

Figure 2.

Hematoxylin and eosin of hippocampus and frontal cortex. (A) Cells in dentate gyrus show normal arrangements and distributions in the sham group. (B) Slight hippocampal changes in the NS-injected rats including neuronal degeneration, nuclear pyknosis and granule cells proliferation. (C) Hippocampal changes in the FeCl2-injected rats including plenty of neuronal loss, swelling, degeneration and death, as well as inflammatory cell infiltration and glial cell proliferation. (D) Cells in frontal lobe show normal arrangements and distributions in the sham group. (E) Slight cellular changes in frontal lobe of the NS-injected rats including neuronal degeneration, nuclear pyknosis and granule cells proliferation. (F) Cellular changes in frontal lobe of the FeCl2-injected rats including plenty of neuronal loss, swelling, degeneration and death, as well as inflammatory cell infiltration and glial cell proliferation. Bottom graphs are enlarged view of the boxs above (magnification, ×400), respectively. NS, normal saline.

Increased expression of p-mTOR and p-P70S6K in rats after intracortical injection of FeCl2

To examine whether mTOR signaling was upregulated in rats after PTE induction, we first carried out a temporal course of experiment with western blotting. As visible in Fig. 3A and B, at baseline, there was a small amount of p-mTOR and p-P70S6K expression in frontal lobe and hippocampus. Of note, both proteins increased significantly at 1 h after the surgery (FeCl2 or NS injection) and peaked at 1 week in the abovementioned regions. Then protein levels of p-mTOR and p-P70S6K decreased to the bottom at 2 weeks (except p-mTOR expression in frontal cortex) while elevated again at 4 weeks (Fig. 3C-F). Furthermore, compared with rats injected with NS, perilesional and hippocampal p-mTOR levels in rats after PTE induction were significantly increased at all time points. Similarly, in addition to p-P70S6K expression in hippocampus at 2 week after surgery, p-P70S6K levels at each time point were higher than those in the NS-injected rats. Consistence with the results of western blotting, immunohistochemistry further demonstrated the higher increased levels of p-mTOR and p-P70S6K in frontal lobe and hippocampus following PTE (Fig. 4). Moreover, both proteins primarily expressed in cytoplasm.

Figure 3.

Temporal course of p-mTOR and p-P70S6K expression in hippocampus and frontal cortex. (A and B) Representative western blot bands of p-mTOR and p-P70S6K expression. (C-F) Quantitative results of p-mTOR and p-P70S6K expression in hippocampus and frontal cortex. Values were shown as the fold changes compared with the sham group. N=6 per group. *P<0.05 vs. the NS-injected group. NS, normal saline; mTOR, mammalian target of rapamycin.

Figure 4.

Time course of p-mTOR and p-P70S6K expression in hippocampus and frontal cortex. Representative immunohistochemical pictures of p-mTOR and p-P70S6K expression in the sham rats, the NS-injected rats and the FeCl2-injected rats at different time points. NS, normal saline; mTOR, mammalian target of rapamycin.

Rapamycin reduced behavioral seizures and attenuated epileptic injury

Similar pattern of seizures was found in the vehicle group as compared with the PTE + rapamycin group, but actually, the PTE rats exerted significant decline of behavioral seizures ranging from 24 h to 4 weeks after treatment with rapamycin (Fig. 5; P<0.05). Additionally, there still existed slight disruptions of cellular arrangement and structure in the PTE + vehicle group, while which were also alleviated greatly both in frontal lobe and hippocampus after rapamycin treatment (Fig. 6A-D).

Figure 5.

Antiepileptogenic effect of rapamycin. The frequency and number of behavioral seizures were significantly reduced after rapamycin treatment in the PTE + rapamycin group as compared to the vehicle group. *P<0.05 vs. the vehicle group. PTE, post-traumatic epilepsy.

Figure 6.

Effect of rapamycin on cellular injury. (A) There still existed slight impairments of cellular arrangement and structure in the vehicle group. (B) Cellular injuries in hippocampus were alleaviated greatly after rapamycin treatment. (C) There still existed slight impairments in frontal lobe after treated with vehicle. (D) Cellular injuries in frontal lobe were alleaviated greatly after rapamycin treatment. Bottom graphs (magnification, ×400) are enlarged view of the boxs above, respectively.

Rapamycin decreased the level of p-mTOR and p-P70S6K in rats after PTE induction

As predicted, the levels of p-mTOR and p-P70S6K were obviously increased in frontal lobe and hippocampus in the vehicle group. Both proteins were significantly reduced in the PTE + rapamycin group as compared to the PTE + vehicle group (except hippocampal p-P70S6K level at 2 weeks). Specifically, perilesional and hippocampal p-mTOR levels decreased significantly at all time points after rapamycin treatment. Similar changes were found in the levels of perilesional p-P70S6K. Moreover, hippocampal p-P70S6K levels at 1 and 24 h, as well as 1 and 4 weeks were also decreased significantly after rapamycin treatment in addition to that at 2 weeks (Figs. 7 and 8).

Figure 7.

Effect of rapamycin on mTOR signaling assessment with western blot. (A and B) Representative western blot bands of p-mTOR and p-P70S6K expression after PTE induction with or without rapamycin treatment. (C-F) Quantitative results of p-mTOR and p-P70S6K in hippocampus and frontal cortex after vehicle or rapamycin treatment. Values were shown as the fold-changes compared to the sham group in experiment 1. N=6 per group. *P<0.05 vs. the vehicle group. mTOR, mammalian target of rapamycin; PTE, post-traumatic epilepsy.

Figure 8.

Effect of rapamycin on mTOR signaling assessment with immunohistochemistry. Representative immunohistochemical pictures of p-mTOR and p-P70S6K in rats after PTE induction with or without rapamycin treatment. mTOR, mammalian target of rapamycin; PTE, post-traumatic epilepsy.

Discussion

The main finding of this study was that the levels of p-mTOR and p-P70S6K, biomarkers of activated mTOR signaling, increased significantly in rats subjected to PTE induction, which was accompanied by obvious behavioral seizures and cellular injury. Of interest, both elevated indicators were decreased remarkably after rapamycin treatment. Moreover, inhibition of mTOR with rapamycin also greatly reduced behavioral seizures over a longer time-period as compared to previously studies (12,19). Our results suggest that the over activation of mTOR signaling may be a crucial pathogenic mechanism participated in the development of FeCl2-induced PTE. Rapamycin provides a antiepileptogenic effect through the inhibition of mTOR signaling.

At present, there are several animal models of PTE, such as controlled cortical impact model (19,22), low Mg2+ model (23), cortical undercut model (24), and FeCl2-induced model (16). In the present study, we adopted the frontal cortex injection of FeCl2-induced PTE model for the following reasons: i) Frontal cortex damage is the most common type of injuries in clinical practice and the pathological change caused by FeCl2 injection is similar to human TBI (17); ii) The model has high success rate, stability and repeatability; and iii) The latency of seizures is short and beneficial to behavioral evaluation and pharmacological intervention. Most of the reasons were further verified in our study. For example, 85.2% rats developed to epileptogenesis after injection of FeCl2. Moreover, behavioral seizures could be induced within as early as an hour and sustained at least 4 weeks after FeCl2 injection.

The mTOR pathway has been reported to involve in several neurological diseases including depressive disorder (25), ischemia brain injury (11,26), brain tumor (27) and epilepsy (28). Here, we provide evidence that the expression of p-mTOR and p-P70S6K, over activation biomarkers of mTOR signaling, strengthened heavily in hippocampus and frontal cortex after PTE induction. Consistence with our results, a study in vitro also verified the upregulation of mTOR signaling after the induction of PTE despite of without investigating the downstream proteins. In addition, literature concerning other type of epilepspy also determined the hyperactivation of mTOR and further found the increased expression of downstream proteins, such as p-P70S6K (28). PTE is a common sequela following craniocerebral injury. However, there is limited effectivity for its treatment. In recent years, rapamycin has been widely applied in experimental researches and neuroprotective effects are found in a number of diseases including TBI (29), hypoxic-ischemic encephalopathy (26), and epilepsy (28,30). In line with the results of these studies, our results indicate that the increased levels of p-mTOR and p-P70S6K were reduced significantly after rapamycin treatment. That is, the over activation of mTOR pathway was markedly inhibited after administration of rapamycin. Meanwhile, the frequency and number of behavioral seizures and epileptic injury were also greatly weakened.

Multiple potential mechanisms may contribute to the antiepileptogenic effects of rapamycin. First, hyperactivation of mTOR/P70S6K signaling promotes oligodendrocyte proliferation and myelination (25), which is essential to the axonal sprouting susceptible to the development of epilepsy (2). Therefore, antiepileptogenic effect was obtained via blocking the mTOR signaling and decreasing the expression of downstream p-P70S6K. Second, induction of synaptic plasticity, resulting from the elevated proteins synthesis in hippocampus following activation of mTOR signaling is a important mechanism for epileptogenesis (31). Rapamycin weaken the frequency and number of seizures through decreasing the levels of certain translation initiation factors and reducing the rate of protein synthesis. Third, as previously reported (32), rapamycin reduce the activation of microglia, a hallmak of neuroinflammation, which can be attibuted to its intrinsic anti-inflammatory effect. Last but no least, although the role of mTOR signaling on neuronal apoptosis is controversial, several studies have demonstrated that inhibition of seizure-induced mTOR signaling with rapamycin could reduce the amount of apoptosis (33).

Meanwhile, we need to notice the limitations of our study. First, electrophysiological examination is still the golden standard for epilepsy diagnosis and is crucial for the response evaluation. So it should be included in the future study. Second, the distribution of p-mTOR and p-P70S6K have not been illustrated in this study. Further tests would be conducted to identify the specific cell types that express the abovementioned biomarkers of activated mTOR signaling.

In summary, our results suggest that there exists over activation of mTOR signaling in a rat model of FeCl2-induced PTE. Inhibition of mTOR signaling with rapamycin significantly reduces the behavioral seizures and then ameliorates epileptic brain injury. It suggests that mTOR signaling pathway may be a potential therapeutic target, and rapamycin can be considered as a promising agent for PTE treatment.