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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Mol Cell Pharmacol. Author manuscript; available in PMC 2010 April 22.
Published in final edited form as:
Mol Cell Pharmacol. 2009 January 1; 1(3): 124–129.
PMCID: PMC2858431

Developing Antiepileptogenic Drugs for Acquired Epilepsy: Targeting the Mammalian Target of Rapamycin (mTOR) Pathway


While current medications for epilepsy are primarily symptomatic treatments that suppress seizures, one of the main goals of future drug development in epilepsy is the identification of antiepileptogenic or disease-modifying therapies that can completely prevent epilepsy or slow its progression. A rational antiepileptogenic strategy is to target primary cell signaling pathways that initially trigger the downstream mechanisms causing epileptogenesis. Recent work implicates the mammalian target of rapamycin (mTOR) pathway as mediating epileptogenesis in a genetic epilepsy, Tuberous Sclerosis Complex (TSC), and suggests that mTOR inhibitors, such as rapamycin, may have antiepileptogenic properties for epilepsy in TSC. As mTOR regulates multiple cellular functions that may contribute to epileptogenesis in general, including ion channel expression, synaptic plasticity, and programmed cell death, mTOR inhibitors might also represent an effective antiepileptogenic therapy for other, more common types of epilepsy, such as acquired epilepsies due to brain injuries. Here, we describe evidence from a recently-published study that mTOR mediates epileptogenesis in a popular animal model of acquired limbic epilepsy due to brain injury following kainate-induced status epilepticus, and that rapamycin has antiepileptogenic effects in this model. Furthermore, putative pathways and mechanisms upstream and downstream from mTOR involved in epileptogenesis in the kainite model are considered, identifying possible additional therapeutic targets. Finally, the potential translational applications of this and other animal model data for developing antiepileptogenic therapies for people with acquired epilepsy due to brain injury are discussed.

Keywords: Epilepsy, Rapamycin, mTOR pathway, Tuberous Sclerosis Complex

Drug development for epilepsy has made substantial progress in recent years. About a dozen new seizure medications have become available for clinical use since the mid-1990’s (1). These antiepileptic drugs have helped control seizures and minimize side effects in many patients. Unfortunately, however, these medications have had minimal impact in reducing the number of people with medically-refractory epilepsy, which continues to represent approximately one-third of all epilepsy patients despite multiple trials of both older and newer medications (2). Furthermore, currently available seizure medications are primarily symptomatic treatments that suppress seizures but do not necessarily correct the underlying brain abnormalities causing epilepsy (epileptogenesis) or improve the long-term prognosis of epilepsy (3). Thus, a holy grail of epilepsy drug research has been the pursuit of disease-modifying or “anti-epileptogenic” drugs that can slow the progression of epilepsy or completely prevent the development of epilepsy in the first place (46).

Many recent antiepileptic drugs were identified through a screening approach, such as via the NIH-sponsored Anticonvulsant Drug Development program, in which thousands of compounds were tested for efficacy in standard assays of acutely-provoked seizures in non-epileptic animals. As a result, current seizure medications are effective in suppressing seizures symptomatically and work through mechanisms that directly decrease neuronal excitability, such as modulation of neurotransmitter receptors and ion channels. However, since most of these drugs were not tested in more chronic assays in epileptic animals, it is not surprising that they may not be as effective in preventing the underlying processes of epileptogenesis. Rather than targeting molecular mechanisms that mediate the end-stage symptoms of epilepsy, a more rational strategy for developing antiepileptogenic therapies is to interrupt the early mechanistic processes that initially trigger the cellular and molecular changes in the brain that eventually lead to seizures. In fact, many types of epilepsy are caused by a remote brain injury, such as a stroke or head trauma, in which the patient starts experiencing seizures only after a prolonged period, often spanning months to years, following the brain injury. During this latent period of epileptogenesis, a number of cellular and molecular changes occur in the brain in response to the injury that promote the eventual development of seizures, but also offer a potential window of opportunity for intervening with antiepileptogenic therapies.

While no such antiepileptogenic treatments have yet been established for clinical use, a number of promising avenues have recently started to emerge from basic research. One of the best examples relates to a cell signaling pathway, the mammalian target of rapamycin (mTOR) pathway, which is increasingly recognized to control a variety of important cellular functions under physiological conditions and to contribute to the pathophysiology of a wide range of different diseases (79). mTOR is a serine-threonine protein kinase that serves as a central regulator of multiple physiological functions that generally relate to cellular growth, proliferation, metabolism, and survival. A number of upstream pathways, such as phosphatidylinositol-3 kinase (PI3K)/Akt (protein kinase B) and AMP-kinase (AMPK), can activate or inhibit mTOR activity, in response to different extracellular stimuli or intracellular signals, including nutrient and energy status, growth factors, and physiological stress (Figure. 1A). Modulation of mTOR by upstream stimuli and pathways is usually mediated through effects on the tuberous sclerosis complex (TSC) gene products, hamartin and tuberin, and the small GTPase Rheb. In turn, mTOR triggers a number of downstream mechanisms, such as ribosomal S6K/S6 and 4EBP1/eIF4E pathway, which directly mediate protein synthesis and ribosomal biogenesis related primarily to cellular growth and metabolism (Figure 1A). Thus, under physiological conditions, mTOR is activated by anabolic or energy-rich states, resulting in increased protein synthesis, cell growth, and metabolism. Conversely, in catabolic or energy-deficient states, mTOR is inhibited, decreasing protein synthesis and growth. Dysregulation of the mTOR pathway has been implicated in a variety of different diseases, ranging from diabetes and obesity to cardiovascular disease, cancer and neurodegenerative disorders (9). Furthermore, from a translational approach, the clinical availability of mTOR inhibitors, such as rapamycin, conveniently allows the involvement of the mTOR pathway in the pathophysiology of disease to be tested and provides potential novel therapeutic agents for these diseases.

Figure 1
Physiological and pathological regulation of the mTOR pathway

Given the diversity of functions regulated by mTOR, abnormal signaling through the mTOR pathway represents a logical candidate for mediating mechanisms of epileptogenesis. For example, mTOR can affect a variety of cellular and molecular processes, such as neurotransmitter receptor and ion channel expression, synaptic plasticity, neuronal death and apoptosis, and neurogenesis, which influence neuronal excitability and epileptogenesis (1016). Perhaps the best example of the role of mTOR in epileptogenesis is seen in Tuberous Sclerosis Complex (TSC), which represents one of the most common types of genetic epilepsy. TSC is caused by mutation of one of two genes, the TSC1 and TSC2 genes, and is characterized by tumor or hamartoma formation in multiple organs (17,18). Epilepsy in TSC is very common and usually intractable to available therapies. Although the mechanisms of epileptogenesis are incompletely understood, recent work from human tissue specimens and animal models of TSC has identified a number of cellular and molecular abnormalities in neurons and glia that likely promote epileptogenesis (19,20). As the TSC gene products, hamartin and tuberin, form a complex that normally inhibits the mTOR pathway, TSC gene mutations lead to abnormal hyperactivation of mTOR, which activates multiple downstream mechanisms that mediate many of the phenotypic features of TSC, such as abnormal cell growth and proliferation and tumor formation (Figure 1B). Accordingly, mTOR inhibitors, such as rapamycin, can decrease tumor growth in animal models (21), as well as in uncontrolled clinical trials in TSC patients (22,23). Similarly, in mouse models of TSC with abnormal neurological phenotypes, mTOR inhibitors can reverse a number of molecular, histological, and behavioral abnormalities that may relate to epileptogenesis, including megenecephaly, neuronal hypertrophy, and astrogliosis (2427). Most remarkably, rapamycin treatment, initiated prior to the onset of seizures, prevents the onset of epilepsy in these mice, indicating a potent antiepileptogenic effect (26).

While TSC is a relatively rare genetic disease, there could be significant overlap between mechanisms of epileptogenesis in TSC and other types of epilepsy, such as more common acquired epilepsies due to brain injury. During the latent period between the initial precipitating brain injury and the subsequent onset of epilepsy, different cellular and molecular changes mediating epileptogenesis may occur that involve mTOR-dependent mechanisms, such as alterations in ion channel expression, aberrant synaptic plasticity, neurogenesis, or apoptosis (Figure 1C). In a recent study, we have begun to test the role of mTOR in a popular animal model of acquired limbic epilepsy due to brain injury. In this model, the glutamate agonist kainate is injected into previously normal mice to induce an acute episode of prolonged seizures lasting a few hours (status epilepticus). After recovery from the status epilepticus, the mice enter a latent period of a few days to weeks, during which there are no observable seizures, but a number of cellular changes occur reflecting brain injury and promoting epileptogenesis. The end of the latent period is heralded by the onset of spontaneous seizures and the mice then have epilepsy.

Consistent with a previous report (28), we first demonstrated that the mTOR pathway is abnormally activated by kainate-induced status epilepticus, both acutely during the episode of status epilepticus and more chronically for a few weeks during the latent period of epileptogenesis (29). Rapamycin treatment prevented this inappropriate mTOR activation and also decreased cellular changes that likely contribute to epileptogenesis in this model, including hippocampal neuronal death, neurogenesis, and axonal sprouting. Correspondingly, mTOR inhibition with rapamycin also reduced the development of spontaneous seizures, indicating an antiepileptogenic effect (29). Thus, these studies suggested that mTOR plays a critical role in activating multiple downstream mechanisms of epileptogenesis in the kainate model of acquired limbic epilepsy and that rapamycin has antiepileptogenic actions in this model (Figure 1C).

Although these results are encouraging in extending the pathophysiological importance of mTOR to acquired epilepsies due to brain injury, a number of issues remain unresolved in this regard. First of all, while in TSC there is a direct link between the TSC gene products and mTOR, the biochemical mechanisms by which the mTOR pathway is activated by kainate-induced status epilepticus is unclear. In theory, a number of signaling pathways upstream from mTOR could be triggered by the initial seizures. As large amounts of glutamate are released during status epilepticus, a rational mechanism might start with stimulation of ionotropic or metabolic glutamate receptors and subsequent activation of the PI3K/Akt pathway (30,31), which in turn can increase mTOR activity (Figure 1C). As pharmacological modulators of PI3K and other upstream signaling molecules are available, discovery of the upstream mechanisms that initiate mTOR activation in response to brain injury might lead to additional antiepileptogenic therapies that complement mTOR inhibitors.

Just as the relevant signaling pathways upstream from mTOR remain to be identified, the critical mechanisms of epileptogenesis downstream from mTOR that mediate the antiepileptogenic effects of rapamycin also need to be better defined. Although experiments from the recent study demonstrated that rapamycin prevented putative mechanisms of epileptogenesis in the kainate model, including neuronal death, neurogenesis, and mossy fiber sprouting (29), these findings are only correlative and do not prove that these aberrant cellular processes cause epileptogenesis in this model and are not simply epiphenomena. A number of other downstream mechanisms that are mTOR-dependent and may contribute to epileptogenesis were not examined in this study, such as ion channel expression, dendritic structure, immune modulation, inflammatory responses, autophagy, and oxidative stress (1216,3234). A major issue is whether rapamycin’s antiepileptogenic efficacy is primarily related to broader neuroprotective properties in reducing the underlying neuronal death and brain injury, or whether mTOR mediates more specific mechanisms of epileptogenesis independent of cell death. Future studies identifying the most critical downstream mechanisms of epileptogenesis regulated by mTOR may also lead to more specific, targeted antiepileptogenic therapies.

The relevance of mTOR in epileptogenesis in other models and types of both genetic and acquired epilepsy is starting to be explored, further expanding the potential applications and impact of mTOR in epilepsy. Closely related to the kainate model, a recent study indicates that rapamycin can inhibit mossy fiber sprouting in the pilocarpine-status epilepticus model of acquired limbic epilepsy (35). mTOR activation has also implicated in preliminary experiments of neonatal seizures (36). In mice with inactivation of the PTEN gene, which, similar to the TSC genes, is an upstream inhibitor of mTOR pathway, rapamycin decreases seizures and reverses underlying brain abnormalities (27,37,38). Finally, in models of traumatic brain injury (TBI), mTOR activity is increased and rapamycin exerts neuroprotective effects (39,40). Although the effect of rapamycin on the development of posttraumatic epilepsy has yet not been specifically reported in TBI models, curcumin, which among other properties has recently been found to be an mTOR inhibitor, retards the progression of epileptogenesis in an animal model of TBI (41,42). If rapamycin is also verified to have antiepileptogenic effects in animal models of TBI, this could have direct translational implications, as antiepileptogenic drug trials in TBI patients are very plausible and clinically-relevant (3,43).

Clinical trials of rapamycin are already in progress studying effects on tumor growth (22,23) and are being planned for epilepsy as a primary endpoint in TSC patients. However, a number of fundamental issues will need to be addressed in the kainate and other animal models before considering an antiepileptogenic drug trial in people with brain injury at risk for epilepsy. First, the existence of a therapeutic window, during which rapamycin will exert antiepileptogenic effects, will need to be defined. For example, what is the longest latency after the initial brain injury (i.e. status epilepticus in the kainate model) at which rapamycin can be initiated in order to still be effective? For how long during the latent period of epileptogenesis does rapamycin need to be administered? Second, even if the efficacy of mTOR inhibitors as antiepileptogenic agents becomes clearly established, more basic science and clinical data are needed about the potential adverse effects of rapamycin, especially in the setting of acute brain injury. Some of the changes in the brain following injury may represent compensatory or adaptive responses promoting recovery from brain injury, such as neurogenesis or synaptic plasticity. Thus, rapamycin could represent a double-edged sword in inhibiting both epileptogenic mechanisms and beneficial, adaptive processes following brain injury. Nevertheless, despite these potential limitations, the recent work with rapamycin is a good sign that drug development for epilepsy is finally shifting from seizure suppression to epilepsy prevention.


Work from the authors has been supported by the National Institutes of Health (K02 NS045583, R01 NS056872), the Tuberous Sclerosis Alliance, and Citizens United for Research in Epilepsy.


Conflicts of Interest

No potential conflicts of interest to disclose.


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