Therapeutic modalities for treatment resistant depression: focus on vagal nerve stimulation and ketamine.

Treatment resistant depression (TRD) is a global health concern affecting a large proportion of depressed patients who then require novel therapeutic options. One such treatment option that has received some attention in the past several years is vagal nerve stimulation (VNS). The present review briefly describes the relevance of this treatment in the light of other existing pharmacological and non-pharmacological options. It then summarizes clinical findings with respect to the efficacy of VNS. The anatomical rationale for its efficacy and other potential mechanisms of its antidepressant effects as compared to those employed by classical antidepressant drugs are discussed. VNS has been approved in some countries and has been used for patients with TRD for quite some time. A newer, fast-acting, non-invasive pharmacological option called ketamine is currently in the limelight with reference to TRD. This drug is currently in the investigational phase but shows promise. The clinical and preclinical findings related to ketamine have also been summarized and compared with those for VNS. The role of neurotrophin factors, specifically brain derived neurotrophic factor and its receptor, in the beneficial effects of both VNS and ketamine have been highlighted. It can be concluded that both these therapeutic modalities, while effective, need further research that can reveal specific targets for intervention by novel drugs and address concerns related to side-effects, especially those seen with ketamine.

INTRODUCTION

Major depressive disorder (MDD) is a serious worldwide public health concern. The point prevalence of MDD is 4.7% (4.4-5.0%) at the global level and 4.0% (3.4-4.6%) within East/Southeast Asia.1) MDD also imposes a huge economic burden. A recent study in South Korea estimates the total cost of the disorder at about 4 billion with USD 153 million being contributed by direct healthcare costs.2) Treatment options for MDD primarily involve antidepressant (AD) drugs. One of the first agents with AD properties, iproniazid, was discovered in 1952. This drug acts by slowing down the enzymatic breakdown of monoamines such as norepinephrine (NE) or serotonin (5-HT) and belongs to a class of ADs called monoamine oxidase inhibitors (MAOIs) due to their mechanism of action. Another class of drugs called tricyclic ADs (TCAs), named based on their three-ring chemical structure, was discovered around the same time.3) Based on mechanism of action, AD drugs can be classified as selective 5-HT reuptake inhibitors (SSRIs), selective NE reuptake inhibitors (selective NRIs) and dual 5-HT/NE reuptake inhibitors (SNRIs), 5-HT modulators and NE/5-HT modulators. All of these classes mainly target central serotonergic and noradrenergic systems whereas MAOIs and dopamine (DA)-NE reuptake inhibitors also affect the dopaminergic system.4,5,6)

MAIN SUBJECTS

Response, Remission, Recovery, Relapse and Recurrence with Reference to Treatment of Major Depressive Disorder

'Response' is defined as a clinically meaningful reduction in symptoms of depression usually seen along with better mood, reduction in pain/distress and improved daily function. It has been defined as a ≥50% reduction in the severity of symptoms that were seen pretreatment, based on standardized rating scales for the severity of depression such as the Hamilton or Montgomery-Asberg Rating Scales for Depression.7,8) 'Remission' is used when the signs and symptoms of depression are either absent or almost absent. Based on the Hamilton Rating Scale for Depression, remission would require a score of ≤5 or 7. 'Recovery' suggests an extended period of remission implying that a major depressive episode (MDE) is not probable in the near future. There is no clear consensus on the duration of remission required to define recovery. The American College of Neuropsychopharmacology Task Force recommends 4 months whereas previously, others have used 6 months of remission to define recovery. Both 'remission' and 'recovery' may be used irrespective of whether the patients are undergoing treatment. 'Relapse' and 'recurrence' both imply the reappearance of an MDE. The term 'relapse' is used if the MDE occurs during remission; however, 'recurrence' occurs only after the onset of recovery.9,10)

The classical AD drugs mentioned earlier are frequently only moderately effective and most studies have found no difference in efficacy between different classes of ADs or even between individual drugs.11) In fact, up to two-thirds of the patient population does not respond to the first prescribed AD. Further, about 15% of the population does not respond to multiple treatment options including psychotherapy.12) These patients are diagnosed with treatment resistant depression (TRD).

Treatment Resistant Depression

The impairment, morbidity and economic burden associated with MDD are further augmented in TRD.13) Over the years, the definition of TRD has been subject to debate; however, the general consensus is that for a diagnosis of TRD, treatment with ADs from different pharmacological classes is needed.14) TRD has been classified by several staging methods that incorporate factors such as treatment trials, severity and chronicity of the disorder. An example of one such model is the Thase and Rush Staging Model (Table 115)), developed as a guideline for psychiatrists and based on the number and classes of ADs that have not produced a response.

Table 1

Thase and Rush Staging Model

Adapted from the article of Thase and Rush15) (J Clin Psychiatry 1997;58(Suppl)13:23-29).

AD, antidepressant; TCA, tricyclic AD; MAOI, monoamine oxidase inhibitor; ECT, electroconvulsive therapy.

Other staging methods or models include the Antidepressant Treatment History Form, the European Staging Model, the Massachusetts General Hospital Staging Model and the Maudsley Staging Method. These models have different advantages and disadvantages leading to varying predictive utility and reliability.16) However, TRD must not be confused with chronic depression.17)

Treatment Options for Treatment Resistant Depression

Pharmacological treatment

Switching strategies

This involves switching treatment from the initially prescribed drug to another AD. The newer prescription may be for an AD from the same class (within-class switching) or from another class with a different mechanism of action (between-class switching). There is a lack of evidence suggesting that one of these two strategies is better than the other to achieve response or remission.10,18,19,20) The first line of treatment is often an SSRI. If this is the case, the second prescribed drug for the between-class switching strategy belongs to one of the following groups: TCAs, mianserin, dual acting agents (such as venlafaxine), MAOIs or agents acting on the dopaminergic and/or noradrenergic systems (such as bupropion and reboxetine).19)

Combination/augmentation strategies

This strategy involves combining one AD with another or with some drug with a different primary indication. Drugs commonly used for augmentation include lithium, bupropion, mirtazapine, atypical antipsychotics, anticonvulsants, DA agonists, stimulants, buspirone, modafinil, pindolol, thyroid hormone, estrogen or testosterone, herbal agents etc. Although these drugs can be beneficial, there are a variety of side-effects associated with most of their use. Upon scanning through data for the response and remission rates, it appears that lithium and liothyronine (a form of triiodothyronine) are most effective as drugs for this strategy.5)

Psychotherapy

Psychotherapy in the form of cognitive behavioral therapy (CBT) is based on the premise that MDD is associated with negative cognitive biases.21) Several studies have shown its effectiveness in reducing vulnerability and in preventing relapse of MDD when used alone,22) in combination with23,24) or sequentially after pharmacotherapy.25) The use of CBT in treating TRD also seems promising.26,27,28,29) Efficacy of psychotherapy may depend on mechanisms underlying the etiology of depression in each patient. Some studies30,31) suggest regional differences in brain activity in response to psychotherapy versus pharmacotherapy.

Somatic therapies

Other non-pharmacological options include electroconvulsive therapy (ECT), repetitive transcranial magnetic stimulation (rTMS), magnetic seizure therapy, deep brain stimulation (DBS) and vagal nerve stimulation (VNS).5,32) The latter two options require surgical intervention. VNS and rTMS were approved by the US Food and Drug Administration (FDA) for treatment of TRD in 2005 and 2008 respectively. The use of DBS for treating TRD is still not FDA-approved and remains in the experimental stage.

Vagal Nerve Stimulation

VNS therapy consists of implantation of a generator connected to bipolar electrodes (Cyberonics Inc., Houston, TX, USA) that deliver chronic intermittent electrical signals at a low frequency to the vagus nerve. The pulse generator is surgically implanted subcutaneously in the anterior chest wall and the electrodes wrapped around the left vagus nerve through an incision in the neck (Fig. 1). The parameters of the stimulation provided by the generator via the electrodes can be programmed and controlled noninvasively using a telemetric wand that is linked to a hand-held computer.

Fig. 1

Illustration depicting the electrodes (negative electrode, positive electrode and anchor tether) wrapped around the left vagus nerve and connected to a Demipulse generator via a thin flexible lead. The Demipulse generator is subcutaneously implanted in the chest region. Figure kindly supplied by Cyberonics, Inc. (Houston, TX, USA) and used with their permission.

The left nerve is preferred to the right for electrode placement as there are more cardiac efferent fibers from the right and stimulation of this side would cause more frequent adverse cardiac effects.33) Further, pre-clinically, we have evaluated the stimulation parameters that we use in our studies, which are the same ones as those used initially in clinical studies, and have observed no significant effects on heart rate and blood pressure.34) Chronic VNS in patients does produce a few side-effects such as voice alteration, cough, pharyngitis, throat discomfort and dyspnea. Other common complications include headache, nausea, vomiting and dyspepsia.33)

Approval of VNS for TRD and clinical studies

VNS therapy is now approved for the treatment of TRD in the United States, Europe, Canada, Mexico, Brazil, Australia and New Zealand (personal communication from Cyberonics Inc.). Clinical studies show promising results with long-term treatment with VNS for patients with TRD. An early 10-week randomized controlled trial of TRD patients with VNS in combination with treatment as usual showed no significant efficacy of VNS over just treatment as usual (TAU).35) However, subsequent treatment of these patients for 9 months or 12 months (for those that initially received sham treatment) produced an increase in the efficacy of VNS over time with response and remission rates of 27.2% and 15.8% respectively.36) In another long-term observational study, George et al.37) compared response and remission rates for patients receiving TAU to rates for patients from the previous study36) who received TAU plus VNS for 1 year. Among the VNS+TAU group, 27% were responders whereas only 13% of the patients in the TAU group responded. Further, the number of patients achieving remission in the VNS+TAU group was twice that in the TAU group. A study conducted in Europe by Schlaepfer et al.38) also showed a reduction in the severity of depression with VNS treatment. This study reported response and remission rates of 37% and 13%, respectively, after 3 months of treatment and 53% and 33%, respectively, after one year of treatment. A more recent re-analysis of this study and additional clinical data confirmed the beneficial effects following VNS in at least one out of three patients suffering from chronic and highly medication-refractory unipolar depression.39) Studies looking at the two-year outcome of VNS treatment show response rates of 42-53% and remission rates of 22-39%.40,41) Several single cases with positive effects of VNS have also been reported.42) Overall, these clinical studies show an increase in efficacy of VNS over time with the effect being sustained in most patients who respond.36,43) Further, another recent clinical study showed that VNS significantly lowered relative risk of suicidal ideation and reduced all-cause mortality and suicide rates by about half as compared to those for patients with just TAU.44)

VNS and dosage

For VNS, 'dosage' refers to a combination of various stimulation parameters, which include current (milliamperes, mA), pulse width (microsec, µs), frequency (hertz, Hz) and the duty cycle (amount of time the stimulation is ON [in seconds] and OFF [in minutes]). These parameters determine the electrical output characteristics. Not many studies have accounted for the effects of different doses of VNS. Aaronson et al.45) addressed this issue by conducting a dose-response study for VNS in TRD patients. They studied the effects of three different doses defined as 'low', 'medium' and 'high' based on the magnitude of the output current (0.25, 0.5-1.0 and 1.25-1.5 mA, respectively) and pulse width (150 µs for 'low' and 250 µs for 'medium' and 'high'). The frequency and duty cycle were identical for all three doses. Patients were assessed at the end of 50 weeks of treatment. There were more frequent reports of suicide attempts among the 'low' dose group than among the 'medium' or 'high' dose groups. Also, patients in the 'low' dose group were significantly more likely to relapse at 50 weeks than patients in the 'medium' and 'high' dose groups combined suggesting a more sustained AD effect of VNS at the higher doses.

Anatomical rationale for use of VNS

The vagus nerve is a mixed nerve with efferent fibers having an autonomic function and afferent fibers carrying sensory information from the periphery to the dorsal medullary complex to the nucleus tractus solitarius (NTS).46) The left vagus nerve bifurcates in the medulla and innervates the NTS bilaterally. The NTS projects to the parabrachial nucleus, cerebellum, dorsal raphae nucleus (DRN), locus coeruleus (LC) and the periaqueductal gray.47,48) There are several projections from these primary areas to limbic, paralimbic and cortical regions. Brain areas activated in response to acute VNS have been studied in rats by immunohistochemical staining of brain slices for c-fos, an immediate early gene product.34,49) These studies were followed by immunohistochemical staining for ΔFosB, an indicator of long-term neuroadaptations, in brain slices from rats treated chronically (2-3 weeks) with VNS.34,50) Collectively, these pre-clinical studies indicate that stimulation of the vagus nerve activates areas of the brain that are involved in mood regulation and implicated in MDD. Using immunohistochemical analysis, we have also compared ΔFosB staining in different brain areas with VNS to that with classical ADs, desipramine and sertraline, and found a higher number of ΔFosB-positive cells in the dorsal raphae, bed nucleus of the stria terminalis, nucleus accumbens and peripeduncular nucleus in the VNS-treated rats.50)

Consistent with these observations, clinical neuroimaging studies (fMRI, PET, SPECT) also show changes in medial temporal regions such as the hippocampus, parahippocampus and amygdala as well as the orbito- and pre-frontal cortices.51,52,53,54,55,56) However, a thorough review of these reports reveals that the changes were bilateral in some studies whereas they were limited to one side in others. The direction of change for some brain regions, such as the amygdala,51,56) was also inconsistent. These few contradictory observations may be due to small sample sizes and differences in the duration and parameters of the VNS treatment used for the studies. In addition, there may be an influence of the varied pharmacological treatments that the participants were undergoing along with VNS therapy.

Theories for depression

There are several hypotheses regarding the cause of depression as well as the mechanisms of action of AD treatments such as the monoaminergic neurotransmission theory, the neurotrophic hypothesis and the neurogenesis theory. Here, we briefly review the current status of research associated with these theories specifically with reference to VNS.

As mentioned earlier, most classical ADs target either the serotonergic and/or noradrenergic systems4,6) and result in an enhancement of neurotransmission in these systems, forming the basis of the monoaminergic neurotransmission theory of depression.57,58,59)

VNS increases 5-HT and NE neuronal firing rates in the DRN and LC, respectively, in a time-dependent manner. Spontaneous firing activity increases in the LC first, after an hour to 3 days of stimulation whereas it increases after 14 days in 5-HT neurons in the DRN. SSRIs cause a time dependent subsensitivity of serotonergic autoreceptors but this does not occur with VNS.60) Reanalysis of these data revealed that VNS enhances the firing rate of 5-HT neurons and the burst firing activity of NE neurons, with a greater effect on NE firing activity.61) Additionally, lesion and pharmacological studies revealed that VNS increases tonic activity of 5-HT neurons in the DRN via noradrenergic neurons in the LC that target α1-adrenergic receptors on the 5-HT neurons.61)

Consistent with the increase in firing activity in NE neurons in the LC, acute VNS treatment also increases NE release in the cortex, medial prefrontal cortex (PFC), amygdala and hippocampus as measured using microdialysis.62,63,64) Chronic administration of VNS for 14 days has been reported to cause an increase in extracellular NE in the PFC and hippocampus. Extracellular levels of 5-HT were only increased in the DRN but not in the PFC or hippocampus.65) In line with these observations, we have shown that the anxiolytic-like and AD-like effects of chronic administration of VNS are abolished by lesioning either serotonergic or noradrenergic systems.66) These results were obtained using the novelty suppressed feeding test (NSFT) and the forced swimming test (FST), widely used to study anxiolytic and AD effects of drugs, respectively.67,68) In fact, the AD-like effect of VNS in the FST had been shown previously by Krahl et al.69) with 30 min of continuous VNS, administered daily for 4 days.

Interestingly, in spite of DA cells in the ventral tegmental area (VTA) decreasing their firing rate in response to VNS, extracellular DA levels in the PFC and nucleus accumbens were increased.65) Thus, in contrast to traditional ADs, VNS does seem to have effects on dopaminergic neurons.

The neurogenesis theory suggests that there is a stress-induced decrease in adult neurogenesis in the hippocampus, leading to depression and this decrease is reversed by AD treatment.70) Biggio et al.71) reported that acute VNS (3 h) increased neurogenesis in the dentate gyrus (of the hippocampus) as seen by an increase in BrdU-positive cells 24 h and 3 weeks post-cessation of VNS. Revesz et al.72) showed that acute (48 h) VNS increased proliferation but did not affect progenitor cell survival within the dentate gyrus. Chronic VNS (4 weeks), however, did not have this effect 3 weeks post-cessation of the treatment,71) so the effect on neurogenesis may be relatively short-lived. A recent study looked at the effects of chronic VNS treatment (8 weeks) on hippocampal neurogenesis in an animal model of depression (bulbectomized rats). The decrease in neuronally differentiated BrdU-positive cells within the dentate gyrus, seen due to bulbectomy, was prevented by VNS. However, there was no increase in BrdU-positive cells upon chronic stimulation in the sham-bulbectomized rats.73)

Unlike positive results with acute VNS, acute treatment with classical ADs does not increase neurogenesis; however, acute ECT does.74) ADs usually require at least 2 weeks to produce an increase in proliferation although this effect has not been consistently reproduced over various studies.75,76,77,78) The neurogenesis theory of depression has been expanded to suggest that plasticity and synaptic remodeling (independent of neurogenesis) in the hippocampus and PFC may be more critical for therapeutic efficacy of ADs.79) Both, acute and chronic VNS increased dendritic arborization of doublecortin-positive (DCX+) neurons. DCX or doublecortin is a microtubule associated protein expressed by neuronal precursor cells and marker for adult neurogenesis80) in the dentate gyrus. This effect was detected 3 weeks post-cessation of treatment and was similar to the effect of chronic treatment with fluoxetine.71,81) Ketamine, a rapidly acting drug with AD-like effects (discussed later), also induces synaptogenesis and synaptic protein synthesis approximately 2 h after treatment.82)

The neurotrophic theory of depression is based on studies that show opposite effects of stress and ADs on expression of certain neurotrophic factors in brain areas related to mood regulation. The most widely studied and perhaps the most relevant neurotrophic factor in this context is brain derived neurotrophic factor (BDNF). Along with BDNF, TrkB, the tyrosine kinase receptor for BDNF (and neurotrophin-4 [NT-4]) has also been studied (Fig. 2). From a functional perspective, the neurotrophic hypothesis is linked to the neurogenesis hypothesis as the increase in expression of neurotrophins with AD treatment may block or reverse the neuronal loss associated with depression.83)

Fig. 2

TrkB signaling. Upon ligand-binding (BDNF or NT-4/5), the receptor (which itself is a tyrosine kinase) undergoes transactivation by phosphorylation at tyrosine residues within the catalytic domain (Y705, is one such residue) and at other tyrosine residues such as Y515 and Y816. Phosphorylation at these latter two residues triggers distinct downstream signaling cascades which can eventually lead to gene transcription, cell proliferation and survival. BDNF, brain derived neurotrophic factor; NT, neurotrophin.

Chronic treatment (21 days) with classical ADs belonging to different classes increases expression of mRNAs for BDNF and TrkB in the hippocampus (CA1, CA3 and dentate gyrus).84,85) Others have reported similar results as well.83) Acute as well as chronic (10 days) treatment with ECT increased expression of mRNA for BDNF and the truncated form of TrkB in the frontal cortex and hippocampus.84) Similarly, chronic (11 weeks) repeated TMS also increased mRNA and immunoreactivity for BDNF in the hippocampus (CA3 and dentate gyrus) and in the parietal and piriform cortices.86) Acute VNS treatment (3 h) increased mRNA for BDNF in the hippocampus as well as in the cortex.62)

Drawing conclusions based on changes in mRNA for BDNF or protein levels can be complicated due to factors such as translation, proteolytic cleavage and release that are not accounted for. Hence, analyzing activation of the receptor, TrkB, may provide additional clues about the effect of AD treatment on BDNF function. We have shown that both acute (2 h) and chronic (14 days) VNS activate the TrkB receptor as evident from its phosphorylation at 3 tyrosine residues (Y705, Y816 and Y515). In contrast, acute and chronic AD treatment caused phosphorylation at Y705 and Y816 but not at Y515.87) Similar results have been shown with AD drugs in mice.88,89) Y705 is the autophosphorylation site whereas Y816 and Y515 are linked with the PLCγ1 and MAPK/PI3K signaling pathways, respectively. Consistent with the phosphorylation of the tyrosine residues, acute VNS as well as ADs caused phosphorylation of PLCγ1, however, this was not maintained with chronic treatments. However, only acute and chronic VNS caused phosphorylation of ERK1/2 and Akt that are downstream of Y515.87,90)

There is an abundance of literature showing that serum levels of BDNF are decreased in patients with MDD and that ADs normalize these levels.91) The source of this BDNF in the periphery, however, is still not clear. There are reports suggesting that BDNF in the periphery may derive from the brain via active transport through the blood brain barrier92) and from cells such as leukocytes and vascular endothelial cells in the periphery.93,94,95) To the authors' knowledge, there have not been many studies looking at serum BDNF levels in VNS treated patients. Lang et al.96) report no change in serum BDNF levels in patients treated for 4 weeks with VNS or rTMS. Considering that the patients had been previously treated with AD drugs, one explanation could be that the serum BDNF levels before initiating VNS/rTMS treatments were already normalized. Also, although patients showed clinical improvement, one could also speculate that a longer duration of treatment may lead to different results.

Ketamine

Both pre-clinical and clinical research have been carried out focusing on other pharmacological agents for TRD rather than the classical ones targeting serotonergic and/or noradrenergic systems. These so called "novel" or "alternative" targets for TRD might include ones aimed at dopaminergic or glutamatergic systems, but are not necessarily limited to them.97,98)

Regarding the glutamatergic system, N-methyl-D-aspartate receptor (NMDA-R) antagonists in particular have long been linked to the pathophysiology of MDD and the mechanism of action of AD drugs.97) The first pre-clinical work testing the hypothesis that various NMDA-R antagonists have AD-like effects was carried out in mice, where the authors showed that such agents caused a significant reduction of immobility in the FST and the tail suspension test,99) two tests with high predictive validity for AD treatments.68,100)

Among NMDA-R antagonists, the anesthetic ketamine in particular is clinically relevant for treatment refractory depression. The first randomized controlled trial investigating the AD properties of a single intravenous low dose of ketamine (0.5 mg/kg) in patients diagnosed with MDD showed a significant improvement in depressive symptoms within 72 hours after ketamine administration, and not with placebo.101) Since this first trial, others have corroborated the rapid AD effects of ketamine administration.101,102,103,104) When given to TRD patients, single subanesthetic dose of ketamine typically improves mood within hours following ketamine administration and can persist, for the most part, for about two weeks.105,106,107,108,109,110,111) It also produces a rapid decrease in suicidal ideation in both bipolar depression and MDD.104,106,112) Rapid-acting pharmacotherapy could readily reduce hospitalization time and allow disabled people to resume their daily routine including being able to work.

It is important to note that aside from the promising and consistent results gained in the clinic, ketamine poses some serious problems with regard to its acute psychotomimetic and physiological (increased blood pressure and heart rate) side effects. In addition, chronic use of ketamine has been associated with dependence.113,114,115)

Sub-anesthetic low dose ketamine can also produce rapid and sustained AD-like responses in rodents. Studies carried out in mice reported a decrease in immobility in the FST shortly after a single systemic injection, with a persistent response for up to one week,116,117,118) analogous to some of its effects previously reported in humans as discussed above.108,109,111,116,117,118)

Pre-clinical studies have focused on the mechanisms of action of ketamine. The AD-like effects of ketamine are blocked by pretreatment with 2, 3-dihydroxy-6-nitro-7-sulfamoyl-benzol[f]quinoxaline-2,3-dione (NBQX), an a-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonist.117) An early study revealed decreased spontaneous activity of GABAergic interneurons and an increased firing rate of glutamatergic pyramidal neurons in the PFC of rats given ketamine,119) suggesting that NMDA-R antagonism by ketamine blocked spontaneous GABAergic activity resulting in enhanced glutamatergic transmission. Stimulation of AMPA receptors leads to activity-dependent BDNF release.120) The use of conditional knockout mice has suggested that BDNF is required for the AD-like effect of ketamine.116) Similar to VNS, ketamine also shows an activation of neurotrophin signaling. In particular studies have shown a rather transient increase in the phosphorylation of the BDNF/NT-4 receptor, namely TrkB, following a single sub-anesthetic injection of ketamine in rodents.116,121) In a randomized control trial with ketamine, plasma BDNF levels were found to be significantly higher in responders compared to that in non-responders.122) However, as mentioned, VNS therapy was not associated with increased plasma BDNF levels.96)

Moreover, both VNS (as mentioned earlier) and ketamine seem to modulate signaling pathways downstream of the TrkB receptor, for example the mammalian target of rapamycin (mTor) within the hippocampus.90,121) Interestingly whereas ketamine cause a rapid and transient activation of the mTor pathway, VNS seems to require more chronic treatment for the same effect.90,121) Pre-clinical studies reviewed by Dwyer and Duman123) report that activation of the mTor pathway following single low-dose of ketamine administration is required to rescue the maladaptative responses to chronic stress.

Some studies have shown a positive correlation between plasma levels of mTor124,125) and its downstream effectors, glycogen synthase kinase-3beta (GSK-3β) and dephosphorylation of eukaryotic elongation factor 2 (e-EF2)125) in patients who responded to ketamine. This has not yet been tested with respect to the VNS-induced mTor signaling activation in humans. Since phosphorylated e-EF2 is associated with inhibition of translation, its dephosphorylation, via mTor signaling activation, leads to increased protein synthesis, including BDNF synthesis.123) It is worth noting that patients carrying a single nucleotide polymorphism, namely Val66Met in the gene encoding for BDNF, show a reduced response to ketamine.126)

CONCLUSION

In conclusion, TRD, is a serious public health concern given the morbidity, and mortality due to suicide, associated with it. With improved and more standardized criteria for its definition, it has become more amenable to proper scientific investigation. This review covered in some detail two treatments for it. One, VNS has been approved for use in many countries but not yet in Korea. The other, ketamine is still in the investigational stage but the clinical data are very encouraging, especially in light of the rapidity of its clinical response. These two treatments do share some effects in common that differ from those produced by traditional AD drugs, e.g., mTor, p70S6 kinase, etc. downstream of the TrkB receptor. The role that such effects play in their effectiveness in TRD, which by definition does not respond to traditional ADs, is an important subject for future research.