Lithium is first-line therapy for bipolar affective disorder and has recently been shown to have protective effects in populations at risk for Alzheimer’s disease (AD). However, the mechanism underlying this protection is poorly understood and consequently limits its possible therapeutic application in AD. Moreover, conventional lithium formulations have a narrow therapeutic window and are associated with a severe side effect profile. Here we evaluated a novel microdose formulation of lithium, coded NP03, in a well-characterized rat model of progressive AD-like amyloid pathology. This formulation allows microdose lithium delivery to the brain in the absence of negative side effects. We found that NP03 rescued key initiating components of AD pathology, including inactivating GSK-3β, reducing BACE1 expression and activity, and reducing amyloid levels. Notably, NP03 rescued memory loss, impaired CRTC1 promoter binding of synaptic plasticity genes and hippocampal neurogenesis. These results raise the possibility that NP03 be of therapeutic value in the early or preclinical stages of AD.
Lithium has been used for more than 60 years in the treatment of bipolar affective disorder and has recently shown disease-modifying properties in individuals at risk for developing Alzheimer’s disease (AD)1, 2, 3, 4 and in AD animal models.5, 6, 7 Although there have been many advances in our understanding of its mechanism of action,8 precisely how lithium confers its protective effects in AD remains poorly understood. Clinical trials support the notion that lithium’s multi-target function can modulate cerebrospinal fluid levels of Aβ, tau, GSK-3β, and stabilize cognition in individuals with AD.2, 4 However, despite appearing as an attractive therapeutic candidate for AD treatment, conventional lithium formulations (lithium carbonate and lithium citrate) have a narrow therapeutic window owing to negative side effects at higher doses and their use in the elderly requires careful monitoring.9, 10
NP03 (issued from the Aonys technology developed by Medesis Pharma, Montpellier, France) is a novel microdose lithium formulation, wherein lithium is encapsulated in reverse water-in-oil microemulsions composed of self-assembled specific polar lipids, surfactant and co-surfactants (lecithin and ethanol), allowing enhanced central nervous system (CNS) uptake.11, 12, 13, 14, 15, 16 With NP03, transmucosal administration permits a significantly lower amount of lithium to be administered (400 × fold lower; blood concentration below detection limit of 0.06 mmol l−1), as this route of administration avoids acid hydrolysis in the gastrointestinal tract and bypasses hepatic metabolism, thus leading to high bioavailability. The Aonys technology has been shown to enhance CNS penetration of the P42 peptide to prevent Huntingtin aggregation in a murine model of Huntington’s disease (HD),12 for efficient CNS targeting of lithium in the same model,11 and CNS targeting of siRNAs in a murine model of prion disease.13 NP03 has previously shown neuroprotective properties in a Huntington’s disease murine model at remarkably low doses while avoiding the well-known adverse side effects of conventional lithium formulations.11
We evaluated whether the NP03 microdose formulation of lithium (40 μg Li per kg) might be efficient in modifying the early Alzheimer-like progressive amyloid pathology in McGill-R-Thy1-APP transgenic rats.17 At the early, pre-plaque stage McGill AD transgenic rats show in vivo disruption of synaptic plasticity in Aβ-burdened neurons18 and cognitive impairment.17, 18, 19, 20, 21, 22 It has also been reported that early intraneuronal Aβ accumulation blocks CRTC1 synaptonuclear transport, resulting in impaired promoter occupancy, and impaired neuroplasticity gene expression.22 In this study, we tested NP03 at the pre-plaque stage since intervening at early pathological stages offers a more promising outcome compared to later stages, by which time the brain has suffered extensive damage.23
Here we report beneficial effects of NP03 in halting the evolving AD pathology in McGill AD transgenic rats and in rescuing early Aβ-driven deficits in learning and memory. NP03 further induced an inactivated GSK-3β profile, and dampened Bace1 (β-site APP cleaving enzyme-1) gene expression and BACE1 activity, rendering lower levels of toxic Aβ42 peptides. NP03 also restored CRTC1 promoter occupancy in synaptic plasticity genes required for learning and memory. Furthermore, it re-established hippocampal neurogenesis in the AD rat transgenic model. These findings thus suggest that NP03 reverses key AD pathologies in an in vivo AD model, and that it may have therapeutic value in the early stages of the disease.
Materials and methods
Full description of Materials and methods is available as Supplementary Materials.
Male and female homozygous McGill-R-Thy1-APP transgenic rats17 were socially housed under 12 h light–dark schedule at 21 °C with free access to food and water. Number of animals is indicated in figure legends. Procedures were approved by the Animal Care Committee of McGill University.
Three-month-old rats received microdose lithium NP03 (40 μg Li per kg; 1 ml kg−1; Medesis Pharma) or vehicle formulation lacking lithium (1 ml kg−1) on rectal mucosa 5 days per week for 8 weeks. A separate group of 250–300 g wild-type rats were treated with increasing doses of lithium (0–600 μg Li per kg) NP03. No changes in weight, drinking behaviour or urination were observed.
Novel object recognition, Morris water maze and auditory fear-conditioning tasks were performed as previously described.19
Determination of brain lithium levels
Brain tissue was collected 3–5 h following NP03 or vehicle administration and processed for analysis by inductively coupled plasma mass spectrometry (ICP-MS) (ICAP-Q, Thermo Fisher Scientific, Waltham, MA, USA).
Immunohistochemistry procedures were performed as previously described.22 Sections were imaged using an Axio Imager 2 microscope (Carl Zeiss Canada, North York, ON, Canada) running Zen Blue software (Carl Zeiss).
Hippocampal tissue was homogenized and Western blot analysis was carried out as previously described.22 The following primary antibodies were applied: anti-phospho-GSK-3βSer9 (5B3; Cell Signaling Technology, Danvers, MA, USA; #9323); anti-total GSK-3β (27C10; Cell Signaling #9315); anti-β-Catenin (6B3; Cell Signaling #9582); anti-βIII Tubulin (Promega, Madison, WI, USA; #G7121); and anti-glyceraldehyde-3-phosphate dehydrogenase (GAPDH, 6C5; EMD Millipore, Etobicoke, ON, Canada, #MAB374).
Protein levels of hippocampal Wnt3a ligand were determined using the electrochemiluminescence-linked immunoassay kit from Meso Scale Discovery (K150SOD; Gaithersburg, MD, USA) following manufacturer’s instructions.
Chromatin immunoprecipitation and gene expression analysis procedures were as previously described.22
BACE1 activity detection assay
BACE1 activity in cortical tissue was assessed using the fluorescence resonance energy transfer (FRET)-based β-secretase (BACE1) Activity Detection Kit (Sigma-Aldrich, St Louis, MO, USA; CS0010).
TBS soluble and insoluble human Aβ40 and Aβ42 ELISA
Levels of soluble and insoluble human Aβ40 and Aβ42 were assessed in cortical homogenates following the manufacturer’s directions (Invitrogen, Carlsbad, CA, USA; KHB3482 and KHB3442).
Coronal sections containing anterior dorsal hippocampus (three sections per animal) were incubated with antibody against doublecortin (DCX) (1:600, C-18, sc-8066, Santa Cruz Biotechnology, Santa Cruz, CA, USA) and Alexa Rhodamine anti-goat. DCX-immunoreactive cells were counted in a blind manner and expressed as a mean number of cells per section for each condition.
Data were analysed using two-way ANOVA to examine effects of NP03 treatment and App transgene and all possible pairwise tests of the group means were examined using Tukey’s post hoc tests. Means of two groups were compared using an unpaired Student’s t-tests (GraphPad Software, La Jolla, CA, USA). Data are reported as mean±s.e.m. Statistical significance was P<0.05.
The McGill-R-Thy1-APP transgenic rat model of AD-like amyloid pathology (AD rats hereafter) expresses the mutated human Aβ precursor protein (APP). It shows intraneuronal Aβ as early as 1 week postnatally, and extracellular plaques appear between 6 and 9 months of age in homozygous animals, spreading from the hippocampus to the cortex (Supplementary Figure 1).17 These AD rats show impaired cellular signaling, long-term potentiation and cognition at the pre-plaque state.17, 18, 19, 22, 24 Thus, we treated AD rats at this time point to assess the ability of NP03 to rescue established Aβ-driven pathology and related cognitive impairment.
We evaluated a microdose formulation of lithium, NP03, in the treatment of AD-like amyloid pathology at the early, pre-plaque stage of the disease. NP03 contains the lithium citrate salt deposited in a water-in-oil microemulsion (Figure 1a). This formulation allows significantly lower levels of lithium to be delivered, avoiding the off-target effects associated with conventional dosing. Thus, AD transgenic rats and their wild-type littermates received either NP03 (40 μg Li per kg; 1 ml kg−1) or vehicle (1 ml kg−1) 5 days per week for 2 months (Figure 1b) starting at 3 months of age. Importantly, no weight changes, a common side effect of lithium, occurred following NP03 treatment (two-way ANOVA, P>0.05; Figure 1c). Brain lithium in rats treated with 40 μg Li per kg NP03 reached 3.36 ng g−1 of brain tissue, as measured by ICP-MS analysis, demonstrating that considerable amounts of lithium reached the CNS across the blood–brain barrier. Of note, the concentration of lithium increased with increasing doses of lithium, suggesting saturation was not reached at 40 μg Li per kg (Figure 1d). Finally, transcript production of the Thy1 promoter-driven APP transgene was not affected by NP03 treatment (t(13)=0.3601; P=0.7246; Figure 1e).
NP03 reversed memory impairments in AD rats
We first assessed the effect of NP03 treatment on learning and memory. During the familiarization phase of the novel object recognition (NOR) task, all rats demonstrated high exploratory behaviour, spending approximately half the allotted time exploring objects (Figure 2a). Following a 30-min intertrial interval, rats were presented with the test phase (Figure 2b) where one familiar object was replaced with a novel object. As expected, wild-type rats showed a clear preference for the novel object with a preference ratio of 40% (chance preference being 20%) while vehicle-treated AD rats demonstrated a significant impairment (Treatment × Transgene interaction: F(1,26)=5.65; P=0.0251). Tukey’s p ost hoc analyses revealed a significant reduction in the novel object preference for the vehicle-treated Alzheimer rats compared to the wild-type control (P<0.05). Importantly, NP03 restored novel object preference in AD rats significantly above the AD vehicle group (P<0.05), and comparable to that of the wild-type control (P>0.05).
Rats were then tested on the Morris water maze task.25, 26 On training Day 1 (Figure 2c), mean platform latencies were not significantly different, ranging 67.00 –85.75 s (Figure 2d), and all groups showed improved performance with training (two-way ANOVA: time effect F(4,135)=12.28; P<0.0001). However, AD rats performed significantly worse on acquisition phase performance on Days 2 (AD vehicle vs WT vehicle: P<0.01) and 3 (AD vehicle vs WT vehicle: P<0.05) compared to the wild type. Again, NP03 rescued performance on Days 2 and 3 in AD rats that performed at the same level as wild-type rats (AD NP03 vs WT vehicle: P>0.05). On the Probe Trial (Figure 2e), AD rats made just as many platform crosses compared to the wild-type rats, indicating that while they took longer over training Days 1–5 to learn the task, they were eventually able to locate the platform, and thus, showed no deficit on the subsequent Probe Trial.
Finally, in the auditory fear-conditioning task, all rats displayed equal baseline freezing in training Context A (CXT-A; Figure 2f; Baseline) and the presentation of a 5-kHz tone elicited no change in freezing, verifying that the tone was initially innocuous (Figure 2f; Tone). As expected, a mild footshock co-terminating with the tone led to an elevation in freezing for all rats (Figure 2f; Post-Shock). When rats were returned to training context (CXT-A) 24 h later they all showed high levels of freezing indicating AD rats were unimpaired in contextual fear memory (Figure 2g).19 When we tested rats in a novel context (Context B, CXT-B) 24 h later all groups again showed baseline freezing (Figure 2h). However, presentation of the 5-kHz tone in CXT-B elicited a high level of freezing in wild-type but not vehicle-treated AD rats. NP03 rescued this cued recall in impaired AD rats. These observations were supported by the results of two-way ANOVA, which revealed a significant Transgene × Treatment interaction (F(1,24)=9.19; P=0.0058), as well as a significant main effect for Treatment (F(1,24)=4.66; P=0.0411), but not for Transgene (F(1,24)=0.07; P=0.7939). Post hoc analyses revealed that vehicle-treated TG rats had lower levels of freezing compared to vehicle-treated WT (P<0.05), while there was no difference between control animals and NP03-treated TG animals (P>0.05). Together our results reveal that NP03 rescued Aβ-induced memory impairments in novel object recognition, spatial learning and amygdala-dependent fear memory.
NP03 inactivated hippocampal GSK-3β and restored native β-catenin
We next investigated the biochemical changes that might account for the observed behavioural restoration by NP03 in AD rats. We first investigated the phosphorylation status of GSK-3β, a multifunctional serine/threonine kinase widely expressed in brain and linked to AD pathology.27, 28, 29 We assessed relative phosphorylation of GSK-3β at serine 9 compared to total GSK-3β as an indicator of GSK-3β inactivation.30 Using quantitative Western blotting we found a significant reduction in the levels of phospho-GSK-3βSer9 in Alzheimer transgenic rats compared to the wild-type (Treatment x Transgene interaction: F(1,23)=8.91; P=0.0066; WT:Veh vs TG:Veh, P<0.05). NP03 reversed this deficit in the AD transgenic rats (TG:Veh vs TG:NP03, P<0.01; WT:Veh vs TG:NP03, P>0.05. Importantly, the ratio of phospho-GSK-3βSer9 to total GSK-3β was significantly reduced in the hippocampus of AD rats relative to wild-type rats, reflecting a release of inhibitory phosphorylation on GSK-3β (Treatment x Transgene interaction: F(1,23)=6.42; P=0.0186; WT:Veh vs TG:Veh, P<0.05). NP03 restored the ratio of phospho-GSK-3βSer9 to total GSK-3β in AD rats (TG:Veh vs TG:NP03, P<0.01; Figure 3a), a finding that is consistent with a previous report that showed NP03 inhibiting GSK-3β in a mouse model of Huntington’s disease.11 GSK-3β phosphorylates several components of the Wnt/β-catenin transduction pathway, including β-catenin, which is subsequently recognized by ubiquitin and targeted for proteasomal degradation.31 We measured levels of the Wnt ligand and found no significant difference between any of the conditions (two-way ANOVA: Treatment: F(1,23)=0.02; P=0.8793; Transgene: F(1,23)=0.28; P=0.5991; interaction: F(1,23)=1.20; P=0.2856; Supplementary Figure 2). However, we did observe a significant decrease in native β-catenin (a GSK-3β substrate) protein in the hippocampus of AD rats (significant main effect for Transgene (F(1,21)=5.82; P=0.0251; WT:Veh and WT:NP03 vs TG:Veh, P<0.05; Figure 3b), suggesting a facilitation of degrading mechanisms of the native form of β-catenin in these rats. We found that NP03 treatment rescued the steady-state levels of β-catenin, coinciding with inactivation of GSK-3β (TG:Veh vs TG:NP03, P<0.05).
NP03 reduced BACE1 activity and the ratio of Aβ42/Aβ40
Wnt/β-catenin signalling supports transcriptional repression of Bace1 by promoting the binding of T-cell factor-4 at Bace1 genetic promoters.32 Thus, in accordance with the observed reduction of native β-catenin, we observed a five-fold increase in Bace1 mRNA in the hippocampus of AD transgenic rats relative to the wild type (Figure 3c) that was diminished to normal levels with NP03 treatment (Treatment × Transgene interaction: F(1,23)=6.91; P=0.0150; WT:Veh vs TG:Veh, P<0.05; TG:Veh vs TG:NP03, P<0.01). In addition, using a FRET-based activity assay, we observed increased substrate cleavage activity by BACE1 in vehicle-treated AD transgenic rats compared to the wild type (Figure 3d). NP03 treatment reduced BACE1 activity in AD rats to baseline levels, a reduction of 12.96%. These observations were supported by the results of a two-way ANOVA, which revealed a significant Transgene × Treatment interaction (F(1,25)=9.547; P=0.0050), as well as a significant main effect for treatment (F(1,25)=6.65; P=0.0162), but not for Transgene (F(1,25)=3.28; P=0.0822). Post hoc analyses revealed that vehicle-treated TG rats had significantly elevated BACE1 activity compared to vehicle- and NP03-treated WT (P<0.05). NP03 reduced BACE1 activity in Alzheimer rats compared to the vehicle-treated AD rats (P<0.01) to a level not significantly different from the WT (P>0.05).
BACE1 cleaves APP to generate Aβ peptides and other APP-derived fragments.33, 34 Accordingly, BACE1 inhibitors have been considered as putative therapeutic agents for the treatment of AD.35 Given the increase in Bace1 gene expression and activity in AD transgenic rats, we subsequently analysed the levels of TBS- and guanidine-soluble human Aβ40 and Aβ42 peptides (Figure 3e). In the TBS-soluble fraction, as expected, Aβ42 peptides and Aβ40 peptides were highly expressed in AD transgenic rats. Importantly, NP03 reduced the levels of soluble Aβ42 in AD transgenic rats (t(12)=2.028; P=0.0327), a decrease of 4.5-fold, while levels of soluble Aβ40 were unchanged (t(12)=6.197; P>0.05). The reduction in Aβ42 led to a significant decrease in the soluble Aβ42/Aβ40 ratio (t(12)=2.187; P=0.0247). Insoluble Aβ42 and Aβ40 peptides were not detected at this early, 5-month time point. Thus, NP03 effectively reduced Bace1 mRNA and activity, and diminished levels of soluble Aβ42 in AD transgenic rats.
NP03 rescued CRTC1 binding at synaptic plasticity-associated gene promoters
In rodent models of AD, the transcription co-regulator CRTC1 is dysregulated early, when Aβ peptides are still intraneuronally confined.22, 36, 37, 38 In a previous study, we showed an Aβ-mediated impairment in CRTC1-dependent gene transcription that was reflected by reduced CRTC1 nuclear translocation, reduced CRTC1 occupancy at synaptic plasticity-associated gene promoters and reduced transcription of plasticity-associated genes in AD transgenic rats.22 As it has been reported that higher concentrations of lithium enhances CRTC1 oligomer formation as well as the interaction between CREB co-activating factors CRTC1 and CREB-binding protein,39, 40, 41 we tested whether NP03 lithium microdoses could reverse the Aβ-driven impairment in CRTC1 promoter occupancy. Thus, consistent with our previous report,22 we found that in AD transgenic rats, genomic promoter occupancy was significantly reduced for Bdnf iv (brain-derived neurotrophic factor) (Figure 3f). These observations were supported by the results of a two-way ANOVA, which revealed a significant main effect for Transgene (F(1,30)=9.50; P=0.0044). Post hoc analyses revealed that vehicle-treated Alzheimer transgenic rats had significantly reduced CRTC1 promoter occupancy at Bdnf iv compared to vehicle- and NP03-treated wild type (P<0.05). NP03 restored CRTC1 Bdnf iv promoter occupancy to a level not significantly different from the wild type (P>0.05). CRTC1 promoter occupancy was also reduced at c-fos in AD transgenic rats (Transgene × Treatment interaction (F(1,29)=5.77; P=0.0229; Figure 3g). Post hoc analyses revealed that vehicle-treated Alzheimer transgenic rats had significantly lower CRTC1 occupancy of c-fos promoters compared to the wild-type vehicle group (P<0.05). NP03 significantly increased CRTC1 occupancy in Alzheimer transgenic rats compared to the vehicle-treated Alzheimer transgenic rats (P<0.05) to a level not significantly different from the wild type (P>0.05). Thus, it is likely that NP03-driven restoration in CRTC1 genomic occupancy contributed to behavioural recovery in AD rats treated with NP03 by facilitating expression of synaptic plasticity-related genes.
NP03 rescued adult hippocampal neurogenesis
The subgranular zone (SGZ) of the hippocampus exhibits persistent neurogenesis into adulthood—a process shown to be impaired with amyloid deposition.42, 43 As Wnt/β-catenin signalling has been reported to regulate adult hippocampal neurogenesis,44 we processed tissue sections containing the SGZ using an antibody specific for the protein doublecortin (Figure 4a), a reliable and specific marker of adult neurogenesis.45 Vehicle-treated AD rats showed impaired SGZ neurogenesis compared to the wild-type groups, as demonstrated by a reduction in the number of DCX+ cells (Treatment × Transgene interaction F(1,12)=8.65; P=0.0124; WT:Veh and WT:NP03 vs TG:Veh, P<0.05; Figures 4b and c). Similarly to the effects reported for conventional lithium in mice,46 and in fitting with its effects on Aβ and the Wnt/β-catenin signalling pathway, we found that NP03 lithium microdoses rescued loss of neurogenesis in AD rats (TG:Veh vs TG:NP03, P<0.01).
This study indicates that microdose lithium NP03 can efficiently reach the brain to rescue cognitive impairments at early stages of AD-like amyloid pathology in AD rats. Importantly, this effect coincided with the inactivation of GSK-3β and a reduction in Aβ42 levels. Furthermore, NP03 blunted BACE1 hyperactivity in AD rats while restoring hippocampal neurogenesis and CRTC1 Bdnf iv and c-fos promoter occupancy. These aspects are critical for the effective CRTC1 transcription as required for learning and memory mechanisms.47, 48 In this regard, our results coincide with recent findings where subclinical concentrations of lithium provoked higher intracellular and extracellular BDNF concentration in hippocampal cell cultures.49 Of note, NP03 treatment did not produce side effects relating to lithium toxicity nor did it provoke adverse effects in wild-type animals. These results support the hypothesis that microdoses of lithium are sufficient to impact Aβ neuropathology by affecting multiple components of the Wnt/β-catenin signalling pathway, among others.
Despite wide use in treatment of bipolar disorder, a major issue with the application of lithium remains its severe side effect profile.9, 10, 50 Lithium has a narrow therapeutic window, and severe side effects preclude its long-term use in elderly patients. Adverse effects of lithium include tremor, nausea, polyuria, polydipsia and weight gain,9 and because of these side effects, lower plasma concentrations are intentionally targeted for maintenance treatment. Here we evaluated a novel lipidic nano-particle formulation of lithium (NP03) that delivers significantly lower amounts of lithium, while allowing enhanced CNS uptake of lithium, avoiding adverse effects without loss of therapeutic efficacy.
The Wnt/β-catenin pathway has been implicated in AD pathogenesis51, 52, 53, 54 and accordingly modulation of this pathway is thought to represent a possible therapeutic strategy in AD. Our results support the hypothesis that lithium modulates Wnt/β-catenin signalling via inactivation of GSK-3β, contributing to a reduction of Bace1 mRNA expression, inhibition of BACE1 and reduction of Aβ neuropathology. Recently, Parr et al.32 showed that activation of Wnt/β-catenin signalling pathway promotes binding of T-cell factor-4, a Bace1 gene repressor, and multiple lines of evidence point to a role of clinical doses of lithium in mimicking Wnt/β-catenin signalling through the inactivation of GSK-3β.51, 55, 56, 57 Furthermore, BACE1 activity is consistently shown to be elevated in AD and in models of Alzheimer amyloidosis.58, 59, 60 NP03 reduced Bace1 expression and activity and it is likely through this mechanism that soluble Aβ42 levels were reduced. The interpretations of the present results are summarized in Figure 5, showing that Aβ-driven hyperactivity of GSK-3β would lead to reduced stability of β-catenin, thereby removing the transcriptional repression of Bace1 by TCF/LEF. This would favour Aβ production via the sequential cleavage of APP by BACE1. Conversely, NP03 inactivates GSK-3β through phosphorylation at Ser 9, restoring β-catenin signalling components, and transcriptional repression of Bace1. This ultimately leads to reduced production of Aβ42 peptides and the consequential diminution of the Alzheimer’s-like amyloid pathology, resulting in improved cognitive outcomes (Figure 5). This model is supported by a recent report showing that inhibition of Wnt signalling induces amyloidogenic processing and aggregation of Aβ42 peptides.61 Thus, notwithstanding the limitations of transgenic models, the reduction in soluble Aβ42 observed here is significant, as dementia severity correlates more closely with presence of soluble Aβ, rather than with fibrillar Aβ deposits in the brain.62
Aβ deposition is a negative regulator of adult hippocampal neurogenesis.42, 43 We found that NP03 can prevent loss of hippocampal neurogenesis at early stages of Aβ neuropathology, consistent with earlier reports using App mutant mice.46 Although it is not known what exact role adult neurogenesis plays in behaviour,64, 65 incorporation of adult-born neurons in the hippocampus SGZ is important for inhibitory modulation of mature granule cells.66 Furthermore, adult neurogenesis has been implicated in pattern separation and the normal processing of information in the hippocampal circuit.67 Thus, it is likely that NP03-rescued cognition in AD rats results in part by the preservation of hippocampal neurogenesis.
Effects of lithium on AD in clinical populations have been reported, although with conflicting results.1, 3 A study administering lithium carbonate (serum levels 0.3–0.8 mmol l−1) for up to 1 year showed no cognitive improvement.68 A second study administering lithium sulphate (serum levels 0.5–0.8 mmol l−1) for 10 weeks, including a 6-week titration phase50 also failed to show benefit. However, a trial assessing lithium at earlier stages of the pathology2 revealed a significant decrease in cerebrospinal fluid p-tau181 and improvement on the ADAS-Cog subscale after 12-month lithium treatment (0.25–0.5 mmol l−1). In a low-dose trial, 300 μg of lithium was given once daily for 15 months4 and while the placebo group deteriorated in MMSE scores, the lithium-treated group remained stable. Together, the clinical studies reveal that the possibility of beneficial effects of lithium in the treatment of AD should not be excluded. Rather, further clinical trials with lithium microdoses within well-defined clinical populations should be undertaken,69 for instance, at early Alzheimer pathological stages and/or in Down syndrome (DS), at the transition from DS-AD asymptomatic to DS-AD symptomatic. Such studies should include biomarker measures, along with ‘self-to-self’ cognitive assessment70 to determine treatment efficacy.
It must be noted that while cognitive impairments and AD-like pathology were reversed by NP03 treatment, our work cannot completely rule out the possibility that the effect of NP03 is of preventative nature and thus NP03 administration would prevent pathology progression, rather than rescuing it. These aspects will be addressed in future studies.
Conventional lithium dosage is associated with a significant adverse side-effect profile including nausea, dizziness, nephrotoxicity, polyuria, polydipsia and tremor.9, 10 Serum lithium levels achieved here were below detection limit of 0.06 mmol l−1. By comparison, this is significantly lower than the levels which are typically targeted for individuals with bipolar disorder, which range between 0.5 and 1.5 mmol l−1.71 This is also lower than the doses targeted in Alzheimer patients, which range from 0.3 to 0.8 mmol l−1.68, 72 Therefore, the justification of NP03 as a less-toxic alternative to conventional lithium stems from the microdose nature of the formulation and its capacity to reach the brain. This is especially important given the long-term treatment required for AD, and its application in elderly populations.50
In our studies, NP03 formulation restored spatial learning, recognition memory and associative learning in a rat model of AD-like amyloid pathology. NP03 reduced brain Aβ42, and proved to be an efficacious inhibitor of BACE1 activity. Finally, NP03 restored neurogenesis and CRTC1 promoter occupancy in synaptic plasticity genes. NP03 did not provoke adverse side effects. With a unique formulation allowing controlled microdose delivery setting it apart from current conventional lithium therapy, NP03 represents a promising therapeutic agent for mild-moderate and foremost for prodromal AD. The emerging literature would indicate that prodromal AD will be safely identified for earlier therapeutic intervention73, 74, 75 and, as such, these cohorts should be suitable candidates for NP03 and alternative microdose lithium therapies.
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This work was supported by grants from the Canadian Institutes of Health Research grant number: 102752 and Centres of Excellence in Neurodegeneration grant number: 01074. We thank Dr A Frosst, the Frosst family and Merck Canada for their continuing support. We thank Dr. Jean-Benoit Charron for his help with chromatin immunoprecipitation experiments. SDC is the holder of the Charles E Frosst/Merck Research Associate position. MFI was the recipient of a Biomedical Doctoral Award from the Alzheimer Society of Canada (2011–2014). HH is the holder of a Fonds de Recherche Sante Quebec Postdoctoral Fellowship. ACC is the holder of the Charles E Frosst/Merck-endowed Chair in Pharmacology and is a Team Leader for the Canadian Consortium on Neurodegeneration in Aging.
The authors declare no conflict of interest.
Supplementary Information accompanies the paper on the Translational Psychiatry website
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Wilson, E., Do Carmo, S., Iulita, M. et al. BACE1 inhibition by microdose lithium formulation NP03 rescues memory loss and early stage amyloid neuropathology. Transl Psychiatry 7, e1190 (2017). https://doi.org/10.1038/tp.2017.169
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