Current Status of Drug Targets and Emerging Therapeutic Strategies in the Management of Alzheimer's Disease.

Alzheimer's disease (AD) is a chronic neurodegenerative disease affecting the elderly. AD is associated with a progressive decline in memory and cognitive abilities, drastic changes in behavioural patterns and other psychiatric manifestations. It leads to a significant decline in the quality of life at personal, household as well as national level. Although AD was described about hundred years back and multiple theories have been proposed, its exact pathophysiology is unknown. There is no cure for AD and the life expectancy of AD patients remains low at 3-9 years. An accurate understanding of the molecular mechanism(s) involved in the pathogenesis of AD is imperative to devise a successful treatment strategy. This review explains and summarises the current understanding of different therapeutic strategies based on various molecular pathways known to date. Different strategies based on anti-amyloid pathology, glutamatergic pathway, anti-tau, neuroprotection through neurotrophic factors and cholinergic neurotransmission have been discussed. Further, the use of anti-inflammatory drugs, nutraceuticals, and dietary interventions has also been explained in the management of AD. It further describes different pharmacological and dietary interventions being used in treating and/or managing AD. Additionally, this article provides a thorough review of the literature for improving the therapeutic paradigm of AD. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

INTRODUCTION

Alzheimer's disease (AD) is the most common cause of dementia and a type of untreatable neurodegenerative condition. It is the third most expensive medical condition [1, 2]. Multiple cognitive and non-cognitive functions get disturbed in AD, thereby impacting the quality of life. A wide range of genetic and environmental factors lead to late-onset AD (LOAD). Beta-amyloid and abnormal tau proteins play a major role in disease development. The basic pathways of the basal forebrain and cerebral cortex are compromised in AD with the neurotransmitter acetylcholine being affected [2]. This degenerative disease is progressive in nature, with the entorhinal cortex being one of the first regions to get affected, which then spreads to other Neighboring parts, such as the hippocampus [3]. The appearance of neurofibrillary tangles (made of tau proteins) and plaques (aggregates of amyloid-beta protein) are the characteristics of the onset of this disease followed by neurodegeneration and synaptic dysfunction [1, 4].

Most clinical studies have focused on reducing the pathogenic amyloid-beta (Aβ) and tau levels. However, such strategies have failed to bring about any long-term relief. The role of Aβ in the normal physiological functioning of the cells, as described by recent research studies have made AD treatment even more complex. Although Aβ pathology has been long thought of as a risk factor for AD, there is still no conclusive evidence of its causal role in AD onset. This has even led some scientists to believe that its aetiology could be due to another pathway that leads to AD, and Aβ might just be one metabolite of its consequence. The mechanism(s) involved in the pathogenesis of AD remain elusive till date. The availability of brain samples from only late-stage AD patients as well as limitations of in vivo models has posed a challenge for pinpointing the molecular changes that take place in prodromal AD. To describe AD, there are many evidence-based theories that have been proposed by researchers. The list includes the theories of free radical damage, inflammatory response, cholinergic damage, and the most popular ones like β-amyloid and anomalous tau protein metabolism, among others.

The lack of understanding of the underlying molecular mechanisms and the unavailability of credible strategies for its early prediction make the prevention and treatment of AD difficult. Understanding the exact pathophysiology of AD would facilitate the finding of appropriate biomarkers and drug‐targets to tackle the growing burden of the disease. The development of efficient and potent therapeutic drugs is the key to tackle the situation. Hence, the search for a diverse range of treatments for this multifactorial disease has shifted the therapy dynamics since the past decade as researchers are inclining towards other non-conventional means of treatment.

ANTI-AMYLOID THERAPEUTIC STRATEGIES

Aβ pathology is one of the major characteristic features of AD, besides tau aggregates. Its role in initiating a cascade of degenerative events is unquestionable. It starts aggregating in the brain of AD patients years before the onset of the symptoms [1]. It is a 4 kD peptide obtained from the integral cellular trans-membrane protein - the amyloid precursor protein (APP). Although not fully understood, APP has its role in a number of cellular processes in the brain ranging from synapse formation, neuroprotection, cell-cell interaction, among others, as observed in various APP knock out experiments [5]. Differential APP processing results in a number of products, each with a distinct role yet to be elucidated. Aβ is generated in the amyloidogenic processing of APP, involving initial cleavage by β-secretase, deviating from the non-amyloidogenic pathway, which employs α-secretase in the initial step (Fig. ). The end-product of β-secretase is cleaved by γ-secretases, generating Aβ peptide of varying residues such as Aβ40, Aβ42 or Aβ38. Several studies have correlated amyloid toxicity with an elevated ratio of Aβ42/Aβ40 species in AD. The presence of an extra two residues Ile41 and Ala42 in Aβ42 affects the hydrophobicity of monomers and may assist in its aggregation and oligomerization. Thus, mutations in genes such as APP and PSEN1 which affect the differential processing of amyloid precursor protein has garnered interest and has led to the development of novel therapeutic measures to modulate the synthesis of APP [6, 7].

Modulating Precursor Synthesis and Aβ Concentration

The elucidation of Aβ synthesis led researchers to target it at various stages of its production. Key enzymes such as γ-secretases and β-secretases were of interest, which led to the development of their respective inhibitors. Early attempts at using γ-secretase inhibitors (GSI) were appealing as it could halt the production of Aβ completely. A number of pre-clinical and clinical trials were conducted using a variety of GSIs. However, these attempts were short-lived as the side effects vastly outnumbered the amelioration offered. Further, the existence of multiple γ-secretase substrates with critical biological functions, in addition to APP, proved a major hindrance. Interaction of γ-secretase with Notch receptors is crucial, as one of its end products, called Notch Intracellular Domain (NICD) is a major transcriptional regulator. Inhibition of NICD is known to cause defects in somite development, neurogenesis, and immune cell maturation, among others in animal studies. GSIs such as Semagacestat and Avagacestat had been of particular interest for their potency and selectivity. However, they faced similar issues for their side effects and efficacy. The rise and fall of GSIs and recognition of the functions of γ-secretase eventually shifted the spotlight towards γ-secretase modulators (GSM). Compared to GSIs, GSMs differ in their activity by regulating the processing of γ-secretases rather than relying on its selectivity towards APP over Notch. Although its interaction with γ -secretases is still not clear, it is believed that it could alter the activity of its proteolytic sub-unit, resulting in a decreased ratio of Aβ42/Aβ40 [6].

Another approach to counter Aβ aggregates is via immunotherapy, which includes active immunisation to produce natural antibodies by stimulating the immune system and passive immunisation through exogenous antibody administration [8]. These antibodies target various intermediary substrates, such as Aβ dimers and oligomers, in the formation of plaques and fibrils (Fig. ). The inspiration for this approach came from individuals having an innate advantage with their immune system successfully defending against the amyloid based pathology, paving the way for immune-based therapy. Not surprisingly, these donors did not display any cognitive impairment, which is a sure sign of AD. As of now, several anti-amyloid antibodies have reached Phase 2 and Phase 3 clinical trials based on their promising outcomes in early in vivo and in vitro experiments. However, human trials have been disappointing so far with a few notable exception(s), making it clear that immunotherapy for AD is still in infancy and needs a mix of creativity and innovation for this strategy to succeed.

Aducanumab (BIIB037)

It is an IgG1 type human monoclonal antibody (mAb) that primarily binds to Aβ aggregates, soluble oligomers and also insoluble fibrils. However, it does not seem to target Aβ monomers. Aducanumab analogue can cross the blood-brain barrier and engage its target efficiently, thus clearing beta-amyloid toxicity. The effects can be monitored effectively by positron emission tomography (PET). Phagocytic activity of microglia enhances the engulfing of amyloid plaques by binding to the Fc region of the antibody. This drug showed good tolerability and safety outcomes since its inception in early clinical trials. Phase 1 trials on patients with mild to moderate AD reported a decrease in Aβ concentration, as well as improved cognitive scores as assessed by Clinical Dementia Rating-Sum of Boxes and Mini-Mental State Examination. In March 2019, the current license holder of this drug - Biogen had to halt the project in Phase 3 trials, as the data accumulated were apparently inconsistent with the predicted trajectory of the outcome. However, soon after, this drug bounced back to relevancy with the surprising announcement by Biogen in the same year (October 2019) after a re-evaluation of its previous trials highlighting its robustness in reducing amyloid pathology. Common side effects include headache associated with amyloid-related imaging abnormalities (ARIA), especially ARIA-E in which fluid deposition occurs, leading to edema. Even though some additional side effects have been reported, including urinary tract infection, nausea, anxiety, cough and upper respiratory tract infection, it still lacks scientific consensus whether the drug has any involvement with it [4, 9-11].

Bapineuzumab

It is a type of humanized immunoglobulin, IgG1 anti-Aβ mAb that binds to the five N-terminal residues and helps in clearing both fibrillary and soluble form of Aβ. Phase 3 trials, however, did not find any significant reduction of CSF Aβ in mild to moderate AD volunteers compared to placebo controlled subjects. It also failed in efficacy scores, with ARIA-E being the notable adversity. Participants also displayed variable symptoms including headache, gastrointestinal problems and psychological confusion [8, 12, 13].

Solanezumab

It is a humanized IgG1 mAb that binds at the mid-domain of Aβ (around residues 16-26) and increases the clearance rate of monomers. Studies in transgenic PDAPP mice disclosed that the drug reduced Aβ burden without binding to the Aβ deposits, suggesting that the soluble pool of Aβ to be the target [8]. However, human trials have repeatedly failed to replicate the outcomes of pre-clinical tests, as noted in several Phase 3 studies. A series of Phase 3 trials initiated by Eli Lilly (EXPEDITION 1, 2 and 3) demonstrated no significant improvement in cognition as well as reduction of Aβ. Moreover, studies also indicate that increasing the dosage could lead to a rise in Aβ concentrations.

Gantenerumab

It is one of the first fully human IgG1 anti-Aβ mAb that binds to a conformational epitope, which is expressed on Aβ fibrils. This epitope encompasses both N-terminal (3-12) and central (18-27) amino acids of Aβ and thus requires that the peptide be folded with its mid-region near the N-terminus. In PS2APP transgenic mice, gantenerumab significantly reduced Aβ plaques by recruiting microglia and prevented new plaque formation without altering plasma Aβ levels [8]. Consistent with pre-clinical observations, Phase 3 trials have shown robust activity in human subjects. PET imaging revealed that almost 51% of the subjects with an early stage and moderate AD displayed a significant reduction in Aβ plaque when gantenerumab was administered for a period of two years [14].

Crenezumab

The drug is engineered on an IgG4 backbone in order to minimize the Fc gamma receptors activation. When tested on transgenic mice, it resulted in the reduction of Fc gamma receptor-mediated activation of microglia, which enabled a decrease in the level of release of pro-inflammatory cytokine tumor necrosis factor-alpha which is responsible for neurotoxicity. Crenezumab attacks at the mid-domain of the Aβ peptide (residues 13-24) and then binds to the multiple conformations of Aβ, i.e., monomers, oligomers, fibrils [8]. Phase 2 trials assessed the pharmacokinetics as well as evaluated the CSF Aβ levels. Although many were unable to meet their goal points, few studies did find a decrease in CSF Aβ concentration. Phase 3 trials such as CREAD 1 and 2 have also ended pre-maturely and await further evaluation [15-17].

GLUTAMATERGIC PATHWAY BASED THERAPY

Glutamate serves as the major excitatory neurotransmitter in the mammalian brain and is involved in memory as well as several executive functions. Its effect has been implicated in proper working of the synapses, neuroprotective pathways and synaptic plasticity, which includes long-term potentiation (LTP) and long-term depression (LTD). Hence, the progressive degradation of glutamatergic connections in Alzheimer's correlates with the loss of the aforementioned cognitive and executive functions. For example, the loss of hippocampal CA1 neurons in AD, an area implicated in LTP and LTD, results in dementia-like symptoms such as memory deficit in LOAD. Increased excitability of neurons is one of the salient features of glutamate dysfunction, which occurs in AD. Convincingly number of evidences have shown a strong association of Aβ with neuronal hyperactivity. Nevertheless, establishing a causal link, like Aβ toxicity, synaptic failure and the eventual collapse of the glutamatergic system, is still an ongoing pursuit. Although the role of soluble oligomeric Aβ in inducing cytotoxicity is undisputed, studies have also found an abnormality in neuronal firing around regions with localised Aβ plaques, especially the hippocampus. This hyperactive state has been correlated with the severity of mild cognitive impairment, as noted by several researchers [18-20]. These functional observations could be related to changes in cellular morphology, as seen in histopathological studies in AD, highlighting the shrinkage of the dendritic tree, axonal dystrophy, enlargement of axon terminals and decrease in dendritic branching. Interestingly, a decreased glutamatergic activity is observed in later stages of AD, which could be attributed to the loss of synaptic function and neuronal death as the disease progresses, leading to a decline in glutamate facilitated stimulation of neurons [19, 21, 22]. A study by Zott and colleagues gave a plausible insight into the perpetuation and spread of the glutamate dyshomeostasis [23]. They noted that neuronal cells with a relatively elevated baseline activity are more susceptible to Aβ mediated hyperactivity. These neurons are termed active neurons and play a key role in initiating a chain of events, which propagates the pathology to other neurons. Indeed, soluble Aβ dimers were shown to selectively disrupt the reuptake of glutamate in the synaptic cleft. Therefore increasing the membrane potential and baseline activity of the post-synaptic neuron makes it susceptible to Aβ. This model also sheds light on epilepsy like phenotype seen both in humans and animal models in early-stage AD [23]. Altered release of glutamate from pre-synaptic boutons could also be related to Aβ accumulation in its vicinity. Sokolow et al. found that Aβ accumulates within the synaptic boutons co-localised with VGluT1, a vesicular glutamate transporter, hinting at a possible interaction, which could modulate glutamate trafficking. Interestingly, downregulation of both VGluT1 and VGluT2 was observed in several in vivo experiments, but a slight upregulation of VGluT1 was seen when acute effects of Aβ were investigated in early stages. Moreover, only patients with mild cognitive impairment (MCI) displayed VGluT2 downregulation, but not VGluT1. This is suggestive of increased vesicular transport of glutamate in the early stages of AD. This is also in line with the early stage hyperactivity and late-stage hypoactivity of the glutamatergic system [21, 24, 25].

Glutamatergic pathology is also attributed to Aβ interactions with glutamate receptors. Among all the known glutamate receptor subtypes, the NMDAR family has displayed a major association with AD pathology. NMDA receptors play a vital role in learning and memory, and hence, their dysfunction leads to the eventual loss of memory and cognition in late-stage AD. NMDARs are blocked by Mg2+ ions, which get removed via subsequent depolarization, leading to the entry of Ca2+ ions and various Ca2+ mediated transductions. Overstimulation of NMDAR by the efflux of glutamate results in heavy Ca2+ influx, which causes excitotoxicity. This further induces cell-apoptotic signals and an increased reactive oxygen species (ROS) production leading to oxidative damage and neurodegeneration. Such excitotoxicity is mostly linked to extra-synaptic NMDARs, whereas synaptic NMDARs, in general, regulate neuroprotective pathways. Soluble Aβ is also shown to preferentially interact with extra-synaptic NMDARs mediating toxic signaling, mainly by interacting with specific subunit GluN2B, which also serves as a promising drug target (discussed later). Glutamate transporters play an important role in AD pathology as its gene expression is significantly suppressed. Neuropharmacalogists are also trying to find better glycine transporter-1 (GlyT1) inhibitors for additional therapeutic benefits. Aβ has been shown to cause downregulation of synaptic NMDARs while increasing the susceptibility of extra-synaptic NMDARs to glutamate (Fig. ); thus, the search for selective NMDAR drugs has remained a crucial research area to explore [21, 26].

Targeting NMDA Receptors

Among the glutamate receptor family, NMDARs are the primary drug targets because of their relatively higher permeability to Ca2+ ions as compared to other ligand-gated ionotropic receptors [27]. Although NMDAR inhibition is an effective therapy, reduced activation of NMDARs may result in a depleted amount of neuroprotective signal transduction. Hence, an ideal glutamatergic drug should have an intermediate affinity, i.e., neither it should bind too strongly disrupting the physiology, learning and memory functioning pathways, nor too weakly for any substantial therapeutic benefit. Memantine is an FDA approved non-competitive NMDAR antagonist with low affinity and has been widely used for its neuroprotective effect, providing symptomatic relief and improving cognitive impairment in patients with moderate to severe AD conditions [28]. The NMDA receptors are composed of various subunits such as GluN1, GluN2, GluN3 and GluN4 heterogeneously. These subunits are present in the receptors depending upon their function and location. Out of these, GluN2 sub-types: GluN2A and GluN2B have been the research focus for their involvement in NMDAR associated with AD. The extra-synaptic NMDARs are comprised mainly of the GluN2B subunit, while synaptic NMDARs are dominantly comprised of GluN2A. Thus, drugs that selectively target GluN2B are ideal as they can specifically act on extra-synaptic NMDA receptors alleviating the excitotoxicity without altering the neuroprotection pathways associated with synaptic NMDARs. Drugs such as ifenprodil, which selectively binds to GluN2B has been experimentally shown to reduce Ca2+ mediated neurotoxicity [29, 30]. These demonstrations have provided incentives for developing a more efficacious drug than the already available memantine.

Targeting Glutamate Transport Channel

The regulation of extra-synaptic glutamate levels is done by excitatory amino acid transport channels (EAATs) which can be found on various glia and neuronal cells, of which the role of astrocytic EAATs is crucial as they comprise 90-95% of the total EAATs in the brain and recycle the majority of glutamate neurotransmitters. In comparison, the amount of neuronal EAATs expressed is relatively low. Excess levels of glutamate are recycled back into glutamine by a process known as a glutamate-glutamine shuttle. Among the five existing subtypes of EAATs, EAAT-2 or glutamate transporter-1 (GLT-1) is predominant and recycles, almost 90% of glutamate [31]. Several studies have reported a marked decrease in GLT-1 expression in AD patients, which has been associated with a decline in cognitive output, as seen with GLT-1 knocked-out mice. In vitro experiments suggest that Aβ might be a causative factor in GLT-1 decline and negatively affect its expression in astrocytes [32-35]. This downregulation of EAATs has been implicated with additional anomalies besides impaired glutamate clearance. Sharma et al. demonstrated alterations in several signaling and metabolic pathways in both neuronal as well as astrocytic EAAT-2 knockout mice [36]. Loss of astrocytic EAAT-2 displayed cognitive as well as spatial memory defect, which is consistent with previous observations. However, neuronal EAAT-2 deletion also displayed late-onset cognitive impairment giving further incentives to look into its role in AD pathogenesis. The transcriptomic analysis also showed that gene expression profile varies between astrocytic and neuronal EAAT-2 knock-outs, with inflammatory and kynurenine pathways (a metabolic pathway associated with tryptophan breakdown and NAD+ production) being disrupted the most among them, respectively. Overall, the deletion of EAAT-2 in the hippocampal region mimics the age-dependent cognitive decline in AD. Such functionality could be regained to an extent when the EAAT-2 expression is restored [36, 37]. Thus, various therapeutic strategies have focused on GLT-1 upregulation, which can be done by targeting its transcription. For instance, beta-lactam antibiotic such as LDN/OSU-0212320, a pyridazine derivative which activates protein kinase C, has been shown to increase GLT-1 gene expression, as well as translation [38, 39]. Such GLT-1 modulating drugs have been used in various other diseases and the current focus has shifted to repurposing their action for the treatment of AD. Riluzole, a drug used to treat ALS, has given positive results when used for AD in pre-clinical trials, having increased glutamate transport, and improved cognition in mice and also downregulated various gene expressions thought to play a role in AD [39].

Targeting Glycine Transporters

Glycine is a co-agonist of NMDARs. Therefore, activation of hyperactive NMDARs can be modulated by altering the level of glycine. This can be achieved by blocking the Glycine transporters present on astrocytic glia and pre-synaptic neurons. GlyT1 has gained attraction because of its close association with NMDA expressing neurons. Glycine transport inhibitor such as sarcosine has been used in the past to treat schizophrenia symptoms, hence, repurposing these drugs for AD might reveal some therapeutic benefit [40]. ASP2535, a GlyT1 inhibitor, was shown to alleviate cognitive impairment in schizophrenia and AD mouse models [41]. Another GlyT1 inhibitor, BI 425809, has entered in Phase-1 trials for AD and is currently being investigated for more therapeutic relief [42].

ANTI-TAU BASED THERAPY

Tau based pathology has been well known and studied since early attempts over the elucidation of AD took place. Tau is a protein that normally binds to microtubule and confers stability to it, which is essential for proper cytoskeletal functioning and cellular trafficking. Tauopathies, which are common in multiple neurodegenerative diseases, result from the formation of intracellular neurofibrillary tangles (NFTs). These are a result of multiple post-translational changes such as hyper-phosphorylation, acetylation, N-glycosylation and C-terminal truncation. Phosphorylated tau has notably been the earliest sign of pathogenesis, which hinders its interaction with tubulin as well as facilitates its relocalization and aggregation. This correlates with the elevation in the levels of tau kinases, such as glycogen synthase kinase - 3β (GSK-3β) or CDK5 in several AD brain samples and serves as a promising site for therapy (discussed later). NFTs are one of the major hallmarks of AD besides Aβ plaques and marks the earliest sign of pathology by its deposition in the entorhinal cortex and hippocampus. The formation of NFT takes place in a series of steps, and results in multiple intermediary fragments, such as pre-tangles, tau oligomers, paired helical filaments, etc., just like Aβ plaques. However, unlike Aβ burden, tau load shows a better correlation to cognitive decline making it an appealing target [43].

Tau, is a major type of microtubule associated proteins (MAPs) which has six isoforms coded by a single gene via alternative splicing. These isoforms are distributed heterogenously throughout the brain and differ in amino acid repeats at the N-terminal coded by different exons. Few studies have suggested that these tau isoforms could have a diverse range of functions in addition to cytoskeletal stabilization such as regulation of synaptic vesicles, nuclear localization, chromatin remodeling, etc. This suggests that tau pathology is not simply a defect in cellular trafficking and there may be other existing pathways, which confer its pathogenesis and symptoms associated with it. It is also known that AD contains a specific mix of tau isoforms (3-repeats and 4-repeats), which separates it from other tau pathologies such as Pick disease. Thus, anti-tau strategies have evolved over time with the knowledge about their underlying mechanisms getting continuously updated [43, 44].

Targeting Tau-phosphorylating Kinases

The involvement of multiple tau phosphorylating kinases has complicated the search for an effective therapeutic target. It is yet to be established if any specific kinase has a major role in tau pathology or whether targeting multiple such kinases would be an appropriate approach. Researchers have identified promising candidates such as GSK-3β, MARK, Fyn and CDK5 in this context [45]. Targeting GSK-3β has yielded positive results encouraging further trials. Tideglusib, a GSK-3β inhibitor, specially reduced tau phosphorylation and showed symptomatic benefits in transgenic mice in vivo [46]. Drugs such as tadalafil, morin, etc. have also been shown to reduce GSK-3β induced tau phosphorylation [47, 48]. Saracatinib, a Fyn kinase inhibitor, has also provided similar alleviations [49].

Targeting Tau Post-translation Modifications

The formation of NFTs also involves the addition of several compounds to tau besides phosphorylation. Acetylation of lysine group in tau has been shown to facilitate its aggregation. Thus, targeting these acetylation enzymes has been proposed as another potential therapy in tau based pathologies [50]. Salsalate, a drug used for the treatment of rheumatoid arthritis, decreased tau aggregates, improved dementia symptoms and reduced shrinkage in the hippocampal region, which can be attributed to its inhibitory effect on the acetyltransferase p300 enzyme [51]. Additionally, targeting other modifications such as tau glycosylation is also an active area of research. It has been proposed that drug action on enzyme O-GlcNAcase (OGA) that reversibly cleave the β-glycosidic O-linkage with carbohydrate N-acetyl glucosamine (GlcNAc), can positively affect tau aggregates and phosphorylation [52]. In fact, OGA inhibitors such as MK-8719 and ASN120290 have shown relief for non-AD tauopathies such as progressive supranuclear palsy (PSP) and few have even entered the Phase-1 trials for further evaluation [53].

Tau-focused Immunotherapy

Antibody-mediated immunotherapy has proven advantageous over other therapeutics, mainly for their specificity towards the toxic species while preserving the normal functioning of tau and its associated enzymes. These antibodies preemptively target tau phosphorylation sites, aggregation epitopes as well as toxic assemblies. The efficacy of these antibodies depends on their endocytosis by the cells, which then directs it to tau aggregates leading to the eventual degradation of the tau-antibody complex by lysosomal mediated autophagy. Two different strategies are employed in tau immunotherapy, namely active and passive immunization. The active vaccine approach uses a self-generated antibody via stimulation of the host's immune system. Although convenient and long-lasting, it is prone to auto-immune damage due to its low specificity. In contrast, passive immunization using monoclonal antibodies has fared better in terms of sheer efficacy and specificity. A study by Carranza and his team displayed a significant reduction of toxic oligomeric tau species in Htau mice after the long term administration of tau oligomer-specific mouse monoclonal antibody (TOMA) [54]. These oligomeric tau aggregates correlate better with cognitive decline than NFTs and have been accepted as a suitable biomarker for tauopathy [54, 55].

Tau-based immunotherapeutics are relatively new, and it is worth noting that most of the ameliorating effects described have only been observed in pre-clinical models. Translating these studies in human trials face a long road ahead. Although with the advent of novel techniques, few drugs did manage to enter Phase I and Phase II trials [55].

ACI-35

It is an active vaccine consisting of 16-mer peptide and is administered via liposomal packaging. It contains tau residue at 393-408 and is phosphorylated at two sites on Ser396 and Ser404. In vivo trials with transgenic mice models, C57BL/6 and P301L resulted in IgG with high specificity towards the phosphorylated tau compared to physiologically normal tau; however, the effect of Ser404p tau was not significant, unlike Ser396p. Studies also highlighted the absence of glial scars and pro-inflammatory markers. It entered a Phase 1b trial in 2015 with the objective of testing its efficacy against mild to moderate AD patients [56, 57]. (Clinical Trial Identifier: ISRCTN13033912).

AADvac-1

It is a synthetic peptide derived from tau residues 294–305, which got its epitope selected using the target site of DC8E8 monoclonal antibody. It is an active vaccine, which yielded positive results with a significant reduction of tau aggregates in pre-clinical trials. Phase-1 trials with an alum-adjuvanted vaccine displayed IgG1 in 29 out of 30 patients. An ongoing Phase 2 study is also currently in progress with mild AD patients [43] (Clinical Trial Identifier: NCT02579252).

BMS-986168

This passive immunization therapy uses a stem cell-derived IgG4 monoclonal antibody. It targets the 9-18 amino acid portion of e-tau fragments (end-terminal fragments) obtained from familial AD patients. Preclinical studies reported a decreased Aβ40 as well as interstitial tau species. Four clinical trials with BMS-986168 have been initiated since 2014. A multiple-ascending-dose Phase 1b trial with 48 patients having PSP yielded a significant decrease in CSF e-tau and showed good tolerability [58]. Biogen also initiated a randomized parallel-group Phase 2 trial with 654 patients displaying MCI, which is expected to run till the year 2024 (Clinical Trial Identifier: NCT03352557).

RG7345

It is a humanized monoclonal antibody, which shows specificity for phosphorylated tau at site Ser422, which is implicated in tau relocation towards the somatodendritic region. An experiment conducted in transgenic TauPS2APP mice showed a reduction of phosphorylated tau [59]. In 2015, it entered a Phase 1 trial with 48 healthy participants for the assessment of its pharmacokinetics. However, the study was later discontinued for unknown reasons. (Clinical Trial Identifier: NCT02281786).

C2N-8E12

This humanized IgG4 antibody targets the tau protein at a 25-30 amino-acid site. In vitro studies displayed a reduced misfolding and propagation of tau aggregates when this antibody was administered [60]. In vivo studies by Yanamandra et al. also found positive results, with improved motor functions, reduction of pathogenic tau and lowered brain degeneration [61]. It entered Phase 1 trials in 2015 with a single-ascending dose test conducted on 30 PSP subjects, with results labelling it safe; however, the tolerability limit was not determined [43]. A Phase 2 trial has also been initiated in 2016 with more than 400 early-stage AD participants for assessment based on several cognitive parameters. (Clinical Trial Identifier: NCT02880956).

LY3303560

Also known as Zagotenemab, this monoclonal antibody preferentially binds to tau clusters compared to monomers, possibly via its interaction with a conformational epitope region. Two Phase 1 trials were initiated on MCI patients by Eli Lilly in 2016 and 2017, respectively, with the goal of CSF antibody level assessment and evaluation of the safety and pharmacokinetics of the drug. A Phase 2 trial has also been initiated in 2018, with 285 participants displaying a progressive decline in cognition for a minimum duration of six months [43]. (Clinical Trial Identifier: NCT03518073).

UCB0107

Developed by UCB Biopharma, this monoclonal antibody targets 235–246 amino acid sites, which falls in the mid-segment of tau aggregates. Studies have implied that targeting the N-terminal segment of tau may result in non-specific binding to degenerated tau fragments, which could hinder clearance and tau seeding. In 2018, UCB0107 entered Phase 1 trials with the aim of testing the efficacy and safety of single ascending doses in healthy male volunteers [43, 62]. (Clinical Trials Identifier: NCT03464227).

RO 7105705

It is a monoclonal IgG4 antibody, which possibly interacts with the Ser409 phosphorylation site. Its research is sponsored jointly by AC Immune and Genentech and it is reported to bind N-terminals of all the conformers of tau, including monomers and oligomers. It entered Phase 1 trials in 2016, which compared the dosage effects on mild to moderate AD subjects with placebo controls. (Clinical Trials Identifier: NCT02820896). A Phase 2 trial also started in February 2019, screening its efficacy on moderate AD patients and is expected to be completed by June 2023 [43, 63] (Clinical Trials Identifier: NCT03828747).

JNJ-63733657

This humanized monoclonal antibody shares a similar mechanism with UCB0107, targeting the mid-region of tau aggregates and removes tau spread and seeding. It entered Phase 1, in 2017, testing its tolerability and efficacy in 64 patients with AD phenotype and healthy subjects [43] (Clinical Trials Identifier: NCT03375697).

NEUROPROTECTION BASED THERAPY

This type of therapy is aimed at potentiating the intrinsic pro-survival signaling that prevents the cells from all kinds of degenerative cascades, making the cells less vulnerable to accumulating damages. With respect to AD, it includes targeting as well as reversing the destructive effects of Aβ, NFT, inflammation, etc. and restoring synaptic plasticity, inhibiting the pro-apoptotic signals, preventing the excitotoxic effects of Ca2+ ion dyshomeostasis, etc. The main highlights that shall be covered here are neurotrophin (NT) receptors that regulate various pro-survival and pro-apoptotic pathways. It uses a wide array of ligands belonging to NT families such as brain-derived neurotrophic factors (BDNFs), nerve growth factors (NGFs), neurotrophin-3 (NT-3), etc. which bind to one of the two types of NT receptors, namely, tyrosine kinase receptors (Trks) and p75 neurotrophin receptors (p75NTR). The same NT family can co-activate both of these types of receptors; however, different isoforms of Trk get activated by only certain NTs, an example being TrkB having the ligand BDNF.

It is plausible that Aβ binds to these neurotropic receptors and initiate cascading events leading to cell death. Inhibiting such interactions by blocking these receptors without disrupting the normal physiology is challenging. However, recent clinical trials have yielded promising results.

p75NTR Based Therapy

The receptor p75NTR is activated differentially by a wide variety of NT molecules, which results in the activation of multiple downstream pathways such as c-Jun N-terminal kinases (JNKs), caspase, etc., leading to either pro-survival signals such as synaptic stability, or degenerative signals such as synaptic pruning. In AD, the degenerative signaling becomes dominant as the p75NTR levels rise and the activating molecules such as pro-NGF levels also increase, which explain the early degeneration of p75 expressing cells [64-67]. The therapy is thus focused on shifting the balance from degenerative to pro-survival signaling. The use of p75 antagonists in pre-clinical trials has proven efficacious and is supported by the experiments where transgenic mice lacking p75 receptors showed a reduction of Aβ induced degeneration [68-70]. Two key drugs, namely LM11A-24 and LM11A-31, have been shown to increase cognition and decrease NFT levels leading to a reduction in the degeneration of cholinergic neurons of the basal forebrain. This positively affected Aβ induced degeneration as well as Aβ induced tau phosphorylation and minimized the Aβ induced CREB and AKT inhibition, which is vital for proper synaptic function [71] (Fig. ). Targeting p75 for anti-tau therapy also has an added benefit as it affects the action of multiple tau phosphorylating kinases without directly inhibiting them and disrupting their normal function [72].

Trk Based Therapy

Trk receptor family includes TrkA, TrkB and TrkC, which are differentially expressed in multiple brain regions such as the entorhinal cortex, hippocampus, basal forebrain, etc. They are activated by different families of NTs. TrkB and TrkC play important roles in various survival pathways, including synapse stabilisation, synapse function, plasticity, LTP, etc. It has been observed that natural agonists of these receptors, such as BDNF (TrkB agonist), progressively decline in the ageing brain and neurodegenerative disorders such as AD. Reduced signaling of these molecules has been associated with major hallmarks of AD, such as Aβ aggregation, NFTs, etc [73-75]. This has invoked attempts to increase the levels of BDNF in patients; however, its low BBB permeability and poor stability have made it a challenging task for researchers [76]. Adopting different diets and physical exercise have shown to positively influence BDNF levels. However, the cognitive benefits imparted by these measures are still under question. Interestingly, a study demonstrated that enhancing BDNF levels in mouse models via exercise is effective in combination with induced neurogenesis in the adult hippocampus [77-81]. Therefore drugs that act as a direct agonists to Trk receptors such as 7, 8-DHF and LM22A-4, which can simulate BDNF effects, have caught the attention of researchers. LM22A-4 has shown similar neuroprotective effects, such as activating synapse functioning pathways (AKT and CREB) [82, 83]. Targeting TrkA receptors, on the other hand, imparts neuroprotection to the cholinergic cell population in the basal forebrain [84]. TrkA ligands such as D3, positively affect the AKT signaling in the hippocampus region, reduced Aβ levels and show improvement in short-term memory [85]. Another TrkA agonist MT2 also is reported to increase cell survival and reduction in amyloid genesis [86].

Modulating the JNK Pathway

JNKs are a family of protein kinases, which activated during stress signals and involved with plasticity, cell apoptosis, senescence, etc. Studies suggest that Aβ aggregates may activate this pathway, especially the JNK3, which results in early degeneration of neuronal cells via activation of apoptotic signals. Its role in generating NFTs via tau phosphorylation has also been suggested [87-89]. Thus, potential therapies include inhibition of Aβ activated JNK downstream signaling. JNK inhibitors such as bentamapimod, tanzisertib, D-JNKi1, etc., have been previously used for non-AD diseases, but are now underway for getting repurposed to see the effect on AD patients [90]. Moreover, experimental data on JNK inhibitors have shown promising results for AD in pre-clinical models. Novel drugs such as CEP-1347 and SP600125 have improved cognition in mouse models as well as lowered Aβ induced cell degeneration [91-93].

CHOLINERGIC NEUROTRANSMISSION BASED THERAPY

Acetylcholinesterase (AChE) is a type of serine hydrolase found at the neuromuscular junctions and also at the cholinergic synapses in the brain. The biological role played by it is in the termination of impulse transmission at cholinergic synapses followed by rapid hydrolysis of the neurotransmitter acetylcholine (ACh) to acetate and choline. In the mammalian brain, the majority of AChE occurs as a tetrameric G4 form, while a marginal quantity exists as the monomeric G1 form [94].

Targeting Acetylcholinesterase

Anti-cholinesterases are a class of drugs that inhibit cholinesterase enzyme from breaking down ACh and this leads to an increase, both in the level and duration of the neurotransmitter action. According to the mode of its action, AChE inhibitors are divided into two groups: irreversible and reversible. Reversible inhibitors, whether competitive or non-competitive, have therapeutic applications, while toxic effects have been associated with irreversible AChE activity modulators. Irreversible inhibitors of AChE are known to result in convulsions, muscular paralysis, bronchial constriction and even death by asphyxiation. Inhibition of AChE activity helps in maintaining the ACh level by decreasing ACh breakdown rate. Therefore, they help in boosting up the cholinergic neurotransmission in regions of the forebrain, which compensates the loss of functioning neurons [94].

Donepezil

It is a selective and reversible AChE inhibitor that functions after binding to the peripheral anionic site. It shows both symptomatic and causative effects in the treatment of AD, possibly by modulating Aβ levels, as seen in animal studies [95]. It is an approved treatment for Alzheimer’s and is used to treat mild to moderate form of AD. Donepezil also improves cognitive function in patients with severe AD symptoms. The drug is found in both the forms of tablet and oral solution that easily cross the blood-brain barrier with a slow rate of excretion. It has a half-life of about 70 hours, so it is prescribed to take it once a day. Tablets are available in 5 and 10 mg dose strengths and the maximum dose is 23 mg per day. Adverse effects include gastrointestinal problems, as well as an increase in cardiac vagal tone, causing bradycardia [94].

Rivastigmine

It is a powerful and low-reversible carbamate inhibitor that functions by blocking the cholinesterase activity after binding to esteratic part of the active site. It has been introduced in Phase 3 clinical trials under the support of Novartis Pharma [2]. Rivastigmine inhibits both BuChE (Butyrylcholinesterase) and AChE, unlike donepezil. It is used for the treatment of mild-to-moderate forms of AD. The drug can be administered orally in the form of capsules and liquid, providing a good absorption with the bioavailability of 40% in the 3 mg dose. It gets eliminated easily through urine and shows few drug-to-drug interactions. Treatment with rivastigmine has beneficial effects in the treatment of AD but has also been shown to negatively impact cognitive function. Side effects prevail with the cholinergic actions of the drug that include nausea, vomiting, diarrhea, anorexia, headache, syncope, abdominal pain and dizziness [94].

Galantamine

It is an alkaloid that is isolated from the plant Galanthus woronowii. It is a selective, competitive as well as rapidly reversible inhibitor of AChE that interacts with the anionic subsite and the aromatic gorge. Galantamine also induces modulation because it is an allosteric ligand at nicotinic cholinergic receptors. Cognitive impairment in Alzheimer’s correlates with loss of nicotinic receptors and this particular effect appears to be a positive point for the treatment. Absorption of galantamine is rapid, with oral bioavailability lying between 80 and 100% and with seven hours half-life. Treatment is initiated with a 4mg dose twice in a day, which is increased gradually. Side-effects include severe gastrointestinal symptoms [94].

Tacrine

It is an aminocridine that specifically interacts with the subtypes of muscarinic and nicotinic receptors. It shows a reversible activity and gets easily absorbed. It gets cleared by the liver during the metabolic process but with low bioavailability of 2% to 3% when administered orally. Multiple doses of tacrine increase its half-life from 1.4 to 3.6 hours. Patients who were on the effective dosage of the drug showed elevated alanine aminotransferase (ALT) than the upper limit [2].

Metrifonate

It carries an irreversible activity, which leads to an increase in its bioavailability in the CNS. It has reached Phase 3 clinical trials for further evaluation. Its mechanism of action relies on its hydrolysis product 2, 2 - dimethyl dichlorovinyl phosphate (DDVP), which binds to the catalytic sites of the enzyme for AChE inhibition. It evades the cytochrome P50 system in plasma and gets absorbed and distributed in the brain rapidly [2].

USE OF ANTI-INFLAMMATORY DRUGS FOR ALZHEIMER’S DISEASE

Altered inflammatory response leading to neurodegeneration has long been studied in AD and their cross-talk with the glial cells has been well implicated in its pathogenesis. Studies have reported elevated levels of cytokines such as TNFα in the AD brain compared to healthy controls, which might downstream a cascade of disruptions in brain metabolism. It is still debatable whether this anomaly is an effect or a cause leading to AD. Epidemiological data suggest that the majority of AD cases are not familial but sporadic in nature and this has prompted researchers to undertake rigorous genetic screening for identifying the risk genes and associated variants. Several studies have demonstrated that certain GWAS genes such as TREM2, CLU, EPHA1, CR1, ABCA7 that are expressed in microglia are highly upregulated in AD condition, which again suggests a strong link to neuro-inflammation. Triggering receptor expressed on myeloid cells 2 (TREM-2) is strongly associated with AD and is possibly a hub gene, regulating a network of other downstream processes. This is supported by the fact that mutations in it, confer a significant risk almost comparable to the widely known APOE ε4 allele. In congruence with this, a study by Sierksma et al. demonstrated the altered microglial expression of a few genes (PC2, TREML2, SYK, GRN, SLC2A5, etc.) in response to Aβ interaction and hinted that their effects may be additive which explains their low genome-wide significance. Thus, it is important to understand the function and downstream regulation of these genes, which could add to the arsenal of effective therapeutics against AD [96, 97].

The role of microglia is quintessential, from clearing the local debris to mediating brain immune response. Generally, microglia stay in a quiescent stage and probe the brain for pathogens and cell debris. Once such an encounter happens, it induces a transition in its morphology, leading to activated microglia state. Although not in consensus, it is believed that in the active state, microglia can adopt a differential characteristic, either taking part in anti-inflammatory (M2) or pro-inflammatory (M1) signaling. M2 state of microglia is neuroprotective in nature, secreting a number of growth factors such as glial-derived neurotrophic factors (GDNF), BDNF and nerve growth factors. In juxtaposition to this, M1 state releases inflammatory mediators as well as free radicals such as ROS, which can cause a number of insults to the surrounding brain region. In AD, Aβ has been shown to interact with microglia and take part in its activation, exacerbating the inflammatory response [98].

Based on the aforementioned role of neuroinflammation in AD, researchers have explored the role of anti-inflammatory drugs as a potential treatment option. Several classes of non-steroidal anti-inflammatory drugs (NSAIDs) have been designed and have garnered attention for their dual role in functioning as GSMs. In vivo experiments have shown that NSAIDs could repress glial activation and cytokine-induced neuroinflammation. Ibuprofen is a well-known NSAID which decreased Aβ plaques and repressed glial activation in animal studies. However, recent meta-analysis questioned its efficacy for its lack of any significant association to cognitive benefit in humans. Other related NSAIDs such as Tarenflurbil and Celecoxib have undergone Phase 3 trials; however, results have mostly been negative. Apart from NSAIDs, glucocorticoids have also been investigated for their anti-inflammatory properties. In vitro and in vivo studies displayed lowered NOS production from microglia as well as decreased Aβ concentration. This, however, failed to show significant benefits in human trials, just like NSAIDs. These studies indicate that there is much room for improvement for anti-inflammatory therapy especially with evidences piling up indicating the role of microglial genes in AD pathophysiology [98-100].

NUTRACEUTICALS AND DIETARY INTERVEN-TIONS

Although the therapeutic potential of the discussed drugs in clinical and pre-clinical trials is undisputed, their benefits are not without complications and drawbacks. For instance, most of the tested histone acetylase inhibitor compounds carry toxic side-effects [101]. Hence, the current paradigm shift towards the natural products and their derivatives has driven a multitude of researches to analyse their efficacy on patients (Table ). These natural compounds are well tolerated with minimal or no side effects. They are easily obtainable and have good bioavailability. Due to their important therapeutic roles, it is quintessential to take nutrition into account during the dietary supplementation in pre-clinical as well as clinical studies as it can lead to inconsistency in results. Individual dietary patterns differ from individual to individual and have given incentives to reconsider previously done epidemiological studies without nutrition adjusted controls.

Resveratrol

It is a polyphenolic compound that is commonly extracted from grapes, blueberries, peanuts, etc. It is a phytoalexin in nature, i.e., it is released in response to pathogens that infect them. Known for its antioxidant properties, it has been the focus of many researchers for its ameliorating effect on cancer, cardiovascular diseases and neurodegenerative diseases such as AD. Recent studies have highlighted its effect on the upregulation of SIRT1, a member of sirtuin proteins, which plays an important role in ageing and vitality. SIRT1 signals various neuroprotective pathways that aid in Aβ clearance and aggregation, ROS scavenging, and facilitation of synaptic plasticity involved in learning, memory and autophagy induction [102-104]. This has been supported by various in vivo and in vitro trials, such as the one carried out by Zhao et al., where it was shown that resveratrol fed rats had a marked reduction in Aβ1-42 level in the hippocampus [105]. Another study showed a reduction in microglial inflammation using a resveratrol diet, which plays an important part in ROS induced degenerative cascade [106].

Curcumin

Curcumin belongs to a family of compounds known as polyphenolic curcuminoids. This natural, yellowish chemical is extracted from Curcuma longa tubers and has been widely used in various industrial sectors, ranging from cosmetics to the food industry for its anti-oxidant and anti-inflammatory properties. Its effect in in vitro and in vivo experiments have shown that it is a strong candidate against AD, following its inhibition of AchE and Beta-secretase 1 (BACE1) [107]. It also works against Aβ oligomerization, possibly via the inhibition of PSEN1 activation [108]. This candidate, however, needs further investigation due to it being less stable and with low bioavailability [109].

Vitamin B

Vitamin B plays an important role in the homocysteine-methionine cycle, which includes the generation of S-adenosylmethionine, a key substrate for the methylation of DNA [110, 111]. DNA methylation epigenetically regulates gene expression, which is relevant because epidemiological studies have linked AD patients with less methylated DNA, leading to over-expression of AD-related genes [112]. Among vitamin B family, vitamin B6, B9 and B12 supplementation have especially been shown with ameliorative properties [113, 114]. However, contrary results have also been shown, in that the intake of only vitamin B is not very efficient in reducing dementia-like symptoms [115]. Even though conflicting data is there, this does not undermine the therapeutic potential of vitamin B supplementation in AD as further validations are still under process.

Other Vitamins

Although not strongly correlated, vitamin C, D and E also have gained traction following epidemiological studies [116]. Vitamin D has been reported to be low in AD patients and linked with dementia and cognitive deficiency. Its role has been implicated in amyloid plaque clearance, anti-inflammation, reducing oxidative stress and offering neuroprotection mediated by vitamin D receptors (VDR) [117]. Vitamin E, like others, has also been reported to have low CSF concentration in AD patients. Its therapeutic potential has been recognised for its anti-oxidative role, having shown reduced ROS induced damage in animal models [118]. Vitamin C, on the other hand, has been reported for its epigenetic regulation of AD-related genes and ROS scavenging property [119].

Genistein

Genistein belongs to the isoflavone group. It is a dietary component rich in plants belonging to the Leguminosae family. It has been the research focus for its protective role in cancer, cardiomyopathies as well as neurological diseases [120, 121]. The most interesting aspect of genistein is its similarity to estrogen through which it imbibes its neuroprotective effects. Estrogen rapidly declines in women after the menopause. This has been correlated with higher than average AD cases in post-menopausal women when compared to men. This has also been supported by symptomatic relief brought about by estrogen therapy in AD patients. However, the results are not without its harmful side-effects, and in some cases, have also been oncogenic in nature [122, 123]. Hence, genistein, with its low side-effects, could serve as a potential alternative and even act as a selective agonist to estrogen receptors specifically located in the hippocampal region involved in learning and memory [124]. Genistein has also been shown to reduce Aβ generation and Aβ induced toxicity via modulating the protein kinase C pathway (PKC) and downregulating β-secretase activity [125].

Calorie Restriction Diet

Changing dietary regimes could have a profound effect in combating various degenerative diseases. Calorie restricted (CR) diet has long been shown to slow down the effects of ageing and Alzheimer's in animal models as well as humans. A reduction of 20-40% in daily calorie intake, which includes decreasing the amount of proteins, carbohydrates and fats (without undernourishment due to lack of essential micronutrients), has resulted in a multitude of benefits. In some cases, it increased the lifespan of rats up to 30% and also improved insulin resistance [126]. In AD mouse models,

CONCLUSION

The past decade has seen a multitude of attempts to push forward the seemingly stagnant status quo in Alzheimer's disease research. While pinpointing the exact aetiology of the disease is important, it is still conceivable to plan interventions based on our limited understanding of AD. Still, we do not know much about the perinatal conditions [130] that can aggravate or program the body of an individual to develop neurodegenerative disorders later in life [131]. AD is multifactorial in nature and raises the question of the feasibility of finding a miraculous all-curing drug. This has led to an array of prophylactic measures, targeting numerous aspects of AD at its various stages of severity (Table ). Such measures include glutamatergic approaches tackling the excitotoxicity, anti-amyloid and anti-tau based medications acting on extracellular and intracellular aggregates, respectively. Further, cholinergic based approaches that reduce the degradation of cholinergic neurons have also been tested. Techniques that enhance neuroprotective signaling and anti-inflammatory medications also have been shown to be promising (Table ). While these pharmacological approaches have undeniable benefits, alternative means of treatment such as nutraceuticals and lifestyle changes resulting in epigenomic maintenance [132] have also grasped attention for their relatively lower side-effects (Table ). How efficacious these measures are and whether they are limited to symptomatic relief is yet an open-ended question that needs rigorous clinical and pre-clinical trials to unveil any meaningful answer.

It is worth pointing out that mitigating AD induced damage via pharmacological interventions relies heavily on its early detection. As yet, no biological marker for AD has been approved for clinical diagnosis. A plethora of molecular and imaging tools have spurted out in recent years, which could gauge the subtle changes that occur years before the onset of this disease. These methods, however, are still in their preliminary stage and their reliability is still under verification. It is known that the two major hallmarks of AD, viz, amyloidosis and tauopathy precede the behavioral identifiers by many decades, such as MCI. The screening methods usually employed include CSF assessment and PET imaging techniques. These diagnostic tools are considered as the gold standard for affirming the AD pathology in both asymptomatic as well as MCI patients. However, their exorbitant cost and invasiveness have incentivized researchers to look for other novel techniques, which could effectively identify diagnostic markers unique to neurodegeneration. Screening plasma-based biomarkers are relatively easy, takes less time and is a lot less invasive. A recent plasma-based amyloid-assay has already shown some efficacy in amyloidosis assessment years before the onset of symptoms. Identifying tau based biomarkers, on the other hand, has been challenging as tauopathy is not unique to AD, as previously discussed. Notwithstanding, a tau fragment, which is phosphorylated at 181 residues (P-tau181), has shown to reliably predict the onset AD [133]. Aside from its robust diagnostic features, recent studies have also validated it as a good prognostic marker, with higher P-tau181 levels correlating effectively with the risk of developing dementia [133, 134]. Thus, plasma-based biomarkers could be a turning point in AD therapeutics even at the prodromal stage [135]. There is one major caveat, however. Neurodegeneration often precedes cognitive deficit and it would appear counter-intuitive for the population to undergo screening for AD detection before the onset of any symptoms. Perhaps, assessment of individual genetic risk profile combined with a routine check-up for approved markers in the future could offer a solution. The experiments in the drug discovery endeavors and further refining the strategies of contemporary and conventional diagnosis would help. Additionally, changes in strategies involved in drug designing, understanding the disease pathways and drug targets would also contribute to finding a possible cure for AD.

Table 1

List of emerging nutraceutical compounds for treatment of Alzheimer's disease.

Nutraceutical Compounds	Type/Effect	Mechanism of action	Model Used/Mode of Study	Source	Refs.
Curcumin(curcuminoid)	Neuroprotective; Reduced Aβ oligomerization and aggregation; Reduction of Tau phosphorylation;Reduced ROS induced damage	BACE1 inhibition; AchE inhibition	-	Curcuma longa plant	[136]
Resveratol(Stilbenoid)	Anti-oxidant; Neuroprotective; reduced Aβ plaques	SIRT1 activation; AMP-phosphokinase pathway activation	Tg19959 mice	Grapes, peanuts, blueberries, red wine etc.	[137, 138]
Quercetin(Flavonol)	Reduced Aβ induced toxicity; Anti-taupathic; Improved Long-term and spatial memory	Modulates pro-apoptotic signaling and increases cell survival	3xTg-AD mice	Ubiquitous among a variety fruits and vegetables such as onions, berries etc.	[139]
Dihydromyricetin (DHM)/ Ampelopsin (AMP) (flavanol)	Anti-inflammatory; Improved learning skills	Modulates AMPK/SIRT1 signaling	Sprague Dawley (SD) male rats	Found majorly in Ampelopsis plants	[140]
Catechin(flavanol)	Anti-oxidative; Anti-inflammatory	Free radical scavenging; Metal ion chelation	Clinical trials (Longitudinal)	Green tea	[141]
Taurin	Reduced Aβ induced toxicity; Improved cognitive skills	Binds to oligomeric Aβ	C57Bl/6 mice	Animal products such as meat and dairy	[142]
Anthocyanin	Suppressed Aβ1–42 cytotoxicity	Inhibition of co-chaperonin GroES fibrills	Neuro2a cells (in vitro)	Bilberry (Vaccinium myrtillus anthocyanoside (VMA))	[143]
Tannic Acid	Reduced β-amyloid oligomer deposits; Enhanced cognition	Inhibition of β-secretase function	PSAPP mouse	Flowering Plant sources such as Rhus semialata	[144]
Arjunolic Acid	Neuroprotection	Anti-cholinesterasic (AChE and BuChE) activity	-	Combretum leprosum roots	[145, 146]
Ferulic Acid(hydroxycinnamic acid)	Anti-β-Amyloid effect	β-secretase modulator	PSAPP mice (in vivo) and N2a cell line (in vitro)	Ubiquitous among a variety of plant cell walls, such as flax seeds, barley etc.	[147]
Genistein	Anti-β-Amyloid effect	Inhibits ubiquilin 1 which downregulates presenilin 1 expression	Daudi, Jurkat, U937 andK562 cell lines	Leguminous plants; soybean products	[148]
Mangiferin	Reduced NFT aggregates; anti-inflammatory; improved episodic and spatial memory	-	APP/PS1 mice	Mangifera indica	[149]

Table 2

List of different therapeutic drugs for combating Alzheimer's disease.

S. No.	Name of Drug		Action of Drug	Clinical Status			Models	Effects		Refs.
1.	CPC-201 (Donepezil + Solifenacin)		Acetylcholine-neurotransmitter based	Phase 2			Patients with AD type dementia	Cholinergic signaling is improved		[150]
2.	Galantamine		Anti-cholinesterase,Allosteric modulator of nAChRs	FDA approved			Patients with dementia related to cerebrovascular disease	Prevent and slow down the symptoms		[151]
3.	Bisnorcymserine		Anti-Butyrylcholinesterase, amyloid protein precursor inhibitor	Phase 1			AD patients above 55 years of age	Neurotransmission of acetylcholine		[152]
4.	TRx0237(LMTX)		Anti-tau	Phase 3			Patients with mild form of AD up to 89 years of age	Inhibits misfolded tau protein aggregation		[153]
5.	NP001		Anti-inflammatory	Phase 1			Neuroinflammation in mild to moderate form of AD patients	Activates the immune system		[154]
6.	Solanezumab		Anti-amyloid	Phase 3			Mild dementia in patients due to AD	Slow down cognitive decline and decrease fibrillary plaques		[155]
7.	BAN2401		Anti-amyloid immunotherapy	Phase 3			Transgenic mouse models	Reduction amyloid beta protofibrils, cognitive decline and APOE4		[156]
8.	Candesartan		Neuroprotective, glial cell functions	FDA approved			Spontaneous hypertensive rats	Targets on vascular functioning, angiotensin II type 1 receptor blocker		[157]
9.	ANAVEX2-73		Anti-tau, metabolic	High dose – Phase 2,Mid dose -Phase 3			In-vivo mouse models of AD	Reduce tau phosphorylation and cell signaling is improved		[158]
10.	Bryostatin-1		Anti-amyloid, prevent tumor growth	Phase 2			Mild to moderate form of AD in patients	Improved cellular processes		[159]
11.	Donepezil		Anti-cholinesterase	FDA approved			Mild to moderate form of AD in patients	Slow down the symptoms of AD		[160]
12.	Memantine		Glutamate – NMDAreceptor antagonist	FDA approved			Moderate to severe form of AD in patients	Slow down the symptoms in learning and memory pathways		[161]
13.	Formoterol		Metabolic	Phase 2			Ts65Dn Mouse model	Improvement in multicellular pathways		[162]
14.	hUCB-MSCs		Regenerative	Phase 1			Zebrafish, murid rodents, nonhuman primates and invertebrates such as Drosophila and C elegans	Regenerating neurons, proliferation of K562 (an erythromyeloblastoid cell line) and the cytokine secretion pattern		[163]
15.	Semorinemab		Anti-tau monoclonal antibody	Phase 2			Mouse models and clinical patients of AD	Targets N-terminus of all six isoforms of human type tau		[164] [https://clinicaltrials.gov/ct2/show/NCT03828747]
S. No.	Name of Drug	Action of Drug			ClinicalStatus	Models			Effects		Refs.
16.	STA-1	Neuroprotective			Phase 2	Patients with vascular dementia, Caenorhabditis elegans			Reduction in oxidative stress		[165]
17.	Probucol	Neuroprotective, anti-inflammatory			Phase 2	Aged male rats (26 months old)			Synaptic functions improve and APOE gene activity is induced		[166]
18.	DAOIB	Neurotransmitter-NMDA based			Phase 2	Behavioral and psychological patients of AD			NMDA activity is enhanced		[153]
19.	Ifenprodil	Neuroprotective			Phase 1	In-vitro and in-vivo models			NMDA receptor antagonist -inhibits receptors containing NR2B subunits		[167]
20.	Riluzole	Neuroprotective, inhibits release of glutamic acid			Phase 2	5XFAD Transgenic mouse models of familial AD			Protection of neurons in brain		[168]
21.	Saracatinib	Anti-tau based therapy			Phase 1	Transgenic mouse models			Fyn kinase inhibitor to inhibit synaptotoxicity		[49]
22.	Morin	Interacts with nucleic acids, proteins and enzymes			-	Rats			Acts on free radicals, reduces oxidative stress and hyperammonemia		[169]

CR was able to enhance cognitive abilities, attenuate Aβ plaques in various brain regions and reduce NFT generation. The results have mostly remained consistent in different mouse strains indicating that CR diet working is not linear and regulates multiple causative factors in AD [127-129].