Advances in Parkinson's Disease: 200 Years Later.

When James Parkinson described the classical symptoms of the disease he could hardly foresee the evolution of our understanding over the next two hundred years. Nowadays, Parkinson's disease is considered a complex multifactorial disease in which genetic factors, either causative or susceptibility variants, unknown environmental cues, and the potential interaction of both could ultimately trigger the pathology. Noteworthy advances have been made in different fields from the clinical phenotype to the decoding of some potential neuropathological features, among which are the fields of genetics, drug discovery or biomaterials for drug delivery, which, though recent in origin, have evolved swiftly to become the basis of research into the disease today. In this review, we highlight some of the key advances in the field over the past two centuries and discuss the current challenges focusing on exciting new research developments likely to come in the next few years. Also, the importance of pre-motor symptoms and early diagnosis in the search for more effective therapeutic options is discussed.

A Little Bit of History

Two centuries have passed since James Parkinson’s Essay on the Shaking Palsy described a handful of patients who showed tremor at rest, bradykinesia and, some of them, akinesia. In his essay, he characterized the motor symptoms of the disease that now takes his name (Parkinson, 1817). Although this was the first description of the disease as a neurological condition, it was not until 50 years later that new scientific evidence obtained by Jean-Martin Charcot contributed to a definition of the clinical and anatomopathological basis of Parkinson’s Disease (PD) (Charcot, 1872). Years later, in 1893, Blocq and Marinescu noticed resting tremor in a patient that resembled parkinsonian symptoms. The tremor was due to a tuberculous granuloma on the right cerebral peduncle that was affecting the ipsilateral Substantia nigra pars compacta (SNc) (Blocq and Marinescu, 1893). It was Brissaud a few years later who suggested that the SNc might be the site affected in PD (Brissaud, 1899). Two decades later, Trétiakoff first reported neuropathological changes in the SNc in PD patients. He observed a large loss of neuromelanin in the SNc resulting from the absence of SNc neurons containing this pigment and also the presence of cytoplasmatic inclusions named Lewy bodies (LB) (Trétiakoff, 1919). These structures had been described some years earlier by James Lewy and, from that moment onward, this feature of PD became the focal point of neuropathological studies on PD (Lewy, 1912). The presence of both loss of dopaminergic neurons in the SNc and LB was established as the anatomopathological hallmark and diagnostic criterion of PD (Postuma and Berg, 2016).

At this point, the diagnostic criteria were established, but the main challenge was to assure successful treatment. The first neurosurgery of the basal ganglia (BG) to treat PD took place in 1940. Between the late 1950s and the mid-1960s many discoveries were made about the existence of dopamine (DA) as a neurotransmitter (Montagu, 1957; Carlsson et al., 1958) and its role in the striatum (Bertler and Rosengren, 1959; Carlsson, 1959; Sano et al., 1959). In 1957, Carlsson reported the first evidence for a functional role for DA, describing the reserpine effect in reducing motor activity in animals, which was reversed by L-3,4-dihydroxyphenylalanine (L-DOPA) administration, a precursor in DA synthesis. DA signaling proved to play a crucial role in motor control by the BG (Carlsson et al., 1957). Soon after this, evidence emerged of the striatal DA deficiency in PD (Sano, 2000). Particularly, Ehringer and Hornykiewicz described a deficit in both the striatum and the SNc in brains from parkinsonian patients (Ehringer and Hornykiewicz, 1960). Furthermore, some studies sustained the presence of a dopaminergic nigrostriatal projections and they also revealed that the dorsolateral striatum mainly receives terminals from SNc neurons. It happens that this area of the striatum is the most affected in PD (Dahlstroem and Fuxe, 1964; Anden et al., 1965). After these discoveries, the L-DOPA era began. During these years, it was demonstrated that intravenous injection of L-DOPA and also small oral doses of L-DOPA in humans had anti parkinsonian effects (Cotzias, 1968). From that moment L-DOPA became the gold-standard treatment for PD, since many authors consistently reported a marked improvement in PD with large oral doses of L-DOPA (Hornykiewicz, 2002). Since then significant progress has been made in the development of new pharmacological and surgical tools to treat PD motor symptoms (Smith et al., 2012).

A new important breakthrough took place in 1983 when Langston and colleagues reported a group of drug users who developed acute parkinsonism after MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) exposure (Langston et al., 1983). These patients developed an acute syndrome indistinguishable from PD. This is due because the MPTP metabolite, MPP+, destroys the dopaminergic neurons in the substantia nigra after a series of alterations in the mitochondrial matrix and the electron transport chain. The SNc of Parkinson patients was also described as exhibiting a marked decrease in complex I activity (Davis et al., 1979; Schapira, 1993). The fact that some PD patients have certain polymorphisms in genes that express subunits of complex I suggests that this could be a vulnerability factor in PD (Kösel et al., 1998; van der Walt et al., 2003). New models based on MPTP intoxication allowed researchers to ascertain PD hallmarks both in vitro and in vivo (Langston, 2017). Due to the achievements of pharmacological DA treatments, search of cell-based DA replacement approaches were initiated with largely disappointing results (Barker et al., 2015). From the surgical and therapeutic point of view, discrete lesions of the BG improved parkinsonism (Meyers, 1942). A monkey model of PD showed motor signs improvement as a result of the chemical destruction of the subthalamic nucleus (STN) (Bergman et al., 1990), with evidence of reversal of experimental parkinsonism by STN lesions. This same year deep brain stimulation (DBS) of the STN became effective for PD treatment (Hammond et al., 2007; Rosin et al., 2011; de Hemptinne et al., 2015).

In the late 1990s, due to the improvement and sophistication of genetic analysis techniques, mutations in SNCA gene codifying for alpha-synuclein (α-syn) protein were identified as the first genetic cause of PD (Polymeropoulos et al., 1997). Once it was clear that SNCA mutations cause parkinsonism, and more than 80 years after the discovery of LB, α-syn protein was found to be the main component of LB (Spillantini et al., 1997, 1998). Later on and based on these discoveries, Braak et al. (2003) proposed a pathological staging of the disease. From that time on, genetic studies have revealed many other mutations in other genes related to PD (PINK1, LRRK2, Parkin, DJ1, etc… see Advances in genetics below). The discovery of different genetic variants affecting the risk of PD has provided the field with a new battery of potential therapies ready to be tested in clinical trials. The initial findings have been followed by intensive research and the identification of several genes linked to PD pathogenesis in the last few years. Developments in genetics and molecular techniques such as CRISPR, have allowed the raise of new experimental models based on the use of transgenic animals presenting mutations associated to PD (Trigo-Damas et al., 2018). These examples open the door to studies where using genetic-based animal models would allow to assess the potential role of α-syn aggregation and spreading, evaluating potential therapeutics, imaging tracers or biomarkers (Dehay et al., 2016; Koprich et al., 2017; Ko and Bezard, 2017; Marmion and Kordower, 2018); also, the cellular models offer unique opportunities for the identification of therapeutic strategies capable of modulating the disease (Lázaro et al., 2017). These new models join the well-known classic neurotoxin based animal models such as MPTP or 6-OHDA that have provided a valuable insight into potential new targets for disease intervention (Blesa et al., 2012; Morissette and Di Paolo, 2018).

At present, catching theories linking alterations in the gut microbiota to PD of the disease open new research areas in the hunt of the etiology of the disease (Sampson et al., 2016). Many efforts are concentrated in decoding the pre-symptomatic phases and turning scientific progresses into disease-modifying therapies for PD (Blesa et al., 2017). In this sense, exciting cutting-edge approaches with less invasive technologies such as gamma knife or focused ultrasound for the treatment of motor symptoms in PD have been advanced (Martínez-Fernández et al., 2018) (see New technologies for the diagnosis, clinical assessment and treatment of Parkinson’s Disease below) (Figure 1).

FIGURE 1

Breakthroughs in Parkinson’s disease history.

Advances in Genetics

The etiology of PD remains largely unknown. The majority of patients are classified as idiopathic PD cases, i.e., arising ‘spontaneously’ or from an unknown cause. Prevalence is estimated at 1% in people above 65 years and increases exponentially in subsequent decades of life (Fahn, 2003) and in fact, aging is considered the major known risk factor. Yet, continuous and intense efforts have been undertaken to improve our incomplete comprehension of the disease. In this context, genetic research has played a pivotal role in elucidating the cause of disease, most especially during the last 20 years. Earlier than that, the genetic contribution to PD was unrecognized because classic reports of PD familial clustering or twin concordance studies were scarce and controversial (Farrer, 2006). It was in 1997 when a linkage study first identified unequivocal familial segregation of the missense mutation A53T in the SNCA gene with an adult-onset autosomal-dominant PD phenotype (Polymeropoulos et al., 1997). Subsequently, other pathogenic missense mutations in SNCA were identified including A30P, E46K, H50Q, G51N, and A53T (Krüger et al., 1998; Zarranz et al., 2004; Lesage et al., 2013; Proukakis et al., 2013). In 1998, another pioneer study reported that the α-synuclein protein was the main component of the proteinaceous aggregates termed Lewy bodies and Lewy neurites which are found in the soma and neurites of the few surviving dopaminergic neurons of the SNpc in PD patients (Spillantini et al., 1997, 1998). The identification of SNCA led to a shift of paradigm in the classification of PD patients into monogenic or familial PD (fPD) cases caused by pathogenic mutations in genes associated with the disease (5–10% of cases), and the vast majority of patients encompassing sporadic PD (sPD) cases (95%). The identification of SNCA was also seminal to set the basis for the subsequent intense genetic cell and animal modeling of the disease in the lab (Singleton et al., 2003; Chartier-Harlin et al., 2004; Ibáñez et al., 2004). More recently, multiplications of the SNCA locus, duplications and triplications, were found to cause PD with an inverse correlation between gene dose and age-at-onset, but a direct effect on disease severity (Chartier-Harlin et al., 2004; Ibáñez et al., 2004; Singleton et al., 2013). Overall mutations in SNCA are uncommon in frequency and lead to a DOPA-responsive early-onset parkinsonism, often severe and with dementia that is pathologically characterized by nigral neurodegeneration and widespread brainstem and cortical LB pathology.

Until date, a total of 23 loci and 19 causative genes have been associated with PD, yet with certain degree of heterogeneity regarding phenotypes (PD only or PD plus syndromes), age-at-onset (juvenile or adult onset), and inheritance mode (autosomal dominant, recessive or X-linked) (Table 1). Whereas some of the genes associated to the PARK loci have not been yet identified (PARK3, PARK10, PARK12, and PARK16), the pathogenicity of a few PD-associated genes still remains controversial due to novelty or to lack of replication of the original study (UCHL1, GIGYF2, EIF4G1, SYNJ1, TMEM230, and CHCHD2). Yet, mutations in the remaining genes, although rare in frequency, have been unequivocally established as PD-causative and account for the majority of autosomal dominant (SNCA, LRRK2, HTRA2, and VPS35) or recessive PD cases (PRKN, PINK1, DJ-1, ATP13A2, PLA2G6, FBXO7, DNAJC6, and VPS13C). Among the dominant genes, the identification by linkage analysis of mutations in the leucine-rich repeat gene (LRRK2) in some PD families with adult onset autosomal-dominant inheritance simultaneously by two groups (Paisan-Ruiz et al., 2004; Zimprich et al., 2004) represented another major milestone in PD research. Subsequently, three different groups identified in parallel the mutation G2019S at the kinase domain of LRRK2 as the most common pathogenic variant of LRRK2-associated PD (Di Fonzo et al., 2005; Hernandez et al., 2005; Kachergus et al., 2005) that remarkably it is found not only in monogenic but also in sPD cases lacking mendelian segregation. The LRRK2-associated PD form uniquely resembles common sPD at the clinical and neuropathological levels, yet with slight clinical differences (Marras et al., 2016; Pont-Sunyer et al., 2017), and eventual pleomorphic pathology (Zimprich et al., 2004). Of note, the penetrance of G2019S mutation is limited but rises progressively with age (Healy et al., 2008; Marder et al., 2015) and has been shown to be modified by additional factors such as genetic risk polymorphisms and other still unknown factors (Trinh et al., 2016; Fernández-Santiago et al., 2018). Moreover, mutations in HtrA Serine Peptidase 2 (HTRA2) (Strauss et al., 2005) and vesicle protein sorting 35 (VPS35) (Vilariño-Güell et al., 2011; Zimprich et al., 2011) are responsible of typical L-DOPA responsive PD, although no neuropathological data is not available yet. On the other hand, mutations in the recessive genes including parkin (PRKN), PTEN-induced putative kinase 1 (PINK1) and DJ-1 are causative of early-onset parkinsonism shearing largely identical clinical phenotypes, but distinct neuropathology. PRKN-associated PD is characterized by pure degeneration in the SNc and locus coeruleus without LB pathology and occasional Tau inclusions (Schneider and Alcalay, 2017), whereas PINK1 mutations lead to nigral neurodegeneration with LB and neurites (Samaranch et al., 2010), and DJ1-associated pathology includes severe degeneration in the SNc and locus coeruleus with diffuse LBs and axonal spheroids (Taipa et al., 2016). In addition, pathogenic mutations in the genes ATPase 13A2 (ATP13A2) (Bras et al., 2012), phospholipase A2 (PLA2G6) (Gregory et al., 2008) F-Box protein 7 (FBXO7) (Shojaee et al., 2008), DNA J Heat Shock Protein Family (Hsp40) Member C6 (DNAJC6) (Edvardson et al., 2012) and Vacuolar Protein Sorting 13 Homolog C (VPS13C) (Lesage et al., 2016) are linked to autosomal recessive, early-onset atypical parkinsonism that often comprises additional clinical features such as pyramidal degeneration, ataxia or dementia, with or without LBs. Overall, although the relative contribution of pathogenic mendelian genes to overall PD is limited, genetic research in PD has been instrumental since it has uniquely permitted the identification of disease molecular alterations, pathophysiological pathways, and candidate therapeutic targets, most of which are believed to be largely common to sPD. Thus genetic findings in PD have undoubtly paved the way out for tackling overall pathology of all PD cases.

Table 1

Summary of genes associated with Parkinson’s disease.

Locus	Gene	Inheritance	Onset	Location	Variants	Function
PARK1/4	SNCA	DominantRisk factor	EO	4q21.3-q22	5 point mutations, multiplications Rep1 risk variant in the promoter	Synaptic vesicles trafficking
PARK2	PARKIN	Recessive	EO	6q25.2-q27	>250 point mutation, ins/de and exon rearrangements	Mitophagy
PARK3	Unknown	Dominant	LO	2p13	?	?
PARK5	UCHL1	Dominant	LO	4p13	1 missense variant in one sibling pair	Proteasome
PARK6	PINK1	Recessive	EO	1p36.12	>100 point mutations, ins/del and exon rearrangements	Mitophagy
PARK7	DJ-1	Recessive	EO	1p36.23	>20 point mutations and deletions	Mitophagy
PARK8	LRRK2	Dominant	LO	12q12	7 point mutations	Autophagy?
		Risk factor			Risk variants p.R1628P and p.G2385R
PARK9	ATP13A2	Recessive	EO	1p36	>20 point mutations	Lysosomes
PARK10	Unknown	Risk factor	?	1p32	?	?
PARK11	GIGYF2	Recessive	EO	2q36-7	7 missense variants	Insulin-like growth factors (IGFs) signaling
PARK12	Unknown	Risk factor	?	Xq21-q22	?	?
PARK13	HTRA2	Dominant	?	2p13.1	1 missense variant	Mitophagy,
PARK14	PLA2G6	Recessive	EO	22q13.1	>18 missense variants	Lipids metabolism
PARK15	FBXO7	Recessive	EO	22q12.3	4 point mutations	Mitophagy
PARK16	Unknown	Risk factor	?	1q32	?	?
PARK17	VPS35	Dominant	LO	16q12	2 point mutations	Endosomes
PARK18	EIF4G1	Dominant	LO	3q27.1	1 missense variant	Protein translation
PARK19	DNAJC6	Recessive	EO	1p31.3	9 missense variants	Endosomes
PARK20	SYNJ1	Recessive	EC	21q22.11	3 missense variants	Endosomes
PARK21	DNAJC13	Dominant	LO	3q22.1	1 missense variant	Endosomes
PARK22	CHCHD2	Dominant	LO/EO	7p11.2	1 missense variant, 1 truncation	Mitochondria-mediated apoptosis and metabolism?
PARK23	VPS13C	Recessive	EO	15q22.2	2 missense variants,l truncation	Mitophagy
–	GBA	AD, AR in GD Risk factor	LO	lq22	>10 missense variants	Lysosomes
–	MAPT	SporadicRisk factor		17q21.31	H1 haplotype increase PD risk and disease severity	Microtubules

In addition to PD-causative mutations, classical candidate gene association approaches or more recently large genome-wide association studies (GWAS) have identified common genetic variants in genes such as SNCA, LRRK2, microtubule-associated protein tau gene (MAPT) or glucosylceramidase beta (GBA) which contribute to increase PD susceptibility (Lill, 2016). The variants in MAPT (Pastor et al., 2000; Golbe et al., 2001; Caffrey and Wade-Martins, 2007) and SNCA (Botta-Orfila et al., 2011; Cardo et al., 2012; Brockmann et al., 2013) loci showed the strongest association with PD risk across populations and most importantly, also at the GWAS level (Simón-Sánchez et al., 2009; Bonifati, 2010; Nalls et al., 2014) correlating not only with higher risk but with increased disease age-at-onset as well (Wang G. et al., 2016). On the other hand, common variants in LRRK2 increase the risk of PD only in Asian populations but not in Europeans (Farrer et al., 2007; Lu et al., 2008). In addition, mutations in GBA which codifies the lysosomal enzyme β-glucocerebrosidase are causative of the recessive lysosomal storage disorder Gaucher’s disease. Both homozygous and heterozygous GBA variants increase the risk of developing PD (Thaler et al., 2017). Moreover, GBA-mutation carriers show a more severe parkinsonism than idiopathic patients, earlier age-at-onset and more frequently dementia (Thaler et al., 2017). Besides genetics, epigenetic alterations have also been suggested to play a role in the pathogenesis of PD in recent years. Thus, abnormal changes in various epigenetic mechanisms regulating gene expression such as DNA methylation (Masliah et al., 2013; Coupland et al., 2014; Fernández-Santiago et al., 2015; Pihlstrom et al., 2015), histones modifications (Park et al., 2016) or microRNAs (miRNAs) (Kim et al., 2007) have been linked to disease, thus opening a new venue of epigenetic research in PD.

From Motor to Non-Motor Symptoms

Motor disturbances in PD have been widely investigated leading to a better diagnosis and origination of validated rating scales and therapies. However, the non-motor symptoms (NMS) of PD also have major importance when evaluating the quality of life of patients and the impact on health economics, attracting a growing interest in the last years. The incidence of NMS augments along with the disease duration, even preceding the motor symptoms or signs by several years. Symptoms such as olfactory dysfunction, REM sleep behavior disorder (RBD), constipation, depression, and pain (Chaudhuri et al., 2006; Tolosa et al., 2009) appear to be clear indicators of a preclinical phase of the disease. This concept is reinforced by studies showing an augmented risk for patients with idiopathic RBD or idiopathic hyposmia to develop a synucleinopathy (Boeve et al., 2001; Iranzo et al., 2014; Sakakibara et al., 2014; Postuma et al., 2017).

In early phases of the disease, some of these NMS still remain in many patients. Up to 21% of patients report pain, depression or anxiety (O’Sullivan et al., 2008). Importantly, in many cases, patients report a major disturbances of these NMS rather than motor ones, in the beginning of the disease (Gulati et al., 2004; Politis et al., 2010).

We currently know that PD involves disorders in several neurotransmitters pathways, including the cholinergic, noradrenergic, and serotonergic systems (Wolters, 2009; Halliday et al., 2011; Jellinger, 2012; Buddhala et al., 2015). This fact could relate symptoms such as depression with the loss of dopaminergic and noradrenergic transmission in the limbic system; and also anxiety and apathy, associated in this case to the low dopaminergic transmission (Thobois et al., 2010). On the other hand, excess of dopaminergic transmission due to DA agonist therapy, can prompt some NMS. Impulse control disorders (ICDs) is one of the most common side effects of dopamine replacement therapy used in PD with an estimated prevalence of 4.9–19% (Voon et al., 2009; Weintraub et al., 2010). ICDs are behavioral addictions including exaggerated behaviors such as gambling or shopping related to the administration of D2/D3 agonists. Research on this topic remains quite reduced and preclinical studies are limited because of the lack of alternatives for the pharmacological treatment. (Voon et al., 2009). It seems that the fact that in PD-ICD patients there is a major denervation in the ventral striatum this leads to an “over-dose” when dopamine is administered in ventral areas and limbic pathways (Weintraub, 2009; Voon et al., 2011). Nevertheless, further studies should be performed in order to achieve a better comprehension of the disorder and the development of successful treatments.

Non-motor fluctuations (uncomfortable anxiety, slowness of thinking, fatigue, and dysphoria) are other psychiatric disorder also DA-dependent, and reported primarily during “OFF” periods and can be reversed with continuous dopaminergic replacement (Chaudhuri and Schapira, 2009).

Nowadays, NMS denote some of the most relevant sources of disability and impairment in quality of life of parkinsonian patients and the acknowledgment of these symptoms become critical for the improvement and advances in the diagnosis of the disease (Chaudhuri et al., 2006). Still, in many cases, NMS of PD are not distinguished in routine clinical evaluations since their origin are not directly related to PD (Shulman et al., 2002).

These circumstances indicate the relevance of developing successful tools to identify NMS, both for the assessment and for their treatment (Grosset et al., 2007). The development of valuable instruments capable of supporting neurologists at the time of diagnosis would also mean a benefit for the rise of valid therapeutic strategies (Seppi et al., 2011) (see Diagnosis and clinical assessment devices below). This is reflected in the scarce therapies available for non-motor deficits (Zesiewicz et al., 2010). Currently, dopaminergic treatments are the most broadly used therapies, but they have no impact on those aspects of the disease that are associated to other neurotransmitter deficits. Conversely, the use of anticholinergics, for example, classically increases the cognitive symptoms of PD, as it does deep brain stimulation surgery (Witt et al., 2008).

To sum up, the increasing prevalence of non-motor complications is far complex marking a new concept in the scenery of PD. These problems are linked with a marked decrease of quality of life of the patients and the social life of their families. Their etiology is multifaceted and still poorly understood. Thus, specific NMS treatments are required, as current treatment options for NMS in PD continue incomplete and large areas remain unfulfilled of therapeutic need.

New Technologies for the Diagnosis, Clinical Assessment and Treatment of Parkinson’s Disease

In the last decade, new technology-based tools and technology-based therapies have been advanced with the objective of refining the diagnosis, clinical assessment and treatment of patients with movement disorders. The development and intricacy of molecular and cellular techniques, as well as extraordinary progress in technology, have marked a milestone in our general understanding of the disease.

Drug Delivery Systems

The clinical use of neuroprotective molecules has been hampered by several issues, and among these, drug delivery to the brain remains a particular challenge. To address these limitations, drug delivery systems and methods that allow enhanced brain delivery of neuroprotective molecules have been investigated. These new technologies offer unprecedented advantages enabling protection of sensitive molecules from degradation and controlled release over days or months. Drug delivery systems can also be engineered to target diseased regions within the body, thereby enhancing the specificity of therapeutics. Therefore, the delivery and efficacy of many pharmaceutical compounds can be improved and their side effects reduced. Among drug delivery systems, microparticles (MPs), nanoparticles (NPs) and hydrogels (HGs) seem to be the most effective in providing neuroprotection, although liposomes and micelles have also been investigated (Figure 2) (Garbayo et al., 2009; Rodríguez-Nogales et al., 2016). MPs and NPs are particulate carrier systems in the micrometer and nanometer size range, respectively. MPs are generally used for the long-term delivery of drugs while NPs are commonly used as carriers of small molecules for targeted and intracellular delivery. On the other hand, HGs are tridimensional polymeric networks that absorb a large amount of water, which becomes their principal component. Formulations can be designed either for local administration into the brain or for systemic delivery to achieve targeted action in the central nervous system. The examples below show that drug delivery systems are in the initial stages of the drug development process, but the potential for using this technology for PD treatment is very high.

FIGURE 2

Drug delivery systems under investigation for Parkinson’s disease treatment.

Drug Delivery Systems for Neurotrophic Factor Therapy

Neurotrophic factors, and glial cell line-derived neurotrophic factor (GDNF) in particular, have been regarded as one of the most promising molecules for PD. In this regard, several delivery systems have been designed focused on increasing GDNF stability and retention in the brain. Several studies have demonstrated the preclinical efficacy of microencapsulated GDNF in different PD animal models (rodents and monkeys) (Garbayo et al., 2009, 2011, 2016). In those studies, a single injection of microencapsulated GDNF achieved long term improvement of motor function and dopaminergic function restoration in parkinsonian monkeys with severe nigrostriatal degeneration. The injectable formulation localized GDNF within the putamen and prevented systemic off-target effects. GDNF showed trophic effects on the nigrostriatal pathway increasing striatal and nigral dopaminergic neurons. Moreover, microencapsulated GDNF did not elicit immunogenicity or cerebellar degeneration. This example demonstrates that MPs are an efficient vehicle for sustained GDNF delivery to the brain. In another approach, vascular endothelial growth factor (VEGF), a potent angiogenic factor with prosurvival effects in neuronal cultures, was combined with GDNF to enhance the action of the latter (Herrán et al., 2013). A pronounced tyrosine hydroxylase (TH) neuron recovery was observed in the SNc of parkinsonian rats. Later, a combinatorial strategy of NPs-containing GDNF and VEGF was locally applied in a partially lesioned rat PD model. Behavioral improvement was observed together with a significant enhancement of dopaminergic neurons both in the striatum and SNc, which corroborates previous work in GDNF and VEGF encapsulation. Interestingly, the synergistic effect of the therapeutic proteins allows dose reduction while still providing neurogenerative/neuroreparative effects (Hernandez et al., 2014). The direct nose to brain administration of GDNF-NPs is another promising trend. One of the most recent examples uses nanoencapsulated GDNF in lipid NPs (Hernando et al., 2018). In order to enhance the target NP delivery to the brain, the nanocarrier surface was modified with a cell-penetrating peptide named TAT. The formulation improved the nose to brain delivery of GDNF, thereby improving motor function recovery and GDNF neuroprotective effects when tested in a mouse PD model. An alternative approach to NPs is the use of liposomes. Uptake of the neurotrophic factor to the brain via intranasal delivery is enhanced when GDNF is encapsulated in a liposomal formulation (Migliore et al., 2014). In order to move forward with nose to brain delivery strategies greater formulation retention in the olfactory region needs to be achieved, together with better targeting of specific brain regions. Finally, another promising approach that has been undertaken for GDNF brain delivery is the use of nanoformulations able to cross the blood brain barrier through receptor-mediated-delivery. This strategy would allow non-invasive drug delivery to the brain. Based on this concept, neuroprotection has been observed after the intravenous administration of a GDNF nanoformulation (Huang et al., 2009). The NPs improved locomotor activity, reduced dopaminergic neuronal loss and enhanced monoamine neurotransmitter levels in parkinsonian rats. A remaining challenge is to target specific brain areas in order to avoid unwanted side effects.

Besides GDNF, other neurotrophic factor such as basic fibroblast growth factor (bFGF) have been evaluated. One example involves gelatin nanostructured lipid carriers encapsulating bFGF that can be targeted to the brain via nasal administration (Zhao et al., 2014). Overall, the nanoformulation stimulated dopaminergic function in surviving synapses and played a neuroprotective role in 6-OHDA hemiparkinsonian rats. A very recent study took advantage of the neuroprotective properties of Activin B, which was administered in a parkinsonian mice using a thermosensitive injectable HG (Li et al., 2016). The biomaterial allowed a sustained protein release over 5 weeks and contributed to substantial cellular protection and behavioral improvement.

Drug Delivery Systems for Stem Cell Therapy

In recent years, stem cells have attracted considerable attention as regards achieving neuroprotection. However, cell therapy has been limited by the low engraftment of the administered cells. By applying a combination of biomaterials, cells and bioactive molecules, brain repair can be facilitated. In an early example, MPs loaded with neurotrophin-3 were used to retain injected adult stem cells in the striatum and to support cell viability and differentiation (Delcroix et al., 2011). When tested in a PD rat model, a potent behavioral recovery was observed together with nigrostriatal pathway protection/repair. Going a step further, BDNF-loaded MPs have been encapsulated in a HG embedded with mesenchymal stem cells for neural differentiation and secretome enhancement (Kandalam et al., 2017). This strategy not only provides neuroprotective BDNF but also stem cells that benefit from that environment by displaying neural commitment and an improved neuroprotective/reparative secretome. Likewise, HGs have also been used to improve dopaminergic progenitor survival and integration after transplantation. A report by T. Wang and co-workers pioneered the development of a composite scaffold made of nanofibers embedded within a xyloglucan HG. The biomaterial was further functionalized with GDNF to improve the niche surrounding the implanted cells (Wang T.Y. et al., 2016). The scaffold enhanced graft survival and striatal re-innervation. A similar strategy was followed by Adil MM, that determined the impact of a heparin/RGD functionalized hyaluronic acid HG on the survival of embryonic stem cell-derived dopaminergic neurons (Adil et al., 2017). These examples demonstrate the potential of biologically functionalized HGs to improve stem cell delivery. Beyond HGs, the use of NPs as a tool to optimize MSC therapeutics was underlined in a recent study by T. Chung and coworkers that successfully developed a dextran-coated iron oxide nanosystem to improve the rescuing effect of mesenchymal stem cells (Chung et al., 2018).

In addition to stem cell delivery, biomaterials can also be used to deliver mesenchymal stem cell secretome at the site of injury. By way of example, adipose mesenchymal stem cell secretome has been encapsulated in a biodegradable injectable HG that was able to increase the controlled release of the neuroprotective factors in a PD-relevant experimental context (Chierchia et al., 2017). NPs can also be used to modulate the subventricular neurogenic niche and boost endogenous brain repair mechanisms using microRNAs. Due to the short half-life and poor stability of these molecules, their efficient delivery into cells is a challenge. NPs can provide a shielded environment and controlled release. One example involves microRNA-124, a potent pro-neurogenic factor for neural stem cells which has been nanoencapsulated, demonstrating the feasibility of this approach as well as its efficacy in parkinsonian mice (Saraiva et al., 2016). The nanoformulation promoted not only neurogenesis but also the migration and maturation of new neurons in the lesioned striatum. Specifically, this example illustrates the potential of nanotechnology for improving not only the safety and efficacy of conventional drugs, but also the delivery of newer drugs based on microRNAs to the brain. Overall, these promising results suggest that biomaterials and drug delivery systems are a valid alternative to enhance stem cell neuroprotective properties. Further studies are needed for the advancement of this technology from preclinical studies to clinical trials.

Nanomedicines for Antioxidant Delivery

Mitochondrial damage and oxidative stress have been proposed as the major contributing factors to PD pathogenesis. Accordingly, coenzyme Q10 has been considered a promising molecule in PD management due to its ability to enhance mitochondrial function. However, its efficacy has been hindered by insolubility, poor bioavailability and lack of brain penetration. In order to solve these issues, a nanomicellar coenzyme Q10 formulation able to stop, but not reverse, ongoing neurodegeneration has shown efficacy in a mouse PD model (Sikorska et al., 2014). Moreover, this neuroprotective treatment activates an astrocytic reaction suggesting that these cells played a significant role in neuron protection. In addition to coenzyme Q10, curcumin counteracts oxidative stress and mitochondrial dysfunction. However, its clinical efficacy has been limited by its poor aqueous solubility, rapid metabolism and inadequate tissue absorption. Piperine has been used as adjuvant to improve curcumin’s bioavailability. Thus, curcumin and piperine amalgamation seems beneficial. Moreover, nanomedicines could also help to enhance drug transport from blood to the brain. In one example, both therapeutics were loaded in a lipid-based nanoformulation blended with different surfactants and orally administered in a PD mouse model (Kundu et al., 2016). A higher density of nigral TH+ neurons was found in the animals treated with dual drug loaded NPs, demonstrating that the system was able to cross the blood brain barrier preventing dopaminergic neuronal degeneration. This may be due to the improved curcumine bioavailability and the synergistic effect exhibited by both drugs. Another strategy to detain oxidative stress and achieve neuroprotection is the use of nanoencapsulated resveratrol (da Rocha Lindner et al., 2015). The nanoformulation was able to attenuate MPTP-induced lipid peroxidation and prevent striatal TH protein decrease in parkinsonian mice. These findings suggest that resveratrol-loaded NPs are a promising nanomedical tool for PD.

Nanomedicines That Interfere With α-syn Expression

Strategies that interfere with α-syn expression in neurons have also received widespread attention. One remarkable approach is the targeted gene therapy proposed by Niu et al. (2017) that has provided effective repair in a PD mice model using magnetic NPs loaded with shRNA plasmid for α-syn. Multifunctional magnetic NPs were effectively delivered through the blood brain barrier, prevented DA neuron degeneration as reflected by TH up-regulation and α-syn down-regulation and inhibited further apoptosis in the brain. Alternatively, suppression of α-syn overexpression has been demonstrated using gold NPs which could load plasmid DNA, cross the blood–brain barrier and target specific cells. For example, the group of Y. Guan achieved successful results in carrying pDNA into the neurons, and thus inhibiting dopaminergic neuron apoptosis (Hu et al., 2018). These approaches have the potential to suppress α-syn expression, providing a highly efficient treatment for PD.

Focused Ultrasound

In the last few years, the use of focused ultrasound (FUS) therapies has been revolutionizing the treatment of neurological disorders. This non-invasive technique consists in the application of focused acoustic energy (ultrasound) on selected brain areas. The MR-guided FUS (MRgFUS) allowed computer calculated targeting and achieved high accuracy with real-time feedback on the effect of the treatment. The first studies using MRgFUS thalamotomy in patients with essential tremor showed a significant clinical reduction in hand tremor (Elias et al., 2016). In PD, MRgFUS is being explored as a way to non-invasively ablate the brain areas responsible for the motor features associated with the disease. In 2014, MRgFUS of the pallidothalamic tract was used in PD patients for the first time, with a significant clinical improvement (Magara et al., 2014). Subsequent studies using MRgFUS in the ventral intermediate thalamic nuclei (Vim) reported a clinically significant reduction in mean UPDRS scores post procedure in PD patients (Schlesinger et al., 2015). In a recent pilot study, MRgFUS unilateral subthalamotomy was reported to be well tolerated and to improve the motor features of noticeably asymmetric PD patients (Martínez-Fernández et al., 2018). The questions of the best target for treating PD symptoms and whether different targets should be chosen for different patients are currently unresolved. Other unanswered questions are the long-term durability of FUS ablation outcomes and the safety and feasibility of bilateral procedures. The possibility of this non-invasive approach, with its immediate and apparently permanent clinical outcome, makes this treatment suitable for an increasing number of patients who are either unable or unwilling to undergo DBS therapy. Large randomized controlled trials are necessary to validate these preliminary findings and to assess the potential use of ablative FUS therapy in the treatment of PD patients. Other applications of FUS that are under current research are the opening of the brain–blood barrier (BBB) or neuromodulation (Krishna et al., 2017). Low-Intensity Ultrasound decreased α-syn in PC12 cells (Karmacharya et al., 2017). And more recently, using a non-invasive approach by combining MRgFUS and intravenous microbubbles and a shRNA sequence targeting α-syn, immunoreactivity of this protein have been decreased in several regions such as hippocampus, SNpc, olfactory bulb, and dorsal motor nucleus (Xhima et al., 2018). This technology could be useful in the near future to alter the progression of LB pathology in combination with improved early diagnosis of the disease.

Deep Brain Stimulation

Device-aided therapies, as levodopa–carbidopa infusion gel (LCIG), subcutaneous apomorphine pump infusion and deep brain stimulation (DBS), are essential tools in the treatment of advanced PD patients. During the last decade, evidence has been obtained regardless of safety, validity and efficacy in large prospective clinical studies (Antonini et al., 2018).

Deep brain stimulation is a surgical therapy that involves the implantation of one or more electrodes in specific regions of the brain. There is substantial and consistent evidence indicating that DBS of both STN and GPi improve motor fluctuations, dyskinesia and quality of life in advanced PD (Rodriguez-Oroz et al., 2005; Follett et al., 2010). Those benefits are maintained for more than 10 years (Zibetti et al., 2011). Additionally, DBS treatment has been evaluated in patients with relatively short disease duration providing better motor outcomes and quality of life compared to the control group receiving best medical treatment (Tinkhauser et al., 2018).

Deep brain stimulation has notably improved due to the development of new neurosurgery approaches (asleep surgery), devices (microelectrodes, directional electrodes), and programming and stimulation algorithms. Particularly relevant is the implementation of the directional electrodes, which leads to a segmented stimulation. They provide a more accurate therapeutic frame and potentially reduce the adverse effects related to DBS (Steigerwald et al., 2016).

The control of fluctuations could be improved and the adverse effects of DBS could be reduced by selective stimulation in a short-time window by using adaptive DBS (aDBS). Thus, aDBS is intended to personalize stimulation by recording local field potentials (LFP) directly from the stimulating electrode, which can only be activated when the LFP beta power exceeds a customized threshold. Therefore, it can modulate the stimulations according to the changes in the LFP beta power. aDBS seems to be more effective than conventional DBS in improving motor scores and controlling levodopa-induced dyskinesias. Further research over more extended time periods and larger cohorts are needed to ensure the benefit and efficacy of this novel strategy (Meidahl et al., 2017).

Diagnosis and Clinical Assessment Devices

The use of new technology-based tools allows quantitative assessment of the motor function of PD patients. Sensors, video-assessment methods or mobile phone applications are some of the techniques that improve the sensitivity, accuracy and reproducibility of the evaluation of PD patients (Espay et al., 2016). Portable devices that include inertial measurement units (IMUs) measure the orientation, amplitude and frequency of movement, as well as the speed of the part of the body where they are located. IMUs are usually made up of accelerometers and gyroscopes, and occasionally magnetometers. IMUs situated in different parts of the patient’s body make a precise record of tremor, bradykinesia, dyskinesias and even gait patterns (Heldman et al., 2014). On the other hand, continual monitoring of the motor status in the domestic environment (regarding baseline motor status, motor fluctuations, and benefit of treatment, among other factors) is also possible by using these technology-based tools (Ossig et al., 2016). These new technology-based systems open up an unexpected range of specific and real-time data, thereby resulting in the prospect of (1) better diagnostic accuracy, (2) more sensitive monitoring of the motor and non-motor symptoms, and (3) more precise adjustments of medical therapies. However, their use is limited in routine clinical practice due to the heterogeneity of the studies, which limit the extrapolation of results, and the high cost of the devices (Sánchez-Ferro et al., 2016).

Conclusion

In the future, population aging in developed countries will increase the burden of neurodegenerative diseases. In the case of PD, where treatment of symptoms needs to be patient-customized, balancing the control of symptoms, drug dose, presence of side effects and patient’s expectations, clinicians and researchers face a situation in which a synergy of medicine and research is urgently needed. In summary, 200 years after the publication of James Parkinson’s essay, our understanding of the disease has made remarkable progress and is still advancing, generating a considerable array of tools. Nowadays, fields such as functional genetics, novel molecular mechanisms, brain imaging and biomarker detection seem to be the major issues guiding our research strategies. Nevertheless, despite the progress made, improved early clinical diagnosis is still necessary and the disease lacks a cure. In this regard, research in drug delivery might provide safer and more effective treatments for PD. Years of research have revealed the need to take into account the role of environmental factors in addition to the genetics when studying PD progression. However, further research is needed to decipher the mechanisms by which this pathology spreads from cell to cell within the brain and from other organs to the central nervous system. Importantly, studies should also address early diagnosis (screening) tools, and more information is needed concerning the differential vulnerability of pathogenic factors affecting dopaminergic neurons.

Author Contributions

NDR, AQ-V, EG, IC-C, RF-S, MM, IT-D, MB-P, and JB reviewed the literature, composed and wrote the manuscript. NDR, IT-D, and JB organized the paper. IC-C and RF-S prepared Table 1. AQ-V prepared Figure 1. EG prepared Figure 2.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.