Inhibitors of MAO-A and MAO-B in Psychiatry and Neurology
- 1Rappaport Faculty of Medicine, Technion, Israel Institute of Technology, Haifa, Israel
- 2Assaf Harofe Medical Center, Affiliated to Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel
Inhibitors of MAO-A and MAO-B are in clinical use for the treatment of psychiatric and neurological disorders respectively. Elucidation of the molecular structure of the active sites of the enzymes has enabled a precise determination of the way in which substrates and inhibitor molecules are metabolized, or inhibit metabolism of substrates, respectively. Despite the knowledge of the strong antidepressant efficacy of irreversible MAO inhibitors, their clinical use has been limited by their side effect of potentiation of the cardiovascular effects of dietary amines (“cheese effect”). A number of reversible MAO-A inhibitors which are devoid of cheese effect have been described in the literature, but only one, moclobemide, is currently in clinical use. The irreversible inhibitors of MAO-B, selegiline and rasagiline, are used clinically in treatment of Parkinson's disease, and a recently introduced reversible MAO-B inhibitor, safinamide, has also been found efficacious. Modification of the pharmacokinetic characteristics of selegiline by transdermal administration has led to the development of a new drug form for treatment of depression. The clinical potential of MAO inhibitors together with detailed knowledge of the enzyme's binding site structure should lead to future developments with these drugs.
Monoamine oxidase (MAO; EC 22.214.171.124.) is a widely distributed mitochondrial enzyme with high expression levels in gastro-intestinal and hepatic as well as neuronal tissues. The enzyme catalyzes the oxidative deamination of a variety of monoamines, both endogenous and exogenous, and has major roles in metabolizing released neurotransmitters, and in detoxification of a large variety of endogenous and exogenous amines. Drugs which inhibit MAO are currently in clinical use for treatment of affective disorders and Parkinson's disease (PD). In this chapter we review recent developments in the basic pharmacology of MAO inhibitors (MAOI) and their clinical usage, and discuss the potential for new drug development in this field.
The overall enzyme reaction of MAO can be represented by the following equation:
The aldehydes produced by the action of MAO are metabolized further by aldehyde dehydrogenase and aldehyde reductase leading to the formation of glycols and carboxylic acids (Westfall and Westfall, 2011). The fact that an aldehyde is formed initially together with H2O2 which can generate reactive oxygen species (ROS) has drawn attention to the possibility that products of the action of MAO may be neurotoxic (Jenner, 2003). In this connection it should be realized that ROS and other reactive species are normally metabolized by scavenger enzymes including catalase and superoxide dismutase, and dysfunction of these enzyme systems may be a factor in neurodegenerative disease (Aluf et al., 2011). The dopaminergic neurons of substantia nigra pars compacta (SNpc) are at risk to oxidative stress because of their tonic activity and dense packing. Their degree of oxidative stress increases in early PD when a portion of the neurons have been lost, and the activity of the remaining ones increases in compensation. This situation was modeled recently in a microdialysis study in which a non-diffusible indicator molecule was perfused through a probe placed in the striatum. Following intraventricular injection of 6-hydroxydopamine in a dose adequate to reduce SNpc dopaminergic cell number by 50%, the level of oxidative stress increased markedly (Aluf et al., 2011), and was reduced following systemic injection of an MAO-A or MAO-B inhibitor (Aluf et al., 2013).
Two isoenzymes are encoded in the human X-chromosomal gene Xp1 123, MAO-A, and MAO-B. The two forms have over 70% homogeneity. Biochemically, the two forms can be differentiated by their substrate and inhibitor specificities; MAO-A shows greater affinity for hydroxylated amines such as noradrenaline (NA) and serotonin (5-hydroxytryptamine, 5-HT), whereas MAO-B shows greater affinity for non-hydroxylated amines such as benzylamine and beta-phenylethylamine (PEA). The amines dopamine (DA) and tyramine show similar affinity for each enzyme form. Clorgyline is a selective inhibitor of MAO-A while selegiline (l-deprenyl) and rasagiline are relatively selective inhibitors of MAO-B. The ratio of selectivity of selegiline and rasagiline for MAO-B is such that in human subjects, doses 2–5 fold higher respectively than the MAO-B selective dose can cause significant inhibition of MAO-A as shown by tyramine pressor responses (Bieck and Antonin, 1994; Goren et al., 2010). Some inhibitors can inhibit both forms of the enzyme (referred to as non-selective inhibitors, although this can cause confusion because the inhibitors are quite selective for MAO as opposed to other enzymes). The precise localization of the two MAO isoforms in brain has not been completely elucidated. Studies using cell cultures (Yu and Hertz, 1983; Carlo et al., 1996) pointed to localization of MAO-A within glial cells, but this is not true for the intact brain, where investigations in both primate and non-primate species have established that the glial enzyme is predominantly type B (Levitt et al., 1982; Denney and Denney, 1985; Westlund et al., 1988). The type A isoform has been localized to several neuronal cell types in primate and rodent species, including NA-ergic neurons of the locus coeruleus, DA-ergic neurons of the substantia nigra pars compacta (SNpc), (Westlund et al., 1993) and striatal medium spiny neurons (Sader-Mazbar et al., 2013). Serotonergic neuronal cell bodies of the raphe nucleus stain positive for MAO-B but the isoform localized to axonal varicosities may be of the A isoform (Denney and Denney, 1985). Selective inhibition of MAO-A leads to increased levels of neurotransmitter within noradrenergic (NA-ergic) and 5-HT-ergic neurons of the CNS, and clinical antidepressant action, while inhibition of MAO-B leads to increased levels of DA in the Parkinsonian brain with partial depletion of DA-ergic neurons in SNpc, and anti-Parkinsonian action (see Finberg, 2014 for a detailed description of these events at the synaptic level).
Many compounds with MAO inhibitory properties are being prepared by researchers, however the present account is limited to a description of the most important drugs from a therapeutic viewpoint, i.e., affective disorders and Parkinson's disease. The chemical structures of drugs mentioned in this review and a brief description of their major characteristics is shown in Table 1.
Molecular Structure of MAO and Mechanism of Enzyme Inhibition
For many years, a formula was searched for without success to explain the selectivity of an inhibitor molecule for MAO-A or MAO-B. The problem was solved when the MAO protein molecule was crystallized by the groups of Edmondson and Sukihara, enabling three-dimensional modeling of the protein and its combining site (Binda et al., 2002, 2007; De Colibus et al., 2005; Son et al., 2008). It was then seen that a two-site cavity structure exists for human MAO-B (hMAO-B), with an entry cavity and a reactive site cavity, whereas in human MAO-A (hMAO-A) the active site cavity is not bipartite and is shorter and wider than the longer and narrower substrate cavity in hMAO-B (De Colibus et al., 2005). The reactive site contains a combining moiety in which the N5 atom of FAD is displayed on the inner surface, and tyrosines 398, and 435 guard the entry gate in hMAO-B (Binda et al., 2002). Knowledge of the three-dimensional aspects of these sites, and the associated amino acid positions, can now be utilized in the design of new inhibitors.
Both reversible and irreversible inhibitors of MAO have been developed in previous years, and are currently in use clinically for treatment of affective and neurological disorders. Irreversible inhibitors are of several types: hydrazines, cyclopropylamines, and propargylamines. In all cases, these drugs combine covalently with the N5 atom of the flavin residue, but the rate of dissociation of the drug-enzyme complex is variable. Detailed mechanisms for the drug-enzyme complex formation have been described. Following recognition of the enzyme pharmacophore by the drug, the inhibitor molecule is metabolized leading to a reactive intermediate which combines covalently with the N5 atom of FAD leading to formation of a drug-receptor adduct, which then undergoes aging and irreversible combination. The term “suicide inhibitor” has been used in description of this type of drug action (see Finberg, 2014).
In general, because these inhibitors will irreversibly inactivate the enzyme, their action can only be reversed by generation of new enzyme molecules, a process which can take days or weeks. In clinical use, the drugs are administered daily, using a dose which alone is adequate to cause only partial enzyme inhibition, but when given daily over several days will cause a cumulative inhibition up to 90% or more of the target enzyme in brain. Continued drug administration ensures that newly-formed enzyme molecules are also inhibited, and that the enzyme activity is maintained at a constant low level. The clinical importance of this type of drug use is that a constant high degree of enzyme inhibition can be maintained over time. In addition, however, on stopping treatment enzyme activity will remain at a low level even after the drug itself has been cleared from the body.
Treatment of Depression with MAO Inhibitors
Non-subtype-Selective Irreversible Inhibitors
The profound antidepressant action of MAOI inhibitors was discovered by chance (Lehmann and Kline, 1983) in tuberculous patients treated with iproniazid, a derivative of the hydrazine compound isoniazid. Further developments led to the introduction into clinical use of several non-subtype-selective irreversible MAO inhibitors including the hydrazines phenelzine and isocarboxazid, the propargylamine pargyline, and the cyclopropylamine tranylcypromine, but these compounds can all lead to potentiation of the cardiovascular effects of the dietary amine tyramine (“cheese effect”). Following realization that the cheese effect can be avoided by dietary counseling, and that MAO inhibitors are in fact excellent drugs for treatment of drug-resistant and atypical depression, use of certain non-subtype-selective inhibitors, in particular tranylcypromine (Parnate), is now seen with increasing frequency. Tranylcypromine has pharmacological properties in addition to inhibition of MAO, in particular inhibition of lysine-specific histone demethylation type 1, and interaction with the endogenous cannabinoid system (Lee et al., 2006; Hill et al., 2008). Phenelzine also has an additional pharmacological property which may be involved in its antidepressant actions, namely blockade of GABA and alanine transaminases (Baker et al., 1991; Todd and Baker, 2008).
In a recent review (Heijnen et al., 2015) of a small number of clinical trials, tranylcypromine was found to be an efficacious and safe drug for the treatment of bipolar depression, when administered with correct dietary counseling. Although cheese effect is a potentially serious reaction, the limitations it imposes on treatment of psychiatric patients have been much exaggerated, because the amounts of tyramine occurring in foodstuffs are quite low, and only a gross violation of normal dietary directions would be likely to cause a fatal, or damaging, reaction (Gillman, 2011). The management of such a hypertensive reaction if it does occur has also been well-documented (Gillman, 2011). In addition to cheese effect, another potential danger is serotonin toxicity syndrome (ST), which can occur following the combination of irreversible MAOI with a drug which has the potential to elevate 5-HT synaptic levels, such as a serotonin-selective reuptake inhibitor (SSRI) (Gillman, 2006). In this context, the relatively long period required for return of MAO activity following cessation of therapy with an irreversible inhibitor is important when a change in therapy is required. If therapy with a SSRI is to be used, there is a danger of ST if these drugs are instituted before MAO activity has returned to normal levels. Following cessation of tranylcypromine administration in healthy subjects, a period of 30 days was required for complete normalization of the pressor response to oral tyramine challenge (Bieck and Antonin, 1988). In the case of rasagiline, using platelet activity of MAO-B as the index, enzyme activity returned to baseline levels 2 weeks after cessation of drug administration in healthy subjects (Thebault et al., 2004). The time required for return of enzyme activity in the brain however, is considerably longer than in the periphery. Using (Denney and Denney, 1985) C-labeled selegiline together with positron emission tomography (PET) the half-time for return of MAO-B binding in the brain following complete blockade of binding by an initial injection of selegiline in a baboon was 30 days (Arnett et al., 1987), and using similar technique, following initial MAO-B inactivation by rasagiline in human subjects, was 40 days (Freedman et al., 2005). Recommended periods (by manufacturer) for wash-out after cessation of tranylcypromine range from 7 to 10 days (Gahr et al., 2013).
The antidepressant effect of MAOI has focused interest on the possibility that altered expression levels of the MAO enzyme could be the cause of some forms of depressive disorders. Polymorphisms in the MAO-A gene have been associated with a number of behavioral traits. Reduced enzyme activity is associated with violent behavior and aggression, whereas over-expression may be linked to depression (Alia-Klein et al., 2008). These facts, together with the well-known biogenic amines hypothesis, provide theoretical background in support of the use of MAOI for treatment of affective disorders. Several studies have attempted to link the MAOA-uVNTR polymorphism, which leads to increased enzyme transcription, with suicidal tendency, but a meta-analysis including 1452 psychiatric patients and 1198 control subjects did not find a significant association (Hung et al., 2012) with this particular trait. In a recent study in which MAO-A expression level (total distribution volume, Vt, of 11C-harmine by PET) was determined in borderline personality disorder (BPD) patients, the MAO-A brain content was correlated with symptom severity (Kolla et al., 2015). Interestingly, MAO-A Vt was increased in prefrontal cortex and anterior cingulate cortex by 43 and 42% respectively in severe BPD subjects in relation to controls.
One of the main restrictions to the clinical use of MAOI for treatment of depression is the cheese effect. In preclinical and clinical studies it was shown that potentiation of the pharmacological effects of tyramine occurs following selective inhibition of MAO-A but not MAO-B (Lader et al., 1970; Finberg and Tenne, 1982; Finberg and Gillman, 2011). This can be attributed to the localization of MAO-A to noradrenergic (as well as serotonergic) neurons (see Finberg, 2014) for detailed review). A corollary to this selective localization of MAO subtypes is that selective inhibitors of MAO-A but not MAO-B are effective antidepressants (Youdim and Finberg, 1983), however no irreversible selective MAO-A inhibitors are in use for treatment of depression.
Reversible Inhibitors of MAO-A
In the 1980s several groups of researchers prepared selective reversible inhibitors of MAO-A (RIMAs) (Tipton et al., 1984) based on the theory that if substrate levels increased as a result of inhibition of the enzyme, the degree of enzyme inhibition would be reversed by increased dissociation of the inhibitor from its combining site, i.e., a reversible inhibitor would possess a built-in safety factor in the case of tyramine ingestion, and therefore reversible inhibitors would not cause cheese effect (Finberg, 2014). The correctness of this notion was confirmed in a number of clinical studies using tyramine challenges in patients (Finberg and Gillman, 2011; Finberg, 2014). Currently, moclobemide is the only RIMA available for clinical use. Although clinical studies carried out in the period following its general release showed an efficacy similar to that of tricyclic antidepressants (TCA) for treatment of depression it was found less effective than irreversible MAOIs (Lotufo-Neto et al., 1999; Shulman et al., 2013). Another reversible selective MAO-A inhibitor with antidepressant properties is methylene blue (Naylor et al., 1987; Ramsay et al., 2007). This interesting drug has several pharmacological actions, including inhibition of nitric oxidase synthase (NOS), and guanylate cyclase (Harvey et al., 2010), and so its antidepressant properties should not be solely ascribed to inhibition of MAO-A.
Selective Inhibitors of MAO-B in Treatment of Depression and Attention Deficit Hyperactivity Disorder (ADHD)
Following introduction of the irreversible selective MAO-B inhibitor selegiline for treatment of PD (see following sections), its efficacy for treatment of depression was examined in several uncontrolled clinical trials, using the MAO-B-selective dose of 10 mg daily, and as was anticipated following the known involvement of mainly serotonergic and noradrenergic neuronal systems in depression, it was not effective. When examined at the higher doses of 30 or 60 mg daily, however, it did have significant antidepressant effect, especially in treatment-resistant depression (Mann et al., 1989; Sunderland et al., 1994). Based on these positive results a pharmacokinetic strategy was developed (selegiline transdermal system, STS) which permits a greater portion of the administered dose to enter the CNS, and reach tissue levels concomitant with inhibition of both MAO-A and MAO-B while avoiding inactivation of gastro-intestinal and hepatic enzyme (Mawhinney et al., 2003). This technique was developed on the basis of preclinical experiments in guinea-pigs (Mawhinney et al., 2003). In order to understand the mechanism of this relative brain selectivity, it is necessary to understand: (a) that selegiline is only MAO-B selective at low dose, and higher doses will inhibit both MAO-A and MAO-B, and (b) the pharmacokinetics of selegiline (Magyar, 2011). This compound is based on the molecule of R(−)methamphetamine, and following systemic administration it is metabolized by cytochrome P450 enzymes in the liver, mainly to R(−)methamphetamine, R(−)amphetamine, and N-desmethylselegiline (Laine et al., 2000; Azzaro et al., 2007). When administered transdermally the first-pass metabolism is largely avoided, and a larger part of the administered dose directly accesses the brain, and binds irreversibly to both MAO-A and MAO-B. Intact molecules of the drug which leave the brain will be metabolized in the liver, but large scale inhibition of MAO isoforms in gastro-intestinal tract and liver will be avoided (Mawhinney et al., 2003), and the formation of potentially damaging amphetamines is reduced. The success of this strategy has been confirmed in human experiments, in which it was shown: a) that STS is an effective antidepressant, and b) that at antidepressant doses it does not cause cheese effect (Azzaro et al., 2006; Blob et al., 2007). Another dose form of selegiline aimed to produce a similar alteration in pharmacokinetics of the drug is the buccally administered solution (Zydis selegiline) which similarly produces effective antidepressant activity without significant tyramine potentiation (Clarke et al., 2003a,b). Its improved pharmacokinetics permit the use of lower doses which confer greater selectivity for MAO-B over MAO-A inhibition. The MAO-B-selective inhibitor rasagiline has been found effective in treatment of PD depression with a greater response at 2 mg/day than the usual dose of 1 mg/day, possibly because of the greater inhibitory effect on MAO-A at the higher dose (Korchounov et al., 2012).
In preclinical studies in rats, rasagiline administered at selective MAO-B-inhibitory dose did not modify DA, NA or 5-HT levels or induce reserpine reversal (Finberg and Youdim, 2002), however in aged mice, chronic administration of an MAO-B-selective dose (0.2 mg/kg daily for 3 weeks) did increase brain levels of DA and reduce DOPAC, and also showed antidepressant-like effects. Interestingly, the drug returned activity in behavioral paradigms such as learning and forced-swim test, which were reduced in the aged animals, to levels seen in young animals (Weinreb et al., 2015). It is of interest that these effects of rasagiline in aged mice were produced also by chronic administration of its major metabolite 1-aminoindan, at a dose of 5 mg/kg daily over 3 months (Badinter et al., 2015). The authors of these articles suggested that the effects of 1-aminoindan indicate an action on catecholaminergic systems which is not the result of MAO inhibition, because ex vivo brain MAO activity was not inhibited; however since it is a reversible MAO inhibitor (Binda et al., 2005) their ex vivo assay of MAO would not be expected to show a change in enzyme activity, because the drug would be washed out or diluted in the brain homogenate used in their assay. On the other hand, the changes in tissue monoamine levels and their metabolites (Mann et al., 1989) are indicative of an inhibition of MAO.
In a placebo-controlled study of 11 children with ADHD selegiline significantly improved attention but not impulsivity (Akhondzadeh et al., 2003; Niederhofer, 2003; Rubinstein et al., 2006). In three studies in which selegiline was compared with methylphenidate in children with ADHD, the two drugs had similar efficacy (Akhondzadeh et al., 2003; Niederhofer, 2003; Mohammadi et al., 2004). Considering the detrimental pharmacology of amphetamine-like drugs used in ADHD, the use of MAO-B inhibitors in this condition warrants further study. Since MAO-B inhibition markedly increases the brain levels of endogenous PEA (“the body's own amphetamine”), this could be an explanation for the selegiline effects observed in the above studies, in addition to inhibition of DA breakdown.
MAOI and Drug Addiction
Use of MAOI in treatment of depression in cocaine-addicted subjects has been proposed, because chronic cocaine administration reduces the activity of monoamine neurotransmitter systems, which are enhanced by MAOI. In addition, by enhancing DA levels MAOI could possibly be used to substitute for the reward-initiating effect of cocaine (Ho et al., 2009). The potential of MAOI to reduce cocaine-induced reward was studied in mice (Ho et al., 2009). The long-term administration of both selegiline (1 mg/kg i.p. daily for 3 weeks) and pargyline (10 mg/kg i.p. daily for 3 weeks) abolished cocaine-supported operant responses whereas long-term treatment with clorgyline (2 mg/kg i.p. daily for 3 weeks) did not. It should be noted that the doses of selegiline and pargyline used were probably adequate to inhibit both MAO-A and MAO-B, as shown by their reduction of dihydroxyphenylacetic acid (DOPAC) and 5-hydroxyindole acetic acid (5-HIAA) levels in frontal cortex, while clorgyline enhanced 5-HT but did not reduce 5-HIAA levels in frontal cortex. The authors proposed that the use of MAO-B inhibitors to curb cocaine reward should be further considered. In a pilot study in human subjects, 10 mg p.o. selegiline daily reduced cocaine consumption but in a subsequent larger study (300 subjects) transdermal selegiline did not significantly reduce consumption. An additional study with transdermal selegiline reduced cocaine-related scores of anger and tension as well as craving but also did not reduce subjective reported rewarding effects of a higher dose of cocaine compatible with binge use in humans (Elkashef et al., 2006; Harris et al., 2009). Clinical studies have not found evidence of abuse liability in humans (Yasar et al., 1996), and in addition it should be noted that selegiline does not induce addictive behavior in monkeys (Winger et al., 1994).
Pharmaco-Therapy of PD Depression
There are a number of considerations relating to the pharmaco-therapy of PD depression, including the stage of the disease, possible interactions with other medications (especially L-dopa, LD), control of the autonomic nervous system, and the disturbed normal balance between the monoamine systems of the brain. In addition, the possibility of cognitive deficits and PD dementia will confuse the understanding of the patient's affective state. In a meta-analysis of 11 controlled clinical trials for pharmacological treatments in PD depression between the years 2004 and 2014 (Sandoval-Rincon et al., 2015), rasagiline was found effective, but at the dose of 2 mg/day, which is higher than the usual dose of 1 mg daily for PD symptomatology.
Neuroprotective Actions of MAOI
All MAOI possess inherent neuroprotective properties because of their inhibition of H2O2 and toxic aldehyde release following oxidative metabolism of amines, however individual inhibitors may possess an intrinsic neuroprotective action in addition. Selegiline was found by Knoll and co-workers to increase the natural life-span of laboratory rats, and subsequently was found to exert an anti-apoptotic effect in a variety of tissues and cells which was independent of MAO inhibition (Tatton and Chalmers-Redman, 1996). It is important to note that the anti-apoptotic properties of desmethylselegiline (the selegiline metabolite which is the active neuroprotective molecule) are superior to those of selegiline, and that R(−)methamphetamine, the major metabolite of selegiline, antagonizes the neuroprotective property of selegiline and desmethylselegiline (Tatton and Chalmers-Redman, 1996). Subsequently, rasagiline was found to also possess neuroprotective properties both in vivo (Aluf et al., 2013) and in vitro (Finberg et al., 1998; Weinreb et al., 2011). Both these molecules increase BCl2 and PKC-epsilon levels, enhance synthesis and release of BDNF and GDNF, and activate additional anti-apoptotic mechanisms (Jenner and Langston, 2011). It is a current unsolved mystery why these small molecules should exert these complex pro-survival effects. One series of studies produced evidence that selegiline binds to GAPDH and prevents the nuclear translocation of this enzyme (Carlile et al., 2000), however the tricyclic selegiline derivative CGP3466 (Omigapil), which does not inhibit MAO, binds GAPDH and prevents its nuclear translocation, possesses anti-apoptotic activity in vitro and in vivo (Waldmeier et al., 2000) but was not effective in clinical trials for PD and ALS. Rasagiline also prevents the pro-apoptotic nuclear translocation of GAPDH (Maruyama et al., 2001). The rasagiline metabolite 1(R)-aminoindan possesses anti-apoptotic activity (at higher concentrations than the parent molecule), and shows a similar spectrum of biochemical mechanisms as described for rasagiline (Bar-Am et al., 2010), however the presence of the propargyl moiety seems to be an important factor in neuroprotection, since propargylamine itself also possesses anti-apoptotic activity, albeit at higher concentrations than are needed with rasagiline or selegiline (Weinreb et al., 2005).
Compound Molecules with MAO Inhibitory and Neuroprotective Properties
Ladostigil (Weinstock et al., 2000) is a compound molecule consisting of a molecule of rasagiline with the addition of a propylcarbamate moiety, which confers cholinesterase-inhibiting properties. The combination of these two moieties in the same molecule produced a drug with inhibitory properties on both enzymes in vivo, while it is ineffective in vitro. An additional fortuitous aspect of this molecule is that its MAO-inhibitory property is brain-selective, so that the likelihood of cheese effect is small. In rats, an oral dose of 75 μmoles/kg daily for 2 weeks inhibits brain cholinesterase by 40% and brain MAO-A and –B by 70% with no significant inhibition of intestinal or hepatic MAO (Weinstock et al., 2000), while higher doses can produce nearly complete inhibition of brain MAO in several species (Youdim et al., 2005).
The active metabolite of ladostigil responsible for the cholinesterase-inhibitory activity is R-MCPAI (6-(N-methyl carbamyloxy)-1(R)-aminoindan hydrochloride), which is formed from ladostigil by CYP-2C19, while MAO inhibitory activity in vivo is due to the metabolite R-HPAI (6-hydroxy-N-propargyl-1(R)-aminoindan mesylate), since ladostigil itself does not inhibit MAO in vitro. Recently the self-limiting inhibitory effect of ladostigil on cholinesterases (maximal inhibition level is 50–55%) has been studied in mice, and found to be the result of rapid hydrolysis of the complex between R-MCPAI and the enzyme, not by limitation in formation of R-MCPAI (Moradov et al., 2015). A slow rate of conversion of ladostigil to R-HPAI in the intestine prevents significant inhibition of intestinal MAO, although following absorption of the parent molecule it is converted to R-HPAI in the brain but to a lesser extent in other tissues.
The drug was also found to possess a variety of neuroprotective and cognitive effects in animal models (Weinreb et al., 2012). Mechanistic studies showed that ladostigil binds to the VDAC mitochondrial complex, protecting against reduction in mitochondrial potential, and activates alpha-secretase leading to production of the non-amyloidogenic form of soluble APP by a MAP-Kinase dependent mechanism, in a similar way to rasagiline (Yogev-Falach et al., 2002). Ladostigil possesses anti-apoptotic properties against apoptosis induced by the naturally-occurring neurotoxin N-methyl(R)salsolinol and the peroxynitrite-generating molecule SIN-1 in SH-SY5Y cells (Maruyama et al., 2003). It also possesses anti-inflammatory properties as shown by its ability to reduce TNFα levels in mouse spleen and macrophages, following LPS stimulation (Moradov et al., 2015) and reduces the extent of gliosis and memory deficits following streptozotocin-induced lesions of the CNS in rats (Shoham et al., 2007). Ladostigil was tested in old rhesus monkeys for cognitive behavioral effects, and was found to improve attention (Buccafusco et al., 2003). Administered to stressed pregnant rats it corrected the depressive behavior of the male offspring (Goelman et al., 2014). The drug is currently in clinical trial for Mild Cognitive Impairment (MCI).
Additional multi-target inhibitors of MAO have been developed with the aim of incorporating iron-chelating activity together with MAO inhibition (Wang et al., 2014). M30 and VAR10303 are both in development for clinical use in neurodegenerative diseases. These compounds are relatively selective inhibitors of brain as opposed to intestinal and liver MAO, with similar degree of inhibitory activity on MAO-A and MAO-B (Gal et al., 2005; Bar-Am et al., 2015). Unlike ladostigil, M30 (Zheng et al., 2005) has potent MAO inhibitory activity in vitro. The reason for the brain selectivity of these compounds has not yet been determined.
Antiparkinsonian Features of MAO-B Inhibitors
Parkinson's disease (PD) is a neurodegenerative disorder primarily of the nigrostriatal DA-ergic pathway that affects the motor system and results in symptoms including uncontrollable tremor, muscle rigidity, slowness of movement (bradykinesia) and postural instability (Lang and Lozano, 1998a). It is estimated that it affects more than 4 million people worldwide (Schapira et al., 2005), significantly shortens life, and affects quality of life (Lang and Lozano, 1998a,b).
Much effort is being directed to development of new drugs with neuroprotective properties for the treatment of neurodegenerative diseases. Prior to initiating a new drug development, evidence of target engagement is desirable. In the case of putative neuroprotective therapies for PD this is not readily accomplished. There are few targets in the CNS that are associated with a possible pathogenic mechanism and are accessible to drug treatment, although as described above, MAOI have potential neuroprotective properties. Another problem is that existing assessment scales have a limited range and are particularly insensitive to detecting the modest change in movement that occurs in the early stages of the disease. Identification of a validated biomarker would be a significant advance in diagnosis and objective measurement of disease progression and drug efficacy. Recently Moloshnikov and coworkers (Molochnikov et al., 2012) reported a disease signature using blood RNA that detects idiopathic PD with a sensitivity of 90%. This may help to improve the selection of PD patients for clinical trials. The population of PD patients selected for inclusion in clinical trials is also critically important. Patients in early disease stages are frequently selected because they are likely to have a larger number of remaining neurons that can potentially be protected or rescued than patients in advanced stages of the disease (Fearnley and Lees, 1991). In addition, patients in early stages of the disease are generally still untreated which avoids the complication of confounding drug action. There is, however, a greater possibility of inaccurate diagnosis in early disease stage and a higher risk of dropout if patients require treatment. Moreover, disease progression is slower in the early stages of the disease, possibly as a result of more efficient functional compensation (Rascol et al., 2011).
Symptoms of PD are improved with DA–replacement therapies such as DA receptor agonists and LD. Over time, however, the benefit of these drugs fluctuates and patients begin to experience loss of benefit with each dose of LD (wearing–off) and involuntary dyskinesia. In addition some parkinsonian symptoms including disturbances of gait and tremor may be resistant to DA-ergic therapy.
The way in which selective inhibition of MAO-A or MAO-B modifies DA release in vivo was studied in the rat by microdialysis. Initial studies were made by single dose administration using non-selective doses of the MAOI. The first study to employ MAO subtype-selective doses of clorgyline, selegiline, and rasagiline given chronically was carried out by Lamensdorf and colleagues (Lamensdorf et al., 1996). This study showed clearly that all three MAOI could increase striatal extracellular levels of DA when given over 3 weeks, although clorgyline caused the greatest elevation in DA levels. In a later study by the same group (Lamensdorf et al., 1999), a differential effect of selegiline was found to increase expression of the DA transporter (DAT), whereas rasagiline and clorgyline did not. In a follow-up study (Sader-Mazbar et al., 2013), the effect of rasagiline and clorgyline on LD-induced DA levels was studied in rats with a unilateral 6-hydroxydopamine (6-OHDA) lesion of the substantia nigra. This study showed clearly that clorgyline again was the most effective MAOI in causing an increase in DA extracellular levels, although rasagiline also elevated DA levels, in a dose level which was selective for MAO-B inhibition. The superior effect of clorgyline in elevating striatal extracellular DA levels is thought to be the result of inhibition of the neuronal MAO, whereas the effectiveness of MAO-B inhibitors in enhancement of LD-induced DA output in the brain with a lesion of the DA-ergic neurons of substantia nigra is thought to be the result of inhibition of glial cell MAO-B (Carlo et al., 1996).
Inhibition of MAO-B may conserve the depleted synaptic levels of DA, and delay the need for treatment with LD in patients with early-stage PD. In patients with advanced-stage PD who experience fluctuations in response to LD, MAO-B inhibition potentiates and prolongs the effect of LD and permits use of a lower dose (Riederer and Laux, 2011).
Irreversible MAOI selective for type B of the enzyme are among the earliest drugs used in PD. They can be used with or without LD (Riederer and Laux, 2011). Both selegiline and rasagiline are beneficial in treating motor symptoms in PD as monotherapy as well as in combination with LD and a decarboxylase inhibitor. The main differences between the two drugs are related to their metabolism, interaction with cytochrome P450 enzymes and quantitative properties at the molecular biologic/genetic level. Rasagiline is more potent as shown in the daily dose necessary for a symptomatic effect: selegiline 5–10 mg daily and rasagiline 1 mg daily.
Selegiline is a useful treatment for PD symptoms both in monotherapy and as adjunct therapy to LD (Riederer et al., 2004). However, selegiline undergoes first-pass metabolism to R(−)amphetamine and R(−)methamphetamine, which have the potential to cause cardiovascular and CNS adverse effects (Gal et al., 2005). The contribution of these metabolites to selegiline's clinical symptomatic effects (Elsworth et al., 1982) and the possibility of adverse cardiovascular reactions (Churchyard et al., 1997), has often been discussed. R(−)amphetamine has about one-tenth the activity of S(+)-amphetamine on the sympathetic nervous system but the enantiomers are equivalent in antagonism of DA uptake in the striatum (Coyle and Snyder, 1969). One clinical study in which the effects of 10 mg of selegiline were compared with equivalent doses of R(−)-amphetamine and R(−)-methamphetamine concluded that only selegiline, and not its metabolites, possesses antiakinetic efficacy in Parkinsonian patients (Elsworth et al., 1982). Moreover, from documentation of side effects in the large clinical trials of selegiline there is no evidence for enhanced cardiovascular risk (Parkinson Study Group, 1989, 1993), as is true also when selegiline is compared to treatment based on LD and DA receptor agonists; however these drugs have never been studied in head-to-head comparison. Long term trials have shown that 30–40% of the daily LD dose can be reduced when the drug is combined with selegiline (Birkmayer et al., 1975; Myllyla et al., 1997). One interesting hypothesis about the good beneficial effect of MAO-B inhibitors is that PEA, which increases in brain after selegiline treatment (Reynolds et al., 1978), may have DA release-promoting activity and by this way contribute to the positive effects on motor features and behavior.
In 1989 Tetrud and Langston published a clinical study based on the discovery that selegiline blocked the development of MPTP-induced parkinsonism in laboratory animals, in which they showed that in 22 PD patients medicated with selegiline and 22 who received placebo the necessity to add LD (rescue drug) occurred in the placebo group after 312.1 days and in the selegiline group after 548.9 days (Tetrud and Langston, 1989). In the DATATOP (Deprenyl and Tocopherol Antioxidative Treatment of Parkinsonism) publications (Parkinson Study Group, 1989, 1993) after 12 months of monotherapy with selegiline or placebo (800 patients), 47% in the placebo group had commenced LD therapy while in the selegiline group only 26%. In addition it is important to mention that in the placebo group the median length of time before patients needed LD was 454 days and in the selegiline group 719 days. In selegiline-treated patients the need for addition of LD therapy was postponed by ~9 months.
Shoulson et al. (2002) published interesting data concerning long term follow up (7 years) of patients in the DATATOP group treated with LD and selegiline, as well as those who received placebo after 3–5 years treatment with selegiline. The conclusions revealed that the wearing-off phenomenon did not improve in the selegiline-treated patients but these patients had less on-off phenomenon or freezing of gait and better motor features with lower total UPDRS (Unified Parkinson's Disease Rating Scores) score. Activities of daily living (ADL), motor scores, LD dosages and use of DA agonists were significantly reduced in the selegiline groups. On the other hand, patients in the placebo group had less dyskinesias than those on selegiline.
It is important to note that, in DATATOP and its extension study it was impossible to distinguish between potential disease–modifying (i.e., neuroprotective) and symptomatic benefits of treatment (Parkinson Study Group, 1996a,b, 1989, 1993; Shoulson et al., 2002). In another study (SELEDO), Przuntek et al. (1999) showed that the length of time in which PD patients treated with selegiline required an increase of 50% in LD dose was 4.9 years, while in placebo-treated patients it was 2.6 years. Myllyla et al. (1992, 1997) reported similar results.
The DATATOP results along with other earlier studies demonstrated a modest symptomatic benefit with selegiline with no significant difference between selegiline and placebo in the occurrence of cardiovascular and other serious adverse events. Long-term post-marketing data, however, have revealed that orthostatic hypotension and hallucinations are seen frequently in selegiline-treated patients, mainly in combination with LD (Perez-Lloret et al., 2013).
A trial in 782 PD patients by the Parkinson's Disease Research Group of the United Kingdom (Lees, 1995; Ben-Shlomo et al., 1998) concluded that the addition of selegiline to ongoing LD therapy provided no additional clinical benefit but was associated with increased motor complications and increased mortality. A follow-up study from the same group examined postural hypotension in a sub-group of patients and found that in 8 out of 22 patients postural hypotension was exacerbated when on selegiline, and this effect was abolished following withdrawal of the drug (Churchyard et al., 1999). When experts who did not participate in the study analyzed the results (Olanow et al., 1998) they found that the conclusions reported were not correct and in fact there was no increase in mortality with selegiline treatment whether administered alone or in combination with LD (Olanow et al., 1998). Considering selegiline treatment in randomized studies it is important to mention a 157-patient, randomized controlled Swedish study of selegiline long-term effects when used in early PD either as monotherapy or in combination with LD. This trial showed that at 7 years, selegiline-treated patients had slower disease progression than their counterparts as measured with UPDRS score. This outcome was observed in the selegiline monotherapy PD patients as well as in those treated in addition with LD (Palhagen et al., 2006), however also in this study, the symptomatic effect of selegiline precludes drawing conclusions about disease modification.
In general, summarizing most of the reports selegiline is well tolerated. Side effects/adverse effects like nausea, vomiting, sleeplessness, dry mouth, orthostatic hypotension and dyskinesias have all been observed in the range of 2–5% of PD patients (Parkinson Study Group, 1993; Reichmann et al., 2000) which is comparable to placebo. Other side effects like headaches, palpitations, dyspneas, confusion, edema, micturition dysfunction, loss of appetite and anxiety have an incidence below 2% (Reichmann et al., 2000).
Waters et al (Waters et al., 2004) examined the effect of Zydis selegiline in a 3 month, randomized, placebo-controlled study in PD patients experiencing motor fluctuations in response to LD and found that it reduced off time by 2.2 h (compared with 0.6 h in the placebo group), without any increase in drug-related adverse events.
Rasagiline is a potent, selective, irreversible inhibitor of MAO-B and in contrast to selegiline has no amphetamine-like metabolites (Finberg et al., 1999). Given in disease models relevant to PD (Bar-Am et al., 2010), rasagiline showed good antiparkinsonian and motor restoration activity as well as neuroprotection properties, and its major metabolite 1-aminoindan is also neuroprotective (see above section on Neuroprotection).
In a 10 week, randomized placebo-controlled pilot (phase 2) trial of rasagiline in patients with early, untreated PD, a dose of up to 4 mg/day was well tolerated. There were no cases of hypertension, bradycardia or other cardiovascular adverse experiences (Marek et al., 1997). One of the early randomized clinical studies comparing rasagiline vs. placebo for advanced PD patients was published in 2000 (Rabey et al., 2000). In this study researchers planned to evaluate the safety, tolerability and clinical effect of rasagiline as adjunct therapy with LD, in a multicenter, double blind, placebo-controlled parallel group study (0.5, 1, and 2 mg/day) lasting 12 weeks, in 70 patients with PD (mean age 57.4 years, mean disease duration 5.7 years; 32 patients had motor fluctuations). A beneficial clinical effect was observed in fluctuating patients treated with rasagiline (all doses) and was expressed as a decrease in total UPDRS score (by 23% in rasagiline-, 8.5% in placebo-treated subjects). The anti-Parkinsonian effect of rasagiline was still evident 6 weeks after stopping treatment at all dose levels. The incidence of adverse effects with rasagiline was similar to those on placebo. Determination of platelet MAO activity (MAO-B) showed nearly complete MAO-B inhibition at all rasagiline dose levels. This study showed that rasagiline (up to 2 mg/day) is well-tolerated and has a beneficial clinical effect in fluctuating patients with PD when given together with chronic LD therapy.
In the TEMPO (Rasagiline mesylate in Early Monotherapy for Parkinson's disease Outpatients) study (Parkinson Study Group, 2002), 404 de novo (untreated) PD patients received either placebo (n = 138), rasagiline 1 mg per day (n = 134) or rasagiline 2 mg per day (n = 132) for 26 weeks. All the patients receiving rasagiline showed statistically significant improvement compared with placebo in the mean change from baseline of the Unified Parkinsons's Disease Rating Scale (UPDRS part I-III) by 4.2 and 3.6 points, in 1 and 2 mg/day groups respectively. Patients on rasagiline showed also a significant and beneficial effect for quality of life as assessed by the Parkinson's Disease Quality of Life (PD-QUALIF) scale.
Considering the results of preclinical studies which suggested that rasagiline may modify the progression of PD (Maruyama et al., 2001; Akao et al., 2002), the TEMPO study was extended into a delayed start trial comparing the effects of early and later initiation of rasagiline on disease progression (Parkinson Study Group, 2004). Three hundred seventy–one subjects from the TEMPO study were included in the 1-year efficacy analysis. Patients who had received rasagiline 1 or 2 mg/day for 6 months received the same dose for a further 6 months, while those who had been treated with placebo for 6 months were given rasagiline 2 mg/day for a further 6 months. This design was adopted in order to compensate for the symptomatic effect of rasagiline, which prevented concluding that the drug had a disease-modifying action when rasagiline-treated patients were compared with those treated with placebo. In this delayed-start trial, it was possible to compare patients who had received rasagiline 2 mg/day for 12 months with those who had received this dose for only 6 months, but all were receiving the drug at the time of neurological assessment at 12 months from start. The result of this trial was that patients who had received rasagiline 2 mg/day for 12 months had a 2.29-unit smaller increase in UPDRS score than those who were treated with rasagiline 2 mg/day for 6 months (P = 0.01). This delayed-start analysis suggested that rasagiline could have a disease-modifying activity.
The ability of rasagiline to improve LD response in more advanced PD patients with motor fluctuations was studied in LARGO (Lasting effect in Adjunct therapy with Rasagiline Given Once daily) (Rascol et al., 2005). In this study 231 individuals, received rasagiline (1 mg daily), 229 received placebo, and 227 received entacapone (200 mg daily). All were treated with LD and a decarboxylase inhibitor. The primary outcome was change in total daily off-time. Other measures included the (CGI) score and the UPDRS scores. Both rasagiline and entacapone reduced mean daily off-time (−1.18 h rasagiline and −1.2 h entacapone vs. placebo −0.4). A significant improvement in clinical global improvement (CGI) scores, and activities of daily living during off-time and motor function during on time was seen with both rasagiline and entacapone. Adverse effects were similar in all groups.
To date the majority of PD clinical studies conducted in patients with motor fluctuations have reported the duration of OFF time during the day with limited evaluation of the severity of PD symptoms during ON time. The irreversible nature of the binding of rasagiline to the essential cofactor of the active site of the MAO-B enzyme means that the duration of its therapeutic action is independent of the drug's half-life and is instead determined by the regeneration rate of MAO-B (Thebault et al., 2004). The Largo study included a subgroup of patients, “UPDRS motor OFF substudy,” for which there was a separate informed consent form. Patients included in this sub-study, were receiving optimum LD + decarboxylase inhibitor therapy, were stable for at least 14 days before study start, and experienced motor fluctuations in which they were in OFF state for at least 1 h every day not including morning akinesia. Additional antiparkinsonian therapy was accepted, with the exception of selegiline, tolcapone and previous treatment with entacapone. At the start of the 18 weeks study patients were randomly assigned to receive placebo, rasagiline 1 mg or entacapone 200 mg in addition to LD and decarboxylase inhibitor. The LD dose could be reduced during the first 6 weeks if dyskinesia worsened. Thereafter the LD dose remained the same for the final 12 weeks of the study (Stocchi and Rabey, 2011). Treatment with rasagiline produced a significant improvement over placebo of 5.64 units in UPDRS motor OFF score (P = 0.013 vs. placebo). By contrast the effect of adjunct entacapone was not significant (P = 0.14 vs. placebo). Retrospective analysis using the Bonferroni correction of UPDRS motor subdomains further revealed that rasagiline but not entacapone, significantly improved bradykinesia (p < 0.001) and showed a trend for improvement in facial expression, speech and axial impairment during OFF time.
In Olanow et al. (2009) conducted a double blind study, with early and delayed start rasagiline (Attenuation of Disease Progression with Rasagiline Given Once-daily, ADAGIO), in order to establish more substantially whether this drug has disease-modifying effect in PD. A total of 1091 untreated PD patients participated in the start of the study; 273 early start rasagiline 1 mg/day, 270 delayed start rasagiline 1 mg/day, 273 early start rasagiline 2 mg/day, and 275 delayed start rasagiline 2 mg/daily. The early start group received the drug for 72 weeks, the delayed start group received placebo for 36 weeks followed by rasagiline for a further 36 weeks.
The putative result required for disease-modification is shown diagrammatically in Figure 1
Figure 1. Schematic of ADAGIO delayed start neuroprotection trial of rasagiline. Treatment with placebo (delayed start group) or rasagiline (early start group) was commenced at time 0. At week 36, the placebo group was changed to rasagiline, and the rasagiline group continued with rasagiline. Adapted from Olanow et al. (2009).
Three endpoints were required to be met in order to permit a positive result: (a) increased slope of the decline in UPDRS in the placebo group with respect to the rasagiline group in the first phase of the study (i.e., week 12–36); (b) a difference between the early- and delayed-start groups in the change in UPDRS score between weeks 12 and 72, and (c) similarity of the slopes of change in UPDRS score with time in the period between weeks 48 and 72. Finite values of UPDRS were fixed for the three endpoints. The conclusions of the study were: “Early treatment with rasagiline at a dose of 1 mg per day provided benefits that were consistent with a possible disease-modifying effect, but early treatment with rasagiline at a dose of 2 mg per day did not. Because the two doses were associated with different outcomes, the study results must be interpreted with caution” (Churchyard et al., 1999).
Following publication of the Adagio results, there has been much discussion about the significance of the data. Rascol et al. published in 2011 a secondary and post-hoc comment on the ADAGIO study (Rascol et al., 2011). In addition to the criterion of UPDRS score, they included changes in non-motor experiences of daily living (ADL), fatigue scales, the need for additional antiparkinsonian therapy, and (UPDRS) subscores, in the data assessment. In addition to the finding that rasagiline therapy delayed the need for additional antiparkinsonian drugs, and improved ADL scores in the 1 mg/daily early start group, they showed that the rate of deterioration in UPDRS scores correlated with baseline scores, patients with low baseline scores deteriorating slower than those with higher baseline scores. A difference in the distribution of low and high baseline UPDRS scores between the 1 and 2 mg daily groups could have contributed to the lack of difference between early and late start groups at the 2 mg dose level.
In 2014, Jankovic et al. (2014) published another post-hoc analysis from the ADAGIO study in which they examined the responses of patients to rasagiline 1 mg/day (n = 288) with those to placebo (n = 588) on key motor symptoms at 36 weeks. In the rasagiline group, significantly better tremor, bradykinesia, rigidity and postural-instability-gait difficulty scores were seen at week 36 by comparison with placebo. While the placebo group deteriorated from baseline by 2.6 points UPDRS at week 36, patients in the rasagiline group improved initially but then returned to baseline values at week 36. At week 72 patients who had received continuous monotherapy with rasagiline experienced a worsening of only 1.6 points. The conclusions of this analysis were that treatment with rasagiline maintained motor function at baseline values for at least a year with significant benefit observed in all key PD motor symptoms.
Safinamide, an orally active alpha-aminoamide derivative, is a novel reversible and highly selective MAO-B inhibitor which is efficacious as add-on therapy to DA agonists in early-stage PD (Stocchi et al., 2004, 2012) and as adjunct to LD in mid- to late-stage PD (Borgohain et al., 2014). In addition to MAO inhibition, the molecule possesses additional pharmacological properties, including state-dependent blockade of voltage-gated sodium and calcium channels, and inhibition of glutamate release in rat hippocampal synaptosomes (Caccia et al., 2006; Stocchi et al., 2006). These properties may be responsible for its demonstrated neuroprotective effect in laboratory animals.
The use of safinamide as adjunct therapy to LD was investigated in mid- to late-stage PD patients with motor fluctuations (Waters et al., 2004). In an initial 6 month trial, safinamide 50 mg (n = 197) or 100 mg (n = 195) daily was studied in relation to placebo (n = 197) and was found to significantly increase ON time without increasing dyskinesia. The study was then continued in the same patient population for an additional 18 months. In the final evaluation of the 2 year period, both safinamide groups had a significant increase in ON-time compared to placebo, which was maintained over the period between 24 and 102 weeks. A non-significant reduction in Dyskinesia Rating Score (DRS) was found for both safinamide groups, but in considering this result, 74% of the population had no to mild dyskinesia at baseline. In the case of the sub-group with more severe dyskinesia (DRS > 4, 36% of the population), safinamide caused a reduction in DRS in relation to placebo, which was significant (P = 0.0317) at the 100 mg daily dose level. Other benefits noted by the investigators in the safinamide group included improvements in ADL, depression, clinical status and quality of life (Borgohain et al., 2014). In an efficacy study reported by Schapira et al. (2013) patients received 100 mg, 200 mg safinamide or placebo added to LD, or DA agonists. In their study the conclusions were that the safinamide group did not attain the primary endpoint of increase in time required for additional drug therapy, however post hoc analysis showed that safinamide was effective in PD therapy in combination with DA agonists.
A number of research groups are aiming to develop other MAO-A and MAO-B reversible inhibitors. A series of chalcone derivatives with reversible MAO-A and MAO-B selective properties was recently described (Minders et al., 2015). The IC50 of the most potent MAO-B inhibitor in this series was 0.067 μM, by comparison with 0.098 μM for safinamide. Further data on in vivo metabolism and efficacy will be required to see whether this compound has therapeutic potential.
Today there is a broad spectrum of therapeutic possibilities for the utilization of MAO-A and -B inhibitors, for the management of PD, and also for the treatment of depression. Novel routes of administration, as well as pro-drugs which are converted to active inhibitors by brain enzymes, are promising directions for development of MAOI with selective action in the brain in order to avoid cheese effect. New drug developments which combine different types of activity in the same molecule, and can possibly be effective in more than one disease condition, may be useful in treatment of both neuropsychiatric and neurological disorders, and mechanism-based drug combinations may improve efficacy in PD and other diseases
JF: Initiated this review, contributed introductory section, mechanisms and section on psychiatric uses, reviewed and submitted article; JR: Contributed section on Parkinson's Disease.
Conflict of Interest Statement
JF was a co-developer of rasagiline and receives financial gain from sales of this drug. Such financial gain did not in any way influence the thoughts and opinions expressed in this article.
The other author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: rasagiline, selegiline, safinamide, depression, Parkinson's disease
Citation: Finberg JPM and Rabey JM (2016) Inhibitors of MAO-A and MAO-B in Psychiatry and Neurology. Front. Pharmacol. 7:340. doi: 10.3389/fphar.2016.00340
Received: 13 May 2016; Accepted: 12 September 2016;
Published: 18 October 2016.
Edited by:Rona R. Ramsay, University of St. Andrews, UK
Reviewed by:Angela J. Grippo, Northern Illinois University, USA
Ken Gillman, PsychoTropical, Australia
Copyright © 2016 Finberg and Rabey. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: John P. M. Finberg, email@example.com