Centrality of striatal cholinergic transmission in basal ganglia function
- 1 Laboratory of Neurophysiology and Plasticity, Fondazione Santa Lucia IRCCS, Rome, Italy
- 2 Department of Neuroscience, University Tor Vergata, Rome, Italy
Work over the past two decades revealed a previously unexpected role for striatal cholinergic interneurons in the context of basal ganglia function. The recognition that these interneurons are essential in synaptic plasticity and motor learning represents a significant step ahead in deciphering how the striatum processes cortical inputs, and why pathological circumstances cause motor dysfunction. Loss of the reciprocal modulation between dopaminergic inputs and the intrinsic cholinergic innervation within the striatum appears to be the trigger for pathophysiological changes occurring in basal ganglia disorders. Accordingly, there is now compelling evidence showing profound changes in cholinergic markers in these disorders, in particular Parkinson’s disease and dystonia. Based on converging experimental and clinical evidence, we provide an overview of the role of striatal cholinergic transmission in physiological and pathological conditions, in the context of the pathogenesis of movement disorders.
The basal ganglia include different interconnected subcortical nuclei that are involved in serving critical motivation, motor planning, and procedural learning function (Graybiel et al., 1994; Yin and Knowlton, 2006; Nicola, 2007; Kreitzer and Malenka, 2008). The striatum represents the main input nucleus of the basal ganglia. It receives excitatory afferents from the cortex and thalamus, and is densely innervated by midbrain dopamine neurons (Bolam et al., 2000; Kreitzer and Malenka, 2008).
The large majority of striatal neurons are GABAergic. Most of these GABAergic neurons are represented by medium spiny projection neurons (MSNs; Izzo et al., 1987). At least three types of GABAergic interneurons have been identified, according to their electrophysiological and neurochemical properties. GABAergic interneurons may colocalize with the calcium-binding proteins parvalbumin or calretinin, or neuropeptide Y, somatostatin, and NADPH diaphorase (Kawaguchi, 1993; Tepper and Bolam, 2004). Accordingly, they have been classified, respectively, as fast-spiking (FS) neurons, persistent and low-threshold spike (PLTS) neurons, or low-threshold spike (LTS) neurons (Kawaguchi et al., 1989; Tepper and Bolam, 2004). A recent study has characterized an additional group of GABAergic interneurons, expressing tyrosine hydroxylase (TH+), which have been electrophysiologically classified into four distinct types (Tepper et al., 2010). Indeed, the existence of TH+ neurons in the striatum of rodents and primates had been reported since the late 1980s (for review, see Ibáñez-Sandoval et al., 2010).
In addition to the numerically prevailing population of GABAergic neurons, the striatum also contains a small percentage of interneurons which provide this area with one of the highest acetylcholine (ACh) levels in the brain (Graybiel, 1990; Mesulam et al., 1992; Contant et al., 1996). These are the large aspiny cholinergic interneurons (ChIs) characterized by dense local axonal arborizations, and by tonic firing activity (Bolam et al., 1984; Wilson et al., 1990; Kawaguchi, 1993; Aosaki et al., 1995; Bennett and Wilson, 1998; Bennett et al., 2000; Zhou et al., 2002).
It has long been known that striatal ChIs play a central role in the basal ganglia circuitry both in the control of voluntary movements and in the pathophysiology of movement disorders, such as Parkinson’s disease (PD), and dystonia (Pisani et al., 2003a, 2007; Aosaki et al., 2010). Indeed, anticholinergic drugs have long been a first choice therapy for PD and dystonia (Duvoisin, 1967; Jankovic, 2006). Here, in light of the most recent findings, we will review the role of ChIs in striatal function and in the pathogenesis of basal ganglia disorders.
Morphological and Electrophysiological Properties of Cholinergic Interneurons
Large aspiny ChIs represent less than 2% of the entire striatal neuronal population. Their neurochemical identification is due to the expression of ChAT, the biosynthetic enzyme for ACh. Morphologically (Figures 1A,B), they are characterized by a large polygonal soma (Ø 20–50 μm), widespread dendritic and axonal fields (Bolam et al., 1984; Smith and Bolam, 1990; Wilson et al., 1990), and a preferential distribution in the matrix area flanking the patches border (van Vulpen and van der Kooy, 1998). These features suggest that ChIs may integrate synaptic inputs over relatively large regions, and act as an associative interneuron in the striatum (Kawaguchi et al., 1995; Miura et al., 2007).
Figure 1. Morphological and electrophysiological properties of striatal cholinergic interneurons. (A) Infrared differential interference contrast image of a cholinergic interneuron in a striatal slice showing the peculiar polygonal shape and large somatic size of this neuronal subtype. (B) Confocal microscope image of a biocytin-loaded cholinergic interneuron. The cell was loaded with 2% biocytin by means of the recording electrode during an electrophysiological experiment. Note the absence of spines along the dendrites. (C) Representative current-clamp recording of the I–V relationship. The arrowhead indicates the prominent Ih evoked by hyperpolarizing current injection. (D) Spontaneous firing activity of a cholinergic interneuron. The inset on the right (gray) shows a single action potential, followed by a prominent AHP (arrow). (E) Table summarizing the main electrophysiological properties characterizing striatal cholinergic interneurons. Data are presented as mean ± SEM; n = 5.
In vitro electrophysiological recordings have described the peculiar membrane properties of ChIs, that distinguish these neurons from all other striatal neuronal subtypes (Figures 1C–E). These include a relatively depolarized resting membrane potential, long-lasting action potential, high input resistance, prominent afterhyperpolarization (AHP) current, and hyperpolarization-activated cation current (Ih; Bolam et al., 1984; Wilson et al., 1990; Kawaguchi, 1993; Aosaki et al., 1995; Bennett and Wilson, 1998; Bennett et al., 2000; Zhou et al., 2002).
These cells are autonomously active, showing a range of spontaneous tonic firing patterns, from irregular single spiking to rhythmic bursting, even in the absence of synaptic input, suggesting that they are intrinsic in origin (Bennett and Wilson, 1999; Bennett et al., 2000; Goldberg and Wilson, 2005; Wilson, 2005; Wilson and Goldberg, 2006; Goldberg et al., 2009). The prevalence of a spiking pattern in any single neuron was shown to be dependent on the underlying Ca2+-activated K+ conductances. In particular, single spiking depends on a medium-duration AHP (mAHP) current generated by rapid SK currents, which are associated with high-voltage-activated (HVA) CaV2.2 Ca2+ channels. On the other hand, periodic bursting is driven by a delayed and slowly decaying AHP (sAHP) current, associated with CaV1 Ca2+ channels (Bennett et al., 2000; Goldberg and Wilson, 2005; Wilson and Goldberg, 2006). The specific association between HVA Ca2+ channel subtypes and the K+ currents underlying the mAHP and sAHP currents is generated by the dynamics of Ca2+ redistribution among cytoplasmic binding sites with different binding kinetics (Goldberg et al., 2009).
Striatal ChIs are recipients of a prominent glutamatergic drive from both the cortex and the centromedian and parafascicular (Cm–Pf) thalamic nuclei (Lapper and Bolam, 1992; Sidibe and Smith, 1999; Thomas et al., 2000), as well as of an extensive dopaminergic innervation from the substantia nigra pars compacta (Olson et al., 1972; Lavoie et al., 1989; Dimova et al., 1993; Smith and Villalba, 2008).
The predominant effect of dopamine on ChIs is mediated by activation of D2-like D2 receptors (Figure 2), which inhibit striatal ACh efflux (DeBoer et al., 1996), by reducing both autonomous action potential firing and synaptic inputs to ChIs. The former effect is achieved by enhancing the slow inactivation of voltage-dependent Na+ channels (Maurice et al., 2004) and by modulating Ih current (Deng et al., 2007). The reduction of synaptic inputs is achieved through inhibition of HVA Ca2+ channel (Yan and Surmeier, 1996; Pisani et al., 2000).
Figure 2. Cholinergic control of striatal medium spiny neuron activity. Simplified cartoon of the striatal circuitry reporting the distribution of muscarinic and nicotinic receptors. Cholinergic receptors regulate the activity of medium spiny neurons both at the postsynaptic level, and presynaptically, by modulating glutamate, dopamine, and acetylcholine neurotransmission.
In addition, striatal ChIs express D1-like D5 subtype receptors (Figure 2; Bergson et al., 1995; Yan and Surmeier, 1997), which are mainly somatodendritic and depolarize the cell by promoting the non-selective opening of cation channels and the closure of K+ channels, thus, in turn, enhancing ACh release (Damsma et al., 1990; Imperato et al., 1993; DeBoer and Abercrombie, 1996; Aosaki et al., 1998; Pisani et al., 2000).
An additional level of control of striatal ACh release is represented by M2/M4 muscarinic autoreceptors (Figure 2). Autoreceptor activation reduces ACh release by closing CaV2 Ca2+ channels which mediate exocytosis, and by increasing opening of Kir3 potassium channels, which hyperpolarize terminals and further reduce Ca2+ channel opening (Yan and Surmeier, 1996; Calabresi et al., 1998b).
Furthermore, ChIs receive extrinsic excitatory serotonergic (Lavoie et al., 1989; Bonsi et al., 2007) and noradrenergic afferents (Pazos et al., 1985; Pisani et al., 2003b), and an intrinsic inhibitory GABAergic innervation from both MSNs and FS interneurons (Bolam et al., 1986; Martone et al., 1992; Aosaki et al., 2010).
Postsynaptic potentials evoked by electrical stimulation of fibers innervating ChIs are mediated by activation of ionotropic NMDA, AMPA, and GABAA receptors. Upon complete inhibition of both the glutamatergic and GABAergic synaptic components, a slow inhibitory synaptic potential is unmasked, which is mediated by a K+ conductance activated by M2-like receptors (Calabresi et al., 1998b).
The activity of striatal ChIs is therefore highly regulated, through a complex interaction between intrinsic properties and the neuromodulatory control exerted by several transmitters.
Origin of the Pause Response in Chi Tonic Firing Activity
Striatal ChIs exhibit a variety of spontaneous firing patterns also during in vivo recordings (Wilson et al., 1990; Reynolds et al., 2004). Indeed, these neurons correspond to the tonically active neurons (TANs) recorded in vivo from the primate striatum, which respond with a pause in their ongoing firing activity to reward-related stimuli (Apicella et al., 1991, 1998; Aosaki et al., 1994; ). Several mechanisms are likely to contribute to this pause response, through the modulation of both intrinsic and synaptic properties of ChIs. It has been suggested that these pauses in firing may be due to AHP currents intrinsically generated via Ih transient deactivation following cortical excitatory synaptic inputs (Reynolds et al., 2004; Oswald et al., 2009). Of interest, Ih is regulated by dopamine (Deng et al., 2007). In fact, it is known that synaptic inputs arising both from the dopaminergic nigrostriatal system and from thalamic nuclei involved in sensorimotor integration modulate the responsiveness of these neurons to reward-related stimuli (Aosaki et al., 1994; Matsumoto et al., 2001). High-frequency stimulation (HFS) of the substantia nigra during in vivo recordings increases the AHP (Reynolds et al., 2004). Similarly, in neurons exhibiting regular firing in vitro exogenous application of dopamine causes a prolongation of a depolarization-induced pause and an increase in the duration of sAHP (Deng et al., 2007). Recent in vitro experimental evidence shed further light on the origin of the pause response in striatal ChIs (Ding et al., 2010). This report showed that high-frequency thalamic stimulation elicits an initial burst followed by a pause in the firing activity of ChIs. Both D2 dopamine and nicotinic ACh (nACh) receptors were shown to be involved in this response. These data suggest that the biphasic response to thalamic stimulation might be driven by the initial excitation of ChIs, which induces ACh release and activation of presynaptic nACh receptors located on dopaminergic terminals (Figure 2); hence the stimulation of dopamine release and D2 receptor activation, which prolongs the AHP by inhibiting Ih and Na+ channel currents (Aosaki et al., 2010).
Striatal ChIs have been shown, both in vivo and in vitro, to undergo long-term plastic changes of synaptic efficacy, which might lastingly influence the pattern of firing activity (Suzuki et al., 2001b; Bonsi et al., 2004; Reynolds et al., 2004; Fino et al., 2008). In slice preparations HFS of glutamatergic afferent fibers induces a long-term potentiation (LTP) of both the AMPA-mediated excitatory and GABAergic inhibitory postsynaptic potentials, which is dependent on D5 receptor activation, and on a critical level of intracellular Ca2+ rise through CaV1 channels (Suzuki et al., 2001b; Bonsi et al., 2004). Interestingly, intracellular recordings of ChIs from striatal slices of rats that have learned a rewarded, externally cued sensorimotor task show an increase in spontaneous GABAA-mediated synaptic activity with respect to untrained animals (Bonsi et al., 2003), further suggesting a role for GABAergic transmission in the generation of the pause response. More recently, spike-timing-dependent plasticity (STDP) protocols were shown to induce bidirectional long-term plasticity in ChIs (Fino et al., 2008). STDP–LTP was mainly presynaptic and involved NMDA-receptor activation, while long-term depression (STDP–LTD) had a postsynaptic origin and involved metabotropic glutamate receptors.
Thus, it is plausible that long-term changes of both glutamatergic and GABAergic synaptic potential amplitude are also involved in the generation of the firing activity pattern (Aosaki et al., 2010).
The pattern of spiking and pauses of ChIs is able to filter the striatal output, by directly and indirectly influencing MSN activity (Phelps et al., 1985; Izzo and Bolam, 1988; Chang and Kita, 1992; Wang et al., 2006; Pakhotin and Bracci, 2007; Bonsi et al., 2008). There is experimental evidence indicating that the pauses in ChIs activity might powerfully enhance the salience of dopamine signaling (Threlfell et al., 2010) and transform the reward signal arising from dopaminergic neurons into a gating signal for LTD induction at MSNs (Wang et al., 2006). Further, the thalamic-induced burst-pause response of ChIs might provide a neural substrate for attentional shift and cessation of ongoing motor activity (Ding et al., 2010). Indeed, the patterned activity of ChIs has been suggested to differentially gate the cortical drive to striatopallidal and striatonigral MSNs. Upon thalamic stimulation, the initial burst response of ChIs triggers the transient suppression of cortical inputs to MSNs, through presynaptic muscarinic M2-class receptor activation, but also initiate a slower, muscarinic M1 receptor-dependent postsynaptic facilitation of striatopallidal MSNs. This facilitation extends during the pause response, when the cortical drive resumes, thus creating a late temporal window when the corticostriatal input can selectively drive activity in the striatopallidal network thought to control action suppression (Ding et al., 2010).
Muscarinic and Nicotinic Modulation of MSN Activity
A very dense cholinergic innervation of the striatum arises from intrinsic ChIs. By tonically firing action potentials at about 5 Hz, these interneurons provide an ongoing ACh signal, that is rapidly terminated by acetylcholinesterase (AChE). ACh may act both at synaptic sites, predominantly onto distal dendrites and spine necks (Bolam et al., 1984; Phelps et al., 1985), and via volume transmission (Descarries et al., 1997; Koos and Tepper, 2002).
In the striatum, different subtypes of nACh receptors have been identified, containing a combination of the α4, α6, α7, and β2, β3 subunits (Wada et al., 1989; Seguela et al., 1993; for review, see Quik et al., 2007). In addition, both M1-like and M2-like muscarinic ACh (mACh) receptors, predominantly the M1 and M4 subtypes, are expressed at high density (Figure 2).
In MSNs, M1 receptor activation enhances NMDA-receptor-mediated currents, promoting cell depolarization and corticostriatal LTP (Calabresi et al., 2000), and increases the synchrony in the NMDA-induced network dynamics, via enhancement of persistent Na+ current (Carrillo-Reid et al., 2009). In addition, M1 receptors modulate HVA Ca2+ currents (Howe and Surmeier, 1995; Galarraga et al., 1999; Olson et al., 2005; Perez-Rosello et al., 2005; Perez-Burgos et al., 2008, 2010). Recently, M1 receptor activation has been suggested to have cell-specific effects on striatopallidal vs. striatonigral MSNs, due to specific characteristics of the downstream effectors (Chen et al., 2006; Shen et al., 2007; Day et al., 2008).
In addition to direct postsynaptic effects on MSNs, presynaptic ACh receptors regulate both glutamate and GABA release from striatal afferents. While mACh receptors inhibit neurotransmitter release, presynaptic nACh receptors exert the opposite effect (Calabresi et al., 1998a; Koos and Tepper, 2002; Zhou et al., 2002; Grilli et al., 2009; McClure-Begley et al., 2009).
The autonomous activity of ChIs ensures a sufficient level of endogenous ACh to tonically activate mACh and nACh receptors, thereby constantly influencing striatal activity. Through mACh receptor activation, ACh provides a presynaptic inhibitory tone on the excitatory glutamatergic drive onto MSNs (Pakhotin and Bracci, 2007). Indeed, a single spike in a ChI is able to induce a significant mACh receptor-mediated depression of glutamatergic synaptic currents in a MSN. However, a mechanism to limit this powerful inhibitory control of ChIs over the glutamatergic input to MSNs has been recently proposed to reside in the nicotinic excitation of striatal GABAergic interneurons (Sullivan et al., 2008).
Overall, nACh and mACh receptors would act to translate the pattern of the ongoing cholinergic activity into a strong influence over striatal output (Koos and Tepper, 2002): nACh receptor activation would rapidly affect the activity of MSNs, while the muscarinic impact might become more evident on a slower time scale, and in particular when additional extrasynaptic volume transmission extends the duration of the ACh signal, such as during periods of more intense cholinergic activity (Singer et al., 2002).
Striatal Acetylcholine and Synaptic Plasticity
Enduring changes in synaptic efficacy at corticostriatal synapses are viewed as the cellular basis underlying motor learning and associative memory processes. HFS of corticostriatal afferents may induce either LTD or LTP at MSN synapses, depending on a variety of cell-specific mechanisms (Calabresi et al., 1992; Lovinger et al., 1993; Surmeier et al., 2009). Induction of LTD and LTP requires an intact nigrostriatal projection, and depends upon both dopamine and ionotropic glutamate receptor subtypes involved (Lovinger, 2010). Complex biochemical processes follow the activation of glutamatergic and dopaminergic receptors and their mutual interplay (Calabresi et al., 1994; Gerdeman et al., 2002).
M1 mACh receptors are abundantly expressed on dendrites and spines of MSNs (Figure 2), and are therefore likely to exert a relevant influence on synaptic plasticity (Hersch et al., 1994; Yan et al., 2001). In fact, activation of postsynaptic M1 muscarinic receptors increases MSN excitability, by reducing dendritic K+ currents (Galarraga et al., 1999; Shen et al., 2005). As a consequence, M1 receptor activation promotes MSN depolarization and plays a permissive role in corticostriatal LTP (Calabresi et al., 1999). Accordingly, the M1 receptor antagonist pirenzepine prevents LTP, whilst methoctramine, an M2-like receptor blocker, enhances the magnitude of this form of synaptic plasticity (Calabresi et al., 2000). In addition, M1 receptor activation reduces the opening of CaV1 channels, in response to depolarization, that is necessary for LTD induction (Calabresi et al., 1994; Choi and Lovinger, 1997; Kreitzer and Malenka, 2005). Indeed, LTD induction requires D2 receptor activation in order to pause ChI firing activity and reduce M1 receptor tone (Wang et al., 2006).
In summary, manipulation of ACh tone is expected to affect the direction of corticostriatal synaptic plasticity. In fact, loss of autoreceptor function in M2/M4 receptor knockout mice increases striatal ACh tone and impairs selectively LTD induction at MSN synapses. Accordingly, in these mice LTD can be restored by reducing ACh levels with hemicholinium-3, which depletes endogenous ACh (Bonsi et al., 2008).
Cholinergic Signaling in Disease States
In the early 1960s anticholinergic drugs were introduced in the pharmacological treatment of PD, according to the evidence of an imbalance between dopaminergic and cholinergic transmission within the striatum (Barbeau, 1962; Duvoisin, 1967; Hornykiewicz and Kish, 1987).
Although the increased striatal ACh level has long been attributed to the removal of tonic inhibitory control by D2 receptors on ChIs (Maurice et al., 2004), recent experimental work has investigated in more detail ChI function in acute dopamine depletion models of PD (Fino et al., 2007; Salin et al., 2009). As expected, in dopamine-depleted animals ChIs displayed an increased excitability in vitro (Fino et al., 2007), and became highly synchronized in firing rhythmic bursts in vivo (Raz et al., 1996, 2001). This altered pattern of activity might result in periodic outbreaks of ACh release into the striatum which might not be readily hydrolyzed by AChE. Such alterations in ACh input are likely to underlie the loss of synaptic plasticity (Pisani et al., 2005) and to contribute to the pruning of spines (Shen et al., 2007) reported in MSNs from dopamine-depleted animals, contributing to imbalanced striatal outflow in the parkinsonian state.
Interestingly, recent experimental evidence revealed a novel mechanism by which mACh receptor signaling would disrupt striatal activity (Ding et al., 2006). “Regulators of G protein signaling” (RGS) proteins are GTPase accelerating proteins (GAPs), which terminate G protein coupling between receptors and effectors. Alterations in dopamine content have been shown to rapidly modify the expression of several RGS proteins. These authors report that dopamine depletion does not alter D2 dopamine receptor signaling in ChIs, but leads to a decreased mACh M4 receptor coupling to Ca2+ channels, thereby modifying ChIs excitability. Moreover, they show that this impaired coupling is caused by the selective upregulation of RGS4 expression (Ding et al., 2006).
A very recent paper by Ding et al. (2011) has suggested unexpected roles for ChIs also in the adverse motor effects, dyskinesias, induced by prolonged treatment of PD patients with the dopamine replacing agent 3,4-L-dihydroxphenylalanine methyl ester (L-DOPA). These authors have shown in PD rodent models that repeated L-DOPA exposure causes activation of extracellular signal-regulated kinase 1/2 (ERK) and, in turn, an increased basal firing rate and dopamine-dependent excitation in striatal ChIs. These specific responses of ChIs to chronic l-DOPA treatment correlated with the expression of dyskinesia. Accordingly, muscarinic receptor antagonism reduced l-DOPA-induced dyskinesia.
As in PD, anticholinergic drugs targeting mACh receptors are also effective in the treatment of another movement disorder, dystonia. DYT1 dystonia is a severe form of inherited dystonia, characterized by involuntary twisting movements and abnormal postures. Although the pathogenesis of this disabling disorder remains to be fully elucidated, an altered coupling of dopaminergic and cholinergic signaling has been recently demonstrated in the striatum of mice over-expressing the human protein torsinA with the mutation responsible for DYT1 dystonia (Pisani et al., 2006). In these mice, D2 receptor activation induces an excitatory, rather than inhibitory, effect in ChIs. This paradoxical effect was associated to an increase in the functional representation of CaV2 Ca2+ channels, that regulate Ca2+ entry and the physiological pacemaking activity of these interneurons, likely enhancing ACh release. Indeed, the activity of endogenous AChE was increased in the striatum of DYT1 mice, suggesting a compensatory mechanism to reduce an increased cholinergic tone. In accordance to the proposed role of ACh levels in determining the direction of corticostriatal synaptic plasticity (Bonsi et al., 2008), the elevation in cholinergic tone in DYT1 mice was correlated to the loss of LTD and synaptic depotentiation, and the enhancement of LTP (Martella et al., 2009). This notion was supported by the observation that these alterations were normalized by lowering ACh tone with hemicholinium-3, a depletor of endogenous ACh. Moreover, the clinical drug trihexyphenidyl as well as pirenzepine, both mACh M1 receptor antagonists, were effective in restoring normal synaptic plasticity. These observations might explain the efficacy of anticholinergic drugs in the treatment of dystonia.
Other Movement Disorders
Functional imaging and post-mortem studies have revealed a significant loss of striatal cholinergic markers in different basal ganglia disorders (Suzuki et al., 2002; Warren et al., 2005; Smith et al., 2006; Kataoka et al., 2010). Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease, caused by a mutation in the gene encoding Huntingtin, characterized by involuntary choreiform movements, behavioral and cognitive impairment. Though striatal ChIs have been reported to be spared during striatal degeneration in HD (Graveland et al., 1985), recent studies suggest that they might be functionally altered. Indeed, the levels of both the vesicular ACh transporter (VAChT) and choline acetyltransferase (ChAT) are markedly decreased in the striatum of HD transgenic mice, as well as in post-mortem striatal tissue from HD patients (Spokes, 1980; Suzuki et al., 2001a; Vetter et al., 2003; Smith et al., 2006). Moreover, in two experimental models of HD, 3-nitropropionic acid-treated rats and R6/2 transgenic mice, striatal ChIs did not express LTP (Picconi et al., 2006). Progressive supranuclear palsy (PSP) is a progressive neurodegenerative disease characterized by accumulation of tau protein and akinetic-rigid features, falls, supranuclear gaze palsy, and subcortical dementia. In this disorder, cholinergic dysfunction is indicated by reduced levels of ChAT and VAChT in post-mortem samples, as well as by loss of striatal ChIs (Suzuki et al., 2002; Warren et al., 2005).
Chronic clinical use of dopaminergic drugs is often associated with the development of different types of motor complications, such as dystonia, parkinsonism, hyperkinesia, and stereotyped behavior. These reactions to dopaminergic agents points to an imbalance between striatal ACh and dopamine levels. Accordingly, the treatment of choice for these complications is represented by cholinergic drugs (Sethi and Morgan, 2007; Cubo et al., 2008). In the case of motor stereotypy, as well as of Tourette’s syndrome (TS), a childhood-onset neuropsychiatric disease characterized by motor and vocal tics (Graybiel and Canales, 2001) and by a reduced striatal volume (Peterson et al., 2003), a cholinesterase inhibitor has been reported to be effective in the clinical practice (Cubo et al., 2008). Notably, a recent stereological analysis of post-mortem brains showed a significant reduction in the number of ChIs in the sensorimotor regions of the striatum in TS patients (Kataoka et al., 2010). Accordingly, a key role of striatal ChIs has been demonstrated in the arrest of cocaine-induced motor stereotypy in a rat model, where pharmacological treatments restoring ACh release rapidly blocked movement dysfunction (Aliane et al., 2010). Interestingly, this study showed that, while the striatal dopamine/ACh balance is effective during the period of strong motor stereotypy (dopamine increases and ACh decreases), it becomes dissociated during the phase of motor recovery. Indeed, in this period dopamine level still remains high, while ACh returns to its basal level mirroring the decreasing intensity of stereotypy, suggesting an important role of cholinergic transmission in the arrest of motor stereotypy. In accordance with this hypothesis, pharmacological blockade of muscarinic receptors as well as lesion of ChIs significantly prolonged motor stereotypy.
Although simplistic, the striatal ACh/dopamine balance view finds support in clinical pharmacological evidence. To date, two major categories of drugs are successfully utilized in the management of most movement disorders: drugs interfering with either dopaminergic or cholinergic function, suggesting that the interplay between these transmitters is relevant to the maintenance of a correct motor control. In our view, a perspective based upon cholinergic dysfunction may prove useful to orientate clinical pharmacological reasoning.
Clues from neurobiology, functional imaging studies and post-mortem data converge to suggest that both pathogenic features and clinical phenomenology of distinct movement disorders are closely related to dysfunction of striatal cholinergic signaling.
To date, therapeutic intervention to most of these disorders is unsatisfactory. In those conditions where an increased cholinergic activity is documented, targeting muscarinic receptors with more selective drugs is warranted. Indeed, both in PD and dystonia, enhancing M2/M4-mediated autoreceptor function, either by developing selective agonists, or by modulating CaV2 Ca2+ channels appears a promising strategy.
The development of new animal models, including transgenic mice, as well as muscarinic and nicotinic receptor knockout mice, is moving research to a level in which the physiology of the receptor subtypes could be addressed in vivo, offering new perspectives for their pharmacological manipulation.
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.
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Keywords: acetylcholine, striatum, interneuron, Parkinson’s disease, dystonia, movement disorders
Citation: Bonsi P, Cuomo D, Martella G, Madeo G, Schirinzi T, Puglisi F, Ponterio G and Pisani A (2011) Centrality of striatal cholinergic transmission in basal ganglia function. Front. Neuroanat. 5:6. doi: 10.3389/fnana.2011.00006
Received: 17 December 2010;
Accepted: 21 January 2011;
Published online: 07 February 2011.
Edited by:Jose L. Lanciego, University of Navarra, Spain
Reviewed by:James M. Tepper, Rutgers, The State University of New Jersey, USA
Enrico Bracci, University of Manchester, UK
Copyright: © 2011 Bonsi, Cuomo, Martella, Madeo, Schirinzi, Puglisi, Ponterio and Pisani. This is an open-access article subject to an exclusive license agreement between the authors and Frontiers Media SA, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
*Correspondence: Antonio Pisani, Department of Neuroscience, University Tor Vergata, Via Montpellier 1, 00133 Rome, Italy. e-mail: email@example.com