Abstract
Neurons in the pedunculopontine nucleus (PPN) exhibit a wide heterogeneity in terms of their neurochemical nature, their discharge properties, and their connectivity. Such characteristics are reflected in their functional properties and the behaviors in which they are involved, ranging from motor to cognitive functions, and the regulation of brain states. A clue to understand this functional versatility arises from the internal organization of the PPN. Thus, two main areas of the PPN have been described, the rostral and the caudal, which display remarkable differences in terms of the distribution of neurons with similar phenotype and the projections that originate from them. Here we review these differences with the premise that in order to understand the function of the PPN it is necessary to understand its intricate connectivity. We support the case that the PPN should not be considered as a homogeneous structure and conclude that the differences between rostral and caudal PPN, along with their intrinsic connectivity, may underlie the basis of its complexity.
Introduction
The pedunculopontine nucleus (PPN) is located in the upper brainstem and has an irregular shape delimited by the borders of its population of cholinergic neurons. The PPN has been conserved in evolution across species and is present in early mammals and amphibians (Marin et al., ; Grillner et al., ). Defined in humans in 1982 (Olszewski and Baxter, ), it is considered a part of the reticular activating system and, as a reticular structure, it has been argued that PPN has no clear boundaries. One of the main characteristics of neurons of the PPN is their long-range axonal projections, reaching numerous targets across the brain, from distant forebrain structures (Woolf and Butcher, 1986; Hallanger and Wainer, ) to the spinal cord (Rye et al., ; Spann and Grofova, 1989). Although initially considered to function as a relay nucleus within ascending activating systems, increasing evidence on the neuronal heterogeneity of the PPN and its local synaptic organization, suggest that this high level of connectivity with functionally distinct neuronal systems underlies an integrative function rather than a role as a simple relay nucleus. An example of this heterogeneous connectivity is the way the PPN is integrated into basal ganglia circuits: distinct functional types of neurons in the PPN innervate basal ganglia and, in turn, basal ganglia projects back to PPN and innervate different neuronal populations. This remarkable interconnectivity has been the subject of previous reviews that have stressed that most structures of the basal ganglia project to, and receive inputs from, the PPN (Pahapill and Lozano, ; Mena-Segovia et al., ). In the present review we will discuss recent evidence on the heterogeneous distribution of neurochemical subtypes of neurons within the PPN and correlate this with data on their connectivity. We will make use of the large amount of information available that describe the anatomical relationship that the PPN maintains with the basal ganglia and that provide evidence of a topographical organization. We will also correlate such organization with the connectivity of the PPN with other neuronal systems to integrate a theory supporting functional domains in the PPN.
Neurochemical Diversity
It has now been widely agreed that the PPN is composed by a mixture of neurons of different sizes, of different neurochemical phenotype and with distinct connectivity. Cholinergic neurons represent a minority of the neurons in the PPN and are intermingled amongst a large number of GABAergic and glutamatergic neurons, which are heterogeneously distributed across its rostro-caudal axis (Mena-Segovia et al., ; Wang and Morales, 2009). A parasagittal view of the PPN illustrates the different distributions of the neuronal populations and therefore better represents the anatomical organization of the PPN. Using external landmarks such as the substantia nigra (SN) and the superior cerebellar peduncle, which maintain a constant spatial relationship with the PPN across different medio-lateral levels, it is possible to follow the distribution of the cell types that compose the PPN. GABAergic neurons are more densely concentrated in the rostral PPN, compared to cholinergic and glutamatergic neurons. In the rat they are detectable from the rostral border of the PPN (limiting the caudal part of the SN) and their density decreases dramatically at a level about 1.2–1.5 mm further caudal (Mena-Segovia et al., ; Figure 1). Such a drop in the density of GABAergic neurons coincides with a change in the cytoarchitecture and organization of cholinergic neurons: bipolar-shaped cholinergic neurons tend to be organized in a layer-like structure close to the SN, where GABAergic neurons are several times more abundant. Following the decline in the number of GABAergic neurons, rounded-shaped cholinergic neurons show a distinct configuration. Instead of lying in the layer-like arrangement, cholinergic neurons show an apparently random distribution and an increased number of processes. The change in density of cholinergic neurons, however, is not as marked as that of the GABAergic neurons or the glutamatergic neurons. In contrast to the rostral PPN, the caudal part of the nucleus has a larger proportion of glutamatergic neurons (Wang and Morales, 2009). Until now, no other neurochemical cell types have been identified although differences have been observed within each neuronal type in relation to the co-expression of other neurochemical markers and their firing properties.
Figure 1
In different regions of the brain including hippocampus (Acsady et al., ; Somogyi and Klausberger, 2005), cortex (Staiger et al., 2004), and basal ganglia (Parent et al., ), neurons that express calcium-binding proteins have been shown to have distinct functional properties despite the fact that they may use the same transmitter. They have thus proved to be useful markers to distinguish sub-populations of neurons. Calcium-binding proteins have also been reported to be expressed by neurons in the PPN in monkeys (Cote and Parent, ; Fortin and Parent, ) and rats (Dun et al., ), and indeed, calbindin and calretinin are expressed by a similar number of neurons to that of cholinergic neurons in the rat PPN (Martinez-Gonzalez et al., ). Although they are rarely expressed in cholinergic neurons, they are commonly expressed by GABAergic and glutamatergic neurons suggesting functional subtypes of GABAergic and glutamatergic neurons.
Significant differences have been observed also in terms of the in vivo firing properties of PPN neurons. Cholinergic neurons show two types of firing patterns: slow-firing cholinergic neurons that are associated to the cortical upstate during slow oscillations, and fast-firing cholinergic neurons that are correlated to the cortical downstate during slow oscillations (Mena-Segovia et al., ). No neurochemical markers of these subtypes have been identified. Neurons that have been identified as non-cholinergic and have been assigned as putative glutamatergic neurons because they give rise to asymmetric synaptic contacts in their targets, also show two main subtypes: fast-firing neurons that are associated with the cortical slow oscillations (Mena-Segovia et al., ), and quiescent (or very slow firing) neurons whose firing is independent of the cortical activity (Ros et al., ). These putative glutamatergic neurons have a different axonal trajectory and pattern of innervation from those of cholinergic neurons, although some targets are shared by both types (notably, the basal ganglia). Other neurons that have not been characterized in terms of their neurochemical nature include tonic firing neurons and irregular firing neurons; it is likely that at least one of these subtypes are GABAergic (Ros et al., ). The correlation between neurochemical subtypes and electrophysiological properties recorded in in vitro experiments is more limited. Three types of neurons have been described on the basis of their membrane properties (A-current type, low-threshold spikes type and mixed A-current plus LTS type; Leonard and Llinas, ; Takakusaki et al., 1997; Saitoh et al., ), although this classification does not seem to be related to their neurochemical nature (and therefore not to their synaptic targets). The different membrane properties, however, are likely to underlie some of the functional differences within each cell subtype.
In summary, each main neuronal type in the PPN is composed of at least two subtypes; the PPN is thus a highly heterogeneous structure at the cellular, molecular, and electrophysiological levels. The different neuronal types are heterogeneously distributed in the PPN, perhaps delineating functional territories (rostral and caudal) determined by a greater density of GABAergic axons arising from the rostral PPN in contrast to a greater density of cholinergic and glutamatergic axons arising from the caudal PPN, thus producing contrasting effects on their target structures.
Internal Structure and Connectivity: The Case for Subdivisions of the PPN
The notion that the PPN is not homogeneous in terms of its cellular organization is not recent; the PPN was originally divided in pars dissipata (rostral) and pars compacta (caudal) on the basis of the density of cholinergic neurons (Olszewski and Baxter, ), which were believed to be the most representative, if not the only, neuronal type in the PPN (Rye et al., ). Other subdivisions included rostral, middle, and caudal thirds, and the inclusion of an area referred to as the midbrain extrapyramidal area (MEA) which receives a dense innervation from the basal ganglia but lies outside the cholinergic borders of the PPN (Steininger et al., 1992). While all of these subdivisions are based on identifiable characteristics in the anatomy of the PPN, it is perhaps the rostral and caudal division that is the most appropriate since it is based on the distribution of all known cell types rather than only the cholinergic neurons. Indeed, GABAergic neurons provide a unique distribution that correlates with the cholinergic pars dissipata and pars compacta subdivisions (Mena-Segovia et al., ). The rostro-caudal division is also the basis for many anatomical studies describing afferents and efferents to and from the PPN, as discussed in the following sections, but essentially does not rely on cell density (as the terms dissipata and compacta denote).
The idea of two functionally distinct regions of the PPN is supported by the distribution of its cell types defined on the basis of neurochemistry and the connectivity of the PPN with other neuronal systems. Thus, two neurochemically distinct projections arising from rostral and caudal PPN diverge, innervating distinct structures, but also converge in others. This functional dichotomy seems to be locally regulated, as suggested by the evidence of axonal collaterals of PPN neurons. Thus, a local synaptic network has been identified after tracing the axons of individually labeled neurons (Mena-Segovia et al., ; Ros et al., ). Both cholinergic and non-cholinergic neurons contribute to this connectivity, although the number of axonal varicosities was found to be greater in cholinergic neurons. Interestingly, a large proportion of PPN projection neurons have axons that travel within the PPN in a rostro-caudal direction, providing local innervation that synaptically links the rostral and the caudal portions. This evidence of a local network of heterogeneous neurochemical nature supports the role of the PPN as an integrator between its input and output systems.
Efferent Connectivity
Neurons of the PPN give rise to long axons that innervate several targets. The longest axons arise from cholinergic neurons and give rise to as many as five or six collaterals that innervate the basal ganglia, thalamus, tectum, and lower brainstem, among other regions (Mena-Segovia et al., ). The axons of non-cholinergic neurons are more restricted in terms of length and number of collaterals (typically two; Ros et al., ). Single-cell labeling experiments, have demonstrated that both cholinergic and non-cholinergic neurons project preferentially to the basal ganglia and that several divisions of the basal ganglia are innervated. Tracer studies have also produced extensive data on the connections of neurons in the PPN (Table 1).
Table 1
| Target brain area | PPN region | References |
|---|---|---|
| BASAL GANGLIA | ||
| STN | Caudal | Nomura et al. (), Carpenter et al. (), Saper and Loewy (), Edley and Graybiel (), Hammond et al. (), Lavoie and Parent (), Bevan and Bolam (), Muthusamy et al. (), Martinez-Gonzalez et al. (), Kita and Kita () |
| EP/GPi | Rostral | Saper and Loewy (), Gonya-Magee and Anderson (), Jackson and Crossman (), Woolf and Butcher (1986), Scarnati et al. (1988), Charara and Parent (), Lavoie and Parent (), Shink et al. (1997) |
| SN | Rostral | Saper and Loewy (), Scarnati et al. (1984, 1987), Sugimoto and Hattori (1984), Woolf and Butcher (1986), Clarke et al. (), Gould et al. (), Nakamura et al. (), Bolam et al. (), Lavoie and Parent (), Futami et al. (), Oakman et al. (), , Charara et al. (), Takakusaki et al. (1996) |
| VTA | Caudal | Sugimoto and Hattori (1984), Oakman et al. (), Charara et al. (), Geisler and Zahm (), Mena-Segovia et al. (), Good and Lupica () |
| STR | Saper and Loewy (), Nakano et al. () | |
| THALAMUS | ||
| MD | Caudal | Steriade et al. (1988), Lavoie and Parent () |
| VA | Caudal | Smith et al. (1988) |
| VL | Caudal | Smith et al. (1988) |
| VM | Caudal | Smith et al. (1988) |
| Pf | Caudal | Sugimoto and Hattori (1984), Kobayashi and Nakamura (), Kobayashi et al. (), Parent and Descarries () |
| DG | Caudal | Parent and Descarries () |
| Rt | Caudal | Parent and Descarries () |
| LM-Sg | Caudal | Hoshino et al. (, ) |
| CM/CL/PV | Caudal | Steriade et al. (1990), Erro et al. (), Krout et al. () |
| TECTUM | ||
| IC | Caudal | Mena-Segovia et al. (), Motts and Schofield () |
| SC | Caudal | Beninato and Spencer (), Hall et al. (), Krauthamer et al. (), Mena-Segovia et al. () |
| FOREBRAIN | ||
| MgPA | Rostral | Semba and Fibiger (1992), Losier and Semba () |
| NbMC | Rostral | Semba and Fibiger (1992) |
| Hypothalamus | Woolf and Butcher (1986), Hallanger et al. (), Ford et al. () | |
| LM-Sg | Hoshino et al. () | |
| RMTg | Jhou et al. () | |
| BRAINSTEM | ||
| PRF | Caudal | Mitani et al. (), Semba et al. (1990), Takakusaki et al. (1996) |
| GiN | Caudal | Mitani et al. (), Rye et al. (), Grofova and Keane (), Martinez-Gonzalez et al. () |
| MVM | Caudal | Skinner et al. (1990b) |
| MRF | Caudal | Nakamura et al. (), Grofova and Keane () |
| NPO | Caudal | Garcia-Rill et al. () |
| Spinal cord | Caudal | Rye et al. (), Spann and Grofova (1989), Skinner et al. (1990a) |
Efferent connectivity of the pedunculopontine nucleus.
Abbreviations: STN, subthalamic nucleus; EP, entopeduncular nucleus; GPi, internal segment of the globus pallidus; SN, substantia nigra; VTA, ventral tegmental area; STR, striatum; MD, mediodorsal; VA, ventral anterior; VL, ventro-lateral; VM, ventro-medial; Pf, parafascicular; DG, dorsal geniculate; Rt, retocular thalamic; LM-Sg, lateralis medialis-suprageniculate; CM, centromedian; CL, centrolateral; PV, paraventricular; IC, inferior colliculus; SC, superior colliculus; MgPA, magnocellular preoptic area; NbMC, nucleus basalis magnocellularis; RMTg, mesopontine rostromedial tegmental nucleus; PRF, pontine reticular formation; GiN, gigantocellular nucleus; MVM, medioventral medulla; MRF, medial reticular formation; NPO, nucleus pontis oralis.
Basal ganglia
Tracer experiments have shown that the STN receives input from the PPN in the cat (Nomura et al., ; Edley and Graybiel, ), rat (Saper and Loewy, ; Hammond et al., ), and monkey (Carpenter et al., ; Lavoie and Parent, ). More recently, tractography studies have confirmed these findings in humans (Muthusamy et al., ). In the monkey and rat, the neurons that project to the STN are located in the caudal PPN (Carpenter et al., ; Martinez-Gonzalez et al., ; Kita and Kita, ). Such projections have been identified to include cholinergic, GABAergic, and glutamatergic components (Bevan and Bolam, ).
The entopeduncular nucleus (EP, in rat and cat, equivalent to the internal segment of the globus pallidus or GPi in the monkey) receives input from the PPN (Saper and Loewy, ; Jackson and Crossman, ; Woolf and Butcher, 1986; Shink et al., 1997), and these projections have an excitatory influence on EP neurons in the rat and cat (Gonya-Magee and Anderson, ; Scarnati et al., 1988). A species-specific difference seems to exist regarding the density of these projections, since they have been reported to be larger in the monkey than in the cat (Edley and Graybiel, ). In the monkey, tracer injections in the GPi give rise to a large number of retrogradely labeled PPN neurons in the rostral PPN, around 40% of which are cholinergic. In contrast, a restricted GPe injection produced a smaller number of labeled neurons in the PPN (Charara and Parent, ). This difference was confirmed by anterograde labeling, Phaseolus vulgaris leucoagglutinin injections in the PPN give rise to a much higher density of anterogradely labeled fibers in the GPi than in the GPe (Lavoie and Parent, ).
The SN pars compacta (SNc) and pars reticulata (SNr) are interconnected with the PPN (Saper and Loewy, ; Woolf and Butcher, 1986). In the rat and monkey, SNc dopaminergic neurons receive direct glutamatergic and cholinergic input from PPN neurons (Sugimoto and Hattori, 1984; Clarke et al., ; Scarnati et al., 1987; Gould et al., ; Bolam et al., ; Futami et al., ; Oakman et al., ; Charara et al., ). These projections emit collaterals that innervate the medial reticular formation in the cat (Nakamura et al., ). Furthermore, the activation of the PPN can elicit an excitatory effect on SN neurons in the rat (Scarnati et al., 1984, 1987), evoking monosynaptic glutamatergic and cholinergic excitatory postsynaptic potentials in dopamine neurons (Futami et al., ) and non-dopamine neurons (Rohrbacher et al., ). In the monkey, the neurons that project to the SN are concentrated in the rostral PPN and about 25% of these are cholinergic. However, very few projecting neurons are located in the caudal PPN (Lavoie and Parent, ). In the rat, cholinergic and non-cholinergic neurons that arborize within the SNc are preferentially located in the rostral PPN (Takakusaki et al., 1996). These projections are mostly ipsilateral (Oakman et al., , ).
The ventral tegmental area (VTA) also receives substantial cholinergic innervation from the PPN in the rat and monkey (Sugimoto and Hattori, 1984; Oakman et al., ; Charara et al., ; Geisler and Zahm, ). In monkeys, retrograde tracing experiments have shown the existence of glutamatergic and GABAergic afferents from the PPN to the VTA (Charara et al., ). In the rat, neurons that send projections to the VTA are concentrated in the caudal PPN, project bilaterally and involve cholinergic (Sugimoto and Hattori, 1984; Oakman et al., ), GABAergic and glutamatergic axons (Mena-Segovia et al., ). In vitro, stimulation of cortical and PPN afferents to the VTA induce glutamatergic synaptic currents in VTA dopaminergic and non-dopaminergic neurons (Bonci and Malenka, ). More recently, it has been described that GABAergic and monosynaptic glutamatergic PPN inputs do not converge on the same VTA neurons (Good and Lupica, ). Nicotinic acetylcholine receptors (nAChR) can also modulate this excitatory synaptic transmission (Good and Lupica, ).
Last but not least, a direct projection from the PPN to the striatum (or caudate/putamen in primates) has been identified in the rat (Saper and Loewy, ) and in the monkey (Nakano et al., ).
Thalamus
The thalamus is heavily innervated by the PPN in the rat (Saper and Loewy, ; Hallanger and Wainer, ), cat and monkey (Parent et al., ), and a large proportion of this output is cholinergic (Sugimoto and Hattori, 1984; Sofroniew et al., 1985; Hallanger et al., ; Hallanger and Wainer, ,; Takakusaki et al., 1996; Oakman et al., ; Parent and Descarries, ). The projections are widespread, innervating several thalamic nuclei (Smith et al., 1988; Steriade et al., 1988; Kolmac and Mitrofanis, ), they are topographically organized in the cat (Steriade et al., 1988) and monkey (Lavoie and Parent, ), and arise from neurons that are predominantly located in the caudal PPN. In the cat and monkey, the majority of the thalamic nuclei receive less than 10% of their PPN innervation from the rostral PPN, with the exception of the mediodorsal thalamic nucleus, which receives up to 20% of its innervation from the rostral PPN (Steriade et al., 1988). The thalamic input from the PPN is both cholinergic and non-cholinergic (Smith et al., 1988; Steriade et al., 1988). Retrograde labeling from the mediodorsal thalamic nucleus produces prominent labeling of non-cholinergic neurons in both the ipsilateral and contralateral PPN in the cat (Smith et al., 1988). The ventro-anterior and the ventro-lateral thalamic nuclei receive between 50 and 75% of their cholinergic afferents from the central–caudal PPN, whereas the ventro-medial thalamic nucleus receives its cholinergic input mainly from the caudal PPN and the laterodorsal tegmental nucleus (Smith et al., 1988). In the rat, the parafasicular nucleus (Pf) receives inputs from the caudal PPN (Sugimoto and Hattori, 1984). The cholinergic innervation to the Pf has a higher density than the innervation to the dosolateral geniculate and reticular thalamic nuclei (Parent and Descarries, ). Individual Pf neurons receive convergent synaptic inputs from the PPN and the SC (Kobayashi and Nakamura, ). In turn, Pf neurons that receive inputs from the PPN project to striatum (Erro et al., ), linking monosynaptically PPN axons to thalamostriatal neurons (Kobayashi et al., ). Cholinergic neurons that project to the thalamus send collaterals to the basal forebrain (Losier and Semba, ), the pontine reticular formation (Semba et al., 1990), the superior and inferior colliculi, and the basal ganglia (Mena-Segovia et al., ). In the cat, glutamatergic and GABAergic neurons of the lateralis medialis-suprageniculate nuclear complex (LM-Sg) receive cholinergic input from the PPN (Hoshino et al., , ). Other thalamic nuclei receive a more heterogeneous mixture of cholinergic and non-cholinergic PPN afferents, such as the centrolateral, centromedial, and paraventricular thalamic nuclei in the rat (Erro et al., ; Krout et al., ).
Other ascending projections
Individual cholinergic neurons of the PPN project to the superior and inferior colliculi in the rat (Mena-Segovia et al., ). The large majority of the cholinergic inputs to the inferior colliculus arise from the ipsilateral PPN and to a less extent, from the LTD. These projections arise from cholinergic neurons that are located in the caudal PPN and include a subpopulation that project to both the ipsilateral and contralateral inferior colliculus in the guinea pig (Motts and Schofield, ). The superior colliculus receives cholinergic and non-cholinergic innervation from the PPN in the rat and cat (Beninato and Spencer, ; Hall et al., ). These afferents arise mainly from the caudal PPN (Beninato and Spencer, ). PPN neurons projecting to the superior colliculus, as identified by antidromic stimulation, are segregated into two groups: those that are sensitive and those that are insensitive to physiological sensory stimuli (Krauthamer et al., ). A small group of neurons located in the rostral PPN have collaterals that innervate the superior colliculus and the LM-Sg in the cat (Hoshino et al., ). In the rat, other ascending targets include the mesopontine rostromedial tegmental nucleus (RMTg; Jhou et al., ).
In the forebrain, the magnocellular preoptic area (MgPA) and the nucleus basalis magnocellularis receive afferents from the PPN (Semba et al., 1988; Losier and Semba, ). The posterior lateral hypothalamus receives cholinergic input from PPN neurons that are scattered throughout the rostro-caudal axis, and GABAergic innervation from neurons that are concentrated in the rostral PPN; the neurochemical nature of the majority of the projection neurons was not identified (Ford et al., ).
Brainstem and other descending projections
Neurons in the PPN make a dense innervation on structures in the lower brainstem, pons, medulla, and spinal cord. The descending projections arise from collaterals of ascending axons, as seen in cholinergic (Mena-Segovia et al., ) and non-cholinergic neurons (Martinez-Gonzalez et al., ), or from non-cholinergic neurons with single descending axons (Ros et al., ). Both cholinergic and non-cholinergic neurons innervate the pontine reticular formation in the rat (Semba et al., 1990; Takakusaki et al., 1996) and the cat (Mitani et al., ). Thus, PPN has been shown to project to the gigantocellular nucleus (GiN) in rats and cats (Mitani et al., ; Rye et al., ; Grofova and Keane, ; Martinez-Gonzalez et al., ), the medioventral medulla (Skinner et al., 1990b), rostral ventro-lateral medulla (Yasui et al., 1990), medial reticular formation, medulla oblongata (Nakamura et al., ; Grofova and Keane, ), and the spinal cord in rats (Rye et al., ; Spann and Grofova, 1989; Skinner et al., 1990a). The majority of the PPN projecting neurons to the spinal cord are non-cholinergic (Skinner et al., 1990a). These descending PPN projections are considered to be directly involved in locomotion since the stimulation of neurons in the caudal PPN leads to a prolonged activation of neurons in the nucleus reticularis pontis oralis and changes in the flexor and extensor nerves in decorticated cats (Garcia-Rill et al., ).
In summary, the ascending projections from the rostral PPN preferentially innervate the EP/GPi, SN and the lateral hypothalamus in the rat, cat, and monkey. In contrast, ascending projections from the caudal PPN innervate the thalamus, STN, VTA, SC, and IC.
Afferent Connectivity
Although the information available on the afferent innervation to the PPN is not as abundant and detailed as it is with regards to its efferents, it is clear that the PPN receives a heterogeneous modulation arising from functionally diverse areas of the brain. Thus, neurons in the PPN receive afferents from structures that include the cortex, thalamus, hypothalamus, pons, cerebellum, medulla, spinal cord, and the basal ganglia (Saper and Loewy, ; Semba and Fibiger, 1992; Table 2).
Table 2
| Origin | Target PPN region | References |
|---|---|---|
| CEREBRAL CORTEX | ||
| FL | Caudal | Semba and Fibiger (1992), Matsumura et al. () |
| PAC | Schofield and Motts (2009) | |
| MPC | Sesack et al. (1989) | |
| CEREBELLUM | ||
| DCN | Hazrati and Parent () | |
| BASAL GANGLIA | ||
| STN | Nauta and Cole (), Jackson and Crossman (), Hammond et al. (), Kita and Kitai (), Granata and Kitai (), Semba and Fibiger (1992), Florio et al. () | |
| EP/GPi | Rostral | Smith et al. (1990), Moriizumi and Hattori (), Semba and Fibiger (1992), Shink et al. (1997), Parent et al. () |
| SN | Rostral | Noda and Oka (), Scarnati et al. (1987), Nakamura et al. (), Granata and Kitai (), Spann and Grofova (1991), Semba and Fibiger (1992), Saitoh et al. () |
| VTA | Haber et al. (), Semba and Fibiger (1992) | |
| STR | Semba and Fibiger (1992) | |
| TECTUM | ||
| SC | Woolf and Butcher (1986), Redgrave et al. (), Semba and Fibiger (1992), Steininger et al. (1992) | |
| BRAINSTEM | ||
| LTDg | Satoh and Fibiger (1986), Cornwall et al. (), Semba and Fibiger (1992) | |
| Contralateral PPN | Semba and Fibiger (1992) | |
| FOREBRAIN | ||
| LC | Jones and Yang () | |
| Habenula | Semba and Fibiger (1992) | |
| RMTg | Jhou et al. () | |
| ZI | Satoh and Fibiger (1986), Semba and Fibiger (1992), Kolmac et al. () | |
| DR | Caudal | Vertes (1991), Steininger et al. (1997) |
Afferent connectivity of the pedunculopontine nucleus.
Abbreviations: FL, frontal lobe; PAC, primary auditory cortex; MPC, medial prefrontal cortex; DCN, deep cerebellar nuclei; STN, subthalamic nucleus; EP, entopeduncular nucleus; GPi, internal segment of the globus pallidus; SN, substantia nigra; VTA, ventral tegmental area; STR, striatum; SC, superior colliculi; LTDg, laterodorsal tegmental nucleus; PPN, pedunculopontine nucleus; LC, locus ceruleus; RMTg, mesopontine rostromedial tegmental nucleus; ZI, zona incerta; DR, dorsal raphé.
The PPN receives a direct input from the cerebral cortex arising from distinct frontal lobe areas involved in motor control in the monkey. These convergent inputs seem to target the dorsal and caudal PPN areas (Matsumura et al., ). In the rat, these afferents have also been demonstrated, although they seem to be less abundant (Semba and Fibiger, 1992). They arise also from the medial prefrontal cortex (Sesack et al., 1989). In addition, cholinergic PPN neurons receive afferents from the primary auditory cortex in guinea pigs (Schofield and Motts, 2009).
Basal ganglia
The PPN receives a direct input from the STN in the rat (Jackson and Crossman, ; Kita and Kitai, ), the cat and the monkey (Nauta and Cole, ). In addition to the anatomical evidence, electrophysiological experiments in the rat have shown that this input is excitatory and it targets neurons in the PPN (Granata and Kitai, ). Furthermore, the STN can modulate PPN activity indirectly through the SNr; this pathway has an inhibitory effect on PPN neurons (Hammond et al., ; Florio et al., ).
Tracer studies show that the EP sends projections that innervate PPN neurons in the rat (Semba and Fibiger, 1992) and in the monkey (Shink et al., 1997). In the latter, the GPi afferents preferentially target NADPH diaphorase-negative neurons in the rostral PPN, establishing symmetric synapses with proximal dendrites. GP afferents to the PPN arise from the caudal GP, in contrast to the rostral GP that projects to the STN (Moriizumi and Hattori, ). GPi axons that innervate PPN neurons arise from type I neurons that are abundant in the center of the GPi (Parent et al., ), although some authors differ on this, finding retrogradely labeled neurons in the whole GP after retrograde tracer injection in the rat STN (Smith et al., 1990). This is particularly relevant because the PPN is involved into a circuit that involves the STN and GP, one of the principal outflows of the basal ganglia.
The PPN also receives afferents from the SN in the rat and cat (Nakamura et al., ; Spann and Grofova, 1991; Semba and Fibiger, 1992), and this input is inhibitory (Noda and Oka, ; Scarnati et al., 1987; Granata and Kitai, ) and mediated by GABA (Saitoh et al., ). It is not clear yet which PPN neurons are the targets of these afferents, but electron microscopy (EM) studies have shown that nigral afferents to the PPN establish synaptic contacts preferentially with non-cholinergic neurons located in the rostral PPN (Spann and Grofova, 1991; Grofova and Zhou, ). Some of these neurons are glutamatergic, and a lower proportion are cholinergic (Grofova and Zhou, ).
Other basal ganglia projections to the PPN include the ventral striatum in monkey (Haber et al., ) and the VTA in rats (Semba and Fibiger, 1992). Indeed, PPN neurons receive a dopaminergic innvervation presumably arising from the mesencephalon in the monkey (Rolland et al., ).
Other afferent systems
The PPN receives afferents from the habenula (Semba and Fibiger, 1992) and the zona incerta (Semba and Fibiger, 1992; Kolmac et al., ), the deep cerebellar nuclei (Hazrati and Parent, ), the mesopontine RMTg (Jhou et al., ) and the superior and inferior colliculi in the rat (Woolf and Butcher, 1986; Redgrave et al., ; Semba and Fibiger, 1992; Steininger et al., 1992).
In the brainstem, tracer studies in the rat have shown that the rostral and caudal portions of the dorsal raphé send projections that innervate the PPN (Vertes, 1991), where they preferentially target non-cholinergic neurons in the caudal PPN (Steininger et al., 1997). The locus coeruleus (Jones and Yang, ) and the laterodorsal tegmental nucleus also innervate the PPN (Satoh and Fibiger, 1986; Cornwall et al., ; Semba and Fibiger, 1992). Furthermore, the PPN receives an input from the contralateral PPN (Semba and Fibiger, 1992).
In summary, the PPN receives afferents from the basal ganglia, cortex, thalamus, cerebellum, forebrain, spinal cord, pons, and the contralateral PPN. The rostral PPN receives inhibitory input from the SN and the EP/GPi. The caudal PPN receives inputs from the dorsal raphé and the motor cortex.
Functional Implications of Topography
The data arising from the connectivity studies show that a significant number of structures have a selective relationship with distinct regions within the PPN. This is clearly evident from the analysis of retrograde and anterograde tracing studies showing the distribution of PPN projecting neurons, although less clear with regards to the distribution of the PPN afferents. Nevertheless, in the case of PPN inputs, two important neuronal systems, the basal ganglia and the cortex, seem to contact neurons in distinct regions of the PPN. Thus, the GABAergic output neurons of the basal ganglia, arising in the SNr and EP/GPi, mainly contact neurons located in the rostral PPN. In contrast, neurons in the cortex and the dorsal raphé preferentially innervate neurons in the caudal PPN. In terms of its efferents, the rostral PPN projects to the SNr, SNc, GPi, and the hypothalamus. In contrast, the caudal PPN projects to the STN, the VTA, the thalamus, and the superior and inferior colliculi (Figure 2).
Figure 2
The differences in connectivity suggest that there is a functional reciprocity in different areas of the PPN with regards to its inputs and outputs. These differences reveal that, (1) the rostral PPN, which contains a significantly larger number of GABAergic neurons, is interconnected with the structures that provide the GABAergic output from the basal ganglia, therefore suggesting a close functional relationship with basal ganglia operations; and (2) the caudal PPN, which contains a larger number of cholinergic and glutamatergic neurons, receives information from cortex and dorsal raphé, and projects to targets in the thalamus and colliculi, suggesting a close relationship with the modulation of brain states mediated through thalamocortical systems. Moreover, it is also the caudal PPN that projects to the STN and to the brainstem locomotor regions involved in gait and posture and the modulation of the muscular tone across different brain states.
Behavioral studies following restricted lesions or selective manipulations in the rostral and caudal PPN have shown functional differences between these two PPN areas that correlate with the functional domains defined by the neurochemical distribution and connectivity (Inglis et al., ; Alderson et al., , ; Andero et al., ). Such functional differences have relevance for deep brain stimulation (DBS) therapy in the PPN in Parkinson's disease patients (Starr et al., 1998; Pahapill and Lozano, ; Nandi et al., ; Benabid, ; Jenkinson et al., ; Stefani et al., 2007). As is evident from the cell types and their efferents, it is most likely that the stimulation of an electrode situated in the rostral PPN will have very different effects to an electrode situated in the caudal PPN.
Conclusion
The PPN is subdivided in two functionally distinct regions: the rostral portion, which is predominantly inhibitory and interconnected with the basal ganglia, and the caudal portion, which is predominantly excitatory and closely related to arousal and motor systems. These two functionally distinct areas are locally regulated and synaptically linked by the local axon collaterals of cholinergic and non-cholinergic neurons. The extent of the interaction between these two regions remains to be determined, but will help to elucidate the common mechanism by which PPN neurons seem to participate in a wide range of behavioral functions.
Statements
Conflict of interest
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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Summary
Keywords
pedunculopontine, brainstem, basal ganglia, reticular activating system, neuronal heterogeneity, synaptic organization, microcircuits, connectivity
Citation
Martinez-Gonzalez C, Bolam JP and Mena-Segovia J (2011) Topographical Organization of the Pedunculopontine Nucleus. Front. Neuroanat. 5:22. doi: 10.3389/fnana.2011.00022
Received
31 December 2010
Accepted
21 March 2011
Published
05 April 2011
Volume
5 - 2011
Edited by
Jose L. Lanciego, University of Navarra, Spain
Reviewed by
Micaela Morelli, University of Cagliari, Italy; Marisela Morales, National Institute of Neurological Disorders and Stroke, USA
Copyright
© 2011 Martinez-Gonzalez, Bolam and Mena-Segovia.
This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
*Correspondence: Juan Mena-Segovia, Medical Research Council Anatomical Neuropharmacology Unit, Department of Pharmacology, University of Oxford, Mansfield Road, Oxford OX1 3TH, UK. e-mail: juan.mena-segovia@pharm.ox.ac.uk
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