Tuesday, August 25, 2015

Control of Speech in Humans

Laryngeal Motor Cortex and Control of Speech in Humans

Kristina Simonyan1,* and Barry Horwitz2

1Departments of Neurology and Otolaryngology, Mount Sinai School of Medicine, New York, NY

2Brain Imaging and Modeling Section, National Institute on Deafness and Other Communication

Disorders, National Institutes of Health, Bethesda, MD


Speech production is one of the most complex and rapid motor behaviors and involves a precise

coordination of over 100 laryngeal, orofacial and respiratory muscles. Yet, we lack a complete

understanding of laryngeal motor cortical control during production of speech and other voluntary

laryngeal behaviors. In recent years, a number of studies have confirmed the laryngeal motor

cortical representation in humans and provided some information about its interactions with other

cortical and subcortical regions that are principally involved in vocal motor control of speech

production. In this review, we discuss the organization of the peripheral and central laryngeal

control based on neuroimaging and electrical stimulation studies in humans and neuroanatomical

tracing studies in non-human primates. We hypothesize that the location of the laryngeal motor

cortex in the primary motor cortex and its direct connections with the brainstem laryngeal

motoneurons in humans, as oppose to its location in the premotor cortex with only indirect

connections to the laryngeal motoneurons in non-human primates, may represent one of the major

evolutionary developments in humans towards the ability to speak and vocalize voluntarily.


motor control; voice; speech; human; non-human primate


Voice is essential for human communication. Starting with the first cry at birth, the vocal

repertoire develops throughout childhood into unique human speech. The development of

the human ability to speak relies on the abilities to listen to speech, comprehend and process

the meaning of the heard words, and coordinate laryngeal, respiratory and orofacial muscles

to communicate speech sounds. Together with body expressions, we use speech and other

vocal gestures to define our needs and thoughts and to project our feelings and emotions.

Research on the mechanism of speech spans the centuries. Commonly, the topic of the brain

basis of speech is discussed in relation to speech perception within the auditory cortex and

speech production within the inferior frontal gyrus (i.e., Broca's area), while the involvement

of the laryngeal motor cortex (LMC) is rarely addressed. Nevertheless, the LMC is

imperative for the control of motor coordination of over 100 muscles for voluntary

production of voice, swallowing and breathing, all of which represent vital functions for our

existence and communication.

*Corresponding author: Kristina Simonyan, M.D., Ph.D. Department of Neurology Mount Sinai School of Medicine One Gustave L.

Levy Place Box 1137 New York, NY 10029 Phone: (212) 241-0656 Fax: (212) 289-4107 kristina.simonyan@mssm.edu.

Simonyan and Horwitz Page 2

In this review, we will first briefly introduce the anatomy and peripheral nervous control of

the larynx as an organ for voice production; we will then review the hierarchical

organization of voice control from brainstem to the LMC with a special focus on the role of

the LMC in the control of voluntary learned voice production and on its interactions with

other brain regions associated with speech control. We will present some hypotheses on the

LMC evolutionary developments in humans and conclude with a summary and future


Larynx and its peripheral nervous control

The larynx as a structure is phylogenetically much older than its role as a vocal organ. The

first vertebrate larynx appeared in the lungfish more than 400 million years ago; however,

the first vocalizations appeared much later with the evolution of anurans about 250 million

years ago.

From a phonatory point of view, voice is produced when the expiratory airflow from the

lungs sets the closed vocal folds of the larynx into vibration, converting aerodynamic power

generated by the thoracic and abdominal muscles (subglottal component) into the basic

sound wave (e.g., acoustic power). This sound wave is further filtered and amplified by oral

articulators, such as pharynx, tongue, palate, lips, and jaw (supraglottal component), and is

emitted from the mouth and nose as sound of voice (Fig. 1A,B).

Voice onset is required for production of vowels and voiced consonants (e.g., b, d), while

voice offset is necessary for production of voiceless consonants (e.g., p, t). During speech

production, voice onset is precisely timed, which allows linguistic distinctions between

voiced and voiceless consonants, such as /d/ versus /t/. Changes in the subglottal pressure

due to changes in lung volume, the elastic properties of the chest wall and the active

contraction of the intercostal and abdominal muscles lead to modulations of voice intensity,

whereas the resonance characteristics of the supraglottal region (e.g., oral and pharyngeal

cavities) influence the spectral properties of the sound.

Vocal fold movements are controlled by intrinsic and extrinsic laryngeal muscles. The

intrinsic laryngeal muscles are confined to the larynx and participate in vocal fold closure

(thyroarytenoid, TA, lateral cricoarytenoid, LCA, and interarytenoid muscles, IA), opening

(posterior cricoarytenoid muscle, PCA), and lengthening (cricothyroid muscle, CT) (Fig.

1C,D). The extrinsic muscles connect the larynx with surrounding structures, such as the

hyoid bone, sternum and pharynx, and raise or lower the larynx within the neck relative to

the spine to modulate vocal fold length, fundamental frequency, oro-pharyngeal resonance

frequencies and formant structure.

All laryngeal muscles, with exception of the IA muscle, receive bilateral motor and sensory

innervation from the superior laryngeal (SLN) and recurrent laryngeal (RLN) nerves

branching from the vagal nerve. While the internal branch of the SLN and the RLN provides

laryngeal sensory innervation, the external motor branch of the SLN innervates the CT

muscle; all other intrinsic laryngeal muscles receive their motor innervation from the RLN.

The extrinsic muscles are primarily innervated from the ansa cervicalis. The motoneurons of

the intrinsic laryngeal muscles are located in the nucleus ambiguus of the brainstem; the

motoneurons of extrinsic muscles are situated near the hypoglossal nucleus. Motor and

sensory nuclei of the subglottal (respiratory muscles) and supraglottal (oro-facial muscles)

components are located in the pons (trigeminal motor nucleus), brainstem (facial nucleus,

hypoglossal nucleus, and nucleus ambiguus), and ventral horn of the spinal cord (cervical,

thoracic and lumbar regions). Bilateral innervation of almost all laryngeal muscles and,

therefore, control of each half of the larynx by both left and right LMC is beneficial in

preventing loss of voluntary voice control in patients with unilateral LMC damage, while

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Two pathways controlling voice production

bilateral LMC lesions render patients unable to speak and sing. On the other hand, damage

to the branches of the vagal nerve results in the unilateral paralysis and paresis of the vocal

fold (Jurgens, 2002).

Central control of voice production is carried out by two parallel pathways: the limbic vocal

control pathway, which is responsible for the control of innate non-verbal and emotional

vocalizations, and the laryngeal motor cortical pathway, which regulates the fine motor

control of voluntary voice production, such as speech and song, as well as voluntary

production of innate vocalizations. These pathways are organized hierarchically, building

from the basic levels in the lower brainstem and spinal cord to the most complex levels in

the anterior cingulate cortex (ACC) and LMC, respectively (Fig. 2).

Voice control develops gradually throughout childhood for the control of speech production.

As we mentioned earlier, the first vocalization occurs at birth as a shriek of the newborn.

This and other types of non-verbal vocalizations in humans, such as an infant's cry and

laughter, represent innate vocal reactions whose acoustic structure is genetically

preprogrammed (Scheiner et al., 2004). This means that infants do not need to hear the

sounds of cry or laughter from others in order to produce them. These basic innate

vocalizations are controlled by the sensory and motor nuclei of the lower brainstem (e.g.,

ambigual, trigeminal, facial, hypoglossal, solitary tract nuclei) and spinal cord (thoracic and

lumbar ventral horn), which are responsible for the basic coordination of laryngeal,

respiratory and articulatory muscle activity (Fig. 2, subsystem I). The reticular formation of

the pons and lower brainstem is another important structure for this type of vocal control. It

plays a dual role in establishing connections between different phonatory nuclei and in

coordinating basic vocal motor activities. Single-unit recording studies in the squirrel

monkey have found that some vocalization-correlated neurons in the reticular formation are

active only during specific vocalizations, while other neurons fire during various types of

vocalizations or change their discharge rate based on the rhythmic frequency modulations of

produced vocalizations (Kirzinger and Jurgens, 1991; Luthe et al., 2000). Furthermore, the

reticular formation dorsal to the superior olive contains a vocalization pattern generator, the

neuronal activity of which co-occurs with the neuronal firing of the phonatory ambigual,

facial and motor trigeminal nuclei (Hage and Jurgens, 2006).

The involvement of the forebrain is not essential for production of innate vocalizations. It

has been reported that even anencephalic infants, who lack the entire forebrain but have an

intact brainstem, are still able to vocally react to painful stimuli (Monnier and Willi, 1953).

However, in older children, innate vocalizations come under voluntary control, sometimes

involving mimicking of vocal utterances. For example, cry can be produced in the absence

of pain or suppressed in the presence of pain. For this higher level of vocal control, that is,

voluntary initiation of innate vocalizations and control of their emotional status, the

brainstem phonatory nuclei and the vocal pattern generator require an input from the higher

brain regions, such as the periaqueductal gray (PAG) and ACC (Fig. 2, subsystem II). The

PAG receives direct projections from the ACC as well as from other cortical and subcortical

regions controlling limbic, sensory, motor, cognitive and arousal systems (Dujardin and

Jurgens, 2005). The PAG projects to the reticular formation of the lower brainstem, thus

representing an neuroanatomical and functional relay station within the ACC-PAG-
brainstem pathway. The PAG plays primarily a gating role in triggering a vocal response

and modulating its intensity, while the ACC is involved in voluntary control of voice

initiation and its emotional intonation. Destruction of the ACC results in a loss of voluntary

control of emotional intonations during speaking, while lesions in the PAG lead to mutism.

Interestingly, destruction of the ACC does not interfere with the production of vocalizations

elicited at the level of the PAG and brainstem reticular formation; however, destruction of

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Localization of the laryngeal motor cortex

the PAG abolishes vocalizations from the ACC but not from the brainstem reticular

formation (Jurgens, 2002). Thus, while the ACC and PAG are important in shaping

voluntary control of voice initiation and emotional modulation, the reticular formation

represents the basic executing level of this pathway.

The highest level within the hierarchy of voice controlling system is represented by the

LMC and its input and output structures (Fig. 2, subsystem III). The ability to learn new

vocalizations is very limited, perhaps impossible, in non-human primates and other

mammals (except whales and dolphins). Their vocalizations are exclusively emotional, with

each type of vocalization conveying only one meaning. In humans, in contrast, the

development of the ability to produce innumerable learned vocal utterances for speech and

song depends on the fine motor control by the LMC. While lesions in this region have

almost no effects on monkey vocalizations, they abolish speech production in human

patients (Jurgens, 2002). Such patients are occasionally able to initiate phonation, such as

grunts, wails and laughs, but do not succeed in voluntary modulations of pitch, intensity and

the harmonious quality of their vocalizations. The preservation of non-verbal vocalizations

in patients with bilateral damage to the LMC may be due to parallel organization of the

LMC and ACC-PAG pathways, one controlling voluntary voice production and the other

controlling the initiation of basic vocal reactions.

For proper coordination of learned vocal patterning and voice initiation, the LMC and ACC-
PAG pathways converge in at least two regions, as found in neuroanatomical studies in non-
human primates. One such region is the ACC itself, which has direct reciprocal connections

with the LMC (Simonyan and Jurgens, 2002, 2005a). The other region is the reticular

formation of the brainstem, which projects directly to the phonatory motoneurons (Hannig

and Jurgens, 2006). Thus, the vocal motor control system seems to be separated into two

parallel pathways for learned and innate vocalizations, coordination and interactions of

which are indispensible for proper voice control.

As we stated earlier, the role of the LMC is essential in the control of voluntary laryngeal

behaviors, both learned, such as speech and song, and innate, such as production on demand

of laughter, coughing, breathing, etc. The ability to control various laryngeal behaviors

voluntarily is most prominent in humans, while other species, including non-human

primates, have limited ability to produce their vocalizations voluntarily.

First observations of the larynx representation within the motor cortex were made in the

1930s. Shortly after the report by Oscar Foester that bilateral vocal fold movements in

humans can be produced with electrical stimulation of the motor strip of one hemisphere

(Foester, 1936), Wilder Penfield and colleagues described the representation of vocalization

in the inferior portion of the motor cortex above the jaw and below the lip muscles

representations (Penfield and Bordley, 1937) (Fig. 3A). Nearly the same somatotopy was

observed in the monkey brain with the representation of the larynx region just above the

Sylvian fissure (Woolsey et al., 1952) (Fig. 3B). On the other hand, electrical stimulation

studies failed to identify the larynx representation in the motor cortex of lower mammals,

such as the dog and cat (Milojevic and Hast, 1964).

Although the implications of the LMC in the control of voice production is significantly

different between humans and non-human primates, much of our understanding about the

organization of the LMC comes from research in non-human primates, primarily in the

rhesus and squirrel monkeys. The LMC in these species is situated between the inferior

branch of the arcuate sulcus anteriorly and the subcentral dimple posteriorly (Hast et al.,

1974) (Fig. 3D). This region contains small populations of neurons that are selectively active

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Laryngeal motor cortical networks

during either conditioned or spontaneous vocalizations (Coude et al., 2009). Among these,

the majority of neurons specific for conditioned vocalization discharge before voice onset,

while a smaller number of neurons are time-locked with voice onset.

The larynx area is surrounded by the representations of the tongue, lip and masticatory

muscles and is considered to be part of the primary motor cortex, although

cytoarchitectonically it corresponds to premotor cortex, area 6, in non-human primates

(Jurgens, 1974; Simonyan and Jurgens, 2002). Electrical stimulation of this region with

simultaneous laryngeal electromyographic (EMG) recordings in the rhesus monkey revealed

that the intrinsic and extrinsic laryngeal muscles have separate representations within the

LMC, i.e. topographical organization (Hast et al., 1974) (Fig. 3D).

More than half a century later after Foester's and Penfield's seminal observations, studies of

the LMC in humans have been recently revived with the advent of non-invasive

neuroimaging techniques. Recent investigations in humans have shown that the LMC is

located more dorsally from the Sylvian fissure (Khedr and Aref, 2002; Rodel et al., 2004)

than originally proposed (Penfield and Bordley, 1937). Similar to non-human primates, the

human LMC is organized topographically, although, compared to the monkey's brain, the

representation of the laryngeal muscles is reversed, with the CT muscle located more

medially than the TA muscle (Rodel et al., 2004). However, in contrast to the monkey,

recent studies have substantially revised the location of the LMC in humans. From the

earlier works of Penfield and colleagues, it is notable that the motor homunculus identifies a

representation of a behavior (vocalization) rather than an organ (larynx) in the inferior

portion of the motor cortex (Fig. 3A). As behavior, vocalization requires not only laryngeal

muscle activity but also orchestrated activity of the respiratory and orofacial movements.

Hence, it is not surprising that, on the map of the motor homunculus, vocalization as

behavior, in contrast to the single organ representation, encompasses quite a large region

within the motor cortex, overlapping with the lip, jaw and tongue representations, without,

however, a specific reference to the larynx. Thus, the location of the human LMC remained

largely unknown until recently. Neuroimaging studies using different vocal tasks were

finally able to separate and localize the laryngeal region within the primary motor cortex

(Brown et al., 2008; Loucks et al., 2007; Rodel et al., 2004; Simonyan et al., 2009; Wilson et

al., 2004), predominantly in the area 4p (Fig. 3C).

The differences in the cytoarchitectonic location of the LMC between humans and non-
human primates deserve special attention. The representation of the LMC in the primary

motor cortex (area 4) in humans, as oppose to its location in the premotor cortex (area 6) in

non-human primates, may represent one of the major evolutionary developments in humans

towards the ability to speak and vocalize voluntarily. The LMC representation in area 4 of

the motor cortex may have enabled the establishment of a unique direct connection between

the LMC and laryngeal motoneurons of the brainstem for faster neuronal transmission and

direct control over the coordinated activity of complex laryngeal, orofacial and respiratory

movements for speech production. In monkeys, this connection is indirect and hence the

control of the brainstem laryngeal motoneurons is limited. We hypothesize that3 this

neuroanatomical difference may underlie the very limited ability of non-human primates to

learn and control their vocalizations voluntarily.

Despite the differences in the representation of the larynx area in the motor cortex and in its

anatomical and functional distinctions between humans and non-human primates, the latter

species still remain a valuable model for studying the neuroanatomical projections of the

LMC using invasive tract tracing techniques. Such investigations in non-human primates

can be considered complimentary to diffusion tensor tractography (DTT) studies in humans

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for categorization of directionality of the LMC connections (efferent vs. afferent), which is

otherwise impossible to define using only the DTT approach. Hence, in the following, we

will review the LMC networks based on studies using both DTT in humans (Simonyan et

al., 2009) and neuroanatomical tract tracing in the rhesus and squirrel monkeys (Jurgens,

1976; Simonyan and Jurgens, 2002, 2003, 2005a, b). We will further review the interaction

of the LMC with the main cortical and subcortical regions indispensible for voluntary voice

production based on neuroimaging studies of voice and speech in humans.

A series of recent investigations have shown that both humans and non-human primates

share a common network of extensive cortical and subcortical connections with the LMC

(Fig. 4). Nearly all cortical connections of the LMC are reciprocal, that is the LMC both

receives and sends information to these regions. The regions reciprocally connected with the

LMC are the surrounding ventral and dorsal premotor, primary motor and somatosensory

cortices at their orofacial and trunkal representations, inferior frontal gyrus (IFG),

ventrolateral and dorsolateral prefrontal cortex, insula, cingulate cortex (CC), supplementary

motor area (SMA), angular (AG), supramarginal (SMG), middle (MTG) and superior

temporal (STG) gyri, claustrum, ventral and mediodorsal thalamus, medial parabrachial

nucleus, deep mesencephalic nucleus and locus coeruleus. The only cortical region

projecting to the LMC without receiving an input from it is the orbital cortex, which is

assumed to have only a very indirect involvement in vocal control (Price, 1996), as well as

subcortically the ventral tegmental area, substantia nigra and raphe nucleus. On the other

hand, the cortical regions that receive projections from the LMC but do not send connections

back are the inferior parietal cortex, posterior parietal operculum and cortex within the

intraparietal sulcus, as well as subcortically the putamen, caudate nucleus, globus pallidus

and brainstem nuclei (i.e., reticular formation and spinal trigeminal, solitary tract and facial


Functionally, the LMC is connected with most of these structures to fulfill its main task - the

voluntary control of voice production. Interconnections of the LMC with the surrounding

somatosensory cortex and inferior parietal cortex are important for integration of

proprioceptive and tactile feedback from the orofacial, respiratory and laryngeal regions

during voice production. Neuroimaging studies of overt and covert voice and speech

production have consistently reported activation of the primary sensorimotor cortex (e.g.,

(Bohland and Guenther, 2006; Horwitz et al., 2003; Loucks et al., 2007; Riecker et al.,

2000). Activation in this region is organized somatotopically with the orofacial and

laryngeal activation occupying the ventral portion of the sensorimotor cortex and the

respiratory activation represented as two discrete loci in the dorsal region of the trunk

representation and in the ventral region overlapping with the laryngeal and orofacial

activation (Brown et al., 2009; Loucks et al., 2007; Simonyan et al., 2007). Interestingly,

only voluntary exhalation, which is required for voice production, but not inhalation elicits

activation of both dorsal and ventral sensorimotor cortex (Ramsay et al., 1993). The

orchestration of simultaneous laryngeal, orofacial and respiratory muscle activity at the

cortical sensorimotor level becomes apparent when one of its components is voluntarily

modulated or altered. A recent study of functional LMC networks during syllable production

showed that when subjects were asked to produce voice with minimal orofacial movements

and at the similar breathing depth, that is the modulation of two out of three components of

voice production system, the LMC displayed reduced functional connectivity with both

orofacial and respiratory sensorimotor cortices to maintain specific level of task production

(Simonyan et al., 2009). The influences of the somatosensory cortex on the motor cortex

become even more apparent when the auditory feedback, another online monitoring system

of correct voice and speech production, is altered and the encoding of auditory input is

challenged, for example, in the presence of very loud noise (Guenther, 2006; Peschke et al.,

2009). These observations suggest that the ventral sensorimotor region contains not only a

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simple ensemble of motor and sensory components of the voice controlling system (e.g.,

laryngeal, orofacial and respiratory), but it also acts as a higher-level centralized region,

coordinating exhalatory airflow necessary for setting the vocal folds into vibration and

modulating the orofacial articulators for voluntary production of different types of vocal


With respect to the inferior parietal cortex, including the SMG and AG, this region

represents one of a few higher-order sensorimotor centers for coordination of both speech

production and comprehension. The inferior parietal cortex is known to be involved in

complex phonological and semantic processing and monitoring of the verbal response to

suppress phonemic errors (e.g., (Fiebach et al., 2007; Hocking et al., 2009; Zheng et al.,


The LMC requires an input from the IFG for motor planning of voice and speech

production. The IFG is another brain region where the control of speech production and

comprehension converge. Its pars orbitalis is involved in the retrieval of semantic

information (de Zubicaray and McMahon, 2009; Tyler et al., 2010) and its pars opercularis

is responsible for hierarchical sequencing of linguistic and non-linguistic sequences

(Tettamanti et al., 2009; Willems et al., 2009) and articulatory preparation to speech

production (Papoutsi et al., 2009; Zheng et al., 2010). Because the IFG is prominent in the

processing of information necessary for long-term preparation of learned oro-motor

sequences, it is not surprising that the IFG is usually active during production of long

sequences of syllables and words (e.g., (Horwitz et al., 2003; Ozdemir et al., 2006; Wise et

al., 1999) and only rarely during production of single syllables (Brown et al., 2008; Ghosh et

al., 2008; Loucks et al., 2007). Despite the fact that the IFG activation is not always

observed in studies of differential complexity of voice and speech production, the strong

functional and structural connectivity between the IFG and LMC seems to be responsible for

motor preparation and processing of all components of speech production (e.g., laryngeal,

orofacial, or respiratory) (Greenlee et al., 2004; Simonyan et al., 2009).

The reciprocal connections of the LMC with the SMA are needed for preparation for vocal

motor command execution. Accordingly, it has been shown that the offset of the late vocal-
related cortical potentials in the SMA precedes those in the LMC pointing to the

involvement of the LMC only after the motor preparatory phase in the SMA (Galgano and

Froud, 2008). The SMA is active during various voluntary laryngeal tasks (e.g., (Ghosh et

al., 2008; Loucks et al., 2007; Ozdemir et al., 2006; Simonyan et al., 2007). More

specifically, it has been shown that activation in the anterior pre-SMA was related to

effortful word selection, activation in the posterior pre-SMA was related to the control of

syllable sequencing, and activation in the SMA proper was related to overt articulation

(Alario et al., 2006). Recently, the SMA has also been identified as a motor component of

the speech monitoring network (van de Ven et al., 2009). Furthermore, electrical stimulation

of this region has been reported to elicit vocalizations in humans (Penfield and Welch, 1951)

but not in monkeys (Jurgens, 2002). Similarly, bilateral lesions in the SMA have no effect

on monkey vocalizations. In contrast, in humans, such lesions severely reduce motivation to

employ propositional speech, whereas nonpropositional (automatic) speech remains almost

intact (so-called transcortical motor aphasia). Functional connections between the LMC and

SMA are left-lateralized and are particularly stronger with the pre-SMA during learned

voice production compared to innate laryngeal behavior, such as breathing (Simonyan et al.,

2009). It, thus, appears that the connectivity between the LMC and the pre-SMA, a region

responsible for processing of higher order motor plans for subsequently ordered movement

execution (Matsuzaka et al., 1992; Shima and Tanji, 1998; Tanji and Shima, 1996), plays a

central role in sequencing and initiation of complex learned vocal movements during speech


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It is important to note that the LMC has a reciprocal structural connection with the ACC but

not with the PAG as identified based on neuroanatomical tract tracing studies in non-human

primates. The lack of connections between the LMC and PAG fits well with the separation

between the two descending pathways controlling voice production, limbic and motor

cortical. Similarly, in the monkey, the PAG blockade has no effect on vocal fold movements

elicited from the LMC as oppose to the drastic effects on vocalization elicited by limbic

structures (Jurgens, 2002). The LMC, thus, seems to control the voluntary voice production

via a pathway by-passing the PAG, although it establishes connections with the ACC for

shaping emotional intonations during speech production. As noted earlier, the connection

between the LMC and ACC serves as one of the two links at which two pathways

controlling innate emotional and learned vocalizations converge.

Another link between the limbic and motor cortical vocal pathways is present at the level of

the brainstem reticular formation, specifically in its dorsal and parvocellular reticular nuclei,

which are further directly connected with laryngeal motoneurons in the nucleus ambiguus,

the articulatory motoneurons in the trigeminal motor, facial and hypoglossal nuclei, and the

expiratory motoneurons in the thoracic and upper lumbar spinal cord (Bernard et al., 1990;

Thoms and Jurgens, 1987; VanderHorst et al., 2001). Combined electrical stimulation and

lesioning studies have shown that bilateral lesions in this region block vocalizations elicited

from the PAG and vocal fold movements elicited from the LMC (Jurgens and Ehrenreich,

2007; Shiba et al., 1997). Because both limbic and motor cortical pathways come together in

the reticular formation of the brainstem, it has been suggested that this region is involved in

vocal motor coordination of both innate and learned voice production (Jurgens and

Ehrenreich, 2007). Its functional properties are more important in vocal motor control in

non-human primates than in humans due to the lack of direct projections from the LMC to

the nucleus ambiguus in the former species and, therefore, their reduced ability to directly

modulate activity of brainstem laryngeal motoneurons (Jurgens, 1976; Simonyan and

Jurgens, 2003). In humans, in contrast, direct connections do exist between the LMC and the

nucleus ambiguus (Iwatsubo et al., 1990; Kuypers, 1958). This direct LMC-ambigual

connection together with the LMC representation in the primary motor cortex seem to be

very recent acquisitions in hominid evolution and may be regarded crucial as prerequisites

for speech control.

In addition to direct LMC-brainstem laryngeal motoneurons connections, the LMC

establishes a widespread network of subcortical connections, most of which project further

down to the brainstem phonatory motoneurons. The putamen receives the strongest of all

telencephalic subcortical projections from the LMC, thus representing the main basal

ganglia output structure of the LMC. Putaminal lesions cause dysarthria and dysphonia in

humans but have no effect on monkey's vocalizations (Jurgens, 2002), suggesting the

involvement of the putamen only in learned voluntary voice and speech production but not

in production of innate vocalizations. Motor cortical connections to the putamen are

somatotopically organized with the leg area projecting to the rostrodorsal putamen, the arm

and trunk occupying its central part, the face area projections to the caudoventral putamen,

and the larynx area connecting with the ventral putamen over a large anterio-posterior extent

(Kunzle, 1975; Simonyan and Jurgens, 2003). It appears that there is an overlap of

projections from the face and larynx areas in the posterior (postcommissural) putamen (i.e.,

part of the sensorimotor functional striatal loop), whereas the putamen rostral to the anterior

commissure (i.e., part of the associative and limbic striatal loops) receives input only from

the LMC. Direct connections of the LMC with all striatal functional subdivisions, including

the sensorimotor, associative and limbic loops, may represent important factors in the

integrative control of different aspects of speech production, ranging from motor control to

motivation and cognitive processing of speech.

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Future Directions

Another subcortical region that is directly connected with the LMC is the thalamus,

specifically its ventral lateral, ventral posterior, medial, and centromedian groups of nuclei.

Single-unit recordings in the ventral thalamus have shown voice and speech-related neuronal

activity (Farley, 1997; McClean et al., 1990). Furthermore, the ventral thalamus has

reciprocal connections with the LMC, IFG and SMA, electrical stimulation of which also

produces vocalization in humans (Penfield and Roberts, 1959). Besides the direct role of the

ventral thalamus in vocal sensorimotor coordination of learned voice production, it

represents an important relay station of the cortico-striato-pallido-thalamo-cortical and

cortico-ponto-cerebello-thalamo-cortical loops for integration of sensorimotor information

from the basal ganglia and cerebellum. Both pathways, finally, connect the LMC with the

laryngeal motoneurons after synapsing in the reticular formation of the brainstem.

In conclusion, the central control of human voice production is organized hierarchically. As

the highest level of this control system, the human LMC is indispensible for the control of

learned but not innate vocalizations. To fulfill its function, the human LMC has direct

connections with the brainstem laryngeal motoneurons, as well as participation in a

widespread network of cortical and subcortical connections, which further indirectly connect

the LMC with laryngeal motoneurons. Thus, voluntary voice production is controlled by the

LMC and is executed through the multiple pathways, both directly and indirectly descending

to the brainstem laryngeal motoneurons. This is supported also by the fact that a combined

interruption of the direct and indirect LMC-motoneuronal pathways abolishes the ability to

produce voice and speech voluntarily, similar to bilateral lesions in the LMC alone (Bauer et

al., 1980; Urban et al., 1996).

Although over the past few years we have seen advances in understanding of the LMC's role

in human voice and speech production, there are still a number of unanswered questions

about its structural and functional organization and interactions with other brain regions in

both healthy humans and patients with neurological voice and speech disorders. In

particular, further research is needed both in humans and non-human primates for

characterization of sub-components of the LMC networks. To date, the LMC projections

have been identified using trans-synaptic tracers, such as 3H-leucine, biotin dextran amine,

and wheat germ agglutinin conjugated with horseradish peroxidase, in non-human primates

and using unconstrained probabilistic DTT in healthy humans. Both techniques provide

information about the projecting regions to and from the LMC but lack information about

whether the given connection between the LMC and the target region is direct or indirect via

other relay stations. To derive a more complete characterization of the LMC structural

networks, neuroanatomical studies using tracers that are transported in a time-dependent

manner to label synaptically-connected neuronal chains (Kelly and Strick, 2000) should be

conducted in non-human primates and further verified in healthy humans using multi-modal

neuroimaging techniques.

Future research should also focus on the organization of functional LMC networks during

different components of laryngeal behaviors and on interactions between limbic and motor

cortical parallel pathways. Similarly, given that speech production, as one of the most rapid

human motor actions, has a strong temporal dimension, the temporal characteristics of the

LMC activity remain to be explored. The significance of these studies is paramount for

future investigations of altered structural and functional links within the central voice

control system in patients with neurological voice and speech disorders.

Another unknown aspect is the laryngeal representation in the primary somatosensory cortex

and its interactions with the LMC. The earlier studies by Penfield and colleagues lacked the

mapping of the larynx representation in the primary somatosensory cortex. Since then, no

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Simonyan and Horwitz Page 10

attempts have been reported to identify the laryngeal somatosensory region, although it is

known that lesions in the inferior postcentral gyrus cause dysarthria due to the interruptions

of kinesthetic and proprioceptive feedback from the phonatory organs (Luria, 1964).

Finally, it is unknown, to date, how different neurotransmitters (e.g., dopamine, GABA)

influence and modulate the human LMC networks during voice and speech production. This

information will be crucial in identifying the target brain regions for the development of new

neuropharmacological options to modulate the LMC activity in patients with neurological

voice problems.


This work was supported by the Extramural and Intramural Programs of the National Institute on Deafness and

Other Communication Disorders, National Institutes of Health (R00DC009620 to K.S.).


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Figure 1. (A) Schematic view of the vocal and respiratory tracts

Voice originates in the larynx. First, the expiratory airflow from the lungs reaches the larynx

through the trachea, where it sets the closed vocal fold tissue into self-excited oscillatations,

due to which the larynx becomes the source of voice sound. Further, pressure from the vocal

fold oscillations is resonated through the vocal tract and radiated from the mouth as voice.

(B) Schematic sequence of events preceding voice production. (1). The vocal folds close

immideatly prior to voice production; (2) subglottal air pressure builds up below the vocal

folds during exhalation; (3) lower and upper edge of the vocal folds separate subsequently

with the release of air and sound generation; (4) the vocal folds re-approximate, starting

from their lower edge, and (5) the vocal folds close completely before the next sound

production. (C) Superior and lateral views of the human larynx. Intrinsic laryngeal muscles

and cartilages. TA – thyroarytenoid muscle; LCA – lateral cricoarytenoid muscle; PCA –

posterior cricoarytenoid muscle; IA – interarytenoid muscle; CT - cricothyroid muscle. The

arrows show the directions of the muscle contractions. (D) Schematic presentation of the

laryngeal muscle function. The left column shows the location of the cartilages and the edge

of the vocal folds when each of the laryngeal muscles is active. The arrows indicate the

directions of the force exerted. 1. thyroid cartilage; 2. cricoid cartilage; 3. arytenoid

cartilages; 4. vocal ligament; 5. posterior cricoarytenoid ligament. The middle column

shows the laryngeal view. The right column shows contours of the frontal section at the

middle of the membranous portion of the vocal fold. The dotted line shows a state in which

no muscle is activated (reprinted from Hirano, 1981 with permission of Springer Science +

Business Media).

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Simonyan and Horwitz Page 15

Figure 2. Hierarchical organization of central voice control in humans and non-human primates

The figure depicts different levels of the voice control system. The lowest level (Subsystem

I) is represented by the brainstem and spinal cord sensorimotor phonatory nuclei. This

subsystem is responsible for the coordination of laryngeal, articulatory and respiratory

control during production of innate vocalizations. The higher level within this system

(Subsystem II) is represented by the PAG, ACC and limbic input structures, such as the

hypothalamus, midline thalamus, amygdala, red nucleus, preoptic region, septum. This

subsystem is responsible for initiation of vocalizations and control of voluntary emotional

vocalizations. The highest level is represented by the laryngeal/orofacial motor cortex with

its input and output regions (Subsystem III). This subsystem is responsible for voluntary

vocal motor control of speech and song production. The dotted lines show simplified

connections between different regions within the voice controlling system.

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Figure 3. Laryngeal motor cortical representation

Schematic views of body representation within the motor cortex (A) in humans (“motor

homunculus” according to (Penfield and Bordley, 1937)) and (B) in the rhesus monkey

(“motor simiculus” according to (Woolsey et al., 1952), reprinted from Fadiga et al., 2000

with permission from Elsevier). (C) The laryngeal motor cortical region in humans as

defined in neuroimaging studies. The colored circles represent the reported peaks of

activation in the following studies of syllable production: orange - (Bohland and Guenther,

2006); purple - (Olthoff et al., 2008); light blue - (Terumitsu et al., 2006); green - (Loucks et

al., 2007); blue - (Brown et al., 2008); red -(Wilson et al., 2004); black - (Simonyan et al.,

2009); white - (Riecker et al., 2008), and yellow - (Peeva et al.). CS - central sulcus. (D) The

laryngeal motor cortical region in the rhesus monkey. Topographical representation of the

laryngeal muscles: cricothyroid - right-angled triangle; thyroarytenoid - circle; combination

of the circothyroid and thyroarytenoid - encircled right-angled triangle, and extrinsic

laryngeal muscles - square. sca - sulcus subcentralis anterior (subcentral dimple) (reprinted

from (Hast et al., 1974) with permission from Elsevier).

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Simonyan and Horwitz Page 17

Figure 4. Cortical and subcortical networks of the laryngeal motor cortex

Block diagrams illustrate the reciprocal (pink box), outgoing (green box) and incoming

(purple box) connections of the laryngeal motor cortex as defined using neuroanatomical

tracing studies in non-human primates and diffusion tensor tractography in humans. Asterisk

(*) indicates that projection from the laryngeal motor cortex to the nucleus ambiguus exists

only in humans but not in non-human primates.

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