Figure 14-1. The location of cranial nerve nuclei and the course of their fibers within the brainstem. The functional components associated with each nucleus and with the fibers to or from that nucleus are color coded in this figure. As described in earlier chapters, a contemporary view of the functional components is based on new concepts of development and focuses on only somatic or visceral and deemphasizes the “general” and “special” designations. Recognizing that either the traditional or contemporary method may be used, the color coding in this and other figures in this chapter for nuclei and fibers is as follows: general somatic efferent (GSE) or somatic efferent (SE), red; general somatic afferent (GSA) or somatic afferent (SA), light red; special visceral efferent (SVE) or somatic efferent (SE), blue; general visceral efferent (GVE) or visceral efferent (VE), light blue; special visceral afferent (SVA) or visceral afferent (VA), green; general visceral afferent (GVA) or visceral afferent (VA), light green; and special somatic afferent (SSA) or somatic afferent (SA), gray. IC, inferior colliculus; IO, inferior olive; SC, superior colliculus. (Modified with permission from Carpenter MB, Sutin J: Human Neuroanatomy, 8th ed. Baltimore, Williams & Wilkins, 1983.)
Laterally adjacent to the SE cell column are the nuclei that collectively constitute the cranial part of the craniosacral division (parasympathetic) of the visceromotor nervous system. These nuclei, with the cranial nerves on which the preganglionic fibers travel, are (1) the dorsal motor vagal nucleus—vagus nerve; (2) the inferior salivatory nucleus—glossopharyngeal nerve; (3) the superior salivatory nucleus—the facial nerve, intermediate part; and (4) the Edinger-Westphal pg (preganglionic cells) nucleus—oculomotor nerve (Fig. 14-1; see also Fig. 10-7). These nuclei share the following characteristics. First, they form a discontinuous column located slightly lateral to the SE nuclei. Second, the neurons in these nuclei give rise to preganglionic axons that terminate in a peripheral ganglion, the cells of which give rise to postganglionic fibers that innervate a visceral structure. Third, because these motor neurons are part of a pathway that innervates a visceral structure (tissue composed of smooth muscle, glandular epithelium, or cardiac muscle or a combination of these), they are classified as visceral efferent (VE). They can most accurately be identified as VE preganglionic parasympathetic as this term completely identifies their structural and functional relationships.
The most lateral motor cell column in the medulla and in the pontine tegmentum is formed by the nucleus ambiguus, the efferents of which travel on the vagus and glossopharyngeal nerves, and by the facial motor nucleus and the trigeminal motor nucleus, related to facial and trigeminal nerves, respectively (Fig. 14-1; see also Fig. 10-7). These motor nuclei also share common characteristics. First, they form a discontinuous column in the more lateral part of the medulla and pontine tegmentum. Their position, as is the case for the SE and VE cell columns, reflects the differentiation of the basal plate in the brainstem (see Fig. 10-8). Second, the muscles innervated by these lower motor neurons originate from paraxial mesoderm that initially migrates into the pharyngeal arches. The muscles of mastication (trigeminal nerve innervation) originate through arch I; the muscles of facial expression (facial nerve innervation), through arch II; the stylopharyngeus muscle (glossopharyngeal nerve innervation), through arch III; and the constrictors of the pharynx, intrinsic laryngeal muscles, palatine muscles (except the tensor veli palatini), and the vocalis (vagal nerve innervation), through arch IV. Third, owing to the fact that these lower motor neurons innervate skeletal muscles that also arose from paraxial mesoderm (see Fig. 10-8), they are classified as somatic efferent (SE).
SENSORY CELL COLUMNS AND NUCLEI
The derivatives of the alar plate that give rise to cranial nerve sensory nuclei of the brainstem are located lateral to the sulcus limitans (see Fig. 10-5 and Fig. 10-6). In contrast to the motor nuclei, which form rostrocaudally oriented but discontinuous cell columns, all three of the sensory nuclei in the brainstem form what can arguably be described as continuous cell columns in the adult. These sensory nuclei–cell columns are located in the lateral aspects of the brainstem.
The most medial of these cell columns is the solitary tract and nucleus, which is the visceral afferent center of the brainstem (Fig. 14-1; see also Fig. 10-7). No matter what cranial nerve returns visceral afferent information to the brainstem, the central processes of these primary afferent fibers contribute to the solitary tract, the fibers of which terminate in the solitary nucleus (Fig. 14-2). Visceral afferent (VA) information is conveyed centrally on the facial, glossopharyngeal, and vagus nerves and consists of taste fibers and fibers conveying visceral sensations from salivary glands and viscera of the thorax and abdomen. The majority of taste input reaches rostral portions of the solitary nucleus (sometimes called the gustatory nucleus), whereas most other visceral sensation enters the caudal portion of the solitary nucleus (sometimes referred to as the cardiorespiratory nucleus) (Fig. 14-2). Because the most rostral cranial nerve that contributes to the solitary tract and nucleus is the facial nerve (a nerve of the pons-medulla junction), the solitary tract and its nucleus are found throughout the medulla but do not extend rostrally beyond the pons-medulla junction.
Figure 14-2. Diagrammatic representation of the solitary tract and nucleus. The functional components associated with rostral versus caudal portions of the tract and nucleus and the cranial nerves conveying this input are shown in letters and numbers of proportionate size for each area.
Immediately and posteriorly adjacent to the solitary tract and nucleus are the medial and spinal vestibular nuclei. These continue rostrally, are joined by the anterior and posterior cochlear nuclei at the pons-medulla junction, and interface in the caudal pons with the superior and lateral vestibular nuclei (Fig. 14-9). This cell column receives sensory input from the vestibulocochlear nerve (cranial nerve VIII) only and subserves the sense of hearing (SA, exteroceptive functional component) and balance and equilibrium (SA, proprioceptive functional component).
The nuclei of the trigeminal sensory system form a continuous cell column extending from the spinal cord–medulla junction to the rostral midbrain (Fig. 14-1; see also Fig. 10-7). The trigeminal sensory nuclei are divided into (1) the spinal trigeminal nucleus (consisting of a pars caudalis, pars interpolaris, and pars oralis), located in the lateral medulla and extending into the caudal pons; (2) the principal sensory nucleus, located at the midpontine level; and (3) the mesencephalic nucleus, extending rostrally into the midbrain at the lateral aspect of the periaqueductal gray (Fig. 14-1; see also Fig. 13-8). As is the case for the solitary tract and nucleus (the visceral receiving center of the brainstem), the principal sensory nucleus and especially the spinal trigeminal nucleus constitute the somatic sensory receiving center of the brainstem. Although somatic afferent (SA) pain and thermal sensations enter the brainstem on four different cranial nerves (trigeminal, facial, glossopharyngeal, and vagus), the central processes of these primary afferent fibers enter the spinal trigeminal tract and terminate in the medially adjacent spinal trigeminal nucleus.
CRANIAL NERVES OF THE MEDULLA OBLONGATA
The cranial nerves that are commonly identified as exiting the medulla are the hypoglossal nerve (cranial nerve XII) through the abducens nerve (cranial nerve VI) (Figs. 14-3 and 14-4). However, in the subsequent discussion, the abducens (VI), facial (VII), and vestibulocochlear (VIII) nerves are considered the nerves of the pons-medulla junction. Consequently, the cranial nerves that are generally associated with only the medulla are the hypoglossal (XII), accessory (XI), vagus (X), and glossopharyngeal (IX) nerves (Figs. 14-3 and 14-4). The unique situation of the accessory nerve is addressed further on.
Figure 14-3. An anterior (ventral) view of the brainstem with particular emphasis on cranial nerves (CN).
Figure 14-4. An anterolateral (ventrolateral) view of the brainstem with special emphasis on cranial nerves (CN). Note the position and relationships of the foramen of Luschka.
Hypoglossal Nerve
The hypoglossal nucleus is located internal to the hypoglossal trigone. Axons of hypoglossal motor neurons pass anteriorly in the medulla along the lateral aspect of the medial lemniscus and the pyramid (see Fig. 11-11) to exit as a series of rootlets from the preolivary fissure as the hypoglossal nerve (Figs. 14-3 and 14-5). They continue through the hypoglossal canal and distribute to the intrinsic muscles of the tongue plus the hyoglossus, palatoglossus, and genioglossus muscles (Fig. 14-6). In addition to the hypoglossal nerve, the hypoglossal canal may also contain an emissary vein and a small meningeal branch to the dura of the posterior fossa from the ascending pharyngeal artery.
Figure 14-5. Axial T2-weighted magnetic resonance image of the medulla showing the roots of the hypoglossal (from the preolivary fissure) and the vagus (from the postolivary or retroolivary fissure) nerves. Compare the shape of the medulla at this level with Figures 14-3 and 14-4.
Figure 14-6. The central origin and peripheral distribution of the hypoglossal nerve (cranial nerve XII). IO, inferior olive.
The blood supply to the hypoglossal nucleus and its exiting fibers is via penetrating branches of the anterior spinal artery. Occlusion of these branches (as in the medial medullary syndrome) may result in paralysis of the genioglossus muscle with deviation of the tongue toward the side of the lesion (the weak side) on protrusion. In addition, the patient experiences a contralateral hemiparesis (corticospinal tract involvement) and a contralateral loss of position sense, vibratory sense, and two-point discrimination (medial lemniscus involvement) because the anterior spinal artery also serves these structures.
Other lesions that may affect hypoglossal function include a lesion of the root of the nerve only (causing tongue deviation to the side of the lesion with no other deficits) and injury to the internal capsule. In the latter case, corticonuclear fibers to hypoglossal motor neurons innervating the genioglossus muscle are predominantly crossed. Consequently, internal capsule lesions may result in a deviation of the tongue to the contralateral side (side opposite the lesion) on protrusion, in concert with other deficits such as a contralateral hemiplegia and a drooping of the facial muscles in the lower quadrant of the contralateral side of the face. See Chapter 25 for examples of lesions that result in hypoglossal nerve dysfunction.
Accessory Nerve
This so-called cranial nerve was historically described as having a cranial part (from the medulla) and a spinal part (from the cervical spinal cord). However, studies have shown that the neurons that innervate the sternocleidomastoid and trapezius muscles are located in the cervical cord only; these muscles are not innervated by motor neurons located in the medulla. For consistency and in recognition of wide usage, the accessory nerve is considered here as a cranial nerve associated with the medulla.
The accessory nerve originates from motor neurons in the cervical spinal cord extending from C1 to C5 (Fig. 14-7). The axons of these neurons exit the lateral aspect of the cord, coalesce to form the nerve (Fig. 14-3), and ascend to enter the cranial cavity via the foramen magnum. As these accessory fibers course through the posterior fossa, they are briefly joined by vagal fibers that originate from the caudal portion of the nucleus ambiguus. These vagal fibers diverge from this temporary association and exit the skull on the tenth cranial nerve. The accessory fibers form the eleventh cranial nerve, receive no contributions from the medulla, and along with cranial nerves IX and X exit the cranial cavity via the jugular foramen (Fig. 14-8).
Figure 14-7. The central nuclei and peripheral distribution of fibers of the accessory nerve (cranial nerve XI) and the vagus nerve (cranial nerve X). Visceral afferent cell bodies (SVA, GVA) collectively form the inferior ganglion, and SA cell bodies collectively form the superior ganglion of cranial nerve X. Gust. nu., rostral portions of solitary nucleus–gustatory nucleus.
Figure 14-8. The right jugular foramen and its contents as viewed from the inside floor of the cranial cavity. The direction and size of the arrows indicate the relative size of structures entering or exiting the foramen. CN, cranial nerve.
The relationship of the accessory nerve to the vagus nerve is similar to the relationship of the seventh nerve to the trigeminal nerve via the chorda tympani. In the latter case, the taste fibers from the anterior two thirds of the tongue travel on the trigeminal nerve and then join the seventh nerve via the chorda tympani. However, throughout their extent, these taste fibers are considered part of the seventh nerve, not the fifth. In like manner, fibers of the accessory nerve temporarily join the vagus and then leave it to exit the skull (Fig. 14-7). These accessory nerve fibers do not originate from the medulla, do not distribute peripherally with the vagus, and have their cells of origin in the cervical spinal cord. What has classically been called the cranial part of the accessory nerve is actually a misnomer; these fibers represent the caudal portions of the vagus nerve to which the accessory nerve temporarily relates. Reflecting the fact that the sternocleidomastoid and trapezius muscles in the human originate from paraxial mesoderm caudal to the fourth arch (not in the fourth arch), the functional component associated with these motor neurons is SE.
Lesions of the root of the accessory nerve result in drooping of the shoulder (trapezius paralysis) on the ipsilateral side and difficulty in turning the head to the contralateral side (sternocleidomastoid paralysis) against resistance. Weakness of these muscles is not especially obvious in cervical cord lesions because a hemiplegia (indicating damage to corticospinal fibers) is the overwhelmingly obvious deficit. However, a lesion of the internal capsule may also result in deficits similar to those described previously owing to interruption of the corticonuclear fibers to the accessory nucleus; these corticonuclear fibers are primarily uncrossed.
Vagus Nerve
The vagus nerve is located at an intermediate position between the midline and lateral aspect of the medulla, exits the postolivary sulcus (Figs. 14-3 to 14-5 and 14-9), and contains both motor and sensory components. This cranial nerve exits the cranial cavity via the jugular foramen (Fig. 14-8) and exhibits two ganglia immediately external to the foramen. The superior ganglion contains the cell bodies of SA fibers, whereas the inferior ganglion contains the cell bodies of VA fibers.
Figure 14-9. Axial T2-weighted magnetic resonance image of the medulla showing the root of the vagus nerve (from the postolivary or retroolivary fissure). Note the location of a portion of the posterior inferior cerebellar artery.
The motor cells in the medulla that distribute their axons on the vagus nerve are located in the dorsal motor nucleus of the vagus (VE parasympathetic preganglionic) and in the nucleus ambiguus (SE) (Fig. 14-7). Preganglionic parasympathetic cells of the dorsal motor nucleus send their axons, via branches of the vagus nerve, to end in terminal (intramural) ganglia located adjacent to or within visceral structures of the trachea and bronchi of the lungs, the heart, and the digestive system to a level just proximal to the splenic flexure of the colon (Fig. 14-7). In general, vagal influence causes constriction of the bronchioles, decreases heart rate, and increases blood flow, peristalsis, and secretions in the gut. Axons of motor neurons in the nucleus ambiguus distribute on branches of the vagus nerve to the constrictor muscles of the pharynx, the intrinsic laryngeal muscles (including the vocalis muscle), the palatine muscles (except the tensor veli palatini, which is innervated by the fifth nerve), and the skeletal muscle in about the upper half of the esophagus (Fig. 14-7). These muscles originate from paraxial mesoderm that migrated into the fourth pharyngeal arch.
The sensory fibers conveyed on the vagus nerve relay somatic and visceral sensations. The somatic sensations are represented by SA input (recognized as pain and thermal sensations) from a small area on the ear and part of the external auditory meatus and from the dura of the posterior cranial fossa (Fig. 14-7). These fibers have their cell bodies in the superior ganglion of the vagus nerve and enter the medulla as part of the vagus, but the central processes of these primary afferent fibers enter the spinal trigeminal tract and synapse in the medially adjacent spinal trigeminal nucleus.
The visceral sensations conveyed by the vagus are represented by VA fibers (Fig. 14-7). Visceral sensations from the heart, aortic arch, pharynx and larynx, lungs, and gut to about the level of the splenic flexure are conveyed by these fibers. Their cell bodies are in the inferior ganglion of the vagus nerve, whereas the central processes of these fibers enter the solitary tract and terminate in the surrounding caudal solitary nucleus (the cardiorespiratory nucleus). The same trajectory is also followed by taste fibers on the vagus. These fibers originate from scattered taste buds on the epiglottis and base of the tongue, have their cell bodies in the inferior ganglion, enter the brainstem on the vagus nerve, and centrally distribute to the rostral solitary nucleus (the gustatory nucleus).
Both sensory (SA, VA) and taste (VA) information conveyed on the vagus nerve is eventually relayed to the sensory cortex, where it is interpreted as, for example, pain from the external auditory meatus, a sense of fullness from the gut, or taste. Details of these central pathways are described in later chapters.
A lesion of the root of the vagus nerve will result in dysphagia, owing to a unilateral paralysis of pharyngeal and laryngeal musculature, and dysarthria, owing to a weakness of laryngeal muscles and the vocalis muscle. There are, however, no lasting demonstrable symptoms specifically related to visceromotor (autonomic) dysfunction. Taste loss is not detectable and cannot be tested, and the small somatosensory loss involving the external auditory meatus and canal may be of little consequence.
Unilateral injury inside the medulla, as with tumors, vascular lesions, or syringobulbia, may give rise to similar deficits (as described earlier) that are due to damage to the nucleus ambiguus. Bilateral lesions of the medulla, although rare, result in aphonia, aphagia, dyspnea, or inspiratory stridor. Such lesions may be life-threatening, especially if they involve the dorsal motor nucleus. Dysarthria may also be seen in patients after thyroid surgery if the recurrent laryngeal nerve has been damaged.
Glossopharyngeal Nerve
The glossopharyngeal nerve exits the medulla at the postolivary sulcus (Fig. 14-10) immediately rostral to the vagus nerve (Figs. 14-3 and 14-4) and leaves the skull via the jugular foramen (Fig. 14-8) along with the vagus and accessory nerves. Like the vagus, the glossopharyngeal nerve has two ganglia: an inferior ganglion containing VA cell bodies and a superior ganglion containing SA cell bodies.
Figure 14-10. Axial T2-weighted magnetic resonance image at the medulla-pons junction showing the root of the glossopharyngeal nerve (from the postolivary fissure). Note the distinct shape of the medulla at this level and the caudal aspect of the basilar pons.
Motor fibers that distribute on the glossopharyngeal nerve originate from the inferior salivatory nucleus (VE preganglionic parasympathetic fibers) and from the nucleus ambiguus (SE fibers) (Fig. 14-11). Axons of cells of the inferior salivatory nucleus exit on the glossopharyngeal nerve and join the tympanic nerve and then the lesser petrosal nerve to synapse with VE postganglionic neurons in the otic ganglion. These postganglionic parasympathetic cells supply secretomotor input to the parotid gland. The contribution of the nucleus ambiguus to the glossopharyngeal nerve serves to innervate the stylopharyngeus muscle (Fig. 14-11). This muscle assists in swallowing and participates in the efferent part of the gag reflex.
Figure 14-11. The central nuclei and peripheral distribution of fibers of the glossopharyngeal nerve (cranial nerve IX). Visceral afferent cell bodies (SVA, GVA) collectively form the inferior ganglion, and GSA cell bodies collectively form the superior ganglion of cranial nerve IX.
Again, as with the vagus nerve, the sensory fibers of the glossopharyngeal nerve are sensory (SA) and visceral (VA) (Fig. 14-11). The SA fibers originate from cutaneous receptors on a small area of the pinna and external auditory canal and on the posterior third of the tongue. These fibers have their cell bodies in the superior ganglion, and their central processes join the spinal trigeminal tract before terminating in the spinal trigeminal nucleus. The visceral afferent (VA) fibers convey information from the parotid gland and the oropharynx, with an especially important input from the carotid body. The carotid body contains chemoreceptors that are sensitive to changing levels of oxygen and carbon dioxide in the blood. The VA fibers have their cell bodies in the inferior ganglion of the glossopharyngeal nerve, and centrally they enter the solitary tract to terminate in the solitary nucleus. Taste from the posterior third of the tongue (Fig. 14-11) is conveyed centrally by VA fibers that also have their cell bodies of origin in the inferior ganglion of the glossopharyngeal nerve. As is the case for all taste fibers, the central processes of these afferent fibers enter the solitary tract and terminate on cells of the surrounding solitary nucleus. All afferent inputs on the glossopharyngeal nerve are eventually transmitted to relay nuclei of the thalamus and on to the sensory cortex, where the information is fully appreciated and interpreted.
Lesions of the ninth cranial nerve are relatively rare but may occur in combination with the vagal and accessory roots at the jugular foramen (Fig. 14-8). Deficits related only to glossopharyngeal nerve damage are largely restricted to a loss of taste from the posterior third of the tongue and a loss of stylopharyngeus contraction on the side of the lesion; this may affect the gag reflex. The gag reflex depends on the integrity of cranial nerves IX and X. In addition, the ninth nerve is subject to glossopharyngeal neuralgia. This disorder is characterized by attacks of intense idiopathic pain arising from the sensory distribution of the nerve (pharynx, caudal parts of the tongue, tonsil, and possibly areas of the middle ear). The attacks may be spontaneous or may result from artificial stimulation of the back of the oral cavity or from swallowing or even talking. Glossopharyngeal neuralgia may be severe and can be seriously disabling.
Jugular Foramen
In addition to containing cranial nerves IX, X, and XI, which pass through approximately its middle third, the jugular foramen also serves as a conduit for other important structures (Fig. 14-8). In general, the foramen can be divided into a rostral and slightly medial area, a middle portion (containing cranial nerves IX, X, and XI), and a caudal and somewhat lateral portion.
The rostromedial portion (Fig. 14-8) contains the continuation between the inferior petrosal sinus and the internal jugular vein. The inferior petrosal sinus, although small, represents a communication between the cavernous sinus and the internal jugular vein. In addition the rostromedial portion of the jugular foramen also contains a meningeal branch of the ascending pharyngeal artery. This small vessel is one source of arterial blood to the meninges of the posterior fossa.
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