Study Guidelines

  • 1.

    The motor nucleus supplies the muscles of mastication.

  • 2.

    The mesencephalic unipolar neurons are proprioceptive.

  • 3.

    The neurons of the principal sensory nucleus receive sensory inputs from the face and underlying mucous membranes.

  • 4.

    The spinal nucleus is of special clinical importance because of its large nociceptive territory.

Trigeminal Nerve

The trigeminal nerve has a very large sensory territory that includes the skin of the face, oronasal mucous membranes, teeth, dura mater, and major intracranial blood vessels. The nerve is also both motor and sensory to the muscles of mastication. The motor root lies medial to the large sensory root at the site of attachment to the pons ( Fig. 17.16 ). The trigeminal (Gasserian) ganglion , near the apex of the petrous temporal bone, gives rise to the sensory root and consists of unipolar neurons.

Details of the distribution of the ophthalmic, maxillary, and mandibular divisions are available in gross anatomy textbooks. Accurate appreciation of their respective territories on the face is essential if trigeminal neuralgia is to be distinguished from other sources of facial pain ( Clinical Panel 21.1 ).

Clinical Panel 21.1
Trigeminal Neuralgia

Trigeminal neuralgia is an important condition occurring in middle age or later, characterised by attacks of excruciating pain in the territory of one or more divisions of the trigeminal nerve (usually II and/or III). The patient (who is usually more than 60 years old) is able to map out the affected division(s) accurately. Because it must be distinguished from many other causes of facial pain, the clinician should be able to mark out a trigeminal sensory map ( Fig. 21.7 ). Attacks are triggered by everyday sensory stimuli such as brushing teeth, shaving, and chewing, and the tendency of patients to wince at the onset of attacks accounts for the French term tic douloureux.

Episodes of paroxysmal facial pain occurring in young adults should raise a suspicion of multiple sclerosis as the cause. Postmortem histology in such cases has revealed demyelination of the sensory root of the trigeminal nerve where it enters the pons. Demyelination of large sensory fibres receiving tactile signals from skin or mucous membranes in the trigeminal territory may cause their exposed axons to come into direct contact with unmyelinated axons serving pain receptors. Animal experiments have shown that this type of contact can initiate ephaptic transmission of action potentials between them. It is now widely accepted that the most frequent aetiology in later years is vascular compression , usually by a ‘sagging’ posterior cerebral artery in transit around the brainstem. The trigeminal CNS/peripheral nervous system (PNS) transition zone (see Chapter 9 ) is several millimetres lateral to the entry zone into the pons, and postmortem histology has provided evidence of the demyelinating effect of chronic pulsatile compression.

Antiepileptic drugs that exert a blocking effect on sodium and/or calcium channels (e.g. carbamazepine) may suffice to keep relapses at bay. Surgery is indicated for those who fail to respond.

A procedure that can be performed under local anaesthesia is electrocoagulation of the affected division, through a needle electrode inserted throughthe foramen rotundum or ovale from below. The intention is to heat the nerve sufficiently to destroy only the finest fibres, in which case analgesia is produced but touch (including the corneal reflex) is preserved.

Fig. 21.7, Trigeminal nerve sensory map.

The final option is to decompress the afflicted nerve root through an intracranial approach whereby neighbouring vessels are lifted away from it.

A surgical procedure of historic interest is medullary tractotomy , whereby the spinal root was sectioned through the dorsolateral surface of the medulla. In successful cases, pain and temperature sensitivity was lost from the face but touch (mediated by the pontine nucleus) was preserved. This procedure was abandoned owing to a high mortality rate associated with compromise of underlying respiratory and cardiovascular centres.

Motor Nucleus ( Figs. 17.16 and 21.1 )

The motor nucleus is the special visceral efferent nucleus supplying the muscles derived from the embryonic mandibular pharyngeal arch. These comprise the masticatory muscles attached to each half of the mandible ( Fig. 21.2 ), along with the tensor tympani, tensor veli palatini, mylohyoid, and the anterior belly of digastric muscle. The nucleus occupies the lateral pontine tegmentum. Embedded in its upper pole is a node of the reticular formation, the supratrigeminal nucleus , which acts as a pattern generator for masticatory rhythm.

Fig. 21.1, Trigeminal nuclei. Left , sensory nuclei; right , motor nucleus, supratrigeminal nucleus.

Fig. 21.2, (A) Masticatory and infrahyoid muscles viewed from the left side. (B) Lateral view of the pterygoid muscles of the left side. Red arrows indicate directions of pull of jaw-closing muscles. Blue arrows indicate directions of pull of jaw openers.

Voluntary control is provided by corticonuclear projections from each motor cortex to both motor nuclei but mainly the contralateral one ( Fig. 17.3 ).

Sensory Nuclei

Three sensory nuclei are associated with the trigeminal nerve: mesencephalic , pontine (principal) , and spinal .

Mesencephalic Nucleus

The mesencephalic nucleus is unique in being the only nucleus in the central nervous system (CNS) that contains the cell bodies of primary unipolar sensory neurons. Their peripheral processes enter the sensory root via the mesencephalic tract of the trigeminal nerve. Some travel in the mandibular division to supply stretch receptors (neuromuscular spindles) in the masticatory muscles. Others travel in the maxillary and mandibular divisions to supply stretch receptors (Ruffini endings) in the suspensory, periodontal ligaments of the teeth.

The central processes of the mesencephalic afferent neurons descend through the pontine tegmentum in the small tract of Probst . Most fibres of this tract terminate in the supratrigeminal nucleus; others end in the motor nucleus or in the pontine sensory nucleus; a few travel as far as the dorsal nucleus of the vagus.

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