The spinal trigeminal nucleus (SpV) is a sensory tract located in the lateral medulla of the brain stem. It is responsible for relaying various sensory modalities including temperature, deep or crude touch, and pain from the ipsilateral portion of the face. SpV incorporates sensory information from different cranial nerves, including the trigeminal nerve/branches (CN V1, V2, and V3), facial nerve (CN VII), glossopharyngeal nerve (CN IX), and vagus nerve (CN X). The spinal trigeminal nucleus is one of three nuclei in the sensory trigeminal nerve pathway. The spinal trigeminal nucleus further subdivides into the pars (subnucleus) caudalis, pars (subnucleus) oralis, and pars (subnucleus) interporalis. Each nucleus serves its own purpose. The pars oralis, one portion of the primary sensory nucleus of the trigeminal nerve, as well as the pars interpolaris are responsible for transmission of discriminative tactile sense from the face. The pars caudalis is responsible for the transmission of pain and temperature from the ipsilateral face. The posterior inferior cerebellar artery (PICA) supplies the lateral portion of the medulla where the SpV is located. Based on the sensory information the spinal trigeminal nucleus integrates and the blood supply to this region, SpV is involved in a few key clinical syndromes.
The primary function of the spinal trigeminal nucleus is to carry temperature, deep or crude touch, and pain from the ipsilateral portion of the face to the ventral posteromedial nucleus of the contralateral thalamus via the anterior trigeminothalamic tract. This sensory information will be relayed from the thalamus to the primary motor cortex via the primary sensory cortex, allowing response to stimuli of the face. This ability to react to noxious stimuli to the face and remove ourselves from harm makes the spinal trigeminal nucleus a pivotal component of the sensory pathway.
The posterior inferior cerebellar artery (PICA) branches from the vertebral artery. PICA is responsible for supplying the spinal trigeminal nucleus in the lateral medulla. Any disruption of blood flow through the vertebral artery or posterior inferior cerebellar artery would interrupt the processing of sensory information from the trigeminal nerve.
The spinal trigeminal nucleus incorporates the sensory information from all three branches of the trigeminal nerve (CN V). CN V1, also known as the ophthalmic nerve, relays sensory information from the face in regions located above the orbit of the eyes. CN V2, also known as the maxillary nerve, is primarily responsible for sensory information between the orbit of eyes and the mouth. The final branch is CN V3, also known as the mandibular nerve. CN V3 has both a sensory component as well as a motor component, however only the sensory component projects to the SpV.
The spinal trigeminal nucleus also consolidates sensory input from the facial, glossopharyngeal, and vagus nerves; this is a minor role of SpV in comparison to its integration of sensory information from the three branches of the trigeminal nerve.
It should be kept in mind that since the spinal trigeminal tract extends inferiorly up to the level of C3, this tract can be involved clinically in a patient having a craniovertebral junction tumor.
Lateral Medullary Syndrome
Lateral medullary syndrome, also known as medullary or posterior inferior cerebellar artery syndrome, occurs due to the occlusion of the posterior inferior cerebellar artery or the vertebral artery. An occlusion to either of these arteries can result in a lack of blood flow to the lateral medulla, the location of the spinal trigeminal nucleus. The primary ischemic events that trigger lateral medullary syndrome can be a result of stenotic blood vessels as is seen in adults, often with other comorbid conditions. In children, however, ischemia can be due to injury to the vertebral artery following a hyperextension neck injury. The lateral medullary syndrome presents with many symptoms including contralateral loss of pain and temperature sensation in the body with ipsilateral Horner syndrome, dysphagia, and loss of sensation in the face. This ipsilateral loss of facial sensation is due to lack of blood supply via the posterior inferior cerebellar artery to the spinal trigeminal nucleus. SpV is responsible for relaying sensory information from the trigeminal nerve to the primary sensory cortex, making it a key player in the presentation of the lateral medullary syndrome.
Trigeminal neuralgia is a condition that most often presents with unilateral, stabbing, and paroxysmal painful sensation from the face along the distribution of the trigeminal nerve. There are myriad theories in regard to the underlying mechanism of this condition. The etiologies have been broken down into idiopathic, primary, and secondary trigeminal neuralgia. Suggested peripheral mechanisms involve defects along the pathway of the trigeminal nerve before entering the brainstem. A recent hypothesis attributes the pain of trigeminal neuralgia to a central mechanism involving the subnucleus oralis of the spinal trigeminal nucleus. This theory has as its basis the characterization of trigeminal neuralgia as focal epileptic and neuronal hyperactivity. An increase in activity at the spinal trigeminal nucleus has been shown to precipitate the pain seen in trigeminal neuralgia in both cats and monkeys. Furthermore, the administration of anti-epileptic medications in cats and monkeys was able to decrease the intensity and duration of the attacks. The difficulty of treatment approaches makes the understanding of trigeminal neuralgia imperative. Though there is not a consensus on the underlying mechanism of trigeminal neuralgia, recent evidence suggests that the spinal trigeminal nucleus, in particular, the subnucleus oralis, plays a vital role in this process.
Chronic Orofacial Pain
Understanding chronic orofacial pain is important as it has been determined as a source of significant psychological distress in patients. This distress is likely because often procedures and medications are unable to provide relief of symptoms. A better understanding of the underlying mechanism may help in creating new solutions to this lack of treatment efficacy. In the processing of orofacial pain, the spinal trigeminal nucleus specifically, the subnucleus caudalis, projects to both the ventral posteromedial thalamic nucleus as well as the parabrachial nucleus. A recent study was conducted in humans to demonstrate changes in synapses of patients with chronic orofacial neuropathic pain. Utilizing T1-weighted MRI imaging, the study showed that alterations in the anatomy of primary synapses of the trigeminal nerve, particularly in the subnucleus oralis, is critical for both the generation and maintenance of chronic pain in the distribution of the trigeminal nerve. These changes included significant regional gray matter volume reduction, a decrease in mean diffusivity, and fractional anisotropy increase. Imaging of the peripheral pathways of the trigeminal nerve showed no significant change in the anatomy in the setting of chronic orofacial pain, thus decreasing the likelihood of its involvement in the pathophysiology of this condition. Anatomical changes to the subnucleus oralis of the spinal trigeminal nerve are responsible for the presentation of chronic orofacial pain.
There is evidence in rats suggesting the presence of oxytocin receptors in both the medulla oblongata and pons. These oxytocin receptors are present in the spinal trigeminal nucleus; however, as is seen with oxytocin receptors in other regions of the medulla and pons, they disappear by postnatal day 10. At the time of birth, there is an increase in the maternal release of oxytocin, likely acting on these oxytocin receptors as well; this indicates an early and transient role of oxytocin in the neuronal development of the neonatal period. The full extent of the effect of oxytocin on neuronal development postnatally is yet to be determined.
|||Huff T,Daly DT, Neuroanatomy, Cranial Nerve 5 (Trigeminal) 2018 Jan; [PubMed PMID: 29489263]|
|||Novy J, Spinal cord syndromes. Frontiers of neurology and neuroscience. 2012; [PubMed PMID: 22377894]|
|||Ruedrich ED,Chikkannaiah M,Kumar G, Wallenberg's lateral medullary syndrome in an adolescent. The American journal of emergency medicine. 2016 Nov; [PubMed PMID: 27246963]|
|||Saleem F,M Das J, Lateral Medullary Syndrome 2020 Jan; [PubMed PMID: 31869134]|
|||Cruccu G, Trigeminal Neuralgia. Continuum (Minneapolis, Minn.). 2017 Apr; [PubMed PMID: 28375911]|
|||Peker S,Sirin A, Primary trigeminal neuralgia and the role of pars oralis of the spinal trigeminal nucleus. Medical hypotheses. 2017 Mar; [PubMed PMID: 28236840]|
|||Lee KH, Facial pain: trigeminal neuralgia. Annals of the Academy of Medicine, Singapore. 1993 Mar; [PubMed PMID: 8363331]|
|||Merrill RL,Goodman D, Chronic Orofacial Pain and Behavioral Medicine. Oral and maxillofacial surgery clinics of North America. 2016 Aug; [PubMed PMID: 27475505]|
|||Okada S,Katagiri A,Saito H,Lee J,Ohara K,Iinuma T,Bereiter DA,Iwata K, Differential activation of ascending noxious pathways associated with trigeminal nerve injury. Pain. 2019 Feb 8; [PubMed PMID: 30747907]|
|||Wilcox SL,Gustin SM,Macey PM,Peck CC,Murray GM,Henderson LA, Anatomical changes at the level of the primary synapse in neuropathic pain: evidence from the spinal trigeminal nucleus. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2015 Feb 11; [PubMed PMID: 25673845]|
|||Murata Y,Li MZ,Masuko S, Developmental expression of oxytocin receptors in the neonatal medulla oblongata and pons. Neuroscience letters. 2011 Sep 20; [PubMed PMID: 21820489]|