Dorsal column–medial lemniscus pathway

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Dorsal column-medial lemniscus pathway
Spinal nerve.svg
The formation of the spinal nerve from the dorsal and ventral roots.
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Originating in peripheral sensory receptors, the dorsal column-medial lemniscus pathway transmits fine touch and conscious proprioceptive information to the brain.
Details
PrecursorNeural tube and crest
SystemSomatosensory system
DecussationMedial lemniscus
ToSensorimotor cortex
FunctionTransmit sensation of fine touch, vibration and proprioception
Identifiers
Latinvia columnae posterioris lemniscique medialis
Acronym(s)DCML, DCML
Anatomical terms of neuroanatomy

The dorsal column–medial lemniscus pathway (DCML) (also known as the posterior column-medial lemniscus pathway (PCML)) is a sensory pathway of the central nervous system that conveys sensations of fine touch, vibration, two-point discrimination, and proprioception (position) from the skin and joints. It transmits information from the body to the primary somatosensory cortex in the postcentral gyrus of the parietal lobe of the brain.[1][2] The pathway receives information from sensory receptors throughout the body, and carries this in nerve tracts in the white matter of the dorsal columns of the spinal cord, to the medulla where it is continued in the medial lemniscus, on to the thalamus and relayed from there through the internal capsule and transmitted to the somatosensory cortex. The name dorsal-column medial lemniscus comes from the two structures that carry the sensory information: the dorsal columns of the spinal cord, and the medial lemniscus in the brainstem.

There are three groupings of neurons that are involved in the pathway: first-order neurons, second-order neurons, and third-order neurons. The first-order neurons are sensory neurons located in the dorsal root ganglia, that send their afferent fibers through the two dorsal columns – the gracile fasciculus, or gracile tract, and the cuneate fasciculus or cuneate tract.[3] The first-order axons make contact with second-order neurons at the gracile nucleus and the cuneate nucleus in the lower medulla. The second-order neurons send their axons to the thalamus. The third-order neurons are in the ventral nuclear group in the thalamus and fibres from these ascend to the postcentral gyrus.

Sensory information from the upper half of the body is received at the cervical level of the spinal cord and carried in the cuneate tract, and information from the lower body is received at the lumbar level and carried in the gracile tract. The gracile tract is medial to the more lateral cuneate tract.

The axons of second-order neurons of the gracile and cuneate nuclei are known as the internal arcuate fibers and when they cross over the midline, at the sensory decussation in the medulla, they form the medial lemniscus. All of the axons in the DCML pathway are rapidly conducting, large, myelinated, alpha delta fibers.[2]

Structure[edit]

The DCML is made up of the axons of first, second, and third-order neurons, beginning in the dorsal root ganglia. These axons from the first-order neurons form the ascending tracts of the gracile fasciculus and the cuneate fasciculus which synapse on the dorsal column nuclei, the second-order neurons in the gracile nucleus and the cuneate nucleus; axons from these neurons ascend as the internal arcuate fibers; the fibers cross over at the sensory decussation and form the medial lemniscus which connects with thalamus; the axons synapse on neurons in the ventral nuclear group which then send axons to the postcentral gyrus in the parietal lobe. The gracile tract carries sensory information from the lower half of the body entering the spinal cord at the lumbar level. The cuneate tract carries sensory information from the upper half of the body (upper limbs, trunk, and neck) entering the spinal cord at the cervical level.[4]

First-order neurons[edit]

Periphery and spinal cord[edit]

The first-order neuron is a pseudounipolar neuron (example here on the left), with a single axon originating from the cell body then splitting into two branches. The body is situated in the dorsal root ganglion, with one axon traveling peripherally to tissue, and one traveling into the dorsal column. On the right is a bipolar neuron.

When an action potential is generated by a mechanoreceptor in the tissue, the action potential will travel along the peripheral axon of the first order neuron. The first order neuron is pseudounipolar in shape with its body in the dorsal root ganglion. The action signal will continue along the central axon of the neuron through the posterior root, into the posterior horn, and up the posterior column of the spinal cord.

Axons from the lower body enter the posterior column below the level of T6 and travel in the midline section of the column called the gracile fasciculus.[5] Axons from the upper body enter at or above T6 and travel up the posterior column on the outside of the gracile fasiculus in a more lateral section called the cuneate fasiculus. These fasciculi are in an area known as the posterior funiculus that lies between the posterolateral and the posterior median sulcus. They are separated by a partition of glial cells which places them on either side of the posterior intermediate sulcus.

The column reaches the junction between the spinal cord and the medulla oblongata, where lower body axons in the gracile tract connect (synapse) with neurons in the gracile nucleus, and upper body axons in the cuneate tract synapse with neurons in the cuneate nucleus.[6]

First-order neurons secrete substance P in the dorsal horn as a chemical mediator of pain signaling. The dorsal horn of the spinal cord transmits pain and non-noxious signals from the periphery to the spinal cord itself. Adenosine is another local molecule that modulates dorsal horn pain transmission [3]

Tracts of the spinal cord, showing the involved tracts of the Dorsal Column Medial Lemniscus System labeled at right.

Second-order neurons[edit]

Brainstem[edit]

The neurons in these two nuclei (the dorsal column nuclei) are second-order neurons.[6] Their axons cross over to the other side of the medulla and are now named as the internal arcuate fibers, that form the medial lemniscus on each side. This crossing over is known as the sensory decussation.

At the medulla, the medial lemniscus is orientated perpendicular to the way the fibres travelled in their tracts in the posterior column. For example, in the column, lower limb is medial, upper limb is more lateral. At the medial lemniscus, axons from the leg are more ventral, and axons from the arm are more dorsal. Fibres from the trigeminal nerve (supplying the head) come in dorsal to the arm fibres, and travel up the lemniscus too.

The medial lemniscus rotates 90 degrees at the pons. The secondary axons from neurons giving sensation to the head, stay at around the same place, while the leg axons move outwards.

The axons travel up the rest of the brainstem, and synapse at the thalamus (at the ventral posterolateral nucleus for sensation from the neck, trunk, and extremities, and at the ventral posteromedial nucleus for sensation from the head).

The second-order neuron begins with the dorsal horn of the spinal cord and decussates to the contralateral spinothalamic tract. Second-order neurons are either nociceptive-specific, which exclusively transmit noxious stimuli, or wide dynamic range (WDR) neurons.  WDR neurons are the most prevalent in the dorsal horn and receive signals from A-beta, A-delta, and C fibers.  In the thalamus, the second-order neuron synapses with the third-order neuron that transmits to the corona radiata and internal capsule to the postcentral gyrus.[5]

Third-order neurons[edit]

Thalamus to cortex[edit]

Axons from the third-order neurons in the ventral posterior nucleus in the thalamus, ascend the posterior limb of the internal capsule. Those originating from the head and the leg swap their relative positions. The axons synapse in the primary somatosensory cortex, with lower body sensation most medial (e.g., the paracentral lobule) and upper body more lateral.

Function[edit]

Discriminative sensation is well developed in the fingers of humans and allows the detection of fine textures. It also allows for the ability known as stereognosis, to determine what an unknown object is, using the hands without visual or audio input. This fine sensation is detected by mechanoreceptors called tactile corpuscles that lie in the dermis of the skin close to the epidermis. When these structures are stimulated by slight pressure, an action potential is started. Alternatively, proprioceptive muscle spindles and other skin surface touch receptors such as Merkel cells, bulbous corpuscles, lamellar corpuscles, and hair follicle receptors (peritrichial endings) may involve the first neuron in this pathway.

The sensory neurons in this pathway are pseudounipolar, meaning that they have a single process emanating from the cell body with two distinct branches: one peripheral branch that functions somewhat like a dendrite of a typical neuron by receiving input (although it should not be confused with a true dendrite), and one central branch that functions like a typical axon by carrying information to other neurons (again, both branches are actually part of one axon).

Clinical significance[edit]

Damage to the dorsal column-medial lemniscus pathway below the crossing point of its fibers results in loss of vibration and joint sense (proprioception) on the same side of the body as the lesion. Damage above the crossing point result a loss of vibration and joint sense on the opposite side of the body to the lesion. The pathway is tested with Romberg's test.

References[edit]

  1. ^ Essentials of Human Physiology by Thomas M. Nosek. Section 8/8ch5/s8ch5_22.
  2. ^ a b O'Sullivan, S. B., & Schmitz, T. J. (2007). Physical Rehabilitation (5th Edition ed.). Philadelphia: F.A. Davis Company.
  3. ^ a b Giuffrida, R; Rustioni, A (1992). "Dorsal root ganglion neurons projecting to the dorsal column nuclei of rats". J. Comp. Neurol. 316: 206–20. doi:10.1002/cne.903160206. PMID 1374085.
  4. ^ Purves, Dale (2011). Neuroscience (5th ed.). Sunderland, Mass.: Sinauer. pp. 198–200. ISBN 9780878936953.
  5. ^ a b Luria, V; Laufer, E (Jul 2, 2007). "Lateral motor column axons execute a ternary trajectory choice between limb and body tissues". Neural development. 2: 13. doi:10.1186/1749-8104-2-13. PMC 1949814. PMID 17605791.
  6. ^ a b Ganong's Review of Medical Physiology. pp. 168–170. ISBN 9780071825108.

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