Ventrobasal complex

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Ventrobasal complex
Details
Identifiers
Latin nuclei ventrobasales
TA A14.1.08.640
FMA 77794
Anatomical terminology

The ventrobasal complex (VB) is a relay nucleus of the thalamus for nociceptive stimuli received from nociceptive nerves. The VB consists of the ventral posteromedial nucleus (VPM) and the ventral posterolateral nucleus (VPL). In some species the ventral posterolateral nucleus, pars caudalis is also a part of the VB. [1] The VB gets inputs from the spinothalamic tract, medial lemniscus, and corticothalamic tract. [2] [3] The main output of the VB is the primary somatosensory cortex.

Thalamus part of diencephalon, which is in turn part of prosencephalon (forebrain)

The thalamus is a large mass of gray matter in the dorsal part of the diencephalon of the brain with several functions such as relaying of sensory signals, including motor signals to the cerebral cortex, and the regulation of consciousness, sleep, and alertness.

Nociception is the sensory nervous system's response to certain harmful or potentially harmful stimuli. In nociception, intense chemical, mechanical, or thermal stimulation of sensory nerve cells called nociceptors produces a signal that travels along a chain of nerve fibers via the spinal cord to the brain. Nociception triggers a variety of physiological and behavioral responses and usually results in a subjective experience of pain in sentient beings.

Nerve enclosed, cable-like bundle of axons in the peripheral nervous system

A nerve is an enclosed, cable-like bundle of nerve fibres called axons, in the peripheral nervous system. A nerve provides a common pathway for the electrochemical nerve impulses called action potentials that are transmitted along each of the axons to peripheral organs or, in the case of sensory nerves, from the periphery back to the central nervous system. Each axon within the nerve is an extension of an individual neuron, along with other supportive cells such as Schwann cells that coat the axons in myelin.

Contents

The VB serves as the main relay for nociceptive stimuli and the modulation of that stimuli to the primary somatosensory cortex. The modulation occurs through different types of receptors present in the VB.

VB Inputs

Spinothalamic tract (STT) cells that project from laminae I and V in the lumbrosacral area of the spinal cord project to the VPL in the VB. [2] STT cells located in the cervical area of the spinal cord are the densest and project from the neck of the dorsal horn to the VPL of the VB. Most projections to the VB are contralateral while only a few projections to the VB are ipsilateral. [2]

Spinal cord long, thin, tubular bundle of nervous tissue and support cells that extends from the brain

The spinal cord is a long, thin, tubular structure made up of nervous tissue, that extends from the medulla oblongata in the brainstem to the lumbar region of the vertebral column. It encloses the central canal of the spinal cord that contains cerebrospinal fluid. The brain and spinal cord together make up the central nervous system (CNS). In humans, the spinal cord begins at the occipital bone where it passes through the foramen magnum, and meets and enters the spinal canal at the beginning of the cervical vertebrae. The spinal cord extends down to between the first and second lumbar vertebrae where it ends. The enclosing bony vertebral column protects the relatively shorter spinal cord. It is around 45 cm (18 in) in men and around 43 cm (17 in) long in women. Also, the spinal cord has a varying width, ranging from 13 mm thick in the cervical and lumbar regions to 6.4 mm thick in the thoracic area.

Excitatory inputs to the VB are medial lemniscal (ML) and corticothalamic (CT) glutamatergic synapses. The ML is a sensory afferent input and the CT is from layer VI of the primary sensory cortex. [3]

The VB also gets inputs from areas in the brain stem which release acetylcholine (ACh) that can modulate activity in the VB. [3]

Acetylcholine chemical compound

Acetylcholine (ACh) is an organic chemical that functions in the brain and body of many types of animals, including humans, as a neurotransmitter—a chemical message released by nerve cells to send signals to other cells [neurons, muscle cells, and gland cells]. Its name is derived from its chemical structure: it is an ester of acetic acid and choline. Parts in the body that use or are affected by acetylcholine are referred to as cholinergic. Substances that interfere with acetylcholine activity are called anticholinergics. Acetylcholine is the neurotransmitter used at the neuromuscular junction—in other words, it is the chemical that motor neurons of the nervous system release in order to activate muscles. This property means that drugs that affect cholinergic systems can have very dangerous effects ranging from paralysis to convulsions. Acetylcholine is also a neurotransmitter in the autonomic nervous system, both as an internal transmitter for the sympathetic nervous system and as the final product released by the parasympathetic nervous system.

VB Outputs

The VB has outputs to the primary somatosensory cortex.

VB Neurons

There are two types of nociceptive neurons that provide input to the VB: nociceptive specific (NS) neurons and wide dynamic range neuron (WDR).

Wide dynamic range neuron

The wide dynamic range neuron(WDR) was first discovered by Mendell in 1966. Early studies of this neuron established what is known as the gate control theory of pain. The basic concept is that non-painful stimuli block the pathways for painful stimuli, inhibiting possible painful responses. This theory was supported by the fact that WDR neurons are responsible for responses to both painful and non-painful stimuli, and the idea that these neurons couldn't produce more than one of these responses simultaneously. WDR neurons respond to all types of somatosensory stimuli, make up the majority of the neurons found in the posterior grey column, and have the ability to produce long range responses including those responsible for pain and itch.

NS neurons respond specifically to a noxious mechanical stimulus, whereas WDR neurons respond to a graded mechanical stimulus. NS and WDR neurons within the VB are somatotopically organized. NS neurons are located more caudally in the VB, while WDR neurons are located more rostrally. All inputs into the VB are contralateral and have two different receptive fields within the VB. The VPM receptive field receives input from the contralateral trigeminal nerve and the VPL receptive field receives input from the contralateral spinal nerve. Each have NS and WDR neurons but terminate either caudally or rostrally respectively. [1]

VB Modulation

Nicotinic ACh Receptors

Nicotinic acetylcholine receptor (nAChRs) are present in the VB. Each nAChR can be made up of different subunits which can cause the receptor to respond to different stimuli. [3] In the VB, nAChRs can contain the subunits α4, α5, α7, and β2. nAChRs that are made up of (α4β2)2α5 are of interest because they decrease neurotransmitter release for corticothalamic (CT) synapses. When nAChRs are activated there is a decrease in synaptic transmission of glutamate from CT neurons. When CT synaptic transmission is decreased by activation of the nAChRs then the activated nAChRs in the VB can selectively enhance information[ further explanation needed ] to the somatosensory cortex through the medial lemniscal tract. [3]

Mu-opioid Receptors

μ-opioid receptor (MORs) are inhibitory receptors that can cause a decrease in pain if activated and are expressed in the VB especially in the VPL. [4] When MORs are activated, by an agonist like DAMGO for example, pain-related behaviors are decreased for a certain amount of time. After 45 minutes rats that were given DAMGO show signs of increased pain behaviors suggesting that opiates activate a pronociceptive system which can lead to increased pain sensitivity after only having one dose of opiates administered. [4] Decrease in pain-related behaviors can be attributed to the activation of MORs in the VB which activates an inhibitory circuit for pain by decreasing the amount or quality of information relayed to the somatosensory cortex. [4] However, there is a complex mechanism between MORs and other receptors in the VB that can lead to a decrease in pain-related behaviors and thus further research is needed to understand exactly how this mechanism works.

GABAB Receptors

GABAB receptors are located in the VB. If a receptor is located presynaptically when activated it causes the suppression of neurotransmitter release. If the receptor is located postsynaptically then when activated it causes inhibitory postsynaptic potential. [5] When GABAB receptors are activated or blocked by baclofen (agonist) or CGP35348 (antagonist) respectively there is a decrease in pain-related behaviors in a dose-dependent manner.[ further explanation needed ] [5] That is, there is less pain-related behavior if a higher dose is given. It is not known if this mechanism is occurring presynaptically or postsynaptically. Further research is needed to distinguish between where the inhibition is being mediated.

Related Research Articles

Trigeminal nerve nerve in human face

The trigeminal nerve (the fifth cranial nerve, or simply CN V) is a nerve responsible for sensation in the face and motor functions such as biting and chewing; it is the largest of the cranial nerves. Its name ("trigeminal" = tri-, or three, and - geminus, or twin: thrice-twinned) derives from the fact that each of the two nerves (one on each side of the pons) has three major branches: the ophthalmic nerve (V1), the maxillary nerve (V2), and the mandibular nerve (V3). The ophthalmic and maxillary nerves are purely sensory, whereas the mandibular nerve supplies motor as well as sensory (or "cutaneous") functions.

Sensory nervous system part of the nervous system responsible for processing sensory information

The sensory nervous system is a part of the nervous system responsible for processing sensory information. A sensory system consists of sensory neurons, neural pathways, and parts of the brain involved in sensory perception. Commonly recognized sensory systems are those for vision, hearing, touch, taste, smell, and balance. In short, senses are transducers from the physical world to the realm of the mind where we interpret the information, creating our perception of the world around us.

Nociceptor

A nociceptor is a sensory neuron that responds to damaging or potentially damaging stimuli by sending “possible threat” signals to the spinal cord and the brain. If the brain perceives the threat as credible, it creates the sensation of pain to direct attention to the body part, so the threat can hopefully be mitigated; this process is called nociception.

Dorsal column–medial lemniscus pathway

The dorsal column–medial lemniscus pathway (DCML) 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. 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.

Primary somatosensory cortex

The primary somatosensory cortex is located in the postcentral gyrus, and is part of the somatosensory system. It was initially defined from surface stimulation studies of Wilder Penfield, and parallel surface potential studies of Bard, Woolsey, and Marshall. Although initially defined to be roughly the same as Brodmann areas 3, 1 and 2, more recent work by Kaas has suggested that for homogeny with other sensory fields only area 3 should be referred to as "primary somatosensory cortex", as it receives the bulk of the thalamocortical projections from the sensory input fields.

Periaqueductal gray

The periaqueductal gray is a nucleus that plays a critical role in autonomic function, motivated behavior and behavioural responses to threatening stimuli. PAG is also the primary control center for descending pain modulation. It has enkephalin-producing cells that suppress pain.

The pretectal area, or pretectum, is a midbrain structure composed of seven nuclei and comprises part of the subcortical visual system. Through reciprocal bilateral projections from the retina, it is involved primarily in mediating behavioral responses to acute changes in ambient light such as the pupillary light reflex, the optokinetic reflex, and temporary changes to the circadian rhythm. In addition to the pretectum's role in the visual system, the anterior pretectal nucleus has been found to mediate somatosensory and nociceptive information.

Thalamocortical radiations

Thalamocortical radiations are the fibers between the thalamus and the cerebral cortex.

Allodynia refers to central pain sensitization following normally non-painful, often repetitive, stimulation. Allodynia can lead to the triggering of a pain response from stimuli which do not normally provoke pain. Temperature or physical stimuli can provoke allodynia, which may feel like a burning sensation, and it often occurs after injury to a site. Allodynia is different from hyperalgesia, an extreme, exaggerated reaction to a stimulus which is normally painful. The term is from Ancient Greek άλλοςállos "other" and οδύνηodúnē "pain".

Lateral spinothalamic tract

The lateral spinothalamic tract, which is a part of the anterolateral system, is a bundle of afferent nerve fibers ascending through the white matter of the spinal cord, carrying sensory information to the brain. It carries pain, crude touch and temperature sensory information to the thalamus. It is composed primarily of fast-conducting, sparsely myelinated A delta fibers and slow-conducting, unmyelinated C fibers. These are secondary sensory neurons which have already synapsed with the primary sensory neurons of the peripheral nervous system in the posterior horn of the spinal cord.

Posterolateral tract

The posterolateral tract is a small strand situated in relation to the tip of the posterior column close to the entrance of the posterior nerve roots. It is present throughout the spinal cord, and is most developed in the upper cervical regions.

Medium spiny neuron

Medium spiny neurons (MSNs), also known as spiny projection neurons, are a special type of GABAergic inhibitory cell representing 95% of neurons within the human striatum, a basal ganglia structure. Medium spiny neurons have two primary phenotypes : D1-type MSNs of the direct pathway and D2-type MSNs of the indirect pathway. Most striatal MSNs contain only D1-type or D2-type dopamine receptors, but a subpopulation of MSNs exhibit both phenotypes.

Group C nerve fiber

Group C nerve fibers are one of three classes of nerve fiber in the central nervous system (CNS) and peripheral nervous system (PNS). The C group fibers are unmyelinated and have a small diameter and low conduction velocity, whereas Groups A and B are myelinated. Group C fibers include postganglionic fibers in the autonomic nervous system (ANS), and nerve fibers at the dorsal roots. These fibers carry sensory information.

Recurrent thalamo-cortical resonance is an observed phenomenon of oscillatory neural activity between the thalamus and various cortical regions of the brain. It is proposed by Rodolfo Llinas and others as a theory for the integration of sensory information into the whole of perception in the brain. Thalamocortical oscillation is proposed to be a mechanism of synchronization between different cortical regions of the brain, a process known as temporal binding. This is possible through the existence of thalamocortical networks, groupings of thalamic and cortical cells that exhibit oscillatory properties.

Tactile discrimination is the ability to differentiate information through the sense of touch. The somatosensory system is the nervous system pathway that is responsible for this essential survival ability used in adaptation. There are various types of tactile discrimination. One of the most well known and most researched is two-point discrimination, the ability to differentiate between two different tactile stimuli which are relatively close together. Other types of discrimination like graphesthesia and spatial discrimination also exist but are not as extensively researched. Tactile discrimination is something that can be either more or less severe in different people and two major conditions, chronic pain and blindness, can affect it greatly. Blindness increases tactile discrimination abilities which is extremely helpful for tasks like reading braille. In contrast, chronic pain conditions, like arthritis, decrease a person’s tactile discrimination. One other major application of tactile discrimination is in new prosthetics and robotics which attempt to mimic the abilities of the human hand. In this case tactile sensors function similarly to mechanoreceptors in a human hand to differentiate tactile stimuli.

Rostral ventromedial medulla

The rostral ventromedial medulla (RVM), or ventromedial nucleus of the spinal cord, is a group of neurons located close to the midline on the floor of the medulla oblongata (myelencephalon). The rostral ventromedial medulla sends descending inhibitory and excitatory fibers to the dorsal horn spinal cord neurons. There are 3 categories of neurons in the RVM: on-cells, off-cells, and neutral cells. They are characterized by their response to nociceptive input. Off-cells show a transitory decrease in firing rate right before a nociceptive reflex, and are theorized to be inhibitory. Activation of off-cells, either by morphine or by any other means, results in antinociception. On-cells show a burst of activity immediately preceding nociceptive input, and are theorized to be contributing to the excitatory drive. Neutral cells show no response to nociceptive input.

Tactile induced analgesia is the phenomenon where concurrent touch and pain on the skin reduces the intensity of pain that is felt.

Meditation and Pain is the study of the physiological mechanisms underlying meditation-specifically its neural components- that implicate it in the reduction of pain perception.

References

  1. 1 2 Natsu Koyama, Yasuo Nishikawa, Toshikatsu Yokota. Distribution of nociceptive neurons in the ventrobasal complex of macaque thalamus. Neuroscience Research 31 (1998) 39-51.
  2. 1 2 3 W.D. Willis Jr. et al. Projections from the marginal zone and deep dorsal horn to the ventrobasal nuclei of the primate thalamus. Pain 92 (2001) 267-276.
  3. 1 2 3 4 5 Yasuyuki Nagumo, Yuichi Takeuchi, Keiji Imoto, Mariko Miyata. Synapse- and subtype-specific modulation of synaptic transmission by nicotinic acetylcholine receptors in the ventrobasal thalamus. Neuroscience Research 69 (2011) 203-213.
  4. 1 2 3 Daniel Humberto Pozza et al. Nociceptive behaviour upon modulation of mu-opioid receptors in the ventrobasal complex of the thalamus of rats. Pain 148 (2010) 492-502.
  5. 1 2 Catarina Soares Potes, Fani Lourenca Neto, Jose Manuel Castro-Lopes. Inhibition of pain behavior by GABAB receptors in the thalamic ventrobasal complex: Effect on normal rats subjected to the formalin test of nociception. Brain Research 1115 (2006) 37-47.