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Somatic nervous system

From Wikipedia, the free encyclopedia
Part of the peripheral nervous system
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Somatic nervous system
1. (Brain)Precentral gyrus: the origin of nerve signals initiating movement.

2. (Cross section ofSpinal cord)Corticospinal tract: Mediator of message from brain toskeletal muscles.

3.Axon: theefferent nerve fiber that carries the command tocontract muscles.

4.Neuromuscular junction:muscle cells are stimulated to contract at this intersection
Details
SynonymVoluntary nervous system
Part ofPeripheral nervous system
Identifiers
FMA9904
Anatomical terminology

Thesomatic nervous system (SNS), also known asvoluntary nervous system, is a part of theperipheral nervous system (PNS) that linksbrain andspinal cord toskeletal muscles under conscious control, as well as tosensory receptors in the skin.[1][2] The other part complementary to the somatic nervous system is theautonomic nervous system (ANS).[3]

The somatic nervous system consists ofnerves carryingafferent nerve fibers, which relay sensation from the body to thecentral nervous system (CNS), and nerves carryingefferent nerve fibers, which relay motor commands from the CNS to stimulatemuscle contraction.[4] Specialized nerve fiber ends calledsensory receptors are responsible for detecting information both inside and outside the body.[3]

Thea- ofafferent and thee- ofefferent correspond to theprefixesad- (to, toward) andex- (out of).

Structure

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There are 43 segments of nerves in the human body.[5] With each segment, there is a pair of sensory and motor nerves. 31 segments of nerves are in the spinal cord and 12 are in the brain stem.[5]Interneurons, also known as association neurons, are present throughout the central nervous system forming links between the sensory and motor fibres.[6]Thus the somatic nervous system consists of two parts:

  • Spinal nerves: They aremixed nerves that carry sensory information into and motor commands out of the spinal cord.[7] The spinal nerves serve as a bridge between the environment and the central nervous system (CNS). These neurons work together to transfer autonomic, sensory, and motor impulses from the spinal cord to the body's other systems. The spinal nerves are arranged into 31 pairs according to the regions of the spinal cord. To be more precise, there are eight pairs ofcervical nerves (C1–C8), twelve pairs ofthoracic nerves (T1–T12), five pairs oflumbar nerves (L1–L5), five pairs ofsacral nerves (S1–S5), and one pair ofcoccygeal nerves. Peripheral nerves are included in the category of peripheral nervous system.[8]
  • Cranial nerves: They are the nerve fibers that carry information into and out of the brain stem.[5] They include smell, eye muscles, mouth, taste, ear, neck, shoulders, and tongue.[7] Partially innervating the head and neck structures are the cranial nerves, which supply afferent and efferent functions. Neural processes connected to certain brainstem nuclei and cortical regions make up cranial nerves, in contrast tospinal nerves, which have neural fibers originating from the spinal grey matter as their roots.[9] The cranial nerves VIII (vestibulocochlear), II (optic), and I (olfactory) are regarded as entirely afferent. The exclusively efferent cranial nerves are XI (spinal accessory), XII (hypoglossal), VI (abducens), IV (trochlear), and III (oculomotor). The remaining cranial nerves, X (vagus), IX (glossopharyngeal), VII (facial), and V (trigeminal), have mixed sensory and motor functions.[10] Anatomically, cranial nerves are numbered from I to XII, which indicates their sequential origin from the caudal to the ventral brainstem. Alternatively, they can be postulated in groups based on the developmental functions they perform (sensory, motor, mixed).[3]

Function

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The somatic nervous system's principal function is to facilitate the organs and striated muscles of the central nervous system so that we can carry out our daily responsibilities.[11]

Theprimary motor cortex, orprecentral gyrus, is home to the higher motor neurons that make up the basic motor pathway.[12] These neurons transmit signals to the lower motor neurons in the spinal cord through axons known as the corticospinal tract. These impulses move to theneuromuscular junction (NMJ) of skeletal muscle via peripheral axons after synapsing with thelower motor neurons through the ventral horn of the spinal cord. A signal that travels to the NMJ, which innervates muscles, is produced by the release of acetylcholine by upper motor neurons.Acetylcholine binds tonicotinic acetylcholine receptors of alpha-motor neurons.[4]

The somatic nervous system controls allvoluntary muscular systems within the body, and the process of voluntaryreflex arcs.[13]

The basic route ofnerve signals within theefferent somatic nervous system involves a sequence that begins in the uppercell bodies ofmotor neurons (upper motor neurons) within theprecentral gyrus (which approximates theprimary motor cortex).[14] Stimuli from the precentral gyrus are transmitted from upper motor neurons, down thecorticospinal tract, tolower motor neurons (alpha motor neurons) in thebrainstem andventral horn of thespinal cord: upper motor neurons release aneurotransmitter calledglutamate from their axon terminal knobs, which is received byglutamate receptors on the lower motor neurons: from there, acetylcholine is released from the axon terminal knobs of alpha motor neurons and received by postsynapticreceptors (nicotinic acetylcholine receptors) of muscles, thereby relaying the stimulus to contract muscle fibers.[15]

Reflex arcs

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Areflex arc is aneural circuit that creates a more or less automatic link between a sensory input and a specific motor output. Reflex circuits vary in complexity—the simplest spinal reflexes are mediated by a two-element chain, of which in the human body there is only one, also called a monosynaptic reflex (there is only one synapse between the two neurones taking part in the arc: sensory and motor). The singular example of a monosynaptic reflex is thepatellar reflex. The next simplest reflex arc is a three-element chain, beginning with sensory neurons, which activateinterneurons inside of the spinal cord, which then activate motor neurons. Some reflex responses, such as withdrawing the hand after touching a hot surface, are protective, but others, such as the patellar reflex ("knee jerk") activated by tapping the patellar tendon, contribute to ordinary behavior.[16]

Clinical significance

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A medical condition known asperipheral neuropathy affects the somatic nervous system's peripheral nerve fibers. They can be divided into congenital and acquired disorders based on the causes. They can also be categorized based on whether themyelin sheath (demyelinating neuropathy) or axons (axonal neuropathy) have the predominant disease. There is a wide range of causes for axonal peripheral neuropathy, most of which are toxic-metabolic in origin and include group B vitamin deficiencies and diabetes.Demyelinating neuropathies do not vary with length. They are frequently immune-mediated, which causes a more widespread involvement of sensorimotor function and an early loss of deep tendon reflexes. When joint position and vibratory sensory loss are present, sensory participation is more selective.

Defects in thecentral nervous system, peripheral nervous system, or muscle itself are the cause of numerous congenital illnesses of sensory and motor function. Owing to the vast territory encompassed by the somatic nerve system, these ailments may manifest as localized in nature, or as broad and systemic.Charcot-Marie-Tooth disease,Myasthenia gravis, andGuillain–Barré syndrome are a few instances of them.[17]

Charcot–Marie–Tooth

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TheCharcot–Marie–Tooth disease group comprises diverse hereditary illnesses that manifest as chronic, progressive neuropathy that affects both the motor and sensory neurons.[18]

Myasthenia gravis

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An autoimmune neurological condition calledmyasthenia gravis is typified by impaired neuromuscular junction communication.[19]

Guillain–Barré syndrome

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A rare but dangerous post-infectious immune-mediated neuropathy isGuillain–Barré syndrome. It is brought on by an autoimmune reaction that destroys peripheral nervous system nerves, leading to symptoms including tingling, weakness, and numbness that can become paralysis.[20]

Signs of somatic nervous system problems

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Depending on whether the damage is to the motor nerves, which regulate movement, or the sensory nerves, which affect the senses, the symptoms of a somatic nervous system problem can differ.[21]

Damage to the motor nerves shows as:

  • Loss of movement control
  • Spasms or cramps in muscles
  • Tremors or twitching
  • Wasting of muscles (muscle atrophy)

The following signs could be present if the sensory system is damaged:

  • Inability to feel things touched
  • Numbness or tingling
  • Sharp or burning pain in the damaged area

Other animals

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Ininvertebrates, depending on the neurotransmitter released and the type of receptor it binds, the response in the muscle fiber could either be excitatory or inhibitory. Forvertebrates, however, the response of askeletal striated muscle fiber to a neurotransmitter – alwaysacetylcholine (ACh) – can only be excitatory.

See also

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References

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  1. ^"Somatic nervous system".qbi.uq.edu.au. 2018-10-09. Retrieved2021-04-22.
  2. ^How does the nervous system work?. Institute for Quality and Efficiency in Health Care. 2016-08-19.
  3. ^abcBarboi, A.C.; Macefield, V.G. (2025). "The autonomic nervous system: Time for a conceptual reframing"?J Physiol. 2025 Nov;603(22):6719-6731. doi: 10.1113/JP288973. Epub 2025 Sep 16. PMID: 40956984; PMCID: PMC12645539.
  4. ^abAkinrodoye MA, Lui F (2022)."Neuroanatomy, Somatic Nervous System".StatPearls. StatPearls Publishing.PMID 32310487. Retrieved12 December 2022.
  5. ^abcRea P (2014-01-01)."Introduction to the Nervous System".Clinical Anatomy of the Cranial Nerves. Academic Press. pp. xv–xxix.doi:10.1016/b978-0-12-800898-0.00019-1.ISBN 978-0-12-800898-0.
  6. ^"Nerve Tissue".SEER Training. United States: National Cancer Institute. Retrieved19 August 2024.
  7. ^abFelten DL, O'Banion MK, Maida MS (January 2016), "9 - Peripheral Nervous System", in Felten DL, O'Banion MK, Maida MS (eds.),Netter's Atlas of Neuroscience (3rd ed.), Philadelphia: Elsevier, pp. 153–231,doi:10.1016/b978-0-323-26511-9.00009-6,ISBN 978-0-323-26511-9
  8. ^Kaiser JT, Lugo-Pic JG (2024)."Neuroanatomy, Spinal Nerves".StatPearls. Treasure Island, Florida: StatPearls.PMID 31194375. Retrieved2024-01-26.
  9. ^Sonne J, Lopez-Ojeda W (2024)."Neuroanatomy, Cranial Nerve".StatPearls. Treasure Island, Florida: StatPearls.PMID 29261885. Retrieved2024-01-26.
  10. ^Traylor KS, Branstetter BF (August 2022). "Cranial Nerve Anatomy".Neuroimaging Clinics of North America. Neuroimaging Anatomy, Part 1: Brain and Skull.32 (3):565–576.doi:10.1016/j.nic.2022.04.004.PMID 35843663.S2CID 250568029.
  11. ^Economo M.N.; Komiyama, T.; Kubota, Y.; Schiller, J. (2024). "Learning and Control in Motor Cortex across Cell Types and Scales."Journal of Neuroscience 2 October 2024, 44 (40) e1233242024;https://doi.org/10.1523/JNEUROSCI.1233-24.2024
  12. ^Lee C, Kim Y, Kaang BK (March 2022)."The Primary Motor Cortex: The Hub of Motor Learning in Rodents".Neuroscience.485:163–170.doi:10.1016/j.neuroscience.2022.01.009.PMID 35051529.
  13. ^Betts JG, Desaix P, Johnson E, Johnson JE, Korol O, Kruse D, et al. (July 16, 2023).Anatomy & Physiology. Houston: OpenStax CNX. Introduction: The somatic nervous system.ISBN 978-1-947172-04-3.
  14. ^Akinrodoye MA, Lui F (2025),"Neuroanatomy, Somatic Nervous System",StatPearls, Treasure Island (FL): StatPearls Publishing,PMID 32310487, retrieved2025-07-02
  15. ^Bertucci P, Arendt D (December 2013)."Somatic and visceral nervous systems - an ancient duality".BMC Biology.11 (1) 54.doi:10.1186/1741-7007-11-54.ISSN 1741-7007.PMC 3639815.PMID 23631570.
  16. ^Dong, D.; Chen, W. (2022). "Deweyan Reflex Arc: the Origins of an idea".Frontiers in Psychology, 13, 829387.https://doi.org/10.3389/fpsyg.2022.829387
  17. ^Waxenbaum JA, Reddy V, Varacallo M (2024)."Anatomy, Autonomic Nervous System".StatPearls. Treasure Island, Florida: StatPearls Publishing.PMID 30969667. Retrieved2024-01-26.
  18. ^Szigeti K, Lupski JR (June 2009)."Charcot-Marie-Tooth disease".European Journal of Human Genetics.17 (6):703–710.doi:10.1038/ejhg.2009.31.PMC 2947101.PMID 19277060.
  19. ^Dresser L, Wlodarski R, Rezania K, Soliven B (May 2021)."Myasthenia Gravis: Epidemiology, Pathophysiology and Clinical Manifestations".Journal of Clinical Medicine.10 (11): 2235.doi:10.3390/jcm10112235.PMC 8196750.PMID 34064035.
  20. ^Nguyen TP, Taylor RS (2024)."Guillain-Barre Syndrome".StatPearls. Treasure Island, Florida: StatPearls Publishing.PMID 30335287. Retrieved2024-01-26.
  21. ^"Somatic Nervous System: What It Is & Function". Cleveland Clinic. Retrieved2024-01-26.
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