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Thoracic diaphragm

From Wikipedia, the free encyclopedia
This article is about anatomic structure. For other uses, see Diaphragm (disambiguation).
Diaphragm
Respiratory system
Details
OriginL1-L3, the xiphoid process, 6-12th rib and their costal cartilages
InsertionCentral tendon
ArteryPericardiacophrenic artery, musculophrenic artery, inferior phrenic arteries
VeinSuperior phrenic vein, inferior phrenic vein
NervePhrenic and lower intercostal nerves
Actionsassists inspiration, depresses costal cartilages
Identifiers
Latindiaphragma
Greekδιάφραγμα
MeSHD003964
TA98A04.4.02.001
TA22327
FMA13295
Anatomical terms of muscle
Structure of Diaphragm shown using a 3D medical animation still shot
Structure of diaphragm shown using a 3D medical animation still shot

The thoracic diaphragm, or simply the diaphragm (/ˈdaɪəfræm/;[1] Ancient Greek: διάφραγμα, romanized: diáphragma, lit. 'partition'), is a sheet of internal skeletal muscle[2] in humans and other mammals that extends across the bottom of the thoracic cavity. The diaphragm is the most important muscle of respiration,[3] and separates the thoracic cavity, containing the heart and lungs, from the abdominal cavity: as the diaphragm contracts, the volume of the thoracic cavity increases, creating a negative pressure there, which draws air into the lungs.[4] Its high oxygen consumption is noted by the many mitochondria and capillaries present; more than in any other skeletal muscle.[3]

The term diaphragm in anatomy, created by Gerard of Cremona,[5] can refer to other flat structures such as the urogenital diaphragm or pelvic diaphragm, but "the diaphragm" generally refers to the thoracic diaphragm. In humans, the diaphragm is slightly asymmetric—its right half is higher up (superior) to the left half, since the large liver rests beneath the right half of the diaphragm. There is also speculation that the diaphragm is lower on the other side due to heart's presence.

Other mammals have diaphragms, and other vertebrates such as amphibians and reptiles have diaphragm-like structures, but important details of the anatomy may vary, such as the position of the lungs in the thoracic cavity.

Structure

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Definition of diaphragm in Blount's 1707 Glossographia Anglicana Nova

The diaphragm is an upward curved, c-shaped structure of muscle and fibrous tissue that separates the thoracic cavity from the abdomen.[6] The superior surface of the dome forms the floor of the thoracic cavity, and the inferior surface the roof of the abdominal cavity.[7]

As a dome, the diaphragm has peripheral attachments to structures that make up the abdominal and chest walls. The muscle fibres from these attachments converge in a central tendon, which forms the crest of the dome.[7] Its peripheral part consists of muscular fibers that take origin from the circumference of the inferior thoracic aperture and converge to be inserted into a central tendon.

The muscle fibres of the diaphragm radiate outward from the central tendon. While the diaphragm is one muscle, it is composed of two distinct muscle regions: the costal, which serves as the driver in the work of breathing, and crural diaphragm, which serves as an "anchor;" attaching the muscle to the lower ribs and lumbar vertebrae. The costal diaphragm is further divided into ventral, medial, and dorsal costal portions. [8][9]

The vertebral part of the diaphragm arises from the crura and arcuate ligaments. Right crus arises from L1-L3 vertebral bodies and their intervertebral discs. Smaller left crus arises from L1, L2 vertebral bodies and their intervertebral discs.[8][7][10] Medial arcuate ligament arises from the fascia thickening from body of L2 vertebrae to transverse process of L1 vertebrae, crossing over the body of the psoas major muscle. The lateral arcuate ligament arises from the transverse process of L1 vertebrae and is attached laterally to the 12th rib. The lateral arcuate ligament also arises from fascia thickening that covers the quadratus lumborum muscle. The median arcuate ligament arises from the fibrous parts of right and left crura where descending thoracic aorta passes behind it. No diaphragmatic muscle arises from the median arcuate ligament.[8] Both adrenal glands lie near the diaphragmatic crus and arcuate ligament.[11]

The costal part of diaphragm arises from the lower four ribs (7 to 10) costal cartilages.[8]

The central tendon of the diaphragm is a thin but strong aponeurosis near the center of the vault formed by the muscle, closer to the front than to the back of the thorax. The central part of the tendon is attached above to pericardium. The both sides of the posterior fibres are attached to paracolic gutters (the curving of ribs before attaching to both sides of the vertebral bodies).[8]

Openings

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Human diaphragm, transverse view from below, showing openings

There are a number of openings in the diaphragm through which structures pass between the thorax and abdomen. There are three large openings — one for the aorta (aortic hiatus),[2] one for the esophagus (esophageal hiatus), and one for the inferior vena cava (the caval opening),[8] as well as a series of smaller openings.[12][13]

The inferior vena cava passes through the caval opening, a quadrilateral opening at the junction of the right and middle leaflets of the central tendon, so that its margins are tendinous. Surrounded by tendons, the opening is stretched open every time inspiration occurs. However, there has been argument that the caval opening actually constricts during inspiration. Since thoracic pressure decreases upon inspiration and draws the caval blood upwards toward the right atrium, increasing the size of the opening allows more blood to return to the heart, maximizing the efficacy of lowered thoracic pressure returning blood to the heart. The aorta does not pierce the diaphragm but rather passes behind it in between the left and right crus.[citation needed]

There are several structures that pierce through the diaphragm, including: left phrenic nerve pierces through the central tendon, greater, lesser, and least thoracic splanchnic nerves pierces through bilateral crura, and lymphatic vessels that pierce throughout the diaphragm, especially behind the diaphragm.[8]

Nerve supply

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The diaphragm is primarily innervated by the phrenic nerve which is formed from the cervical nerves C3, C4 and C5.[7] While the central portion of the diaphragm sends sensory afferents via the phrenic nerve, the peripheral portions of the diaphragm send sensory afferents via the intercostal (T5–T11)[8] and subcostal nerves (T12).[citation needed]

Blood supply

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Arteries and veins above and below the diaphragm supply and drain blood.

From above, the diaphragm receives blood from branches of the internal thoracic arteries, namely the pericardiacophrenic artery and musculophrenic artery; from the superior phrenic arteries, which arise directly from the thoracic aorta; and from the lower internal intercostal arteries. From below, the inferior phrenic arteries supply the diaphragm.[7]

The diaphragm drains blood into the brachiocephalic veins, azygos veins, and veins that drain into the inferior vena cava and left suprarenal vein.[7]

Variation

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The sternal portion of the muscle is sometimes wanting and more rarely defects occur in the lateral part of the central tendon or adjoining muscle fibers.

Development

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The thoracic diaphragm develops during embryogenesis, beginning in the third week after fertilization with two processes known as transverse folding and longitudinal folding. The septum transversum, the primitive central tendon of the diaphragm, originates at the rostral pole of the embryo and is relocated during longitudinal folding to the ventral thoracic region. Transverse folding brings the body wall anteriorly to enclose the gut and body cavities. The pleuroperitoneal membrane and body wall myoblasts, from somatic lateral plate mesoderm, meet the septum transversum to close off the pericardio-peritoneal canals on either side of the presumptive esophagus, forming a barrier that separates the peritoneal and pleuropericardial cavities. Furthermore, dorsal mesenchyme surrounding the presumptive esophagus form the muscular crura of the diaphragm.

Because the earliest element of the embryological diaphragm, the septum transversum, forms in the cervical region, the phrenic nerve that innervates the diaphragm originates from the cervical spinal cord (C3,4, and 5). As the septum transversum descends inferiorly, the phrenic nerve follows, accounting for its circuitous route from the upper cervical vertebrae, around the pericardium, finally to innervate the diaphragm.

Function

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Real-time magnetic resonance imaging showing effects of diaphragm movement during breathing

The diaphragm is the main muscle of respiration and functions in breathing. During inhalation, the diaphragm contracts and moves in the inferior direction, enlarging the volume of the thoracic cavity and reducing intra-thoracic pressure (the external intercostal muscles also participate in this enlargement), forcing the lungs to expand. In other words, the diaphragm's movement downwards creates a partial vacuum in the thoracic cavity, which forces the lungs to expand to fill the void, drawing air in the process.

Cavity expansion happens in two extremes, along with intermediary forms. When the lower ribs are stabilized and the central tendon of the diaphragm is mobile, a contraction brings the insertion (central tendon) towards the origins and pushes the lower cavity towards the pelvis, allowing the thoracic cavity to expand downward. This is often called belly breathing. When the central tendon is stabilized and the lower ribs are mobile, a contraction lifts the origins (ribs) up towards the insertion (central tendon) which works in conjunction with other muscles to allow the ribs to slide and the thoracic cavity to expand laterally and upwards.

When the diaphragm relaxes (moves in the superior direction), air is exhaled by elastic recoil process of the lung and the tissues lining the thoracic cavity. Assisting this function with muscular effort (called forced exhalation) involves the internal intercostal muscles used in conjunction with the abdominal muscles, which act as an antagonist paired with the diaphragm's contraction. Diaphragm dysfunction is a well-known factor associated with various complications in patients, such as prolonged respiratory failure, difficulties in weaning from mechanical ventilation, extended hospitalization, increased morbidity, and mortality.[15] Studies have reported that a thin diaphragm leads to greater lung compliance, which can contribute to respiratory failure. Furthermore, reduction in diaphragm thickness during the early stages of disease can serve as a prognostic marker in sepsis patients, and COVID-19 patients.[16][17]

The diaphragm is also involved in non-respiratory functions. It helps to expel vomit, feces, and urine from the body by increasing intra-abdominal pressure, aids in childbirth,[18] and prevents acid reflux by exerting pressure on the esophagus as it passes through the esophageal hiatus.

In some non-human animals, the diaphragm is not crucial for breathing; a cow, for instance, can survive fairly asymptomatically with diaphragmatic paralysis as long as no massive aerobic metabolic demands are made of it. [citation needed]

Clinical significance

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Paralysis

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If either the phrenic nerve, cervical spine or brainstem is damaged, this will sever the nervous supply to the diaphragm. The most common damage to the phrenic nerve is by bronchial cancer, which usually only affects one side of the diaphragm. Other causes include Guillain–Barré syndrome and systemic lupus erythematosus.[19]

Herniation

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Main articles: Hiatus hernia and Congenital diaphragmatic hernia

A hiatus hernia is a hernia common in adults in which parts of the lower esophagus or stomach that are normally in the abdomen pass/bulge abnormally through the diaphragm and are present in the thorax. Hernias are described as rolling, in which the hernia is beside the oesophagus, or sliding, in which the hernia directly involves the esophagus. These hernias are implicated in the development of reflux, as the different pressures between the thorax and abdomen normally act to keep pressure on the esophageal hiatus. With herniation, this pressure is no longer present, and the angle between the cardia of the stomach and the oesophagus disappear. Not all hiatus hernias cause symptoms however, although almost all people with Barrett's oesophagus or oesophagitis have a hiatus hernia.[19]

Hernias may also occur as a result of congenital malformation, a congenital diaphragmatic hernia. When the pleuroperitoneal membranes fail to fuse, the diaphragm does not act as an effective barrier between the abdomen and thorax. Herniation is usually of the left, and commonly through the posterior lumbocostal triangle, although rarely through the anterior foramen of Morgagni. The contents of the abdomen, including the intestines, may be present in the thorax, which may impact development of the growing lungs and lead to hypoplasia.[20] This condition is present in 0.8 - 5/10,000 births.[21] A large herniation has high mortality rate, and requires immediate surgical repair.[22]

Imaging

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X-ray of chest, showing top of diaphragm.

Due to its position separating the thorax and abdomen, fluid abnormally present in the thorax, or air abnormally present in the abdomen, may collect on one side of the diaphragm. An X-ray may reveal this. Pleural effusion, in which there is fluid abnormally present between the two pleurae of the lungs, is detected by an X-ray of the chest, showing fluid collecting in the angle between the ribs and diaphragm.[19] An X-ray may also be used to reveal a pneumoperitoneum, in which there is gas in the abdomen.

An X-ray may also be used to check for herniation.[20]

Significance in strength training

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The adoption of a deeper breathing pattern typically occurs during physical exercise in order to facilitate greater oxygen absorption. During this process the diaphragm more consistently adopts a lower position within the body's core. In addition to its primary role in breathing, the diaphragm also plays a secondary role in strengthening the posture of the core. This is especially evident during deep breathing where its generally lower position increases intra-abdominal pressure, which serves to strengthen the lumbar spine.[23][better source needed]

The key to real core stabilization is to maintain the increased IAP while going through normal breathing cycles. [...] The diaphragm then performs its breathing function at a lower position to facilitate a higher IAP.[23]

[better source needed]

Therefore, if a person's diaphragm position is lower in general, through deep breathing, then this assists the strengthening of their core during that period. This can be an aid in strength training and other forms of athletic endeavour. For this reason, taking a deep breath or adopting a deeper breathing pattern is typically recommended when lifting heavy weights.

Other animals

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Diaphragm and pleural cavities in amphibian (left), bird (center), mammal (right). a, mandible; b, genio-hyoid; c, hyoid; d, sterno-hyoid; e, sternum; f, pericardium; g, septum transversum; h, rectus abdominis; i, abdominal cavity; j, pubis; k, esophagus; l, trachea; m, cervical limiting membrane of abdominal cavity; n, dorsal wall of body; o, lung; o', air-sac.[24]

The existence of a membrane separating the pharynx from the stomach can be traced widely among the chordates. Thus the model organism, the marine chordate lancelet, possesses an atriopore by which water exits the pharynx, which has been claimed (and disputed) to be homologous to structures in ascidians and hagfishes.[25] The tunicate epicardium separates digestive organs from the pharynx and heart, but the anus returns to the upper compartment to discharge wastes through an outgoing siphon.

Thus the diaphragm emerges in the context of a body plan that separated an upper feeding compartment from a lower digestive tract, but the point at which it originates is a matter of definition. Structures in fish, amphibians, reptiles, and birds have been called diaphragms, but it has been argued that these structures are not homologous. For instance, the alligator diaphragmaticus muscle does not insert on the esophagus and does not affect pressure of the lower esophageal sphincter.[26] The lungs are located in the abdominal compartment of amphibians and reptiles, so that contraction of the diaphragm expels air from the lungs rather than drawing it into them. In birds and mammals, lungs are located above the diaphragm. The presence of an exceptionally well-preserved fossil of Sinosauropteryx, with lungs located beneath the diaphragm as in crocodiles, has been used to argue that dinosaurs could not have sustained an active warm-blooded physiology, or that birds could not have evolved from dinosaurs.[citation needed] An explanation for this (put forward in 1905), is that lungs originated beneath the diaphragm, but as the demands for respiration increased in warm-blooded birds and mammals, natural selection came to favor the parallel evolution of the herniation of the lungs from the abdominal cavity in both lineages.[24]

However, birds lack diaphragms. They do not breathe in the same way as mammals and do not rely on creating a negative pressure in the thoracic cavity, at least not to the same extent. They rely on a rocking motion of the keel of the sternum to create local areas of reduced pressure to supply thin, membranous airsacs cranially and caudally to the fixed-volume, non-expansive lungs. A complicated system of valves and air sacs cycles air constantly over the absorption surfaces of the lungs so allowing maximal efficiency of gaseous exchange. Thus, birds do not have the reciprocal tidal breathing flow of mammals. On careful dissection, around eight air sacs can be clearly seen. They extend quite far caudally into the abdomen.[27]

See also

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This article uses anatomical terminology.

References

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Public domain This article incorporates text in the public domain from page 404 of the 20th edition of Gray's Anatomy (1918)

  1. ^ "Definition of 'diaphragm'". collinsdictionary.com.
  2. ^ a b Campbell NA (2009). Biology: Australian Version (8th ed.). Sydney: Pearson/Benjamin Cumings. p. 334. ISBN 978-1-4425-0221-5.
  3. ^ a b Spencer's pathology of the lung (5th ed.). New York: McGraw-Hill. 1996. p. 1. ISBN 0071054480.
  4. ^ "Medical Illustrations and Animations, Health and Science Stock Images and Videos, Royalty Free Licensing at Alila Medical Media". www.alilamedicalmedia.com.[full citation needed]
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  6. ^ Oliver, Kaitlin A.; Ashurst, John V. (2024), "Anatomy, Thorax, Phrenic Nerves", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30020697, retrieved 2024-08-26
  7. ^ a b c d e f g h i Drake RL, Vogl W, Tibbitts AW (2005). Gray's anatomy for students. illustrations by Richardson PR. Philadelphia: Elsevier/Churchill Livingstone. pp. 134–135. ISBN 978-0-8089-2306-0.
  8. ^ a b c d e f g h i j k l m Ryan S (2011). "Chapter 3". Anatomy for diagnostic imaging (Third ed.). Elsevier Ltd. p. 117. ISBN 9780702029714.
  9. ^ Poole, David (1 June 1997). "Diaphragm structure and function in health and disease". Medicine and Science in Sports and Exercise. 29 (6): 738–754. doi:10.1097/00005768-199706000-00003. PMID 9219201. Retrieved 29 November 2023.
  10. ^ Moore K (2014). Clinically Oriented Anatomy (7th ed.). Baltimore: Walters Kluwer. p. 306.
  11. ^ Perrier ND, Boger MS (5 December 2005). "2: Surgical Anatomy". Adrenal Glands: Diagnostic Aspects and Surgical Therapy (PDF). Springer Science & Business Media. ISBN 9783540268611. Archived from the original (PDF) on 3 March 2022. Retrieved 3 March 2022.
  12. ^ Sinnatamby CS (2011). Last's Anatomy (12th ed.). Elsevier Australia. p. 186. ISBN 978-0-7295-3752-0.
  13. ^ a b Moore KL, Dalley AF, Agur AM (2017). Essential Clinical Anatomy. Lippincott Williams & Wilkins. p. 536. ISBN 978-1496347213.
  14. ^ a b Nason LK, Walker CM, McNeeley MF, Burivong W, Fligner CL, Godwin JD (March 2012). "Imaging of the diaphragm: anatomy and function". Radiographics. 32 (2): E51 – E70. doi:10.1148/rg.322115127. PMID 22411950.
  15. ^ Supinski GS, Morris PE, Dhar S, Callahan LA (April 2018). "Diaphragm Dysfunction in Critical Illness". Chest. 153 (4): 1040–1051. doi:10.1016/j.chest.2017.08.1157. PMC 6026291. PMID 28887062.
  16. ^ Corradi F, Isirdi A, Malacarne P, Santori G, Barbieri G, Romei C, et al. (April 2021). "Low diaphragm muscle mass predicts adverse outcome in patients hospitalized for COVID-19 pneumonia: an exploratory pilot study". Minerva Anestesiologica. 87 (4): 432–438. doi:10.23736/S0375-9393.21.15129-6. PMID 33594871. S2CID 263501203.
  17. ^ Emekli E, Bostancı Can EZ (April 2023). "Prognostic Value of Diaphragm Diameter, Muscle Volume, and Bone Mineral Density in Critically Ill COVID-19 Patients". Journal of Intensive Care Medicine. 38 (9): 847–855. doi:10.1177/08850666231169494. PMC 10099913. PMID 37050868.
  18. ^ Mazumdar MD. "Stage II Of Normal Labour". Gynaeonline. Archived from the original on 24 February 2010. Retrieved June 12, 2018.
  19. ^ a b c Colledge NR, Walker BR, Ralston SH, eds. (2010). Davidson's principles and practice of medicine (21st ed.). Edinburgh: Churchill Livingstone/Elsevier. pp. 644, 658–659, 864. ISBN 978-0-7020-3085-7.
  20. ^ a b Hay WW, ed. (2011). Current diagnosis & treatment : pediatrics (20th ed.). New York: McGraw-Hill Medical. p. 602. ISBN 978-0-07-166444-8.
  21. ^ Chandrasekharan PK, Rawat M, Madappa R, Rothstein DH, Lakshminrusimha S (2017-03-11). "Congenital Diaphragmatic hernia - a review". Maternal Health, Neonatology and Perinatology. 3: 6. doi:10.1186/s40748-017-0045-1. PMC 5356475. PMID 28331629.
  22. ^ Nguyen L, Guttman FM, De Chadarévian JP, Beardmore HE, Karn GM, Owen HF, Murphy DR (December 1983). "The mortality of congenital diaphragmatic hernia. Is total pulmonary mass inadequate, no matter what?". Annals of Surgery. 198 (6): 766–770. doi:10.1097/00000658-198312000-00016. PMC 1353227. PMID 6639179.
  23. ^ a b "Diaphragm function for core stability » Hans Lindgren DC". hanslindgren.com.
  24. ^ a b Keith A (1905). "The nature of the mammalian diaphragm and pleural cavities". Journal of Anatomy and Physiology. 39 (Pt 3): 243–284. PMC 1287418. PMID 17232638.
  25. ^ Kozmik Z, Holland ND, Kalousova A, Paces J, Schubert M, Holland LZ (March 1999). "Characterization of an amphioxus paired box gene, AmphiPax2/5/8: developmental expression patterns in optic support cells, nephridium, thyroid-like structures and pharyngeal gill slits, but not in the midbrain-hindbrain boundary region". Development. 126 (6): 1295–1304. doi:10.1242/dev.126.6.1295. PMID 10021347.
  26. ^ Uriona TJ, Farmer CG, Dazely J, Clayton F, Moore J (August 2005). "Structure and function of the esophagus of the American alligator (Alligator mississippiensis)". The Journal of Experimental Biology. 208 (Pt 16): 3047–3053. doi:10.1242/jeb.01746. PMID 16081603.
  27. ^ Dyce KM, Sack WO, Wensing CJ (2002). Textbook of Veterinary Anatomy (3rd ed.). Philadelphia: Saunders.

Public Domain This article incorporates text from a publication now in the public domain: Chambers, Ephraim, ed. (1728). Cyclopædia, or an Universal Dictionary of Arts and Sciences (1st ed.). James and John Knapton, et al. {{cite encyclopedia}}: Missing or empty |title= (help)

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