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Small intestine

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Small intestine
Small intestine and surrounding structures
Details
Part ofGastrointestinal tract
SystemDigestive system
ArterySuperior mesenteric artery, jejunal arteries, ileal arteries
VeinHepatic portal vein, superior mesenteric vein
NerveCeliac ganglia, vagus[1]
LymphIntestinal lymph trunk
Identifiers
Latinintestinum tenue
MeSHD007421
TA98A05.6.01.001
TA22933
FMA7200
Anatomical terminology
Major parts of the
Gastrointestinal tract
Upper gastrointestinal tract
Lower gastrointestinal tract
See also

The small intestine or small bowel is an organ in the gastrointestinal tract where most of the absorption of nutrients from food takes place. It lies between the stomach and large intestine, and receives bile and pancreatic juice through the pancreatic duct to aid in digestion. The small intestine is about 5.5 metres (18 feet) long and folds many times to fit in the abdomen. Although it is longer than the large intestine, it is called the small intestine because it is narrower in diameter.

The small intestine has three distinct regions – the duodenum, jejunum, and ileum. The duodenum, the shortest, is where preparation for absorption through small finger-like protrusions called villi begins.[2] The jejunum is specialized for the absorption through its lining by enterocytes: small nutrient particles which have been previously digested by enzymes in the duodenum. The main function of the ileum is to absorb vitamin B12, bile salts, and whatever products of digestion that were not absorbed by the jejunum.

Structure

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Size

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The length of the small intestine can vary greatly, from as short as 3 metres (10 feet) to as long as 10.5 m (34+1⁄2 ft), also depending on the measuring technique used.[3] The typical length in a living person is 3–5 m (10–16+1⁄2 ft).[4][5] The length depends both on how tall the person is and how the length is measured.[3] Taller people generally have a longer small intestine and measurements are generally longer after death and when the bowel is empty.[3]

Small bowel dilation on CT scan in adults[6]
<2.5 cm Non-dilated
2.5-2.9 cm Mildly dilated
3–4 cm Moderately dilated
>4 cm Severely dilated

It is approximately 1.5 centimetres (5⁄8 inch) in diameter in old after 35 weeks of gestational age,[7] and 2.5–3 cm (1–1+1⁄8 in) in diameter in adults. On abdominal X-rays, the small intestine is considered to be abnormally dilated when the diameter exceeds 3 cm.[8][9] On CT scans, a diameter of over 2.5 cm is considered abnormally dilated.[8][10] The surface area of the human small intestinal mucosa, due to enlargement caused by folds, villi and microvilli, averages 30 square metres (320 sq ft).[11]

Parts

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Labeled diagram of the small intestine and its surrounding structures

The small intestine is divided into three structural parts.

  • The duodenum is a short structure ranging from 20–25 cm (8–10 in) in length, and shaped like a "C".[12] It surrounds the head of the pancreas. It receives gastric chyme from the stomach, together with digestive juices from the pancreas (digestive enzymes) and the liver (bile). The digestive enzymes break down proteins and bile emulsifies fats into micelles. The duodenum contains Brunner's glands, which produce a mucus-rich alkaline secretion containing bicarbonate. These secretions, in combination with bicarbonate from the pancreas, neutralize the stomach acids contained in gastric chyme.
  • The jejunum is the midsection of the small intestine, connecting the duodenum to the ileum. It is about 2.5 m (8 ft) long, and contains the circular folds, and intestinal villi that increase its surface area. Products of digestion (sugars, amino acids, and fatty acids) are absorbed into the bloodstream here. The suspensory muscle of duodenum marks the division between the duodenum and the jejunum.
  • The ileum: The final section of the small intestine. It is about 3 m long, and contains villi similar to the jejunum. It absorbs mainly vitamin B12 and bile acids, as well as any other remaining nutrients. The ileum joins to the cecum of the large intestine at the ileocecal junction.[citation needed]

The jejunum and ileum are suspended in the abdominal cavity by mesentery. The mesentery is part of the peritoneum. Arteries, veins, lymph vessels and nerves travel within the mesentery.[13]

Blood supply

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The small intestine receives a blood supply from the celiac trunk and the superior mesenteric artery. These are both branches of the aorta. The duodenum receives blood from the coeliac trunk via the superior pancreaticoduodenal artery and from the superior mesenteric artery via the inferior pancreaticoduodenal artery. These two arteries both have anterior and posterior branches that meet in the midline and anastomose. The jejunum and ileum receive blood from the superior mesenteric artery.[14] Branches of the superior mesenteric artery form a series of arches within the mesentery known as arterial arcades, which may be several layers deep. Straight blood vessels known as vasa recta travel from the arcades closest to the ileum and jejunum to the organs themselves.[14]

Microanatomy

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Main article: Gastrointestinal wall
Micrograph of the small intestine mucosa showing the intestinal villi and crypts of Lieberkühn.

The three sections of the small intestine look similar to each other at a microscopic level, but there are some important differences. The parts of the intestine are as follows:

This cross section diagram shows the 4 layers of the small intestine wall.
Layer Duodenum Jejunum Ileum
Serosa 1st part serosa, 2nd–4th adventitia Normal Normal
Muscularis externa Longitudinal and circular layers, with Auerbach's (myenteric) plexus in between Same as duodenum Same as duodenum
Submucosa Brunner's glands and Meissner's (submucosal) plexus No BG No BG
Mucosa: muscularis mucosae Normal Normal Normal
Mucosa: lamina propria No PP No PP Peyer's patches
Mucosa: intestinal epithelium Simple columnar. Contains goblet cells, Paneth cells Similar to duodenum, but the intestinal villus is long Similar to duodenum, but the intestinal villus is short

Gene and protein expression

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About 20,000 protein coding genes are expressed in human cells and 70% of these genes are expressed in the normal duodenum.[15][16] Some 300 of these genes are more specifically expressed in the duodenum with very few genes expressed only in the small intestine. The corresponding specific proteins are expressed in glandular cells of the mucosa, such as fatty acid binding protein FABP6. Most of the more specifically expressed genes in the small intestine are also expressed in the duodenum, for example FABP2 and the DEFA6 protein expressed in secretory granules of Paneth cells.[17]

Development

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See also: Development of the digestive system

The small intestine develops from the midgut of the primitive gut tube.[18] By the fifth week of embryological life, the ileum begins to grow longer at a very fast rate, forming a U-shaped fold called the primary intestinal loop. The loop grows so fast in length that it outgrows the abdomen and protrudes through the umbilicus. By week 10, the loop retracts back into the abdomen. Between weeks six and ten the small intestine rotates anticlockwise, as viewed from the front of the embryo. It rotates a further 180 degrees after it has moved back into the abdomen. This process creates the twisted shape of the large intestine.[18]

  • First stage of the development of the intestinal canal and the peritoneum, seen from the side (diagrammatic). From colon 1 the ascending and transverse colon will be formed and from colon 2 the descending and sigmoid colons and the rectum.
    First stage of the development of the intestinal canal and the peritoneum, seen from the side (diagrammatic). From colon 1 the ascending and transverse colon will be formed and from colon 2 the descending and sigmoid colons and the rectum.
  • Second stage of development of the intestinal canal and peritoneum, seen from in front (diagrammatic). The liver has been removed and the two layers of the ventral mesogastrium (lesser omentum) have been cut. The vessels are represented in black and the peritoneum in the reddish tint.
    Second stage of development of the intestinal canal and peritoneum, seen from in front (diagrammatic). The liver has been removed and the two layers of the ventral mesogastrium (lesser omentum) have been cut. The vessels are represented in black and the peritoneum in the reddish tint.
  • Third state of the development of the intestinal canal and peritoneum, seen from in front (diagrammatic). The mode of preparation is the same as in Fig 400
    Third state of the development of the intestinal canal and peritoneum, seen from in front (diagrammatic). The mode of preparation is the same as in Fig 400

Function

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Food from the stomach is allowed into the duodenum through the pylorus by a muscle called the pyloric sphincter.

Digestion

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The small intestine is where most chemical digestion takes place. Many of the digestive enzymes that act in the small intestine are secreted by the pancreas and liver and enter the small intestine via the pancreatic duct. Pancreatic enzymes and bile from the gallbladder enter the small intestine in response to the hormone cholecystokinin, which is produced in the response to the presence of nutrients. Secretin, another hormone produced in the small intestine, causes additional effects on the pancreas, where it promotes the release of bicarbonate into the duodenum in order to neutralize the potentially harmful acid coming from the stomach.

The three major classes of nutrients that undergo digestion are proteins, lipids (fats) and carbohydrates:

  • Proteins are degraded into small peptides and amino acids before absorption.[19] Chemical breakdown begins in the stomach and continues in the small intestine. Proteolytic enzymes, including trypsin and chymotrypsin, are secreted by the pancreas and cleave proteins into smaller peptides. Carboxypeptidase, which is a pancreatic brush border enzyme, splits one amino acid at a time. Aminopeptidase and dipeptidase free the end amino acid products.
  • Lipids (fats) are degraded into fatty acids and glycerol. Pancreatic lipase breaks down triglycerides into free fatty acids and monoglycerides. Pancreatic lipase works with the help of the salts from the bile secreted by the liver and stored in the gall bladder. Bile salts attach to triglycerides to help emulsify them, which aids access by pancreatic lipase. This occurs because the lipase is water-soluble but the fatty triglycerides are hydrophobic and tend to orient towards each other and away from the watery intestinal surroundings. The bile salts emulsify the triglycerides in the watery surroundings until the lipase can break them into the smaller components that are able to enter the villi for absorption.
  • Some carbohydrates are degraded into simple sugars, or monosaccharides (e.g., glucose). Pancreatic amylase breaks down some carbohydrates (notably starch) into oligosaccharides. Other carbohydrates pass undigested into the large intestine for further handling by intestinal bacteria. Brush border enzymes take over from there. The most important brush border enzymes are dextrinase and glucoamylase, which further break down oligosaccharides. Other brush border enzymes are maltase, sucrase and lactase. Lactase is absent in some adult humans and, for them, lactose (a disaccharide), as well as most polysaccharides, is not digested in the small intestine. Some carbohydrates, such as cellulose, are not digested at all, despite being made of multiple glucose units. This is because the cellulose is made out of beta-glucose, making the inter-monosaccharidal bindings different from the ones present in starch, which consists of alpha-glucose. Humans lack the enzyme for splitting the beta-glucose-bonds, something reserved for herbivores and bacteria from the large intestine.

Absorption

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Digested food is now able to pass into the blood vessels in the wall of the intestine through either diffusion or active transport. The small intestine is the site where most of the nutrients from ingested food are absorbed. The inner wall, or mucosa, of the small intestine, is lined with intestinal epithelium, a simple columnar epithelium. Structurally, the mucosa is covered in wrinkles or flaps called circular folds, which are considered permanent features in the mucosa. They are distinct from rugae which are considered non-permanent or temporary allowing for distention and contraction. From the circular folds project microscopic finger-like pieces of tissue called villi (Latin for "shaggy hair"). The individual epithelial cells also have finger-like projections known as microvilli. The functions of the circular folds, the villi, and the microvilli are to increase the amount of surface area available for the absorption of nutrients, and to limit the loss of said nutrients to intestinal fauna.

Each villus has a network of capillaries and fine lymphatic vessels called lacteals close to its surface. The epithelial cells of the villi transport nutrients from the lumen of the intestine into these capillaries (amino acids and carbohydrates) and lacteals (lipids). The absorbed substances are transported via the blood vessels to different organs of the body where they are used to build complex substances such as the proteins required by our body. The material that remains undigested and unabsorbed passes into the large intestine.

Absorption of glucose in the small intestine

Absorption of the majority of nutrients takes place in the jejunum, with the following notable exceptions:

Immunological

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The small intestine supports the body's immune system.[20] The presence of gut flora appears to contribute positively to the host's immune system. Peyer's patches, located within the ileum of the small intestine, are an important part of the digestive tract's local immune system. They are part of the lymphatic system, and provide a site for antigens from potentially harmful bacteria or other microorganisms in the digestive tract to be sampled, and subsequently presented to the immune system.[21]

Clinical significance

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See also: Gastrointestinal disease

The small intestine is a complex organ, and as such, there are a very large number of possible conditions that may affect the function of the small bowel. A few of them are listed below, some of which are common, with up to 10% of people being affected at some time in their lives, while others are vanishingly rare.

Other animals

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The small intestine is found in all tetrapods and also in teleosts, although its form and length vary enormously between species. In teleosts, it is relatively short, typically around one and a half times the length of the fish's body. It commonly has a number of pyloric caeca, small pouch-like structures along its length that help to increase the overall surface area of the organ for digesting food. There is no ileocaecal valve in teleosts, with the boundary between the small intestine and the rectum being marked only by the end of the digestive epithelium.[22]

In tetrapods, the ileocaecal valve is always present, opening into the colon. The length of the small intestine is typically longer in tetrapods than in teleosts, but is especially so in herbivores, as well as in mammals and birds, which have a higher metabolic rate than amphibians or reptiles. The lining of the small intestine includes microscopic folds to increase its surface area in all vertebrates, but only in mammals do these develop into true villi.[22]

The boundaries between the duodenum, jejunum, and ileum are somewhat vague even in humans, and such distinctions are either ignored when discussing the anatomy of other animals, or are essentially arbitrary.[22]

There is no small intestine as such in non-teleost fish, such as sharks, sturgeons, and lungfish. Instead, the digestive part of the gut forms a spiral intestine, connecting the stomach to the rectum. In this type of gut, the intestine itself is relatively straight but has a long fold running along the inner surface in a spiral fashion, sometimes for dozens of turns. This valve greatly increases both the surface area and the effective length of the intestine. The lining of the spiral intestine is similar to that of the small intestine in teleosts and non-mammalian tetrapods.[22]

In lampreys, the spiral valve is extremely small, possibly because their diet requires little digestion. Hagfish have no spiral valve at all, with digestion occurring for almost the entire length of the intestine, which is not subdivided into different regions.[22]

Society and culture

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In traditional Chinese medicine, the small intestine is a yang organ.[23]

Additional images

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Wikimedia Commons has media related to Small intestine.
  • Small intestine in situ, greater omentum folded upwards.
    Small intestine in situ, greater omentum folded upwards.
  • Tissue layers (mucosa, submucosa and muscularis)
    Tissue layers (mucosa, submucosa and muscularis)

References

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  1. ^ Nosek, Thomas M. "Section 6/6ch2/s6ch2_30". Essentials of Human Physiology. Archived from the original on 2016-03-24.
  2. ^ human body | Britannica.com
  3. ^ a b c DiBaise, John K.; Parrish, Carol Rees; Thompson, Jon S. (2016). Short Bowel Syndrome: Practical Approach to Management. CRC Press. p. 31. ISBN 9781498720809.
  4. ^ Tortora, Gerard (2014). Principles of Anatomy & Physiology. USA: Wiley. pp. 913. ISBN 978-1-118-34500-9. ..its length is about 3m in a living person and about 6.5m in a cadaver due to loss of smooth muscle tone after death.
  5. ^ Standring, Susan (2016). Gray's Anatomy. UK: Elsevier. p. 1124. ISBN 978-0-7020-5230-9. ..and has a mean length of 5 metres (3 - 8.5 metres) when measured intraoperatively in the living adult (Tietelbaum et al 2013).
  6. ^ Jacobs, S.L.; Rozenblit, A.; Ricci, Z.; Roberts, J.; Milikow, D.; Chernyak, V.; Wolf, E. (2007). "Small bowel faeces sign in patients without small bowel obstruction". Clinical Radiology. 62 (4): 353–357. doi:10.1016/j.crad.2006.11.007. ISSN 0009-9260. PMID 17331829.
  7. ^ Debora Duro, Daniel Kamin (2007). "Overview of short bowel syndrome and intestinal transplantation". Colombia Médica. 38 (1).
  8. ^ a b Ali Nawaz Khan (2016-09-22). "Small-Bowel Obstruction Imaging". Medscape. Retrieved 2017-02-07.
  9. ^ "Abdominal X-ray - Abnormal bowel gas pattern". radiologymasterclass.co.uk. Retrieved 2017-02-07.
  10. ^ Gazelle, G S; Goldberg, M A; Wittenberg, J; Halpern, E F; Pinkney, L; Mueller, P R (1994). "Efficacy of CT in distinguishing small-bowel obstruction from other causes of small-bowel dilatation". American Journal of Roentgenology. 162 (1): 43–47. doi:10.2214/ajr.162.1.8273687. ISSN 0361-803X. PMID 8273687.
  11. ^ Helander, Herbert F; Fändriks, Lars (2015). "Surface area of the digestive tract – revisited". Scandinavian Journal of Gastroenterology. 49 (6): 681–689. doi:10.3109/00365521.2014.898326. ISSN 0036-5521. PMID 24694282. S2CID 11094705.
  12. ^ Drake, Richard L.; Vogl, Wayne; Tibbitts, Adam W.M. Mitchell; illustrations by Richard; Richardson, Paul (2005). Gray's anatomy for students. Philadelphia: Elsevier/Churchill Livingstone. p. 273. ISBN 978-0-8089-2306-0.
  13. ^ Drake, Richard L.; Vogl, Wayne; Tibbitts, Adam W.M. Mitchell; illustrations by Richard; Richardson, Paul (2005). Gray's anatomy for students. Philadelphia: Elsevier/Churchill Livingstone. p. 271. ISBN 978-0-8089-2306-0.
  14. ^ a b Drake, Richard L.; Vogl, Wayne; Tibbitts, Adam W.M. Mitchell; illustrations by Richard; Richardson, Paul (2005). Gray's anatomy for students. Philadelphia: Elsevier/Churchill Livingstone. pp. 295–299. ISBN 978-0-8089-2306-0.
  15. ^ "The human proteome in small intestine - The Human Protein Atlas". www.proteinatlas.org. Retrieved 2017-09-26.
  16. ^ Uhlén, Mathias; Fagerberg, Linn; Hallström, Björn M.; Lindskog, Cecilia; Oksvold, Per; Mardinoglu, Adil; Sivertsson, Åsa; Kampf, Caroline; Sjöstedt, Evelina (2015-01-23). "Tissue-based map of the human proteome". Science. 347 (6220): 1260419. doi:10.1126/science.1260419. ISSN 0036-8075. PMID 25613900. S2CID 802377.
  17. ^ Gremel, Gabriela; Wanders, Alkwin; Cedernaes, Jonathan; Fagerberg, Linn; Hallström, Björn; Edlund, Karolina; Sjöstedt, Evelina; Uhlén, Mathias; Pontén, Fredrik (2015-01-01). "The human gastrointestinal tract-specific transcriptome and proteome as defined by RNA sequencing and antibody-based profiling". Journal of Gastroenterology. 50 (1): 46–57. doi:10.1007/s00535-014-0958-7. ISSN 0944-1174. PMID 24789573. S2CID 21302849.
  18. ^ a b Schoenwolf, Gary C.; Bleyl, Steven B.; Brauer, Philip R.; Francis-West, Philippa H. (2009). "Development of the Urogenital system". Larsen's human embryology (4th ed.). Philadelphia: Churchill Livingstone/Elsevier. p. 237. ISBN 9780443068119.
  19. ^ Silk DB (1974). "Progress report. Peptide absorption in man". Gut. 15 (6): 494–501. doi:10.1136/gut.15.6.494. PMC 1413009. PMID 4604970.
  20. ^ "Intestinal immune cells play an unexpected role in immune surveillance of the bloodstream". Massachusetts General Hospital. 13 December 2012. Archived from the original on 16 October 2018. Retrieved 28 August 2013.
  21. ^ Canny, G. O.; McCormick, B. A. (2008). "Bacteria in the Intestine, Helpful Residents or Enemies from Within?". Infection and Immunity. 76 (8): 3360–3373. CiteSeerX 10.1.1.596.7265. doi:10.1128/IAI.00187-08. ISSN 0019-9567. PMC 2493210. PMID 18474643.
  22. ^ a b c d e Romer, Alfred Sherwood; Parsons, Thomas S. (1977). The Vertebrate Body. Philadelphia, PA: Holt-Saunders International. pp. 349–353. ISBN 978-0-03-910284-5.
  23. ^ Porter [ed.], Roy (1997). Medicine : a history of healing. [S.l.]: Diane Pub Co. p. 104. ISBN 9780756751432. {{cite book}}: |last1= has generic name (help)

Bibliography

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