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Small intestine

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.

Small intestine
Diagram showing the small intestine and surrounding structures
Details
Part ofGastrointestinal tract
SystemDigestive system
ArterySuperior mesenteric artery
VeinHepatic portal vein
NerveCeliac ganglia, vagus[1]
LymphIntestinal lymph trunk
Identifiers
Latinintestinum tenue
MeSHD007421
TA98A05.6.01.001
TA22933
FMA7200
Anatomical terminology
[edit on Wikidata]

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 edit

Size edit

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+12 ft), also depending on the measuring technique used.[3] The typical length in a living person is 3–5 m (10–16+12 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 (58 inch) in diameter in newborns after 35 weeks of gestational age,[7] and 2.5–3 cm (1–1+18 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 edit

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 edit

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 edit

 
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 edit

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 edit

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]

Function edit

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

Digestion edit

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 edit

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 simple columnar epithelial tissue. 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 edit

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 edit

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 edit

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 edit

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

Additional images edit

References edit

  1. ^ Nosek, Thomas M. . 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. ^ . 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 edit

  • Sherwood, Lauralee (2006). Fundamentals of physiology: a human perspective (Third ed.). Florence, KY: Cengage Learning. p. 768. ISBN 978-0-534-46697-8.
  • Solomon et al. (2002) Biology Sixth Edition, Brooks-Cole/Thomson Learning ISBN 0-03-033503-5
  • Townsend et al. (2004) Sabiston Textbook of Surgery, Elsevier ISBN 0-7216-0409-9
  • Thomson A, Drozdowski L, Iordache C, Thomson B, Vermeire S, Clandinin M, Wild G (2003). "Small bowel review: Normal physiology, part 1". Dig Dis Sci. 48 (8): 1546–64. doi:10.1023/A:1024719925058. PMID 12924651. S2CID 37494914.
  • Thomson A, Drozdowski L, Iordache C, Thomson B, Vermeire S, Clandinin M, Wild G (2003). "Small bowel review: Normal physiology, part 2". Dig Dis Sci. 48 (8): 1565–81. doi:10.1023/A:1024724109128. PMID 12924652. S2CID 42442830.

External links edit

  • Small intestine at the Human Protein Atlas

small, intestine, small, intestine, small, bowel, organ, gastrointestinal, tract, where, most, absorption, nutrients, from, food, takes, place, lies, between, stomach, large, intestine, receives, bile, pancreatic, juice, through, pancreatic, duct, digestion, s. 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 Small intestineDiagram showing the small intestine and surrounding structuresDetailsPart ofGastrointestinal tractSystemDigestive systemArterySuperior mesenteric arteryVeinHepatic portal veinNerveCeliac ganglia vagus 1 LymphIntestinal lymph trunkIdentifiersLatinintestinum tenueMeSHD007421TA98A05 6 01 001TA22933FMA7200Anatomical terminology edit on Wikidata 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 Contents 1 Structure 1 1 Size 1 2 Parts 1 3 Blood supply 1 4 Microanatomy 1 5 Gene and protein expression 1 6 Development 2 Function 2 1 Digestion 2 2 Absorption 2 3 Immunological 3 Clinical significance 4 Other animals 5 Society and culture 6 Additional images 7 References 8 Bibliography 9 External linksStructure editSize edit 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 lt 2 5 cm Non dilated2 5 2 9 cm Mildly dilated3 4 cm Moderately dilated gt 4 cm Severely dilatedIt is approximately 1 5 centimetres 5 8 inch in diameter in newborns 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 edit 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 edit 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 edit Main article Gastrointestinal wall nbsp Micrograph of the small intestine mucosa showing the intestinal villi and crypts of Lieberkuhn 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 nbsp This cross section diagram shows the 4 layers of the small intestine wall Layer Duodenum Jejunum IleumSerosa 1st part serosa 2nd 4th adventitia Normal NormalMuscularis externa Longitudinal and circular layers with Auerbach s myenteric plexus in between Same as duodenum Same as duodenumSubmucosa Brunner s glands and Meissner s submucosal plexus No BG No BGMucosa muscularis mucosae Normal Normal NormalMucosa lamina propria No PP No PP Peyer s patchesMucosa 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 shortGene and protein expression edit 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 edit 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 nbsp 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 nbsp 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 nbsp 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 400Function editFood from the stomach is allowed into the duodenum through the pylorus by a muscle called the pyloric sphincter Digestion edit 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 edit 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 simple columnar epithelial tissue 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 nbsp Absorption of glucose in the small intestineAbsorption of the majority of nutrients takes place in the jejunum with the following notable exceptions Iron is absorbed in the duodenum Folate Vitamin B9 is absorbed in the duodenum and jejunum Vitamin B12 and bile salts are absorbed in the terminal ileum Vitamin B12 will only be absorbed by the ileum after binding to a protein known as intrinsic factor Water is absorbed by osmosis and lipids by passive diffusion throughout the small intestine Sodium bicarbonate is absorbed by active transport and glucose and amino acid co transport Fructose is absorbed by facilitated diffusion Immunological edit 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 editSee 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 Small intestine obstruction or obstructive disorders Meconium ileus Paralytic ileus Volvulus Hernia Intussusception Adhesions Obstruction from external pressure Obstruction by masses in the lumen foreign bodies bezoar gallstones Infectious diseases Giardiasis Ascariasis Tropical sprue Tape worm Diphyllobothrium latum Taenia solium Hymenolepis nana Hookworm e g Necator americanus Ancylostoma duodenale Nematodes e g Ascaris lumbricoides Other Protozoa e g Cryptosporidium parvum Cyclospora Microsporidia Entamoeba histolytica Bacterial infections Enterotoxigenic Escherichia coli Salmonella enterica Campylobacter Shigella Yersinia Clostridium difficile antibiotic associated colitis Pseudomembranous colitis Mycobacterium Mycobacterium avium paratuberculosis disseminated Mycobacterium tuberculosis Whipple s disease Vibrio cholera Enteric typhoid fever Salmonella enterica var typhii and paratyphoid fever Bacillus cereus Clostridium perfringens gas gangrene Viral infections Rotavirus Norovirus Astrovirus Adenovirus Calicivirus Neoplasms cancers Adenocarcinoma Carcinoid Gastrointestinal stromal tumor GIST Lymphoma Sarcoma Leiomyoma Metastatic tumors especially SCLC or melanoma Small intestine cancer Developmental congenital or genetic conditions Duodenal intestinal atresia Hirschsprung s disease Meckel s diverticulum Pyloric stenosis Pancreas divisum Ectopic pancreas Enteric duplication cyst Situs inversus Cystic fibrosis Malrotation Persistent urachus Omphalocele Gastroschisis Disaccharidase lactase deficiencies Primary bile acid malabsorption Gardner syndrome Familial adenomatous polyposis syndrome FAP Other conditions Crohn s disease and the more general inflammatory bowel disease Typhlitis neutropenic colitis in the immunosuppressed Coeliac disease sprue or non tropical sprue Mesenteric ischemia Embolus or thrombus of the superior mesenteric artery or the superior mesenteric vein Arteriovenous malformation Gastric dumping syndrome Irritable bowel syndrome Duodenal peptic ulcers Gastrointestinal perforation Hyperthyroidism Diverticulitis Radiation enterocolitis Mesenteric cysts Peritoneal Infection Sclerosing retroperitonitis Small intestinal bacterial overgrowth EndometriosisOther animals editThe 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 editIn traditional Chinese medicine the small intestine is a yang organ 23 Additional images edit nbsp Wikimedia Commons has media related to Small intestine nbsp Small intestine in situ greater omentum folded upwards nbsp Tissue layers mucosa submucosa amp muscularis References edit Nosek Thomas M Section 6 6ch2 s6ch2 30 Essentials of Human Physiology Archived from the original on 2016 03 24 human body Britannica com 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 Tortora Gerard 2014 Principles of Anatomy amp 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 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 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 Debora Duro Daniel Kamin 2007 Overview of short bowel syndrome and intestinal transplantation Colombia Medica 38 1 a b Ali Nawaz Khan 2016 09 22 Small Bowel Obstruction Imaging Medscape Retrieved 2017 02 07 Abdominal X ray Abnormal bowel gas pattern radiologymasterclass co uk Retrieved 2017 02 07 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 Helander Herbert F Fandriks 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 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 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 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 The human proteome in small intestine The Human Protein Atlas www proteinatlas org Retrieved 2017 09 26 Uhlen Mathias Fagerberg Linn Hallstrom Bjorn M Lindskog Cecilia Oksvold Per Mardinoglu Adil Sivertsson Asa Kampf Caroline Sjostedt 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 Gremel Gabriela Wanders Alkwin Cedernaes Jonathan Fagerberg Linn Hallstrom Bjorn Edlund Karolina Sjostedt Evelina Uhlen Mathias Ponten 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 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 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 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 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 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 Porter ed Roy 1997 Medicine a history of healing S l Diane Pub Co p 104 ISBN 9780756751432 a href Template Cite book html title Template Cite book cite book a last1 has generic name help Bibliography editSherwood Lauralee 2006 Fundamentals of physiology a human perspective Third ed Florence KY Cengage Learning p 768 ISBN 978 0 534 46697 8 Solomon et al 2002 Biology Sixth Edition Brooks Cole Thomson Learning ISBN 0 03 033503 5 Townsend et al 2004 Sabiston Textbook of Surgery Elsevier ISBN 0 7216 0409 9 Thomson A Drozdowski L Iordache C Thomson B Vermeire S Clandinin M Wild G 2003 Small bowel review Normal physiology part 1 Dig Dis Sci 48 8 1546 64 doi 10 1023 A 1024719925058 PMID 12924651 S2CID 37494914 Thomson A Drozdowski L Iordache C Thomson B Vermeire S Clandinin M Wild G 2003 Small bowel review Normal physiology part 2 Dig Dis Sci 48 8 1565 81 doi 10 1023 A 1024724109128 PMID 12924652 S2CID 42442830 External links editSmall intestine at the Human Protein Atlas Retrieved from https en wikipedia org w index php title Small intestine amp oldid 1197640061, wikipedia, wiki, book, books, library,

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