Structure The structure and function of the GI tract can be described both by
gross anatomy and
microscopic anatomy (histology). The tract itself is divided into upper and lower tracts, and the intestines into
small and
large intestines.
Upper gastrointestinal tract The upper gastrointestinal tract consists of the
mouth,
pharynx,
esophagus,
stomach, and
duodenum. The exact demarcation between the upper and lower tracts is the
suspensory muscle of the duodenum. This differentiates the embryonic borders between the foregut and midgut, and is also the division commonly used by clinicians to describe
gastrointestinal bleeding as being of either "upper" or "lower" origin. Upon
dissection, the duodenum may appear to be a unified organ, but it is divided into four segments based on function, location, and internal anatomy. The four segments of the duodenum are as follows (starting at the stomach, and moving toward the jejunum):
bulb, descending, horizontal, and ascending. The suspensory muscle of the duodenum suspends the superior border of the ascending duodenum from the
diaphragm, and serves as an important anatomical landmark showing the formal division between the duodenum and the jejunum, the first and second parts of the small intestine, respectively. This is a thin muscle which is derived from the
embryonic
mesoderm.
Lower gastrointestinal tract The lower gastrointestinal tract includes most of the
small intestine and all of the
large intestine. In
human anatomy, the
intestine (
bowel or
gut; Greek:
éntera) is the segment of the gastrointestinal tract extending from the
pyloric sphincter of the
stomach to the
anus and as in other mammals, consists of two segments: the
small intestine and the
large intestine. In humans, the small intestine is further subdivided into the
duodenum,
jejunum, and
ileum. The large intestine is subdivided into the
cecum, and
ascending,
transverse,
descending, and
sigmoid colons,
rectum, and
anal canal.
Small intestine The
small intestine is a tubular structure around 6 to 7 m long, that begins at the
duodenum, and ends at the
ileum. Its
mucosal area in an adult human is about . The combination of the
circular folds, the villi, and the microvilli increases the absorptive area of the mucosa about 600-fold, making a total area of about for the entire small intestine. Its main function is to absorb the products of digestion (including carbohydrates, proteins, lipids, and vitamins) into the bloodstream. There are three major divisions: •
Duodenum: A short structure (about 20–25 cm long The large intestine begins at the cecum, where the
appendix is located. This is also the start of the colon as the
ascending colon in the back wall of the abdomen. At the
right colic flexure (
hepatic flexure) (the flexed portion of the ascending and
transverse colon) it runs across the abdomen in the transverse colon, passing below the diaphragm. At the
left colic flexure (
splenic flexure) the flexed portion of the transverse and
descending colon, it descends down the left side of the abdomen. It reaches the
sigmoid colon which is a loop of the colon closest to the rectum and continues to the rectum and
anal canal.
Development The gut is an
endoderm-derived structure. At approximately the sixteenth day of human development, the
embryo begins to fold
ventrally (with the embryo's ventral surface becoming
concave) in two directions: the sides of the embryo fold in on each other and the head and tail fold toward one another. The result is that a piece of the
yolk sac, an
endoderm-lined structure in contact with the
ventral aspect of the embryo, begins to be pinched off to become the
primitive gut. The yolk sac remains connected to the gut tube via the
vitelline duct. Usually, this structure regresses during development; in cases where it does not, it is known as
Meckel's diverticulum. During
fetal life, the primitive gut is gradually patterned into three segments:
foregut,
midgut, and
hindgut. Although these terms are often used in reference to segments of the primitive gut, they are also used regularly to describe regions of the definitive gut as well. Each segment of the gut is further specified and gives rise to specific gut and gut-related structures in later development. Components derived from the gut proper, including the
stomach and
colon, develop as swellings or dilatations in the cells of the primitive gut. In contrast, gut-related derivatives — that is, those structures that derive from the primitive gut but are not part of the gut proper, in general, develop as out-pouchings of the primitive gut. The blood vessels supplying these structures remain constant throughout development.
Histology The gastrointestinal tract has a form of general histology with some differences that reflect the specialization in functional anatomy. The GI tract can be divided into four concentric layers in the following order: •
Mucosa •
Submucosa •
Muscular layer •
Adventitia or
serosa Mucosa The
mucosa is the innermost layer of the gastrointestinal tract. The mucosa surrounds the
lumen, or open space within the tube. This layer comes in direct contact with digested food (
chyme). The mucosa is made up of: •
Epithelium – innermost layer. Responsible for most digestive, absorptive and secretory processes. •
Lamina propria – a layer of
loose connective tissue. Unusually cellular compared to most connective tissue •
Muscularis mucosae – a thin layer of
smooth muscle that aids the passing of material and enhances the interaction between the epithelial layer and the contents of the lumen by agitation and
peristalsis The mucosae are highly specialized in each organ of the gastrointestinal tract to deal with the different conditions. The most variation is seen in the epithelium.
Submucosa The
submucosa consists of a layer of
dense irregular connective tissue with large blood vessels, lymphatics, and nerves branching into the mucosa and
muscular layer. It contains the
submucosal plexus, an
enteric nervous plexus, situated on the inner surface of the
muscularis externa.
Muscular layer The
muscular layer consists of an inner circular layer and a
longitudinal outer layer. The circular layer prevents food from traveling backward and the longitudinal layer shortens the tract. The layers are not truly longitudinal or circular, rather the layers of muscle are helical with different pitches. The inner circular is helical with a steep pitch and the outer longitudinal is helical with a much shallower pitch. Whilst the muscularis externa is similar throughout the entire gastrointestinal tract, an exception is the stomach which has an additional inner oblique muscular layer to aid with grinding and mixing of food. The muscularis externa of the stomach is composed of the inner oblique layer, middle circular layer, and the outer longitudinal layer. Between the circular and longitudinal muscle layers is the
myenteric plexus. This controls peristalsis. Activity is initiated by the pacemaker cells, (myenteric
interstitial cells of Cajal). The gut has intrinsic peristaltic activity (
basal electrical rhythm) due to its self-contained enteric nervous system. The rate can be modulated by the rest of the
autonomic nervous system. Over 600 of these genes are more specifically expressed in one or more parts of the GI tract and the corresponding proteins have functions related to digestion of food and uptake of nutrients. Examples of specific proteins with such functions are
pepsinogen PGC and the
lipase LIPF, expressed in
chief cells, and gastric
ATPase ATP4A and
gastric intrinsic factor GIF, expressed in
parietal cells of the stomach mucosa. Specific proteins expressed in the stomach and duodenum involved in defence include
mucin proteins, such as
mucin 6 and
intelectin-1.
Transit time The time taken for food to transit through the gastrointestinal tract varies on multiple factors, including age, ethnicity, and gender. Several techniques have been used to measure transit time, including radiography following a
barium-labeled meal, breath
hydrogen analysis,
scintigraphic analysis following a
radiolabeled meal, and simple ingestion and spotting of
corn kernels. It takes 2.5 to 3 hours for 50% of the contents to leave the stomach. The rate of digestion is also dependent of the material being digested, as food composition from the same meal may leave the stomach at different rates. Total emptying of the stomach takes around 4–5 hours, and transit through the colon takes 30 to 50 hours.
Immune function The gastrointestinal tract forms an important part of the
immune system.
Immune barrier The surface area of the digestive tract is estimated to be about 32 square meters, or about half a badminton court. Fundamental components of this protection are provided by the
intestinal mucosal barrier, which is composed of physical, biochemical, and immune elements elaborated by the intestinal mucosa. Microorganisms also are kept at bay by an extensive immune system comprising the
gut-associated lymphoid tissue (GALT). There are additional factors contributing to protection from pathogen invasion. For example, low
pH (ranging from 1 to 4) of the stomach is fatal for many
microorganisms that enter it. Similarly,
mucus (containing
IgA antibodies) neutralizes many pathogenic microorganisms. Other factors in the GI tract contribution to immune function include
enzymes secreted in the
saliva and
bile.
Immune system homeostasis Beneficial bacteria also can contribute to the homeostasis of the gastrointestinal immune system. For example,
Clostridia, one of the most predominant bacterial groups in the GI tract, play an important role in influencing the dynamics of the gut's immune system. It has been demonstrated that the intake of a high fiber diet could be responsible for the induction of
T-regulatory cells (Tregs). This is due to the production of
short-chain fatty acids during the fermentation of plant-derived nutrients such as
butyrate and
propionate. Basically, the butyrate induces the differentiation of Treg cells by enhancing
histone H3 acetylation in the promoter and conserved non-coding sequence regions of the
FOXP3 locus, thus regulating the
T cells, resulting in the reduction of the inflammatory response and allergies.
Gastrointestinal microbiota depicted in various regions of the gastrointestinal tract The large intestine contains multiple types of
bacteria, and other
microorganisms that can break down molecules the human body cannot process alone, demonstrating a
symbiotic relationship. These microbes are responsible for gas production at
host–pathogen interface, which is released as
flatulence. Intestinal bacteria can also participate in biosynthesis reactions. For example, certain strains in the large intestine produce vitamin B12; an essential compound in humans for things like DNA synthesis and red blood cell production. However, the primary function of the large intestine is
water absorption from digested material (regulated by the
hypothalamus) and the reabsorption of
sodium and nutrients. Beneficial
intestinal bacteria compete with potentially harmful
bacteria for space and nutrients, as the intestinal tract has limited resources. A ratio of 80–85% beneficial to 15–20% potentially harmful bacteria is proposed for maintaining
homeostasis. An imbalanced ratio results in
dysbiosis.
Detoxification and drug metabolism Enzymes such as
CYP3A4, along with the
antiporter activities, are also instrumental in the intestine's role of
drug metabolism in the detoxification of
antigens and
xenobiotics. ==Other animals==