| STRUCTURE
OF THE GI TRACT WALL
|
|
| General
structure
Fig 17-6 |
Mucosa:
(1) Surface: Highly convoluted. From the stomach on, there is a single layer of epithelial cells linked by tight junctions. The epithelium contains numerous ducts that act as exocrine glands and also has some endocrine glands. (2) Lamina propria: a supporting layer that has small blood vessels, nerves and lymph ducts. (3) Muscularis mucosa: thin smooth muscle layer. Submucosa: Contains submucous nerve plexus and blood vessels and lymph ducts. Muscularis externa: Contains (1) A circular smooth muscle layer whose contraction narrows the lumen. (2) A longitudinal smooth muscle layer whose contraction shortens the tube. (3) Myenteric plexus: a nerve network between the two muscle layers. Serosa: Thin layer of cells and connective tissue that surround the gut wall. These are anchored to the abdominal wall with connective tissue. |
| Intestinal
surface
Fig 17-7, 17-8 |
The surface is made larger for more absorption of nutrients by various structures: The villi are finger like projections. The surface of each villus has microvilli which increase the surface area as hairlike projections. The small intestine has a surface area of 300 m2, about 600 times more than a plain tube of the same size. |
| Epithelial cell replacement | The epithelial surfaces are continuously being replaced. About 17 billion cells are replaced each day, and the whole epithelium in 5 days. The cells differentiate into mature cells as they migrate to the top of the villus, where they are sloughed off. |
| Nutrient movement from the epithelial layer | Each villus has an arteriole, a venule and a lymph duct (lacteal). After passing through the epithelium, the fat enters the lacteal and goes into the lymph system, which drains into the venous system. The other nutrients go into the venules then into the hepatic portal vein into the liver. Some of the nutrients are processed there. The nutrients then continue form the liver to the heart and then to the body. |
| DIGESTION AND ABSORPTION | |
| Carbohydrates
Table 17-2 |
Intake
is 250-800 grams per days in our diet.
About 2/3s is starch, a plant polysaccharide. Most of the rest is sucrose (table sugar) and lactose (milk sugar) (disaccharides). Cellulose is another plant polysaccharide. It cannot be digested and is referred to as fiber. Starch digestion: Begins in the mouth with salivary amylase which continues to work in the stomach. Starch is digested in the small intestine by pancreatic amylase. The end result is a disaccharide, maltose, and short glucose chains. Sucrose, lactose, maltose and the glucose chains are broken down into monosaccharides: glucose, fructose and galactose, by enzymes on the microvilli of the small intestine. The sugars then cross the epithelium into the blood. This is by active transport or facilitated diffusion. The sugars are too big for simple diffusion across the membrane. |
| Protein | 40-50
g of protein is required to supply essential amino acids. An American diet
contains about 125 g of protein daily.
Enzymes, mucus, and broken down epithelial cells also are a protein source. Protein digestion: begins in the stomach with pepsin and in the small intestine with trypsin and chymotrypsin secreted by the pancreas. Also in the small intestine carboxypeptidase and aminopeptidase pull off amino acids that can be absorbed into the epithelium. Amino acids are transferred into the epithelium by secondary active transport coupled to sodium transport. Chains of 2-3 amino acids can be absorbed as well. Small proteins can be transported by endocytosis and exocytosis. |
| Fat
17-9,
17-10
17-11
17-12 |
25-160
grams/day in our diet.
Fat digestion takes place almost entirely in the small intestine. The main digestive enzyme is pancreatic lipase. Triacylglycerol ----> monoglyceride + 2 fatty acids Large lipid droplets are converted to smaller emulsion droplets by emulsification and then to micelles (even smaller). Emulsification (fat breakdown) requires mechanical disruption and emulsifying agents which prevent smaller droplets from reaggregating. Phospholipid in food and bile salts are the emulsifying agents. They are amphipathic (have polar and non-polar ends). The non-polar end binds to the emulsion droplet. The polar end is exposed to the surface and prevents the droplets from reuniting. When a micelle breaks down it releases its lipid molecules into solution. These can diffuse across the intestinal epithelium. As more lipids diffuse into the epithelium, micelles break down to release more. In the epithelial cells fatty acids and monoglycerides are reassembled into triacylglycerol in the smooth endoplasmic reticulum (ER) and released as fat droplets called chylomicrons into the interstitial space on the other side. The chylomicrons also contain other lipids such as cholesterol and fat soluble vitamins (A,D,E,K). The chylomicrons diffuse from the interstitial space into the lacteals. The lymph eventually empties into the systemic veins. |
| Vitamins | Fat
soluble vitamins are transported in chylomicrons as are the fat molecules.
Water soluble vitamins are absorbed by diffusion or carrier mediated transport. However, B12 must bind to a protein called intrinsic factor produced in the stomach. This complex is absorbed on specific cells in the small intestine. |
| Water
and minerals
Iron |
Water
is the most abundant substance in chyme. Most water is reabsorbed in the
wall of the small intestine, which is very permeable to water. Water
follows solutes via osmosis.
Sodium is the most abundant solute in chyme. It is absorbed using Na,K-ATPase pumps similarly to the renal tubules. Chloride and bicarbonate are co-transported with sodium. The absorption of other minerals also occurs but their transport processes are too detailed to cover in this course. About 10% of ingested iron is absorbed into the blood every day. Most iron transported into the epithelial cells is bound to ferritin and stored as such. Iron in the GI epithelial cells is released back into the intestine when the cells slough off. Iron released into blood is bound to transferrin which circulates in the body. When more iron is needed, as in blood loss, ferritin synthesis drops, and the absorbed iron then goes into the blood to be used in hemoglobin. Too much iron in the body tends to accumulate in tissues and not be released as waste. |