CHAPTER 24    DIGESTIVE SYSTEM

 

Digestion--breaking down of food into molecules small enough to enter body cells

 

FIGURE 24.1 P. 897—Very general diagram of organs of digestion

 

Organs of digestion are divided into 2 groups:

 

A. Gastrointestinal (GI) tract (alimentary canal)--continuous tube passing through the ventral body cavity from mouth to anus. The GI tract contains the food while it is in the body, until it is either absorbed or eliminated. Total length is about 30 feet.

   1. Mouth

   2. Pharynx

   3. Esophagus

   4. Stomach

   5. Small intestine (SI)

   6. Large intestine (LI)

 

B. Accessory structures---not part of the tube

   1. Teeth---chewing

   2. Tongue---handling food and swallowing

   3. Salivary glands

   4. Liver                       Produce or store secretions, add

   5. Gallbladder             them to GI tract through ducts,

   6. Pancreas                 never touch food

 

Gastroenterology--structure, function, diagnosis & treatment of diseases of the stomach and intestines

     Gastro-  stomach

     Entero-  intestine

 

6 basic activities of the digestive system:

 

1. Ingestion--taking in food

2. Secretion---7 liters/day---water, acid, buffers, enzymes

3. Mixing and movement of food (propulsion) along the GI tract

4. Digestion--mechanical and chemical breakdown

   a. Mechanical digestion--chewing, mixing, etc.

   b. Chemical digestion--splitting of ingested carbohydrate, protein and lipid

       molecules into smaller molecules that can be absorbed and used by cells

5. Absorption--passage of digested food into the cardiovascular or lymphatic systems for distribution to cells

6. Defecation--elimination of indigestible material  (feces)

 

 

LAYERS OF THE GI TRACT WALL

 

The wall of the GI tract from esophagus to anal canal has the same 4 basic layers:

   1. Mucosa--mucous membrane that lines the GI tract

      a. Epithelium--next to food

         1) Non-keratinized stratified squamous--mouth, pharynx, esophagus, anal canal--protection

         2) Simple columnar--rest of tract, absorption and secretion

 

      b. CT layer called the lamina propria--support, provides blood supply and contains many immune cells. The lymphatic tissue of this area is called the mucosa-associated lymphoid tissue (MALT)

 

      c. Muscularis mucosae—very thin layer of smooth muscle, helps form the ridges and folds of the mucosa

 

   2. Submucosa--areolar CT that binds the mucosa to the third layer and contains the submucosal plexus (plexus of Meissner), the part of the enteric nervous system

concerned with control of secretion, vasomotor nerves, and the muscularis mucosae. This layer may also contain glands and lymphatic tissue.

 

   3. Muscularis

      a. Skeletal muscle of the mouth, pharynx, and upper esophagus aids in chewing and swallowing

      b. Skeletal muscle of the anal canal (external sphincter) permits voluntary control

of defecation

      c. Smooth muscle throughout the rest of the tract--contractions help break down food, mix it with digestive secretions and propel it along the GI tract. 2 layers:

         1) Inner sheet of circular fibers

         2) Outer sheet of longitudinal fibers

      d. Also contains the other ENS nerve plexus, the myenteric plexus of Auerbach, which is the major control of GI tract motility.

 

   4. Serosa--outermost layer--serous membrane of simple squamous epithelium (mesothelium) and CT.

      a. Esophagus---outer covering is the adventitia, areolar CT only

      b. Below the diaphragm the serosa forms the visceral peritoneum.

 

Peritoneum--the largest serous membrane of the body and consists of a layer of mesothelium (simple squamous epithelium) and underlying CT

   Visceral peritoneum--covers organs, forming their serosa

   Parietal peritoneum--lines the abdominal cavity

The peritoneal cavity is a potential space between the 2 layers. Contains a small amount of serous fluid for lubrication. (Abnormally large amount of this fluid is called ascites). Peritonitis is inflammation of the peritoneum.

 

Some organs, such as the kidneys, lie behind the peritoneum on the posterior abdominal wall (retroperitoneal).

 

The peritoneum forms several large folds that bind organs to each other and to the abdominal walls, and also carry blood vessels, lymphatics and nerves to various organs.

   1. Mesentery--binds the small intestine to the abdominal wall (a loose attachment)

 

   2. Mesocolon--binds large intestine (much closer attachment)

 

   3. Falciform ligament--attaches liver to the anterior abdominal wall and the

diaphragm

 

   4. Lesser omentum--suspends the stomach (lesser curvature) and duodenum from

the liver

 

   5. Greater omentum--originates from the greater curvature of the stomach and drapes over the transverse colon and small intestine. Contains large quantities of adipose tissue and lymphatic nodes and nodules.

 

                                     FIGURE 24.4 P. 900-901

 

ORGANS OF DIGESTION

1. MOUTH--(oral/buccal cavity) 

   a. Cheeks—form lateral walls and terminate in the lips. The zone where the mucous membrane from the inside and skin from the outside meet is called the vermilion (red part of the lips). A midline fold, the labial frenulum, attaches lip to gum. The area from lips/cheeks to gums/teeth is the vestibule of the oral cavity. The opening between mouth and pharynx is the fauces.

 

   b. Roof of the mouth—formed anteriorly by the hard palate and posteriorly by the soft palate. The uvula hangs from the soft palate and closes off the nasopharynx during swallowing.

 

 

2. SALIVARY GLANDS—secrete small amounts of saliva at all times and more when food is present. Saliva lubricates, dissolves and begins the chemical breakdown of food. Mucous membrane of the mouth and tongue contains many small salivary glands, but most saliva comes from the 3 paired major salivary glands:

 

   a. Parotid glands—inferior and anterior to the ears, secretion reaches the mouth by Stenson's duct, which runs across the masseter muscle and empties into the mouth opposite the upper 2nd molars.

 

   b. Submandibular glands—beneath the base of the tongue--empty into the floor of the mouth by Wharton's ducts.

 

   c. Sublingual glands—superior to submandibulars and also empty into the floor of the mouth by ducts of Rivinus.

 

 

Saliva is 99.5% water and 0.5% solutes (ions, lysozyme, mucus, salivary amylase, and lingual lipase). Composition:

   Parotids—watery liquid containing large amounts of salivary amylase

   Submandibular—thicker & mixture of salivary amylase and mucus

   Sublingual—mostly mucus

 

Water in saliva dissolves the food so it can be tasted. Along with mucus, lubricates food. Lysozyme destroys some bacteria. Chloride ions activate salivary amylase.

 

Secretion of saliva is under nervous control only (no hormones). Average amount is 1000-1500 ml per day. Parasympathetic impulses increase secretion, sympathetic decrease.

 

The presence of food in the mouth causes an increase in parasympathetic impulses and an increase in secretion of saliva. The sight, smell, thought of food may also increase secretion.

 

 

3. TONGUE—composed of skeletal muscle covered by mucous membrane. The lingual frenulum attaches tongue to floor of mouth. The top and sides of the tongue are covered by papillae. Lingual glands on top of the tongue secrete an enzyme, lingual lipase, which begins the digestion of fats. The tongue manipulates food during chewing and aids in swallowing.

 

 

4. TEETH (dentes)—located in alveolar processes of mandible & maxillae. Gums (gingivae) cover these processes. The periodontal ligaments are CT that lines the sockets and binds the tooth roots in place. 3 portions of a tooth:

 

   a. Crown—exposed portion above the gum line and covered by enamel (hardest substance in the body) composed of calcium phosphate and calcium carbonate.

 

   b. Neck—at gum line between crown and root

 

   c. Root—each tooth has 1-3 roots that are embedded in the socket. The root is covered by cementum.

 

 

Dentin and cementum are living CTs of the tooth and have living cells associated with them. The enamel is classified as a cellular secretion and does not contain cells.

 

The inside of a tooth is composed of dentin, a calcified CT that encloses a central hollow area, the pulp cavity. This contains the pulp, the non-calcified living tissue of the tooth. Blood vessels, nerves, and lymphatics enter the apical foramen (an opening at the tip of the root) and pass through the root canal to the larger pulp cavity.

                              FIGURE 24.7  P. 905

 

 

Humans have 2 sets of teeth:

   a. Deciduous (primary, milk, baby) teeth--20 in all and erupt from 6 months-2years of age. Lost and replaced over ages of 6-12 years.

   b. Permanent (secondary) teeth--32 teeth that appear from the age of 6 years to adulthood. Includes 4 types of teeth:

      1) Incisors--2 pairs on midline--chisel-shaped for cutting

      2) Cuspids (canines)--1 pair with a pointed surface (cusp)--used to tear or shred food

      3) Premolars (bicuspids)--2 pairs, 2 cusps each--crushing and grinding

      4) Molars--3 pairs, 4 cusps each--crushing and grinding. The 3rd molars are commonly called the wisdom teeth. Modern human jaws often do not have room for them to erupt (impacted wisdom teeth).

                               FIGURE 24.8  P. 907

 

 

DIGESTION IN THE MOUTH

   a. Mechanical—chewing (mastication) reduces the food to smaller pieces and mixes it with saliva. A “mouthful” of food forms a soft mass called a bolus.

   b. Chemical—2  enzymes 

      1) Salivary amylase—initiates the breakdown of starches

      2) Lingual lipase begins digestion of triglycerides (the form of fat we eat the most of)

 

5. PHARYNX—food being swallowed passes through the pharynx (oropharynx & laryngopharynx)

 

Swallowing (deglutition)—moves food from mouth to stomach in 3 stages:

   a. Voluntary—bolus moved into oropharynx by movement up and back of tongue

   b. Pharyngeal stage—involuntary and moves bolus into the esophagus. Epiglottis and uvula close off respiratory passages.

 

These movements are coordinated by the deglutition center in the medulla.

 

   c. Esophageal stage--through esophagus to stomach

 

 

6. ESOPHAGUS—muscular collapsible tube with typical layers except no true serosa. The outer layer is known as the adventitia and has no epithelial layer. The functions are transportation of food and secretion of mucus for lubrication (no enzymes, no absorption). It penetrates the diaphragm at the esophageal hiatus. The upper esophageal sphincter in the pharynx opens during swallowing to allow food to enter. Peristalsis (wave-like muscle contractions) moves the food down the esophagus. At the lower end the lower esophageal (cardiac) sphincter opens to allow food into the stomach. If this sphincter fails to close, acid stomach contents may leak upward into the esophagus (heartburn).

 

 

7. STOMACH—enlargement of the GI tract with 4 areas:    

   a. Cardia—surrounds esophageal opening—if this upper portion slips up through the esophageal hiatus this is a hiatal hernia.

   b. Fundus—above and to the left of the cardia

   c. Body—large central portion

   d. Pylorus—connects to duodenum and contains the pyloric sphincter, which must open to allow stomach contents to move into the SI

 

 

 

 

 

 

 

 

 

 

 

 

When the stomach is empty, the mucosa lies in thick ridges called rugae, which flatten out as it fills. The stomach mucosa contains a layer of simple columnar cells with many gastric pits extending down to the lamina propria and connecting to the gastric glands.

                                    FIGURE 24.12  P. 868

 

 

Gastric glands contain 4 kinds of cells:

   a. Chief (zymogenic) cells—secrete pepsinogen and gastric lipase

   b. Parietal cells—secrete HCl and intrinsic factor (necessary for the absorption of Vitamin B12)

   c. Mucous neck cells—secrete mucus

The secretion of these 3 types of cells mixes in the duct (gastric pit) as it moves into the stomach, where it is called gastric juice. About 2000-3000 ml per day is secreted.

   d. G cells—do not contribute to gastric juice--these are endocrine cells and secrete the hormone gastrin

 

The muscularis of the stomach has 3 layers:

   a. Outer longitudinal

   b. Middle circular

   c. Inner oblique—extra layer not found in rest of tube

This allows the stomach to move in a variety of ways to churn and mix food.

 

DIGESTION IN THE STOMACH

 

a. Mechanical—after food enters, frequent peristaltic mixing waves pass over the stomach. Food mixes with gastric juice and is then known as chyme. Mixing waves become gradually stronger. Eventually the waves force chyme against the pyloric sphincter. A little of the most liquid chyme is squirted into the duodenum as the sphincter opens briefly. Most of the chyme remains in the stomach and undergoes further mixing, then a little more is moved into the duodenum as the stomach is slowly emptied. Chyme remains in the stomach 2-6 hours, depending on content. Meals high is carbohydrate leave fastest, protein next fastest and high fat meals remain the longest.

 

b. Chemical digestion 

   1) HCl—kills microbes, unfolds proteins (a preliminary step in digestion) and activates pepsinogen

 

   2) Pepsin is the protein-digesting enzyme of the stomach. It breaks peptide bonds and splits proteins into fragments called peptides. It can act only in a very acid pH (about 2). Pepsin is secreted in an inactive form, pepsinogen. This protects the secreting cells themselves from digestion by the enzyme. It becomes active only in the stomach, where lining cells are protected by a thick layer of alkaline mucus.

 

   3) Gastric lipase—acts in the digestion of milk fats--important in babies, limited role in adults

 

 

REGULATION OF GASTRIC MOTILITY AND SECRETION

3 phases:

   a. Cephalic phase—initiated in the cortex by the sight, smell, taste or thought of food. Parasympathetic impulses increase all secretions of the gastric glands and increase motility. Emotions (fear, anger, tension) may interfere with this by generating sympathetic impulses.

 

   b. Gastric phase—occurs when food actually enters the stomach.

      1) Nervous—food stretches the stomach and stimulates stretch receptors in the wall. Also chemoreceptors sense that the pH has risen as non-acid food enters. Both of these trigger parasympathetic impulses that increase peristalsis and secretion of gastric juice. As the pH returns to normal and then later food moves into the small intestine, these receptors stop triggering impulses until more food arrives.

 

      2) Hormonal—distention of the stomach, partially digested proteins, and caffeine all stimulate the G cells and cause the secretion of gastrin. This hormone stimulates secretion of gastric juice, increases stomach motility and acts on the sphincters (contraction of the lower esophageal sphincter and relaxation of the pyloric and ileocecal sphincters).

 

   c. Intestinal phase—this occurs when food moves to the duodenum and results in inhibition of gastric secretion and motility. The intestinal phase slows gastric digestion and the movement of chyme so the duodenum won't be overloaded.

 

 

REGULATION OF GASTRIC EMPTYING

 

Gastric emptying is under both neural and hormonal control.

 

Factors that encourage :

     1) Distention of the stomach

     2) Presence in the stomach of partially digested proteins, alcohol, and caffeine

     3) Gastrin

 

Factors that slow:

     1) Enterogastric reflex—this is initiated by the presence of food in the SI. It inhibits parasympathetic impulses to the stomach and decreases gastric secretion and motility.

      2) Hormonal—presence of chyme containing glucose and fatty acids in the small intestine causes enteroendocrine cells in the wall of the SI to release 2 hormones:

         a) Secretin—decreases gastric secretions

         b) Cholecystokinin (CCK)—inhibits stomach emptying

 

 

ABSORPTION IN THE STOMACH

Only a few substances are absorbed through the stomach wall:

Water                       Certain drugs (aspirin)

Electrolytes               Alcohol

8. PANCREAS—accessory structure of major importance to digestion in the SI. Lies retroperitoneal, posterior to the greater curvature of the stomach and consists of a head, a body and a tail. Two large ducts carry pancreatic secretions to the duodenum:

     a. Pancreatic duct (duct of Wirsung)—larger and joins the common bile duct from the liver and gallbladder

     b. Accessory duct (duct of Santorini)—directly from pancreas to duodenum

                                FIGURE 24.14  P. 917

 

The gland is made up of small clusters of exocrine cells called pancreatic acini which secrete pancreatic juice. Scattered among the acini are islets of Langerhans, which are the endocrine portion (1%).

 

 

Pancreatic juice contains mostly water, sodium bicarbonate and a number of  enzymes. About 1200-1500 ml per day is secreted. Functions:

     a. Buffers the acidic chyme to slightly alkaline

     b. Stops the action of pepsin

     c. Provides the following enzymes:

        1) Pancreatic amylase

        2) Trypsin

        3) Chymotrypsin

        4) Carboxypeptidase

        5) Elastase

        6) Pancreatic lipase

        7) Ribonuclease

        8) Deoxyribonuclease

 

The pancreatic protein digesting enzymes are also secreted in an inactive form and activated in the SI. If these enzymes become activated within the pancreas they would digest the gland itself. This sometimes occurs (acute pancreatitis).

     Trypsinogen—inactive form of trypsin—activated by enterokinase, an enzyme secreted by cells of the SI

     Chymotrypsinogen

     Procarboxypeptidase   all activated by trypsin

     Proelastase

 

 

 

REGULATION OF PANCREATIC SECRETION

 

     Nervous—during the cephalic and gastric phase of gastric digestion, the vagus nerve also sends impulses to the pancreas to increase secretion.

      Hormonal

     a. Acidic chyme entering the SI causes enteroendocrine cells in the SI mucosa to release secretin, which stimulates flow of pancreatic juice rich in bicarbonate ions.

     b. Partially digested fats and proteins entering the SI cause other enteroendocrine cells to secrete cholecystokinin (CCK). CCK stimulates pancreatic juice rich in enzymes.

 

9. LIVER—2nd largest organ of the body, located under the diaphragm and covered by peritoneum and dense CT. Divided into 2 principal lobes, a larger right and a smaller left, separated by the falciform ligament. Also 2 smaller lobes, the caudate and quadrate.

 

The liver is made up of many small functional units called lobules, which consist of hepatocytes (specialized epithelial cells) arranged in plates around a central vein. Instead of capillaries, blood passes through larger vessels called sinusoids, which contain Kupffer's cells that phagocytize worn-out blood cells, bacteria and certain toxic substances.

 

Bile is secreted by the hepatocytes and enters bile caniculi that empty into bile ductules. Bile ductules merge to form larger bile ducts and eventually form the right and left hepatic ducts, which unite and leave the liver as the common hepatic duct. The common hepatic duct is joined by the cystic duct from the gallbladder to form the common bile duct, which along with the pancreatic duct enters the duodenum at the hepatopancreatic ampulla (ampulla of Vater).

                              

   FIGURE 24.14  P. 917 (again)

 

Blood from both the hepatic artery and the hepatic portal vein enters the liver sinusoids, where hepatic cells remove oxygen, nutrients and certain poisons and Kupffer's cells also function. As the blood travels through the liver:

     Nutrients are stored or modified

     Poisons are stored or detoxified

     Products manufactured by hepatic cells and some nutrients are secreted into the blood

 

Blood drains into the central vein of the lobule and then the hepatic vein. Often branches of the hepatic portal vein, the hepatic artery, and a bile duct travel together through the liver and form a portal triad at the corners of liver lobules.

 

Hepatocytes secrete 800-1000 ml of bile daily. It is a yellow, brownish or olive green liquid that consists mostly of water with:

     Bile salts          Lecithin

     Bile acids          Bile pigments

     Cholesterol         Ions

 

Bile is both an excretory (waste) product and a digestive secretion. Bile salts act in the emulsification and absorption of fats. Emulsification is the breakdown of large fat globules into tiny droplets. Bilirubin is the principal bile pigment and is a waste product of RBC breakdown. In the intestine, bilirubin is broken down to stercobilin, which gives the brownish color to feces.

 

Jaundice is a yellowish coloration of skin, mucous membranes and the sclera due to a buildup of bilirubin.

     a. Prehepatic (hemolytic) jaundice---rapid excess production of bilirubin

     b. Hepatic jaundice---liver malfunction

     c. Extrahepatic (obstructive) jaundice---blockage of bile drainage

 

REGULATION OF BILE SECRETION---small amounts are produced at all times)

   1. Nervous--parasympathetic impulses delivered by the vagus nerve increase production

   2. Hormonal--secretin stimulates secretion

   3. Increased blood flow through the liver increases secretion

   4. Presence of large amounts of bile salts in the blood increases secretion

 

 

PHYSIOLOGY OF THE LIVER

   1. Carbohydrate metabolism—very important in maintaining normal blood glucose level. Converts glucose to glycogen back to glucose as needed. Can also convert certain amino acids, lactic acid and other sugars to glucose when needed.

   2. Lipid metabolism--breaks down fatty acids to generate ATP. synthesizes lipoproteins and cholesterol, converts some cholesterol to bile salts

   3. Protein metabolism—loss of just this function could be fatal in a few days. Converts ammonia, a highly toxic byproduct of protein breakdown, to urea, which is less toxic. Urea is then removed by the kidneys. Also synthesizes most plasma proteins (globulins, albumin, clotting factors).

   4. Removal of drugs and hormones

   5. Excretion of bilirubin

   6. Synthesis of bile salts

   7. Storage of glycogen, vitamins, minerals

   8. Phagocytosis

   9. Activation of Vitamin D

 

10. GALLBLADDER--small sac on the ventral surface of the liver that stores and concentrates bile by absorbing water and ions. The wall contains smooth muscle fibers which can contract to squeeze bile into the duodenum through the cystic duct and then the common bile duct.

When the SI is empty, a sphincter closes the hepatopancreatic ampulla so bile backs up into the gallbladder for storage. Food in the SI stimulates secretin of CCK, which causes contraction of the gallbladder and the opening of the sphincter.

                           FIGURE 24.14  P.  917   (AGAIN) 

 

 

SEE SUMMARY OF DIGESTIVE HORMONES

               TABLE  24.8    P. 939

Where are they produced?

Where do they act?

What do they do?

Remember, the same hormone may affect more than one target.

 

 

 

11. SMALL INTESTINE--most of digestion and absorption occur here. It totals about 10 feet in a living person (21 feet in a cadaver) and is divided into 3 sections:

     a. Duodenum (10 inches)—begins at pylorus

     b. Jejunum (3 feet)

     c. Ileum (6 feet)—joins the LI at the ileocecal valve (sphincter)

 

The SI is highly adapted for digestion and absorption.

Modifications for absorption:

      a. Intestinal mucosa is arranged in permanent ridges called circular folds which cause the chyme to spiral

 

      b. Mucosa forms villi, fingerlike projections that increase surface area. Inside each villus are CT, blood vessels and a lacteal (special lymphatic vessel) to pick up absorbed nutrients.

 

      c. Microvilli—extremely tiny projections of just the plasma membrane of the lining cells that also increase the surface area. Cannot be distinguished individually through a light microscope but give a fuzzy appearance called the brush border.

                                  FIGURE 24.18  P. 923 

  

Secretions:

a. Intestinal glands (crypts of Lieberkuhn)—these are deep crevices  in the mucosa lined with glandular epithelium. They secrete the watery fluid called intestinal juice, which helps dissolve and further liquefy the chyme.

 

b. Intestinal lining cells secrete the following enzymes (called brush border enzymes):

         1) Maltase

         2) Sucrase

         3) Lactase

         4) a-dextrinase

         5) Peptidases

            a) Aminopeptidase

            b) Dipeptidase

         6) Nucleosidases

         7) Phosphatases

 

b. Goblet cells of the mucosa secrete mucus

c. Duodenal (Brunner's ) glands of the submucosa secrete a special

   alkaline mucus

d. Paneth cells in the intestinal glands secrete lysozyme and carry on phagocytosis

e. Enteroendocrine cells secrete digestive hormones

 

The lamina propria of the SI contains large amounts of lymphatic tissue (mucosa associated lymphatic tissue or MALT) to prevent bacteria from entering the blood. Some lymphatic nodules are in groups called Peyer's patches, esp. in the ileum.

 

 

MECHANICAL DIGESTION IN THE SI

2 types of movements occur:

     a. Segmentation is the major movement—it is a localized contraction in areas containing food to mix chyme with digestive juices and bring material in contact with the mucosa for absorption. It occurs due to contraction of circular muscle fibers.

 

     b. Peristalsis—propels chyme onward. In the small intestine, this is a wave of peristalsis known as a migrating motility complex (MMC). Beginning just past the stomach, each MMC travels slowly the entire length of the small intestine. Chyme remains in the SI for 3-5 hours.

 

 

CHEMICAL DIGESTION IN THE SMALL INTESTINE

     1) Carbohydrates

          a. Some of the starches in the food are broken down by salivary amylase. Remaining digestible starches are broken down into fragments by pancreatic amylase. The brush border enzyme a-dextrinase splits glucose units off the starch fragments.

          b. Ingested sucrose, lactose, and maltose are split into monosaccharides by the brush-border enzymes sucrase, lactase, and maltase. Many individuals do not produce enough lactase to completely break down the lactose, which leads to lactose intolerance.

     2) Proteins—pancreatic protein digesting enzymes take up where pepsin of the stomach leaves off. Two brush-border enzymes, aminopeptidase and dipeptidase, complete the process of breaking the protein down to individual amino acids.

     3) Lipids—In adults, the entire fat-digesting process is carried out by pancreatic lipase, acting on fats emulsified by bile salts. Triglycerides are broken down by removing 2 of the 3 fatty acids, leaving 2 fatty acids and a monoclygeride.

     4) Nucleic acids—ribonuclease and deoxyribonuclease in pancreatic juice break down RNA and DNA into pentoses, phosphates, and nitrogenous bases.

 

 

REGULATION OF SI SECRETION & MOTILITY

 

Local reflexes in response to the presence of chyme are most important. Intestinal distension and parasympathetic impulses increase motility. Sympathetic impulses decrease secretion and motility.

 

A hormone, vasoactive intestinal polypeptide (VIP) stimulates production of intestinal juice.

 

12. LARGE INTESTINE--extends from ileum to anus and is about 5 feet long. It is attached to the posterior body wall by mesocolon. The 4 regions are:

      Cecum

      Colon

      Rectum

      Anus

A sphincter (ileocecal valve) regulates movement of chyme from the

SI to the LI. A blind pouch, the cecum, hangs down from the junction of the ileum and LI and ends in a twisted tube, the vermiform appendix.

 

The large intestine continues from this area as the colon: ascending to hepatic flexure, transverse to splenic flexure, descending  and sigmoid. The rectum is the last 8 inches of the LI and terminates as the anal canal. The anus is the opening to the outside and contains 2 sphincters, the internal involuntary and the external voluntary.

                                FIGURE 24.22  P. 932

 

 

Digestion is mostly complete when chyme enters the LI, so little secretion or absorption occur. The muscularis has 3 bands of thickened longitudinal muscles called taenia coli which run most of the length of the LI. Contraction of these bands gathers the colon into a series of pouches called haustra and gives it a puckered appearance.

 

 

MECHANICAL DIGESTION

 

The ileocecal valve regulates the passage of chyme from the ileum into the LI. Immediately after a meal the gastroileal (ileogastric) reflex causes a strong wave of peristalsis that sends any chyme present in the ileum into the LI.

 

In the LI one movement that occurs is haustral churning. One pouch fills and then its walls contract to send the chyme on into the net pouch. Peristalsis also occurs at a slow rate. Mass peristalsis occurs in response to filling of the stomach (gastrocolic reflex). This drives colon contents into the rectum.

 

 

CHEMICAL DIGESTION

The last stage of chemical digestion involves the action of bacteria in the LI. Any remaining carbohydrates are fermented with production of gas. Remaining proteins are also broken down. Bilirubin is decomposed to urobilinogen. Bacteria produce some of the B vitamins and vitamin K, which we absorb.

 

Chyme remains in the LI for 3-10 hours, becoming solid or semisolid as much of the remaining water is absorbed. It is then called feces and contains water, salts, sloughed-off mucosal cells, bacteria, and undigested food. Absorbed in the LI:

     Water

     Vitamins

     Electrolytes

About 1/2 to 1 liter of water enters the LI daily. All but 100-200 ml of it is reabsorbed.

 

DEFECATION

Mass peristalsis pushes feces from sigmoid colon to rectum. Distension of the rectum stimulates stretch receptors which initiate a defecation reflex, which causes contraction of the longitudinal muscles of the rectum and relaxation of the internal sphincter. At this point defecation occurs in infants and small children. We develop voluntary control of the external sphincter and can delay defecation until a convenient time as we mature. In this case feces moves back into the sigmoid colon until another wave of mass peristalsis occurs.

 

DIETARY FIBER

Consists of indigestible plant materials--cellulose, lignin, pectin--found in fruits, vegetables, grains and beans.

   Insoluble fiber--does not dissolve in water--fruit & vegetable skins, wheat and corn bran. Important in keeping foods moving through the digestive tract and may reduce the risk of colon cancer, gallstones, etc.

 

   Soluble fiber--dissolves in water--found in beans, oats, barley, broccoli, prunes, apples and citrus fruits. Seems to help lower cholesterol levels (binds bile salts and prevents their reabsorption).

    

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

CHAPTER 24  SUMMARY OF CHEMICAL DIGESTION AND ABSORPTION

 

Chemical digestion is the result of various enzymes acting to chemically break down food molecules.

 

 TABLE 24.54  P. 927—VERY IMPORTANT—THIS TABLE WITH BLANKS WILL BE ON YOUR HOUR EXAM

 

Absorption---occurs once food molecules are broken down to a form that can pass through the cells of the mucosa into the blood or lymphatic vessels

 

   90% of absorption occurs in the SI

   10% occurs in the stomach and LI

 

CARBOHYDRATES are broken down to monosaccharides and absorbed into capillaries of the villi, some by active transport and some by facilitated diffusion.

 

PROTEINS are broken down to amino acids and absorbed by active transport. A few dipeptides and tripeptides are absorbed into cells and broken down there.

 

LIPIDS are broken down to monoglycerides and fatty acids and absorbed by simple diffusion. Most lipids enter the lacteals and are transported in the lymphatic system to the subclavian vein. Bile salts are necessary.

 

WATER

About 9.3 liters enter the SI each day, about 2.3 liters from ingested liquids and 7 liters from digestive secretions. 8 - 8.5 liters are absorbed in the SI and most of the rest in the LI. Only about .1 liters per day is excreted from the digestive tract. Water is absorbed by osmosis.

 

VITAMINS

   A. Fat-soluble vitamins (ADEK) are absorbed along with ingested dietary fats (cannot be absorbed with no fat in GI tract).

   B. Water-soluble vitamins (BC) are absorbed by simple diffusion except for B12. It must combine with intrinsic factor and the combination is absorbed by receptor-mediated endocytosis.