Digestive System-Chapter 26 Flashcards

1
Q

Describe the major functions of the digestive tract

A

The major functions are ingestion, motility, secretion, digestion (mechanical digestion and chemical digestion), absorption and elimination.

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2
Q

Define mechanical digestion

A

It occurs when ingested material is physically broken down into smaller units by chewing and mixing without changing their chemical structure.

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3
Q

Define chemical digestion

A

It involves specific enzymes to break chemical bonds to change larger complex molecules into smaller molecules that can then be absorbed.

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4
Q

Describe the organization of the digestive system.

A

It has two separate categories of organs: the gastrointestinal (GI) tract (also called the digestive tract, or alimentary canal) form a continuous tube that includes the oral cavity, pharynx, esophagus, stomach, small intestine, and large intestine and ends at the anus. The accessory digestive organs include the salivary glands, liver, and pancreas. Also, the teeth, tongue and gallbladder.

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5
Q

Identify the layers of the gastrointestinal tract wall

A

They are the mucosa (inner lining), the submucosa, the muscularis, and the outermost tunic may be either the adventitia or a serosa.

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6
Q

Describe the structure and function of the mucosa

A

The mucosa is the inner-lining mucous memebrane. It consists of an epithelium, an underlying lamina propria, and a thin layer of muscularis mucosae. The epithelium is in contact with the contents of the lumen and it allows for secretion and absorption.

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7
Q

Describe the structure and function of the submucosa

A

The submucosa is composed of areolar and dense irregular connective tissue. Many large blood vessels, lymph vessels, and nerves are withing the submucosa. In the last region of the small intestine, MALT is present.

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8
Q

Describe the structure and function of the muscularis

A

The muscularis contains two layers of smooth muscle. The cells of the inner layer are oriented circumferentially around the GI tract and are called the inner circular layer. The cells of the outer layer are oriented lengthwise along the GI tract and are called the outer longitudinal layer. The enteric nervous system are located between the two layers and detect both changes in the GI tract wall and the chemical makup of the contents of the lumen. The function of the muscularis is to mix and propel the contents within the GI tract.

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9
Q

Describe the two types of movement that occur in the digestive system.

A

1) Peristalsis-the alternating contraction sequence of both the inner circular and outer longitudinal muscle layers for the purpose of propelling ingested materials through the GI tract. 2) Mixing-the “back-and-forth,” or kneading motion that occurs at any point in time within different regions but lacks directional movement. Mixing is for the purpose of blending ingested materials with the secretions within the GI tract.

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10
Q

Explain how the enteric nervous system is involved in regulating digestion.

A

Both the submucosal nerve plexsus and the myenteric nerve plexus together compse the enteric nervous system. Sensory neurons within these plexuses (housed within the GI tract wall) detect both changes in the GI tract wall (e.g., stretch), and chemical makeup of the contents of the lumen. THus, this system is composed of both sensory and motor neurons of the autonomic nervous system.

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11
Q

Explain how the central nervous system is involved in regulating digestion

A

Sensory input from both mechanoreceptors and chemoreceptors is relayed to the CNS in response to stimulation. Autonomic motor output is then relayed through three cranial, and vagus nerves, to different digestive system effectors, such as salivary glands, the pancreas, and the muscularis layers in the GI tract wall. The result is coordinated secretory and smooth muscle contractions involved in digestive responses.

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12
Q

Explain how hormones are involved in regulating digestion.

A

Gastrin in the stomach stimulates the contractile activity of muscle in the gastric wall, increases release of HCl from parietal cells, and also stimulates contraction of the pyloric sphincter to slow stomach emptying. Secretin is released from the small intestine in response to an increase in chyme activity. It causes the release of an alkaline solution from both the liver and ducts of the pandreas that help neutralize the acidic chyme. Chymottrypsinis activated by trypsin (from chymotrypsinogen) and it breaks the bonds between specific amino acids within the protein to produce smaller strands of amino acides called peptides

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13
Q

Describe the structure and function of mesenteries.

A

The structure of mesenteries refers to the double-layer of peritoneum (connective tissue) that supports, suspends and stabilizes the intraperitoneal GI tract organs. Blood vessels, lymph vessels, and nerves are sandwiched between the two folds and supply the digestive organs.

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14
Q

Identify the four major mesentaries.

A

The greater omentum (which covers most of the abdominal organs); the lesser omentum (connects the superomedial surface of the stomach and the proximal end of the duodenum to the liver); the falciform ligament (a peritoneal fold that attaches the liver to the internal surface of the anterior abdominal wall); and the mesentery proper (a fan-shaped fold of peritoneum that suspends most of the small intestine from the internal surface of the posterior abdominal wall).

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15
Q

Describe the structure of the oral cavity and its accessory structures.

A

The oral cavity is the mouth and is the entrance to the GI tract. There are two distinct spatial regions: the vestibule (or buccal cavity) is the space between the gums, lips, and cheeks, and the oral cavity proper lies central to the teeth.The oral cavity is bound laterally by the cheeks, anteriorly by the teeth and lips, and it leads posteriorly into the oropharynx. The cheeks contain the buccinator muscles. The internal surfaces of both the superior and inferior lips are attached to the gingivae (gums) by a thin mucosa fold in the midline, called the labial frenulum. The palate forms the superior boundar of the oral cavity and acts as a barrier to separate it from the nasal cavity. The anterior 2/3 is hard and bony (the hard palate), and the posterior 1/3 is soft and muscular (soft palate). The hard palate exhibits transverse palatine folds (or friction ridges); the uvula is the posterior part of the soft palate and is a conical median projection; the fauces represent the opening between the oral cavity and the oropharynx; the tongue is formed primarily from skeletal muscle. Both extrinsic and intrinsic muscles move the tongue; papillae are small projections that cover the superior surface of the tongue; The lingual frenulum is a thin vertical mucous membrane that attaches the tongue to the floor of the oral cavity; collectively the intrinsic salivary glands are the buccal glands of the cheeks, lingual glands of the tongue, and labial glands of the lips.

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16
Q

Describe the function of the oral cavity and its accessory structures.

A

The main function of the oral cavity is to ingest food, and here it undergoes the initial processes of mechanical and chemical digestion. The buccinator muscles of the cheeks compress the cheeks against the teeth to hold solid materials in place during mastication; the palatine folds assist the tongue in manipulating ingested materials prior to swallowing; when swallowing the soft palate and the uvula elevate to close off the posterior entrance into the nasopharynx and prevent ingested materials from entering the nasal region; the tongue manipulates and mixes ingested materials during chewing and helps compress the partially digested materials against the palate to assist in mechanical digestion. The tongue also performs important function in both swallowing and in speech production. The teeth are responsible for mastication. The intrinsic salivary glands contribute to the production of saliva.

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17
Q

Explain what mastication is.

A

Mastication is mechanical digestion in the oral cavity, or chewing. It requires the coordinated activities of teeth, skeletal muscles in lips, tongue, cheeks, and jaws that are controlled by nuclei within the medulla oblongata and the pons, collectively called the mastication center.

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18
Q

Describe the components of saliva.

A

Saliva is composed of 99.5% water and a mixture of solutes. Saliva is formed as water and electrolytes are filtered from capillaries through cells (acini) of a salivary gland. Other components are added by acinar cells, including salivary amylase, mucin, and lysozyme.

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19
Q

Explain how salivation is activated.

A

The salivary nuclei within the brainstem regulate salivation. Input to the salivary nuclei is received from chemoreceptors or mechanoreceptors in the upper GI tract. THese receptors detect various types of stimuli, including the introduction of sbstances into the oral cavity, especially those that are acidic; and arrival of foods into the stomach lumen, especially foods that are spicy or acidic. Input is also received by the salivary nuclei from the higher brain center in response to the thought, smell, or sight of food.

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20
Q

Describe the structure and function of the pharynx.

A

The pharynx is a funnel-shaped, muscular passageway with distensible lateral walls, Three skeletal muscle pairs called the superior, middle, and inferior pharyngeal constrictors form the wall of the pharynx. The oropharynx and laryngopharynx are lined with nonkeratinized stratified squamous epithelium that provides protection against the abrasiive activities associated with swallowing ingested materials. The function of the pharynx is to serve as the passageway for both air and food.

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21
Q

Describe the structure and function of the espophagus.

A

The esophagus is a normally collapsed, tubular passageway. It is about 25 cm long in an adult. The superior esophageal sphincter is a contracted ring of circular skeletal muscle at the superior end of the esophagus. It is the area where the esophagus and the pharynx meet. It is closed during inhalation of air, so air does not enter the esophagus and instead enters the larynx and trachea. The inferior esophageal sphincter is at the inferior end of the stomach. It isn’t strong enough alone to prevent materials from refluxing back into the esophagus; instead, the muscle of the diaphragm at the esophageal opening contract to help prevent materials from regurgitating from the stomach. The mucosa of the esophagus is lined with a nonkeratinized stratified squamous epithelium. There is a submucosa and muscularis. THe muscularis is unique in that it contains a blend of both skeletal and smooth muscle. The function of the esophagus is as a passageway for food into the stomach.

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22
Q

List the phases of deglutition (swallowing).(swallowing).

A

The voluntary phase, the pharyngeal phase, and the esophageal phase.

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23
Q

Describe the voluntary phase of deglutition.

A

The voluntary phase occurs after ingestion. Ingested materials and saliva mix in the oral cavity. Chewing forms a bolus. Transverse palatine folds help direct the bolus posteriorly toward the oropharynx.

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24
Q

Describe the pharyngeal phase of deglutition.

A

The arrival of the bolus at the entryway to the oropharynx initiates the pharyngeal phase. It is involuntary. Tactile sensory receptors around the fauces are stimulated by the bolus and initiate sensory input ot the swallowing center in the medulla. Newve signals are then relayed to effectors to cause the following responses: 1) entry of bolus into the oropharynx; 2) elevation of the soft palate and uvula to block the passageway between the oropharynx and nasopharynx; 3) elevation of the larynx by the hyoid muscles in the neck to move the epiglottis to cover the laryngeal opeining (this prevents ingestede material from entering the larynx and trachea); 4) inhibition of the respiratory center in the medulla to assure that a breath is not taken during swallowing. The bolus passes quickly and involuntarily through the pharynx to the esophagus-about 1 second elapses in this phase.Sequential contraction of the pharyngeal constrictors decreases the diameter of the pharynx, beginning at its superior end and moving toward its inferior end. This creates a pressure difference, forcing swallowed material from the pharynx into the esophagus.

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25
Q

Describe the esophageal phase of deglutition.

A

It is also involuntary. It is the time during which the bolus passes through the esophagus and into the stomach-about 5-8 seconds. The presence of the bolus within the lumen of the esophagus stimulates sequential peristaltic waves of muscular contraction that assist in propelling the bolus toward the stomach. The superior and inferior esophageal sphincters are usually closed at rest. . When the bolus is swallowed, these sphincters relax to allow it to pass through the esophagus. Nerve signals to the inferior esophageal sphincter after passage of the bolus cause it to contract, preventing reflux of materials and fluids from the stomach into the esophagus.

26
Q

Describe the anatomy of the stomach.

A

The stomach is a muscular J-shaped organ. It is composed of 4 regions: 1) cardia-a small narrow superior entryway into the stomach lumen from the esophagus; 2) fundus-the dome-shaped region lateral and superior to the esophageal connection with the stomach; 3) body-the largest region of the stomach; 4) pylorus-a narrow, medially directed, funnel-shaped pouch that forms the terminal region of the stomach. It’s opening into the duodenum of the small intestine is called the pyloric orifice. Surrounding this is a thick ring of circular smooth muscle called the pyloric sphincter. THe internal stomach lining is composed of numerous gastric folds. THe greater omentum and the lesser omentum are the two serous membranes associated with the stomach.

27
Q

List the cells found in the gastric epithelium and gastric glands.

A

1) surface mucous cells; 2) mucous neck cells; 3) parietal cells; 4) chief cells; and 5) G-cells.

28
Q

Describe the secretions of surface cells.

A

They continuously secrete an alkaline product containing mucin. Mucin becomes hydrated, producing a 1 to 3 mm mucus layer. This layer helps to prevent ulceration of the stomach lining upon exposure to both the high acidity of the gastric fluid and gastric enzymes.

29
Q

Describe the secretions of mucous neck cells.

A

They produce an acidic mucin that helps maintain the acidic conditions resulting from the secretion of HCl by parietal cells.

30
Q

Describe the secretions of parietal cells (also called oxyntic cells).

A

They secrete two substances into the lumen of the stomach. 1) intrinsic factor-it is required for absorption of vitamin B12 in the ileum. 2) HCl is not formed within the parietal cell (it would destroy the cell). Instead, it forms from H and Cl secreted across the parietal cells’ surface. HCl converts pepsinogen into active pepsin; kills most microorganisms that enter the stomach; contributes to the breakdown of plant cell walls and animal connective tissue; and denatures proteins.

31
Q

Describe the secretions of chief cells (also called zymogenic cells, or peptic cells.

A

They produce and secretepackets of zymogen granules primarily containing pepsinogen. Pepsinogen is the inactive precursor of the proteolytic enzyme pepsin. Pepsin must be produced in this inactive from to prevent the destruction of chief cell proteins. Pepsin chemically digests denatured proteins into smaller peptide fragments (oligopeptides). Chief cells also produce gastric lipase, an enzyme that has a limited role in fat digestion.

32
Q

Describe the secretions of G-cells (enteroendocrine cells).

A

THey secrete gastrin hormone into the bloodstream. Gastrin stimulates stomach secretions and motility. Other enteroendocrine cells produce other hormones, such as somatostatin, a peptide hormone that modulates the function of nearby enteroendocrine and exocrine cells.

33
Q

Distinguish between gastric mixing and gastric emptying.

A

1) Gastric mixing-a form of mechanical digestion that changes the semidigested bolus into chyme. Contractions of the stomach’s thick muscularis layer churn and mix the bolus with the gastric secretions, leading to a reduction in the size of swallowed particles. 2) gastric emptying-the movement of acidic chyme from the stomach through the pyloric sphincter into the duodenum, which is facilitated by the progressive thickening of the muscularis layer in the pylorus region. As a wave of peristaltic muscular contraction moves through the pylorus toward the pyloric sphincter, a pressure gradient is established that drives the stomach contents toward the small intestine.

34
Q

List the three phases involved in the regulation of gastric activity.

A

1) Cephalic phase; 2) gastric phase; and 3) intestinal phase.

35
Q

Describe the cephalic phase.

A

It primarily involves the cephalic reflex, which is a nervous system reflex initiated by the thought, smell, sight, or taste of food. Nerve signals from the higher region of the brain are sent to the hypothalamus, which then relays nerve signals to the medulla, which increases vagal stimulation of the stomach, causing both an increase in contractile force in the gastric wall and secretory activity of the gastric glands. The stomach ‘growling’ is this phase.

36
Q

Describe the gastric phase.

A

It involves the processes following the bolus reaching the stomach. It is regulated by both the nervous system via the gastric reflex and the endocrine system through the release of gastrin hormone. Baroreceptors in the wall of the stomach detect increased distension in the wall, and chemoreceptors detect both protein and an increase in pH of gastric contents. Nerve signals are relayed directly to the medulla, resulting in an increase in both stomach motility and secretory activity of gastric cells. The presence of food in the stomach also causes release of gastrin. Gastrin further stimulates the contractile activity of muscle in the gastric wall and increases the release of HCl from parietal cells. Gastrin also stimulates contraction of the pyloric sphincter to slow stomach emptying.

37
Q

Describe the intestinal phase.

A

It involves the processes following the chyme reaching the small intestine, a phase regulated by both the nervous system and the endocrine system. It involves the intestinal reflex and the release of cholecystokinin (CCK) and secretin. The intestinal reflex opposes the gastric and cephalic reflexes. It protects the small intestine from being overloaded with chyme. CCK and secretin are hormones that decrease both stomach motility and secretory activity and inhibit the release of gastrin. This slows down the emptying of the stomach.

38
Q

Gastrin-describe the stimulus for secretion, the secreting organ/cell type, and the function.

A

Gastrin are secreted by G-cells. The presence of food (especially protein) causes the release of gastrin. Gastrin enters the bloodstream and circulates back to the stomach to further stimulate the contractile activity of muscle in teh gastric wall and it increases the release of HCl from parietal cells. It also stimulates contraction of the pyloric sphincter to slow stomach emptying.

39
Q

Cholecystokinin (CCK)-describe the stimulus for secretion, the secreting organ/cell type, and the function.

A

It is released by the small intestine. It is sttimulated by fatty chyme. It stimulates the smooth muscle in the gallbladder wall to strongly contract, causing the release of concentrated bile. It also stimulates the pancreas to release pancreatic juice, and stimulates to relaxation of the smooth muscle within the hepatopancreatic ampulla, allowing entry of the bile and pancreatic juice into the small intestine. Finally, it also inhibits both stomach motility and release of gastric secretions.

40
Q

Secretin-describe the stimulus for secretion, the secreting organ/cell type, and the function.

A

It is released from the small intestine primarily in response to an increase in chyme acidity. It causes the release of an alkaline solution that contains HCO3- from both the liver and ducts of the pnacreas. This alkaoline fluid helps neutralize acidic chyme. Secretin also hinhibits gastric secretions and motility.

41
Q

Describe the organization of hepatocytes in the liver.

A

The liver is partitioned into thousands of small, polyhedral hepatic lobules, with are the structural and functional units of the liver. WIthin the hepatic lobules are the liver cells, the hepatocytes.In cross section, a hepatic lobule loods like a side view of a bicycle wheel. The central vein is like the hub of the wheel. At the circumference of the wheel (where the tire would be) are the portal triads. Cords of hepatocytes make up the numerous spokes of the wheel, and they are bordered by hepatic sinusoids.

42
Q

Describe the flow of blood through the liver.

A

The cells of the liver are served by a dual blood supply; one is oxygenated and the other is deoxygenated. The hepatic artery is a branch of the celiac trunk that carries oxygenated blood to the liver. The hepatic portal vein, as part of teh hepatic portal system, carries blood from the capillary beds of the GI tract, spleen and pncreas. It brings approx. 75% of the blood volume to the liver. Blood from the branches of these two vessels mixes in the hepatic sinusoids as it passes into and through the hepatic lobules The blood then flows slowly toward the central vein, that drains the blood flow from the lobule. Central veins collect the blood and merge throughout the liver to form numerous hepatic veins that eventually empty into the inferior vena cava..

43
Q

Describe the functions of bile.

A

Bile salts and lecithin function in the mnechanical digestion of lipids, allowing more efficient chemical digestion of triglycerides.

44
Q

Describe the functions of the gallbladder.

A

It is a saclike organ that stores, concentrates, and releases bile that the liver produces.

45
Q

Distinguish between pancreatic islets and pancreatic acini in terms of structure and function.

A

Pancreatic islets contain areterioles and venules, and alpha cells (which secrete glucagon) and beta cells (which secrete insulin). Pancreatic acini are saclike arrangements of acinar cells, that secrete amylase, lipase, proteases and nucleases. THey also contain duct cells that serete HCO3-.

46
Q

Describe the function of pancreatic amylase

A

Digests starch

47
Q

Describe the function of pancreatic lipase

A

Digests fats

48
Q

Describe the function of trypsinogen, chymotrypsinogen, and procarboxypeptidase (inactive proteases).

A

When activated, they digest protein.

49
Q

Describe the function fo nucleases.

A

They are necessary for the digestion of nucleic acids (DNA and RNA).

50
Q

Describe the structure of the small intestine.

A

It is a coiled, thin-walled tube. It consists of three specific segments: the duodenum, jejunum, and ileum. 1) duodenum-form the first segment, approx. 10 in. long and originates at the pyloric sphincter. 2) jejunum-approx. 7.5 feet in length, about two-fifths of the small intestine length. it is the primary region within the small intestine for chemical digestion and nutrient absorption; 3) ileum-the last region. anout 10.8 feet, forms approx. 3/5 of the length. The mucosal and submucosal tunics of the sm. intestine are thrown into internal circular folds (also called plicae circulares), that extend inward toward the lumen. They help increase the surface area through which nutrients are absorbed. There are small fingerlike projections, villi. They also increase surface area. There are also microvilli.

51
Q

Explain the function of the goblet cells.

A

They produce mucin.

52
Q

Describe the digestion of carbohydrates by the brush border enzymes.

A

The completion of starch breakdown is accomplished by the brush border enzymes. They include dextrinase and glucoamylase. They break the bonds between glucose subunits of oligosaccharides. Maltase breaks the bond between the two glucose molecules that compose maltose.

53
Q

Describe the digestion of proteins by the brush border enzymes.

A

The brush border enzyme dipeptidase breaks the final bond between the two amino acids of a dipeptide so that both may be absorbed. Aminopeptidase generates free amino acids from the amino end of peptides.

54
Q

Describe how fats are absorbed across the intestinal wall.

A

1) Bile salts released from the liver and gallbladder emulify lipid droplets to form micelles. 2) Pancreatic lipase functions within micelles to digest each triglyceride into a monoglyceride and two free fatty acids. 3) Monoglycerides and free fatty acids enter an epithelial cell, while bile salts remain in the intestinal lumen to be reabsorbed and reclycled. 4) Triglyceride molecules are reassembled within epithelial cells. Lipids are then wrapped with protein to form chylomicron. Chylomicrons are are packaged within secretory vesicles and then exocytosed from the cells and absorbed into lacteals.

55
Q

Describe the structure and function of intestinal crypts (also known as intestinal glands, or crypts of Lieberkuhn).

A

They are invaginations of mucosa. These mucosal cells secrete intestinal juice.

56
Q

Describe the structure and function of the duodenal glands (also called the submucosal, or Brunner gland).

A

THey are housed within the submucosa layer and found found only in the proximal duodenum. THis gland produces a viscous, alkaline, mucus secretion that protects the duodenum from the acidic chyme.

57
Q

Distinguish between peristalsis and segmentation.

A

1) Segmentation-mixes chyme with accessory gland secretion through a “back-and-forward” motion. 2) peristalsis-propels material within the GI lumen by alternating contraction of the circular and longitudinal muscle layer in small regions.

58
Q

Describe the gastroilial reflex.

A

It moves the contents from the ileum into the cecum in response to food entering the stomach.

59
Q

Describe the digestion and absorption of carbohydrates.

A

IN the oral cavity, salivary amylase breaks the chemical bonds between glucose molecules to partially digest the starch molecule. 1)Pancreatic amylase is produced by the pancreas and secreted into the small intestine; 2) pancreatic amylase continues digestion of starch that began in the oral cavity; 3) brush border enzymes complete the breakdown of starch to individual glucose molecules, and are responsible for the digestion of disaccharides.

60
Q

Describe digestion and absorption of proteins.

A

It begins within the stomach. Pepsin is released and denatures proteins to facilitate their chemical breakdown. 1_Proteolytic enzymes are released from the pancreas; 2) Enteropeptidase activates trypsinogen to trypsin; trypsin then activates other proteolytic enzymes; 3) Activated pancreatic proteolytic enzymes break proteins into peptides and amino acids; 4) brush border peptidases break peptides tinto single amino acids to be absorbed through epithelial cells into blood.

61
Q

Describe the structure and function of the large intestine.

A

See diagrams fore structure. The large intestine absorbs water and electrolyes from the remaining digested material that enters into it. The large intestine then stores fecal material until it is eliminated through defecation.

62
Q

Describe the types of mevements that occur in the large intestine and the reflexes that control those movements.

A

1)Peristaltic movements-they are usually weak and sluggish, but otherwise they resemble those that occur in the wall of the small intestine. 2) haustral churning-occurs after a relaxed haustrum fills with digestede or fecal material until distension stimulates reflex contraction in the muscularis. THese contraction increase churnin and move the material to more distal haustra. 3) Mass movements-powerful, peristaltic-like contraction that propel fecal material tward the rectum. It is initiated by the gastocolic reflex (which in turn is initiated by distension in the stomach). A wave of contraction beinins in the middle of the transverse colon, forcing a large amount of fecal matter into the descending colon, sigmoid colon and the rectum. 4) Defectation reflex-filling of the rectum initiates the urge to defecate. This stimulus results in transmission of nerve signals from the receptors to the spinal cord. IN response, parasympathetic output increass to both the sigmoid colon and rectum, while it decreases to the internal anal sphincter.