Chapter 005
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Transcript of Chapter 005
Williams' Basic Nutrition & Diet Therapy
Chapter 5
Digestion, Absorption, Transport and Metabolism
Copyright © 2013 Mosby, Inc., an imprint of Elsevier Inc. All rights reserved. 1
14th Edition
Lesson 5.1: Digestion and the Digestive Organs
1. Through a balanced system of mechanical and chemical digestion, food is broken down into smaller substances and the nutrients are released for biological use.
2. Special organ structures and functions accomplish these tasks through the successive parts of the overall system.
2Copyright © 2013 Mosby, Inc., an imprint of Elsevier Inc. All rights reserved.
Digestion (p. 64)
Basic principles Principle of change
• The body cannot use food as it is eaten.• Food must be changed into simpler substances to be
absorbed and then used by cells to sustain life. Principle of wholeness
• The parts of the digestive process comprise a continuous whole.
• Food components travel through the gastrointestinal (GI) system until they are delivered to cells or excreted.
3Copyright © 2013 Mosby, Inc., an imprint of Elsevier Inc. All rights reserved.
Digestion (cont’d) (p. 65)
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Mechanical and Chemical Digestion (p. 65)
Mechanical and chemical actions make up the digestive process.
Food must undergo these changes to be delivered to cells.
Specific actions occurring during digestion of carbohydrates, proteins, and fats are discussed in other chapters.
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Mechanical Digestion (p. 66)
Mechanical digestion: gastrointestinal motility Muscles in GI wall produce:
• Tonic contractions, which produce continuous movement• Periodic muscle contraction and relaxation, which mix
food mass and move it forward
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Mechanical Digestion (cont’d)(p. 66)
Mechanical digestion: gastrointestinal motility (cont’d) Nerves from esophagus to anus:
• Control muscle tone in wall• Regulate rate and intensity of contractions• Coordinate various movements
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Chemical Digestion (p. 66)
Chemical digestion: gastrointestinal secretions Hydrochloric acid and buffer ions: produce the correct pH
necessary for enzyme activity Enzymes: specific digestive proteins for breaking down
nutrients Mucus: lubricates and protects the GI tract tissues and helps
mix the food mass Water and electrolytes: carry and circulate the products of
digestion through the tract and into the tissues Bile: divides fat into smaller pieces to assist fat enzymes
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Case Study
Tim eats a meal consisting of the following foods: Grilled Chicken with lemon seasoning Baked potato with broccoli and cheese Mixed greens with lemon juice and olive oil and
parmesan cheese 1 cup of unsweetened ice tea
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Digestion in the Mouth and Esophagus (p. 66)
Mechanical digestion Mastication breaks down food Food is swallowed and passes down esophagus Muscles at tongue base facilitate process Gastroesophageal sphincter at stomach entrance
relaxes, allowing food to enter, then constricts to retain food
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Digestion in the Mouth and Esophagus (cont’d) (p. 66)
Chemical digestion Salivary glands secrete material containing
salivary amylase or ptyalin Ebner’s glands at the back of the tongue secrete a
lingual lipase Salivary glands also secrete a mucous material to
lubricate and bind food particles, facilitating the swallowing of the food bolus
Secretions from the mucous glands in the esophagus help move food toward the stomach
11Copyright © 2013 Mosby, Inc., an imprint of Elsevier Inc. All rights reserved.
Case Study (cont’d)
Explain what is happening in the mouth and esophagus in regard to Tim’s meal
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Digestion in the Stomach (p. 67)
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Digestion in the Stomach (cont’d) (p. 67)
Mechanical digestion Under sphincter control, the food enters upper
portion of the stomach (fundus) Stomach muscles knead, store, mix, and propel
food mass forward By the time food mass reaches the lower portion
of the stomach (antrum), it is a semiliquid acid/food mix called chyme
Pyloric valve slowly releases chyme into the first section of the small intestine (duodenum)
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Digestion in the Stomach (cont’d) (p. 67)
Chemical digestion: three types of acid secretions Hydrochloric acid: parietal cells in the stomach
lining secrete acid to promote gastric enzyme activity
Mucus: secretions protect the stomach lining from the erosive effect of the acid and also bind and mix the food mass and help move it along
Enzymes: pepsinogen is secreted by stomach cells and is activated by acid to become pepsin, a protein-splitting enzyme
15Copyright © 2013 Mosby, Inc., an imprint of Elsevier Inc. All rights reserved.
Case Study (cont’d)
Explain what is happening to Tim’s meal in the stomach at this time.
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Digestion in the Small Intestine (p. 67)
Mechanical digestion Peristaltic waves push food forward Pendular movements stir chyme Segmentation rings chop food mass into lumps Longitudinal rotation rolls food in spiral motion,
mixing it Surface villi motions stir and mix chyme
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Digestion in the Small Intestine (cont’d) (p. 68)
Chemical digestion: pancreatic enzymes Carbohydrate: pancreatic amylase converts starch
to maltose and sucrose Protein: trypsin and chymotrypsin split large
protein molecules into small peptide fragments and eventually into single amino acids; carboxypeptidase removes end amino acids from peptide chains
Fat: pancreatic lipase converts fat to glycerides and fatty acids
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Digestion in the Small Intestine (cont’d) (p. 68)
Chemical digestion: intestinal enzymes Carbohydrate: Disaccharidases convert
disaccharides into monosaccharides. Protein: Enterokinase activates trypsinogen from
the pancreas to become trypsin; amino peptidase removes end amino acids from polypeptides; dipeptidase splits dipeptides into amino acids.
Fat: Intestinal lipase splits fat into glycerides and fatty acids.
19Copyright © 2013 Mosby, Inc., an imprint of Elsevier Inc. All rights reserved.
Case Study (cont’d)
Explain how Tim’s meal is progressing through the intestine with each enzyme activity.
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Digestion in the Small Intestine (cont’d) (p. 68)
Chemical digestion Mucus: protects mucosal lining Bile: emulsifying agent, aids fat digestion and
absorption Hormones: secretin for alkaline environment,
cholecystokinin triggers release of bile
21Copyright © 2013 Mosby, Inc., an imprint of Elsevier Inc. All rights reserved.
Digestion in the Small Intestine (cont’d) (p. 69)
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Case Study (cont’d)
What role does bile play in the digestive process of Tim’s meal?
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Lesson 5.2: Absorption and Metabolism
3. Absorption, transport, and metabolism allows for the distribution, use, and storage of these nutrients throughout the body.
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Absorption and Transport (p. 69)
At this point in the process: Carbohydrates: reduced to simple sugars
(glucose, fructose, galactose) Fats: changed into fatty acids and glycerides Proteins: changed into single amino acids Vitamins and minerals: liberated from food
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Case Study (cont’d)
Discuss the final products formed from digestion of Tim’s meal that can be readily used by the cells
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Absorption and Transport (cont’d) (p. 69)
Amount of nutrients consumed depends on bioavailability: Amount of nutrient present Competition between nutrients for absorption sites Form in which nutrient is present
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Small Intestine (p. 71)
Small intestine: three absorbing structures Mucosal folds: surface of small intestine piles into
many folds Villi: small, fingerlike projections Microvilli: cover each villus
Make inner surface 600 times greater than outer surface of intestinal wall
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Small Intestine (cont’d) (p. 72)
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Absorption Processes (p. 71)
Simple diffusion: particles move outward in all directions toward areas of lesser concentration
Facilitated diffusion: uses a protein channel for carrier-assisted movement of larger particles
Active transport: carrier partner (e.g., sodium) moves particles across a membrane
Pinocytosis: larger materials are engulfed by a cell
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Absorption Processes (cont’d)(p. 72)
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Absorption in the Large Intestine (p. 73)
Water: main absorptive task of large intestine is to absorb water; small amount remains for feces
Dietary fiber: contributes bulk to help form feces Macronutrients and micronutrients: absorbed to
lymph or blood
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Transport (p. 73) Vascular system: veins and arteries
Carry water-soluble nutrients, oxygen, other vital substances
Transport wastes for removal Portal circulation first carries nutrients to liver for
cell enzyme work Lymphatic system
Carries non–water-soluble fatty materials Lymph vessels in villi absorb materials Route to larger lymph vessels Eventually to blood stream through thoracic duct
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Metabolism (p. 73)
At this point, individual macronutrients in food: Have been broken down Absorbed into bloodstream or lymphatic system Next, nutrients can be converted into energy or
stored
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Energy for Fuel (p. 73)
Mitochondria of cells is where metabolism takes place
Two forms of metabolism Catabolism: breaking down of larger substances
into smaller units Anabolism: building up of larger substances from
smaller units
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Energy for Fuel (cont’d) (p. 73)
Metabolic processes ensure that the body has energy in the form of adenosine triphosphate (ATP)
Metabolism of glucose from carbohydrates yields less energy than metabolism of fat, but glucose is the body’s primary source of energy
Protein can be an energy source, but it is relatively inefficient
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Stored Energy (p. 74)
Energy beyond that needed at present is stored for future
Glucose is converted to glycogen via glycogenesis, stored in liver or muscles
When glycogen reserves are full, excess is stored as fat via lipogenesis
Excess protein/amino acids converted to glucose via gluconeogenesis
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Stored Energy (cont’d) (p. 74)
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Errors in Digestion and Metabolism (p. 75)
Genetic defects: cell is missing enzyme controlling metabolism of a specific nutrient Phenylketonuria (PKU)
• Enzyme responsible for metabolizing essential amino acid phenylalanine is missing
• Untreated, causes permanent mental retardation and CNS damage
• With proper treatment, affected children may have normal and healthy lives
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Errors in Digestion and Metabolism (cont’d) (p. 75)
Genetic defects (cont’d) Galactosemia
• Enzyme responsible for metabolizing galactose to glucose is missing
• All sources of lactose must be eliminated from diet• Untreated, can cause brain and liver damage• Screening and treatment can enable normal life
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Errors in Digestion and Metabolism (cont’d) (p. 77)
Genetic defects (cont’d) Glycogen storage diseases (GSD)
• Group of rare genetic defects• Absence of enzymes required for synthesis or
breakdown of glycogen• Form of disease depends on enzyme missing
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Other Intolerances or Allergies (p. 78)
Not genetic inborn errors of metabolism Rather, caused by food intolerances or
allergies Lactose intolerance: deficiency of any of the
disaccharidases in small intestine• Insufficient lactase to break down milk• Abdominal cramping and diarrhea
Produces containing lactose must be avoided
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Other Intolerances or Allergies (cont’d) (p. 78)
Allergies Inappropriate immune responses Not necessarily a problem with digestion or
metabolism Covered in Chapter 18
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