Ch. 66 Digestion and Absorption in the GI Tract

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A comprehensive set of flashcards covering key concepts, enzymes, transporters, anatomical adaptations, and clinical correlations related to gastrointestinal digestion and absorption, formatted as question-and-answer for effective exam review.

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29 Terms

1
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What chemical process is the basis for digestion of macronutrients?

Hydrolysis—the addition of water to break large molecules into absorbable units.

  • Carbos become monosaccharides

  • proteins become small peptides and amino acids

  • fats become 2-monoglycerides and fatty acids

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What are the two types of digestion? Describe both

Luminal or cavity

  • occurs in lumen of GI trat

  • enzymes from salivary glands, stomach, pancreas

Membrane or contact

  • come in contact with brush border of enterocytes for absorption to occur

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During luminal (cavital) digestion, where do the digestive enzymes originate?

Salivary glands, stomach, and pancreas.

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Which phase of digestion occurs on the brush-border surface of enterocytes?

Membrane (contact) digestion.

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Where can you find the enzymes listed and what do they breakdown?

  1. Pepsin

  2. Amylase

  3. Enterokinase

  4. a-amylase

  5. elastase

  1. stomach - proteins

  2. pancreas - sugars

  3. intestinal mucosa - fats and proteins

  4. salivary glands - sugars

  5. pancreas - proteins

<ol><li><p>stomach - proteins</p></li><li><p>pancreas - sugars</p></li><li><p>intestinal mucosa - fats and proteins</p></li><li><p>salivary glands - sugars</p></li><li><p>pancreas - proteins</p></li></ol><p></p>
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What brush-border enzyme converts trypsinogen to trypsin?

Enteropeptidase (enterokinase).

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Name the three macroscopic/microscopic structures that together increase small-intestinal surface area ~1,000-fold.

Folds of Kerckring - controlled by muscularis mucosa

villi

microvilli

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What is the average total surface area of the small intestine?

Approximately 250–400 m² (about a tennis court).

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Which small-intestinal crypt cell type secretes antimicrobial compounds?

Paneth cells.

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What are the cells of the cypt of Lieberkuhn?

Mucous cells - secrete mucus lubricating and protecting the intestinal surfaces

Intestinal stem cells - differentiate into the specialized cells of intestinal epithelium (renew throughout life)

Paneth cells - secrete antimicrobial compounds to protect against pathogens - maintains gastrointestinal barrier

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Describe the life cycle of the small intestine enterocytes

  1. Live within the villi and have cell turnover 3-6 days

  2. cell types in villus: secretory cells, endocrine cells, goblet cells, mature absorptive epithelial cells

  3. cells in enterocyte divide and migrate up the crypts become mature absorptive cells

  4. enterocytes are shed into lumen to become part of ingesta to be digested and absorbed

<ol><li><p>Live within the villi and have cell turnover 3-6 days</p></li><li><p>cell types in villus: secretory cells, endocrine cells, goblet cells, mature absorptive epithelial cells</p></li><li><p>cells in enterocyte divide and migrate up the crypts become mature absorptive cells</p></li><li><p>enterocytes are shed into lumen to become part of ingesta to be digested and absorbed</p></li></ol><p></p>
12
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List the four main mechanisms for transporting substances across the intestinal epithelium.

Active transport

  • Primary active transport

  • secondary active transport

Passive diffusion

facilitated diffusion

endocytosis - allows large proteins (immunoglobulins) to be absorbed in babies (does not occur in adults except in ileum for B12 absorption)

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  1. Where are bile salts and vitamin B₁₂ predominantly absorbed?

  2. Ethanol, NSAIDS, aspirin

  3. water and electrolytes

  4. nutrients, vitamins, ions, water, electrolytes

  1. Ileum

  2. stomach

  3. colon

  4. duod and jejunum

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Which step is rate-limiting in carbohydrate assimilation?

Absorption across the enterocyte membrane.

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What enzyme initiates starch digestion in the mouth?

Salivary α-amylase.

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Where does final enzymatic breakdown of lactose and sucrose occur?

At the brush border of enterocytes.

17
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Describe carbohydrate breakdown in the small intestine

  1. Starches

  2. Lactose

  3. Sucrose

  1. Starches are broken down by a-amylase enzyme in the saliva and pancreatic amylase and become glucose

  2. Lactose is broken down in the brush border by lactase and becomes glucose and galactose

  3. Sucrose is broken down in the brush border by sucrase to fructose

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<p>Describe carbohydrate absorption </p><ol><li><p>Glucose and galactose</p></li><li><p>Fructose</p></li></ol><p></p>

Describe carbohydrate absorption

  1. Glucose and galactose

  2. Fructose

  1. both are absorbed by secondary active transport using the energy from the Na/K pump

    1. the two will compete for a spot in the membrane carrier SodiumGLUT (SGLUT) 1

  2. Fructose diffuses through facilitated diffusion with GLUT-5 using the concentration gradient

<ol><li><p>both are absorbed by secondary active transport using the energy from the <u>Na/K pump</u></p><ol><li><p>the two will compete for a spot in the membrane carrier SodiumGLUT (SGLUT) 1</p></li></ol></li><li><p>Fructose diffuses through facilitated diffusion with GLUT-5 using the <u>concentration gradient</u></p></li></ol><p></p>
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Which transporter mediates Na⁺-dependent uptake of glucose and galactose?

SGLUT-1 (secondary active cotransport).

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Fructose enters enterocytes primarily via which transporter and mechanism?

GLUT-5 via facilitated diffusion (no energy required).

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What carbohydrate malabsorption disorder is most common worldwide? What causes it?

Lactose intolerance (primary adult hypolactasia).

Casued by absense of brush border lactase

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What are the 3 locations of digestion of proteins to amino acid occuring?

Intestinal lumen

  • stomach - pepsin digest collagen

  • Small intestine

Brush border (of intestinal lumen)

Cytoplasm of mucosal cells

<p>Intestinal lumen</p><ul><li><p>stomach - pepsin digest collagen</p></li><li><p>Small intestine </p></li></ul><p>Brush border (of intestinal lumen) </p><p>Cytoplasm of mucosal cells</p><p></p>
23
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Describe the activation and destruction of proteases (enzyme that breaks down peptides and proteins)

In general, proteolytic enzymes are activated and destroyed rapidly

  1. Enterokinase is activated by trypsinogen

  2. Trypsinogen becomes trypsin and is autocatalytic (it can autogenerate trypsinogen (positive feedback loop)

  3. Trypsin (THE KEY) activates other proenzymes (green box)

  4. Proteolytic enzymes digest themselves

<p>In general, proteolytic enzymes are activated and destroyed rapidly</p><ol><li><p>Enterokinase is activated by trypsinogen</p></li><li><p>Trypsinogen becomes trypsin and is autocatalytic (it can autogenerate trypsinogen (positive feedback loop)</p></li><li><p>Trypsin (THE KEY) activates other proenzymes (green box)</p></li><li><p>Proteolytic enzymes digest themselves</p></li></ol><p></p>
24
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Describe the process of protein digestion

  1. Protein is broken down by pepsin and pancreatic proteases into Di- and Tri- peptides, large peptides, and free amino acids

  2. Di and Tri peptides enter the cell through carriers and can leave as amino acids or in small amounts

  3. Large peptides enter the cell with peptidases and leave in small amounts

  4. free amino acids enter the cell with a carrier and leave as amino acids

<ol><li><p>Protein is broken down by pepsin and pancreatic proteases into Di- and Tri- peptides, large peptides, and free amino acids</p></li><li><p>Di and Tri peptides enter the cell through carriers and can leave as amino acids or in small amounts</p></li><li><p>Large peptides enter the cell with peptidases and leave in small amounts</p></li><li><p>free amino acids enter the cell with a carrier and leave as amino acids</p></li></ol><p></p>
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Which disease is characterized by inability to absorb neutral amino acids yet still absorbs them as di-/tri-peptides?

Hartnup disease.

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Name the 3 abnormalities of protein assimilation

Pancreatic insufficiency

  • pancreatitis or CF

  • Decreased absorption leading to increased N in the stool from increased protein contents

Congenital absence of trypsin

  • no trypsin causes protein malabsorption

Hartnup disease

  • can’t absorb neutral amino acids (tryptophan) but can still be absorbed as di and tri peptides and absorbed with a carrier into the cell

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How are lipids assimilated?

Triglyceride in the duodenum will be broken down into fatty acid and 2-monoglyceride.

In the enterocyte it will be put back together as a triglyceride

MORE DETIAL

  • For triglycerides to be absorbed, first they are emulsified - broken down to increase surface area.

  • Enzymatic digestion - to become the monoglyceride and fatty acid so they can diffuse into the enterocyte

  • Reconstitution in enterocyte

    • Will bind to apoprotein and enter the lymph vessel

<p>Triglyceride in the duodenum will be broken down into fatty acid and 2-monoglyceride.</p><p>In the enterocyte it will be put back together as a triglyceride</p><p>MORE DETIAL</p><ul><li><p>For triglycerides to be absorbed, first they are emulsified - broken down to increase surface area.</p></li><li><p>Enzymatic digestion - to become the monoglyceride and fatty acid so they can diffuse into the enterocyte</p></li><li><p>Reconstitution in enterocyte</p><ul><li><p>Will bind to apoprotein and enter the lymph vessel</p></li></ul></li></ul><p></p>
28
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Which two molecules act as main emulsifying agents for dietary fat?

Bile salts and lecithin (a phospholipid).

29
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Familial lipoprotein lipase deficiency

is a genetic disorder that results in the impaired breakdown of triglycerides due to a lack of the enzyme lipoprotein lipase. This leads to elevated levels of triglycerides in the blood, increasing the risk of pancreatitis.

  • hypertriglyceridemia