The Gastrointestinal System

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75 Terms

1
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What are the four histological layers of the GI tract?

Mucosa, submucosa, muscularis externa, serosa/adventitia.

2
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What type of epithelium lines the oesophagus?

Moist stratified squamous epithelium.

3
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Which sphincter prevents gastric reflux into the oesophagus?

Lower oesophageal (cardiac) sphincter.

4
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What are rugae in the stomach?

Mucosal folds allowing expansion.

5
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What is the primary function of the small intestine?

Nutrient digestion and absorption (90% of nutrients).

6
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Which glands are found in the submucosa of the duodenum?

Brunner’s glands (mucus-secreting).

7
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What are Peyer’s patches and where are they located?

Lymphoid follicles in the ileum submucosa (immunity).

8
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What structures increase surface area in the small intestine?

Plicae circulares and villi.

9
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What is the predominant cell type in large intestine crypts?

Goblet cells (mucus secretion).

10
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What are taeniae coli in the large intestine?

Three bands of longitudinal muscle forming haustra.

11
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What is the function of haustra in the large intestine?

Permit expansion and elongation.

12
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Which sphincter in the anal canal is voluntary?

External anal sphincter (skeletal muscle).

13
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What is the role of the ileocecal valve?

Prevents backflow from large intestine to ileum.

14
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Which part of the GI tract is primarily retroperitoneal?

Duodenum (except superior part).

15
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What are epiploic appendages in the large intestine?

Fat-filled pouches on the serosa.

16
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What are the main functions of GI secretions?

Chemical digestion, lubrication, signalling, protection, enzyme activation, waste excretion.

17
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What enzyme in saliva begins carbohydrate digestion?

Salivary amylase.

18
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What are symptoms of xerostomia (dry mouth)?

Difficulty swallowing, speech issues, increased dental caries, oral infections.

19
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Which gastric cell secretes HCl and intrinsic factor?

Parietal cell.

20
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At what pH is pepsinogen activated to pepsin?

~2 (acidic, via HCl).

21
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What is the role of gastric mucus?

Forms a protective barrier against acid and pepsin.

22
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What neutralizes stomach acid in the duodenum?

Pancreatic bicarbonate (NaHCO₃, pH 7.1–8.2).

23
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How is trypsinogen activated in the duodenum?

By enteropeptidase (brush border enzyme).

24
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Which pancreatic hormone promotes glucose uptake?

Insulin (β cells).

25
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What tissue type are hepatocytes (bile-producing cells)?

Epithelial.

26
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What is the primary function of bile salts?

Emulsify lipids for digestion and absorption.

27
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How does the gallbladder concentrate bile?

Absorbs water and ions.

28
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Which brush border enzyme activates trypsinogen?

Enteropeptidase.

29
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What triggers the cephalic phase of secretion?

Sight, smell, taste, or thought of food.

30
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What effect do CCK and secretin have on gastric secretions?

Inhibit gastric acid and pepsin secretion.

31
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What are the types of passive transport?

Simple diffusion (e.g., oxygen, fatty acids), facilitated diffusion (e.g., sodium, glucose).

32
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What drives secondary active transport?

Na⁺ gradient created by Na⁺/K⁺ ATPase.

33
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How are glucose and galactose absorbed?

Secondary active transport via Na⁺-glucose cotransporter (SGLT1)

34
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Which monosaccharide uses facilitated diffusion?

Fructose (via GLUT5).

35
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Symptoms of lactase deficiency?

Bloating, diarrhoea, gas.

36
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Why are carbohydrates digested at the brush border?

Ensures monosaccharides are produced near absorption sites.

37
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How are amino acids absorbed?

Na⁺-dependent cotransporters or facilitated diffusion.

38
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What enzyme digests most lipids in adults?

Pancreatic lipase.

39
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Why do chylomicrons enter lymph?

Too large for blood capillaries; lymphatics transport to bloodstream.

40
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How are fat-soluble vitamins absorbed?

Via micelles, simple diffusion.

41
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How is vitamin B12 absorbed?

Binds intrinsic factor, absorbed by endocytosis in ileum.

42
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How does bile duct blockage cause vitamin E deficiency?

Reduces micelle formation, impairing fat-soluble vitamin absorption.

43
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How is calcium absorption regulated?

By vitamin D and parathyroid hormone (PTH).

44
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How is water absorbed?

Osmosis, following solute gradients (95% in small intestine).

45
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What causes malabsorption in celiac disease?

Gluten damages villi/brush border; treated with gluten-free diet.

46
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What is the liver’s dual blood supply?

Hepatic artery (oxygen-rich, ~25%), hepatic portal vein (nutrients/toxins, ~75%).

47
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How is blood drained from the liver?

Via 3 hepatic veins into inferior vena cava.

48
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What is the hepatic portal system’s role?

Delivers nutrients/toxins from GI tract to liver for processing without returning to heart.

49
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What structures form the portal triad?

Hepatic artery, portal venule, bile duct.

50
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What are sinusoids?

Specialised capillaries carrying blood from hepatic artery/portal vein to central vein; fenestrated for metabolite transfer.

51
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What do Kupffer cells do?

Macrophages in sinusoids; phagocytose pathogens, debris, old RBCs.

52
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What is the role of stellate cells?

Store vitamin A; produce collagen in disease, causing fibrosis.

53
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What happens in Phase I detoxification?

Cytochrome P450 enzymes add polar groups (oxidation, reduction, hydrolysis); may produce toxic metabolites.

54
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How is bilirubin processed?

Conjugated with glucuronic acid in liver, becomes water-soluble, excreted in bile.

55
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What causes neonatal jaundice?

Immature liver lacks glucuronyl transferase, leading to unconjugated bilirubin buildup.

56
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How does the liver maintain blood glucose?

Glycogenesis (glucose → glycogen), glycogenolysis (glycogen → glucose), gluconeogenesis (from amino acids/triglycerides).

57
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What hormones regulate carbohydrate metabolism?

Insulin (anabolic, glycogenesis), glucagon (catabolic, glycogenolysis/gluconeogenesis).

58
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What lipids does the liver synthesise?

Triglycerides (stored/transported as VLDL), cholesterol (hormones, membranes), phospholipids.

59
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What is the urea cycle’s purpose?

Converts toxic ammonia to urea for excretion.

60
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What are jaundice symptoms?

Yellow skin/eyes, dark urine, pale stools.

61
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What are the main functions of the urinary system?

Waste disposal, osmoregulation, blood volume/pressure/pH regulation, hormone production.

62
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Where are the kidneys located?

Posterior abdominal wall, retroperitoneal, ~12th rib, left slightly higher.

63
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What is the blood supply to the kidneys?

Renal arteries (from aorta, 20-25% cardiac output); drain via renal veins to inferior vena cava.

64
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What is the nephron’s role?

Functional unit; filters blood, reabsorbs/excretes to form urine.

65
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What structures form the renal corpuscle?

Glomerulus (capillary network), Bowman’s capsule (visceral/parietal layers).

66
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What can pass through the filtration membrane?

Water, sodium, glucose, chloride; blocks RBCs, large proteins.

67
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What is the role of the proximal convoluted tubule?

Reabsorbs ~65% of filtrate (glucose, sodium, amino acids, water).

68
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How does the Loop of Henle function?

Counter-current multiplier; descending limb reabsorbs water, ascending limb reabsorbs sodium/potassium/chloride.

69
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What does ADH do in the kidneys?

Inserts aquaporins in collecting duct, increases water reabsorption, concentrates urine.

70
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What is the other name for ADH, and its effect?

Vasopressin; causes vasoconstriction, increases blood pressure.

71
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Outline the RAAS pathway.

Renin converts angiotensinogen to angiotensin I; ACE converts to angiotensin II; stimulates aldosterone, vasoconstriction.

72
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What is the effect of RAAS on blood pressure?

Increases via vasoconstriction and sodium/water reabsorption.

73
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How does the sympathetic nervous system affect kidneys?

Reduces sodium/water excretion, increases angiotensin II, constricts afferent arterioles.

74
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What do natriuretic peptides do?

Increase sodium/water excretion, reduce blood volume/pressure (ANP, BNP, CNP).

75
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How much filtrate is produced vs. urine excreted daily?

~180 L filtered, ~2 L urine excreted.