Digestive Physiology Flashcards

(72 cards)

1
Q

four process of the digestive system

A
  1. secretion
  2. digestion
  3. motility
  4. absorption
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2
Q

anatomy of the digestive system

A

oral cavity

salivary glands

esophagus

gallbladder

liver

pancreas

stomach

small and large intestine

rectum

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3
Q

upper gastrointestinal tract

A
  • begins the digestion of food
  • minimal macronutrient absorption here
  • mechanical and chemical digestion
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4
Q

saliva

A

Complex solution containing the enzyme salivary amylase (in babies also some lingual lipase**)​

Also composed of water, mucus and ions​

3 major glands secrete saliva and each gland secretes a different composition of fluid​

  • Parotid gland​: watery saliva
  • Submandibular gland: mixed saliva and mucus
  • Sublingual gland​: mainly mucus
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5
Q

stages of swallowing

A

After appropriate mechanical and chemical digestion, the bolus must be passed to the stomach via the esophagus​

  1. Voluntary stage​

Decisions for how much to chew and when to begin the process of swallowing​

  1. Pharyngeal stage​

Closing off of the nasal cavity and trachea, involuntary​

  1. Esophageal stage​

Movement of food down the esophagus, involuntary

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6
Q

mastication

A

the mechanical digestion of the good into a bolus

chemical digestion also occurs in the mouth

  • enzyme salivary amylase: digests carbohydrates
  • enzyme lingual lipase: digests fat *but doesnt begin until it reaches the stomach*
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7
Q

peristalsis

A
  • co-ordinate contraction of the muscles in the esophagus
  • involuntary control
  • propels bolus toward the stomach (gravity not necessary)
  • secondary paristalsis initiated bolus is lodged items in the esophagus
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8
Q

summary of mouth digestion

A

secretion: saliva of varying composition

digestion: chemical (amylase and lipase)

mechanical - mastication

motility: mastication in mouth peristalsis in esophagus

absorption: minimal

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9
Q

stomach

A
  • acts as a reservior for bolus before it enters the intestine
  • muscular contractions for mechanical breakdown
  • bolus is liquefied to enhance enzymatic digestion
  • secretion of 2-3 L of gastric juices
  • gastric juices contributed by a number of cell types
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10
Q

basic stomach anatomy

A

esophagus

low esophageal sphincter

cardia

fundus

pylorus/pyloric sphincter

antrum

rugue

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11
Q

layers of the stomach

A

1. Mucosa

  • single layer of cells that can be endocrine or exocrine
  • large folds called rugue and also invaginations called pits

2. Submucosa

  • contains a neural network (submucosal plexus)
  • connective tissue to adhere mucosa to smooth muscle layer

3. Smooth muscle (muscularis externa)

  • circular muscle, longitudinal muscle to change shape of the stomach
  • contains a neural network (myeteric plexus)

4. Serosa

  • external layer of densa connective tissue
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12
Q

exocrine & endocrine cells of the stomach

A

exocrine cells

1. Mucus neck cells

  • secretes mucus and bicaronate

2. Chief cells

  • secretes pepsinogen and gastric lipase

3. Parietal cells (oxyntic cells)

  • secretes H+ and Cl- (HCl), intrinsic factor

endocrine cells

1. G cells

  • secretes the hormone gastrin
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13
Q

exocrine and endocrine cells of stomach

A

exocrine cells

  1. Mucus neck cells
    - secretes mucus and bicaronate
  2. Chief cells
    - secretes pepsinogen and gastric lipase
  3. Parietal cells (oxyntic cells)
    - secretes H+ and Cl- (HCl), intrinsic factor

endocrine cells

  1. G cells
    - secretes the hormone gastrin
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14
Q

stomach mechanical digestion

A

Propulsion

Grinding

Retropulsion

bolus to chyme

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15
Q

stomach chemical digestion

A

secreted gastric juices contains hydrochloric acid (HCl)

lingual lipase *activated by HCl - lipid digestion begins

secreted pepsinogen converted to pepsin (because of HCl)

pepsin - protein digestion

secreted gastric lipase - lipid digestion

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16
Q

small intestine

A
  1. duodenum
  2. jejunum
  3. ileum
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17
Q

functions of acid in the stomach

A
  1. activation of lingual lipase - lipid digestion can occur
  2. activation of pepsin (from pepsinogen) - protein digestion can occur
  3. inactivation of salivary amylase - carbohydrate digestion stops
  4. kills microbes
  5. denatures (unwraps folded structure) proteins
  6. stimulus secretion of hormones
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18
Q

layers of the small intestine

A
  1. Mucosa
    - contains mixed population of epithelial cells, small blood vessels and lymph vessels
    - invaginations called crypts folds called villi
  2. Submucosa
    - contains a neural network (submucosal plexus)
  3. Smooth muscle (muscularis)
    - layers of smooth muscle (circular and longitudinal)
    - contains a neural network (myenteric plexus)
  4. Serosa
    - thin layer of connective tissue
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19
Q

motility of the small intestine

A

segmentations

  • special localized contractions for mixing chyme with digestive juices
  • increases the interactions of particles of food in chyme with absorptive cells of the mucosa layer

peristalsis

  • propels chyme from the pyloric sphincter towards the large intestine
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20
Q

cell types of the small intestine

A
  1. Absorptive cells
    - epithelial cells with microvilli
  2. Goblet cells
    - secretes mucus
  3. Intestinal gland cells
    - secretes alkaline watery mucus
  4. Paneth cells
    - secretes lysozyme
  5. S cells
    - secretes secretin
  6. CCK cells
    - secretes cholecystokinin (CCK) stimulates release of bile
  7. K cells
    - secretes glucose dependent insulinotrophic peptide (GIP) stimulates release of insulin
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21
Q

microvilli

A
  • also called brush border (fuzzy appearance)
  • increases surface area for absorption of nutrients
  • cells on the microvilli have enzymes called brush border enzymes
  • final digestion of some nutrients to allow for absorption
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22
Q

brush border enzymes

A
  1. Lactase
  2. Sucrase
  3. Maltase
  4. Aminopeptidase
    - removes one amino acid from the end of a protein
  5. Dipeptidase
    - cuts a dipeptide into two single amino acids
  6. Enteropeptidase
    - cuts trypsinogen into trypsin
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23
Q

large intestine

A
  • completes absorption, usually water
  • highly populated by bacteria, benefical for completing nutrient extraction via fermentation if any nutrients remain
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24
Q

motility of the large intestine

A

i. Gastroileal reflex
- presence of food in the stomach stimulates the opening of the ileocecal valve (neural reflex)
ii. Haustral churning
- mixing of large intestine contents from one haustrum to the next
- allows for optimal absorption of mostly water from the lumen contents
iii. Peristalsis & mass peristalsis
- unidirectional movement of lumen contents out of the large intestine

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25
pancreas
epithelial cell clusters called **acinar cells** and cells that form the ducts **(ductal cells)** make exocrine secretions exocrine secretion into ducts converge to form the pancreatic duct, which joins to the common bile duct, and secretions go into the duodenum
26
exocrine secretions of the pancreas
**from ductal cells** i. bicarbonate - neutralizes the acid from the stomach **from acinar cells** ii. pancreatic amylase - digestion of carbohydrates iii. pancreatic lipase - digestion of lipids iv. trypsinogen → trypsin → protein digestion v. chymotrypsinogen → chymotrypsin → protein digestion vi. procarboxypeptidase → carboxypeptidase - digestion of proteins vii. prophospholipase → phospholipase - digestion of phospholipids viii. procolipase → colipase - aids in lipid digestion but not an enzyme
27
lumen of small intestine
pancreatic duct - pancreatic secretions (include inactive zymogens) → trypinogen → trypsin (activated by enteropeptidase in brush border) → zymogens - chymotrypsinogen, procarboxypeptidase, prophospholipase, procolipase → activated enzymes (activated by trypsin) - chymotrypsin, carboxypeptidase, phospholipase, colipase
28
endocrine secretions of the pancreas
islets of langerhans 1. insulin - from beta cells 2. glucagon - from alpha cells 3. somatostatin - from delta cells
29
blood flow of liver
blood → Aorta → Hepatic artery - supplies oxygen to liver → Digestive tract artery - to capillaries of the intestines capillaries of intestines connect to the Hepatic portal vein with the nutrients → the blood then goes to the liver (capillaries of liver) → reconnect as Hepatic vein to the inferior vena cava
30
liver
made up of mostly hepatocytes (liver cell type) many functions including secretion of bile which is important for lipid digestion blood flow to liver has a special arrangement - oxygen rich blood artery - nutrient rich blood portal system
31
hepatocytes
hepatocytes secrete bile into a vessel called a bile canaliculus (plural - bile canaliculi) these small vessels gather together and join to form a hepatic duct, which eventually forms the common hepatic duct blood from the hepatic artery and blood from the hepatic portal vein merge together into vessels called sinusoids sinusoids join together to form the central vein, and then the hepatic vein
32
functions of the liver
1. synthesis of bile (contains bile salts) - functions to aid in lipid digestion 2. excretion of bilirubin - waste product derived from hemoglobin 3. metabolism of carbohydrates, lipids and proteins - nutrients for storage, or converting nutrients into each other 4. processing of drugs and hormones **components of bile** 1. bile salts 2. cholesterol 3. bile pigments (bilirubin) 4. water and ions
33
the gallbladder
the liver makes bile and stores bile in the gallbladder gallbladder and common hepatic duct connect to bile duct the common bile duct connects to the duodenum with a sphincter of Oddi pancreatic duct joins to the common bile duct and also share the sphincter of Oddi
34
regulation of gastrix motility and secretions
hormonal and neural communication organized into phases of regulation phase named by the location of initation in the tract
35
cephalic phase
**stimulus** - sight, smell and tase of food **neural control** - through medulla oblongata, activation of the submucosal plexus neurons (secretions) and myenteric plexus neurons (motility) increased secretions from: - salivary glands (saliva), stomach (ie HCl) and intestine (ie mucus) increased motility of: - stomach and small intestine
36
gastric phase
**stimulus** - presence of a bolus in the stomach causing stretching, presence of amino acids **neural control** - sensory infomation to the submucosal plexus (secretions) and to the myeteric plexus (motility) **hormonal control** - gastrin (G cells) **both cause:** increased secretions from: - stomach (ie HCl) and intestine (ie mucus) increased motility of: - stomach & increased gastric emptying
37
intestinal phase
**stimulus** - presence of chyme in the intestine **neural control** - sensory information to the submuscosal plexus (secretions), and myenteric plexus (motility) **hormonal control** - secretin (S cells), CCK (CCK cells), GIP (K cells) increased secretions from: - intestine (ie mucus) and pancreas - bicarbonate from ductal cells \*secretin - digestive enzymes from acinar cells \*CCK - insulin from beta cells \*GIP \*\*endocrine pancreas
38
intestinal phase inhibits the gastric phase
decreased secretions from: stomach (ie HCl) decreased motility of: stomach & decreased gastric emptying
39
carbohydrate sources
**simple** - monosaccharides (glucose, galactose and fructose) - disaccharides (lactose, sucrose, and maltose) **complex** - starch (plant storage of glucose) - glycogen (animal storage of glucose)
40
carbohydrate digestion (chemical)
salivary amylase - starch → maltose **pancreas** pancreatic amylase - starch → maltose **lactase** → lactose into glucose + galactose **sucrase** → sucrose into glucose + fructose **maltase** → maltose into x2 glucose
41
carbohydrate enzyme mechanisms
starch - **amylase** → maltose + maltotriose maltose - **maltase** → 2 glucose lactose - **lactase** → glucose + galactose sucrose - **sucrase** → glucose + fructose
42
carbohydrate absorption
fructose uniporter
43
protein sources
animal sources and plant sources amino acids - have 20 different kinds single amino acids can be organized as essential and non-essential **dipeptides** - 2 amino acids bonded together **tripeptides** - 3 amino acids bonded together **polypeptides** - many amino acids bonded together
44
protein digestion (chemical)
**pepsin** - polypeptides → smaller peptides **pancreas -** trypsin, chymotrypsin, carboxypeptidase **aminopeptidase****, dipeptidase**
45
protein enzyme mechanisms
pepsin, trypsin, chymotrypsin endopeptidase → cut into 3 - bond peptide and 4 bond peptide **aminopeptidase** → cuts the amino terminus side of the polypeptide **carboxypeptidase** → cuts the carboxy terminus side of the polypeptide
46
protein absorption
amino acid + sodium symporter di-, tri-peptide + hydrogen symporter with peptidase in the cell di-, tri-peptides are turned into single amino acids **sodium + hydrogen antiporter** (sodium enters cell) the amino acids cross into the blood by amino acid uniporter **Na/K ATPase** (sodium leaves cell into extracellular fluid)
47
lipid sources
triglycerol/triglycerides - glycerol and 3 fatty acids fatty acids are variable in length (4-24 carbons), 18 carbons most common can be saturated (double bond) or unsaturated (no double bond)
48
lipid digestion (chemical)
**lingual lipase** - from saliva (active in acidic pH) **gastric lipase** - from chief cells in the mucosa of stomach **pancreatic lipase + colipase** - pancreas **bile** - liver
49
bile salts
bile solution - has bile salts that coat the fat droplet (keep lipids separated) triglycerides - lipase with colipase (breaks down triglycerides into) diglycerides, monoglycerides and free fatty acids
50
fat absorption
micelles (lipid droplets surrounded by bile salts) break into fatty acids and monoglycerides fatty acids and monoglycerides can diffuse across the intestinal cell membranes once inside the intestinal cells, fatty acids and monoglycerides reform into triglycerides chylomicrons are the re-packaging of lipids within cells into carriers to allow for transport in the body (first lymphatic vessels by exocytosis, eventually blood)
51
vitamin classifications
**fat-soluble vitamins** vitamin A, D, E, K **water-soluble vitamins** vitamin C, B vitamins, \*vitamin B12 (moved across membrane through transporter)
52
lipid absorption
lipid droplet + bile salt → micelles micelles are broken down into fatty acids (monoglyceride) fatty acids can diffuse into cell then are repackaged into vesicles and exocytosis into a lymphatic vessel
53
glycolysis, citric acid and electron transport system to create ATP
in cytoplasm a little ATP and **pyruvic acid** is created by glycolysis (10 steps) in the mitochondria pyruvic acid + CoA is turned into Acetyl CoA Acetyl CoA is then used in the citric acid cycle to make some CO2 and some ATP H+ & high energy electrons are used in the electron transport system which creates ATP
54
carbohydrate fates
**ATP production** - glucose is oxidized into ATP (glycolysis) **Amino acid synthesis** - converted to some amino acids if needed (protein anabolism) **glycogen synthesis** - storage of glucose (glycogenesis) **triglyceride synthesis** - when glucose is in excess (lipogenesis)
55
glucose uptake
cells of the body take glucose from the blood to make ATP glucose uniporters (present in the membranes of most body cells) move glucose from a region of high concentration (blood) into a region of low concentration (cell)
56
glycogenesis
**glycogenesis - storage of glucose** some cells have a large capacity to store glucose as glycogen - skeletal muscle - liver some cells, like the brain cannot store glycogen (fed state)
57
glycogenolysis
**glycogenolysis - breakdown of glycogen** glycogen is converted Glucose 6-phosphate to be used for the production of ATP (step 1 of glycolysis) liver is unique because it can continue to form glucose which can then be released into the circulation (fasted state)
58
gluconeogenesis
**gluconeogenesis** **- formation of new glucose** liver can create new glucose molecules from non-carb sources from amino acids\*, lactic acid and glycerol (part of triglycerides)
59
lipid fates
stored in adipose tissue as fat deposits (triglycerides) oxidized to produce ATP formation of structural molecules - phospholipids, myelin sheaths **triglyceride storage** 98% of our energy needed for daily use is stored in triglycerides distribution is mostly sub-cutaneous
60
lipolysis
**lypolysis - breakdown of triglycerides into glycerol and fatty acids**
61
lipogenesis
**lipogenesis - formation of triglycerides from non-lipid sources** liver and adipose cells can make triglycerides from glucose and amino acids
62
ketones
**ketogenesis** ketone bodies are formed by joining two **Acetyl Coenzyme A** molecules together liver cells (hepatocytes) can make ketone bodies (ketogenesis) which diffuse into the blood some cells (heart and kidney cortex) prefer ketone bodies to produce ATP (fasted state)
63
protein anabolism
**protein anabolism** - formation of proteins from amino acids most components of our bodies is made up of proteins - enzymes, hormones, structural components, transporters (fed state)
64
protein catabolism
**protein catabolism** - breakdown of proteins into amino acids liver cells can covert amino acids to fatty acids, ketone bodies or glucose (fasted state)
65
glucose absorptive (fed) state
**stored in skeletal muscle** glycogenesis glucose → glucose-6-phosphate → glycogen **most tissues** glucose uptake **liver** glycogenesis lipogenesis - from extra glucose → triglyceride **adipose tissue** triglyceride from liver goes to circulation and into adipose tissues
66
fatty acids & glycerol absorptive (fed) state
**liver** fatty acids & glycerol from circulation → triglycerides → back into circulation **adipose tissue** fatty acids & glycerol from circulation → triglycerides + triglycerides from circulation
67
amino acid absorptive (fed) state
**skeletal muscle** amino acids from circulation to proteins **(protein anabolism)** **adipose tissue** extra amino acids from circulation to fatty acids → glycerol → tryglycerides
68
post-absorptive (fasted) state
**liver** glycogen → glucose → circulation lactic acid from skeletal muscle → glucose **nervous tissue** glucose → ATP ketones → ATP **other tissues** glucose → ATP fatty acids → ATP **heart** ketones → ATP **skeletal muscle** glycogen → ATP + lactic acid proteins → (protein catabolism) amino acids → glucose (liver) **adipose tissue** triglycerides → glycerol + fatty acids glycerol → liver → glucose fatty acids → liver → ketones (ketongenesis)
69
how are triglycerides digested
**mouth** - lingual lipase (inactivated) **stomach** - lingual lipase (activated by HCl) - HCl untangles the proteins **intestines** -
70
how is protein digested
**mouth** - nothing **stomach** - aminopeptidase - dipeptidase - trypsin - chymotrypsin - carboxypeptidase **intestines** -
71
how is sucrose digested
**mouth** - nothing **stomach** - nothing **intestines** - sucrase
72
how is lactose digested
**mouth -** nothing **stomach** - nothing **intestine** - lactase **absorption** - glucose and galactose use same symporter (with Na) - fructose has uniporter