3.3 Gastric enteroendocrine Flashcards

1
Q

what does secretion of gastrin do

A
  • Inc HCl secretion care0 8 3 activators

- Stimulates gastric emptying (minor effect)

  • Stimulates parietal cell maturation
  • Stimulates chief cells to secrete pepsinogen
  • INC intestine muscle contraction
  • Relaxes ileocecal valy and stimulates mass movements
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2
Q

what does secretion of histamine do

A
  • secreted from enterochromaffin cells
  • inc parietal cells HCl release (one of the 3 thigns needed to activates secretion of HCl)
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3
Q

what does secretion of serotonin do

A
  • from enterochromaffin like cells
  • inc contraction of stomach muscle

(makes 90% of total body serotonin, SSRI)

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4
Q

what does release of Somatostatin do

A
  • inhibits secretion from stomach and pancreas
  • inhibts small intestine absorption
  • inhibits gall bladder and liver release of bile
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5
Q
A
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6
Q

describe the regulation of gastric secretion

A
  • neural & hormonal mechansims that alter secretions
  • Stimulatory and Inhibitory events occur in phases
    • Cephalic (reflex) phase: few min prior to food entry (short)
    • Gastric phase: food entering stomach t0 3-4 hours later
    • intestinal phase: brief sitmulatory effect as partially digested food enters duodenum, followed by inhibitory effects
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7
Q

describe the Cephalic Phase of gastric digestion

A
  • starts with sight, smell, taste or thgouht of food
  • > CNS sends impulse via CNX
  • Stim mucous cells -> muscus, Chief cells -> pepsinogen, Parietal cells -> HCl, and G cells to make Gastrin
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8
Q

describe the Hastric phase of gastric secretion

A
  • can be triggered by
    • psrtially digested proteins, caffeine, inc in pH
      • acts on G cells to secrete gastrin which encourages all the stomach actions
    • Chemo and stretch receptors
      • trigger mucous, chief, parietal and G cells
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9
Q

describe the intestinal phase of gastric secretion

A
  • decreased pH (more acidic) or prescence of lipids and carbs caues release of secretin, GIP and CCK -> goes in blood stream and inhibits chief and parietal cells, and peristalsis
  • duodenal stretch & chemoreceptors act via enterogastic reflax and inhibt myenteric plexus
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10
Q

describe the gross anatomy of the small intestine

A

* major organ of digestion and absorption

  • diameter: 2.5-4cm
  • Duodenum: 25cm, jejunum (upper left) 2.5m, ileum (lower right) 3.5 m
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11
Q

what surface modifcation are made to the SI to increase SA

A
  • need inc SA for nutrient abs
  • circular fold (plicae circulares) ~1 cm deep (ones you can see)
  • villi 1mm high (on folds make it look fuzzy)
  • microvilli ~100-2000nm high
  • total SA of SI = 200m2
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12
Q

describe the structure of the intestinal mucosa

A
  • Absorptive cells (simple columnar epithelium)

goblet cells and enteroendocrine cells in epithelium

  • lacteal running thi middle
  • Paneth cells: found deep in crypts that release antimicrobial agents
  • villus epithelium replaced every 2-4 days
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13
Q

what are the modifcations in the diff regions of the SI

A
  • Duodenum: in submucosa -> secretes bicar
    • Duodenal glands
    • Serosa
    • muscularis externa
  • Ileum
    • aggregated lymphoid modules (big colelction of lymphocytes
  • Jejunum

* call have plicucircularis

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14
Q

describe the secretions of your SI

A
  • secreted in response to distension or iritation of mucosa by hypertonic or acidic chyme
  • slightly alkaline pH (7.4-7.8) & isotonic with blood plasma
  • largely water, enzyme-poor, but contains mucus
  • facilitates transport and absorption of nutrients
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15
Q

describe the process of digestion in the small intestine

A
  • Chyme from stomach contains
  • > patially digested carbohydrates & proteins
  • > undigested fats (lipase so far has been minmal
  • spends 3-6 h in SI: most water is absorbed, all nutriends are absorbed
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16
Q

what are the requirements for digestion and absorptoin in the small intestine

A
  1. Slow delivery of acidic, hypertonic chyme
  2. Delivert of bile, enzymes & bicarbonate ions from liver and pancreas
  3. mixing
17
Q

how are things released into SI

A
  1. Propfulsion: peristaltic waves move from fundus -> pylorus (starts @ cardiac region)
  2. Grinding: Most vigorous peristalsis and mixing occur close to pylorus
  3. Retropulsion: pyloric end of stomach act as pump to deliver 3mL of chyme to duodenum, when it closes material that doesnt go throuhg splashes back (helps with mixing)
18
Q

describe the ileocecla sphincter/valve

A
  • closed when chyme exerts backward pressure (prevents regurgitation into ileum
  • relaxes to admit chyme into LI when
  • > gastroileal reflex enhances force of segmentation in ileum
  • > gastrin increase motility of ileum
19
Q

describe the liver

A
  • largest gland in body (3 lbs)
  • 4 lobes based on surface features (8 based on vascular & biliary suply)
  • right, left, caudate and quadrate lobe
  • has a falciform ligament (actually a mesentary)
20
Q

what does the calciform ligament do

A

Suspends liver from diaphragm & anterior abdominal wall (a mesentery)

Separates right & leftl obes
Round ligament (ligamentum teres): Remnant of fetal umbilical vein
21
Q

How does blood get to the liver

A

blood enters liver at Porta hepatis via

  1. Hepatic arteries
  2. Hepatic portal veins
    - blood exits liver through hepatic veins (into IVC)

*have two capillary networks in row: artery -> cap -> vein -> vap

22
Q

locations of hepatic veins and arteries

A
23
Q

Describe the microscopic anatomy of Liver

shape of lovules

A
  • liver lobules: hexagonal structure
  • filter & process nutrient rich blood
  • copmosed of plates of hepatocytes radiating from longitudinal central vein
24
Q

liver microscopic anatomy

describe the innervation

A
  • middle central vein
  • Portal triad: at each corner of lobule (bile duct, branch of hepatic portal bein and branch of hepatic artery)
  • liver sinusoids (leaky capillaries between hepatic plates)
  • kupffer cells (stellate macrophages)
25
Q

describe Kupffer cells

A

aka stellate macrophages

  • in liver sinusoids
  • self-sustaining population of macrophages within liver
  • remove debris (bacteria, worn out blood cells)
  • act as gate keeper for mmune response (in addition to lymphoid tissues)
26
Q

what are the functions of hepatocytes

A

Process blood borne nutrients

Synthesize & secrete hormones

Storage

Performdetoxification

Immune surveillance

Produce bile

27
Q

describe hepatocyte function for processing blood borne nutrients

A
  • metabolism: carbohydrates, proetins and fats
  • metabolism & detoxification of enobiotics (CYP450)
  • use aa to make plasma proteinsL albumins, lipoproteins (VLDL, LDL, HDL), alpha/beta globulins for transport, clotting proteins (fibrinogen & prothombin), anti-clotting proteins
  • makes immune proteins
  • amkes apoproteins (lipoprotein metabolism)
  • convers unconjugates bilirubin (indirect) to conjugated bilirubin (direct)
28
Q

role of hepatocytes to synthesize and secrete hormones

A

Insulin-like growth factor 1 (Growth hormone mediator)

Angiotensinogen (Blood pressure & fluid balance)

Thrombopoietin (platelet production)
Hepcidin (iron homeostasis)

29
Q

role of hepatocytes for storage

A

store:

Fat soluble vitamins (A, D, K, E) & Vit B12

  • iron & copper
  • store glycogen (glycogenesis); makes glucose from non carb sources (gluconeogenesis

^ release when needed (glycogenolysis)

  • fat
30
Q

role of hepatocytes in detoxificaiton

A
  • turn ammonia (NH3) -> urea

*ammonia is toxic to CNS (crosses BBB)

sources of ammonia: colon, kidneys, erythrocyte breakdown, muscle breakdown

31
Q

role of hepatocytes in immune surveillance

A

Kupffer cells (aka stellate macrophages) destroy bacteria, worn out erythrocytes & other foreign substances in blood

32
Q

role of hepatocytes in bile production

+ what is in bile

A

* Hepatocytes produce ~900mL of bile/day (~500 mg bile acids)

*Yellow-green alkaline solution containing

  1. water 65%-97%
  2. Bile salts (bile acid (hydrophobic) conjugated w/ taurine r glycine (hydrophilic)
    - > Primary acids synthesized by liver from cholesterol (cholic & chenodeoxycholic acids)
    - > Secondary bile acids synthesized from primary bile acids by colonic bacterial enzymes (deoxycholic & lithocholic acids)
  3. Bilirubin (conjugated/direct)-> metabolism by small intestines bacteria produces sterobilin
  4. phospholipids
  5. electrolytes (Na, Ca, HCO3)
  6. Xenobiotics
  7. IgA
33
Q

describe the biliary tree

A
  • right and left hepatic druct feed into the common hepatic duct
  • the common hepatic duct and cystic duct from the gall bladder feed into bile duct -> pacreas
34
Q

what is the gall bladder

A

Thin-walled muscular sac on a n inferior/anterior surface of liver

Stores & concentrates bile by absorbing its water & ions

*doesnt make bile just holds onto it

35
Q

describe hte functional relationship involved in the storage and ejection of bile

A
  1. Liver continuously secretes bile
  2. Bile is stores & concentrated in the gallbladder
  3. Duodenum releases CCK whcih triggers dilation of hepatopancreatic sphincter & contraction of gall bladder

*ejects bile into duodenum thru duodenal ampulla

  1. Bile salt emulsificating lipid droplet in digestive tract lumen
36
Q

describe enterohepatic circulation

A
  1. Bile salts (cholic & chenodeoxycholic acids) are secreted into duodenum
  2. As bile salts travel through small intestine they allow lipid digestion & absorption to occur (bc of emulsification)
  3. 95% of bile salts are reabsorbed by ileum
  4. Reabsorbed bile salts travel via hepatic portal bein back to liver *only 5% of bile salts are newly synthesized each time

*blood goes to liver so bile salts recycled

37
Q
A