Ch. 15 - Gastrointestinal Physiology Flashcards

1
Q

What is the extrinsic nervous control of the GI tract?

A

Mostly Vagus CN X, parasympathetic

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2
Q

What are the Intrinsic nevous controls of the GI tract?

A
  • Myenteric Plexus “Auerbach’s plexus” - between outer longitudinal and middle circular muscle layers
  • Submucous Plexus “Meissner’s plexus” - between the middle circular layer and the mucosa
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3
Q

What is released by the small intestine in response to chime entering the duodenum?

A
  • Secretin
  • CCK
  • GIP
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4
Q

What cells release pepsinogen?

A

Chief cells - pepsinogen is converted to pepsin in presence of HCl

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5
Q

What cells release Intrinsic Factor?

A

Parietal cells - binds vitamin B12 to allow for its absorption in terminal ileum

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6
Q

What can peptic ulcers result from?

A
  • High HCl
  • Low mucous
  • H. pylori
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7
Q

What are the phases of Gastric Secretion?

A
  • Cephalic phase
  • Gastric phase
  • Intestinal phase
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8
Q

What phase of gastric secretion begins with smell, sight, taste or thought of food?

A

Cephalic Phase

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9
Q

What increases and decreases gastric emptying?

A
  • Increases
    • Eating, gastric distension, gastrin, vagal input (parasympathetic)
  • Decreases
    • CCK, Secretin, GIP, duodenal distension (enterogastric reflex)
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10
Q

What hormones are produced in the duodenum?

A
  • CCK
  • Secretin
  • GIP
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11
Q

What are the 3 major types of GI contractions?

A
  1. Peristalsis
  2. Segmentation (mixing)
  3. Tonic contractions
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12
Q

What is the most common type of GI contraction in the small intestine?

A

Segmentation (mixing)

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13
Q

How are disaccharides absorbed?

A

Na+ cotransport (secondary actie transporters - driven by the sodium gradient)

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14
Q

Where is bile made, stored and what stimulates its’ release?

A
  • Made by liver
  • Stored in gall bladder
  • Stimulated by CCK
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15
Q

What is the key enzyme of cholesterol synthesis?

A

HMG CoA Reductase

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16
Q

How is cholesterol synthesis regulated in the liver?

A

Negative feedback mechanism - statin allosterically inhibits HMG CoA Reductase

17
Q

Why can’t skeletal muscle deliver glucose to the bloodstream?

A

It lacks glucose-6-phosphatase

18
Q

What are the different Glucose transporters associated with? (GLUT1-4)

A
  • GLUT 1 - erythrocytes
  • GLUT 2 - renal, small intestine, liver, pancreatic B cells
  • GLUT 3 - neurons, placenta
  • GLUT 4 - insulin regulated, adipose, striated muscle tissue
19
Q

Where does most of the gluconeogenesis occur?

A

In the liver/kidneys

In prolonged starvation - kidneys become major glucose-producing organs

20
Q

What is the role of glucokinase and where is it only found?

A

It converts glucose to glucose-6-phosphate just like hexokinase – found only in liver

21
Q

What is the first location to spot jaundice?

A

Under the tongue

22
Q

What are some prehepatic, hepatic and posthepatic causes of jaundice?

A
  • Prehepatic
    • hemolytic anemia, malaria
  • Hepatic
    • hepatitis, alcoholic liver disease, primary biliary cirrhosis
  • Posthepatic
    • Choledocholithiasis (gall stones), Pancreatic head cancer
23
Q

What 2 enzymes are needed for alcohol metabolism?

A
  • Alcohol dehydrogenase
  • Acetaldehyde dehydrogenase (to acetate)
24
Q
A