Pancreas/Gall Bladder Physiology Flashcards

(48 cards)

1
Q

What cells in the pancreas secrete digestive enzymes?

A

Acinar cells

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2
Q

What cells in the pancreas secrete bicarbonate?

A

Centroacinar and duct cells

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3
Q

What proteases are secreted by the pancreas?

A

Trypsinogen
Chymotrypsinogen
Proelastase
Procarboxypeptidase A and B

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4
Q

What amylolytic enzymes are secreted by the pancreas?

A

Amylase (pancreatic amylase)

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5
Q

What lipase are secreted by the pancreas?

A

lipase
Nonspecific esterase
Prophospholipase A2

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6
Q

What nucleases are secreted by the pancreas?

A

Deoxyribonuclease

Ribonuclease

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7
Q

What is the role of colipase?

A

Works with lipase to activate it.

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8
Q

What are the granules called that hold enzymes in the pancreas?

A

Zymogen granules

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9
Q

What two ions are exchanged as a part of the duct function?

A

Bicarbonate pushed out for chloride being brought in

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10
Q

What transporter is important for Cl homeostasis in the centroacinar cells?

A

CFTR

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11
Q

During the cephalic/gastric phase, what stimulates acinar cells?

A

ACh, GRP from vagal centers

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12
Q

In the intestinal phase, what changes in enzyme output is seen?

A

30% enzyme output increased to 70%

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13
Q

What cells secrete CCK? What activates them?

A

I cells activated by CCK-RP and monitor peptide

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14
Q

What cells secrete secretin? What activates them?

A

S cells activated by H+

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15
Q

What is the intracellular pathway by which acinar cells increase content discharge?

A

Ca mostly

Then cAMP

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16
Q

What activates CCK-RP release?

A

Amino acids and fatty acids in lumen

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17
Q

What are four things that CCK does?

A

Gall bladder contraction
Pancreas acinar secretion
Stomach reduced emptying
Sphincter of Oddi relaxation

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18
Q

What activates trypsinogen?

A

Enteropeptidase

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19
Q

What enzyme is mutated in hereditary pancreatitis? What is its role?

A

PRSS1 gene

Trypsinogen gene mutation that prevents trypsin elimination

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20
Q

What are some effects of pancreatitis?

A

Abdominal pain from pancreatic autodigestion
Increased serum lipase and amylase
Steatorrhea and fat-soluble vitamin insufficiency
Malignancy, diabetes, infx

21
Q

Why does oral glucose lead to higher insulin levels than IV glucose?

A

GLP1 is released from L cells in the intestine and GIP from K cells

22
Q

What happens to satiety when someone lacks sleep?

A

Leptin levels lower, decreasing satiety and inducing hyperphagia and overeating

23
Q

What four hormones stimulate insulin secretion of beta cells in the islets of langerhans? Which are negative regulators?

A

GLP-1, gastrin, cholecystokinin, and acetylcholine

Negative regulators: somatostatin, norepinephrine

24
Q

What molecules are satiety signals at the hypothalamus?

A

GLP1, CCK, Insulin, Leptin

25
What molecule stimulates appetite and decreases energy expenditure?
Ghrelin
26
What produces ghrelin?
Fundus of stomach
27
What are the major functions of the liver?
Processing all ingested nutrients, detoxification Metabolism of carbs, fats, proteins Buffers glucose Synth of factors important for circulatory system Bile formation for uptake and excretion of lipophilic molecules
28
What cells synthesize bile?
Hepatocytes
29
What is the hepatic triad?
Portal vein, hepatic artery, bile duct
30
What is a Kupffer cell?
Macrophage of the liver
31
Where are chylomicron remnants sieved into?
Space of Disse
32
What is the role of stellate cells?
Produce collagen | Store lipids like Vitamin A
33
What synthetic cells are hyperactive in cirrhosis? | What does that cause?
Stellate cells | Irreversible deposition of excess collagen
34
What causes stellate cells to be hyperactive in cirrhosis?
Oxidative stress causes Kupffer cells to release cytokines inducing collagen production
35
What is hepatic encephalopathy?
When toxins enter blood stream because of too much shunting
36
What facilitates excretion of hydrophobic molecules?
Bile salts
37
Describe the pathway of bile salts
``` Secreted into bile duct Concentrated in gall bladder Passes to duodenum Reabsorbed from ileum into portal vein Goes back to liver ```
38
How much of the bile salts are lost in feces?
5%
39
What enzyme is critical for cholesterol conversion into bile acid?
7-a-hydroxylase
40
What must be added to a bile acid to become a bile salt?
Glycine or taurine
41
What bacterial product of bile salts must be sulfated and excreted?
Lithocholic acid
42
After leaving the canaliculi, where does bile go? What lines these ducts?
Canals of Hering | Lined with cholangiocytes
43
What is taken out and added in the canals of Hering
Glucose and amino acids removed | IgA and mucus added
44
What causes bile to be concentrated in the gall bladder?
Na and Cl pumped out of bile, water follows osmotic gradient
45
What transporter is responsible for conjugated bile salt uptake from the GI lumen? Where is it found?
Apical sodium-dependent bile salt transporter | Foundin Ileum
46
What transporter is responsible for taking up conjugated bile salts from the sinusoids?
Na dependent taurocholate transporter
47
What are causes of cholestasis (impaired bile secretion)?
Primary Biliary Cirrhosis (destruction of cholangiocytes) Primary Sclerosing Cholangitis (inflammation of bile ducts) Pregnancy (progesterone reduces GB smooth muscle tone)
48
What are some effects of cholestasis?
Metabolic dysfunction (bile accumulation in liver) Itching (bile in plasma) Hypercholesterolemia Deficiency of ADEK