Digestion and Absorption in GI Flashcards

1
Q

Where is the lactase enzyme located?

A

Brush border

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2
Q

What is lactose intolerance?

A
  • Failure to digest dairy carbohydrates
  • 75% of lactose can pass unabsorbed through the intestines
  • The lactose in the small intestine is vonverted to SCFAss and H gas in the lumen resulting in the lumen holding water in causing Osmotic diarrhea
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3
Q

What does lactase turn lactose into?

A

Glucose and Galactose

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4
Q

What digestion occurs in the mouth?

A

Breakdown of starch with salivary amylase

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5
Q

How does the intestinal mucosa relate to the function of the SI? Where are the villi longest?

A
  • Its ideal for absorbing large amounts of nutrients as the villi and microvilli increase the surface area
  • Duodenum has the longest villi
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6
Q

How is the lumen surface of the SI arranged?

A

Longitudinal folds called folds of kerckring

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7
Q

Describe the path startch takes to glucose?

A
  • Alpha amylase breaks starch into maltose
  • Maltase breaks maltose into glucose
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8
Q

How are glucose and galactose absorbed?

A
  • Na/K ATPase creates a gradient
  • Secondary active transport through SGLT1 takes in Glu and Gal
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9
Q

How is Fructose absorbed?

A

GLUT5 via facilitated diffusion

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10
Q

How do carbohydrates get from the lumen to the blood?

A

Via facilitated transport with GLUT2

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11
Q

What is the purpoe of a D-xylose test?

A
  • D-xylose is drank after an overnight fast and urine is collected for five hours
  • We look to see how much is excreted in the urine, if absorption is disrupted there will be little in the urine
  • D-xylose is usually absorbed by active Na co transport and passsive diffusion
  • This measures the absorptive capacity of duodenum specific to sugars
  • Absorbed but not utilized
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12
Q

What test do you use to look for lactose intolerance?

A

Hydrogen breath test following an oral Lactose test

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13
Q

In general, what causes protein assimilation disorders?

A

Deficiency of pancreatic enzymes or defect in transporters of intestinal epithelial cells

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14
Q

In a patient who has congenital trypsin absence what will levels of their other pancreatic enzymes look like?

A
  • There are no pancreatic enzymes as they are secreted as zymogens and activated by Trypsin. If ther is no trypsin you will not have Chymotrypsin, Elastase, Carboxypeptidase A or Carboxypeptidaase B.
  • Only the zymogen form
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15
Q

What is Cystinuria?

A
  • A defect in the SLC3A1 transporter or absence of di basica AA transporter SLC7A9
  • This results in Lys, Ard, Cysteine and Ornithinie not being reabsorbed at the proximal tubule
  • Resulting in AA secreted in the urine/feces
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16
Q

What is Hartnup disease?

A
  • Intestines can absorb neutral AA’s such as Trp
  • The symptoms are similar to pellagra, Dementia, Diarrhea and Dermatitis, photosensitivity, short stature, urine high in neurtral AA’s

AR disorder of SLC6A19 gene

17
Q

How is CF related to the pancreas?

A
  • Cystic Fibrosis occurs when theres a defect in CFTR channel which is a Cl channel on apical membrane of the duct cells
    • This can result in loss of Bicarb secretion, which protects the pancreas and results in acute and chronic pancreatitis as enzymes cant move from ducts
18
Q

Where does pepsin come from?

A
  • Chief cells from the stomach secrete pepsinogen and it gets activated into Pepsin at low pH
    • it does 10-20% of protien breakdown
19
Q

What enzymes come from the pancreas and what do they do?

A
  • Trypsin, Chymotrypsin, Carboxypeptidase, elastase
  • Breaks proteins down into di and tripeptides and some AA
  • Trypsin and chymotrypsin break down in to small polypeptides
  • Carboxypeptidase cleaves AA at the carboxyl end
20
Q

What enzymes come from the brush border of the SI?

A

`Aminopolypeptidase and dipeptidases

The AA, Di and Trie peptides are then absorbed into the enterocytes

21
Q

What enzyme activates Trypsionggen and where does it come from?

A

Enterokinase from the brush border