22- Digestion & Absorption Flashcards
This is a failure in ability to digest dairy carbohydrates.
Lactose Intolerance
In lactose intolerance, the brush border ________ enzyme activity is deficient or absent resulting in undigested and unabsorbed lactose.
Lactase
In low lactase activity, the lactose will not be absorbed in the small intestine. This causes it to be converted to ________ and ________, producing acetate, butyrate, and propionate in the lumen. This causes water to hold in the lumen and ________ _______ results. Ferments into methane and H+ gas.
SCFAs
Hydrogen
Osmotic Diarrhea
What are the major primary sugars in the human diet?
Sucrose
Lactose
Starch
What are the major secondary sugars in the human diet/
Amylose Glycogen EtOH/Alcohol Lactic Acid Pyruvic Acid Pectins Dextrins
This major sugar in the human diet has no digestive enzymes.
Cellulose
In the mouth, this is where we begin breaking down starch by the use of the enzyme _______ _______. This breaks it down into Maltose and 3-9 polymers of Glucose.
Salivary Amylase
In the small intestine, most of the starch breaks down here by the use of the enzyme ________ ________. This breaks it down into Maltose and 3-9 polymers of Glucose. Many disaccharides reach the small intestine intact.
Pancreatic Amylase
Brush border enterocytes has specific hydrolases that complete the process of breaking down carbohydrates. What are Maltose, Trehalose, Lactose, and Sucrose broken down into and by what enzymes?
Maltose (via Maltase) — Glucose + Glucose
Trehalose (via Trehalase) — Glucose + Glucose
Lactose (via Lactase) — Glucose + Galactose
Sucrose (via Sucrase) — Glucose + Fructose
Absorption of carbohydrates occurs via co-transport mechanisms and facilitated diffusion. What are these forms of transport and what are their transporter names?
– Na/K ATPase creates concentration gradient for secondary active transport for Glucose and Galactose (co-transporter SGLT1)
– Facilitated diffusion for Fructose (GLUT5)
– Facilitated diffusion into blood (GLUT2)
Which carbohydrates utilize SGLT1, GLUT5, and GLUT2?
SGLT1 = Glucose and Galactose
GLUT5 = Fructose
GLUT2 = Glucose, Galactose, and Fructose
Explain how we can test for CHO assimilation problems.
After overnight fasting, patient ingests 25g D-xylose and their urine is collected for the next 5 hours. Absorption is normal if less than 4 g is excreted in the 5 hours.
***D-xylose absorbed by both Na+ cotransport and passive diffusion
This occurs due to a deficiency of pancreatic enzymes, specifically a lack of proteases (i.e., trypsinogen).
Chronic Pancreatitis
This occurs due to the absence of trypsin. All pancreatic enzymes are gone.
Congenital Trypsin Absence
This occurs due to defects in transport (SLC3A1) or absence of di-basic AA transporter (SLC7A9). Thus, cysteine, lysine, arginine, and ornithine are not reabsorbed at the proximal tubule. This occurs in 1:7,000 live births and is due to an intestinal deficiency. The AAs are secreted in the feces.
Cystinuria
***Cysteine builds up and forms stones in kidney, bladder, and ureter. High levels of it in the urine.
This occurs when a person cannot absorb neutral AAs. Symptoms resemble pellagra (niacin deficiency). It is an autosomal recessive genetic disorder. Symptoms include diarrhea, mood changes, neurological problems, red scaly skin, photosensitivity, short stature, and high levels of neutral AAs in urine.
Hartnup Disease
***i.e., Tryptophan in the urine
This occurs due to mutations in the CFTR gene, which is a regulated Cl- channel on apical membrane of duct cells. It’s important in sweat, digestive fluid, and mucous production. Without it, fluids that should be thin become thick. Loss of HCO3- secretion. Pancreas problems persist and present early.
Cystic Fibrosis
In the stomach, ________ is secreted as ________ which is activated at low pH (2-3). It is responsible for 10-20% of protein breakdown but is not essential for protein digestion.
Pepsin
Pepsinogen
The pancreas mostly breaks proteins down into di- and tripeptides and some amino acids. What are the enzymes in the pancreas?
Trypsin
Chymotrypsin
Carboxypeptidase
Elastase
What does Trypsin and Chymotrypsin break down ________ ________.
Small Polypeptides
What does Carboxypeptidase cleave AAs into?
Carboxyl ends
What enzymes are present in the small intestines for protein digestion?
Aminopolypeptidase
Dipeptidases
In the small intestines, di- and try-peptides are absorbed into _________.
Enterocytes
Pancreatic enzymes are secreted as _________ activated by either Enterokinase (Trypsinogen) or Trypsin itself.
Zymogens
***These are inactive substance activated by another enzyme (Trypsinogen or Trypsin in this case)
For protein absorption, there are separate ________ and separate ________ ________ mechanisms for each amino acid type (neutral, acidic, basic, imino). The amino acids can’t just go through by themselves!
Co-transporters Facilitated Diffusion (of dipeptides and tripeptides)
For protein absorption, ________ establishes a Na+ gradient for co-transport. There can also be _____-dipeptide or ______-tripeptide cotransporters.
Na/K ATPase
H+
H+
Antibodies can develop against a gluten component, called ________. This leads to destruction of small intestine villi (atrophy), and hyperplasia of the intestinal crypts. This leads to malabsorption related to deficiencies in folate, iron, calcium, and Vitamins A, B12, and D.
Gliadin
How can we manage problems with the antibodies against gliadin?
Maintain a gluten-free diet
If there is a loss or decreased number of intestinal epithelial cells, that means there is a reduced microvilli surface area. Fat absorption is impaired due to the loss, and there is excess fat in feces (steatorrhea). Nutritional deficiencies in _______ and _______ also occur.
Folate
Vitamin B12
***Remember, this is greasy poops!
How can we treat poor fat absorption due to decreased intestinal epithelial cells?
Treatment with tetracycline (antibiotic) and folate for 6 months
The structure of the intestinal mucosa is ideal for absorption of large amounts of nutrients. The lumen surface of small intestine is arranged in longitudinal folds called _______ _______ _______ and the villi and microvilli increase surface area for absorption. Villi are longest in the ________.
Folds of Kerckring
Duodenum