Malabsorption Clinical Cases Flashcards
how much dietary fluid does the average person take in per day
and how many received by the small intestine due to secretions
1-2 litres dietary
6-7 litres from secretions
describe the absorption by enterocytes of the small intestine on the apical surface
1) on apical lumen side
HCO3- / Cl- antiport = chloride into the cell and HCO3 out into lumen
Na+/H+ antiport = Na into the cell and H+ into the lumen
Na+/glucose symport both into the cell from the lumen
describe the absorption by enterocytes on the basal side
cl- / K+ freely leak out from cell into the interstitial space
Na+/K+ ATPase pumping Na out the cell and K init the cell
glucose freely moves out from cell into interstitium
describe how ORT works
glucose and sodium enter cell via symport which means water follows it into the cell (water potential in the cell becomes more negative which is the driving force)
Na/K atpase of basal aspect sodium out and K into cell
k leaks back out and glucose leaks out followed by water
what are the two processes that pull water into the cell from the lumen
increase in luminal osmotic pressure resting from influx of ions
crypt cells secrete electrolytes which contain the CFTR gene
cystic fibrosis transmembrane conductance regulator
describe the structure of vilis with crypts
villi stick out with microvilli which absorb
crypts of liberkuhn secrete
how long does cell migration to the villus tip take
3-4 days and then they apoptosis
describe how water is secreted in crypt cells
Na/K on basal membrane make na into intersitium and k into cell
K leaks out on basal to intersistium
symporter on basal aspect transports 2 cL into the cell and 1 Na and 1 K
(secondary active transport)
elevated cAMP active CFTR chloride channel which allows Cl into the lumen
this draws sodium paracellularly into the lumen
cl and Na increase in the lumen brings water with it
what is impaired digestion
pancreatic insufficiency (CF, chronic pancreatitis) lack of bile (liver disease, biliary obstruction) lack of intestinal enzymes (lactose intolerance)
what is impaired absorption
damage to absorptive surface (coeliac disease, crohns disease)
decrease to absorptive ares (intestinal resection )
inherited defects such as SLT1 mutation
what are the 4 mechanisms for causing diahorrea
secretory
osmotic
inflammatory
abnormal motility
what is borbygmi
loud bowel sounds
how can you diagnose for lactose intolerance
consume dairy products and no increase in blood glucose with flatulance and abdominal pain
why do you get the symptoms of lactose intolerance
lactose build up and bacterial fermentation
water moves into lumen via osmosis
where is the CFTR gene located
chromosome 7