GIT physiology Flashcards

1
Q

Gastric Secretion
What factors regulate gastric secretion?

A

Can divide this answer into either neural and hormonal or do it via stages i.e.
cephalic/gastric/intestinal. We have done it in order of what happens as you eat food
because its easier to remember.
Cephalic phase - mediated via the vagus nerve. The sight, smell or taste of food excites
the vagus nuclei, which excites parasympathetic neurons in the stomach that release
ACh onto parietal cells to stimulate secretion. Vagal efferents also stimulate gastrin
release from G cells.
Gastric Phase - food in the stomach triggers local receptors which activate post
ganglionic neurons. These neurons stimulate parietal cells to produce acid.
Intestinal phase - fats, carbohydrates and acid in the duodenum inhibit gastric acid
secretion and pepsin secretion as well as motility by neural and hormonal mechanisms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What does the parietal cell do?

A

● Parietal cell is stimulated by histamine (from ECL cells) and gastrin (from G cells)
as well as vagal efferents
● H+ ions are pumped out by H/K/ATPase
● Cl- ions follow to combine with H+ in the lumen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Digestion of carbohydrates
Describe the enzymes required for the digestion of carbohydrates and their
location

A

● Mouth - salivary amylase
● Duodenum - Pancreatic amylase
● Brush border of the small intestine - oligosaccharidases i.e. lactase, sucrase,
maltase, isomaltase
● The final oligosaccharides are metabolised to one of the final hexoses (i.e.
glucose, fructose) in the small intestine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Please describe how carbohydrates are absorbed from the GI tract

A

Two phases - first into the mucosal cell from the lumen, then into the ECF and blood
from the cell.
● Glucose and galactose undergo ‘secondary active transport’ with sodium via
SGLT1 and SGLT2 co transporters. A low concentration of sodium inhibits
transport.
● Glucose and Galactose can also go via ‘facilitated diffusion’ into the cells via
GLUT-2
● Fructose can go via ‘facilitated diffusion into the cell via GLUT-5 and then
GLUT-2 to blood

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Digestion and absorption of lipids
Describe the enzymes required for the digestion of lipids and their location

A

● Lingual lipase - active in the stomach on triglycerides
● Pancreatic lipase - requires colipase for maximal activity, acts on triglycerides
● Pancreatic bile-salt activated lipase - triglycerides, cholesterol esters, some
vitamins and phospholipids
● Cholesteryl ester hydrolase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What other process is involved in the digestion of lipids?

A

● Emulsification
● Micelle formation - these are formed from bile salts, lecithin and monoglycerides
surrounding fatty acids and cholesterol
● Transport of lipids through the unstirred layer to the brush border of mucosal cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Please describe how lipids are absorbed through the GI tract

A

● Two phases
● First phase - lipids go into the intestinal mucosal cell and second phase into the
interstitial fluid and thus into the capillaries and portal blood as free fatty acids
(FFAs) or into lymphatics as chylomicrons
● They move into the enterocytes via passive diffusion and carriers
● They move out of enterocytes into the interstitial fluids depending on the size
○ <12 carbons goes directly into portal blood
○ >12 carbons are re-esterified to triglycerides or cholesterol esters &
packaged in chylomicrons

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Digestion of Proteins
Describe the enzymes required for digestion of protein in the gastrointestinal tract
and their location

A

● In the stomach - pepsinogens are activated by gastric acid to produce pepsins
and these cleave the bond between amino acids to yield polypeptides
● Small intestine - proteins are digested by powerful proteolytic enzymes from the
pancreas and intestinal mucosa. These include endopeptidases (trypsin,
chymotrypsin & elastase - which recognize specific amino acids in the middle of
the peptide) and exopeptidases which yield amino acids (by recognizing and
acting on one or two terminal amino acids)
● Brush border - amino, carboxy, endo and dipeptidases cleave peptides into
amino acids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How are proteins absorbed from the GI tract?

A

● Two phases
○ 1 Into the mucosal cell
○ 2 Into interstitial fluid and then into capillaries and portal blood

● There are seven transport systems for moving amino acids into enterocytes: five
require sodium co-transport and there are two sodium independent transporters
● Absorption of protein is rapid in the duodenum and jejunum and then slow in the
ileum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How does protein absorption and digestion differ in infa nts and young children
compared to adults?

A

Infants absorb more undigested protein, which results in passive immunity via absorption
of antibodies. However, this also results in more food allergies in this age group.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Glucose
What factors influence glucose homeostasis?

A

● Glucose absorption from the intestine
● Uptake from the periphery - muscle, fat, brain, RBCs, liver
● Reabsorption in the kidney
● Gluconeogenesis in the liver - as determined by the actions of insulin and
glucagon

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What happens to glucose homeostasis in the absence of insulin?

A

● Hyperglycaemia due to a number of factors
○ decreased peripheral uptake of glucose into muscle and fat
○ reduced glucose uptake by the liver
○ increased glucose output by the liver and lack of glycogen synthesis

● The intake of glucose by the brain, GIT , kidney and RBCs remains unchanged

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

By what mechanism does glucose cause the release of insulin?

A

● Taken up by specific GLUT 2 transporter in beta cells of the pancreas
● Glucose is converted to pyruvate, then metabolised to glutamate via the citric
acid cycle which primes insulin granules for release
● Production of ATP triggers (via K efflux) a Ca influx which causes the granules to
be released

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Iron
How is iron absorbed from the GIT?

A

● In the stomach, gastric acid causes a reduction of Fe3+ (ferric form) to Fe2+
(ferrous form) and formation of soluble complexes
● The duodenum is the major site of absorption
● Fe3+ is converted to Fe2+ by ferric reductase
● Fe2+ is transported into enterocytes via the apical membrane iron transported
(DMT1)
● Dietary haeme is transported into the enterocyte by heme transporter
● Heme oxidase releases Fe2+ from heme
● Some intracellular Fe2+ is converted to Fe3+ and bound to ferritin
● The remainder binds to basolateral Fe2+ transporter ferroportin and transported
to interstitial fluid aided by hephaestin (Hp)
● Then it is converted to the ferric form (Fe3+) and bound to transferrin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What factors reduce iron absorption from the GIT?

A

● Dietary factors - phytic acids in cereals, oxalates and phosphates bind to Fe to
produce insoluble compounds
● Surgical factors - partial gastrectomy (via reduction of gastric acid), duodenal
surgery or illness e.g. ulcers (via reduced site of absorption)
● Physiological - high iron stores, recent high iron diet, degree of erythropoiesis
● Drugs - antacids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How is iron transported?

A

Free Fe2+ (ferrous) bound to transferrin

17
Q

Calcium
How does the body regulate plasma calcium?

A

● Works via a feedback loop
● 1,25-dihydroxycholecalciferol (1,25DHCC, from Vit D) increases Ca absorption in
the GIT and kidneys
● PTH mobilises Ca from bone, increases Ca resorption in the kidneys and
increased 1,25 DHCC in the kidneys
● Calcitonin (from thyroid) inhibits bone resorption, increases calcium excretion in
the urine

18
Q

How is the synthesis of 1,25 DHCC regulated?

A

● 1,25 DHCC is formed in the kidneys by 1-alpha-hydroxylase.
● Low Ca increases PTH which stimulates 1-alpha- hydroxylase and increases
1,25DHCC formation
● Low phosphate directly stimulates 1-alpha-hydroxylase
● High Ca/High PO4 inhibits 1,25 DHCC (increasing the inactive form 24,25DHCC
instead)

19
Q

Water and Electrolytes
Explain the mechanisms of absorption and secretion of water and electrolytes in
the GIT

A

Absorption
● After meals, fluid is taken up due to coupled transport of nutrients e.g. glucose
and water
● Between meals - NcCl enters across the apical membrane via the coupled
activity of Na/H exchanger and a Cl/HCO3 exchanger
● In the distal colon, Na enters the epithelial cells via epithelial Na channels
(eNAC) which is electrogenic

Secretion
● Cl- secretion occurs continuously in the small intestine and colon
● Cl uptake occurs via Na/K/2Cl co-transporter and is secreted into the lumen via
Cl channels (CFTR = cystic fibrosis transmembrane conductance regulator)
● Water endogenous secretions is approx 7L per day, intake is 2L and the amount
reabsorbed is 8.8L. Balance is in the stools approx 200ml

20
Q

Exocrine pancreas
List the enzymes secreted from the exocrine pancreas and give at least 3
examples of the substrates that these enzymes work on

A

● Trypsin- proteins, polypeptides
● Chymotrypsins - proteins, polypeptides
● Elastase - elastin and some proteins
● Carboxypeptidase A and B - proteins and polypeptides
● Colipase - fat droplets
● Pancreatic lipase - triglycerides
● Bile salt acid lipase - cholesterol esters
● Pancreatic alpha amylase - starch
● Ribonuclease - RNA
● Deoxyribonuclease - DNA
● Phospholipase A2 - phospholipids

21
Q

Describe the regulation of pancreatic juice secretion

A

● Primarily under hormonal control
● Secretin acts on the duct to cause production of copious amounts of alkaline
pancreatic juice, which is poor in enzymes. Exerts effects via cAMP. Also
stimulates bile secretion.
● As the flow of pancreatic juice increases is becomes even more alkaline because
the exchange of HCO3- for Cl- in the distal duct is inversely proportional to flow
● Cholecystokinin (aka moves the gallbladder) acts on acinar cells to cause release
of zymogen granules and pancreatic juice rich in enzymes. Also relaxes the
sphincter of oddi. Secrete by I cells in the mucosa of the upper small intestine.
● Acetylecholine (The rest and digest transmitter) also stimulates the release of
zymogen granules. ACh is also involved in vagal nerve mediated pancreatic
secretion via the sight/smell of food.

22
Q

Describe the composition of pancreatic juice

A

Cations, anions, bicarb (HCO3-), digestive enzymes - released as proenzymes which
are activated by brush border enzymes

23
Q

What hormone is secreted by delta cells of the pancreas?
Somatostatin:

A

● Half life of 3 minutes, stimulated by food intake.
● Decreases the motility of upper GIT, reduces secretion and absorption of GIT and
inhibits glucagon and insulin release by the pancreas.
● Extends the period of time over which food nutrients can be absorbed from the
GIT into blood.
● Inhibits growth hormone (which is where the name comes from).

24
Q

Liver
List the principal functions of the liver

A

● Bile formation (500ml/day)
● Synthetic function - makes proteins, coagulation factors, albumin
● Inactivation/detoxification - drugs, toxins, circulating substances
● Nutrient/vitamin absorption/metabolism/control - amino acids, lipids, fat soluble
vitamins
● Immune function - especially against gut organisms, via the Kupffer
cells/macrophages in the sinusoidal epithelium

25
Q

How is bilirubin produced in the body?

A

● Formed by the breakdown of hame from haemoglobin
● Heme is converted to biliverdin and then on to bilirubin

26
Q

How is bilirubin metabolised?

A

● Bound to albumin in the circulation
● Dissociates in the liver and free bilirubin enters the liver cells via OATP (Organic
Anion Transport Polypeptide)
● Conjugated within liver cells - by glucoronyl-transferase located in the smooth ER
to convert bilirubin into bilirubin-diglucoronide which is the water soluble form
● This soluble form is transported against the gradient to the bile canaliculi and
then into the intestine (small amounts <5% leak back into the blood)
● Intestinal bacteria acts on the bilirubin-diglucoronide it to convert mostly to
urobilinogens and unconjugated bilirubin which are excreted by the gut
● Some bile pigments/urobilinogen and unconjugated bilirubin are reabsorbed in
the portal circulation, where most are then re-secreted. This is what is referred to
as the enterohepatic circulation
● Small amounts of urobilinogen are excreted in the urine and stercobilin is
excreted in the faeces

27
Q

Describe the composition of bile

A

● 97% water
● Bile pigments - conjugated bilirubin and biliverdin
● Bile salts - colic acid, chenodeoxycholic acid, deoxycholic acid, lithocholic acid
● Inorganic salts
● Others: cholesterol, fatty acids, lecithin, fat