GI Theme 3 Flashcards
What is the structure of amylose ?
linear polymer of alpha 1-4 glycosidic links
What is the structure of amylopectin ?
branched polymer with alpha 1-4 and alpha 1-6 glycosidic links
Where can you find alpha amylase ?
pancreatic juice and saliva
What does amylase hydrolyse and what cant it ?
hydrolyses alpha 1-4 links
cant hydrolyse alpha 1-6 links or alpha 1-4 linkks close to terminal branches ?
Starch digestion release what
maltose
maltotriose
alpha limit dextrins
What are alpha limit dextrins?
branched polymers of glucose 5-9 units long
formed due to the inability of amylase to hydrolyse alpha 1-4 links next to branch points
What happens to alpha limit dextrins in the mouth ?
they can be taken up by bacteria and used as an energy source
The length of time food is in the mouth detemrines what ?
how much maltose and maltotriose is released
they are carcinogenic
What carbohydrate digestion takes place in the stomach ?
none- acidic pH inhibits alpha amylase
What carbohydrate digestion takes place in the duodenum ?
pancreatic alpha mylase
digests remaining starch into maltose , maltotriose and alpha limit dextrins
Which is faster salivary alpha amylase or pancreatic alpha amylase ?
pancreatic alpha amylase
What is the role of oligosaccharidases ?
on the brush border
they further digest the maltose, maltotriose and the alpha limit dextrins
Where can you find oligosaccharidases ?
in the duodenum and the jejunum
What does isomalatase (alpha dextrinase) do ?
hydrolyse alpha 1-6 links that amylase csnt
What does maltase do ?
hydrolyse maltose and maltotriose into glucose
What does lactase do ?
hydrolyse lactose into glucose and galactose
What does sucrase do ?
hydrolyse sucrose into glucose and fructose
What are the end products of digestion with oligosaccharidases ?
monosaccahrides- glucose , fructose and galactose which can be absorbed by the duodenum and jejunum
Where does the absorption of monosaccahrides occur ?
duodenum and upper jejunum
How are glucose and galactose actively uptaken ?
by sodium-glucose transporter 1
What type of active transport does the sodium-glucose transporter use ?
secondary active transport
What creates the electrochemical gradient in sodium-glucose active transport ?
Na/K ATPase
basolateral membrane
How do glucose and galactose leave the epithelial cell ?
glucose transporter protein 2
How is the entry of galactose and glucose into the epithelial cell mediated ?
by the presence of sodium in the GI lumen
How does fructose enter and leave the intestinal epithelial cell ?
enters using facilitated diffusion - glucose transporter 5
exits using glucose transporter 2
What is sucrase-isolmaltase deficiency ?
low levels of sucrase and isomaltase in the brush border
intolereane to starch and sucrose
fructose and glucose are tolerated
What is glucose-galactose malabosprtion syndrome ?
mutation in SGLT-1
fructose can be given
What type of transport is SGLT?
secondary active trnasport
symport
What is the type of transport with GLUT proteins ?
facilitated diffusion
uniport
What are alpha limit dextrins hydrolysed by ?
isomaltase
How is pepsinogen converted to pepsin ?
by protons
How much protein does pepsin digest ?
15%
What is pro elastase ?
converted to elastase
digests serine in elastin
What are the peptidases ?
aminopeptidase
dipeptidase
dipetidyl aminopeptidase- cleaves a dipeptide from end of the dipeptide
How can small peptides be further hydrolysed ?
by peptidases in the cytosol
What is present on the apical membrane to provide gradients for peptide transport ?
Na/H transporters
What are the amino acid transport systems on the apical membrane ?
5 dependent on Na - active
2 are facilitated
7 in total
What are the amino acid transport systems on the basolateral membrane ?
5
3 are Na independent - efflux of amino acids into blood
2 are Na dependent - active
How do fat soluble vitamins diffuse ?
diffuse acorss the brush border membrane
Where is vit B12 absorbed ?
ileum
How is B12 found in foods ?
bound to proteins
What happens to b12 in the stomach ?
released and binds to R proteins - high affinity
What is intrinsic factor ?
vitamin b12 binding protein
secreted by gastric parietal cells
binds to B12 with less affinity than R proteins
What degrades the R - protein B12 complexes ?
pacnreatic proteases
What happens to the B12 afte degradation from R proteins ?
binds to IF- resist protease degradation
What happens to the B12 afte degradation from R proteins ?
binds to IF- resist protease degradation
What does the brush border of the ileum contain ?
receptors for B12- IF complexes
What might happen in pancreatic insuffficinecy ?
no degradation from R proteins
B12 deficiency might occur
What is the B12 carrier ?
transcobalamine II
What inhibits gastric emptying locally ?
CCK - lipid present in the duodenum
What emulsifies lipids ?
bile salts and lecithin
What is the purpose of emulsification ?
increase the surface area for water soluble enzymes to act
What are the lipolytic enzymes found in pancreatic juice ?
pancreatic lipase
co-lipase
cholesterol esterase
phospholipase A
How is pancreatic lipase inhibited ?
bile salts bind to fat surface and prevent lipase binding
What does co lipase do ?
displaces bile salts on the fat surface enabling lipase to fucntion
What are the products of triglyceride break down ?
2-monoglyceride
2 x NEFA
What does cholesterol esterase do ?
cleaves a fatty acid from cholesterol esters
What does phospholipase A2 do ?
turns phsopholipids into lypophospholipid and NEFA
What is micelle formation ?
bile salts form micelles with the products of fat digestion
What do the bile salts act as in micell formation ?
surfactant
What is the structure of micelles ?
lipid molecules arranged in a spherical form
Where does absorption of lipids take place ?
in the ileum and the jejunum
What is the unstrirred layer ?
mucus layer
with microvilli between the lumen and the brush border
molecules pass through and become more disorgansied as they approach the apical membrane
What lipid transport occurs at the brush border membrane ?
cholesterol transporter mediates facilitated transport
microvilli membrane fatty acid binding protein transports long chain fatty acids by secondary active transport - Na/K ATPase
What is the role of cytosolic transport membrane ?
transport the products of lipid digestion to the smooth endoplasmic reticulum
What are the cytosolic lipid transport proteins ?
fatty acid binding protein and sterol carrier
What happens to lipids in the smooth endoplasmic reticulum ?
they are esterified again
enter pre chylomicrons
go to golgi
too large to leave across the basement membrane
lacteals - lymphatic capillaries- large enough - empty into the lymph and the the blood by the thoracic duct
Where does absorption of bile salts occur ?
in the terminal ileum
How are conjugated bile salts actively taken up ?
by an Na bile duct co transporter
How do bile salts enter the blood ?
they re enter the portal blood
bound to albumin
return to the liver
How does fructose get from the gut to the blood ?
enters via facilitated diffusion and then leaves bu GLUT 5
What are the brush border peptidases ?
aminopeptidase
dipeptidase
dipeptidyl aminopeptidase
Where does lipid break down occur in the GI tract ?
stomach
duodenum
jejunum
What 2 substances are responsible for emulsification ?
bile salts and lecithin
What is the role of R protein ?
to protect IF from gastric acid
Which compounds predominantly contribute to micelle formation ?
bile salts
What is the mechanism whereby lipids in the duodenum prevent gastric emptying ?
CCK
what are anciliary organs of digestion
pancreas, gallbladder and liver
how long is the human gut
5m long
how is the sa increased in the human gut
folds and microvilli in the SI
outline the journey through the gut
Oesophagus Pyloric sphincter and stomach Upper small intestine Lower small intestine Caecum Colon Rectum
what are the GI Tract Disorders
Physical (blockages/strictures/ fat deposition)
Functional (nerve-peristalsis/muscle)
Environmental insult (infections, toxins, DNA mutations)
Immune-related ( defence becomes attack)
Unknown aetiology
All may have metabolic implications
what disorder affect the whole length of the GI tract
GI cancers
Crohns disease
what disorders move down the GI tract
oesophagus:
- Dysphagia (difficulty swallowing)
Oesophageal stricture/tumours
Oesophageal varices (liver disease)
Oesophageal reflux/indigestion
Barret’s oesophagus
what is dysphagia
oropharygeal
- neuromuscular disorders or stroke
- cant close trachea
- choking
- aspiration pneumonia
- anxiety, anorexia
- dehydration
how can dysphagia be managed
soft diet
pureed diet
thickened fluids
PEG- feeding tube, long term feeding
what happens in dysphagia
food can go to lungs
what is oesophageal stricture
food sticking after swallowing caused by - achalasia -astrictures -present with dysphagia
how can oesophageal stricture be treated
dietery management
surgical
what is Gastroesophogeal Reflux Disease (GORD)
Reflux of gastric contents through lower oesophageal sphincte
what is Chronic: GORD
potential progression to Barret’s Oesophagus/cancer
what can GORD be aggrevated by
Spicy and fatty foods, tomatoes, onion, garlic
Caffeine and alcohol, carbonate drinks
Obesity and pregnancy
what is Laryngo-pharyngeal Reflux (LPR)
refluxate that travels above the upper oesophageal sphincter
is LPR physiological
no
How is GORD linked to erosive tooth wear
Intrinsic acids from the stomach can travel to the mouth and can damage enamel and dentin
how is erosive tooth wear managed in those with GORD
dental treatment & PPI therapy
what is hiatus hernia
stomach protrudes up to chest cavity
what is dyspepsia
discomfort in upper abdomen thta is food related
what is the cause of dyspepsia
peptic ulcer (by bacterial infection- helicobacter pylori)
what is the treatment for peptic ulcers
single 14 dyacourse combinatin therapy leading to healing
why are 2 antibiotics needed to treat peptic ulcers
h pylori can be antibiotic resistant
what is perniciuos anaemia
automimmune destrcution of gastric parietal cells that produce IF
what happens to rbc in pernicious aneamia
large
what are the symptoms of pernicuous anaemia
extreme fatigue shortness of breath pins and needles muscle weakness mood swings memory
how is pernicuous anaemia treated
vit b injection every 3 mnths
what are the oral symptoms of B12 deficiency
atrophic glossitis (sore and red beefy tongue)
mouth ulcers
angualr chleiltis
what is coeliac disease
autoimmune resposne to gluten and gliadin proteins
- wheat, rye, barley. oats
what happens in coeliac disease
damage to villi which affects absorption of nutrients
what are the complication in coeliac disease
anaemia
osteoporosis
neurological conditions
increased risk of small bowel cancer and intestinal lymphoma
how is coelaic disease managed
complete avoidance of gluten
gluten free breads
iron calcium and folate supplement
what crohns disease
inflammatory disease
what causes crohns disease
genetics
inapropirate immune response to commensal bacteria
environmental trigger
where can crohns disease occur
any where in gi tract from mouth to anus