Week 8 Integrating Human Physiology Flashcards

1
Q

Secretion during the pre-ingestive cephalic phase

A

Initiated when receptors in the head (cephalic) are stimulated by thought, sight, small and taste of food.

Before we even eat anything!

Involves the parasympathetic nervous system (Vagus) short: only lasts a few minutes

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2
Q

What is stimulated during this cephalic phase ?

A

Same responses as ACTUAL eating, but normally weaker)

Saliva production (24h a day, but 2/3 in early cephalic phase)

Gastric acid (1/3 of max capacity) (protein digestion)

Gallbladder contraction (start to release bile to absorb fat)

Pancreatic exocrine (enzymes) and endocrine function (hormones, e.g. insulin spike)

Why is it important ?
Feed forward mechanism:
Prepares the body for influx of food

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3
Q

Secretion stimulated by food in the stomach

A

Parietal cells:
• Secretion of HCl (breaks down food) • pH 1-2 (very acidic, corrosive!)
Chief cells:
• Secretion of pepsinogen (protein digestion) • Secretion of lipase (lipid digestion)
Mucous cells:
• Production of the mucus-bicarbonate layer (protect us from low gastric acid)

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4
Q

The bicarbonate-mucus layer

A

Continuously mucus production (goes down the gut) • Bicarbonatecatcheshydrogen,releaseofgasandwater
“Bicarbonate buffer system”

Critical for protection of the
mucosa (mucus barrier)
& makes it watery (good for digestion)

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5
Q

Secretion in the small intestine

A

Presence of food stimulates secretion
HCO3- secretions neutralise acidic chyme (stomach contents) (Bicarbonate can come from pancreas and duodenal glands)
Enzymes work in alkali range not low pH
Secretion of digestive enzymes and bile

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6
Q

Pancreatic exocrine secretion

A

Exocrine cells (Acini) connected to duct

Produce pancreatic juice, watery solution of digestive enzymes and HCO3- (optimizes pH for enzymes)
Enzymes:
Proteases secreted in inactive form to prevent auto-digestion Amylase (starch) / lipases (triacylglycerol) secreted in active form

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7
Q

Bile from the gall bladder – reservoir for bile

A

yellow/green bitter/alkaline solution
Contains: bile salts, bile pigments (bilirubin/biliverdin), cholesterol, neutral fats, phospholipids and electrolytes

Function of bile is emulsification of dietary fat
2 process to regulate/release bile secretion:
• Cephalic phase: Paras. NS (vagus)
stimulates the bladder to constrict of
smooth muscle & relaxation of sphincter

• Presence of nutrients triggers hormones (CCK) via blood to constrict bladder

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8
Q

Digestion & Absorption

A

Water absorption
Water crosses lipid-rich membranes by diffusion through aquaporins
lipid bilayer

Water absorption
Water crosses lipid-rich membranes by diffusion through aquaporins
lipid bilayer

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9
Q

Carbohydrate Digestion

A

Break down starch to glucose
glucose digestion begins in mouth with secretion of
salivary α-amylase (1,4 bond) (only short, then swallowed)
Enzymatic activity inhibited in stomach due to low pH
Most of digestion happens due
to pancreatic amylase,but doesn’t liberate glucose!!! only short-chain glucans

Absorption of glucose from duodenum stimulates pancreatic exocrine secretion (α-amylase) via release of hormones (CCK, secretin) “nutrient stimulated process”

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10
Q

Carbohydrate digestion & absorption at the brush border

A

Enzymes liberate monosaccharides from disaccharides in the diet and glucan from starch digestion
Only glucose, galactose and fructose can be absorbed in humans

Monosaccharides are released in really close proximity to their transporters (efficient absorption)
They don’t have to travel far, no malabsorption

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11
Q

Protein Digestion

A

e.g. piece of meat:
• Mechanical disruption by chewing and gastric
motility (increase surface and break down structure)
Stomach parietal cells
• Protein denaturation by HCl (break bonds and folding) leaving large polypeptides
Stomach chief cells
Pepsinogen pH < 5 Pepsin (inactive) (active)
Mix of small peptides and amino acids sensed in duodenum CCK-induced release of pancreatic peptidases into duodenum; endo & exo peptidases

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12
Q

Pancreatic Peptidases act in the Duodenum

A

We don’t wanna digest ourself!

Trypsinogen (inactive) > Enterokinase > Trypsin (active)
V
Proenzyme (inactive) > Enzyme (active)

Endopeptidases
(break middle of chain)
trypsinogen chymotrypsinogen proelastase

Exopeptidases
(breaking terminal ends)
procarboxypeptidase A
procarboxypeptidase B

70 % oligopeptides: 30% free amino acids

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13
Q

Protein Absorption: 3 Transport Mechanisms

A

Na+ dependent amino acid transport (4 types)
• H+ co-transport with small peptides e.g. di-tri peptides (Pept1)
• Larger peptide fragments moved by transcytosis (minor)
• Intracellular/Cytoplamic peptidases, most peptides leave cell as free amino acid
We can absorb free Amino acids and small peptide chains!

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14
Q

Fat digestion - Initiation

A

Whole process is heavy on enzymes…….
In the mouth: saliva containing lingual lipase (taste of fat (evolution?), not important nutritionally in humans)
Few digestion products stimulate the stomach to release enzymes and CCK from sI (feed forward mechanism)

In the stomach:
release of gastric lipase & motility-> Emulsification surface area increase

Fatty acids in duodenum-> Cholecystokinin (hormone)
(from action of gastric lipase)
/\

Bile release
(gallbladder contraction, relaxion of sphincter of odi)

3 Pancreatic enzymes
Triacylglycerol hydrolase Cholesterol ester hydrolase Phospholipase A2

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15
Q

Bile is important for Emulsification

A

Doesn’t contain enzymes, but important for digestion
• Bile salts crucial in increasing (and maintaining) the
surface area for lipase action
• Prevent droplets to merge into big one again

Hydrophobic tail and hydrophobic head, repel each other

Micelles

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16
Q

Products of 3 Pancreatic enzymes

A

Triacylglycerol > TG hydrolase > 2-MAG + 2 x fatty acids

Cholesterol ester> Cholesterol ester hydrolase> Cholesterol + fatty acid

Lecithin> Phospholipase A2 > Lysolecithin + fatty acid

“pancreatic lipase actually made up of 3 separate enzymes”

17
Q

Lipid absorption processes (Jejunum)

A

Within lumen of SER chylomicron forms and moves by exocytoses through the basolateral membrane entering lacteal

18
Q

What about medium &
short chain fatty acids (> 12 carbons) ?

A

Water soluble; absorbed directly into capillary and into hepatic portal circulation bound to albumin

19
Q

Summary

A

TheGItractallowsustodigestandabsorbalmost everything we eat (little malabsorption):
• Secretion (digestion is based on enzymes, bile salts (aqueous environment), fluids for pH (enzymes), mucus is vital for protection)
• Digestion (breakdown of large to small molecules)
• Absorption (uptake of nutrients into the enterocyte and
ultimately the body)
2. To allow this each segment is unique and must function independently “Segmental heterogeneity” (meal changes
continuously (pH, nutrients, consistency &content, gut adapts to deal with it)