digestion and absorption + mass transport Flashcards

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1
Q

define digestion

A
  • the hydrolysis of large, insoluble molecules into smaller molecules that can be absorbed across cell membranes . (cells lining the intestine)
  • digestive enzymes break bonds in macromolecules into monomers
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2
Q

which enzymes are involved in carbohydrates digestion ? where are they found ?

A
  • amylase in mouth
  • maltase, sucrase, lactase in membrane of smell intestine.
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3
Q

what’s the role of amylase ?

A
  • breaks down starch into maltose by catalysing the hydrolysis of glycosidic bonds
  • made in salivary glands and pancreas
  • salivary glands secrete amylase into mouth (starch begins hydrolysed )
  • pancreas secretes amylase into small intestine - remaining starch digested
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4
Q

what’s the role of disaccharides ?

A
  • (maltese) break down disaccharides into monosaccharides in small intestine. —> some attached to epithelial cells lining oleum (membrane-bound disaccharides )
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5
Q

what are the substrates and products of carbohydrate digestive enzyme ?

A
  • amylase = starch into smaller polysaccharides
  • maltase = hydrolysed maltose to 2 glucose molecules
  • sucrase = hydrolyses sucrose into glucose + fructose.
  • lactase = hydrolysed lactose into glucose * galactose.
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6
Q

where are lipids digested ?

A
  • the small intestine.
  • lipase synthesised in pancreas and released into small intestine.
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7
Q

what needs to happen before lipids can be digested ?

A
  • must be emulsified by bile salts produced by liver .
  • this breaks down large fat molecules into smaller, soluble molecules called micelles (increasing surface area to speed up digestion)
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8
Q

how are lipids digested ?

A
  • lipase hydrolyses the ester bond between monoglycerides and fatty acids.
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9
Q

what’s the role of micelles ?

A
  • help move digested lipid towards the epithelium .
  • dynamic structures - continually breaking apart and reforming (they split out monoglycerides + fatty acids —> pass thru bilayer via simple diffusion)
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10
Q

how/where are proteins digested ?

A
  • protease breaks down into amino acids by hydrolysing peptide bonds
  • some protease made in pancreas + released into small intestine
  • others made in cell lining stomach and released into stomach .
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11
Q

what enzymes are involved in protein digestion ? what are their roles?

A
  • endopeptidases = break between specific amino acid in middle of a polypeptide = converts longer poly into shorter ones
  • exopeptidases = break between specific amino acids at the end of a polypeptide = releases individual amino acid - transported into ileum epithelial cells
  • dipeptidases = break dipeptides into amino acids = exopep that hydrolyse peptide bonds in dipeptide
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12
Q

how are certain molecules absorbed into ileum despite a negative concentration gradient ?

A
  • through co-transport.
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13
Q

which molecules require co-transport?

A
  • amino acids + monosaccharides.
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14
Q

explain how sodium ions are involved in co-transport .

A
  • sodium ions (Na+) are actively transported out of cell into the lumen, creating a diffusion gradient.
  • nutrients taken up into cells along with Na+ ions
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15
Q

why do fatty acids and monoglycerides not require co-transport ?

A
  • the molecules are nonpolar so can easily diffuse across the membrane of epithelium cells.
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16
Q

describe the structure of haemoglobin .

A
  • globular , water soluble. consists of 4 polypeptide chains, each carrying a haem group containing iron ion . (quaternary structure )
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17
Q

describe the role of haemoglobin .

A
  • present in RBCs = oxygen molecules bind to the haem groups and are carried around the body to where they needed in respiring tissues
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18
Q

name 3 factors affecting oxygen-haemoglobin binding .

A

1) partial pressure/ concentration of oxygen.

2) partial pressure/ concentration of carbon dioxide .

3) saturation of haemoglobin with oxygen.

19
Q

how does partial pressure of oxygen affect oxygen-haemoglobin binding ?

A
  • as partial pressure of oxygen increases, the affinity between haemoglobin for oxygen also increases, so oxygen binds tightly to haemoglobin
  • when partial pressure is low, oxygen is released from haemoglobin .
20
Q

how does partial pressure of carbon dioxide affect oxygen-haemoglobin binding ?

A
  • as partial pressure of CO2 increases, the conditions become acidic causing haemoglobin to change shape
  • affinity of haemoglobin for oxygen this decreases , so oxygen released from haemoglobin
  • known as Bohr effect
21
Q

what does it mean when the graph has a sigmoid / S-shape ?

A
  • binding of the first oxygen molecule causes oxygen to change shape + u cover other oxygen binding sites

—> easier further O2 molecules bind and known - cooperative binding

22
Q

how does saturation of haemoglobin with oxygen affect oxygen-haemoglobin binding?

A
  • hard for the first oxygen molecule to bind
  • once it does , changes the shape to make it easier for second and third molecules to bind. = positive cooperativity
  • then slightly harder for fourth oxygen molecule to bind as there’s low chance of finding a binding site .
23
Q

explain the bohr effect

A
  • haem affinity for oxygen changes at diff concentrations of CO2
  • higher partial pressures of CO2 = haem has lower affinity for oxygen : causing oxyhaem to dissociate more readily

—> useful : tissues with high rates of respiration will be producing larger amounts CO2 - ensures oxygen unloaded from haem at respiring tissues

  • high CO2 conc shifts dissociation curve to right
24
Q

explain why oxygen binds to haemoglobin in lungs.

A
  • partial pressure of oxygen is high
  • low conc of CO2 in the lungs, so affinity is high
  • positive cooperativity (after first oxygen molecule binds, binding is subsequent molecules easier)
25
Q

explain why oxygen released from haemoglobin in respiring tissues .

A
  • partial pressure of oxygen is low
  • high conc of CO2 in respiring tissues, so affinity decreases
26
Q

what do oxygaemoglobin dissociation curve show.

A
  • saturation of haemoglobin with oxygen (in %), plotted against partial pressure of oxygen (in kPa)
  • organisms that live low oxygen environments have dissociation curve lies to left (haem good at binding to O2 when partial pressure low)
  • active organisms - dissociation curve lies to right (haem good releasing O2 at higher partial pressures so cells use it to respire )
27
Q

how does CO2 affect position of an oxyhemoglobin dissociation curve ?

A
  • curve shifts to right as haemoglobins affinity for oxygen has decreased.
28
Q

name 3 common features of a mammalian circulatory system.

A

1) suitable medium for transport, water-based to allow substances to dissolve .

2) means of moving medium and maintaining pressure throughout the body . such as the heart

3) means of controlling flow so remains unidirectional, such as valves .

29
Q

relate the structure of the chambers to their function.

A
  • atria - thin-walled and elastic, so can stretch when filled with blood
  • ventricles - thick muscular walls pump blood under high pressure - left ventricle thicker than right as it has to pump
    blood all way around body.
30
Q

what is the role and structure of the arteries ?

A
  • carry blood away from heart to various organs of body
  • need to cope with high pressure generated from heart forcing out blood with each heartbeat —> thick muscular wall containing lots elastic tissue
  • inner lining arteries called endothelium - folded allowing artery to expand help withstand high pressure
  • small lumen ensures high pressure maintained
31
Q

describe the role and structure of veins

A
  • carry blood from organs of body towards heart
  • blood flowing much lower pressure so veins have larger lumen and much thinner walls containing little elastic fibres / muscle tissue
  • valves prevent slow-moving blood from flowing backwards
  • contraction of nearby body muscles helps blood to flow through veins
32
Q

describe what is the role and structure of capillaries

A
  • connect arteries and veins
  • substances move out of blood to body tissues =(O2, glucose, mineral ions) -> waste products (CO2 + H2O) move out body tissues and into capillaries
  • small holes (pores) enable exchange of substances
  • walls one cell thick - reduces diffusion distance for these substances
  • large no. capillaries (capillary beds) increases surface area available for exchange
33
Q

why are two pumps (left and right) needed instead of one?

A
  • to maintain blood pressure around whole body.
  • when blood passes thru narrow capillaries of lungs, pressure drops sharply so not be flowing strongly enough to continue around body
  • it’s returned to heart to increase pressure .
34
Q

what is tissue fluid ?

A
  • watery substance containing glucose, amino acids, oxygen and other nutrients . supplies these to cells whilst removing any waste products .
  • doesn’t contain things too big to be forced out of capillary so no RBC / large proteins
35
Q

how is tissue fluid formed ?

A
  • as blood pumped through increasingly small vessels , this creates hydrostatic pressure which forces fluid out of capillaries
  • bathes the cells, then returns to capillaries when hydrostatic pressure is low enough.
36
Q

define what’s meant by the cardiac cycle

A
  • coordinated sequence of contractions + relaxations by heart muscle causing blood to move from atria into ventricles and then arteries.
  • muscle contraction = systole
  • relaxation = diastole
37
Q

describe what happened during cardiac disatole .

A
  • heart relaxes
  • blood enters atria, increasing pressure + pushing open atrioventricular valves
  • this allows blood to flow into ventricles — pressure in heart lower than in arteries, so semilunar valves remain closed
38
Q

describe what happens during 1. atrial systole

A
  • atria contact while ventricles relax
  • decreases volume inside atria which increases pressure —> increased pressure forces atrioventricular valves open and pushes blood into ventricles .
39
Q

describe what happens during ventricular systole

A
  • ventricles contact
  • pressure increases, closing atrioventricular valves = prevent back flow, + opening semilunar valves ,
  • blood flows into arteries .
40
Q

describe what happens during disastole

A
  • both atria and ventricles relaxes = low pressure in both chambers
  • since pressure higher in arteries than heart chambers—> semi lunar valves forced closed : prevents blood flowing backwards into ventricles
  • blood returned heart - atria filled blood
41
Q

name the nodes involved in heart contraction and where they situated

A
  • SAN (sinoatrial node) - wall of right atrium
  • AVN (atrioventricular node ) = in between 2 atria
42
Q

what does myogenic mean?

A
  • hearts contraction initiated from within muscle itself , rather by nerve impulses
43
Q

explain how heart contracts

A
  • SAN initiates + spreads impulse across atria, so they contract
  • AVN receives , delays , and conveys impulse down bundle of His
  • impulse travels into Purkinje fibres - branch across ventricles so contract from bottom up
44
Q

why does the impulse need to be delayed ?

A
  • if impulse spread straight from atria into ventricles = not be enough time for all blood to pass thru and for valves to close