Transport Flashcards

1
Q

What is a solute?

A

Substance dissolved in water e.g. ions, glucose, vitamins, drugs

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2
Q

Why doe solutes need to be transported across the membrane?

A

Oxygen for respiration, food through gut, maintaining & changing membrane potential

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3
Q

What is circulation?

A

Movement in blood

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4
Q

What is transport?

A

Substance crossing a membrane

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5
Q

What are the factors affecting the ability of substances to cross the membrane?

A

Permeability & electro-chemical gradient

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6
Q

In what way does electrical gradient influence the movement of molecules crossing the membrane?

A

Inside of cell is negative relative to outside (similar conc. of +ve ions, more -ve ions) - resting membrane potential= -70mV
Forces -ve ions out & +ve ions in

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7
Q

In what way does chemical gradient influence the movement of molecules crossing the membrane?

A

Substances move from to low conc.

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8
Q

What is passive diffusion?

A

Hydrophobic substance & gases - move in direction of electro-chemical gradient - no energy or carrier proteins

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9
Q

What is facilitated diffusion?

A

Ions & hydrophobic substances can’t cross membrane even with electro-chemical gradient - require carrier proteins

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10
Q

What law dictates the rate of diffusion?

A

Fick’s Law of Diffusion

dn/Dt = PΔc
P=permeability
Δc =electro-chemical gradient

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11
Q

What is the limitation of diffusion

A

Can only occur at a small distance e.g. cell =10μm = 0.05 seconds - 1m = 15 years

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12
Q

What are the different types of carrier proteins

A

Channels (regulated & non-regulated)
Transporters (uniporter, symporter, antiporter)
Pumps (ATP-pump)

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13
Q

Which channel proteins are passive & which are active?

A

Channels & uniporters are passive
Symporters, antiporters, ATP-pumps are active

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14
Q

Explain channel proteins?

A

Pores in membrane - specificity for a single substance e.g. Na2+ & H2O - passive - follow electro-chemical gradient - regulated=gated & non-regulated=constitutive (always open)

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15
Q

Explain uniporters?

A

Passive - bind to & move large molecules e.g. glucose - follow electro-chemical gradient - regulated by insertion & removal of uniporters from cell membrane - e.g. insertion of GluT1 for glucose in the kidneys - more selective than channel & prevent similar shapes molecules from entering

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16
Q

What type of active transport are symporters & antiporters?

A

2° Active Transport

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17
Q

What is 2° active transport?

A

Use energy stored in conc. gradient established by 1° active transport

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18
Q

What is a symporter?

A

Moves 2 molecules across membrane in the same direction - Na+ & glucose transporter

19
Q

What is an antiporter?

A

Moves 2 molecules across membrane in opposite directions

20
Q

What is active transport?

A

Uses energy to move against conc. gradient

21
Q

What is an ATP pump?

A

E.g. Na+ extruded against gradient - ATP used - maintain cell volume, nerve impulses, & muscle contraction

22
Q

What type of transport is an ATP pump?

A

1° active transport

23
Q

What is resting membrane potential?

A

-70mV - imbalance of ions (cation conc. equal - K+ inside & Na+ outside - trapped anions inside)

24
Q

What are trapped anions?

A

Negatively charged ions - proteins (17-), organic phosphate (-), ATP (4-) - can’t pass through membrane explained by Fick’s Law (P=0, ∆c is high - rate of diffusion still 0)

25
Q

What maintains resting membrane potential?

A

Na+/K+ pump - use ATP to pump 3 Na+ out of cell & 2 K+ into cell

26
Q

What is osmosis?

A

Water moves across aquaporins from regions of low osmolarity to high osmolarity

27
Q

What is the concentration of water?

28
Q

What is osmolarity?

A

Amount of solute dissolved in 1kg of water (1L) - 1 mole solute in 1L = 1 Osmolar (Osm)
*1 mole NaCL in 1L water = 2 Osm (dissociates in water)

29
Q

How is osmolarity measured?

A

Depression of freezing point - 1 Osm will depress freezing point by 1.86°
E.g. plasma freezes @ -0.52° = 280 mOsm

30
Q

How does osmolarity affect RBCs?

A

RBCs contain aquaporins & cytoplasm has osmolarity of 280 mOsm - solution of 280 mOsm isosmotic/isotonic no osmosis occurs - Osmolarity ECF < ICF (hypotonic, hypoosmotic) water rushes in & cell swells, lysis - Osmolarity ECF > ICF (hypertonic, hyperosmotic) water rushes our & crenation

31
Q

How does glucose have to travel from intestine to muscle cells?

A

Leave intestine (pass 4 lipid membranes & interstitial space) circulate via blood system, & leave blood & enter muscle cells (cross 3 lipid membranes & interstitial space)

32
Q

How are epithelial cells polarised?

A

Apical domain (facing lumen), tight junction (impermeable to water - tight & leaky), basolaterlal domain (face basal lamina)

33
Q

What are the conditions of the cell & ECF and in terms of glucose & sodium?

A

ICF - High glucose & low sodium
ECF - low glucose & high sodium

Glucose cant enter cell from intestine via diffusion (∆c<0) but can exit via diffusion through basolaterlal layer (∆c>0) however p=0 (need carrier proteins)
Na+ can enter cell from lumen via diffusion(∆c>0), can only exit via active transport (∆c<0) - needs carrier proteins as P=0

34
Q

Explain the Glu/Na+ transporter?

A

1) 1° Active Transport - ICF [Na+] kept low by Na+ pump in basolaterlal layer
2) 2° Active Transport - low Na+ creates a conc gradient - Na+ enters via Na+/glucose symporter on apical membrane - energy released is captured by symporter & allows glucose to enter against the conc. gradient
3) Facilitated diffusion - Glucose uniporter allows glucose to leave via basolaterlal membrane down a conc. gradient & enter interstitial space

35
Q

Other examples of co-transporters?

A

Amino acids via Na+/Amino Acid transporter
Folate via H+/Folate transporter

36
Q

Explain bulk absorption of water

A

Large amounts of water from lumen of intestine to interstitial space via leaky tight junctions - proximal tubule & small intestine - needs on osmotic gradient - constitutive process - Na+ move into cell via Na+/Glu symporter, Cl- follows due to electrical imbalance - water follows

37
Q

Explain regulated absorption of water

A

Small volumes via transcellular pathways - collecting ducts - tight junctions impermeable - moves via aquaporins (channel proteins) - AQP-1 located in basolateral membrane

38
Q

What happens to the aquaporins when ADH is absent?

A

AQP-1 in basolateral membrane - AQP-2 retained in secretory vessels in cytoplasm - water can’t be reabsorbed & urine is dilute

39
Q

What happens to the aquaporins when ADH is present?

A

AQP-2 is inserted into apical membrane - water reabsorbed (AQP-2 provide permeability follows osmotic gradient) - urine concentrated & water retained

40
Q

Explain healthy water secretion & loss vs. diarrhoea?

A

Healthy - 20L secreted - 19.9L reabsorbed, 0.1L lost as feaces
Diarrhoea - secretion increased & reabsorption decreased

41
Q

Explain Oral Rehydration Therapy?

A

H2O only - interstitial fluid [Na+] too low
H2O & Na+ - no Na+ channels in lumen
Glucose, Na+. & H2O - Na/Glu symporter - water will follow via leaky tight junctions

42
Q

Explain Sweating?

A

H2O secretion - 1)Cl- exported 2)Na+ follows 3) Water follows

43
Q

Explain exocytosis?

A

Secretion of proteins (insulin), insertion of membrane proteins (Na+ pump), & release of neurotransmitters - mRNA from nucleus moves to ribosome & translation occurs - Polypeptide move to lumen of sER - transport vesicle breaks off sER & brought to cis face of Golgi apparatus - Exits via vesicles from trans face of Golgi - insertion or secretion

44
Q

Explain endocytosis?

A

Uptake of bacteria/virus in macrophage & uptake of LDL cholesterol in liver - vesicles merge with cell membrane & release substances (protein) - travel to lysosome to be broken down & recycled or removed