(10) - Epithelial Transport Flashcards

1
Q

(Key Points)

  1. reabsorption (and secretion) involves crossing which 2 barriers?
  2. The tubular epithelium can be crossed in how many steps?
  3. Most metabolically important substances can not penetrate lipid membrances and must do what?
A
  1. the tubule epithelium and the endothelial cells lining the peritubular capillaries
  2. 1 or 2
  3. must move via specific integral membrane proteins - transporters or channels
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2
Q

(Key Points)

  1. What is the lynchpin of reabsorption in the proximal tubule?
  2. Hydraulic pressure in peritubular capillaries in peritubular capillaries is low and oncotic pressure high, thus facilitating what?
  3. Are there limits to the max rate at which solutes can be reabsorbed?
A
  1. movement of Na from the tubular lumen to the serosa
  2. reabsorption of filtrate
  3. yes
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3
Q

how can you tell these apart - check blood levels (if high its diabetes)

A
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4
Q

disease of the proximal tubule where all of this stuff is messed up

is genetic in this dog

A
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5
Q
A

if he doesn’t go over this later might want to go back to this - cause he said a decent amount about this

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6
Q

almost everything that is filtered will be reabsorbed

A

this varies a good amount

if you really want to get rid of something completely need to used secretion - cause not all blood subjected to filtration (?)

if you gave too much PAH - would still have some left becuase secretion can only get rid of so much because there is only so much energy and transporters

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7
Q
A
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8
Q

(Crossing the Epithelial Barrier)

  1. how many steps?

(Paracellular route)

  1. how many steps?
  2. how does it get through?

(Transcellular route)

  1. how many steps?

5-6. what are they?

A
  1. one or two
  2. single step
  3. substance goes “around” cells through matrix of tight junctions
  4. two steps
  5. across apical membrance facing lumen
  6. across basolateral membrane
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9
Q

1-4. What four ways do substances move across membranes and cells?

A
  1. diffusion
  2. transporters
  3. channels (a holes - things can move in bulk - aquaporin)
  4. active transport (use ATP)
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10
Q

(Movement by diffusion)

  1. what kind of movement?
  2. permeable membrane
  3. what are the two driving forces?
  4. applies to movement across what two things?
A
  1. “brownian”
  2. concentration, electrical
  3. paracellular (some transcellular) and across capillary walls (endothelial barrier)
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11
Q

(Movement by transporters)

  1. are tranpsorters extremely specific?
  2. faster or slower than channels?

why?

  1. What are the 3 general types?
A
  1. many of them are
  2. slower

binds substance stronger (for specificity)

carrier protein undergoes more elaborate conformational change

  1. uniport, symport and antiport, primary active transport
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12
Q

(uniporters)

  1. what kind of diffusion?

follows what?

what facilitates movement?

  1. permit movement of single solute
  2. solute binds to site alternately available to one side and then the other side of the membrane
A
  1. facilitated

electrochemical gradient

transporter protein

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13
Q

(Symporters and Antiporters)

A
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14
Q

big picture thing to see here

Na is carrying glucose in, carrying AA in, bunch of metablic anions in, and exchange of Na for H (which will combine with HCO-3 - which makes CO2 and water)

thing that runs the whole system is the NA-K ATPase pump - this establishes the gradient (keeps Na low in intra and K high in intra

all movement based on very low Na in cell

A
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15
Q

(Movement by channels)

  1. Channels can move large amounts of substances how fast across membranes?
  2. what is specificity like?
  3. How is movement through the pore controlled?

(pic is slide before)

A
  1. rapidly
  2. low
  3. opening and closing the pore
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16
Q

(Secondary Active Transport)

  1. Secondary because what?
  2. energy from what?
  3. energetics of Na distribution always favor what?
A
  1. ATP not hydrolyzed
  2. transport of another solute (often sodium)
  3. entrance to the cell
17
Q

(Primary Active transporters)

  1. Moves 1 or more solutes up electrochemical gradient using what?

(Sodium pump: Na-K-ATPase)

  1. maintains what?
A
  1. energy from ATP hydrolysis
  2. low Na and high K intracellular stoichiometry (3 Na to K for every ATP)
18
Q
A
19
Q
A

C

20
Q

(Hydrostatic Flow, Osmosis and Oncotic Pressure)

A
21
Q
A

B

22
Q

(The Renal Tubular Epithelia Barrier)

  1. solute permeability less than or more than that of water for all solutes?
  2. thus.. what contribute to driving water flux?
  3. What is net flux (the direction)?
A
  1. less than
  2. all solutes (small ions, glucose, proteins (oncotic pressure))
  3. renal tubule –> capillary lumen
23
Q

(Reabsorption: Transport Mechanisms)

  1. most transport in kidneys is what?
  2. most reabsorption occurs where?

(most movement essentially iso-osmotic)

  1. glomerular filtrate - same or different as plasma?
  2. is proximal tublue reabsorption iso-osmotic?
  3. Distal nephron - water and solute absorption are usually what?
A
  1. reabsorption
  2. PT
  3. nearly the same
  4. yes
  5. divergent (this occurs because in the ascending limb there is no movement of water…Na can be moved without water following at around)
24
Q

(PT Reabsorption)

(Reabsorption in PT is mostly of what…)

1-2. what two things?

  1. Are PT cells permeable to water?
  2. what does water follow?
A
  1. sodium
  2. anions to maintain electoneutrality (chloride and bicarbonate)
  3. highly permeable
  4. the solute
25
Q

(Interstitium to Caps)

(Solute and water move into capillaries)

1-2. under what pressures?

  1. Rapid blood flow in peritubular capillaries does what?
A
  1. capillary hydraulic pressure
  2. plasma oncotic pressure
  3. sweeps away solute and electrolytes
26
Q
A
27
Q
A

C

28
Q
A

this happens over the entire body

29
Q

(Transcellular Transport)

  1. Involves crossing how many membranes?
  2. which ones?
  3. are transporters same or different in each?
  4. transcellular transport requires that the epithelial cells be what?
A
  1. two
  2. apical and basolateral
  3. different
  4. polarized (apical and basolateral membranes are not the same - promtoes net movement of Na from lumen to interstitium)

(in pictured he said something about loss of brush border causing change in polarity)

30
Q

he talked about this a fair amount

A
31
Q

(Key Points)

  1. most transcellular transport in the proximal tubules results from what?
A
  1. active transport of Na across basolateral surface of PT cells
32
Q

1-3. What are three kinds of passive reabsorption?

A
  1. simple diffusion
  2. paracellular transport
  3. non-ionic transport
33
Q

(Passive reabsorption)

  1. occurs by simple diffusion
    (example: urea)
  2. urea reabsorbed in what tubular segments?
  3. Reabsorption in proximal tubules is by what route?

3-4. Reabsprotion determind by what two things?

A
  1. most of them
  2. paracellular route
  3. concentration gradient (tubular lumen –> interstitium)
  4. permeability of tight junctions
34
Q

(Key point)

  1. passive reabsorption fo urea is facilitated by what?
  2. This causes urea concentration to increase where?
A
  1. greater removal of sodium with water (isotonic) upstream
  2. downstream (thus facilitating diffusion down concentration gradient)