What is Resorbed Where and Why Flashcards

1
Q

Describe the primary filtrate

A

As it leaves the renal corpuscle, the primary filtrate is iso-osmotic to the
plasma and has approximately the same composition as far as small
molecules are concerned

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2
Q

What happens in the proximal tubule?

A

-Sodium is pulled through by the basal pump
-Glucose, amino acids etc are pulled through by the sodium gradient.
-Phosphate etc are pulled through by the sodium gradient.
-Potassium is dumped into
tubule lumen, again due to
the basal pump
-HCO3- is recovered, with a
bit of H+ cycling, again powered by the sodium gradient.

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3
Q

Where is water in the Proximal tubule?

A
All of this solute movement
tries to lower the osmolarity
of the tubule, so water flows
passively from the tubule to
counteract this (through aquaporins)
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4
Q

Where is chloride in the proximal tubule?

A

Chloride also leaves passively to stop its concentration
rising in the tubule
-Charge (sodium)
concentration gradient (water)

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5
Q

How is the proximal tubule adapted to its function?

A

-Microvilli
-Pack a lot of length into a small space
=Large surface area

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6
Q

What does the proximal tubule achieve overall?

A

-65% recovery of sodium, chloride, phosphate, calcium, amino acids…
-Slightly higher percentage of glucose
-Some recovery of water (65%)
=Concentration of urine still iso-osmotic
=No control of acid/base

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7
Q

Why do we need to concentrate the urine and recover more ions?

A
  • Renal filtrate flow 1.2L/min = 1700L/day
  • Proximal tubule recovery 65% so loss would be 35% of 1700L = 595L
  • Human drinks around 2L/day and eats 3g salt
  • Without concentration, would need to drink 595L/day and eat 2kg salt
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8
Q

How does the kidneys concentrate urine?

A
  1. Do not have water pump
  2. Na+/K+ ATPase
  3. SLCs and ion channels that can parasitize the Na+ gradient to move ions and small molecules about
  4. Osmosis- water follows ions
    Therefore need to provide more destination more concentrated than urine to recover water= area in tissues more concentrated in ions
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9
Q

How is the rest of the tubule adapted to make a concentrated area of ions?

A

-Tight junctions so water cannot passively diffuse across- to make a super-concentrated area of ions
-No aquaporins so water cannot travel across
=hypertonic basal side area of ions as ion transport still occurs

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10
Q

Describe the Loop of Henle

A

-Thin walled loop structure
=descending limb down towards middle if kidney (medulla)
=ascending limb, thickening at end

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11
Q

Compare the descending and ascending limbs of the Loop of Henle

A
  • Descending thin limb= permeable to water, impermeable to ions and urea (doesn’t pump ions)
  • Ascending thin limb= impermeable to water, permeable to ions (active transport) and urea
  • Thick ascending limb= active recovery of ions (driven by Na pump)- makes the area very salty for the descending limb
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12
Q

Describe water movement in the descending limb and why it occurs

A

-Lots of aquaporins in descending limb so water drawn out of descending limb
=urine more concentrated
-Locally very hypertonic as many ions in concentrated urine recovered in ascending limb
*positive feedback system

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13
Q

What typical osmolarity values are associated with the Loop of Henle?

A
  • 0.29 osmole/kg in renal corpuscle
  • 1.4 in descending limb as tubular contents gets much more concentrated
  • 0.1 in thick ascending limb as gets more diluted because so much has been recovered
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14
Q

What does the mechanism of the Loop of Henle recover?

A

-10% filtered water
-25% Na+ and Cl-
=75% water and 90% NaCl recovered so far from urine

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15
Q

How does the kidneys stop the high osmolarity of the Henle’s loop area being washed away?

A
  1. Loops in same area and all renal corpuscles elsewhere (0.29 renal corpuscles so cortex, 1.4 medulla)
  2. Organised blood system (main transport system that could cause problems)
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16
Q

How does the kidney stop out hypertonic region being swept away by blood flow in the tissues?

A

-The blood vessels emerging from the glomerulus go on to
form a secondary capillary system – the vasa recta
-Blood comes in up the concentration gradient and goes out the exact opposite way
=afferent arteriole, leaves glomerulus as afferent arteriole- goes down past the ascending limb and wraps around the loop of Henle of the same nephron

17
Q

Describe counter current exchange

A
  • As blood comes down, enters hypertonic region so water drawn out, ions diffuse into it passively
  • Blood more concentrated as it reaches bottom
  • Up around descending limb= moving away from hypertonic region so ions given back and picks up water
  • Oxygen short-circuits to ascending capillary so medulla is oxygen poor
18
Q

Describe the urine concentration in the distal tubule

A
  • Active ion pumping in distal tubule to recover more salt

- Very dilute urine (losing salt not raising in volume)

19
Q

Describe the anatomy of the distal tubule

A
  • For developmental reasons considered end of nephron
  • Leads directly onto branched urine collecting duct system
  • Collecting duct leads from cortex back through hypertonic zone and medulla of kidney to renal pelvis (basin-like urine collecting system in middle of kidney)
20
Q

Why is water reabsorbed from the collecting duct?

A

As the collecting duct takes urine back through the hypertonic zone= area of osmotic gradient which will pull water out into the medulla

  • At top of collecting duct, water from dilute urine can equilibrate with plasma
  • More salt recovery occurs (2-5%)
  • Up to 24% of the filtered water recovered here (up to 99% recovered overall)
21
Q

Why is the water reabsorption regulated?

A

-Sometimes dont want to recover all the water you can
-Not all extra fluid as perspiration so volume of urine increases
-Active, evaporation of perspiration= short of water so recover more
=Homeostasis

22
Q

How is water reabsorption regulated in the collecting duct?

A
  • Presence of aquaporins in cell membrane

- Either on plasma membrane (to mediate transport) or taken into vesicles inside cell to store them

23
Q

What is water regulation mediated by?

A

-AVP or vasopressin hormone

24
Q

Describe the transport of urea

A
  • In collecting duct cells
  • Passive transporters for urea
  • Very concentrated in urine so diffuses down concentration gradient out of urine to aid hypertonic area of medulla
25
Q

How does the function of the loop of Henle depend on its anatomical arrangement?

A

-Separation between normal and hypertonic zones
-Route to pass again through hypertonic route
=Normal zone on outside of organ and hypertonic zone near place that urine collects
=Group several units around central urine collecting place

26
Q

Describe the anatomy of the kidney

A

-Cortex (renal corpuscles, PCT and DCT)
-Medulla (LoH, collecting duct)
-Renal pyramids drain into renal papilla into renal pelvis
Calyces= big branches of pelvis
-Kidneys surrounded by tough capsule for protection

27
Q

How is there individual variation in artery supply to the kidney?

A

-Sometimes renal artery will break up into arterioles before it has reached the kidney

28
Q

Why are the kidneys sensitive to ischaemia?

A

-The long runs of parallel arteries/ arterioles and veins/venules mean
that there is counter current exchange of oxygen, so that much gets shunted from artery to vein before the blood enters capillaries
-Low renal oxygen -> erythropoietin release -> more red cells made in bone marrow

29
Q

What things can be altered in the filtration of the kidneys/ urine production?

A
  1. Blood flow to glomerulus
  2. Na+ recovery
  3. Urea recovery by collecting duct
  4. Water permeability of collecting duct
  5. Acid-base balance in collective duct
30
Q

How can blood flow to and in the kidney be controlled?

A
  1. Systemic blood pressure
  2. Constriction of afferent arterioles (lowers glomerulus pressure)
  3. Constriction of efferent arterioles (raises glomerulus pressure- also in diabetic changes in vessels)
31
Q

What are the limits of the kidney’s ability to regulate blood flow in the glomerulus?

A
  • 80 to 180 mmol pressure= safe window which management can hold pressures steady
  • If too high= glomerular pressure to high
  • Too low= filtration cant be remained at same rate
32
Q

What are the mechanisms that control pressure?

A
  1. Direct pressure sensing in the afferent arteriole (myogenic mechanism)
  2. Monitoring the performance of the nephron (tubuloglomerular feedback)
33
Q

Describe the myogenic mechanism

A

Stretch activated cation channels depolarize membrane and cause
smooth muscle to contract: fast and protective against acute surges

34
Q

Describe the tubuloglomerular feedback mechanism

A

Central heating takes measurement of room in order to feedback performance of system to boiler
-Measure by assessing salt concentration in distal tubule, feed information back to control constriction of arterioles

35
Q

What are the problems with tubuloglomerular feedback?

A

We need this control to be nephron-by nephron, not global, so we can’t have a
signal diffusing long distances.

36
Q

What is the solution for the tubuloglomerular problem?

A

Arrange a nephron so that the end of the distal tubule makes ‘kissing contact’ with the arterioles entering the glomerulus

  • A special zone of the distal tubule (macula densa) forms where the contact is made with specialised cells
  • Together= juxtaglomerular apparatus
37
Q

How does the macula densa work?

A

-Elevated glomerular blood pressure
=Filtrate flows faster
=Less time for solute recovery in PCT and LoH
=More NaCl remains in the distal tubule
=Macula densa cells pump out more NaCl than they usually can as more available
=Juxtaglomerular cells release adenosine
=Afferent arteriole constricts in response to adenosine