GFR physiology Flashcards

1
Q

Factors affecting GFR

A
  • Sympathetic VC causes afferent and efferent vasconstriction and decrease in GFR
  • Catacholamines - Constrict firstly the afferent
  • Angiotensin II - Constricts the efferent at low
  • Both afferent and efferent at high pressures
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2
Q

What are the BP values the kidney can autoregulate at?

A

60-130mmHg

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3
Q

Why is reabsorption favoured in the peritubular capillaries

A
  • Due to efferent arteriole offering resistance along entire duration there is large decrease hydrostatic pressure (15mmHg)
  • Due to some plasma being filtered through capillaries there is an increase in plasma proteins and therefore plasma colloid osmotic pressure in capillaries
  • Low hydrostatic in efferent and high osmotic pressure results in the favour in absorption
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4
Q

Describe the molecules involved in carrier mediated transport systems, Tm, maxiumun transport capacity system

A
  • Glucose, amino acids, organic acids, sulphate, phosphate
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5
Q

What is the renal threshold?

A

Plasma level at which saturation occurs

e.g = 10 for glucose

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6
Q

What other substances use Tm mechanism

A

Sulphate and phosphate

  • Set at such a level that normal plasma causes saturation
  • Any increase in this normal level will cause plasma to be excreted
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7
Q

What percentage of Na is absorbed in proximal tubule and by what means?

A
  • 65-75% by active transport
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8
Q

Explain the absorption of sodium from the lumen to the Interstitial fluid?

A
  • Na passivley diffuses at the apical membrane due to the low concentation in the tubule cells
  • Active Na/K pumps are located on the basolateral membrane, this decreases Na within the cells providing the concentration gradient for Na to move passivley in from the tubule
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9
Q

Why is Na permabile at the tubule cells and not most other places in the body

A
  • Due to large amount of Na channels and surface area offered by microvilli
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10
Q

How do anions such as Cl diffuse

A
  • Passivley due to the concentration gradient provided by the Na/K pump transporter
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11
Q

Why is Na so significant in reabsorption?

A

Determines the gradient of the other ions, and establishs the gradients of the other ions, anything that decreases active transport of Na, will disrupt the whole system

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12
Q

Na reabsorption with glucose

A

Na is involved with the reabsorption of glucse

  • The SGLT2 transporter faciliates the movment of glucose into the cell against its concentration gradient
  • Passes via GLUT 1 into the intersitial fluid
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13
Q

What substances are reabsorbed in the kidney tubule?

A
  • Sulphates, amino acids, sulphate, lactate, phosphate, FA

-

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14
Q

How are substances secreted?

A
  • Tm Carrier mechanisms
  • Not very specfic, ie organic acid mechainism which secretes lactic and uric acid can also be used for penicilln asprin and PAH
  • Organic base mechanisms for choline & creatinine can be used for morphine/atrophine
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15
Q

What is the normal K value?

A
  • 4 mmoles/L
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16
Q

What happens above 5.5

A
  • Resting membrane potential decreases, membrane gets excited and ventricullar vibrillation occurs
  • Calcium gluconate
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17
Q

What happens when K below 3.5

A
  • Hypokalemia,
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18
Q

Where is K reabsorbed and secreted

A
  • Reabsorbed in the proximal

- Excreted in the distal tubule

19
Q

How is K regulated

A
  • By aldosterone secreted in the zona glomerularis, Increased K secretion and Na reabsorption
  • H ions are also secreted to make up for losses
20
Q

How is albumin reabsorbed?

A

Via the Tm mechanism in the proximal tubule

21
Q

How are drugs not reabsorbed considering the are highly nonpolar and not lipid soluble

A
  • The liver metabolises them to polar compounds
22
Q

What substances are reabsorbed 100%

A
  • Glucose, amino acids, FA’s
23
Q

Maximum concenration of urine that can be produced

A

1200-1400 mOsmoles

24
Q

What is the obligotory waste product and water loss values

A

600mOsmoles / 500mOsmoles

25
Q

Describe the loop of henle

A
  • Removes water on descending

- Removes NaCl on the ascending

26
Q

Describe the fluid entering into the loop of henle

A

Enters at 300mOsmoles
Leaves at 100mOsmoles
200mOsmoles difference at any level between intestitium and ascending limb

27
Q

What has the loop of henle achieved

A
  • It has concentrated the interstitial gradient

- 2

28
Q

Describe the counter current exchangers

A
  • The vesa recta acts as a counter current exchanger,
  • Arranged as a hairpin loop, means it does not interfere with the interstitial gradient
  • They reabsorb the water while not interfering with the interstitial gradient
29
Q

What are the functions of the counter current exchanger

A
  • Provide O2 to the medulla
  • Do not disturb the interstitial gradient
  • Removes volume from the interstitium 36/L day
30
Q

What type of hormone is ADH and where is it released from?

A
  • ADH is a peptide hormone released from the posterior pituitary of the hypothalamus
  • It is secreted by the Supraoptic and paraventricular nuclei
31
Q

Where are osmoreceptor located

A
  • The anterior pituitary gland
32
Q

What triggers the release of ADH

A
  • A Increase in osmolarity via stretch sensitive ion channels
  • Cell dehydration due to trying to balance the hypertonic fluid
33
Q

What is the normal plasma osmorality

A

280 - 290

34
Q

Describe the sensitivity of plasma regulatirty

A
  • A mere change of 2.5% outside of the normal 280-290 will result in a large secretion of ADH
35
Q

Describe effective osmorality

A

Osmorality - Non penetrating and penetrating solutes
Tonicity - Non penetrating solutes
- An increase in osmorality that does not increase in tonicty will not cause in increase in ADH secretion

  • i.e Freely permable substances like urea will not create and osmotic drag are not produce osmotic drag or increase ADH secretion
36
Q

How is water reabsorbed at the collecting ducts?

A
  • ADH binds to receptors triggering exocytosis or aquaporin 2 pores into the apical membrane
  • Water is then absorbed via osmosis
37
Q

If ADH is present maximally

A
  • Water is reabsorbed into the interstitum due to the high concentration created by the multipliers
  • H20 is then reabsorbed back via the vasa recta\
  • Highly concentrated, small volume of urine created
38
Q

In the absence of ADH

A
  • ## Collecting duct is impermeable to H20, creating a large volume of dilute urine compensating for ADH excess
39
Q

Explain urea recycling

A
  • Movement of H20 out of the CD greatly concentrates the urea
  • CD membranes are relatively permeable to urea particullarly towards tips
  • Urea is reabsorbed back down its concentration gradient at medullary tips where it acts to reinforce the the intertitium gradient
  • The occurs in an anti-diuresis where high levels of ADH, urea is reaborbed to the thin ascending LoH, Ureamia occurs
  • Urea also has an osmotic effect on water so its important its reabsorbed
40
Q

Describe the other way osmorlatiy is regulated

A

Low and high pressure receptors

  • Low located in the L and R atria of the great veins
  • High located in the Carotid and aortic arch baroreceptors
41
Q

Describe the effect of decrease of volume on receptors

A
  • They normally have a constant inhibitory discharge on ADH, when ECF decreases this discharge stops
  • A moderate decrease in blood pressure will effeect the L and R atria receptors
  • When there is a change in MBP the carotid and aortic baroreceptors will be affected
  • This will increase ADH secretion
42
Q

What other stimuli increase ADH

A
  • Pain, emotion, stress, exercise, nicotine, morphine, following traumatic surgery
43
Q

What main stimuli depresses ADH release

A
  • Alcohol depresses ADH secretion
44
Q

Describe average volumes of fluid

A

Bowmans capsule - 180L/day, 300mOsm
End of proximal tubule - 54L/day, 300mOsm
End of loop of henle - 16L/day, 100mOsm
Collecting duct - 1.5L/day, 50-1200 mOsm