test 8 part 2 Flashcards

(31 cards)

1
Q

Reabsorption – Proximal Tubule

A

 65% of filtered load of sodium & water reabsorbed

 Little less percentage for chloride

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2
Q

Proximal Tubule Cellular Ultrastructure

A
  • Contain large number of mitochondria to support extensive active transport activity
  • Luminal (apical) brush border
     Provides huge surface area for rapid diffusion
     Contains extensive number of protein carrier molecules
  • Basolateral border
     Contains extensive number channels in between cells providing huge surface area
     Contains extensive amount of N-K ATPase
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3
Q

First half of tubule of proximal reabsorption

A

 Extensive co-transport of sodium with glucose and amino acids
 Sodium reabsorption carries glucose, bicarb, organic ions leaving chloride resulting in increasing [Cl-]
 105 mEq/L increases to 140 mEq/L

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4
Q

Second half of tubule of proximal reabsorption

A

 Most glucose & amino acids have been reabsorbed –
 Electrochemical gradient
 Sodium reabsorption drives chloride reabsorption
 High chloride concentration favors chloride diffusion

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5
Q

Sodium concentrations thorugh the tubule vs quantity

A

 Total quantity of sodium in tubule changes but concentration does not change because water reabsorption matches sodium reabsorption
 Total osmolarity does not change for the same reason
 Proximal tubule highly permeable to water

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6
Q

Glucose & amino acid concentrations through proximal tubule

A
  • decrease due to extensive reabsorption
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7
Q

Creatinine & Urea concentrations through the proximal tubule

A
  • concentrated because they are not reabsorbed
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8
Q

Total amount of Na+, Cl-, HCO3-,glucose, amino acids in tubule

A

decreases

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9
Q

Total amount of creatinine and urea in tubule

A

does not change

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10
Q

Secretion of Organic Acids & Bases

A

 Many end products of metabolism are secreted by proximal tubule
catecholamines
 Many drugs & toxins secreted
 Para-aminohippuric acid also secreted
 90% of PAH in renal blood flow is removed
-PAH can be used to determine renal blood flow

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11
Q

Functional Segments of the Loop of henle

A
  1. Thin descending segment
  2. Thin ascending segment
  3. Thick ascending segment
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12
Q

Thin Descending & Ascending Segment

A

 Thin epithelial membrane
 No brush border
 Few mitochondria
 Minimal metabolic level

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13
Q

Thin Descending Segment

A

 Highly permeable to water
 Moderately permeable to most solute
 Allows diffusion of water and solutes (No active reabsorption)
 20% of water reabsorption occurs in the loop of Henle

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14
Q

Thick Ascending Segment

A

 Thin and thick ascending segment impermeable to water (lumen is hypo-osmotic)
 Part of mechanism for concentrating urine
 Thick epithelial cells with high concentration of mitochondria
 High level of metabolic activity
 Able to reabsorb sodium, chloride, & potassium (Approx 25% of filtered load)
 Also reabsorbs calcium, bicarb, and magnesium

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15
Q

Thick Ascending Segment: Sodium Reabsorption

A

 Driven by N-K ATPase in basolateral border of tubule cells
 Two transport mechanisms move sodium from tubular lumen
 1 Na-2Cl-1K co-transport mechanism (all move into the cell) (PRIMARY MEANS OF MOVING SODIUM OUT OF LUMEN INTO TUBULAR CELLS)
 Na-H counter-transport mechanism

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16
Q

Loop Diuretics

A

 Loop diuretics inhibit the action of the 1Na- 2Cl-1K co-transport mechanism
- Less sodium reabsorption
 Less water reabsorption in later segments of the nephron
 Less potassium reabsorption with potential loss of potassium

17
Q

Paracellular reabsorption of what solutes

A

 Sodium
 Potassium
 Magnesium
 Calcium

18
Q

Na-Cl-K co-transport mechanism

A

 Isoelectric BUT K able to diffuse back into lumen via potassium channels creating +8 mV positive charge in tubule lumen

19
Q

Early Distal Tubule

A

 Macula densa forms first part of tubule
 Provides feedback control for GFR and blood flow (for its own nephron)
 Solute reabsorption: Yes
 Water reabsorption: NO
 Diluting segment of distal tubule
 5% of filtered load for sodium & chloride reabsorbed here
 Driven by Na-K ATPase in basolateral border of tubular cells
 Na-Cl co-transport mechanism moves Na+ and Cl- into cell down [Na+] gradient
 Chloride diffuses out of cell via chloride specific channels

20
Q

Thiazide diuretics

A
  • inhibit this Na-Cl co-transport mechanism in the early distal tubule
     Reduces sodium and chloride reabsorption
     Ultimately reduces water reabsorption in later segments of nephron
21
Q

Functional Characteristics – Late Distal Tubule and Cortical Collecting Tubule

A

 Membranes impermeable to urea
 Some reabsorption of urea will occur in medullary collecting ducts
 Sodium reabsorption and potassium secretion controlled by various hormones especially aldosterone
 Able to secrete hydrogen ions against large concentration gradient (1000:1)
 Proximal tubule moves hydrogen ions against small gradient (4:1 to 10:1)
 Water permeability controlled by concentration of antidiuretic hormone (ADH, aka vasopressin)
 No ADH - no water permeability – excrete dilute urine

22
Q

Principal cells

A

 Reabsorb sodium & water

 Secrete potassium

23
Q

Intercalated cells

A

 Reabsorb potassium

 Secrete hydrogen

24
Q

two types of cells in the Late Distal Tubule and Cortical Collectin Tubule

A

 Principal cells

 Intercalated cells

25
Principal Cell Activity
 Na-K ATPase in basolateral borders of tubule cells drives activity  Sodium follows concentration gradient into the cell through Na specific channels  Potassium follows concentration gradient out of cell into tubular lumen through K specific channels
26
Potassium Sparing Diuretics - Aldosterone antagonists
 Mineralocorticoid receptor antagonists  Compete with aldosterone receptor sites which inhibits sodium reabsorption and potassium secretion  Spironolactone & eplerenone
27
Potassium Sparing Diuretics - Sodium Channel Blockers
 Inhibit entry of sodium into cell which reduces amount of sodium transported by Na-K ATPase  Also reduces secretion of potassium as action of Na-K ATPase decreases  Amiloride & triamterene
28
Intercalated Cell Activity – Hydrogen Ions
 Secretion controlled by H-ATPase transporter – tubular border  Presence of carbonic anhydrase allows conversion of CO2 and H2O to hydrogen and bicarb ions  Chloride also secreted following electrochemical gradient  Bicarb reabsorbed using Cl-HCO3 - counter-transport mechanism following the Cl- gradient into the cell – basolateral border  CO2 moved freely between cell and interstitial fluid  Potassium is also reabsorbed
29
Meduallary Collecting Ducts
 Reabsorb approximately 10% of filtered water and sodium  Determines final concentration of solutes and urine concentration  Epithelial cells smooth with few mitochondria  Water permeability controlled by ADH  Urea is reabsorbed via specific urea transporters which moves urea into the interstitial spaces thus affecting osmolarity  Secretes hydrogen ions (like cortical collecting tubule)
30
Solute Concentrations graph
- anything above one = tubular concentration is higher than plasma concentration - Less reabsorption - more secretion - or both
31
Inulin
- neither secreted or reabsorbed (plasma concentration and inulin concentration in boweman's capsule is the same)  Provides indication of water reabsorption  [Inulin] of 3 means that 1/3 of the water remains in the tubule (2/3 has been reabsorbed)