Nephron Physiology Flashcards

1
Q

PTH effects on proximal convoluted tubule

A

Inhibits Na/PO4 cotransport; Phosphate excretion

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2
Q

AngII on proximal convoluted tubule

A

Stimulates Na/H exchange; Reabsorbs Na, H2O, and HCO3-

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3
Q

65-80% of Sodium Reabsorbed

A

Proximal Tubule

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4
Q

Tonicity of Proximal Tubule

A

Isotonic

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5
Q

Reabsorbs all of the glucose, AA and most of HCO3, Na, Cl, PO4, K and H2O

A

Proximal tubules

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6
Q

Passive reabsorbs H2O via medullary hypertonicity; impermeable to Na. Concentrating segment making urine hypertonic

A

Thin descending loop of Henle

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7
Q

Indirectly induces paracellular reabsorption of Mg and Ca; potential is generated by K

A

Thick ascending limb of Henle

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8
Q

Impermeable to H2O

A

Thick ascending limb of Henle

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9
Q

Reabsorbs Na/K/2Cl

A

Thick ascending limb of Henle

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10
Q

10-20% Na reabsorbed

A

Thick ascending limb of Henle

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11
Q

Actively absorbs NaCl and makes urine hypotonic

A

Early distal convoluted tubule

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12
Q

PTH effects on Early distald Convoluted tubule

A

Increases Calcium reabsorption with Ca/Na-exchange

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13
Q

5-10% Na reabsorbed

A

Early Distal Convoluted tubule

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14
Q

Reabsorbs Na in exchnage for secreting K and H

A

Collecting tubules, in response to aldosterone

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15
Q

Insertion of sodium channel on luminal side

A

Aldosterone, collecting tubule

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16
Q

V2 receptor

A

ADH in collecting tubule

17
Q

Inserts aquaporin H2O on luminal side

A

ADH in collecting tubule

18
Q

3-5% Na reabsorbed

A

Collecting tubule

19
Q

Block ENaC in Collecting tubule

A

Amiloride, Triamterene

20
Q

Thiazide Diuretics

A

Block Na/Cl cotransporter in Early convoluted tubule

21
Q

Loop Diuretics

A

Blook Na/K/2Cl channel in TAL

22
Q

Reabsorptive defect in PCT; associated with increased excretion of nearly all amino acids, glucose, HCO3-, and PO4

A

Fanconi Syndrome

23
Q

Causes of Fanconi Syndrome

A

Hereditary defects like Wilson dx, ischemia, and nephrotoxins/drugs

24
Q

Reabsorptive defect in TAL; affects Na/K/2Cl cotransporter causing hypokalemia, metabolic alkalosis with hypercalciuria

A

Bartter Syndrome (autosomal recessive)

25
Resorptive defect of NaCl in DCT; leads to hypokalemia and metabolic alkalosis without hypercalciuria
Gitelman Syndrome (autosomal recessive)
26
Increased Na reabsorptionin distal and collecting tubules by increasing ENaC. Causes HTN, hypokalemia, metabolic alkalosis, decreased aldosterone
Liddle Syndrome
27
Tx of Liddle Syndrome
Amiloride