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
Q

Resorptive defect of NaCl in DCT; leads to hypokalemia and metabolic alkalosis without hypercalciuria

A

Gitelman Syndrome (autosomal recessive)

26
Q

Increased Na reabsorptionin distal and collecting tubules by increasing ENaC. Causes HTN, hypokalemia, metabolic alkalosis, decreased aldosterone

A

Liddle Syndrome

27
Q

Tx of Liddle Syndrome

A

Amiloride