Acute Renal Tubular Acidosis Flashcards
The proximal tubule reabsorbs
HCO3 (90%) Ca Glucose Amino acids NaCl H20
Action of carbonic anhydrase inhibitors
They block reabsorption of HCO3; useful in alkalinizing urine
Main pathophysio of renal tubular acidosis
Transport defects in the reabsorption of bicarbonate and the excrertion of hydrogen ion
Features of Renal tubular acidosis
Metabolic acidosis
Normal anion gap
Hyperchloremia
Hypokalemia
Difference in the measured cations and anions in serum, plasma, or urine
Anion gap
Normal anion gap
12+- 2 mEq/L
Primary physiologic regulator of net acid secretion
Extracellular pH
T or F. In RTA there is academia so the urine is also acidic
False, urine is basic because there is difficulty in acidification of urine
TorF. For every 1 HCO3 absorbed 1 H secreted
True
Transporter used in H secretion into tubular lumen for renal acidification
NHE3
Approximately 85% of filtered HCO3 is absorbed by the
Proximal tubule
remaining 15% of the filtered HCO3 is reabsorbed in the
thick ascending limb and in the outer medullary collecting tubule
How is ammonium produced
Catabolism of glutamine in the proximal tubule
Transporter for ammonia
None, it passivel diffuses in and out of the cell
Luminal NH4 is partially reabsorbed in the ________
Thick ascending limb
The thick ascending limb reabsorbs abt 15% of the filtered HCOR through
Na H apical exchange
major site of H+ secretion and is made up of the medullary collecting duct (MCT) and the cortical collecting duct
Collecting tubule
main cells involved with H+ secretion in the CT
Alpha intercalated cells
Luminal exchanger in beta intercalated cells
Cl/HCO3
Most important site of urinary acidification
Medullary portion of the collecting duct
T or F: Increased urine ammonium levels is probably a renal cause
False: extrarenal
If decreased- renal
Difference of metabolic acidosis in diarrhea and RTA
In RTA there’s Low excretion of urinary NH4 as compared to high excretion in diarrhea
Fanconi syndrome is often due to generalized proximal tubular dysfunction manifested by
Glycosuria
Generalized aminoaciduria
Phosphaturia
Type of RTA where there’s isolated bicarbonate defect
Proximal RTA
Nephrolithiasis, nephrocalcinosis and bone disease are common in this type of RTA
Distal RTA (type 1)
Disorder leading to HCMA secondary to impaired proximal reabsorption of filtered bicarbonate
pRTA