acid and base Flashcards

1
Q

what are the volatile and non-volatile acids produced with respect to blood an renal systems

A
  1. volatile acid
    1. CO2
  2. nonvolatile acid
    1. phsophoric, lactic and sulfuric
    2. ketoacids produced on pathological conditions
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2
Q

what are the three mechanisms (general) for handeling the pH and what is the normal pH?

A
  1. mechanisms
    1. intracellular and extracellular buffering
    2. respiratory compensation alteration in breathing depth and rate
    3. renal compensation
  2. pH
    1. acidemiea<7.37-normal-7.42
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3
Q

What is the description of a buffer?

A

Buffer

  1. weak acid conjugated to a weak base
  2. resist pH change
  3. main in the ECF = HCO3-
    1. buffers volatile and nonvolatile acids
  4. main buffer in ICF = proteins, inorganic phosphates and organic phosphate
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4
Q

what are the main buffering sources of ICF and ECF?

A

Buffer

  1. weak acid conjugated to a weak base
  2. resist pH change
  3. main in the ECF = HCO3-
    1. buffers volatile and nonvolatile acids
  4. main buffer in ICF = proteins, inorganic phosphates and organic phosphate
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5
Q

explain what it means to be below the pK.

A
  1. titratable acids refers to acids that can be titrated with NaOH to a pH of 7.4 (that of normal plasma)
    1. pH=pK, [conjugatebase]=[conjugate acid]
      1. this is where buffering capacity is the greatest
    2. below pKa
      1. more of the ocmpound is in acid form
      2. adding more OH- convertrs tha acid to its conjugate base and combint the H with OH- = increasing the pH.
      3. climbing above pKa value depeletes the acid and accumulates the conjugate base
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6
Q

Where if the buffering capacity the greatest for a buffer?

A
  1. titratable acids refers to acids that can be titrated with NaOH to a pH of 7.4 (that of normal plasma)
    1. pH=pK, [conjugatebase]=[conjugate acid]
      1. this is where buffering capacity is the greatest
    2. below pKa
      1. more of the ocmpound is in acid form
      2. adding more OH- convertrs tha acid to its conjugate base and combint the H with OH- = increasing the pH.
      3. climbing above pKa value depeletes the acid and accumulates the conjugate base
        3.
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7
Q

Kidneys rol in acid-base homeostasis (2-general description)

A
  • roles
    • reabsorb filtered HCO3
    • compensate forbuffer lost by conjugation to nonvolatile acids in plasma
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8
Q

what is a better term to describe the absorption of bicarb? why?

A
  1. becarbonate reabsorption aka reclamation
    1. rather tha absorption, the filtered moiety is destroyed and a new one is produced in its stead.
  2. reclamation occurs in PT or excreted
    1. when in doubt, choose PT
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9
Q

Where does reclamation of bicarb occur?

A
  1. becarbonate reabsorption aka reclamation
    1. rather tha absorption, the filtered moiety is destroyed and a new one is produced in its stead.
  2. reclamation occurs in PT or excreted
    1. when in doubt, choose PT
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10
Q

decribe the location and process of bicarb reclamation

A
  1. apical
    1. tubular brush border = carbonic anhydrase cleaves HCO3- -> H2O + CO2
      1. OH- combines with excreted H+ and generates water
      2. HCO3- combines with H+ and generates H2CO3-> reacts with CA-> H2O +CO2= inert and moves through membrane
  2. intracellular
    1. carbonic anhydrase recombines CO2 and H2O to generate HCO3 and H
    2. H is pumped into the lumen, Na/H exchanger (antiporter)
    3. HCO3 is pumped into the interstitium- mainly occurs in TAL, a little in PT
      1. Na/HCO3 symptorter
      2. Cl/HCO3 antiporter
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11
Q

what enzymes/transporters are active on the apical and basolateral side of the PT cells?

A
  1. apical
    1. tubular brush border = carbonic anhydrase cleaves HCO3- -> H2O + CO2
      1. OH- combines with excreted H+ and generates water
      2. HCO3- combines with H+ and generates H2CO3-> reacts with CA-> H2O +CO2= inert and moves through membrane
  2. intracellular
    1. carbonic anhydrase recombines CO2 and H2O to generate HCO3 and H
    2. H is pumped into the lumen, Na/H exchanger (antiporter)
    3. HCO3 is pumped into the interstitium- mainly occurs in TAL, a little in PT
      1. Na/HCO3 symptorter
      2. Cl/HCO3 antiporter
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12
Q

what are the three locations for H excretion?

A
  1. PT- little
    1. H/NA antiporter
  2. TAL- many
    1. Na/H antiporter
  3. MCD
    1. K/H antiporter
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13
Q

What is the cost to neutralize an acid? how is this managed?

A
  1. acids are neutralized in the blood at a cost of base
    1. new base synthesized to replace that loss
    2. lowest urine pH=4.4
  2. protons bound to buffers, most commonly to form dihydrogen phosphate
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14
Q

Describe how dihydrogen phosphate is formed in the kidneys. Why does it make a really good buffer?

A

generation of New HCO3- by forming a titratable acid

  • HPO2(conjugate base)+H-> H2PO4-(conjugate acid)
  1. properties
    1. pK=6.8
      1. this means it holds onto the H as the pH drops
    2. conjugate base has a high rate of excretion, freely filtered
    3. conjugate acid is not absorbed
  2. HCO3 is secreted on the basolateral side (NOT THE APICAL)
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15
Q

during dihydrogen phosphate generatation, where is the HCO3 secreted and the H secreted?

A

generation of New HCO3- by forming a titratable acid

  • HPO2(conjugate base)+H-> H2PO4-(conjugate acid)
  1. properties
    1. pK=6.8
      1. this means it holds onto the H as the pH drops
    2. conjugate base has a high rate of excretion, freely filtered
    3. conjugate acid is not absorbed
  2. HCO3 is secreted on the basolateral side (NOT THE APICAL)
    1. generated from free OH- and CO2
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16
Q

why is dihydrogen phosphrus titratable and ammonium not?

A
  1. not filtered
    1. produced along with OH- in the epithelial cell by metabolism of Glutamine
  2. during the glut metabolism
    1. HCO3- secreted into the basolateral side
      1. OH- and CO2 combine via carbonic anhydrase
    2. NH4+
      1. intracellularly seperates = ammonia + H+
        1. ammonia is lipid soluble and diffuses across the membrane
      2. recombines in the lumen
      3. pK >9
        1. conjugate acid is very stable and does not dissociate urine
        2. is not titratable, becuase pK is above 7
17
Q

Formation of a new HCO3- from an nontitrable acid. Describe the mechanism.

A
  1. not filtered
    1. produced along with OH- in the epithelial cell by metabolism of Glutamine
  2. during the glut metabolism
    1. HCO3- secreted into the basolateral side
      1. OH- and CO2 combine via carbonic anhydrase
    2. NH4+
      1. intracellularly seperates = ammonia + H+
        1. ammonia is lipid soluble and diffuses across the membrane
      2. recombines in the lumen
      3. pK >9
        1. conjugate acid is very stable and does not dissociate urine
        2. is not titratable, becuase pK is above 7
18
Q

Describe the titrable acid and non titrable acid

  1. where-formed/secreted/reabsorped(only one)
A
  1. titrable acid synthesis-reclaimation (H2PO4)
    1. PT-formed
    2. DCT -formed
    3. IMCD-formed
  2. non titratable acid synthesis
    1. PT-formed/secreted
    2. tDLH- secreted
    3. TAL--REABSORPTION
    4. OMCD-secreted
19
Q

Formed in the PT, reabosored in the TAL and secreted in the PT, tDLH, and OMCD

A
  1. titrable acid synthesis-reclaimation (H2PO4)
    1. PT-formed
    2. DCT -formed
    3. IMCD-formed
  2. non titratable acid synthesis
    1. PT-formed/secreted
    2. tDLH- secreted
    3. TAL--REABSORPTION
    4. OMCD-secreted