Week 1: Glomerular filtration and Regulation of renal blood flow and GFR Flashcards

1
Q

Apply the starling equation that describes fluid movement across the capillary walls in a form applicable to glomerular capillaries.

A

GFR=Kf(Pgc-Pbs)-(Ogc-Obs)
Pgc=hydrostatic pressure go glomerular capillary
Pbs=Bowman’s space hydrostatic pressure
Ogc: oncotic pressure of glomerular capillary

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2
Q

Discuss how and why each of the variables on the right side of the Starling equation changes as a function of distance along the glomerular capillary

A

GFR=Kf(Pgc-Pbs)-(Ogc-Obs)

  • starling forces favor filtration all along glomerular capillaries
  • further along the glomerular capillary, the glomerular capillary oncotic pressure increases, decreasing the pressure driving filtration (from -28 to-35mmHg from afferent to efferent)
  • hydrostatic pressure of gc kept high throughout, slight 2mmHg drop
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3
Q

How does varying Ra change GFR and RBF?

A
  • Constrict afferent arteriole: decreases GFR, decreases RBF (e.g. to maintain GFR during high bp)
  • Constrict efferent arteriole: increases GFR, decreases RBF (e.g. AngII)
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4
Q

Differentiate how molecular size and electrical charge on glomerular pores affects filtration of solutes.

A
  • glomerulus is like sieve. Selectivity determined by size and charge
  • endothelial cell surface coat contains negatively charged proteoglycans: charge selectivity
  • Basement membrane has size and charge selectivity
  • slit diaphragms have size selectivity
  • clearance: cationic>neutral>anionic
  • filtration barrior repel (-) charged macromolecules
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5
Q

Summarize the role of nephron-nephrin interaction in setting of the dimensions of the filtration slit.

A

-Nephrin molecules from opposite foot processes make the slit diaphragm. Disulfide bonds.

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6
Q

Explain what is meant by autoregulation of GFR and renal blood flow.

A

-regulation and maintenance of constant RBF and GFR by control of afferent arteriolar resistance when arterial BP is varied between 90-180mmHg

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7
Q

ID the arteriole that mediates auto regulation and the two mechanisms that modulate the resistance of this arteriole to achieve auto regulation.

A
  • The afferent arteriole
    1. Myogenic mechanism: intrinsic property of smooth muscle to contract when stretched
  • increased perfusion pressure–> causes afferent arteriolar resistance to increase and diameter of arteriole to decease to normalize flow rate
  • decreased perfusion pressure–> Ra decreases and radius increases to normalize flow
    2. Tubuloglomerular feedback: macula densa cells sense transport of NaCl by NaK2Cl transporters in TALH
  • if [NaCl] deliver too high, signals sent to constrict afferent arteriole–> decrease GFR
  • if [NaCl] deliver too low, signals turned off
  • Unrelated: when [NaCl] too low at macular dense, signals sent to increase renin in JG cells.
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8
Q

What are factors that affect GFR?

A

changes in the following:

  • Glomerular capillary pressure is a fxn of afferent and efferent arteriolar resistance, blood pressure
  • Kf is influenced by SNS, AngII
  • Plasma protein concentraiton (Ogc) is due to extra renal changes in protein synthesis.
    1. Sympathetic stimulation: increases Ra and Re, decreases Kf (activated by baroreceptors when bp low)
    2. AngII constrictions both but favors increases Re (when ECF volume low)
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9
Q

What are stimuli that increase NaCl at macula densa?

A
  1. increase arterial pressure–>decreased NaCl reabsorption in PT (increased NaCl in tubular lumen)–>stimulates TGF–> decreases GFR and RBF
  2. increased GFR (increased perfusion pressure)–>increase NaCl deliver via filtration–> activates TGF–> decreases GFR to control levels
  3. anything that decreases NaCl reabsorption in PT or TALH increases volume flow to macular densa–>activates TGF–>reduces GFR
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