Week 1: Glomerular filtration and Regulation of renal blood flow and GFR Flashcards
Apply the starling equation that describes fluid movement across the capillary walls in a form applicable to glomerular capillaries.
GFR=Kf(Pgc-Pbs)-(Ogc-Obs)
Pgc=hydrostatic pressure go glomerular capillary
Pbs=Bowman’s space hydrostatic pressure
Ogc: oncotic pressure of glomerular capillary
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
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
How does varying Ra change GFR and RBF?
- 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)
Differentiate how molecular size and electrical charge on glomerular pores affects filtration of solutes.
- 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
Summarize the role of nephron-nephrin interaction in setting of the dimensions of the filtration slit.
-Nephrin molecules from opposite foot processes make the slit diaphragm. Disulfide bonds.
Explain what is meant by autoregulation of GFR and renal blood flow.
-regulation and maintenance of constant RBF and GFR by control of afferent arteriolar resistance when arterial BP is varied between 90-180mmHg
ID the arteriole that mediates auto regulation and the two mechanisms that modulate the resistance of this arteriole to achieve auto regulation.
- 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.
What are factors that affect GFR?
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)
What are stimuli that increase NaCl at macula densa?
- increase arterial pressure–>decreased NaCl reabsorption in PT (increased NaCl in tubular lumen)–>stimulates TGF–> decreases GFR and RBF
- increased GFR (increased perfusion pressure)–>increase NaCl deliver via filtration–> activates TGF–> decreases GFR to control levels
- anything that decreases NaCl reabsorption in PT or TALH increases volume flow to macular densa–>activates TGF–>reduces GFR