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Renal Blood Flow

Renal Blood Flow. Total renal blood flow: TRBF ~ 1270 ml/min ~ 20-25% of CO (5000 ml/min) ~ 90% to cortex Total renal plasma flow: TRPF ~ 700 ml/min (Hct ~ 0.45) Filtration fraction ~ 20% (GFR = 125 / 700 ml/min) The low medullary flow is due to high resistance of the vasa recta.

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Renal Blood Flow

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  1. Renal Blood Flow

  2. Total renal blood flow: TRBF ~ 1270 ml/min ~ 20-25% of CO (5000 ml/min) ~ 90% to cortex • Total renal plasma flow: TRPF ~ 700 ml/min (Hct ~ 0.45) • Filtration fraction ~ 20% (GFR = 125 / 700 ml/min) • The low medullary flow is due to high resistance of the vasa recta. • Low flow is required to maintain the medullary concentration gradient.

  3. Autoregulation: • Both RBF and GFR remain relatively constant in spite of marked changes in arterial blood pressure. • Over mean arterial pressure from 80 to 180 mm Hg, both RBF and GFR change little. • This phenomenon is called autoregulation as it is the result of intrinsic renal mechanisms and it does not depend on nerves or on extrarenal hormones.

  4. Regulation of GFR prevents changes in solute & water excretion with changes in arterial BP. However, 1. Autoregulation is not perfect, changes of renal artery pressure do cause changes in RBF and GFR. 2. Autoregulation is virtually absent at mean arterial pressures < 70 mmHg. 3. Despite autoregulation, RBF & GFR can be significantly altered by the sympathetic nervous system and the renin-angiotensin system.

  5. The afferent arterioles regulation of renal vascular resistance - these effects are seen in both isolated and transplanted kidneys. Therefore the mechanisms are totally intrarenal. Factors include 1. myogenic mechanism 2. tubulo-glomerular feedback 3. sympathetic control 4. angiotensin II 5. intrarenal baroreceptors 6. macula densa 7. renal SNS 8. intrarenal prostaglandins

  6. 1. Myogenic Mechanism: Elevated arterial pressure causes increased stretch of the afferent arteriole. The afferent arteriole constricts in response to the stretch, thereby increasing its resistance. This brings both the RBF and the GFR back toward normal. One possible mechanism is distortion of the plasma membrane and opening of Ca2+ channels with a subsequent increase in [Ca2+].

  7. 2. Juxtaglomerular (JG) apparatus The TAL makes contact with the angle between the afferent and efferent arterioles of that nephron. The TAL cells that face the glomerulus are enlarged and specialized: they comprise the macula densa. Other components are a. the mesangial cells of the glomerulus b.the granular cells (juxtaglomerular cells) of the afferent and efferent arterioles  renin

  8. Tubulo-Glomerular Feedback Primarily regulates GFR, changes in RBF being secondary. Increased renal artery pressure  leads to 1. increased PGC 2. increased NFP & GFR 3. increased flow in PT, loop & macula densa

  9. Cells of the macula densa detect the increased rate of flow, possibly in response to increased luminal [Na+], [Cl-], or osmolality. These cells release several vasoconstrictor mediators, a. angiotensin II  permissive effects b. prostaglandins c. adenosine  afferent arteriolar constriction

  10. 3. Sympathetic Control: There is a rich SNS supply to kidney, afferent > efferent arterioles. a.SNS tone is reflexly mediated by aortic and carotid sinus baroreceptors. 1. -receptors  vasoconstriction 2. -receptors are relatively inert, adrenaline causes only vasoconstriction Both afferent & efferent arterioles are innervated.  SNS tone immediately raises BP, but also decreases Na+ & H2O excretion via GFR.

  11. b.  SNS tone can also be mediated by venous baroreceptorsin the atria and great veins c. Other reflexes can also increase SNS outflow, 1.peripheral chemoreceptors - hypoxia 2. CNS - exercise, emotional, hypercarbia

  12. 4. Angiotensin II: • Powerful constrictor of both afferent & efferent arterioles. Greater effect on efferent arteriole. Decreases RBF > GFR GFR/RBF ratio as does the SNS. • Causes contraction of mesangial cells, therefore reduces KF & GFR. • Serum concentration is directly determined by renal renin release. • The final common pathway is decreased [Ca2+] in the cytosol stimulating renin release.

  13. 5. Intrarenal Baroreceptors: Renin secreting granular cells act as baroreceptors, measuring pressure in the late afferent arteriole. Secretion is inversely related to arteriolar pressure.

  14. 6. Renal Sympathetic NS: Produces both indirect and direct effects. a. indirect  afferent arteriolar constriction and decreased glomerular pressure  decreased NaCl load leaving the loop & reaching the macula densa. b. direct 1 receptors on the granular cells. Sensitivity of the direct effect greater than the indirect effect

  15. 7. Prostaglandins: PGE2 & PGI2 are potent vasodilators, especially on the afferent arteriole. They dampen the effects of increased SNS tone and angiotensin II, both of which cause increased PG synthesis in addition to vasoconstriction. Thus, both autoregulation and renal PG's minimise any reduction in RBF & GFR induced by changes in BP, sympathetic activity, and angiotensin II

  16. The End

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