1 / 36

DILUTING AND CONCENTRATING MECHANISM AND CLEARANCE

DILUTING AND CONCENTRATING MECHANISM AND CLEARANCE. URINARY BLOCK 313. Dr. Shaikh Mujeeb Ahmed Assistant Professor AlMaarefa College. Objectives . Describe the factors that determine the ability of loop of Henle to creat osmotic medullary gradient

claus
Download Presentation

DILUTING AND CONCENTRATING MECHANISM AND CLEARANCE

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. DILUTING AND CONCENTRATING MECHANISMAND CLEARANCE URINARY BLOCK 313 Dr. ShaikhMujeeb Ahmed Assistant Professor AlMaarefa College

  2. Objectives • Describe the factors that determine the ability of loop of Henle to creat osmotic medullary gradient • Identify countercurrent multiplier and countercurrent exchange systems in concentrating and diluting urine • Explain changes in osmolarity of tubular fluid in the various segments of the loop of Henle when concentrated urine is being produced. • Describe the role of ADH on the ability of the kidney to produce either a dilute or a concentrated urine. • Discuss the micturition reflex.

  3. Urine Excretion • Depending on the body’s state of hydration, the kidneys secrete urine of varying concentrations. • Too much water in the ECF establishes a hypotonic ECF. • A water deficit establishes a hypertonic ECF. • This function is determined by the amount of water reabsorption in the renal tubules.

  4. Urine Concentration & Dilution • Water reabsorption is obligatory in the proximal(65%) tublues and Loop of Henle(15%). • The final adjustment of the urine volume and osmolarity depends on the extent of facultative water reabsorption in the Collecting Ducts, which is depends on:- • The blood level of antidiuretic hormone (ADH). • The Medullary interstitium (MI) hypertonicity (Medullary concentration gradient).

  5. Urine Concentration Requirements for forming a concentrated urine are: • High level of ADH (increase permeability) • High osmolarity of the renal medullary interstitial fluid (osmotic gradients)

  6. Driving force for H2O reabsorption • Driving force for water reabsorption throughout the entire length of tubules is an osmotic gradient between tubular lumen and surrounding interstitial fluid.

  7. Urine Excretion • A large, vertical osmotic gradient is established in the interstitial fluid of the medulla (from 100 to 1200 mosm/liter) • This osmotic gradient exists between the tubular lumen and the surrounding interstitial fluid.

  8. Urine Concentration & Dilution What is the process by which renal medullary interstitial fluid becomes hyperosmotic? This process involves the operation of the medullary countercurrent system

  9. Medullary Countercurrent system • Juxta medullary nephrons • long loop of henleestabilishes a vertical osmotic gradient (Countercurrent multiplier) , • their vassa recta preserve this gradient while providing blood to renal medulla,( Countercurrent exchanger) • collecting ducts of all nephrones use the gradient in conjunction with the hormone vassopressin, to produce urine of varying concentration (osmotic equilibrating device) . • Collectively this entire functional organization is known as medullary countercurrent system

  10. Countercurrent Multiplication • Comparing the descending and ascending limbs of the loop of Henle • The descending ling is highly permeable to water but does not extrude sodium for reabsorption. • The ascending limb actively transports NaCl out of the tubular lumen into the surrounding interstitial fluid. It is impermeable to water. Therefore, water does not follow the salt by osmosis. • There is a countercurrent flow produced by the close proximity of the two limbs.

  11. Countercurrent Multiplication

  12. Countercurrent Multiplication

  13. Countercurrent Multiplication

  14. Countercurrent Multiplication

  15. Countercurrent Multiplication

  16. Countercurrent Multiplication

  17. Countercurrent Multiplication

  18. BENEFITS OF COUNTERCURRENT MULTIPLICATION • It establishes a vertical osmotic gradient in the medullary interstitial fluid. This gradient, in turn, is used by the collecting ducts to concentrate the tubular fluid so that a urine more concentrated than normal body fluids can be excreted. • Second, the fact that the fluid is hypotonic as it enters the distal parts of the tubule enables the kidneys to excrete a urine more dilute than normal body fluids.

  19. Role of Vasopressin • Vasopressin-controlled, variable water reabsorption occurs in the final tubular segments. • 65 percent of water reabsorption is obligatory in the proximal tubule. In the distal tubule and collecting duct it is variable, based on the secretion of ADH. • The secretion of vasopressin increases the permeability of the tubule cells to water. An osmotic gradient exists outside the tubules for the transport of water by osmosis. • Vasopressin works on tubule cells through a cyclic AMP mechanism. • During a water deficit, the secretion of vasopressin increases. This increases water reabsorption. • During an excess of water, the secretion of vasopressin decreases. Less water is reabsorbed. More is eliminated.

  20. Mechanism of action of Vasopressin

  21. Urea Recirculation • Urea is passively reabsorbed in proximal tubule. • In the presence of ADH, water is reabsorbed in distal and collecting tubules, concentrating • urea in these parts of the nephron. • The inner medullary collecting tubule is highly • permeable to urea, which diffuses into the • medullary interstitium. • ADH increases urea permeability of medullary • collecting tubule.

  22. Recirculation of Urea Absorbed from Medullary Collecting Duct into Interstitial Fluid Figure 28-5; Guyton and Hall

  23. Regulation of H2O reabsorption in response to H2O deficit

  24. Regulation of H2O reabsorption in response to H2O Excess

  25. Countercurrent exchange within the vasarecta conserves the medullary verticalosmotic gradient.

  26. The Vasa Recta Preserve Hyperosmolarity of Renal Medulla • The vasa recta • serve as • countercurrent • exchangers • Vasa recta blood • flow is low • (only 1-2 % of • total renal • blood flow) Figure 28-3; Guyton and Hall

  27. Renal Failure • Causes of renal failure • Infectious organisms • Toxic agents • Inappropriate immune responses • Obstruction of urine flow • An insufficient renal blood supply

  28. Micturition • Urine stored in bladder is eliminated by micturition • Urine in bladder stimulates stretch receptors • Stimulated stretch receptors signal smooth muscle in bladder wall by parasympathetic neurons • Contraction of bladder pushes urine out of the body • Micturition reflex • Relaxation of external urethral sphincter muscle allowing urine to pass through urethra and out of the body • Under voluntary control but cannot be delayed indefinitely • Urinary incontinence • Inability to prevent discharge of urine

  29. Urinary Bladder and Its Innervation Figure 26-6; Guyton and Hall

  30. Normal Cystogram There are 3 phases of vesicular pressure changes Initial 10 cm of H2O rise in pressure for 10-50 ml of urine collection Second phase last until the bladder volume is 400ml Third phase shows the sharp rise in the intravesicle pressure Micturition contractions begin to appear at a urine volume about 150 ml. Desire to void urine occurs when the bladder is full. Figure 26-7; Guyton and Hall

  31. Reflex and Voluntary Control of Mictrurition

  32. Abnormalities of micturition Atonic Bladder Caused by Destruction of Sensory Nerve Fibers. • Micturition reflex cannot occur if the sensory nerve fibers from the bladder to the spinal cord are destroyed. • Person loses bladder control • Instead of emptying periodically, the bladder fills to capacity and overflows a few drops at a time through the urethra. This is called overflow incontinence. • A common cause of atonic bladder is crush injury to the sacral region of the spinal cord. • Certain diseases can also

  33. Automatic Bladder Caused by Spinal Cord Damage Above the Sacral Region. • Typical micturition reflexes can still occur. • They are no longer controlled by the brain. • During the first few days to weeks the micturition reflexes are suppressed because “spinal shock” (sudden loss of facilitative impulses from the brain stem and cerebrum). • Gradually typical micturition reflexes return; then, periodic (but unannounced) bladder emptying occurs. • Some patients can still control urination in this condition by stimulating the skin (scratching or tickling) in the genital region, which sometimes elicits a micturition reflex.

  34. Uninhibited Neurogenic Bladder Caused by Lack of Inhibitory Signals from the Brain. • Which results in frequent and relatively uncontrolled micturition. • From partial damage in the spinal cord or the brain stem that interrupts most of the inhibitory signals. • Facilitative impulses passing continually down the cord -even a small quantity of urine elicits an uncontrollable micturition reflex, thereby promoting frequent urination.

  35. References • Human physiology by Lauralee Sherwood, seventh edition • Text book physiology by Guyton &Hall,11th edition • Text book of physiology by Linda .s contanzo,third edition

More Related