Kidney functions

From Iusmphysiology

Revision as of 21:43, 24 March 2011

Kidney functions

The National Kidney Disease Education Program

• 300K+ people have end stage kidney disease.
• It is expensive to take care of end stage kidney disease: 28 billion in 2010 (8% of the Medicare/caid budgets).
• 11% of the US population has chronic kidney disease.
• Testing and therapy for chronic kidney disease are inadequately applied.

Homeostasis

• Claude Bernard suggested the idea of homeostasis: "constancy of the internal milieu is the essential condition to a free life".
• Walter Canon developed the idea of homeostasis and gave it said name.
• Homer Smith explains why the kidney filters everything and then has to reabsorb most of it.
  • "Recognizing that we have the kind of blood we have because we have the kind of kidneys we have, we must acknowledge that our kidneys constitute the major foundation of our physiological freedom."
• Recall that mammal (and all land animals) came from sea animals.
• The kidneys have evolved from an environment where there was too much water (sea) to an environment where there is too little water (land).
  • And many diverse animals keep their ions (Na, K, Ca, Mg, and Cl) at very consistent proportions.

Drinking urine is good for you

• Drinking urine is NOT good for you!

Kidney functions

• The kidneys have many functions, all of which focus on homeostasis of the fluid.
• The kidneys regulate the osmotic pressure of the body fluids by retaining or losing water.
• The kidneys regulate concentrations of 8 major ions / molecules: Na, K, Mg, Ca, Cl, HCO3- (and therefore H+), phosphate (PO3-) and sulfate (SO4-).
• The kidneys eliminate waste products and foreign compounds (think drugs and urea).
• The kidneys regulate extraceullar fluid volume.
• The kidneys regulate arterial blood pressure.
• The kidneys have specialized metabolic functions:
  • Gluconeogenesis
  • Degradation of polypeptide hormones
• The kidneys add important substances to the blood:
  • Erythropoietin
  • 1,25OH VitD (calcitriol)
  • Prostaglandins and thromboxane
  • Renin
  • Kallikrein

Erythropoietin

• Erythropoietin (EPO) is released by cells of the renal cortex in response to hypoxia.
• EPO (erythropoietin) acts on the bone marrow to increase RBC proliferation, matruation and release.
• As more RBCs are made, oxygen carrying capacity goes up.
• In chronic renal disease, too little EPO is generated by the kidney and anemia results.
• In blood doping, EPO was used to increase oxygen carrying capacity until we became able to determine the difference between endogenous and exogenous EPO.
• Treatment of anephritic patients with EPO is far more effective than the cycles of transfusion that would otherwise be required.

Vitamin D

• Vitamin D is hydroxylated once at the liver and once at the kidney.
  • Recall that 7-dehydrocholesterol is obtained from the diet, converted to vitamin D3 at the skin, hydroxylated at the 25 position at the liver, and then at the 1 position in the kidney.
• The kidney adds the second hydroxyl group at the 1 position.
• Calcitriol (1,25OH vit D) is the biologically active form of vitamin D.
  • Cacitriol causes increased Ca absorption at the gut and increased Ca mobilization at the bone (by potentitiating PTH's action, from the parathyroid).

• In renal disease, vitamin D is not hydroxylated well and so the body has too little biologically active vitamin D (calcitriol).
  • As the kidney fails, increased phosphate in the blood (hyperphosphatemia) and decreased renal tubular mass lead to decreased ability of the kidney to hydroxylate 25OH VitD to calcitriol (1,25 vit D3).

• Decreased calcitriol generation has a series of effects (literally, a series):
  • This results in poor calcium absorption at the gut.
  • Because there is poor Ca absorption at the gut, there is also hyperparathyroidism as the parathyroid works overtime to signal to the gut and bone to keep the Ca levels high despite poor absorption.
  • And because the parathyroid is calling on the bone to release lots of Ca to keep serum levels normal, the bone becomes demineralized (bone disease).
  • Finally, there is vascular calcification.

Why is there calcium calcification?
"Patients with chronic kidney disease are at risk for vascular calcification because of multiple risk factors that induce vascular smooth muscle cells to change into a chondrocyte or osteoblast-like cell; high total body burden of calcium and phosphorus due to abnormal bone metabolism; low levels of circulating and locally produced inhibitors; impaired renal excretion; and current therapies." per JASN

Prostaglandins and Thromboxanes

• Prostaglandins and thromboxanes are made from phospholipds via cyclo-oxygenase enzymes like COX1 and COX2.
• Cyclo-oxygenase enzymes (COX1 and COX2) are constitutively activated in the kidney.
• The kidneys make lots of prostaglandins and thromboxanes which have effects on the kidney, itself.
• Prostaglandins:
  • Prostaglandins increase renal blood flow.
  • Prostaglandins increase Na excretion (increases water reabsorption, increases blood pressure).
  • Prostaglandins increase renin release (increases water reabsorption, increases blood pressure).
    • Recall that renin converts angiotensinogen to angiotensin 1 which gets converted to antiotensin 2 (by ACE in the lung) which causes blood vessels to constrict (elevates blood pressure) and causes release of aldosterone (from the glomerulosa zone of the adrenal cortex) which causes the kidney to reabsorb more Na and therefore more water (elevates blood pressure).
  • Prostaglandins inhibit the actions of ADH on the kidney (decreases water absorption, decreases blood pressure).
    • Recall that ADH (anti-diuretic hormone, AVP arginine vasopressin, from the posterior pituitary) causes the kidney to reabsorb water.
• Thromboxanes are vasoconstrictors (increases blood pressure).

Renin-angiotensin system

• The overall scheme is that angiotensin is present in the blood, renin cuts it into angiotensin 1, ACE cuts angiotensin 1 into angiotensin 2.
  • Note that angiotensinogen comes from the liver, renin comes from the kidney, and ACE (angiotensin converting enzyme) comes from the liver.

Did Homor Smith explain why it makes sense that one enzyme should come from the liver and the other from the lungs?

• Angiotensin 2 is all about increasing blood pressure and therefore has effects on the vasculature (think constriction), the adrenal cortex (think aldosterone, and the brain (think thirst).
  • Angiotensin 2 causes vasculature to constrict, thus increasing the blood pressure.
  • Angiotensin 2 causes the adrenal cortex (the zona glomerulosa) to release aldosterone which causes the kidney to increase Na reabsorption (and therefore water reabsoprtion), thus increasing the blood pressure.
  • Angiotensin 2 causes the brain to release AVP (arginine vasopressin = ADH) which causes the kidney to put more aquaporin proteins on the renal tubule epithelial cells which increases water reabsorption, thus increasing the blood pressure.

• ACE inhibitors inhibit the conversion of angiotensin 1 to angiotensin 2 and thus help keep blood pressure low (by decreasing water reabsorption mostly and also by decreasing vascular constriction).

Renal kallikrein enzyme system

• The renal-kallikrein system serves to dilate the vasculature (so it has mostly an opposite affect as the renin-angiotensin system, in terms of the vasculature).
• The general pathway is kininogen to kinins via kallikrein, then kinins to inactivated peptides via kininases.
  • Kininogens are made primarily by the liver, but also by some other tissues.
  • Kallikrein is made by the kidney.
  • The active molecules are the kinins, like bradykinin.
  • Bradykinin increases production of NO and prostaglandins and is therefore a potent vasodilator.
    • Recall that the kidney makes lots of prostaglandins through the cyclo-oxygenase genes.

• ACE (recall that it converts angiotensin 1 to angiotensin 2 which goes on to increase blood pressure in many ways) is a kininase so it helps to increase blood pressure by getting rid of the kinins (like bradykinin) that are floating around trying to decrease the blood pressure.

The nephron

• The nephron is the basic structural and functional unit of the kidney.
• Each kidney is supplied by a renal artery, a renal vein, and a ureter which enter at the renal hilus.
• The outside of the kidney is the renal capsule.
• Deep to the capsule is the cortex.
• Within the cortex framework are medullary pyramids in which are the medulla.
• The beginning of the drainage structures are the minor calyces, then the major calyces, then the renal pelvis, and finally the ureter.
  • The area of the renal pelvis and the calyces combined is the renal sinus.

Blood vessels of the kidney

• Recall that there is the cortex and medulla of the kidney.
  • The cortex and medulla are histologically distinct.
  • Within the medulla, we define two distinct areas: the outer medulla and the inner medulla.

• The kidney blood supply is specialized to allow the kidney to perform it's filtering duties.
• Each nephron has its own blood artery and vein.
• The overall flow is renal artery -> arcuate artery -> cortical radial artery -> afferent arteriole (one for each glomerulus) -> glomerulus (either a superficial cortical glomerulus or a juxtamedullary glomerulus) -> efferent arteriole -> peritubular arteries -> arcuate vein -> renal vein.
  • The peritubular capillaries deliver oxygen to the cells of the tubule and serve to reabsorbed material from the interstitial fluid back into the blood.
  • The superficial cortical glomerulus and the juxtamedullary glomerulus differ in their function and in their location within the kidney.
  • The descending vasa recta provide another route for blood.
    • The descending vasa recta branch off the efferent arterioles (that is, distal to the glomerulus) of the juxtamedullary glomeruli.
    • The descending and ascending vasa recta lie parallel to an individual tubule.

• Note that the bowman's capsule is the set of epithelial cells that surround the gomerular capillaries.

• The functional unit of the kidney is the nephron, of which there are about 1 million in each kidney.
  • 85% of the nephrons proceed from the superficial cortex to the outer medulla and have superficial cortical glomeruli.
  • 15% of the nephrons proceed from the deep cortex to the inner medulla and have juxtamedullary glomeruli.

Renal osmolarity gradient

• The through filtration and blood flow, the kidney maintains an osmotic gradient along the cortex-medulla axis.

Blood flow to the kidneys is high

• 25% of the cardiac output goes to the kidneys.
• High blood flow is important for driving a high filtration rate.
  • The 3 liters of plasma is filtered every 24 minutes (which is 50-60 times per day).

Major processes involved in urine formation

• The blood is "filtered" at the glomerulus; small particles flow out of the blood into the "filtrate".
• Some material from the filtrate is "reabsorbed" in the kidney tubule; epithelial cells reabsorb ions and such back into the interstitial fluid / blood.
• Some materials are "secreted" into the filtrate; epithelial cells can put metabolites and such into the filtrate (urine).

Proximal tubule

• The proximal tubule is the epithelial tract that is nearest the glomerulus.
• The proximal tubule is a specialized tissue for reabsorption and secretion:
  • Neighboring epithelial cells have tight junctions to keep "stuff" from passing without an active transport mechanism (either reabsorption or secretion).
  • The epithelial cells have microvilli (a brush border) to increase the surface area and the ability to reabsorb / secrete.
  • The epithelial cells have many microvilli to produce lots of ATP for all the active transport that must occur.
  • The epithelial cells sit on a basement membrane to provide structure and order to the single layer of cells.

The juxtaglomerular apparatus (JGA)

• The juxtaglomerular apparatus is important for two major functions: the release of renin and feedback on the tubulo-glomerular feedback.
  • Recall that the release of renin will convert angiotensinogen to AT1 (angiotensin 1) which will get converted to angiotensin 2 (at the lungs by ACE) which will cause blood vessels to constrict and aldosterone to be released, thus increasing blood pressure.
• The juxtaglomerular apparatus is called an apparatus because it functions by the coordinated activity of three cell types from two separate structures of one nephron.
  • Macula densa cells are epithelial cells found on the thick ascending tubule of the nephron.
    • Macula densa cells seem to be more columnar in shape than their more cuboidal, normal endothelial cells.
  • Extraglomerular mesangial cells are also found on the thick ascending tubule.
  • Granular cells (also called juxtaglomerular cells) are endothelial cells found in the wall of the afferent arteriole.

Tubulo-glomerular feedback

• Tubulo-glomerular feedback describes how the concentration of NaCl in the tubule (that is, in the filtrate) can be used to affect the GFR (glomerular flow rate) by changing the diameter of the afferent arterioles that lead to the glomerulus.
  • Note that this it taking place within a single nephron; as the tubule ascends back toward the cortex, it passes by it's own glomerulus and therefore can have a very rapid affect on the GFR.
  • The macula densa cells detect the NaCl concentration in the tubule and send molecular signals to the afferent arterioles.

***Sensing of the NaCl concentration is a model of filtrate flow.
Are flow rate and NaCl concentration two separate sensing mechanisms for the macula densa cells?

• Why detect the NaCl?
  • Recall that the tubule is all about reabsorbing important ions and molecules from the filtrate, including Na and Cl (the body doesn't want to lose them).
  • So if NaCl concentration is high at the distal tubule (that is, near the macula densa), then we know the filtrate needs to move more slowly in order to reabsorb more of the Na and Cl.
  • If NaCl concentration is low at the distal tubule, then we know the filtrate can be moved along more quickly.
  • Now recall that the flow rate of the filtrate is a function of glomerular filtration rate which is a function of the blood pressure difference between the afferent and efferent arterioles of the glomerulus.
  • So, we should change the blood pressure of the afferent arteriole if we want to change the flow rate of the filtrate (and therefore affect the reabsorption levels).

• The macula densa cells can respond to both high and low NaCl concentrations:
  • When NaCl concentrations are high, filtrate flow rate is too slow. The macula densa cells signal to the granular cells to release renin.
    • Recall that renin will increase blood pressure systmeically because angiotensin 2 causes vasoconstriction and aldosterone release at the adrenal gland.
    • It makes sense that low flow rate should lead to release of renin by the granular cells because increased blood pressure (at the afferent arteriole) causes an increase in filtrate formation (increased blood flow will push more fluid through the fenestrations at the glomerulus and thus generate more filtrate).

So this wouldn't cause immediate vasoconstriction, right, b/c renin would have to cut angiotensinogen up and then that would have to go to the lung and then back to the kidney as angiotensin 2, right?

• • • Note that macula densa cells signal to granular cells via PGE2, a prostaglandin produced by COX2 in the macula densa cells.
    • The granular cells of the afferent arteriole are well named because they have granules full of renin.
  • When NaCl concentration levels are high, filtrate flow is too fast. The macula densa cells signal to the endothelial cells of the afferent arteriole to vasoconstrict.
    • ATP is released by the macula densa cells and is converted to adenosine (a vasoconstrictor) to decrease blood flow of the afferent arteriole and thus decrease filtrate production.
    • Adenosine binds to the A1 receptors of the endothelial cells of the afferent arteriole to cause vasoconstriction.

Angiotensin 2

• Recall that angiotensin 2 causes systemic vasoconstriction and release of aldosterone at the adrenal cortex (glomerulosa).
• At low concentrations, angiotensin 2 causes efferent arteriole constriction.
  • This causes a decrease in renal blood flow (RBF).
  • This will cause an increase in the difference between the afferent arteriole blood pressure and the efferent arteriole blood pressure, and thus and increase in GFR.
• At high concentrations (as in trauma and emergencies), both the afferent and efferent arterioles vasoconstrict.
  • This causes a decrease in RBF (renal blood flow).
  • This causes a decrease in GFR (glomerular filtration rate).
    • This makes sense because you want to conserve all the fluid you can in an emergency.
  • Angiotensin 2 levels are severely elevated in emergency situations because sympathetic nerves directly stimulate the granular cells of the juxtamedullary apparatus to release their renin and thus much more angiotensin 2 is generated than when macula densa cells signal for renin release.

Micturition = Urination

• Micturition is a voluntary control in adults.
• Children do not obtain voluntary control of micturition until 2-3 years of age.
• The tension in the wall of the bladder adjusts as the bladder fills to keep pressure from building up.
• One generally feels the need to micturate at about 150-250 ml and loses control of voluntary micturition at 700 ml.
• The ureters have a smooth muscle layer that forces urine along the tract.
  • This is important for outer space travel and to counteract the counter pressure of the fluid already in the bladder.

Renal plasma clearance

• One measure of renal function is the renal plasma clearance, defined as ml plasma / min that are cleared of a substance.

• The renal plasma clearan