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Kidneys are major excretory organ

Pg 961
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urinary system c25

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Kidneys are major excretory organ Pg 961 though the lungs and skin do some as well
Kidneys also react as essential regulators of volume an chemical makeup of blood; maintaining proper balance between water and sals, and acids and bases
Other Renal functions include gluconeogenesis during prolonged fasting; Producing the hormones renin and erythropoietin; Metabolizing vitamin D to it's active form
RENIN acts as an enzyme to help regulate blood pressure and kidney funtion
ERYTHROPOIETIN stimulates red blood cell production
Urinary system includes kidneys, urinary bladder, plus 3 tubelike organs (paired ureters, and rurethra) (transportation channels)
Renal Hilum ureter, renal blood vessels, lymphatics, and nerves all converge here
Three layers of supported tissue around kidney renal fascia, perirenal fat capsule, fibrous capsule
Renal fascia outer layer, dense fibrous connective tissue; anchors kidney to surrounding structures
Perirenal fat capsule fatty mass that surrounds the kidney and cushions it against blows
Fibrous capsule transparent capsule that prevent infections in surrounding regions from spreading to the kidney
Hydronephrosis backup of urine
3 distinct regions of the kidney cortex, medulla and pelvis
Renal cortex Pg 962 most superficial; light in color and has granular appearance.
Renal Medulla Pg 962 deep to cortex; darker, reddish-brown; exhibits cone shaped tissue masses called RENAL PYRAMIDS or MEDULLARY PYRAMIDS; pyramids appear striped due to almost entirely of parallel bundles of microscopic urine collecting tubules and capillaries
Renal columns separate pyramids. each pyramid and its surrounding cortical tissue constitutes on of approximately eight LOBES of a kidney
Renal Pelvis funnel-shaped tube; continuous w/ ureter leaving the hilum;
Major calyces branching extensions of the pelvis form 2 or 3 major CALYCES; cup shaped area that enclose papillae
Calyces collect urine which drains to papillae,; empty into pelvis; the flows from pelvis to ureter; this moves it to the bladder to store;
Walls of calyces, pelvis, and ureter contain smooth muscle that contracts rhythmically to propel urine by PERISTALSIS
Pyel/itis infection of renal pelvis and calyces
Pyel/o/nephr/itis infections that affect entire kidney
Kidneys have rich blood supply true
Renal arteries Pg 963 deliver 1/4 of total cardiac output (1200ml) to the kidneys each minute (at rest)
Renal arteries issue at right angles from the abdominal aorta, and the right renal artery is longer than the left because the aorta lies to the left of the midline
Segmental arteries pg964 Renal arteries divide to 5
Interlobar arteries each segmental artery branches further to form these in renal sinus
Arcuate arteries branched from interlobar arteries, in medulla-cortex junction; arch over bases of medullary pyramids
Cortical radiate arteries pg964 radiate outward from the arcuate arteries to supply the cortical tissue
90% of blood entering kidney perfuses the renal cortex true
Afferent Arterioles branch from cortical, radiate arteries begin a complex arrangement of microscopic blood vessels; KEY ELEMENTS of kidney function
Veins pretty much trace the pathway of the arterial supply in REVERSE
Blood leaving the renal cortex Pg 964 drains into cortical radiate, arcuate, interlobar, and finally renal veins
Renal veins issue from kidney and empty into vena cava
Left renal vein is almost twice as long as right true
Renal Plexus network of autonomic nerve fibers and ganglia, ; provides the nerve supply of the kidney and its ureter
Renal plexus is supplied by sympathetic fibers from the most inferior thoracic and fist lumbar splanchnic nerves which course along w/ the renal artery to reach the nerve; the SYMPATHETIC VASOMOTOR fibers regulate renal blood flow by adjusting the diameter of renal arterioles and also influence the urine-forming role of the nephrons
Nephrons STRUCTURAL and FUNCTIONAL units of the kidneys
Each kidney contains over 1 mission nephrons (blood processing units) they carry out the process that forms urine
1000's of collecting ducts, each of which collects fluid from several nephrons and conveys it to the renal pelvis
Glomerulus in each nephron; tuft of capillaries
Renal tubule has a cup-shaped end which called the Glomerular capsule (or Bowman's capsule); which is blind and completely surrounds glomerulus
Renal capsule Glomerular capsule and the enclosed glomerulus
Endothulium of the glomerular capillaries if FENESTRATED (penetrated by many pores) so they are very porous
Filtrate (plasma derived fluid) raw material that renal tubules process to form urine
External parietal layer of glomerular capsule simple squamous epithelium; simply contributes to capsule structure, and plays NO PART in forming FILTRATE
Visceral layer pg966 clings to glomerular capillaries; consists of highly modified, branching epithelial cells called PODOCYTES
Foot processes where Podocytes terminate; intertwine as they cling to the basement membrane of the glomerus
Filtration slits Clefts or openings between the foot processes
Capsular space filtrate enter here through the slits
remainder of Renal tubule has 3 major parts: proximal convoluted tubule (PCT); Loop of Henle; distal convoluted tubule
Proximal convoluted tubule (PCT) Pg966 exit from glomerular capsule; elaborately coiled;
loop of Henle (Nephron loop or Henle's loop) hairpin loop coming from the PCT
Distal convoluted tubule (DCT) last part of tubule that empty into a collecting duct
collecting ducts receives filtrate from many nephrons; runs through pyramids(gives striped appearance); as they approach the renal pelvis, they fuse together and deliver urine into the minor calyces via papillae of the pyramids.
Renal tubule consist of single layer of polar epithelial cells on basement membrane; but each region has a unique cellular anatomy;
Walls of PCT cuboidal epithelial cells w/ large mitochondria; luminal(exposed) side bear dense microvilli
brush border dramatically increases the surface area and capacity for reabsorbing water and solutes
U-shaped loop of Henle has ascending and descending limbs
Descending limb of loop of Henle proximal part is continuous w/ proximal tubule and its cells are similar
Thin segment the rest of the descending limb, is simple squamous epithelium freely permeable to water;
Ascending loop of Henle becomes cuboidal or even low columnar
Thick segment ascending part of loop of Henle where it becomes cuboidal or columnar
In some nephrons, the thin segment if sound only in descending limb. In others, it extends into ascending limb as well
Epithelial cells of the DCT are cuboidal and confined to the cortex, but they are thinner and almost entirely lack microvilli
Transition between DCT and collecting duct marked by appearance of a heterogeneous collection of cells.
Cell types in collecting ducts INTERCALATED CELLS, (cuboidal cells w/ abundant microvilli) and more numerous PRINCIPLE CELLS which have sparse/short microvilli
Principle cells help maintain body's water and Na+ balance
Nephrons; divided into two major groups cortical nephrons and juxtamedullary nephrons
Cortical nephrons 85% of nephrons; located entirely in cortex (except small part in the loop of Henle)
Juxtamedullary nephrons originate close to the cortex-medulla junction; play an important role in kidney's ability to produce concentrated urine; their loops of Henle deeply invade the medulla; their thin segment are much more extensive than those of cortical nephrons
Nephron capillary beds Pg 966 renal tubule of every nephron is closely associated w/ 2 capillary beds; glomerulus and peritubular
Glomerulus in which the capillaries run in parallel, specialized for filtration; differs from all other capillary beds in the body in in that it is both fed and drained by arterioles
Afferent arteriole arise from cortical radiate arteries; run through renal cortex;
BP is extremely high in glomerulus because arterioles are high-resistance vessels; afferent arteriole has a larger diameter that the efferent
Peritubular capillaries pg968 arise from the efferent arterioles draining the glomeruli; cling closely to adjacent renal tubules and empty into nearby venules; LOW PRESSURE, POROUS capillaries that readily absorb solutes and water from tubule cells as these substances are reclaimed
Efferent arterioles serving the Juxtamedullary nephrons tend not to break up into meandering particular capillaries. Instead the form bundles of straight vessels called VASA RECTA
Vasa Recta (straight vessels) extend deep into medulla paralleling the longer loops of Henle; thin-walled; Play important role in forming concentrated urine
In summary microvasculature of the nephrons consists of 2 capillary beds separated by intervening efferent arterioles; Glomerulus produces filtrate; Peritubular reclaims most of that filtrate
Vascular resistance in Microcirulation Pg 968 Blood flow encounters high resistance
Renal BP declines from 95mm Hg in the renal arteries to 8mm Hg or less in the renal veins
Resistance of the afferent arterioles protects the glomeruli form large fluctuations in systemic BP
Resistance in the efferent arterioles reinforces the high glomerular pressure and reduces the hydrostatic pressure in the peritubular capillaries
Juxtaglomerular Apparatus Pg 968 most distal portion of the ascending limb of loop of Henle lies
JGA includes granular cells and macula densa granular cells (also called juxtaglomerular (JG) cells)
Granular cells enlarged smooth muscle cells w/ prominent secretory granules contain renin; ACT AS mechanoreceptors that sense the BP in the afferent arteriole
Macula densa group of tall, closely packed cells of the ascending limb of the loop of Henle that lies adjacent to granular cells
Macula densa are chemoreceptors that respond to changes in the NaCl content of the filtrate
Extraglomerular mesangial cells interconnected by gap junctions and may pass signals between macula dense and granular cells
Filtration membrane Pg 969 lies between blood and interior of glomerular capsule; porous allows free passage of water and solutes smaller that plasma proteins
3 layers of filtration membrane fenestrated endothelium of the glomerular capillaries; visceral membrane of the glomerular capsule, made of podocytes which have filtration slits between their foot processes; and between these two layers is the basement membrane composed of fused basal
Fenestrations (capillary pores) allow passage of plasma but not blood cells; basement membrane restricts all but smallest proteins;
Structural makeup of basement membrane confers electrical selectivity on the filtration process
Urine formation Pg 969-970 3 major processes; glomerular filtration tubular reabsorption in renal tubes tubular secretion in renal tubes
Maintain volume and chemical makeup kidneys dump free blood into a separate container (renal tubes and collecting ducts)
next From there, the kidneys reclaim (by tubular reabsorption) everything the body needs to keep (almost everything)
next some things are selectively added to the container (by tubular secretion ) fine tuning the bodies chemical balance
of the 1200 ml of blood that passes through the glomeruli each minute some 650ml is plasma; about one-fifth of this (120-125) is forced into the renal tubules
Kidneys consume 20-25% of all oxygen used by the body at rest true
Filtrate contains everything found in blood plasma EXCEPT proteins
Urine contains mostly metabolic wastes and unneeded substances.
The kidneys process 180L (47 gallons) of blood derived fluid daily of this amount less than 1% typically leave the body as urine
Glomerular Filtration Pg 970 passive process ; hydrostatic pressure forces fluids and solutes through; "simple mechanical filter", because filtrate formation doe not consume metabolic energy
Glomerulus filtration membrane has a large surface area and is thousands of times more permeable to water and solutes
Glomerular BP higher than that in other capillary beds (55mm Hg as opposed to 18 mm Hg); Resulting in a much higher net filtration pressure
As a result of these differences, the kidneys produce 180L of filtrate daily, in contrast to the 2 to 4 L formed daily by all other capillary beds combined
Molecules smaller than 3nm in diameter such as water, glucose, amino acids and nitrogenous wastes; pass freely form the blood into the glomerular capsule
Keeping plasma proteins in capillaries due to colloid osmotic pressure of the glomerular blood
proteins or blood cells in the urine indicates a problem with the filtration membrane True
Net Filtration Pressure (NFP) Pg 971 responsible for filtrate formation
Glomerular hydrostatic pressure (HPg) glomerular BP; chief force pushing water and solutes out of the blood and across filtration membrane.
HPg is opposed by two forces colloid osmotic (oncotic) pressure of glomerular blood (OP); capsular hydrostatic pressure (HP)
Glomerular filtration Rate (GFR) volume of filtrate formed each minute
Factors governing filtration rate total surface area available for filtration Filtration membrane permeability NFP (10mm Hg)
Normal GFR ,in adults, in both kidneys is 120-125 ml/min true
Glomerular pressure drop of only 18%, stops filtration altogether
GFR is directly proportional pg972 to the NFP; any change in pressure changes both;
Increase in arterial(and glomerular) BP in the kidneys INCREASES the GFR in the absense of regulation
Regulation of Glomerular filtration Pg 972 GFR is regulated by both intrinsic and extrinsic controls.
Kidneys need constant GFR to do their job on the other hand; the body needs constant BP and therefore a constant blood volume
Intrinsic controls (renal autoregulation) act locally within the kidney to maintain GFR
Extrinsic controls (by nervous and endocrine system) maintain BP
In extreme changes in BP (less than 80, higher than 180) extrinsic controls take precedence over intrinsic controls
Intrinsic controls (Renal autoregulation) adjusting its own resistance to blood flow; 2 types of controls- myogenic mechanism and tubuloglomerular feedback mechanism
Myogenic mechanism reflects tendency of vascular smooth muscle to contract when stretched
Increasing systemic BP causes the AFFERENT arterioles to constrict which restricts blood flow into glomerulus and prevents glomerular BP from rising to damaging levels
Declining systemic BP causes dilation of afferent arterioles and raises glomerular hydrostatic pressure both responses help maintain a normal GFR
Tubuloglomerular feedback mechanism autoregulation ; directed by the MACULA DENSE cells of the JUXTAGLOMERULAR apparatus
When GFR increases there is insufficient time for reabsorption and the concentration of NaCl in the filtrate remains high. This causes the macula dense to release vasoconstrictor chemical (probably ATP) that causes tense constriction of the afferent arteriole
Extrinsic Controls; Neural and Hormonal Mechanisms Pg 972 purpose is to maintain systemic BP; sometimes to the detriment of the kidneys!
Sympathetic nervous system controls volume of extracellular fluid is normal-sympathetic nervous system is at rest-the renal blood vessels are DIALATED and renal auto regulation mechanisms prevail
During extreme stress or emergency , neural controls may overcome renal autoregulatory mechanisms true
Renin-angiotensin Mechanism triggered when various stimuli cause the granular cells to release the hormone RENIN
Renin acts enzymatically on ANGIOTENSINOGEN; converting it to ANGIOTENSIN I; this, in turn, is converted to ANGIOTENSIN II by ANGIOTENSIN CONVERTING ENZYME(ACE)
Angiotensinogen plasma globuloin made by the liver
Angiotensin II acts to; potentent vasoconstrictor; activates smooth muscle of arterioles throughout the body, raising mean arterial BP
Angiotensin II acts to stimulate hypothalamus to release hormone and activate the hypothalamic thirst center, both of which increase blood volume
Angiotensin II acts to stimulate reabsorption of Na+. Both directly by acting on renal tubules and indirectly by triggering the release of aldosterone from the adrenal cortex; Because water follows Na+, blood volume and BP rise
Angiotensin II acts to pg973 increases fluid reabsorption by decreasing peritubular capillary hydrostatic pressure; this pressure drop occurs because the efferent arterioles constrict and the downstream drop in hydrostatic pressure allows more fluid to move back into the peritubula
Angiotensin II acts to targets the glomerular mesangial cells, causing them to contract and reduce the GFR by decreasing the total surface area of tglomerular capillaries available for filtration
REMEMBER: ALL of the effects of Angiotensin II are aimed at RESTORING blood volume and BP! The vasoconstrictor and stimulating reabsorption of Na+ are most important
Triggers for RENIN release Pg 974 Reduced stretch of the granular cells; Stimulation of the granular cells by input from activated macula densa cells: Direct stimulation of granular cells via B1-adrenergic receptors by renal sympathetic nerves
Other factors affecting GFR Prostaglandin E2 (PGE2); Intrarenal angiotensin II; Adenosine
Prostaglandin E2 (PGE2) vasodialatory paracrine counteracts vasoconstriction by norepinephrine and angiotensin II within the kidney. The adaptive value of these opposing action is to prevent renal damage while responding to body demands to increase peripheral resistance
Intrarenal angiotensinII Although we think of angiotensin II as a hormone; the kidney makes it's own, locally acting angiotensin IIthat reinforces effects of hormonal angiotensin II. Dampens resulting renal vasoconstriction by causing PGE release
Adenosine released as such or produced extracellularly form ATPreleased by macula dense cells. Although it functions as a vasodilator systemically, adenosine CONSTRICTS the renal vasculature
anuria low urinary output (less than 50ml/day); may indicate that glomerular BP is too low to cause filtration
Renal failure and anuria can also result from nephrons cease to function; acute nephritis, transfusion reactions, crush injuries
Tubular Reabsorption (reclamation process) pg974 Selective trans/epitheilial process.;
Reabsorbed sustances follow either the Trans/cellular or Para/cellular route
Trans/cellular Route substances move through the LUMINAL MEMBRANE, the CYTOSOL, and BASOLATERAL MEMBRANE; then to the endo/thelium of the peritubular capillaries
Movement in paracellular route between the tubule cells is limited due to tight junctions.
In Proximal Nephron tight junctions are "leaky" and allow some important ions through (Ca, Mg, K, and some Na)
Virtually all Organic nutrients are completely reabsorbed REABSORPTION of WATER and many ions is continuously regulated and adjusted in response to hormonal signals
Reabsorption Process is either passive(no ATP) or active(at least one step driven by ATP directly or indirectly)
Sodium Reabsorption Pg 974 SODIUM IONS are single most ABUNDANT CATION 80% of energy used for active transport is devoted to their reabsorption.
Sodium reabsorption is ACTIVE and via TRANS/CELLULAR route
2 basic processes that promote active Na reabsorption occur in each tubule segment; 1. Na actively transoported OUT of tubule cell by PRIMARY ACTIVE transport (a Na -K ATPase pump present in basalateral membrane)
From there; Na is swept by bulk flow of water into adjacent peritubular capillaries; Flow is RAPID due to low hydrostatic pressure and high osmotic pressure
Most PROTEINS remain IN blood instead of being filtered out into the tubule True
SECONDARY active transport (symport or antiport carriers) ACTIVE PUMPING of Na+ from tubule cells results in a strong ELECTROCHEMICAL gradient that favors its passive entry at the luminal face via secondary active transport or;
via FACILITATED DIFFUSION through channels, this occurs because 1) pump maintains the intracellular Na concentration at low levels, and 2) the K pumped into the tublu cells almost immediately diffuses out into the interstitial fluid via leakage channels, leaving interior tubule cell w/ NET NEGATIVE charge
Reabsorption of Nutrients, Water, and Ions Pg 975 Reabsorption of Na by primary active transport provides energy and means for reabsorbing almost every other substance, even WATER
Secondary active transport ("push" comes from gradient created by Na+ -K+ pumping at basolateral membrane) pg975 glucose, amino acids, lactate, and vitamins; Luminal carrier moves Na DOWN concentration gradient as it co transports (SYMPORTS) another solute
Cotransported (SYMPORTED) solutes diffuse across basolateral memebrane before moving into the peritubular capps
Transport Maximum (Tm) (reported in mg/min) reflects number of transport proteins in the renal tubules available to ferry each substance; Generally plenty of transporters; Tm high for glucose and few for substance of no use
when Transport are saturated (all bound to substances) the excess is excreted in urine; that is what happens to someone HYPERGLYCEMIC because of DM
Passive tubular reabsorption Pg 975 encompasses osmosis, diffusion, and facilitated diffusion; substances move DOWN electrochemical gradients WITHOUT ATP.; establishes strong osmotic gradient, and water moves by osmosis into peritubular capps
Aquaporins transmembrane proteins; form water channels across cell membranes
Aquaporins in continuously water-permeable regions such as PCT, constant components of tubule cell membranes; makes body "obliged" to absorb water in the proximal NEPHRON regardless of its state of over- or under hydration.
this water flow is called Obligatory water reabsorption true
Aquaporins are virtually absent in luminal membranes of collecting duct UNLESS antidiuretic hormone is present
as Water leaves tubules concentration of solutes in filtrate increases and begin to follow gradients into peritubullar capps
Solute following solvent phenomenon ; explains the passive reabsorption of a number of solutes present in the filtrate; also explains in part why lipid-soluble drugs and environmental toxins are difficult to excrete;
since lipid-soluble compounds can generally pass through membranes they will follow their concentration gradients and be reabsorbed, even if this is "not desirable"
Reabsorption capabilities of Renal Tubules and Collecting Ducts pg976 Pg976 PROXIMAL CONVOLUTED TUBULE, LOOP OF HENLE, DISTAL CONVOLUTED TUBULE
Proximal convoluted tubule PCT cells most active in reabsorption; Normally absorb all glucose, lactate, and amino acids and 65% of Na and water; 80% of bicarbonate, 60% of Cl, and 55% of K.
Bulk of reabsorption of electrolytes is accomplished by the time filtrate reaches loop of Henle nearly ALL uric acid and 1/2 of urea are reabsorbed in PCT, BUT, both are later secreted back into filtrate
Loop of Henle permeability changes dramatically; here, for the 1st time water reabsorption IS NOT coupled to solute reabsorption.
Water can leave the DESCENDING loop but not ASCENDING loop where aquaporins are scarce or absent in the tubule membrane.
Permeability differences play a vital role in kidney ability to form dilute and concentrated urine True
Rule of water is it leaves descending (but not ascending) limb of Henle and OPPOSITE is true for SOLUTES
Virtually NO solute reabsorption occurs in the descending limb, but both active and passive reabsorption of solute occus in the ascending limb.
In THIN PORTION of ascending limb Na moves passively down gradient created by water reabsorption
Na+ -K+ -2Cl symporter is main means of Na entry at lumina surface in THICK PORTION of ascending limb true
Na -K ATPase operates at basolateral membrane to create ionic gradient that drives the symporter.
Thick ascending limb also has Na -H antiporters
50% of sodium passes via paracellular route in thick region true
Distal Convuluted tubule and Collecting ducts pg978 Pg978 by time DCT is reached only 10% of originally filtered NaCl and 25% of water remain in tubule
Most reabsorption from this point on depends on the bodies needs and is regulated by hormones (mainly aldosterone for Na, ADH for water, and PTH for Ca
In absence of ADH, the collecting duct is relatively impermeable to water so reabsorption of more water depends on presence of ADH, which insert aquaporins
Aldosterone "fine tunes" reabsorption of remaining Na decreased BV or BP, low extracellular Na concentration (hyponatremia), or high extracellular K concentration (hyperkalemia) can cause adrenal cortex to release aldosterone to the blood
Except for hyperkalemia (which directly stimulates the adrenal cortex to secrete aldosterone) these conditions promote the renin-angiotensisn mechanism,w which in turn prompts the release of aldosteone
little or no Na leaves the body in urine w/ aldosterone without aldosterone, much less Na is is reabsorbed , resulting in Na losses of about 2% of Na filtered daily an amount IMCOMPATIBLE WITH LIFE
Aldosterone's Role (conserve Na) increase BV , and therefor BP, by enhancing Na reabsorption. Also reduces K concentrations because it induced reabsorption of Na is couple to K secretion in principal cells. That is Na enters K moved into lumen
Atrial natriuretic peptide (ANP) reduces Na, thereby decreasing BV and BP; Released by cardiac atrialcells when BV or BP is elevated, ANP exerts sever effects that lower Na content
Failure of tubule cells to reabsorb some solutes is an important way of clearing plasma of unwanted substances another way is TUBULAR SECRETION
Tubular Secretion essentially reabsorption in reverse; H, K NH, creatinine and certain organic acids either move into the filtrate from the peritubular capps through the tubule cells or are synthesized in the tubule cells and secreted.
Urine eventually exerted contains both filtered and secreted substances. with one major exception, (K) the PCT is the MAIN site of SECRETION, but the cortical parts of the COLLECTING DUCTS are also active
Tubular secretion is important for; Pg 978 Disposing of substances Eliminating undesirable substances Ridding the body of excess K Controlling blood pH
Regulation of Urine Concentration and volume pg979 Pg 979 crucial renal function is to keep the solute concentration of body fluids constant
Osmolality is number of solute particles dissolved in 1 kg of water and reflects solution's ability to cause osmosis
1 osmol (equivalent to 1 mole of particles) because this is a fairly large unit, the milliosmol (mOsm) equal to 0.00l osmol, is generally used
Kidneys keep the solute load of body fluids constant at 300 mOsm the osmotic concentration of blood plasma, by regulating urine concentration and volume
Countercurrent mechanisms fluid flows in opposite direction through adjacent segments of the same tube connected by a hairpin turn
Countercurrent mechanisms are 1) the interaction between flow of filtrate through ascending and descending limbs of long loops of Henle of juxtameduallary nephrons (the COUNTER CURRENT MULTIPLIER. 2) the flow of blood through the ascending and descending portions of the vasa recta
Vasa Recta blood vessels are the countercurrent exchanger
Osmolality of filtrate entering PCT is identical to plasma, 300 mOsm because of PCT reabsorption of water and solutes, filtrate is still iomotic w/ plasma by the time it reaches the descending limb.
Osmolality increases from 300 to 1200 mOsm in the deepest part of the medulla true
filtrate in the loops of Henle and blood in the vasa recta - first descend an then ascend through parallel limbs true
Countercurrent multiplier functions because of two factors Pg979 1)descending limb of loop is relatively impermeable to solutes and freely permeable to water 2) ascending limb is permeable to solutes, but not to water
Uria recycling and the Medullary Osmotic Gradient pg981 Pg 981 Urea enters the filtrate by facilitated diffusion in ascending thin limb; water reabsorbed; now highly concentrated is transpired by facilited diffusion out of tubule into IF of the medulla, forming pool of urea; recycles back into thin limb
ADH, stimulates exertion of urine, enhances urea transport in medullary collecting duct. When ADH is present, urea recycling is enhanced, medullary osmotic gradient is enhanced and more concentrated urine can be formed
Countercurrent Exchanger (vasa recta function as this) Pg 981 maintaining gradient ; blood flow is sluggish;passive exchanges w/ IF. as blog flows into medullary depths, it LOSES water and GAINS sal (hypersonic). as it emerges from medulla to cortex, it picks up water and loses salt
Water picked up by ascending vasa includes not only water lost from descending vasa, but water reabsorbed form loop As a result, volume of blood at the end of the vasa recta is GREATER than at the beginning
Vessels of the vasa recta act as countercurrent exchangers; this system does not create the medullary gradient, but it protects it by preventing rapid removal of sal an removing reabsorbed water
Formation of Dilute or Concentrated Urine Pg 981 w/o gradient you would not be able to raise the concentration of urine above 300 mOsm; as a result you would not be able to EXCRETE excess solutes to lower your body's osmolality
ADH ( Inhibits diuresis, or urine output) controlling reabsorption of water from filtrate order to adjust the body's osmalality
Dilute Urine When ADH is not ring released; the collecting ducts remain essentially impermeable to water du to absence of aquaporins in luminal cell membranes, and no further water reabsorption occurs
Na and selected other ions can be removed from the filtrate by DCT and collecting duct cells so that urine becomes even more dilute before entering the renal pelvis osmolality of urine can plunge as low as 50 mOsm about one sixth the concentration of glomerular filtrate or blood plasma
Concentrated Urine formation of concentrated urine depends on medullary osmotic gradient and the presence of ADH
In distal tubules filtrate osmolality is 100 mOsm as filtrate flows through the collecting ducts and is subjected to hyperosmolar conditions, water rapidly leaves followed by urea
Depending on amount of ADH released urine concentration my rise as high as 1200 mOsm, the concentration of IF in the deepest part of the medulla
Maximal ADH secretion, up to 99% of water is reabsorbed and returned to blood, half a liter per day of highly concentrated urine is excreted
Ability of our kidneys to produce such concentrated urine is critically tied to our ability to survive w/o water
Facultative water reabsorption Water reabsorption that depends on the presences of ADH
ADH release is enhanced by any event that raises plasma osmolality above 300 mOsm, such as sweating diarrhea, or reduced BV or BP
Release of ADH is the "signal" to produce concentrated urine that opens the door for water reabsorption (through aquaporins) Kidneys ability to respond to signal depends on the high medullary osmotic gradient
Diuretics Pg 982 several types; chemicals that enhance urinary output
osmotic diuretic substance that is not reabsorbed and that carries water out with it
Alcohol, essentially a sedative, encourages diuresis by inhibiting release of ADH other diuretics increase urine flow by inhibiting Na reabsorption and the obligatory water reabsorption that normally follows.
also, caffeine and many prescribed drug for hypertension or edema of congestive heart failure common diuretics inhibit Na associated symporters.
Loop diuretics (like furosemide(lasix) are powerful because they inhibit formation of the medullary gradient by acting as the ascending limb of Henle's loop. THIAZIDES are less potent and act at the DCT
Renal Clearance Pg 984 refers to volume of plasma that is cleared of a particular substance in a given time(usually 1 min)
Renal Clearance Test are done to determine the GFR which allows us to detect glomerular damage and followw the progress of renal disease
Renal clearance rate (RC) in ml/min is calculated RC = UV/P where U = concentration of the substance in urine V = flow rate of urine formation P=concentration of the substance in plasma
Insulin freely filtered and neither reabsorbed nor secreted by the kidneys; is standard used to determine the GFR
Inulin (polysaccharid w/ a molecular weight of 5000 has a renal clearance value equal to GFR; when inulin is fused such that its plasma concentration is 1mg/ml(P = 1mg/ml), then generally U =125 mg/ml, and V = 1 ml/min. Therefor RC = (125 x 1)/1 = 125 ml/min
Meaning that in 1 minute the kidneys have removed (cleared) all inulin present in 125 ml of plasma
chronic renal disease GFR of less than 60 ml/min for at least three months
Renal failure GFR <15 ml/min; filtrate formation decreases or stops completely
Urine Pg 984 color and transparency; UROCHROME, a pigment that results from the body's destruction of hemoglobin
More concentrate the urine, the deeper the yellow color abnormal color (pink or brown) eating certain foods or presence in the urine of bile pigments or blood
cloudy urine indicated a urinary tract infection
odor in urine fresh is slightly aromatic, but let stand it develops ammonia odor as bacteria metabolize its urea solutes
uncontrolled DM urine smells fruity because of its acetone content
pH of urine usually slightly acidic (pH 6) changes in body metabolism or diet may cause the pH to vary form 4.5 to 8.0.
A predominantly acidic diet that contains large amount of protein and whole wheat products produces acidic urine Vegetarian (alkaline) diet, prolonged vomiting, and bacterial infection of the urinary tract all cause the urine to become alkaline
Specific gravity urine is water plus solutes, a given volume has a greater mass than the same volume of distilled water; ratio of mass to mass of equal volueme of distilled water is SPECIFIC GRAVITY; distilled water 1.0; Urine ranges from 1.001 to 1.035
Chemical Composition Pg 985 95% water; 5% solutes;
largest component of urine by weight, apart form water, is UREA derived from the normal breakdown of amino acids
Nitrogenous wastes in urea, include uric acid (end product of nucleic acid metabolism) and creatinine (metabolite of creatine phosphate which stores energy for regeneration of ATP. Found in large amounts in skeletal muscle tissue
Normal solute constituents of urine (order of decreasing concentration) urea, Na, K, PO, SO, creatinine, and uric acid; much smaller but highly variable amounts of Ca, Mg, and HCO are also present
High concentrations of any solute or the presence of abnormal substances such as blood proteins, WBCs(pus), or bile pigments may indicate pathology true
Ureters Pg 985 Slender tubes that convey urine from kidney to bladder; begins at L2 as continuation of renal pelvis
Any increase in bladder pressure compresses and closes the distal ends of the ureters
Ureter wall has three layers transitional epithelium of its lining MUCOSA is continuous w/ that of kidney pelvis superiorly and bladder medially; Middle MUSCULARIS two smooth muscle sheets (internal longitudinal layer, external circular layer)cont'd
An additional smooth muscle layer, the extrnal longitudial layer, arrears in lower third of ureter. The ADVENTITIA covering the ureter's external surface is typical fibrous connective tissue true
Ureter plays an active role in transporting urine; incoming urine distends ureter and stimulates muscularis to contract, propelling urine into bladder
Urine DOES NOT reach the bladder through gravity alone strength and frequency of peristaltic waves are adjusted to the rate of urine formation
Each ureter is INNERVATED by both SYMPATHETIC and PARASYMPATHETIC fibers BUT neural control of peristalsis appears to be insignificant compared to the way ureteral smooth muscle responds to stretch
Bladder Pg 986 smooth, collapsible, muscular sac; stores urine temporarily;
interior of the bladder has openings for both ureters and urethra
Trigone smooth, triangular region of the bladder base outlined by these three openings; Important clinically because INFECTIONS tend to persist here
Bladder wall has 3 layers mucosa(transitional epithelium) Thick muscular layer Fibrous adventitia (except on its superior surface)
Detrusor muscle muscular layer; consists of intermingled smooth muscle fibers arranged in inner and outer longitudinal layers and a middle circular layer
Rugae bladder folds
Moderately full bladder 12cm (5inches); holds 500 ml (1 pint); Can hold double; When tense w/ urine it can be palpated well above the pubi symphysis; MAX capacity 800-1000ml
Urethra Pg 987 thin-walled muscular tube; drains urine from bladder to outside body; epithelium of mucosal linin is pseudostratified columnar;but Near the bladder it becomes transitional epithelium; near external opening changes to stratified squamous
Internal urethral sphincter at bladder-urethra junction; thickened detrusor smooth muscle; involuntary; UNUASUAL in that contraction OPENS, relaxation CLOSES it
External urethral sphincter surrounds urethra as it passes through the UROGENITAL DIAPHRAGM; skeletal muscle; voluntarily controlled
Levator ani muscle of pelvic floor also serves as a voluntary constrictor of the urethra
Female urethra Female urethra 3-4cm(1.5 in); tightly bound to anterior vaginal wall by figrous connective tissue
External urethral orifice external opening; lies anterior to vaginal opening and post to clit
Male urethra 20cm(8in); 3 regions
Prostatic urethra (1inch) runs w/in prostate
Membranous urethra runs through the urogenital diaphragm, extends about 2cm from prostate to beginning of penis
Spongy urethra (15cm) passes through the penis and opens at the tip via EXTERNAL URETHRAL orfice
Micturition (urinate) Pg 988 In order for this to occur; detrusor muscle must contract, internal urethral sphincter must open, external urethral sphincter must open
Detrusor muscle and its internal urethral sphincter composed of smooth muscle; innervated by both Para and Sympathetic nervous systems, which have opposing actions
External urethral sphincter is skeletal muscle; is innervated by the somatic nervous system
Spinal reflex coordinate the process of micturition urine accumulates, bladder distends activating stretch receptors; impulses travel vi avisceral afferent fibers to sacral region of spinal cord; cont'd
Visceral afferent impulses, relayed by sets of interneurons, excite parasym neurons and inhibit symp neurons as a result, detrusor muscle contracts nad internal sphincter opens; Visceral afferent impulses also inhibit tonically active somatic effernts that keep the external urethral sphincter closed
by age 2 descending circuits have matured enought to begin to override relexive urination Pons has two centers that participate in control of urination; PONTINE STORAGE center inhibits, PONTINE MICTURITION center promotes this reflex
lower bladder volumes activate the pontine storage center which acts to inhibit urination by suppressing parasym and enhancing symp output to bladder
Choose not to void reflex bladder contractions subside
Developmental Aspects Pg 988 3 different sets of kidneys develop from the UROGENITAL rigdges, paired elevations of the intermediate mesoderm that give rise to both urinary organs and reproductive organs
Pronephros (4th week)first tubule system forms then quickly degenerate as second, lower set apprears; NEVER function; gone by 6th week
Pronephric duct connects pronephros to cloaca; it is retained and used by later developing kidneys
The cloaca is the terminal part of the gut that opens to the body exterior true
Mesonephros (middle kidney) 2nd renal system claims the pronephric duct (now called mesonephric duct); these degenate once the 3rd set makes their apperance
Metanephros (after Kidneys) 3rd set; 5th week; URETERIC BUDS push superiorly from mesonephric duct
Ureteric ducts become ureters
Mestanephric kidneys excrete urine by 3rd month true
as metanephros develope cloaca subdivides to form the future rectum and anal canal and the UROGENITAL SINUS, into which urinary and genital ducts empty
Urinary bladder and the Urethra develope from urogenital sinus
Hypospadias male infants only; orifice is located on the ventral surface of the penis
Polycystic kidney disease (PKD) disorder; presence of many fluid filled cysts in kidneys; cause renal failure
adult urine output 1500 ml/day
Created by: tammiemcconnell
 

 



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