Chapter 25 Urinary System Flashcards

1
Q

Urinary system organs

A
  • kidneys are major excretory organs
  • urinary bladder is the temporary storage reservoir for urine
  • ureters transport urine from the kidneys to the bladder
  • urethra transports urine out of the body
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2
Q

kidney functions

A
  • removal of toxins, metabolic wastes, and excess ions from the blood
  • regulation of blood volume, chemical composition, and pH
  • gluconeogenesis during prolonged fasting
  • endocrine function
  • activation of vitamin D
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3
Q

endocrine functions

A
  • renin- regulation of blood pressure and kidney function

- erythropoietin (EPO)- regulation of RBC production

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4
Q

renal cortex

A

a granular superficial region

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5
Q

renal medulla

A

-the cone shaped pyramids separated by renal columns

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6
Q

renal pelvis

A

the funnel-shaped tube within the renal sinus, continuous with the ureter

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7
Q

urine flow

A

-urine flow from pyramid -> minor calyces -> major calyces -> renal pelvis -> ureter

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8
Q

nephrons

A
  • structural and functional units that form urine
  • about 1 million per kidney (correction pyramid)
  • 2 main parts:
  • renal corpuscle
  • renal tubule
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9
Q

renal corpuscle

A

-capsule (bowman’s) and glomerulus

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10
Q

renal tubule

A

-prox and distal convoluted tubule, nephron loop and collecting duct

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11
Q

two types of nephrons

A
  • cortical nephrons

- juxtamedullary nephrons

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12
Q

cortical nephrons

A
  • 85% of nephrons
  • almost entirely in the cortex
  • has short loop of henle and glomerulus
  • efferent arteriole supplies peritubular capillaries
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13
Q

juxtamedullary nephrons

A

-long loops of henle deeply invade the medulla
-outside the cortex
-important in the production of concentrated urine
efferent arteriole supplies vasa recta

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14
Q

nephron capillary beds: glomerulus

A
  • afferent arteriole -> glomerulus -> Efferent arteriole (only place in body)
  • specialized for filtration
  • blood pressure is high because:
  • arterioles are high pressure
  • afferent arterioles are larger in diameter than efferent arterioles
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15
Q

nephron capillary beds: peritubular capillaries

A
  • low pressure
  • porous
  • meandering
  • associated with cortical nephron
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16
Q

nephron capillary beds: vasa recta

A
  • long and straight vessel loops of Henle
  • juxtamedullary nephrons
  • formation of concentrated urine
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17
Q

renal tubule

A
  • glomerular capsule
  • proximal convoluted tubule (PCT)- functions in reabsorption and secretion
  • loop of Henle- descending and ascending limbs
  • distal convoluted tubule (DCT)- secretion
  • collecting duct- receives filtrate from many nephrons
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18
Q

juxtaglomerular complex (JGC)

A
  • one per nephron
  • important in regulation of filtrate formation and blood pressure
  • involved modified portion of the:
  • distal portion of the ascending limb of the loop of henle
  • afferent (sometimes efferent) arteriole
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19
Q

juxtaglomerular complex: granular cells

A
  • wall of afferent arteriole
  • mechanoreceptors (monitor BP)
  • secrete enzyme renin
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20
Q

juxtaglomerular complex- macular dense cells

A
  • cells in ascending limb of tubule

- chemoreceptors monitor NaCl of filtrate entering the distal convoluted tubule

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21
Q

filtration membrane

A
  • porous membrane between the blood and the capsular space
  • consists of:
    1. fenestrated endothelium (pores) of the glomerular capillaries
    1. visceral membrane of the glomerular capsule (podocytes with foot processes and filtration slits)
    1. basement membrane- negatively charged basement membrane repels large plasma proteins
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22
Q

which of the following is not associated with the renal corpuscle

A
  • a podocyte
  • a vasa recta**
  • a fenestrated capillary
  • an efferent arteriole
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23
Q

which of the following is true about the macula dense cells

A
  • they are mechanoreceptors
  • they are found in the wall of the arteriole
  • they monitor NaCl content*
  • all of the above
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24
Q

mechanisms of urine formation

A
    1. glomerular filtration- “clean out closet”- passive nonselective
    1. tubular reabsorption- returns all glucose and amino acids, 99% of water, salt, and other components to the BLOOD
    1. tubular secretion- reverse of reabsorption - selective addition to urine
25
Step 1- glomerular filtration
- passive, nonselective process (no ATP) - filtration membrane (Efficient) - large plasma proteins are not filtered and function to maintain colloid osmotic pressure of the blood - net filtration pressure (NFP) = pressure responsible for filtration - negative pressure drives filtration - glomerular filtration rate due to 3 factors: - net filtration pressure - total surface area (large) - membrane permeability
26
Regulation of glomerular filtration rate
- GFR is tightly regulated to serve 2 crucial needs - 1. kidneys need a constant GFR to make filtrate - 2. body as a whole needs a constant BP - the 2 are closely related, if GFR increases, urine output increases which reduced blood volume and BP - GFR is tightly controlled by two types of mechanisms - INTRINSIC CONTROLS - EXTRINSIC CONTROLS
27
intrinsic controls of GFR
- renal autoregulation - act locally within the kidney - maintains a nearly constant GFR when MAP (mean arterial pressure) is in the range of 80-100 mm Hg - two types of renal autoregulation - myogenic mechanism- (stretch) - tubuloglomerular feedback mechanism, which senses changes in Na concentration of filtrate
28
extrinsic controls of GFR
-nervous and endocrine mechanisms that maintain blood pressure, but affect kidney function
29
intrinsic controls: myogenic mechanism
- increased systemic BP stretches vascular smooth muscle -> constriction of afferent arterioles - prevents glomerulus BP from rising - protects glomeruli from damaging high BP - decreased systemic BP -> dilation of afferent arterioles - helps maintain normal GFR
30
intrinsic controls: tubuloglomerular feedback mechanism
- macula densa cells (in walls of ascending limb, salt monitoring)- flow dependent - if GFR increases, filtrate flow rate increases in the tubule - NaCl concentration in filtrate will be high because of insufficient time for reabsorption - macula dense cells respond to increased NaCl by releasing a chemical that vasoconstricts the afferent arteriole -> decreased GFR (slows down rate of flow) - the opposite occurs if GFR decreases and causes vasodilation of afferent arterioles
31
tubuloglomerular mechanism of autoregulation
- 1. GFR increases - 2. increased filtrate flow - 3. flow past macula dense increases (in JGC) - 4. release of vasoactive chemicals - 5. afferent arteriole contracts - 6. resistance in afferent arteriole increases - 7. hydrostatic pressure in glomerulus decreases - 8. GFR decreases
32
extrinsic controls: sympathetic nervous system
- under normal conditions at rest: renal blood vessels are dilated and renal autoregulation (intrinsic) mechanisms prevail - under extreme stress (low BP shock - need to maintain BP): - norepinephrine and epinephrine are released - both cause constriction of afferent arterioles which inhibit filtration of afferent arterioles which inhibit filtration and renin is released - goal: restore blood volume and pressure
33
summary of intrinsic control
- myogenic mechanism- if increased BP, stretches arteriole wall, causes constriction and decreases BP - tubuloglomerular feedback- if GFR increases, will have increased flow rate, NaCl will be high, macula dense cells (ascending limb) will detect and release a chemical for constriction
34
which of the following factors contributes to the higher filtration rate in the glomerular capillaries compared with other capillary beds
- the glomerular capillaries are fenestrated - the diameter of the efferent arteriole is smaller than the diameter of the afferent arteriole - the visceral layer of the glomerular capsule is very porous - all of the above contribute*
35
where does filtration occur in the nephron
- glomerular capsule* - proximal convoluted tubule - loop of henle - distal convoluted tubule
36
extrinsic controls renin-angiotensin-aldosterone
- main mechanism for raising BP** - low BP causes granular cells to release renin - renin assists in changing angiotensinogen to angiotensin 2
37
effects of angiotensin 2
- 1. constricts arteriolar smooth muscle, causing MAP to rise - 2. triggers aldosterone secretion from adrenal cortex- stimulates the reabsorption of Na+ (Na moves into blood, water follows, conserves blood volume) - 3. stimulates the hypothalamus to release ADH (antidiuretic hormone) and activates the thirst center
38
step 2. tubular reabsorption
- a selective process that begins in the proximal convoluted tubule - all organic nutrients are reabsorbed - water and ion reabsorption are hormonally regulated - includes active (requires ATP) and passive transport - different areas of the tubules have different absorptive capabilities - if not for tubular reabsorption all our plasma would drain away as urine in 30 mins
39
reabsorption of nutrients, water, and ions
- Na+ reabsorption- active transport - organic nutrients (glucose, AA, vitamins)- by secondary active transport (carriers) -> when the carriers are saturated, the excess of that substance is excreted (glucose in urine is sign of DM) - water- reabsorbed by osmosis- aided by pores called aquaporins
40
resabsorptive capabilities of renal tubules and collecting ducts
- PCT- site of most reabsorption (ions, water, nutrients) - loop of henle- descending limb- H20 - ascending limb- Na, K, Cl - DCT and collecting duct: - hormonally regulated - Na- aldosterone - water- ADH - Ca- parathyroid hormone
41
which of the following general functions can be assigned to the renin-angiotensin-aldosterone system
- water conservation - blood pressure elevation - lowering blood sodium levels - both a and b* - all of the above
42
if systemic BP is extremely low, epinephrine is released form adrenal medulla. This type of control is called
- extrinsic* - myogenic mechanism - intrinsic - tubuloglomerular feedback
43
step 3: tubular secretion
- eliminates undesirable substances (e.g. urea and uric acid) - disposes of substances such as drugs - rids the body of excess K+ - controls blood pH by altering amounts of H+ or HCO3- in urine - these solutes move from peritubular capillaries into filtrate
44
regulation of urine concentration and volume
- kidneys make adjustments to keep solute concentration constant, whether dehydrated or overhydrated - osmolality of body fluids: - the kidneys maintain osmolarity of plasma at about 300 mOsm, using countercurrent mechanisms - allow the kidneys to vary urine concentration
45
countercurrent mechanism
- occurs when fluid flows in opposite directions in two adjacent segments of the same tube - filtrate flow in the loop of henle - blood flow in the vasa recta - fluid flows in the opposite direction through two adjacent parallel sections of a nephron loop
46
countercurrent multiplier: loop of henle
- DESCENDING LIMB: reabsorption of water - freely permeable to H20 NOT salt - filtrate osmolality increases to about 1200 mOsm - ASCENDING LIMB: reabsorption of salt - selectively permeable to solutes - impermeable to water and pumps out salt - filtrate osmolality decreases to 100 mOsm - filtrate is diluted in the ascending loop
47
dehydrated- maximal ADH
- if ADH is present, aquaporins are inserted in collect ducts - water is reabsorbed back into capillaries
48
the descending limb of the nephron loop ___
- is not permeable to water - is freely permeable to sodium and urea - pulls water by osmosis into the lumen of the tubule - contains fluid that becomes more concentrated as it moves down into the medulla*
49
at the collecting ducts, which hormone is required for the reabsorption of Na
- antidiuretic hormone (ADH) - parathyroid hormone - atrial natriuretic peptide - aldosterone
50
diuretics
- chemicals that enhance the urinary output - osmotic diuretics- substances not reabsorbed (e.g. high glucose in a diabetic patients, water follows glucose) - ADH inhibitors such as alcohol - substances that inhibit Na reabsorption and obligatory H2O reabsorption such as caffeine and many drugs
51
physical characteristics of urine
- color and transparency: - clear, pale to deep yellow - cloudy urine may indicate a UTI - pink urine= blood - odor: - slightly aromatic when fresh - develops ammonia odor upon standing - may be altered by some drugs and vegetables - diabetics= fruity smelling
52
ureters
- convey urine from kidneys to bladder - enter the base of the bladder through the posterior wall - as bladder pressure increases, distal ends of the ureters close, preventing backflow of urine
53
urinary bladder
- muscular sac for temporary storage of urine - collapse when empty; rugae (folded walls) appear - trigone (inferior portion of bladder)- infections tend to persist in this region
54
urethra
- sphincters: - internal urethral sphincter- involuntary (smooth muscle) at bladder- > urethra function -> internal sphincter opens - external urethral sphincter- voluntary (skeletal) muscle surrounding the urethra as it passes through the pelvic floor
55
drinking too much alcohol results in a headache the next day. Why does this happen
- alcohol stimulates pain receptors in the brain - alcohol stimulates sodium reabsorption - alcohol stimulates aldosterone secretion - alcohol inhibits ADH secretion* i think
56
urine flows from kidney to bladder via
- nephrons - urethra - ureter * - loop of henle
57
micturition
- urination or voiding - three simultaneous events - 1. contraction of detrusor muscle by ANS - 2. opening of internal urethral sphincter by ANS - 3. opening of external urethral sphincter by somatic nervous system
58
reflexive urination infants
- distention of bladder activates stretch receptors - excitation of parasympathetic neurons in reflex center of spinal cord - contraction of the detrusor muscle - opening of internal sphincter - inhibition of somatic pathways to external sphincter, allowing its relaxation (opening)
59
pontine control centers mature between ages 2-3
- pontine storage center inhibits micturition- inhibits parasympathetic pathways and excites sympathetic and somatic efferent pathways - pontine micturition center promotes micturition- excites parasympathetic pathways and inhibits sympathetic and somatic efferent pathways