WEEK NINE - Functions of the urinary system and anatomy of the kidney Flashcards

1
Q

State the components of the urinary system

A

SIX organs

2 x kidneys
2 x ureters
Urinary bladder
Urethra

Primary Function = prediction and excretion of urine

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2
Q

FVEBP

State and describe 5 functions of the kidneys other than urine formation

A
  1. Blood plasma filtration
    Blood filter which excretes harmful toxic waste products
  2. Regulation of blood volume
    Conserves water or eliminates it in urine
  3. Production of ERYTHROPOIETIN
    Stimulate RBC production in red bone marrow
  4. Regulation of BP
    Kidneys secrete renin - helps bp by activating renin angiotensin-aldosterone pathway
  5. Regulate blood pH
    Kidneys excrete H+ and reabsorb HCO3 = helps maintain acid-base balance of body fluids
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3
Q

Describe the location and gross anatomy of the kidneys

A

kidneys = bean shaped retroperitoneal organs which lay lay against posterior abdominal wall at level of T12 –> L3
* R kidney = slightly lower due to R lobe of liver above

  • lateral surface = convex
  • medial surface concave w slit [hilum]
  • ~150g
  • 11cm long x 6cm wide x 3cm thick

THREE CT LAYERS
1. renal fascia [outer]
* binds to abdominal wall

  1. perirenal fat capsule [mid]
    * cushions kidney and holds it in place
  2. fibrous capsule [inner]
    * encloses kidney - protects from trauma and infection
  • the renal parenchyma consist of two zones = OUTER renal CORTEX + INNER renal MEDULLA
  • renal columns divide the medulla into 6-10 pyramids, with each papilla found nestled in the minor calyx
  • 2 or 3 minor calyx –> major calyx
  • 2 or 3 major calyx –> **renal pelvis **
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4
Q

Name the major nitrogenous wastes and state their sources

A
  1. urea
    made from protein catabolism of AA –> deamination of NH2 = ammonia [NH3] –> converted to urea by LIVER
  2. uric acid
    - nucleic acid catabolism
  3. creatinine
    creatine phospahte metabolism
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5
Q

Trace the flow of blood through the kidneys & identify the vessels

A

abdominal aorta > renal a. > segmental a. > interlobar a. > arcuate a. > cortical radiate a. > afferent arterioles > glomerulus > efferent arteriole > peritubular capillaries OR vasa recta > cortical radiate v./interlobular v > arcuate v > interlobar v > renal v. > IVC

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6
Q

Describe the nephron and its 2 parts (renal corpuscle and renal tubule)

A

NEPHRON = functional unit of kidneys - responsible for urine formation. found in renal pyramid ~ 1.2 million nephrons/kidney
- TWO types of nephrons
1. cortical
- found in OUTER 2/3. of cortex [~85% of nephrons]

  1. juxtamedullary
    - inner 1/3 of cortex
    - 15% of nephrons

**RENAL CORPUSCLE **
glomerulus
- specialised capillary network in phrone = filters plasma + produces filtrate [1st step in urine formation]

bowman’s capsule [around glomerulus]
- two layered capsule with capsular space
- visceral layer = comprised of podocyte cells which make up epithelial lining

**RENAL TUBULE **
- proximal convoluted tubule [PCT] = simple cuboidal epithelium w/ microvilli

  • nephron loop
    primarily in medulla w/ :
    THICK segment –> simple cuboidal epithelium = active transport of saltsTHIN segment = simple squamous epithelium –> highly permeable to water
  • distal convoluted tubule [DCT]
    found at end of nephron loop
    simple cuboidal epithelium - NO microvilli
  • collecting duct
    receives filtrate from multiple DCTs
    CDs merge w/ eachother = papillary ducts
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7
Q

Describe the filtration membrane and the process by which the kidney filters the blood plasma

A

Almost any molecule < 3nm can pass freely through filtration membrane
Eg water, electrolytes, AAs, nitrogenous wastes and vitamins
- 99% reabsorbed = only 1/2L of urine is formed/day

THREE BARRIERS
1. Fenestrated endothelium of glomerular capillaries
- 70-90nm filtration pores
- HIGHLY permeable type of capilary
- allows passage of water, AAs, glucose, electroyltes
- EXCLUDES LARGER moleciles eg blood cells, plasma proteins from filtrate

  1. Basement membrane [proteoglycan gel]
    - LARGER than 8nm
    - repels some smaller molecules due to NEGATIVE CHARGE. eg albumin
    - small protein bound solutes DONT pass
  2. Filtration slits of podocyte
    - pedicel extensions wrap around capillary to form barrier w/ 30nm filtration slits
    - NEGATIVELY charged = repels anions
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8
Q

Explain the forces/factors that promote and oppose filtration

A

PROMOTES&raquo_space;
Blood hydrostatic pressure
[BHP] = 60 mmHg outwards = much higher than most other capillaries. –> results from a large afferent arteriole vs small efferent arteriole at glomerulus

OPPOSES»
Capsular hydrostatic pressure
[CP]= 18 mmHg inwards pressure
- results from high rate of filtration and accumulation of fluid in capsule

Colloid Osmotic Pressure
[COP]
- 32 mmHg inwards pressure
- filtrate is almost protein free hence NO significant COP

Net filtration pressure [NFP] = 60-32-18=10 mmHg
- 60 mmHg OUT [blood hydrostatic pressure]
- 32 mmHg IN [colloid osmotic pressure]
-18 mmHg IN [capsular pressure]
= net filtration pressure [NFP] = 10 mmHg OUT

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9
Q

Describe how renal autoregulation controls glomerular filtration rate

A

= Ability of nephron to adjust to own BF and GFR w/o external control
TWO MECHANISMS
**1. Myogenic Mechanism **
- based on smoo.musc contraction tendency when stretched
- aims to regulate BF ensuring relatively constant production of urine
^ BP = stretches afferent arterioles = vasoconstriction
v BP in afferent arteriole = vasodilation

2. Tubuloglomerular Feedback
- HIGH GFRs = LESS reabsorption of NaCl in renal tubules
- Macula densa detects ^ in fluid flow and ^ NaCl levels in DCT
- Macula densa secretes paracrine signal –> stims juxtaglomerular cells [JG] = inhibit release of nitric oxide = vasoconstriction of afferent arteriole

Negative Feedback Control of
GFR
1. High GRF
2. Rapid flow of filtrate in renal tubules + ^ NaCl reabsoprtion
3. Sensed by macula densa cells
4. Paracrine secretion –> JG cells [inhibits release of nitric oxide]
5. Constriction of afferent arteriole
6. Reduced GFR

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10
Q

Describe how the nervous system controls glomerular filtration rate

A

symp. nerve fibres richly innervate renal blood vessels >
strenuous exercise, circulatory shock and fight/flight responses stimulate vasoconstriction of afferent arterioles
- because blood is redirected to heart/brain/skeletal muscles –> GFR/urine output = DECREASED

symp.control can also initiated renin release when BP is decreased

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11
Q

Describe how the renin-angiotensin-aldosterone mechanism acts to control blood pressure

A

if BP DECREASES dramatically > JG cells secrete renin
>renin converts angiotensinogen to angiotensin I
>angiotensin I converted to active hormone - angiotensin II by angiotensin-convertine-enzyme [ACE] in lungs

**angiotensin II **
> potent vasoconstrictor = ^ mean arterial BP bodywide
> constricts aff.art. = ^/maintains GFR desite low BP
> constriction of eff.art = v BP in peritubular caps = ^ NaCl reabsoprtion/H20 retention = ^ body wide BP
> stimulates adrenal cortex to secrete aldosterone in DCT and CD = ^ Na reabsorption/H2o retention
>stims post.pit to secrete ADH = stims H2o reab. in DCT, aquaporin synthesis in CD
> stimulates water intake via thirst

** ^ NaCl/Na/ H2O reabsorption/retention = ^ BP**

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12
Q

Describe tubular reabsorption and how it takes place

A

Removes useful water/solutes [eg NaCl, water, Glucose] from filtrate → returning them to blood
- PCT reabsorbs greater variety of chemicals than any other part of nephron and reabsorbs 65% of filtrate to preitubular capps
> great length, prominent microvilli and abundant mitochondria = active transport

Routes of tub.reab.
1. transcellular
- pass through cytoplasm via aquaporins

  1. paracellular
    - substances pass through leaky tight junctions between cells
  2. water abosrbed by osmosis carries some other solutes [solvent drag]

NaCl reabsorption [two mechanisms]
> uses symports which bind Na+ to another solute eg AA, glucose
> antiports which pull Na+ into cell whilst H+ is pumped out [Na+H+ antiport is activated by** angiotensin II **= IMPORTANT INFLUENCE ON REABSOPRTION]

Water
>reabsorbed both by transcellular route via aquaporins
>also reabsorbed by paracellular route via osmosis
>2/3 of water is reabsorbed in PCT at constant rate [obligatory water reabsorption]

Glucose
> co-transported into epithelium w/ Na+ via Na-glucose transporteres
> 100% reabsorption in healthy subjects

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13
Q

Describe tubular secretion and state solutes that are excreted

A

tub.sec. = removes additional wastes from peritubular capillary blood –> secretes them to filtrate
> eg urea, creatinine, bile salts, ammonia, catecholamines, drugs [morphine, penicillin, aspirin]

tub.sec. = TWO functions
1. waste removal
2. acid-base balance
[regulate pH]
- ^ secretion of H+ and ^ reabsorption of HCO3- = INCREASED PH

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14
Q

Describe how the nephron regulates water conservation

A

nephron = responsible for regulating water cons. reab useful substances and excreting waste products

  1. PCT
    - majority [65%] of water is reab here due to great length, microvilli and mitochondria which aid active transport
  2. loop of Henle/ nephron loop
    - countercurrent exchange mechanism creates osmotic/salinity gradient from 300 mOsm/L in the cortex to 1200 mOsm/L in the medulla
    - thin desc limb = permeable to water = water reab –> interstitial fluid = ^ osmo
    - thick asc limb permeable to solutes NOT water = NaCl pumped out = ^ osmo
    - as water moves from low–> high osmolarity, the countercurrent exchange mechanism promotes water reab
    - think portion of loop reab. 15% water from filtrate
    - reabsorbs 25% of electrolytes - Na+, K+, Cl- remaining in filtrate
    [K+ = secreted back –> tubular fluid via Na+/K+ pump /// NaCl stays in tissue fluid of medulla]

DCT
- fluid arriving in DCT still contains 20% of the water and 7% of the salts from filtrate
- further water reab. occurs, as regulated by hormones such as ADH, aldosterone, angiotensin II, ANP, PTH

CD
- the permeability of the CD is controlled by ADH which is secreted in events of dehydration.
- ADH synthesises aquaporins in the CD making the membrane more permeable to water and promoting water reab.
- as the filtrate travels down the increasingly salty medulla water is reab. = via osmosis

DCT and CD reabsorb variable amounts of water/salt as regulated by hormones - aldosterone, atrial natriuretic peptides [ANP], ADH, parathyroid hormone [PTH]

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15
Q

Discuss the roles of aldosterone, atrial natriuretic peptide (ANP) and parathyroid hormone (PTH) on kidney function

A

ALDOSTERONE [salt retaining steroid hormone secreted by adrenal cortex on kidneys]
- acts to MAINTAIN/^ BP **
- secreted when Na+ FALLS or K+ rises in blood [LOW BP]
- also secreted in renin-angiotensin-aldosterone mechanism from drop in BP [
angiotensin II **stimulates aldosterone secretion]

  • acts on thick segment of nephron loop, DCT and cortical portion of CD
  • promotes Na+/water/Cl- reab. and K+ sec.
    -effect = body retains NaCl/water = **maintains BP/volume **

ANP [sec. - atrial myocardium of heart from ^ BP]
- act to REDUCE BP/VOL by excreting more salt/water in urine
1 dilates aff.art, constricts eff.art = **^ GFR **
2 inhbit renin/aldosterone secretion
3 inhibit secretion of **ADH **
4 inhibits NaCl reabsorption by CD

PTH ** [secreted by parathyroid glands from Ca defieincy -hypocalcemia**]
- acts on PCT to **^ phosphate excretion **
- act on **thick **segment of ascending nephron loop + DCT to **^ Ca reabsoprtion **
- ^ phosphate content and **LOWERs Ca+ content in urine = ^ Ca. Conc in blood **= maintains calcium homeostasis

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16
Q

Explain how the collecting duct and antidiuretic hormone (ADH) regulate the volume and concentration of urine

A

CD
- produces hypertonic urine via TWO mechanisms
1 osmolarity of ECF in lower medulla = **4x as higher **than cortex [Countercurrent Exchange Mechanism]
2 medullary portion of CD = more permeable to water due to ADH synthesis of aquaporins
= as urine moves through increasingly hypertonic medulla, water = reab. via osmosis = hypertonic urine

**ADH / Vasopressin **
- responds to dehydration
- stimulates hypothalamus > post.pit > release of ADH
1 - ^ # of aquaporins in CD = ^ water reab.
2 - if ADH level elevated > 24hrs, **more aquaporins are manufactured **to respond = further raising water permeability of CD
» if you are well hydrated/excess water in body –> ADH secretion falls, aquaporins are removed from CD = less water reab. = urine more dilute

17
Q

Explain how the kidney establishes an osmotic gradient in the renal medulla that enables the collecting duct to function

A

Countercurrent multiplication in the loops of Henle of juxtamedullary nephrons are largely responsible for developing osmotic gradient which produces hypertonic urine.

the countercurrent exchange occurs because blood flows in opposite directions in adjacent parallel caps - desc + asc loops of henle.

as the filtrate flows down into the medulla, water = reab. as the desc is water permeable - leaving an increasingly salty filtrate. Solutes such as NaCl are not reab = ^ osmo in interstitial fluid

as the filtrate travels to the asc limb, NaCl is pumped into the interstitial fluid = further ^ osmo.

nephron loop produces an osmolarity gradient from ~300 mOsm/L at the cortex to 1200 mOsm/L near the papilla.

18
Q

Describe the composition and properties of urine

A

normal vol = 1-2L/day
polyuria = >2L/day
oliguria = <500mL/day
anuria = 0-100 mL/day

composition
- 95% water
- 5% solutes [urea, NaCl, KCl, creatinine, uric acid]

specific gravity range = 1.001 - 1.028

colourless-deep amber colour range
yellow colour from urochrome

odour - bacteria degrades urea to ammonia

pH 4.5 - 8.2 **[usually 6] **

19
Q

Describe the anatomy of the ureters, urinary bladder, and male and female urethra

A

**URETERS **
- ~25cm long x 2
- from renal pelvis –> passes posterior to bladder and enters from below via mucosal valves
- lumen = very narrow and easily obstructed - max diameter of 1.7cm near bladder
- THREE LAYESR
1 outer adventitia [CT]

2 **middle muscularis **
two layers of smoo.musc over most of length BUT **THIRD **layer found in lower ureter

3 **inner mucosa **
transitional epithelium

URINARY BLADDER
located in pelvic cavity, posterior to pubic symphysis

OUTER parietal peritoneum
MIDDLE THREE LAYERS smoo.musc = detrusor muscle
INNER mucosa - transitional epithelium w/ rugae
- the opening of the ureters and urethra = trigone
- bladder = highly distensible - rugae flatten and epithelium things to 2-3 layers to allow expansion
- capacity = 500-800mL MAX

**M URETHRA **
18cm long
internal/external urethral sphincter
THREE REGIONS
1. prostatic urethra [receives semen during orgams]
2. membranous urethra [passes through pelvic cavity
3. spngy/penile urethra

**F URETHRA **
3-4 cm long
- external urethral orifice
[between vaginal orifice and clitoris]

  • internal urethral sphincter
    [detrusor muscle thickened, smoo.musc. involuntary control]
  • external urethral sphincter
    [skeletal musc, voluntary control]
20
Q

Explain how the nervous system controls the voiding of urine

A

**INVOLUNTARY MICTURITION REFLEX **
1. 200mL of urine in bladder = activate stretch receptors, send aff. signals –> sacral SC
2. signals return to bladder from S2/S3 segments of SC via parasym fibres in pelvic nerve
3. eff. signals excite detrusor muscle
4. eff signals relax internal **urethral sphinter **

**VOLUNTARY MICTURITION REFLEX **
1. micturition centre in pons receives signals from stretch receptors
2. if urination appropriate –> pons returns signal to **spinal interneurons = excites detrusor and relax internal urethral sphincter = pee **
3. if urination NOT appropriate –> pons excites interneurons that keep external urethral sphincter contracted = **no pee **