Lecture 6: Physiology of Micturition and Assessment of Renal Function Flashcards

1
Q

what is micturition?

A
  • the process of eliminating water and electrolytes from the urinary system, commonly known as urinating.
  • it has two distinct pahses: the storage/continence pahse, when urine is stored in the bladder; and the voiding phase, where urine is released through the urethra.
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2
Q

describe the control of the storage/continence phase of micturition

A
  • the storage phase of micturition is controlled at the highest level by continence centres of the brain.
  • these in turn control the continence centres of the spinal cord.
  • the storage of urine requires relaxation of the detrusor muscle of the bladder and simultaneous contraction of both the internal urethral sphincters (IUS) and external urethral sphincters (EUS).
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3
Q

the bladder and internal urethral sphincters are under the control of which nervous system?

A

autonomic nervous system

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4
Q

the external urethral sphincters (EUS) are under the control of which nervous system?

A

somatic nervous system
- can therefore be voluntarily opened or closed to control micturition.

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5
Q

describe the pathway from the brain to the bladder, in controlling the storage/continence phase of micturition

A
  • to stimulate storage, impulses from the cerebral cortex travel to the pons.
  • from the pontine continence centre, signals are sent to sympathetic nuclei in the spinal cord (T10-L2), and finally to the detrusor muscle and IUS of the bladder via the hypogastric nerve (roots T10-L2).
  • at the bladder, this stimulates: relaxation of the detrusor muscle via stimulation of beta-3-adrenoceptors in the fundus and body of the bladder.
  • contraction of the IUS, via stimulation of alpha-1-adrenoceptors at the neck of the bladder.
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6
Q

discuss the somatic innervation of the EUS during the storage phase

A
  • impulses travel to the EUS via the pudenal nerve (S2-S4) to nicotinic (cholinergic) receptors on the striated muscle, resulting in its contraction > prevents any urine from leaking out.
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7
Q

describe the treatment of incontinence secondary to neurological insults

A
  • anticholinergics (e.g. oxybutynin, tolterodine) > reduce parasympathetic input to the bladder. Side effects such as dry mouth or constipation, increased risk of falls.
  • beta-3-adrenoceptor agonists (e.g. Mirabegron): bind to beta-3 receptors on the detrusor muscle to cause relaxation, increasing the bladder’s capacity to store urine.
  • other possible therapies: botulinum toxin A injection, sacral nerve stimulation, surgical procedures such as augmentation enterocystoplasty or urinary diversion.
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8
Q

what is the urinary flow rate in a full bladder in men and women?

A

20-25ml/s in men
25-30ml/s in women

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9
Q

what is the capacity of the bladder and at what volume is the voiding phase stimulated?

A

capacity varies from roughly 300-550ml
afferent nerves in the bladder wall signal the need to void the bladder at around 400ml of filling

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10
Q

the passing of urine is under which control?

A

parasympathetic

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11
Q

describe the voiding phase of micturition

A
  • upon stretching of the bladder, afferent signals ascend through the spinal cord and project to the pontine micturition centre and cerebrum.
  • upon the voluntary decision to urinate, neurons of the pontine micturition centre fire to excite the sacral preganglionic neurons.
  • subsequent parasympathetic stimulation to the pelvic nerve > release of ACh > M3 receptors > contraction of detrusor muscle > increased intra-vesicular pressure.
  • pontine micturition centre also inhibits Onuf’s nucleus > reduction in sympathetic stimulation to IUS > relaxation.
  • finally, a concious reduction in voluntary contraction of EUS from the cerebral cortex > distension of urethra > passing of urine.
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12
Q

what is urinary retention?

A

the inability to void the bladder i.e. being unable to urinate

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13
Q

list the causes of urinary retention

A
  • benign prostatic hyperplasia (BPH)
  • nerve dysfunction
  • infection e.g. UTI
  • constipation
  • drugs e.g. anticholinergics, antidepressants ad opioids.
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14
Q

what are the complications of urinary retention?

A
  • urinary incontinence
  • nocturia (the need to urinate at night)
  • hydronephrosis - high pressure in the bladder can push urine back up ureters into the kidneys > expansion of the renal pelvises.
  • kidney failure
  • sepsis
  • bladder rupture
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15
Q

what is the treatment for urinary retention in an acute setting?

A
  • urinary catheterisation
  • prostatic stenting
  • suprapubic cystostomy
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16
Q

urine remaining in the male urethra is expelled by contractions of which muscle?

A

bulbocavernosus muscle

17
Q

what do plasma clearance tests determine?

A

the ability of the kidney to clear the plasma of various substances

18
Q

how is GFR measured?

A

GFR = [urine production (ml/minute) x substance concentration in the urine (mg/L)] / substance concentration in plasma (mg/ml)

19
Q

in a healthy adult, the GFR is approximately…

A

120ml/min

20
Q

which substances are commonly used to measure GFR and why?

A
  • creatinine and inulin
  • they are inert, freely filtered and freely excreted substances and remain in a steady state in the bloodstream
21
Q

how is renal plasma flow measured?

A
  • PAH is an organic acid that is completely filtered and secreted by the kidney.
  • it is given by IV infusion and is used to measure renal plasma flow (PAH does not change renal plasma flow).
  • Effective renal plasma flow (eRPF) = urine concentration of PAH x (urine flow rate/plasma concentration of PAH)
22
Q

the renal plasma flow is approx…

A

600 ml/min
- however, not all of this renal plasma flow can pass through the filtration barrier at once, approx 20% is filtered to join the filtrate (120ml/min). Over 24 hours, this equates to approx 173 litres of filtrate, majority is reabsobed leaving 1.2ml/min of urine output (1% of the filtrate).