micturition Flashcards

1
Q

what is micturition ?

A

the act of urination

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2
Q

what happens to the ureter when urine enters ?

A
  • distends it and smooth muscles around contract
  • Peristaltic waves in ureter occur
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3
Q

why does urine enter obliquely into the bladder ?

A
  • Prevents reflux of urine back into ureters by passive flap-valve effect
  • Ureteric peristalsis is myogenic and NOT under CNS control
  • Coordination required between peristalsis and changing urine volume
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4
Q

what are the two sphincters of the bladder ?

A

Internal Sphincter
* Extension of detrusor muscle  NOT under voluntary control

External Sphincter:
* Two striated muscles (compressor urethrae & bulbocavernosus) surrounding urethra
* these muscles are responsible for continence
under conscious, voluntary control

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5
Q

describe the bladder

A
  • Lining – transitional epithelium
  • Bladder muscle - detrusor
  • Impermeable to salt & water
  • Permeable to lipophilic molecules
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6
Q

what are kidney stones ?

A
  • Most common disorder of urinary tract
  • Develop from crystals that precipitate from urine within urinary tract
  • Normal urine contains inhibitors (citrate) to prevent this
  • Calcium is present in nearly all stones (80%), usually as calcium oxalate or less often as calcium phosphate.
  • Others made up of uric acid (<10%), struvite (<10%), cysteine (<5%).
  • not the same as gall stones
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7
Q

what are kidney stones caused by ?

A
  • excess dietary intake of stone-forming substances
  • poor urine output/obstruction
  • altered urinary pH
  • low concentration of inhibitors
  • infection
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8
Q

what are the symptoms of ureterolithiasis ( Kidney stone disease) ?

A
  • Dysuria (painful urination)
  • Haematuria - blood in urine
  • Loin pain/back pain
  • Reduced urine flow
  • Urinary tract obstruction: pressure reaches 50mmHg - causes considerable pain “renal colic”
  • If stone approaches tip of urethra – intense pain can inhibit micturition – “strangury”
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9
Q

describe the 3 types of bladder innervation

A
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10
Q

describe the efferent innervation of the detrusor muscle

A

sympathetic pathway (green lines):
* NA inhibits parasympathetic ganglia via α-receptors, indirectly causing detrusor relaxation.
* NA also acts on β-receptors (β-Rs) directly, further promoting detrusor relaxation (also affects the trigone area).

Parasympathetic pathway (red lines):
* ACh acts on nicotinic receptors at the ganglion.
* Parasympathetic post-ganglionic neurons release ACh and ATP:
* ACh acts on muscarinic receptors to contract the detrusor.
* ATP acts on purinergic receptors to also contract the detrusor.
* Atropine blocks muscarinic receptors, inhibiting detrusor contraction.

Final effect:
* Sympathetic activation → detrusor relaxation (prevents urination).
* Parasympathetic activation → detrusor contraction (promotes urination).

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11
Q

describe the efferent innervation of the sphincters

A

Internal sphincter control:
Sympathetic (green line):
* Noradrenaline (NA) acts on α1 receptors → contracts internal sphincter (prevents urination).

Parasympathetic (red line):
* Nitric Oxide (NO) and Acetylcholine (ACh) cause relaxation of the internal sphincter (allows urination).

External sphincter control:
* Somatic control (blue line):
* ACh acts on nicotinic receptors to keep the external sphincter closed.
* continuous ACh activity maintains contraction of the external sphincter.

Final effect:
* Sympathetic activation → internal sphincter contraction (urine retention).
* Parasympathetic activation → internal sphincter relaxation (urine release).
* Somatic control keeps the external sphincter closed voluntarily until urination is desired.

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12
Q

what are the types of afferent (sensory) nerve fibres ?

A

A fibres: sense tension in detrusor:
i. Filling of bladder
ii. Detrusor contraction
- bladder fullness, discomfort

C fibres: respond to damage & inflammatory mediators
- PAIN (urgent desire to micturate)

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13
Q

describe the afferent sensory innervation of the bladder

A

Main afferent pathway is via pelvic nerve (parasympathetic):
* Small myelinated Aδ–fibres  micturition reflex
* Stretch receptors - signal wall tension
* Volume receptors - signal bladder filling
* Unmyelinated C fibres - endings in/near epithelium
* Nociceptors - pain (e.g. during infection of bladder lining – cystitis; excessive distension)

Hypogastric (sympathetic) & Pudendal (somatic) pathways:
* Nociceptors
* Flow receptors (external sphincter)

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14
Q

describe the filling of the bladder

A

Initially – bladder empty
* Sphincters closed
(continuous) activity sympathetic & somatic nerves)
* Bladder pressure low

Arrival of urine
* Detrusor relaxes progressively
(sympathetic activity inhibiting parasympathetic transmission)
* Little increase in pressure
* Sphincters still closed

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15
Q

describe emptying of the bladder

A
  1. Micturition is an autonomic reflex
    e.g. in babies (<18months), adults with spinal cord transected above sacral region
  2. Reflex is modified by voluntary control
    Inhibited or initiated by higher centres in the brain
    Maturation of bladder complete by >6 years
  3. Basic circuits act as on/off switches to alternate between 2 modes of operation: storage and elimination
  4. Disease/injury/ageing to nervous system in adults disrupts voluntary control of micturition
    - bladder hyperactivity & urge incontinence
    - stress incontinence
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16
Q

describe the micturition reflex

A

Bladder filling:
* As the bladder fills, receptors in the bladder wall detect tension and begin to “fire off” signals.
* Aδ-fiber afferents send sensory information to the spinal cord.

Reflex activation:
* The parasympathetic efferent pathway is activated.
* Acetylcholine (ACh) and Nitric Oxide (NO) cause detrusor contraction and internal sphincter relaxation.

External sphincter control:
* Tonic contraction of the external sphincter is inhibited, allowing urine to pass.
* This is due to the removal of somatic (voluntary) input.

Urine flow reinforcement:
* Flow receptors in the urethra are activated by urine movement, exciting pudendal afferents.
* This reinforces the micturition reflex to ensure the bladder empties completely.

Sacral reflex importance:
* The sacral reflex is crucial in sustaining micturition until the bladder is empty.

Final Effect:
* Detrusor muscle contracts.
* Internal sphincter relaxes.
* External sphincter relaxes, allowing urine flow.
* Bladder empties completely due to reflex reinforcement.

17
Q

describe the voluntary modification of this reflex

A

Conscious control:
* External sphincter & levator ani muscle can be contracted voluntarily to delay urination.
* Sympathetic firing to the bladder & internal sphincter can be increased, enhancing retention.
* Parasympathetic transmission can be inhibited, disrupting the positive feedback loop that facilitates bladder emptying.
* Internal sphincter tightens, preventing involuntary leakage.

Factors that can halt urination:
* Strangury (urethral pain due to urethritis or renal calculi) can involuntarily stop the urine stream.
* Pinching the glans penis can reflexively inhibit micturition.

Night-time bladder control:
* If the bladder reaches full capacity at night, the pontine micturition center (PMC) and arousal center detect it, waking you up to urinate.

18
Q

describe voluntary control of micturition

A
  • The bladder is contained in the floor of the abdominal cavity

By contracting abdominal muscles:
* The increased intra-abdominal pressure is transmitted to the bladder and urethra.
* Reflex contraction of peri-urethral striated muscles also helps compress the urethra ⇒ micturition reflex aided

19
Q

what is the importance of emptying the bladder ?

A

Urine
* Normally sterile
* Occasional bacterial entry
* Complete emptying restores sterility
* Bacteria in retained urine seeds fresh urine
* Retained urine - clinical infection (UTI)

  • Repeated infections can destroy renal function if ascend to kidney
20
Q

what is a UTI ?

A
  • Can happen anywhere along the urinary tract
  • UTIs have different names, depending on area of infection:
  • Bladder – an infection in the bladder is called cystitis or a bladder infection
  • Kidneys – an infection of one/both kidneys is called pyelonephritis
  • Ureters – rarely the site of infection
  • Urethra – an infection of the urethra is called urethritis
21
Q

what are the risk factors of UTIs ?

A
  • More common in women because of short urethra
  • Common in men over 40 due to prostatic disease, causing bladder outflow obstruction
  • Diabetes mellitus
  • long-term catheterisation
  • pregnancy
  • enlarged prostate
  • prolonged immobility
  • kidney stones
  • bowel incontinence
  • advanced age
22
Q

what are the problems of an aging bladder ?

A

Slow urine stream:
* Prostate enlargement (BPH -benign prostatic hyperplasia)
* most common cause of lower urinary tract symptoms in men (25% of men > 40yrs)
* Slow urine stream → incomplete emptying → infection

Incontinence:
Causes
* Weakening of sphincters (e.g. stress incontinence)
Common in women after child-birth, weakened pelvic floor muscles
* Failure of nervous control
* Overactive bladder (OAB) – detrusor contracts spastically – results in sustained high bladder pressure – urge incontinence

Consequence:
* Socially embarrassing
* Diminishes self-esteem
* Reduces quality of life

23
Q

what are the treatments for bladder problems ?

A
  1. Anti-muscarinics  relax smooth muscle & ↓ detrusor contraction
    * (eg non-specific muscrarinic receptor antagonist Oxybutynin – wide ranging side effects)
  2. Bladder retraining (used for stress & urge incontinence)
    * Timetable & Kegel exercises
  3. Surgery
    * Bladder neck suspension
    * botulinum toxin/collagen injections into muscles around urethra → relaxes bladder (OAB)
  4. Sacral Nerve Stimulation (SNS)
    * implanted neurostimulation system
    * electrical impulses to sacral nerve
  5. Stem cell therapy
    * Frauscher et al (2004) cultured stem cells into bladder wall ⇒ 90% no leakage
    * Limited by supply of stem cells (bone marrow)
  6. Tissue engineered bladder
    * Synthetic and natural scaffolds to form 3D structure using human tissue.
    * Currently in phase II trials.