Physiopathologie de l’hyperactivité vésicale

  • J. Kerdraon
  • A. Manunta
  • P. Coignard
  • L. Siproudhis
Article de Synthèse / Review Article

Résumé

L’hyperactivité vésicale est définie comme un trouble de la continence associant une urgenturie avec ou sans incontinence, et fréquemment associée à une pollakiurie et à une nycturie. Un ensemble d’observations récentes permet en effet, désormais, d’établir que l’hyperactivité vésicale correspond d’abord à une anomalie du traitement sensoriel régulant la continence. Les différents cadres étiopathogéniques chez l’homme partagent un ensemble de désordres similaires au niveau de l’urothélium, des nerfs et du muscle lisse du détrusor. Ces désordres s’inscrivent pour partie dans le cadre d’une neuroplasticité orchestrée par les facteurs de croissance nerveuse.

Mots clés

Hyperactivité vésicale Urgenturie Pathophysiologie Neuroplasticité 

Pathophysiology of bladder overactivity

Abstract

Overactive bladder (OAB) is characterised by the storage symptoms of urgency, with or without incontinence, and usually with urinary frequency and nocturia. Recent findings establish that OAB may first refer to abnormal sensory processing of continence. The various pathologic conditions associated with OAB share common features of altered function of urothelium, innervation and detrusor smooth muscle, and may partly rely on growth factors that orchestrate neural plasticity.

Keywords

Overactive bladder Urgency Pathophysiology Neuroplasticity 

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Références

  1. 1.
    Abrams P, Cardozo L, Fall M, et al (2002) The standardisation of terminology of lower urinary tract function: report from the Standardisation Sub-committee of the International Continence Society. Neurourol Urodyn 21(2):167–78CrossRefPubMedGoogle Scholar
  2. 2.
    Fall M, Geirsson G, Lindström S (1995) Toward a new classification of overactive bladders. Neurourol Urodyn 14(6):635–46CrossRefPubMedGoogle Scholar
  3. 3.
    de Groat WC (1997) A neurologic basis for the overactive bladder. Urology 50(6A Suppl):36–52CrossRefPubMedGoogle Scholar
  4. 4.
    Brading AF (1997) A myogenic basis for the overactive bladder. Urology 50(6A Suppl):57–67CrossRefPubMedGoogle Scholar
  5. 5.
    Griffiths D, Derbyshire S, Stenger A, et al (2005) Brain control of normal and overactive bladder. J Urol 174(5):1862–7CrossRefPubMedGoogle Scholar
  6. 6.
    Araki I, Du S, Kamiyama M, et al (2004) Over expression of epithelial sodium channels in epithelium of human urinary bladder with outlet obstruction. Urology 64(6):1255–60CrossRefPubMedGoogle Scholar
  7. 7.
    O’Reilly BA, Kosaka AH, Knight GF, et al (2002) P2X receptors and their role in female idiopathic detrusor instability. J Urol 167(1):157–64CrossRefPubMedGoogle Scholar
  8. 8.
    Yoshida M, Homma Y, Inadome A, et al (2001) Age-related changes in cholinergic and purinergic neurotransmission in human isolated bladder smooth muscles. Exp Gerontol 36(1):99–109CrossRefPubMedGoogle Scholar
  9. 9.
    Geirsson G, Fall M, Lindström S (1993) Toward a new classification of overactive bladders. Neurourol Urodyn 14(6):635–46Google Scholar
  10. 10.
    Seki S, Sasaki K, Igawa Y, et al (2004) Suppression of detrusorsphincter dyssynergia by immunoneutralization of nerve growth factor in lumbosacral spinal cord in spinal cord injured rats. J Urol 171(1):478–82CrossRefPubMedGoogle Scholar
  11. 11.
    Steers WD, Kolbeck S, Creedon D, Tuttle JB (1991) Nerve growth factor in the urinary bladder of the adult regulates neuronal form and function. J Clin Invest 88(5):1709–15CrossRefPubMedGoogle Scholar
  12. 12.
    Krenz NR, Meakin SO, Krassioukov AV, Weaver LC (1999) Neutralizing intraspinal nerve growth factor blocks autonomic dysreflexia caused by spinal cord injury. J Neurosci 19(17):7405–14PubMedGoogle Scholar
  13. 13.
    Clemow DB, Steers WD, Tuttle JB (2000) Stretch-activated signaling of nerve growth factor secretion in bladder and vascular smooth muscle cells from hypertensive and hyperactive rats. J Cell Physiol 183(3):289–300CrossRefPubMedGoogle Scholar
  14. 14.
    Hohlfeld R, Kerschensteiner M, Stadelmann C, et al (2000) The neuroprotective effect of inflammation: implications for the therapy of multiple sclerosis. J Neuroimmunol 107(2):161–6CrossRefPubMedGoogle Scholar
  15. 15.
    Fowler CJ, Jewkes D, McDonald WI, et al (1992) Intravesical capsaicin for neurogenic bladder dysfunction. Lancet 339(8803):1239CrossRefPubMedGoogle Scholar
  16. 16.
    Sui GP, Rothery S, Dupont E, et al (2002) Gap junctions and connexin expression in human suburothelial interstitial cells. BJU Int 90(1):118–29CrossRefPubMedGoogle Scholar
  17. 17.
    Drake MJ, Mills IW, Gillespie JI (2001) Model of peripheral autonomous modules and a myovesical plexus in normal and overactive bladder function. Lancet 358(9279):401–3CrossRefPubMedGoogle Scholar
  18. 18.
    Drake MJ, Hedlund P, Harvey IJ, et al (2003) Partial outlet obstruction enhances modular autonomous activity in the isolated rat bladder. J Urol 170(1):276–9CrossRefPubMedGoogle Scholar
  19. 19.
    Coolsaet BL, Van Duyl WA, Van Os-Bossagh P, De Bakker HV (1993) New concepts in relation to urge and detrusor activity. Neurourol Urodyn 12(5):463–71CrossRefPubMedGoogle Scholar

Copyright information

© Springer-Verlag France 2010

Authors and Affiliations

  • J. Kerdraon
    • 1
    • 2
  • A. Manunta
    • 2
  • P. Coignard
    • 1
  • L. Siproudhis
    • 2
  1. 1.Service de rééducation neurologique adulteCMRRF KerpapePloemeur cedexFrance
  2. 2.Pavillon Pointeau du Ronceray, centre de référence spina bifidaCHU PontchaillouRennesFrance

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