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Am J Physiol Regul Integr Comp Physiol (January 26, 2006). doi:10.1152/ajpregu.00742.2005
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Submitted on October 20, 2005
Accepted on January 25, 2006

Impact of the State of Arousal and Stress Neuropeptides on Urodynamic Function in the Freely Moving Rat

Darcie A Kiddoo1, Rita J Valentino2*, Stephen Zderic1, Arjunan Ganesh3, Steven C Leiser2, Lance Hale2, and Dimitri E Grigoriadis4

1 Surgery, The Children's Hospital of Philadelphia, Philadelphia, PA, USA
2 Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA
3 Anesthesiology and Critical Care Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA, USA
4 Neurocrine Biosciences Inc., San Diego, CA, USA

* To whom correspondence should be addressed. E-mail: valentino{at}email.chop.edu.

Cortictropin-releasing factor (CRF) is a neurotransmitter in Barrington's nucleus neurons. These neurons can co-regulate parasympathetic tone to the bladder (to modulate micturition) and brain noradrenergic activity (to affect arousal). To identify the role of CRF in the regulation of micturition, the effects of CRF agonists and antagonists on urodynamics in the unanesthetized rat were characterized. Rats were implanted with bladder and intrathecal (i.t.) or intraperitoneal (i.p.) catheters under isofluorane anesthesia. Cystometry was performed in the unanesthetized, unrestrained state at least 24 h later. In some cases, cortical electroencephalographic activity (EEG) was recorded simultaneously to assess arousal state. During cystometry, the state of arousal often shifted between waking and sleeping and urodynamic function changed depending on the state. Micturition threshold, bladder capacity, and micturition volume were all increased during sleep. CRF receptor agonists, CRF and urocortin 2, increased bladder capacity and micturition volume in awake, but not sleeping rats. Conversely, the CRF1 receptor antagonists, antalarmin and NBI 30775, increased urinary frequency and decreased bladder capacity in awake rats. The present results demonstrate a profound effect of the state of arousal on urodynamic function and suggest that simultaneous monitoring of EEG and cystometry may provide a useful model for studying nocturnal enuresis and other urinary disorders. Additionally, the results provide evidence for an inhibitory influence of CRF in the spinal pathway on micturition. Targeting the CRF system in the spinal cord may provide a novel approach for treating urinary disorders.




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