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      The Role of the Mucosa in Normal and Abnormal Bladder Function

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      1 , 2
      Basic & clinical pharmacology & toxicology

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          Abstract

          The internal face of the detrusor smooth muscle wall of the urinary bladder is covered by a mucosa, separating muscle from the hostile environment of urine. However, the mucosa is more than a very low permeability structure and offers a sensory function that monitors the extent of bladder filling and composition of the urine. The mucosa may be considered as a single functional structure and comprises a tight epithelial layer under which is a basement membrane and lamina propria. The latter region itself is a complex of afferent nerves, blood vessels, interstitial cells and in some species including human beings a muscularis mucosae. Stress on the bladder wall through physical or chemical stressors elicits release of chemicals, such as ATP, acetylcholine, prostaglandins and nitric oxide that modulate the activity of either afferent nerves or the muscular components of the bladder wall. The release and responses are graded so that the mucosa forms a dynamic sensory structure, and there is evidence that the gain of this system is increased in pathologies such as overactive bladder and bladder pain syndrome. This system therefore potentially provides a number of drug targets against these conditions, once a number of fundamental questions are answered. These include how is mediator release regulated; what are the intermediate roles of interstitial cells that surround afferent nerves and blood vessels; and what is the mode of communication between urothelium and muscle – by diffusion of mediators or by cell-to-cell communication?

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          Author and article information

          Journal
          101208422
          31859
          Basic Clin Pharmacol Toxicol
          Basic Clin. Pharmacol. Toxicol.
          Basic & clinical pharmacology & toxicology
          1742-7835
          1742-7843
          18 July 2017
          05 August 2016
          October 2016
          14 August 2017
          : 119
          : Suppl 3
          : 57-62
          Affiliations
          [1 ]School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK
          [2 ]Department of Biological, Biomedical and Analytical Sciences, University of the West of England, Bristol, UK
          Author notes
          Author for correspondence: Christopher H. Fry, School of Physiology, Pharmacology & Neuroscience, Faculty of Biomedical Sciences, University of Bristol BS8 1TD, Bristol, UK ( chris.fry@ 123456bristol.ac.uk )
          Article
          PMC5555362 PMC5555362 5555362 nihpa893036
          10.1111/bcpt.12626
          5555362
          27228303
          4ba551d0-e297-4e0e-bc5f-8cfc338cf3a9
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