Browse by author
Lookup NU author(s): Professor David Neal,
Professor James Gillespie
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
Purpose: The aim of this study was to investigate stretch activated channels in human detrusor using hypo-osmolar solutions to produce cell deformation. Stretch activated channels could provide another mechanism by which detrusor myocytes may be coupled. Materials And Methods: Human detrusor removed at surgery was dissected into strips and also enzymatically digested and cultured. Strips (5 x 1 x 1 mm.) were mounted in an organ bath and perfused with gassed Tyrode's. Hypo-osmolar solutions were made by removal of NaCl. Gadolinium (Gd3+), a blocker of stretch activated channels (SACs), and diltiazem, an L-type Ca2+ channel antagonist were used at 10 μM concentrations. Mean data ± S.E.M. are expressed as a percentage of maximal tension produced by 1 μM carbachol for each patient. Enzymatically disaggregated, human detrusor was cultured in flasks, passaged and placed on glass coverslips. Once confluent the cells were incubated with the Ca2+ sensitive fluorochrome Fura-2AM. Coverslips were placed in a bath on the stage of EPI-fluorescence microscope and solutions were perfused through the bath (5 ml. per minute, 35C, pH 7.4). Changes in fluorescence emission ratio (proportional to changes in cytosolic Ca2+) were measured. Results: Hypo- osmolar solutions produced a tension increase in the strips and a Ca2+ influx in the cells. In the strips in paired experiments Gd3+ and diltiazem significantly reduced the response to hypo-osmolar solution (87% ± 16% v 51% ± 12.5%, p = 0.003, n = 10 for Gd3+), and (69% ± 11% v 37% ± 9%, p = 0.001, n = 9 for diltiazem). In Ca2+ free solution responses were significantly reduced (65% ± 10% v 21% ± 8%, p = 0.001, n = 9). In the cells in paired experiments, 10 μM Gd3+ significantly reduced the elevation of cytosolic Ca2+ in response to hypo-osmolar solutions (median 0 v 0.38 (62 cells, n = 7 bladders)), as did Ca2+ free hypo-osmolar solution (median 0 v 0.44 (46 cells, n = 7)). 10 μM diltiazem (L-type Ca2+ channel antagonist) did not influence the response to hypo-osmolar solution (p = 0.14, median 0.5 v 0.54 (31 cells, n = 4)). Conclusions: Hypo-osmolar solutions produced a tension increase in human detrusor that appears to be dependent on upon influx of Ca2+ through stretch activated channels (SACs), influx of Ca2+ through L-type Ca2+ channels and also on release of intracellular Ca2+.
Author(s): Gillespie JI; Neal DE; Masters JG
Publication type: Article
Publication status: Published
Journal: Journal of Urology
Print publication date: 01/08/1999
ISSN (print): 0022-5347
ISSN (electronic): 1527-3792
Publisher: Elsevier Inc.
PubMed id: 10411091
Altmetrics provided by Altmetric