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|Title:||Enhancement of rat bladder contraction by artificial sweeteners via increased extracellular Ca2+ influx|
Elliott, Ruth A.
Tincello, Douglas G.
|Citation:||Toxicology and Applied Pharmacology, 2006, 217 (2), pp.216-224|
|Abstract:||Introduction: Consumption of carbonated soft drinks has been shown to be independently associated with the development of overactive bladder symptoms (OR 1.62, 95% CI 1.18, 2.22) [Dallosso, H.M., McGrother, C.W., Matthews, R.J., Donaldson, M.M.K., 2003. The association of diet and other lifestyle factors with overactive bladder and stress incontinence: a longitudinal study in women. BJU Int. 92, 69–77]. We evaluated the effects of three artificial sweeteners, acesulfame K, aspartame and sodium saccharin, on the contractile response of isolated rat detrusor muscle strips. Methods: Strips of detrusor muscle were placed in an organ bath and stimulated with electrical field stimulation (EFS) in the absence and presence of atropine, and with α,β methylene ATP, potassium, calcium and carbachol. Results: Sweeteners 10−7 M to 10−2 M enhanced the contractile response to 10 Hz EFS compared to control (p < 0.01). The atropine-resistant response to EFS was marginally increased by acesulfame K 10−6 M, aspartame 10−7 M and sodium saccharin 10−7 M. Acesulfame K 10−6 M increased the maximum contractile response to α,β methylene ATP by 35% (± 9.6%) (p < 0.05) and to KCl by 12% (± 3.1%) (p < 0.01). Sodium saccharin also increased the response to KCl by 37% (± 15.2%) (p < 0.05). These sweeteners shifted the calcium concentration–response curves to the left. Acesulfame K 10−6 M increased the log EC50 from −2.79 (± 0.037) to −3.03 (± 0.048, p < 0.01) and sodium saccharin 10−7 M from −2.74 (± 0.03) to 2.86 (± 0.031, p < 0.05). The sweeteners had no significant effect on the contractile response to carbachol but they did increase the amplitude of spontaneous bladder contractions. Discussion: These results suggest that low concentrations of artificial sweeteners enhanced detrusor muscle contraction via modulation of L-type Ca+2 channels.|
|Appears in Collections:||Published Articles, Dept. of Cancer Studies and Molecular Medicine|
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