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  4. The effects of uranyl ions on neuromuscular transmission in the urinary bladder of the normal and streptozotocin-diabetic mouse
 
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The effects of uranyl ions on neuromuscular transmission in the urinary bladder of the normal and streptozotocin-diabetic mouse

Journal
Naunyn-Schmiedeberg's Archives of Pharmacology
Journal Volume
354
Journal Issue
6
Pages
773-778
Date Issued
1996
Author(s)
SHING-HWA LIU  
Lin-Shiau S.-Y.
DOI
10.1007/BF00166904
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029825280&doi=10.1007%2fBF00166904&partnerID=40&md5=09789f10d809ab1ea8fe3f828b0f0cd4
https://scholars.lib.ntu.edu.tw/handle/123456789/431203
Abstract
The depressant effects of uranyl nitrate on the nerve-evoked muscle contraction of urinary bladder isolated from normal and streptozotocin-diabetic mice were compared. The non-cholinergic component of the evoked bladder contraction (in the presence of atropine) was specifically sensitive to the suppressive effect of uranyl nitrate. In contrast, the cholinergic component remaining after treatment with α,β-methylene ATP was rather insensitive to uranyl nitrate. The contractile responses induced by KCl, acetylcholine and ATP were also not affected by uranyl nitrate, indicating a presynaptic site of action. High Ca2+ and calmodulin inhibitors (trifluoperazine, diltiazem and W7) antagonized the suppressive effects of uranyl ions. These results suggest that the depressant effect of uranyl nitrate is mediated by a reduction of prejunctional non-cholinergic transmitter release through the calcium-calmodulin pathway. In contrast to the normal bladder, the urinary bladder of streptozotocin-diabetic mice revealed not only weaker neurogenic contractile responses to electrical field stimulation, but also a profound reduction in the depressant effect of uranyl nitrate. These findings suggest that the Ca2+ regulation of non-cholinergic neurotransmission in mouse urinary bladder may be impaired in the diabetic state.
Subjects
Diabetes; Non-cholinergic; Uranyl ion; Urinary bladder
SDGs

[SDGs]SDG3

Other Subjects
acetylcholine; adenosine triphosphate; alpha,beta methyleneadenosine triphosphate; atropine; calcium; calmodulin inhibitor; diltiazem; n (6 aminohexyl) 5 chloro 1 naphthalenesulfonamide; potassium chloride; trifluoperazine; uranyl nitrate; animal model; animal tissue; article; bladder; controlled study; dose response; electrostimulation; in vitro study; male; mouse; neuromuscular transmission; nonadrenergic noncholinergic nerve; nonhuman; streptozocin diabetes
Publisher
Springer Verlag
Type
journal article

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