Literature DB >> 29392751

A systematic review of urinary bladder hypertrophy in experimental diabetes: Part I. Streptozotocin-induced rat models.

Ebru Arioglu Inan1, Johanne H Ellenbroek2, Martin C Michel3.   

Abstract

AIMS: To better understand the genesis and consequences of urinary bladder hypertrophy in animal models of diabetes. This part of a three-article series will analyze urinary bladder hypertrophy in the diabetes mellitus type 1 model of rats injected with streptozotocin (STZ).
METHODS: A systematic search for the key word combination "diabetes," "bladder" and "hypertrophy" was performed in PubMed; additional references were identified from reference lists of those publications. All papers were systematically extracted for relevant information.
RESULTS: A total of 39 studies were identified that quantitatively reported on bladder hypertrophy in rats upon injection of STZ; of which several reported on multiple time points yielding a total of 83 group comparisons. Bladder hypertrophy was found consistently, being fully developed as early as 1 week after STZ injection (bladder weight 188 ± 59% of matched control). Hypertrophy was similar across sexes and STZ doses (35-40 vs 50-65 mg/kg) but appeared greater with Wistar rats than other rat strains. The extent of bladder hypertrophy was not correlated to blood glucose concentrations, but normalization of blood glucose concentration by insulin treatment starting early after STZ injection prevented hypertrophy; insulin treatment starting after hypertrophy had established largely reversed it.
CONCLUSIONS: Bladder size approximately doubles after STZ injection in rats; the extent of hypertrophy is not linked to the severity of hyperglycemia but largely reversible by restoration of euglycemia.
© 2018 The Authors. Neurourology and Urodynamics Published by Wiley Periodicals, Inc.

Entities:  

Keywords:  bladder; diabetes; hypertrophy; insulin; rat strain; streptozotocin

Mesh:

Year:  2018        PMID: 29392751     DOI: 10.1002/nau.23490

Source DB:  PubMed          Journal:  Neurourol Urodyn        ISSN: 0733-2467            Impact factor:   2.696


  7 in total

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Authors:  Ching-Chung Liang; Steven W Shaw; Yung-Hsin Huang; Tsong-Hai Lee
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2.  Daidzein attenuates urinary bladder dysfunction in streptozotocin-induced diabetes in rats by NOX-4 and RAC-1 inhibition.

Authors:  Ankit P Laddha; Yogesh A Kulkarni
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2022-05-11       Impact factor: 3.195

Review 3.  Established and emerging treatments for diabetes-associated lower urinary tract dysfunction.

Authors:  Betül R Erdogan; Guiming Liu; Ebru Arioglu-Inan; Martin C Michel
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2022-05-12       Impact factor: 3.195

4.  Time-dependent functional, morphological, and molecular changes in diabetic bladder dysfunction in streptozotocin-induced diabetic mice.

Authors:  Xu-Feng Yang; Jing Wang; Yi-Fei Xu; Fang-Jun Chen; Li-Yao Tang; Wen-Kang Ren; Li-Jun Fu; Bo Tan; Ping Huang; Hong-Ying Cao
Journal:  Neurourol Urodyn       Date:  2019-04-20       Impact factor: 2.696

5.  The Effect of Low-Intensity Extracorporeal Shockwave Treatment on the Urinary Bladder in an Experimental Diabetic Rat Model.

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6.  Analysis of 16 studies in nine rodent models does not support the hypothesis that diabetic polyuria is a main reason of urinary bladder enlargement.

Authors:  Zeynep E Yesilyurt; Jan Matthes; Edith Hintermann; Tamara R Castañeda; Ralf Elvert; Jesus H Beltran-Ornelas; Diana L Silva-Velasco; Ning Xia; Aimo Kannt; Urs Christen; David Centurión; Huige Li; Andrea Pautz; Ebru Arioglu-Inan; Martin C Michel
Journal:  Front Physiol       Date:  2022-08-08       Impact factor: 4.755

7.  Functional and Immunofluorescence Evaluations of Vascular and Neural Integrities in Urinary Bladder of Streptozotocin-Induced Diabetic Mice.

Authors:  Mi-Hye Kwon; Min-Ji Choi; Fang-Yuan Liu; Fitri Rahma Fridayana; Lashkari Niloofar; Guo Nan Yin; Ji-Kan Ryu
Journal:  Int Neurourol J       Date:  2022-09-30       Impact factor: 3.038

  7 in total

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