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A comparison of urinary bladder weight in male and female mice across five models of diabetes and obesity

Introduction: Diabetes often leads to lower urinary tract dysfunction. The most frequently assessed parameter of urinary bladder dysfunction in animal models of diabetes is an enlargement of the bladder, which is consistently observed in type 1 and less consistently in type 2 diabetes. The vast majo...

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Autores principales: Erdogan, Betül R., Michel, Martina B., Matthes, Jan, Castañeda, Tamara R., Christen, Urs, Arioglu-Inan, Ebru, Michel, Martin C., Pautz, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986474/
https://www.ncbi.nlm.nih.gov/pubmed/36891264
http://dx.doi.org/10.3389/fphar.2023.1118730
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author Erdogan, Betül R.
Michel, Martina B.
Matthes, Jan
Castañeda, Tamara R.
Christen, Urs
Arioglu-Inan, Ebru
Michel, Martin C.
Pautz, Andrea
author_facet Erdogan, Betül R.
Michel, Martina B.
Matthes, Jan
Castañeda, Tamara R.
Christen, Urs
Arioglu-Inan, Ebru
Michel, Martin C.
Pautz, Andrea
author_sort Erdogan, Betül R.
collection PubMed
description Introduction: Diabetes often leads to lower urinary tract dysfunction. The most frequently assessed parameter of urinary bladder dysfunction in animal models of diabetes is an enlargement of the bladder, which is consistently observed in type 1 and less consistently in type 2 diabetes. The vast majority of studies on bladder weight in animal models of diabetes and obesity has been performed in males, and no studies have directly compared this outcome parameter between sexes. Methods: Therefore, we have compared bladder weight and bladder/body weight ratio in five mouse models of obesity and diabetes (RIP-LCMV, db/db, ob/ob (two studies), insulin receptor substrate 2 (IRS2) knock-out mice and mice on a high-fat diet; pre-specified secondary analysis of a previously reported study). Results: In a pooled analysis of the control groups of all studies, females exhibited slightly lower glucose levels, lower body weight, and lower bladder weight, but bladder/body weight ratio was similar in both sexes (0.957 vs. 0.986 mg/g, mean difference 0.029 [−0.06; 0.118]). Among the six diabetic/obese groups, bladder/body weight ratio was similar in both sexes in three but smaller in female mice in three other groups. The mRNA expression of a panel of genes implied in the pathophysiology of bladder enlargement and/or fibrosis and inflammation did not differ systematically between sexes. Conclusions: We conclude that sex differences in diabetes/obesity-associated bladder enlargement may be model dependent.
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spelling pubmed-99864742023-03-07 A comparison of urinary bladder weight in male and female mice across five models of diabetes and obesity Erdogan, Betül R. Michel, Martina B. Matthes, Jan Castañeda, Tamara R. Christen, Urs Arioglu-Inan, Ebru Michel, Martin C. Pautz, Andrea Front Pharmacol Pharmacology Introduction: Diabetes often leads to lower urinary tract dysfunction. The most frequently assessed parameter of urinary bladder dysfunction in animal models of diabetes is an enlargement of the bladder, which is consistently observed in type 1 and less consistently in type 2 diabetes. The vast majority of studies on bladder weight in animal models of diabetes and obesity has been performed in males, and no studies have directly compared this outcome parameter between sexes. Methods: Therefore, we have compared bladder weight and bladder/body weight ratio in five mouse models of obesity and diabetes (RIP-LCMV, db/db, ob/ob (two studies), insulin receptor substrate 2 (IRS2) knock-out mice and mice on a high-fat diet; pre-specified secondary analysis of a previously reported study). Results: In a pooled analysis of the control groups of all studies, females exhibited slightly lower glucose levels, lower body weight, and lower bladder weight, but bladder/body weight ratio was similar in both sexes (0.957 vs. 0.986 mg/g, mean difference 0.029 [−0.06; 0.118]). Among the six diabetic/obese groups, bladder/body weight ratio was similar in both sexes in three but smaller in female mice in three other groups. The mRNA expression of a panel of genes implied in the pathophysiology of bladder enlargement and/or fibrosis and inflammation did not differ systematically between sexes. Conclusions: We conclude that sex differences in diabetes/obesity-associated bladder enlargement may be model dependent. Frontiers Media S.A. 2023-02-20 /pmc/articles/PMC9986474/ /pubmed/36891264 http://dx.doi.org/10.3389/fphar.2023.1118730 Text en Copyright © 2023 Erdogan, Michel, Matthes, Castañeda, Christen, Arioglu-Inan, Michel and Pautz. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Erdogan, Betül R.
Michel, Martina B.
Matthes, Jan
Castañeda, Tamara R.
Christen, Urs
Arioglu-Inan, Ebru
Michel, Martin C.
Pautz, Andrea
A comparison of urinary bladder weight in male and female mice across five models of diabetes and obesity
title A comparison of urinary bladder weight in male and female mice across five models of diabetes and obesity
title_full A comparison of urinary bladder weight in male and female mice across five models of diabetes and obesity
title_fullStr A comparison of urinary bladder weight in male and female mice across five models of diabetes and obesity
title_full_unstemmed A comparison of urinary bladder weight in male and female mice across five models of diabetes and obesity
title_short A comparison of urinary bladder weight in male and female mice across five models of diabetes and obesity
title_sort comparison of urinary bladder weight in male and female mice across five models of diabetes and obesity
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986474/
https://www.ncbi.nlm.nih.gov/pubmed/36891264
http://dx.doi.org/10.3389/fphar.2023.1118730
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