Effects of Elastase Digestion on the Murine Vaginal Wall Biaxial Mechanical Response.

elastic fibers mechanical testing pelvic floor disorders vaginal wall women's health

Journal

Journal of biomechanical engineering
ISSN: 1528-8951
Titre abrégé: J Biomech Eng
Pays: United States
ID NLM: 7909584

Informations de publication

Date de publication:
01 Feb 2019
Historique:
received: 10 04 2018
pubmed: 20 11 2018
medline: 20 11 2018
entrez: 20 11 2018
Statut: ppublish

Résumé

Although the underlying mechanisms of pelvic organ prolapse (POP) remain unknown, disruption of elastic fiber metabolism within the vaginal wall extracellular matrix (ECM) has been highly implicated. It has been hypothesized that elastic fiber fragmentation correlates to decreased structural integrity and increased risk of prolapse; however, the mechanisms by which elastic fiber damage may contribute to prolapse are poorly understood. Furthermore, the role of elastic fibers in normal vaginal wall mechanics has not been fully ascertained. Therefore, the objective of this study is to investigate the contribution of elastic fibers to murine vaginal wall mechanics. Vaginal tissue from C57BL/6 female mice was mechanically tested using biaxial extension-inflation protocols before and after intraluminal exposure to elastase. Elastase digestion induced marked changes in the vaginal geometry, and biaxial mechanical properties, suggesting that elastic fibers may play an important role in vaginal wall mechanical function. Additionally, a constitutive model that considered two diagonal families of collagen fibers with a slight preference toward the circumferential direction described the data reasonably well before and after digestion. The present findings may be important to determine the underlying structural and mechanical mechanisms of POP, and aid in the development of growth and remodeling models for improved assessment and prediction of changes in structure-function relationships with prolapse development.

Identifiants

pubmed: 30453317
pii: 2716276
doi: 10.1115/1.4042014
pmc: PMC6298538
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM103629
Pays : United States

Informations de copyright

Copyright © 2019 by ASME.

Auteurs

Akinjide R Akintunde (AR)

Department of Biomedical Engineering,Lindy Boggs Center Suite 500,Tulane University,New Orleans, LA 70118e-mail: aakintun@tulane.edu.

Kathryn M Robison (KM)

Mem. ASMEDepartment of Biomedical Engineering,Lindy Boggs Center Suite 500,Tulane University,New Orleans, LA 70118e-mail: krobison@tulane.edu.

Daniel J Capone (DJ)

Department of Biomedical Engineering,Lindy Boggs Center Suite 500,Tulane University,New Orleans, LA 70118e-mail: dcapone@tulane.edu.

Laurephile Desrosiers (L)

Department of Female Pelvic Medicineand Reconstructive Surgery,UQ Ochsner Clinical School,1514 Jefferson Highway,New Orleans, LA 70121e-mail: laurephile.desrosiers@ochsner.org.

Leise R Knoepp (LR)

Department of Female Pelvic Medicineand Reconstructive Surgery,UQ Ochsner Clinical School,1514 Jefferson Highway,New Orleans, LA 70121e-mail: lknoepp@ochsner.org.

Classifications MeSH