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

Author:

Akintunde Akinjide R.1,Robison Kathryn M.2,Capone Daniel J.1,Desrosiers Laurephile3,Knoepp Leise R.3,Miller Kristin S.2

Affiliation:

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

2. Mem. ASME Department of Biomedical Engineering, Lindy Boggs Center Suite 500, Tulane University, New Orleans, LA 70118 e-mail:

3. Department of Female Pelvic Medicine and Reconstructive Surgery, UQ Ochsner Clinical School, 1514 Jefferson Highway, New Orleans, LA 70121 e-mail:

Abstract

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.

Funder

National Institute of General Medical Sciences

Division of Civil, Mechanical and Manufacturing Innovation

Tulane University

Publisher

ASME International

Subject

Physiology (medical),Biomedical Engineering

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