Around 80% of women experience vaginal tears during labour when the diameter of the vagina must increase to allow the passage of a full-term baby. Current techniques for evaluating vaginal tears are qualitative and often lead to an incorrect diagnosis and inadequate treatment, severely compromising the quality of life of women. In order to characterize the failure properties of the vaginal tissue, whole vaginal tracts from rats ( n = 18) were subjected to free-extension inflation tests until rupture using a custom-built experimental set-up. The resulting deformations were measured using the digital image correlation technique. Overall, the strain and changes in curvature in the hoop direction were significantly larger relative to the axial direction. At a failure pressure of 110 ± 23 kPa (mean ± s.d.), the hoop and axial stresses were computed to be 970 ± 340 kPa and 490 ± 170 kPa, respectively. Moreover, at such pressure, the hoop and axial strains were found to be 12.8 ± 4.4 % and 6.4 ± 3.7 % , respectively. Rupture of the vaginal specimens always occurred in the hoop direction by tearing along the axial direction. This knowledge about the rupture properties of the vaginal tissue will be crucial for the development of clinical approaches for preventing and mitigating vaginal tearing and the associated short- and long-term traumatic conditions.

No abstract

No abstract

No abstract

Thoracic aortic aneurysm is characterized by dilation of the aortic diameter by greater than 50%, which can lead to dissection or rupture. Common histopathology includes extracellular matrix remodeling which may affect transmural mass transport, defined as the movement of fluids and solutes across the wall. We measured in vitro ascending thoracic aorta mass transport in a mouse model with partial aneurysm phenotype penetration due to a mutation in the extracellular matrix protein fibulin-4 ( Fbln4E57K/E57K, referred to as MU-A [aneurysm] or MU-NA [non-aneurysm]). To push the aneurysm phenotype, we also included MU mice with reduced levels of lysyl oxidase ( Fbln4E57K/E57K;Lox+/-, referred to as MU-XA [extreme aneurysm]) and compared all groups to wild-type (WT) littermates. The phenotype variation allows investigation of how aneurysm severity correlates with mass transport parameters and extracellular matrix organization. We found that MU-NA ascending thoracic aortae have similar hydraulic conductance ( Lp) to WT, but 397% higher solute permeability ( ω) for 4 kDa FITC-dextran. In contrast, MU-A and MU-XA ascending thoracic aortae have 44-68% lower Lp and similar ω to WT. The results suggest that ascending thoracic aortic aneurysm progression involves an initial increase in ω, followed by a decrease in Lp after the aneurysm has formed. All MU ascending thoracic aortae are longer and have increased elastic fiber fragmentation in the extracellular matrix. There is a negative correlation between diameter and Lp or ω in MU ascending thoracic aortae. Changes in mass transport due to elastic fiber fragmentation could contribute to aneurysm progression or be leveraged for treatment.