Vaginal
atrophy (VA) is the thinning and drying of the vaginal
walls, which can lead to a variety of symptoms. VA is usually initiated
by decreasing estrogen levels in post-menopausal women; so, the traditional
treatment of VA is hormone therapy (HT). Here, we sought nonhormonal
therapies aimed at treating this condition safely and effectively.
Collagen is an excellent biomaterial and has important biological
functions in skin and mucosal tissues. In particular, collagen can
bind to epithelial cells to promote proliferation and differentiation.
In this study, recombinant protein T16, which was derived from human
type III collagen to provide potent cell-adhesion activity, was used
as a safe alternative therapy to treat VA in ovariectomy rat models.
After T16 was administered intravaginally for 2 weeks, the autologous
collagen arrangement was improved in the epithelium and muscle layer
of the rat vagina, and the thickness of epithelium tissue also increased
significantly. Compared with the sham group, collagen therapy was
found to influence the expression levels of several important proteins
in the vaginal tissue, resulting in the upregulation of TIMP-1, Collagen
I, Collagen III, Ki-67, VEGF, and AQP-2 and the downregulation of
MMP-1 and IL-6. Cells in the collagen treatment group exhibited better
proliferation and less apoptosis properties. These results not only
provide support for additional animal experiments to further evaluate
collagen therapy in VA treatment but also suggest the potential for
wide applications of collagen biomaterials with high cell-adhesion
activities.