Safety of multiple administrations of spermicidal LL-37 antimicrobial peptide into the mouse female reproductive tract

Author:

Lee Seung Gee1,Kiattiburut Wongsakorn1,Burke Schinkel Stephanie C1,Angel Jonathan123,Tanphaichitr Nongnuj14ORCID

Affiliation:

1. Chronic Disease Program, Ottawa Hospital Research Institute , Ottawa, ON, Canada

2. Department of Biochemistry, Microbiology, Immunology, Faculty of Medicine, University of Ottawa , Ottawa, ON, Canada

3. Division of Infectious Diseases, Department of Medicine, The Ottawa Hospital , Ottawa, ON, Canada

4. Department of Obstetrics/Gynecology, Faculty of Medicine, University of Ottawa , Ottawa, ON, Canada

Abstract

Abstract We have previously demonstrated spermicidal activity of LL-37 antimicrobial peptide on mouse/human sperm and its contraceptive effects in female mice. With its microbicidal action against Neisseria gonorrhoeae, LL-37 warrants development into a multipurpose prevention technology (MPT) agent for administering into the female reproductive tract (FRT). However, it is important to verify that multiple administrations of LL-37 do not lead to damage of FRT tissues and/or irreversible loss of fecundity. Herein, we transcervically injected LL-37 (36 µM–10× spermicidal dose) into female mice in estrus in three consecutive estrous cycles. A set of mice were sacrificed for histological assessment of the vagina/cervix/uterus 24 h after the last injection, while the second set were artificially inseminated with sperm from fertile males 1 week afterwards, and then monitored for pregnancy. Mice injected with PBS in parallel were regarded as negative controls, whereas those injected with vaginal contraceptive foam (VCF, available over the counter), containing 12.5% nonoxynol-9, served as positive controls for vaginal epithelium disruption. We demonstrated that the vagina/cervix/uterus remained normal in both LL-37-injected and PBS-injected mice, which also showed 100% resumption of fecundity. In contrast, VCF-injected mice showed histological abnormalities in the vagina/cervix/uterus and only 50% of them resumed fecundity. Similarly, LL-37 multiply administered intravaginally caused no damage to FRT tissues. While our results indicate the safety of multiple treatments of LL-37 in the mouse model, similar studies have to be conducted in non-human primates and then humans. Regardless, our study provides an experimental model for studying in vivo safety of other vaginal MPT/spermicide candidates.

Funder

Canadian Institutes of Health Research

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Obstetrics and Gynecology,Genetics,Molecular Biology,Embryology,Reproductive Medicine

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