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Updated: Jul 26, 2025

Collection of Post-mating Semen from the Female Reproductive Tract and Measurement of Semen Liquefaction in Mice
Published on: November 18, 2017
Safety of multiple administrations of spermicidal LL-37 antimicrobial peptide into the mouse female reproductive
Seung Gee Lee1, Wongsakorn Kiattiburut1, Stephanie C Burke Schinkel1
1Chronic Disease Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
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.
Insights
Repeated administration of LL-37 antimicrobial peptide in female mice did not cause reproductive tract damage or impair fertility. This supports LL-37
Area of Science:
- Reproductive biology and immunology
- Antimicrobial peptide research
- Contraceptive development
Background:
- LL-37 antimicrobial peptide exhibits spermicidal and microbicidal properties.
- LL-37 is a candidate for a multipurpose prevention technology (MPT) for the female reproductive tract (FRT).
- Safety of repeated LL-37 administration in the FRT requires investigation to prevent tissue damage and infertility.
Purpose of the Study:
- To evaluate the safety of multiple transcervical administrations of LL-37 in female mice.
- To assess potential damage to the vagina, cervix, and uterus after repeated LL-37 exposure.
- To determine if repeated LL-37 administration affects the resumption of fecundity.
Main Methods:
- Female mice received transcervical injections of LL-37 (10× spermicidal dose) over three consecutive estrous cycles.
- Histological assessments of reproductive tissues were performed 24 hours post-injection.
- Pregnancy rates were monitored after artificial insemination one week post-injection.
- Controls included PBS (negative) and nonoxynol-9 vaginal contraceptive foam (positive).
Main Results:
- LL-37 and PBS injections resulted in normal histology of the vagina, cervix, and uterus.
- Mice treated with LL-37 or PBS showed 100% resumption of fecundity.
- Vaginal contraceptive foam (nonoxynol-9) caused histological abnormalities and reduced fecundity to 50%.
Conclusions:
- Multiple intravaginal administrations of LL-37 are safe in the mouse model, causing no FRT tissue damage or loss of fertility.
- LL-37 demonstrates potential as a safe agent for vaginal MPTs.
- Further studies in non-human primates and humans are necessary to confirm safety and efficacy.
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