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

IF 3.6 2区 医学 Q2 DEVELOPMENTAL BIOLOGY Molecular human reproduction Pub Date : 2023-06-30 DOI:10.1093/molehr/gaad023
Seung Gee Lee, Wongsakorn Kiattiburut, Stephanie C Burke Schinkel, Jonathan Angel, Nongnuj Tanphaichitr
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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.

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向小鼠雌性生殖道多次施用杀精 LL-37 抗菌肽的安全性。
我们之前已经证明了 LL-37 抗菌肽对小鼠/人类精子的杀精活性及其对雌性小鼠的避孕效果。LL-37 对淋病奈瑟菌有杀微生物作用,因此值得开发成一种多用途预防技术(MPT)制剂,用于女性生殖道(FRT)的给药。然而,重要的是要验证多次注射 LL-37 不会导致 FRT 组织受损和/或不可逆转的生育能力丧失。在此,我们对发情的雌性小鼠连续进行了三个发情周期的经管注射 LL-37(36 µM-10×杀精剂量)。一组小鼠在最后一次注射 24 小时后被处死,以对阴道/宫颈/子宫进行组织学评估;第二组小鼠在 1 周后用可育雄性小鼠的精子进行人工授精,然后监测是否怀孕。同时注射 PBS 的小鼠被视为阴性对照组,而注射含有 12.5% 壬炔醇-9 的阴道避孕泡沫(VCF,可在柜台购买)的小鼠被视为阴道上皮破坏的阳性对照组。我们证实,注射 LL-37 和注射 PBS 的小鼠的阴道/宫颈/子宫均保持正常,而且 100%恢复受孕。相反,注射 VCF 的小鼠的阴道/宫颈/子宫出现组织学异常,只有 50% 的小鼠恢复了生育能力。同样,阴道内多次注射 LL-37 也不会对 FRT 组织造成损害。虽然我们的研究结果表明在小鼠模型中多次使用 LL-37 是安全的,但类似的研究还需要在非人灵长类动物和人类中进行。无论如何,我们的研究为研究其他候选阴道杀多巴胺/杀精剂的体内安全性提供了一个实验模型。
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来源期刊
Molecular human reproduction
Molecular human reproduction 生物-发育生物学
CiteScore
8.30
自引率
0.00%
发文量
37
审稿时长
6-12 weeks
期刊介绍: MHR publishes original research reports, commentaries and reviews on topics in the basic science of reproduction, including: reproductive tract physiology and pathology; gonad function and gametogenesis; fertilization; embryo development; implantation; and pregnancy and parturition. Irrespective of the study subject, research papers should have a mechanistic aspect.
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