Tideglusib, a prospective alternative to nonoxynol-9 contraceptive

Q2 Medicine
Zhiting Chen , Niyan Shu , Yuzhu Wang , Yiting Yang , Zhiyu Shao , Fang Tian , Minjie Xia , Zhikai Wang , Xin Wang , Xing Feng , Xianliang Huang , Weihua Li , Heguo Yu , Hua Diao
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引用次数: 3

Abstract

Objectives

We aimed to evaluate the antifertility activity and vaginal irritation effects of tideglusib in vivo using rabbit models and to evaluate the cytotoxical effects of tideglusib to sperm, vaginal cells and vaginal bacteria (L. acidophilus) in vitro.

Study design

We treated female rabbits with vaginal tideglusib 1 mM, nonoxynol-9 (N-9) or vehicle control (Poloxamer 407). In experiment 1, we sacrificed females (n = 6 each) after 10 days of daily administration and assessed vaginal histological changes using Eckstein irritation score. In experiment 2, females (n = 9 each) received estradiol benzoate to induce ovulation 24 h prior to vaginal treatment followed by introduction of a fertile male. These females underwent necropsy at the 21st day to assess pregnancy status. In experiment 3, we used an HTM-TOX IVOS sperm motility analyzer and scanning electron microscopy (SEM) to evaluate the effect of tideglusib on human sperm samples. In experiment 4, we evaluated the effect of tideglusib on lactobacillus and vaginal cell growth in vitro.

Results

The total irritation score of tideglusib vs. N-9 was 3.4 ± 2.07 vs. 7.8 ± 3.82, p <.05. The pregnancy rate of tideglusib, N-9 and control group was 11.1%, 0% and 88.9%, respectively. Tideglusib exhibited a dose-dependent spermostatic/spermicidal activity, and the minimum effective concentrations of tideglusib and N-9 were 8.724 ± 3.047 μM and 219.75 ± 41.78 μM, respectively. SEM and transmission electron microscopy revealed acrosomal membrane impairments caused by tideglusib. Tideglusib was much less toxic to vaginal cells and L. acidophilus than N-9 in vitro.

Conclusions

Evaluation using rabbit models indicated that tideglusib is a prospective spermicidal contraceptive with low vaginal irritation effects.

Implications

Tideglusib or tideglusib analogues may be a contraceptive with perspective to replace N-9. It is possible for a spermicide to balance spermicidal activity and vaginal/cervical irritation effects very well.

Abstract Image

Abstract Image

Abstract Image

Tideglusib,一种有前景的壬苯醇醚-9避孕药替代品
目的利用家兔模型,研究藻绿素的抗生育活性和阴道刺激作用,并在体外研究藻绿素对精子、阴道细胞和阴道细菌(嗜酸乳杆菌)的细胞毒作用。研究设计我们用阴道tideglusib 1 mM、壬氧醇-9 (N-9)或对照物(poloxam407)治疗雌性家兔。在实验1中,我们在每天给药10 天后处死女性(n = 6人),并使用Eckstein刺激评分评估阴道组织学变化。在实验2中,雌性(n = 各9只)在阴道治疗前24 小时接受苯甲酸雌二醇诱导排卵,然后引入有生育能力的雄性。这些雌性在第21天进行尸检以评估妊娠状况。在实验3中,我们使用HTM-TOX IVOS精子活力分析仪和扫描电镜(SEM)来评估tideglusib对人类精子样本的影响。在实验4中,我们评估了tideglusib对体外乳酸菌和阴道细胞生长的影响。结果tideglusib与N-9的总刺激评分分别为3.4 ± 2.07 vs. 7.8 ± 3.82,p < 0.05。替地格鲁菌组、N-9组和对照组的妊娠率分别为11.1%、0%和88.9%。Tideglusib和N-9的最小有效浓度分别为8.724 ± 3.047 μM和219.75 ± 41.78 μM。扫描电镜和透射电子显微镜显示顶体膜损伤引起的潮汐glusib。Tideglusib对阴道细胞和嗜酸乳杆菌的毒性远低于N-9。结论对家兔模型的评价表明,甲氨苄是一种有前景的杀精避孕药,对阴道刺激作用小。意义替格卢昔或替格卢昔类似物可能是一种有希望取代N-9的避孕药。杀精剂可以很好地平衡杀精活性和阴道/宫颈刺激效应。
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来源期刊
Contraception: X
Contraception: X Medicine-Obstetrics and Gynecology
CiteScore
5.10
自引率
0.00%
发文量
17
审稿时长
22 weeks
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