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从鸡矢藤中提取的孕酮竞争性 CatSper 激活剂。

Competitive CatSper Activators of Progesterone from Rhynchosia volubilis.

机构信息

School of Pharmacy, Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Institute of Life Science and School of Life Science, Nanchang University, Key Laboratory of Reproductive Physiology and Pathology in Jiangxi Province, Nanchang, China.

出版信息

Planta Med. 2022 Sep;88(11):881-890. doi: 10.1055/a-1542-0151. Epub 2021 Aug 6.

Abstract

The root was widely used for contraception in folk medicine, although its molecular mechanism on antifertility has not yet been revealed. In human sperm, it was reported that the cation channel of sperm, an indispensable cation channel for the fertilization process, could be regulated by various steroid-like compounds in plants. Interestingly, these nonphysiological ligands would also disturb the activation of the cation channel of sperm induced by progesterone. Therefore, this study aimed to explore whether the compounds in affect the physiological regulation of the cation channel of sperm. The bioguided isolation of the whole herb of has resulted in the novel discovery of five new prenylated isoflavonoids, rhynchones A - E (1:  - 5: ), a new natural product, 5'--methylphaseolinisoflavan (6: ) (H and C NMR data, Supporting Information), together with twelve known compounds (7:  - 18: ). Their structures were established by extensive spectroscopic analyses and drawing a comparison with literature data, while their absolute configurations were determined by electronic circular dichroism calculations. The experiments of intracellular Ca signals and patch clamping recordings showed that rhynchone A (1: ) significantly reduced cation channel of sperm activation by competing with progesterone. In conclusion, our findings indicat that rhynchone A might act as a contraceptive compound by impairing the activation of the cation channel of sperm and thus prevent fertilization.

摘要

该植物的根在民间医学中被广泛用于避孕,尽管其抗生育的分子机制尚未被揭示。在人类精子中,据报道,精子的阳离子通道,受精过程中不可或缺的阳离子通道,可以被植物中的各种类甾体化合物调节。有趣的是,这些非生理配体也会干扰孕激素诱导的精子阳离子通道的激活。因此,本研究旨在探讨[植物名称]中的化合物是否会影响精子阳离子通道的生理调节。对[植物名称]全草的生物导向分离导致了五个新的prenylated isoflavonoids,rhynchones A - E(1:-5:)的新发现,一种新的天然产物,5'-甲基 phaseolinisoflavan(6:)(H 和 C NMR 数据,支持信息),以及十二个已知化合物(7:-18:)。通过广泛的光谱分析和与文献数据的比较建立了它们的结构,而它们的绝对构型则通过电子圆二色性计算确定。细胞内 Ca 信号和膜片钳记录实验表明,rhynchone A(1:)通过与孕酮竞争显著降低了精子阳离子通道的激活。总之,我们的研究结果表明,rhynchone A 可能通过损害精子阳离子通道的激活来发挥避孕作用,从而防止受精。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5490/9439852/3170510da560/10-1055-a-1542-0151-if0210pm01.jpg

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