Competitive CatSper Activators of Progesterone from Rhynchosia volubilis

Author:

Xiang Jin1,Kang Hang2,Li Hong-Gang3,Shi Yu-Long45,Zhang Ya-Li6,Ruan Chang-Lei1,Liu Lin-Hui1,Gao Han-Qi1,Luo Tao2,Hu Gao-Sheng6,Zhu Wei-Liang45,Jia Jing-Ming6,Chen Jia-Chun1,Fang Jin-Bo1

Affiliation:

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

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

3. Institute of Reproductive Health/Center of Reproductive Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

4. CAS Key Laboratory of Receptor Research & Drug Discovery and Design Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China

5. School of Pharmacy, University of Chinese Academy of Sciences, Beijing, China

6. School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China

Abstract

AbstractThe root Rhynchosia volubilis 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 R. volubilis affect the physiological regulation of the cation channel of sperm. The bioguided isolation of the whole herb of R. volubilis has resulted in the novel discovery of five new prenylated isoflavonoids, rhynchones A – E (1 – 5), a new natural product, 5′-O-methylphaseolinisoflavan (6) (1H and 13C 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 Ca2+ 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.

Funder

the Fundamental Research Funds for the Central Universities

the Special funds for central government to guide local scientific and Technological Development

the National Natural Science Foundation of China

the Open Funds of State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics of China

the National Key Research and Development Plan of China

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Reference40 articles.

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2. Chemical constituents from Rhynchosia volubilis;J Xiang;Chin Tradit Herbal Drugs,2020

3. New Isoflavonoids from the extract of Rhynchosia precatoria (Humb. & Bonpl. ex Willd.) DC. and their antimycobacterial activity;E W Coronado-Aceves;J Ethnopharmacol,2017

4. Prenylated isoflavonoids from Rhynchosia edulis;I V Ogungbe;Nat Prod Commun,2011

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