| Autor: |
Carlson EJ; Department of Medicinal Chemistry (E.J.C., G.I.G., J.E.H.) and Institute for Therapeutics Discovery and Development (G.I.G., J.E.H.), University of Minnesota, Minneapolis, Minnesota., Georg GI; Department of Medicinal Chemistry (E.J.C., G.I.G., J.E.H.) and Institute for Therapeutics Discovery and Development (G.I.G., J.E.H.), University of Minnesota, Minneapolis, Minnesota hawkinso@umn.edu georg@umn.edu., Hawkinson JE; Department of Medicinal Chemistry (E.J.C., G.I.G., J.E.H.) and Institute for Therapeutics Discovery and Development (G.I.G., J.E.H.), University of Minnesota, Minneapolis, Minnesota hawkinso@umn.edu georg@umn.edu. |
| Jazyk: |
angličtina |
| Zdroj: |
Molecular pharmacology [Mol Pharmacol] 2022 Jan; Vol. 101 (1), pp. 56-67. Date of Electronic Publication: 2021 Oct 30. |
| DOI: |
10.1124/molpharm.121.000349 |
| Abstrakt: |
The cation channel of sperm (CatSper) is the principal entry point for calcium in human spermatozoa and its proper function is essential for successful fertilization. As CatSper is potently activated by progesterone, we evaluated a range of steroids to define the structure-activity relationships for channel activation and found that CatSper is activated by a broad range of steroids with diverse structural modifications. By testing steroids that failed to elicit calcium influx as inhibitors of channel activation, we discovered that medroxyprogesterone acetate, levonorgestrel, and aldosterone inhibited calcium influx produced by progesterone, prostaglandin E 1 , and the fungal natural product l -sirenin, but these steroidal inhibitors failed to prevent calcium influx in response to elevated K + and pH. In contrast to these steroid antagonists, we demonstrated for the first time that the T-type calcium channel blocker ML218 acts similarly to mibefradil, blocking CatSper channels activated by both ligands and alkalinization/depolarization. These T-type calcium channel blockers produced an insurmountable blockade of CatSper, whereas the three steroids produced antagonism that was surmountable by increasing concentrations of each activator, indicating that the steroids selectively antagonize ligand-induced activation of CatSper rather than blocking channel function. Both the channel blockers and the steroid antagonists markedly reduced hyperactivated motility of human sperm assessed by computer-aided sperm analysis, consistent with inhibition of CatSper activation. Unlike the channel blockers mibefradil and ML218, which reduced total and progressive motility, medroxyprogesterone acetate, levonorgestrel, and aldosterone had little effect on these motility parameters, indicating that these steroids are selective inhibitors of hyperactivated sperm motility. SIGNIFICANCE STATEMENT: The steroids medroxyprogesterone acetate, levonorgestrel, and aldosterone selectively antagonize progesterone- and prostaglandin E 1 -induced calcium influx through the CatSper cation channel in human sperm. In contrast to T-type calcium channel blockers that prevent all modes of CatSper activation, these steroid CatSper antagonists preferentially reduce hyperactivated sperm motility, which is required for fertilization. The discovery of competitive antagonists of ligand-induced CatSper activation provides starting points for future discovery of male contraceptive agents acting by this unique mechanism.
(Copyright © 2021 by The Author(s).) |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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