Targeting the retinoid signaling pathway with YCT-529 for effective and reversible oral contraception in mice and primates.

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Tác giả: Akash Bakshi, Narsihmulu Cheryala, Sanny S W Chung, Gunda I Georg, Soma Maitra, Nadja Mannowetz, Md Abdullah Al Noman, Debra J Wolgemuth, Henry L Wong

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: England : Communications medicine , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 711649

BACKGROUND: The retinoic acid receptor alpha (Rarα) has been validated as a male contraceptive target by genetic knockouts resulting in male sterility. The effects on spermatogenesis in the absence of RARα resemble the loss of RAR signaling in vitamin A deficiency, and the mice are otherwise normal. The effects on spermatogenesis in animals treated orally with the dual RARα/RARγ antagonist BMS-189453 closely phenocopies the absence of RARα function. Notably, the resulting male sterility is reversible. We, therefore, wished to identify RARα-selective inhibitors for potential male non-hormonal contraception. METHODS: YCT-529 was investigated for RARα selective inhibition, physicochemical characteristics, oral bioavailability, and pharmacokinetic properties in mice and non-human primates. It was assessed in mouse mating trials to determine the most effective dosing regimen to induce infertility in male mice and in male non-human primates to reduce sperm levels. RESULTS: Characterization of YCT-529 shows suitable biochemical, physicochemical, and pharmacokinetic properties for in vivo testing. YCT-529 inhibits mouse fertility of male mice within 4 weeks of oral administration, correlating with disrupted spermatogenesis demonstrating specific inhibition of the RARα pathway. Within 6 weeks after cessation of dosing, mouse fertility reverses. Furthermore, YCT-529 inhibits sperm production in a non-human primate model within 2 weeks of oral dosing without adverse side effects. Within 10-15 weeks after cessation of dosing, non-human primates' sperm counts fully reverses. CONCLUSIONS: These results lay the groundwork for evaluating YCT-529 in human clinical trials.
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