18th International İstanbul Scientific Research Congress, İstanbul, Türkiye, 28 Aralık 2025, ss.27, (Özet Bildiri)
Seasonal anestrus
in ewes results from photoperiod-mediated suppression of hypothalamic GnRH
pulsatility, leading to reduced LH secretion and cessation of ovulatory
activity. To maintain flock fertility and sustain lamb production during this
period, estrus synchronization remains essential, and progestagen-based
protocols are widely employed for this purpose. However, despite their
practical effectiveness, these steroidal treatments present notable drawbacks,
including residue concerns, welfare issues, and environmental impact,
highlighting the need for alternative non-steroidal approaches. Recent advances
in reproductive neuroendocrinology have identified several non-steroidal
compounds capable of reactivating the reproductive axis by targeting central
regulatory pathways. Among these, kisspeptin analogs directly stimulate
KISS1R-expressing neurons, inducing robust GnRH/LH secretion and reinitiating
cyclic ovarian activity. Dopamine antagonists facilitate reproductive
activation by suppressing the heightened dopaminergic inhibition originating
from A15 neurons, thereby indirectly enhancing GnRH pulsatility and follicular
progression. Aromatase inhibitors, on the other hand, transiently suppress
estradiol synthesis, thereby reducing the inhibitory feedback exerted on the
hypothalamic GnRH neurons and facilitating increased GnRH release. Collectively,
evidence indicates that these non-steroidal strategies target the major
neuroendocrine bottlenecks underlying seasonal anestrus through kisspeptin,
dopaminergic, and estrogen-feedback modulation. Their short-acting profiles
reduced welfare concerns, and lack of steroid residues position them as
promising next-generation tools for estrus induction and synchronization in
anestrous ewes. This presentation will summarize their mechanisms of action,
current efficacy data, and potential integration into reproductive management
programs.