Arcuate nucleus‐specific progesterone receptor knockdown in female mice is sufficient to induce <scp>PCOS</scp> ‐like hyperactivity in the reproductive axis

mice and assessed HPG axis function. Females with GABA-specific PR knockout (GABAPRKO) exhibited delayed vaginal opening and fewer estrous cycles compared to controls, but LH pulse frequency and P4 negative feedback were unaffected. In contrast, females with AAV-Cre-mediated knockdown of PR specifically in the ARC exhibited increased LH pulse frequency in comparison to control and AAV-Cre off-target animals. ARC-specific PR knockdown also resulted in significantly decreased estrous cycle frequency, increased cycle length, reduced time spent in proestrus, and impaired P4 negative feedback, but no change in testosterone levels. These data show that reduced PR signalling in the ARC of adult female mice is sufficient to drive hyperactivity within the HPG axis and mimic some but not all reproductive features of PCOS. The subtle reproductive deficits in GABAPRKO may reflect compensatory mechanisms or the involvement of multiple neuronal phenotypes in P4 negative feedback. Together, this work supports the ARC as a critical site for P4 negative feedback regulation of the reproductive axis.

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Publication Details

Journal
Journal of Neuroendocrinology
Published
2026-04-01
DOI
https://doi.org/10.1111/jne.70181
Primary Topic
Hypothalamic control of reproductive hormones
Type
article
Field-Weighted Citation Impact
0.00

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article

Arcuate nucleus‐specific progesterone receptor knockdown in female mice is sufficient to induce PCOS ‐like hyperactivity in the reproductive axis

Kelly A. Glendining, Elodie Kip, Rebecca E. Campbell, Kyoko Potapov et al.
Journal of Neuroendocrinology
Hypothalamic control of reproductive hormones
article

Arcuate nucleus‐specific progesterone receptor knockdown in female mice is sufficient to induce PCOS ‐like hyperactivity in the reproductive axis

Kelly A. Glendining, Elodie Kip, Rebecca E. Campbell, Kyoko Potapov, Melanie Prescott
article en

Abstract

mice and assessed HPG axis function. Females with GABA-specific PR knockout (GABAPRKO) exhibited delayed vaginal opening and fewer estrous cycles compared to controls, but LH pulse frequency and P4 negative feedback were unaffected. In contrast, females with AAV-Cre-mediated knockdown of PR specifically in the ARC exhibited increased LH pulse frequency in comparison to control and AAV-Cre off-target animals. ARC-specific PR knockdown also resulted in significantly decreased estrous cycle frequency, increased cycle length, reduced time spent in proestrus, and impaired P4 negative feedback, but no change in testosterone levels. These data show that reduced PR signalling in the ARC of adult female mice is sufficient to drive hyperactivity within the HPG axis and mimic some but not all reproductive features of PCOS. The subtle reproductive deficits in GABAPRKO may reflect compensatory mechanisms or the involvement of multiple neuronal phenotypes in P4 negative feedback. Together, this work supports the ARC as a critical site for P4 negative feedback regulation of the reproductive axis.

Journal of NeuroendocrinologyVol. 38(4)
University of Otago (NZ)
Health Research Council of New Zealand, Marsden Fund
Gender equality
Openalex Percentile: Top 17%
Hypothalamic control of reproductive hormones
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