Prenatal androgen treatment impairs the suprachiasmatic nucleus arginine-vasopressin to kisspeptin neuron circuit in female mice

• Published in: Frontiers in endocrinology (Lausanne) Vol. 13; p. 951344
• Main Authors: Jamieson, Bradley B, Moore, Aleisha M, Lohr, Dayanara B, Thomas, Simone X, Coolen, Lique M, Lehman, Michael N, Campbell, Rebecca E, Piet, Richard
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 05.08.2022
• Subjects: androgen receptor; Androgens - metabolism; Androgens - pharmacology; Animals; Arginine; Arginine Vasopressin - metabolism; circadian; Endocrinology; Female; GnRH; Gonadotropin-Releasing Hormone - genetics; Gonadotropin-Releasing Hormone - metabolism; Humans; Kisspeptins - genetics; Kisspeptins - metabolism; LH surge; Luteinizing Hormone - metabolism; Mice; Neurons - metabolism; PCOS; Polycystic Ovary Syndrome - chemically induced; Polycystic Ovary Syndrome - genetics; Polycystic Ovary Syndrome - metabolism; Pregnancy; Suprachiasmatic Nucleus - metabolism; tract-tracing; Vasopressins - metabolism; PCOS; circadian; androgen receptor; electrophysiology; tract-tracing; LH surge; GnRH
• ISSN: 1664-2392; 1664-2392
• DOI: 10.3389/fendo.2022.951344

Polycystic ovary syndrome (PCOS) is associated with elevated androgen and luteinizing hormone (LH) secretion and with oligo/anovulation. Evidence indicates that elevated androgens impair sex steroid hormone feedback regulation of pulsatile LH secretion. Hyperandrogenemia in PCOS may also disrupt the preovulatory LH surge. The mechanisms through which this might occur, however, are not fully understood. Kisspeptin (KISS1) neurons of the rostral periventricular area of the third ventricle (RP3V) convey hormonal cues to gonadotropin-releasing hormone (GnRH) neurons. In rodents, the preovulatory surge is triggered by these hormonal cues and coincident timing signals from the central circadian clock in the suprachiasmatic nucleus (SCN). Timing signals are relayed to GnRH neurons, in part, projections from SCN arginine-vasopressin (AVP) neurons to RP3V neurons. Because rodent SCN cells express androgen receptors (AR), we hypothesized that these circuits are impaired by elevated androgens in a mouse model of PCOS. In prenatally androgen-treated (PNA) female mice, SCN expression was significantly increased compared to that found in prenatally vehicle-treated mice. A similar trend was seen in the number of -positive SCN cells expressing . In the RP3V, the number of kisspeptin neurons was preserved. Anterograde tract-tracing, however, revealed reduced SCN neuron projections to the RP3V and a significantly lower proportion of RP3V neurons with close appositions from SCN fibers. Functional assessments showed, on the other hand, that RP3V neuron responses to AVP were maintained in PNA mice. These findings indicate that PNA changes some of the neural circuits that regulate the preovulatory surge. These impairments might contribute to ovulatory dysfunction in PNA mice modeling PCOS.