RFamide-Related Peptide Neurons Modulate Reproductive Function and Stress Responses

• Published in: The Journal of neuroscience Vol. 41; no. 3; pp. 474 - 488
• Main Authors: Mamgain, Asha, Sawyer, India L, Timajo, David A M, Rizwan, Mohammed Z, Evans, Maggie C, Ancel, Caroline M, Inglis, Megan A, Anderson, Greg M
• Format: Journal Article
• Language: English
• Published: United States Society for Neuroscience 20-01-2021
• Subjects: Ablation; Animals; Control theory; Feedback loops; Female; Fertility; Fertility - physiology; Gene Knock-In Techniques; Gene Silencing; Genotype; Glucocorticoids; Glucocorticoids - metabolism; Luteinizing hormone; Luteinizing Hormone - metabolism; Male; Mice; Mice, Inbred C57BL; Neurons; Neurons - physiology; Neuropeptides - genetics; Neuropeptides - physiology; Peptides; Puberty; Reproduction - physiology; Reproductive cycle; Restraint, Physical; Secretion; Sex Characteristics; Sexual Maturation - physiology; Stress; Stress response; Stress, Psychological - physiopathology; stress; HPA axis; puberty; RFRP; fertility; reproduction
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/jneurosci.1062-20.2020

RF-amide related peptide 3 (RFRP-3) is a neuropeptide thought to inhibit central regulation of fertility. We investigated whether alterations in RFRP neuronal activity led to changes in puberty onset, fertility, and stress responses, including stress and glucocorticoid-induced suppression of pulsatile luteinizing hormone secretion. We first validated a novel RFRP-Cre mouse line, which we then used in combination with Cre-dependent neuronal ablation and DREADD technology to selectively ablate, stimulate, and inhibit RFRP neurons to interrogate their physiological roles in the regulation of fertility and stress responses. Chronic RFRP neuronal activation delayed male puberty onset and female reproductive cycle progression, but RFRP-activated and ablated mice exhibited apparently normal fertility. When subjected to either restraint- or glucocorticoid-induced stress paradigms. However, we observed a critical sex-specific role for RFRP neurons in mediating acute and chronic stress-induced reproductive suppression. Female mice exhibiting RFRP neuron ablation or silencing did not exhibit the stress-induced suppression in pulsatile luteinizing hormone secretion observed in control mice. Furthermore, RFRP neuronal activation markedly stimulated glucocorticoid secretion, demonstrating a feedback loop whereby stressful stimuli activate RFRP neurons, which in turn further activate the stress axis. These data provide evidence for a neuronal link between the stress and reproductive axes.