Abstract

The circadian clocks within the hypothalamic–pituitary–gonadal axis control estrous cycles in female rodents. The suprachiasmatic nucleus (SCN), where the central clock is located, generates daily signals to trigger surge release of luteinizing hormone (LH), which in turn induces ovulation. It has been observed in aged rodents that output from the SCN such as neuronal firing activity is declined, and estrous cycles become irregular and finally stop. Circadian clock mutants display accelerated reproductive aging, suggesting the complicated interplay between the circadian system and the endocrine system. To investigate such circadian regulation of estrous cycles, we construct a mathematical model that describes dynamics of key hormones such as LH and of circadian clocks in the SCN and in the ovary, and simulate estrous cycles for various parameter values. Our simulation results demonstrate that reduction of the amplitude of the SCN signal, which is a symptom of aging, makes estrous cycles irregular. We also show that variation in the phase of the SCN signal and changes in the period of ovarian circadian clocks exacerbates the aging effect on estrous cyclicity. Our study suggests that misalignment between the SCN and ovarian circadian oscillations is one of the primary causes of the irregular estrous cycles.

Highlights

  • The circadian clocks within the hypothalamic–pituitary–gonadal axis control estrous cycles in female rodents

  • Aging effects on the circadian system are evident in neural activity of the suprachiasmatic nucleus (SCN) and subparaventricular zone (SPZ), both of which are essential for circadian output from the ­SCN24

  • We show that accelerated aging in circadian clock mutants is at least partly due to misalignment between the SCN and ovarian circadian oscillations, which further reduces synchrony of a population of ovarian cellular oscillators

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Summary

Introduction

The circadian clocks within the hypothalamic–pituitary–gonadal axis control estrous cycles in female rodents. The suprachiasmatic nucleus (SCN), where the central clock is located, generates daily signals to trigger surge release of luteinizing hormone (LH), which in turn induces ovulation It has been observed in aged rodents that output from the SCN such as neuronal firing activity is declined, and estrous cycles become irregular and stop. LH shifts the phase of the Per[1] rhythm in a circadian-time-dependent manner, yielding a phase response curve (PRC) to ­LH18 These experimental observations suggest that LH signals entrain individual ovarian clocks and maintain their synchronization, which might be required to establish the high-amplitude circadian oscillation of the ovary as a whole and to maintain the rhythmic ovulatory sensitivity to LH. This concept is consistent with the observation that the rhythmicity in mRNA levels of VIP, one of major peptides acting as the SCN output, is attenuated with ­age[30]

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