Abstract

Adolescence is a critical period of development with increased sensitivity toward psychological stressors. Many psychiatric conditions emerge during adolescence and animal studies have shown that that acute stress has long-term effects on hypothalamic-pituitary-adrenal axis function and behavior. We recently demonstrated that acute stress produces long-term electrophysiological changes in locus coeruleus and long-lasting anxiety-like behavior in adolescent male rats. Based on prior reports of increased stress sensitivity during adolescence and increased sensitivity of female locus coeruleus toward corticotropin releasing factor, we hypothesized that the same acute stressor would cause different behavioral and physiological responses in adolescent female and adult male and female rats one week after stressor exposure. In this study, we assessed age and sex differences in how an acute psychological stressor affects corticosterone release, anxiety-like behavior, and locus coeruleus physiology at short- and long-term intervals. All groups of animals except adult female responded to stress with elevated corticosterone levels at the acute time point. One week after stressor exposure, adolescent females showed decreased firing of locus coeruleus neurons upon current injection and increased exploratory behavior compared to controls. The results were in direct contrast to changes observed in adolescent males, which showed increased anxiety-like behavior and increased spontaneous and induced firing in locus coeruleus neurons a week after stressor exposure. Adult males and females were both behaviorally and electrophysiologically resilient to the long-term effects of acute stress. Therefore, there may be a normal developmental trajectory for locus coeruleus neurons which promotes stress resilience in adults, but stressor exposure during adolescence perturbs their function. Furthermore, while locus coeruleus neurons are more sensitive to stressor exposure during adolescence, the effect varies between adolescent males and females. These findings suggest that endocrine, behavioral, and physiological responses to stress vary among animals of different age and sex, and therefore these variables should be taken into account when selecting models and designing experiments to investigate the effects of stress. These differences in animals may also allude to age and sex differences in the prevalence of various psychiatric illnesses within the human population.

Highlights

  • Adolescence is an important period of transition between childhood and adulthood and is a sensitive period for stressor exposure

  • Previous findings from our lab have shown that a single episode of combined restraint and predator odor stress in adolescent male rats leads to specific changes in locus coeruleus (LC) physiology and anxiety-like behavior (Borodovitsyna et al, 2018a, 2020)

  • These unexpected results may be due to the elevated plus maze being inherently stressful, and, as blood was collected after behavior scoring, may have elevated serum corticosterone beyond baseline even in the control animals.One week after stress, corticosterone concentration returned to levels similar to baseline in all groups, regardless of the treatment (Figures 2A, 3A, 4A, 5A), which indicates that the stressor does not result in chronic dysregulation of the HPA axis

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Summary

Introduction

Adolescence is an important period of transition between childhood and adulthood and is a sensitive period for stressor exposure (van Dijken et al, 1993). A surge of gonadal hormones during puberty renders the adolescent HPA axis more susceptible to stress. It takes almost twice as long for adolescent rats to return to the normal baseline plasma concentration of the stress hormone corticosterone during recovery after stress when compared to adults (Romeo et al, 2004a,b). Adolescence in humans is characterized by an increase in the baseline concentration of the primary stress hormone in humans, cortisol, and an increase in the stress reactivity of the HPA axis (Adam, 2006). Female rats have been shown to have higher baseline plasma corticosterone levels and increased responsiveness to stressors compared to males (Kitay, 1961). A human study has shown that stress anticipation leads to higher levels of cortisol release in males than females (Kirschbaum et al, 1992)

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