Abstract

It is well known that glucocorticoid receptor (GR) signaling regulates the hypothalamic-pituitary-adrenal (HPA) axis, and GR expression level is associated with HPA axis activity. Recent studies revealed that microRNA- (miR-) 18 and/or 124a are candidate negative regulators of GR in the brain. The Kampo medicine Yokukansan (YKS) can affect psychological symptoms such as depression and anxiety that are associated with stress responses. In this study, we evaluated the effect of YKS on miR-18 and 124a and GR levels in mice exposed to stress. We found that YKS pretreatment normalized elevated plasma corticosterone levels in stress-exposed mice. In addition, GR mRNA levels were downregulated in the brain following stress exposure. While miR-124a expression levels were not altered in the hypothalamus of stress-exposed mice, miR-18 levels decreased in the hypothalamus of YKS-pretreated mice after stress exposure. Finally, GR protein levels in the paraventricular nucleus (PVN) of the hypothalamus after stress exposure recovered in YKS-pretreated mice. Collectively, these data suggest that YKS normalizes GR protein levels by regulating miR-18 expression in the hypothalamus, thus normalizing HPA axis activity following stress exposure.

Highlights

  • Hypothalamic-pituitary-adrenal (HPA) axis activation is one of the key responses following physiological stress [1,2,3,4,5]

  • The HPA axis is reliably activated by stress exposure, and it is well known that this increases plasma corticosterone levels for up to 6 h after stress exposure [14, 23, 26]

  • We provide the first evidence that YKS downregulates miR-18 expression in the hypothalamus after stress exposure and normalizes glucocorticoid receptor (GR) protein levels in the paraventricular nucleus (PVN), affecting HPA axis activity

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Summary

Introduction

Hypothalamic-pituitary-adrenal (HPA) axis activation is one of the key responses following physiological stress [1,2,3,4,5]. Corticosteroids provide negative feedback to the HPA system at the level of the hippocampus, hypothalamus, and pituitary gland by activating glucocorticoid receptors (GRs) [6,7,8,9]. The mineralocorticoid receptor has a high affinity for corticosterone [10]. GR has a low affinity for corticosterone and is rarely activated in resting conditions. GR expression is a crucial indicator of stress response indicator [10,11,12,13,14]. Little is known about the molecular mechanisms regulating GR expression in the hypothalamus

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