Abstract

Stress is an important neurological input for successful life. However, chronic stress and stress hormones could be a cause of various neurological disorders including anxiety disorders. Therefore, there have been many efforts to find effective materials for curing stress-induced neurological disorders. In this study, we examined the effect of Hydrangea macrophylla (HM) on corticosterone-induced neurotoxicity, stress-induced anxiety in mice and suggested a possible active ingredient of HM. HM protected cortical neurons against neurotoxicity of corticosterone (CORT), a stress hormone. HM also blocked CORT-induced hippocampal synaptic deficit via regulating Akt signaling. Oral administration of HM improved chronic restraint stress-induced anxiety in Elevated Plus maze test along with reduction of plasma corticosterone and TNF-α levels. Moreover, HM reduced stress-induced neuroinflammation and oxidative stress. Thunberginol C, an active ingredient of HM, also prevented CORT-induced neuronal cell death and restraint stress-induced anxiety. Moreover, thunberginol C reduced plasma TNF-α level and neuroinflammation and oxidative stress. Collectively, HM could be a good candidate for preventing stress-induced neurological disorders and thunberginol C may be an active ingredient of HM for this purpose.

Highlights

  • Stress can be either beneficial or harmful to the human body depending on its duration.In the brain, short-term stress is known to enhance cognition, which seems to be related to the long-term potentiation (LTP) improvement effect [1,2,3]

  • Since corticosterone is an important substance for inducing various neuropsychiatric diseases due to stress, animal experiments were conducted based on the expectation that Hydrangea macrophylla (HM) could improve anxiety symptoms caused by stress

  • We found that HM and thunberginol C have anti-stress effects

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Summary

Introduction

Short-term stress is known to enhance cognition, which seems to be related to the long-term potentiation (LTP) improvement effect [1,2,3]. Long-term stress is known to cause many neuropsychiatric symptoms, such as lowering cognition, increasing anxiety, and even causing depression [4,5,6]. The challenge is to develop a variety of neuropsychiatric disorders’ therapeutics through research on materials that could block the changes in brain function caused by long-term stress [7,8,9]. Cortisol is a powerful steroid, and it is known that high concentrations of cortisol can cause neuronal cell death, synaptic function deterioration, and cognitive decline in Antioxidants 2022, 11, 234.

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