Abstract

Mustard leaf (Brassica juncea var. crispifolia L. H. Bailey) has been reported to have psychological properties such as anti-depressant activities. However, studies on chronic stress and depression caused by restraint have not been conducted. Therefore, this study aimed to evaluate the effects of a mustard leaf (ML) extract on chronic restraint stress (CRS) in mice. Male mice were subjected to a CRS protocol for a period of four weeks to induce stress. The results showed that the ML extract (100 and 500 mg/kg/perorally administered for four weeks) significantly decreased corticosterone levels and increased neurotransmitters levels in stressed mice. Apoptosis by CRS exposure was induced by Bcl-2 and Bax expression regulation and was suppressed by reducing caspase-3 and poly (ADP-ribose) polymerase expression after treatment with the ML extract. Our results confirmed that apoptosis was regulated by increased expression of brain-derived neurotrophic factor (BDNF). Additionally, cytokine levels were regulated by the ML extract. In conclusion, our results showed that the ML extract relieved stress effects by regulating hormones and neurotransmitters in CRS mice, BDNF expression, and apoptosis in the brain. Thus, it can be suggested that the studied ML extract is an agonist that can help relieve stress and depression.

Highlights

  • The modern society is exposed to excessive stress and diseases due to heavy workload, difficult human relationships, and career fatigue

  • Our results showed that the mustard leaf (ML) extract relieved stress effects by regulating hormones and neurotransmitters in chronic restraint stress (CRS) mice, brain-derived neurotrophic factor (BDNF) expression, and apoptosis in the brain

  • Weight loss was not affected by the ML extract

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Summary

Introduction

The modern society is exposed to excessive stress and diseases due to heavy workload, difficult human relationships, and career fatigue. The CRS method was confirmed to suppress behavioral and physiological functions that caused the retraction of dendrites i CA3 pyramidal neurons [1,2,3,4]. Dendritic retraction caused by stress is due to the reduction in brain-derived neurotrophic factor (BDNF) synthesis and mRNA expression of hippocampal neurotrophic elements. The synthesis of BDNF in the hippocampus is regulated by several neurotransmitters and hormones, whose secretion is controlled by external stimuli and stress [8,9]. Neurotransmitters are secreted from the hypothalamus in the CNS and include dopamine (DA), serotonin (5-hydroxytryptamine; 5-HT), and norepinephrine (NE), which regulate physiological activities such as emotional state, Nutrients 2020, 12, 3640; doi:10.3390/nu12123640 www.mdpi.com/journal/nutrients

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