saiko -ka- ryukotsui -borei-to在减轻小鼠社交失败压力引起的焦虑严重程度中的潜在作用。

IF 0.9
PCN reports : psychiatry and clinical neurosciences Pub Date : 2025-08-19 eCollection Date: 2025-09-01 DOI:10.1002/pcn5.70191
Yoshikazu Kitai, Leo Gotoh, Hikaru Hori
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引用次数: 0

摘要

目的:重度抑郁症是一个日益受到全球关注的问题,治疗方案有限。社会压力有助于其发展,但药物预防和缓解仍未得到充分探索。本研究探讨了“saiko -ka- ryukosu -borei-to”(SRBT)对社交失败应激小鼠抑郁和焦虑样行为的影响。方法:C57BL/6J小鼠连续10天,每天10分钟与较大、更具攻击性的ICR小鼠相互作用,诱导SDS。每次实验结束后,小鼠立即口服SRBT、氟西汀(Flu)或生理盐水(Sal),并分别被分配到SD-SRBT、SD-Flu和SD-Sal组。正常对照(NC)组为未接触SDS的Sal小鼠。第11天,对四组大鼠进行行为学评估,包括升高加迷宫(EPM)测试、悬尾测试(TST)和社会互动测试(SIT)。同时测量血浆皮质酮水平。结果:SDS显著增加了EPM的焦虑样行为,SD-Sal组和SD-Flu组的张开臂时间缩短。这种效果在SD-SRBT组中不太明显。虽然SD-Flu组表现出与SD-Sal组相似的焦虑样行为,但在张开手臂的时间上没有观察到显著差异。SDS不会在SIT或TST中诱发社交回避或抑郁样行为,也不会改变血浆皮质酮水平。结论:SRBT具有减轻社会压力焦虑的作用。然而,需要进一步的持续评价和调查来评估SRBT的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The potential role of Saiko-ka-ryukotsu-borei-to in mitigating the severity of anxiety induced by social defeat stress in mice.

The potential role of Saiko-ka-ryukotsu-borei-to in mitigating the severity of anxiety induced by social defeat stress in mice.

The potential role of Saiko-ka-ryukotsu-borei-to in mitigating the severity of anxiety induced by social defeat stress in mice.

The potential role of Saiko-ka-ryukotsu-borei-to in mitigating the severity of anxiety induced by social defeat stress in mice.

Aim: Major depressive disorder is a growing global concern with limited treatment options. Social stress contributes to its development, yet pharmacological prevention and mitigation remain underexplored. This study examined the effects of Saiko-ka-ryukotsu-borei-to (SRBT) on depressive and anxiety-like behaviors in mice exposed to social defeat stress (SDS).

Methods: C57BL/6J mice were subjected to daily 10-min interactions with larger, more aggressive ICR mice for 10 consecutive days to induce SDS. Immediately following each session, mice were orally administered SRBT, fluoxetine (Flu), or saline (Sal), and were assigned to the SD-SRBT, SD-Flu, and SD-Sal groups, respectively. Mice that received Sal without SDS exposure served as the normal control (NC) group. On the 11th day, behavioral assessments, including the elevated plus maze (EPM) test, tail suspension test (TST), and social interaction test (SIT), were conducted across the four groups. Plasma corticosterone levels were also measured.

Results: SDS significantly increased anxiety-like behavior in the EPM, as shown by reduced open arm time in the SD-Sal and SD-Flu groups. This effect was less evident in the SD-SRBT group. Although the SD-Flu group showed similar anxiety-like behavior to the SD-Sal group, no significant difference in open arm time was observed. SDS did not induce social avoidance or depressive-like behavior in the SIT or TST, nor did it alter plasma corticosterone levels.

Conclusion: This study suggested that SRBT has the potential to mitigate anxiety caused by social stress. However, further ongoing evaluation and investigation are required to assess the effectiveness of SRBT.

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