toll样受体7刺激后小鼠抑郁样行为增强。

Yasunori Kubo, Yoshiki Yanagawa, Machiko Matsumoto, Sachiko Hiraide, Hiroko Togashi
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引用次数: 0

摘要

toll样受体(TLR) 7识别病毒单链RNA并通过产生I型干扰素(ifn - α和ifn - β)触发抗病毒免疫反应。已知ifn - α能诱发各种精神变化,如抑郁症状;然而,与TLR7激活的相关性仍有待确定。在本研究中,我们通过强迫游泳试验(FST)和悬尾试验(TST)对TLR7特异性配体咪喹莫特对小鼠抑郁样行为的影响进行了研究。米喹莫特(50微克/体,i.p)治疗后,FST和TST的静止时间均显著延长了2小时,表明TLR7激活增强了小鼠的抑郁样行为。此外,咪喹莫特诱导海马ifn - α mRNA表达,而它阻止了Schaffer-CA1通路的长期增强(即海马突触可塑性)。此外,TLR7 mRNA在海马中的表达高于全脑。这些发现表明,TLR7激活可能通过增加ifn - α表达和改变海马突触可塑性来增强小鼠的抑郁样行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced depressive-like behaviors after Toll-like receptor 7 stimulation in mice.

Toll-like receptor (TLR) 7 recognizes viral single-stranded RNA and triggers anti-viral immune responses through the production of type I interferons (IFNs) IFN-alpha and IFN-beta. IFN-alpha is known to induce various psychiatric changes such as depressive symptoms; however, the correlation with TLR7 activation remains to be determined. In this study, we examined the effect of imiquimod, a TLR7 specific ligand, on depressive-like behaviors evaluated by the forced swim test (FST) and the tail suspension test (TST) in mice. Immobility durations were significantly prolonged in both FST and TST by 2 h after imiquimod treatment (50 microg/body, i.p.), indicating that TLR7 activation enhanced depressive-like behaviors in mice. In addition, imiquimod induced IFN-alpha mRNA expression in the hippocampus, whereas it prevented long-term potentiation in the Schaffer-CA1 pathway (i.e., hippocampal synaptic plasticity). Moreover, TLR7 mRNA expression in the hippocampus was higher than that in the whole brain. These findings suggest that TLR7 activation enhances depressive-like behaviors in mice, possibly through increasing IFN-alpha expression and altering synaptic plasticity in the hippocampus.

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