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美金刚通过抑制嗅球切除小鼠中的Kir6.1通道改善抑郁样行为。

Memantine Improves Depressive-like Behaviors via Kir6.1 Channel Inhibition in Olfactory Bulbectomized Mice.

作者信息

Moriguchi Shigeki, Inagaki Ryo, Shimojo Hirotsugu, Sugimura Yoshihiko, Fukunaga Kohji

机构信息

Research Center for Pharmaceutical Development, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan; Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.

Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.

出版信息

Neuroscience. 2020 Aug 21;442:264-273. doi: 10.1016/j.neuroscience.2020.06.002. Epub 2020 Jun 10.

Abstract

Aberrant depressive-like behaviors in olfactory bulbectomized (OBX) mice have been documented by previous studies. Here, we show that memantine enhances adult neurogenesis in the subgranular zone of the hippocampal dentate gyrus (DG) and improves depressive-like behaviors via inhibition of the ATP-sensitive potassium (K) channel in OBX mice. Treatment with memantine (1-3 mg/kg; per os (p.o.)) for 14 days significantly improved depressive-like behaviors in OBX mice, as assessed using the tail-suspension and forced-swim tests. Treatment with memantine also increased the number of BrdU-positive neurons in the DG of OBX mice. In the immunoblot analysis, memantine significantly increased phosphorylation of CaMKIV (Thr-196) and Akt (Ser-473), but not ERK (Thr-202/Tyr-204), in the DG of OBX mice. Furthermore, phosphorylation of GSK3β (Ser-9) and CREB (Ser-133), and BDNF protein expression levels increased in the DG of OBX mice, possibly accounting for the increased adult neurogenesis owing to Akt activation. In contrast, both the improvement of depressive-like behaviors and increase in BrdU-positive neurons in the DG following treatment with memantine were unapparent in OBX-treated Kir6.1 heterozygous (+/-) mice but not OBX-treated Kir6.2 heterozygous (+/-) mice. Furthermore, the increase in CaMKIV (Thr-196) and Akt (Ser-473) phosphorylation and BDNF protein expression levels was not observed in OBX-treated Kir6.1 +/- mice. Overall, our study shows that memantine improves OBX-induced depressive-like behaviors by increasing adult neurogenesis in the DG via Kir6.1 channel inhibition.

摘要

先前的研究已记录了嗅球切除(OBX)小鼠中异常的抑郁样行为。在此,我们表明美金刚可增强海马齿状回(DG)颗粒下区的成体神经发生,并通过抑制OBX小鼠的ATP敏感性钾(K)通道来改善抑郁样行为。用美金刚(1 - 3毫克/千克;口服(p.o.))治疗14天可显著改善OBX小鼠的抑郁样行为,这通过悬尾试验和强迫游泳试验进行评估。美金刚治疗还增加了OBX小鼠DG中BrdU阳性神经元的数量。在免疫印迹分析中,美金刚显著增加了OBX小鼠DG中CaMKIV(Thr - 196)和Akt(Ser - 473)的磷酸化,但未增加ERK(Thr - 202/Tyr - 204)的磷酸化。此外,OBX小鼠DG中GSK3β(Ser - 9)和CREB(Ser - 133)的磷酸化以及BDNF蛋白表达水平增加,这可能是由于Akt激活导致成体神经发生增加的原因。相比之下,在OBX处理的Kir6.1杂合子(+/-)小鼠中,美金刚治疗后抑郁样行为的改善和DG中BrdU阳性神经元的增加均不明显,但在OBX处理的Kir6.2杂合子(+/-)小鼠中并非如此。此外,在OBX处理的Kir6.1 +/-小鼠中未观察到CaMKIV(Thr - 196)和Akt(Ser - 473)磷酸化以及BDNF蛋白表达水平的增加。总体而言,我们的研究表明美金刚通过抑制Kir6.1通道增加DG中的成体神经发生来改善OBX诱导的抑郁样行为。

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