Suppr超能文献

慢性使用氟西汀超过 6 周会减少成年小鼠侧脑室下区的神经发生。

Chronic treatment with fluoxetine for more than 6 weeks decreases neurogenesis in the subventricular zone of adult mice.

机构信息

Division of Systems Medical Science, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.

出版信息

Mol Brain. 2011 Mar 8;4:10. doi: 10.1186/1756-6606-4-10.

Abstract

BACKGROUND

Recent studies indicate that chronic treatment with serotonergic antidepressants upregulates adult neurogenesis of the dentate gyrus (DG). In contrast, some studies claimed that there was very little alteration of neurogenesis in the subventricular zone (SVZ) by the antidepressants. Since almost all of those studies treated animals with drugs for 2 to 4 weeks as chronic treatment models of antidepressants, it is possible that antidepressant treatments for longer periods would affect adult neurogenesis in the SVZ.

RESULTS

In the present study, we examined the effects of long-term (up to 9 weeks) administration of fluoxetine (FLX), a selective serotonin reuptake inhibitor, on cell proliferation and survival in the DG and the SVZ of adult mice. As reported previously, in the DG of mice treated with FLX for 3, 6, or 9 weeks that were also injected with 5-bromodeoxyuridine (BrdU) in the last 3 days before perfusion, the numbers of Ki67- and BrdU-positive cells, which are cell proliferation markers, were significantly upregulated even at 3 weeks after the onset of the FLX treatments, and these increases were sustained in mice treated with FLX for 9 weeks. On the other hand, in the SVZ, we found a small, insignificant decrease in the numbers of Ki67- and BrdU-positive cells at 3 weeks, followed by highly significant decreases in the numbers of Ki67- and BrdU-positive cells at both 6 and 9 weeks. Furthermore, among olfactory newly generated cells that survived for 3 weeks after BrdU injection, the number of new cells was decreased at 9 weeks of FLX treatment.

CONCLUSIONS

These results demonstrate that long-term (more than 6 weeks) treatment with FLX has the opposite effect on neurogenesis in the SVZ than it does in the DG. The results also suggest that the decrease in neurogenesis in the SVZ might be involved in some aspects of the drugs' therapeutic effects on depression. In addition, our findings raise the possibility that some of the side effects of antidepressants might be mediated by decreased adult neurogenesis in the SVZ.

摘要

背景

最近的研究表明,慢性使用血清素抗抑郁药会增加齿状回(DG)的成年神经发生。相比之下,一些研究声称抗抑郁药对侧脑室下区(SVZ)的神经发生几乎没有改变。由于几乎所有这些研究都将动物用药物处理 2 到 4 周作为抗抑郁药的慢性治疗模型,因此长期(长达 9 周)使用抗抑郁药可能会影响 SVZ 中的成年神经发生。

结果

在本研究中,我们研究了长期(长达 9 周)使用氟西汀(FLX),一种选择性血清素再摄取抑制剂,对成年小鼠 DG 和 SVZ 中的细胞增殖和存活的影响。如前所述,在接受 FLX 治疗 3、6 或 9 周的小鼠的 DG 中,在灌注前的最后 3 天内注射 5-溴脱氧尿苷(BrdU),细胞增殖标志物 Ki67 和 BrdU 阳性细胞的数量在 FLX 治疗开始后 3 周时显著上调,并且这些增加在接受 FLX 治疗 9 周的小鼠中持续存在。另一方面,在 SVZ 中,我们发现 3 周时 Ki67 和 BrdU 阳性细胞的数量略有下降,随后在 6 周和 9 周时 Ki67 和 BrdU 阳性细胞的数量显著下降。此外,在 BrdU 注射后存活 3 周的新嗅觉生成细胞中,FLX 治疗 9 周后新细胞数量减少。

结论

这些结果表明,长期(超过 6 周)使用 FLX 对 SVZ 中的神经发生产生的影响与 DG 中的相反。研究结果还表明,SVZ 中神经发生的减少可能与药物治疗抑郁症的某些方面有关。此外,我们的研究结果提出了这样一种可能性,即抗抑郁药的一些副作用可能是由 SVZ 中成年神经发生减少介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cf7/3060120/949f1d1f7414/1756-6606-4-10-1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验