Car1基因敲除小鼠表现出抗抑郁样行为,同时伴有肠道微生物群紊乱。

IF 1.8 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell Biochemistry and Biophysics Pub Date : 2024-09-28 DOI:10.1007/s12013-024-01509-0
Chong Chen, Jianjun Chen, Ke Cheng, Peng Xie
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引用次数: 0

摘要

重度抑郁症(MDD)是一种严重的精神疾病,其发病机制尚不清楚。碳酸酐酶将二氧化碳转化为碳酸盐和质子,在各种大脑功能中发挥作用。碳酸酐酶1(Car1)的含量特别高,可能与间质部位的微生物群有关。我们培育了碳酸酐酶1缺陷小鼠,以探索抑郁样行为与肠道微生物群之间的关系。行为测试证实了 Car1-/- 小鼠的抑郁样行为。收集了 Car1-/- 和 WT 小鼠的粪便样本,并通过 16S rRNA 基因测序确定了两组之间不同的微生物群成分。与 WT 小鼠相比,Car1-/- 小鼠在尾悬试验(TST)中表现出明显增加的不运动性。肠道微生物群的组成在门级上存在差异,包括p_类杆菌科、p_毛细管菌科、p_固着菌科和p_泛酸菌科。在科一级,Car1-/-小鼠与WT小鼠相比,在八个微生物群组中的丰度有显著差异。Car1缺乏与抑郁样行为和肠道微生物群失调有关,可能与抑郁样表型有关。
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The Car1 Knockout Mice Exhibit Antidepressant-like Behaviors Accompanied with Gut Microbiota Disturbance.

Major depressive disorder (MDD) is a severe mental disorder with largely unknown mechanisms. Carbonic anhydrases convert CO2 to carbonates and protons, playing roles in various brain functions. Carbonic anhydrase 1 (Car1) is particularly abundant and may be linked to microbiota at interstitial sites. We developed Car1-deficient mice to explore the relationship between depression-like behaviors and gut microbiota. Behavioral tests confirmed depression-like behavior in Car1-/- mice. Fecal samples from Car1-/- and WT mice were collected, and 16S rRNA gene sequencing identified distinct microbiota components between the groups. Car1-/- mice exhibited significantly increased immobility in the tail suspension test (TST) compared to WT mice. The gut microbiota composition differed at the phylum level in p_Bacteroidetes, p_Verrucomicrobia, p_Firmicutes, and p_Tenericutes. At the family level, Car1-/- mice had significantly different abundances in eight microbiota groups compared to WT mice. Car1 deficiency is associated with depressive-like behavior and gut microbiota dysbiosis, potentially linked to depressive-like phenotypes.

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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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