Department of Psychiatry, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Traditional Chinese Medicine), Hangzhou, China.
CNS Neurosci Ther. 2023 Jun;29 Suppl 1(Suppl 1):115-128. doi: 10.1111/cns.14091. Epub 2023 Jan 17.
Most of the previous studies have demonstrated the potential antidepressive and anxiolytic role of prebiotic supplement in male subjects, yet few have females enrolled. Herein, we explored whether prebiotics administration during chronic stress prevented depression-like and anxiety-like behavior in a sex-specific manner and the mechanism of behavioral differences caused by sex.
Female and male C57 BL/J mice on normal diet were supplemented with or without a combination of fructo-oligosaccharides (FOS) and galacto-oligosaccharides (GOS) during 3- and 4-week chronic restraint stress (CRS) treatment, respectively. C57 BL/J mice on normal diet without CRS were used as controls. Behavior consequences, gut microbiota, dysfunction of gut and brain-blood barriers, and inflammatory profiles were measured.
In the 3rd week, FOS + GOS administration attenuated stress-induced anxiety-like behavior in female, but not in male mice, and the anxiolytic effects in males were observed until the 4th week. However, protective effects of prebiotics on CRS-induced depression were not observed. Changes in the gene expression of tight junction proteins in the distal colon and hippocampus, and decreased number of colon goblet cells following CRS were restored by prebiotics only in females. In both female and male mice, prebiotics alleviated stress-induced BBB dysfunction and elevation in pro-inflammatory cytokines levels, and modulated gut microbiota caused by stress. Furthermore, correlation analysis revealed that anxiety-like behaviors were significantly correlated with levels of pro-inflammatory cytokines and gene expression of tight junction proteins in the hippocampus of female mice, and the abundance of specific gut microbes was also correlated with anxiety-like behaviors, pro-inflammatory cytokines, and gene expression of tight junction proteins in the hippocampus of female mice.
Female mice were more vulnerable to stress and prebiotics than males. The gut microbiota, gut and blood-brain barrier, and inflammatory response may mediate the protective effects of prebiotics on anxiety-like behaviors in female mice.
大多数先前的研究表明,益生元补充剂对男性具有潜在的抗抑郁和抗焦虑作用,但很少有女性参与研究。在此,我们探讨了在慢性应激期间给予益生元是否以性别特异性的方式预防抑郁样和焦虑样行为,以及性别引起行为差异的机制。
正常饮食的雌性和雄性 C57BL/J 小鼠分别在 3 周和 4 周慢性束缚应激(CRS)期间补充或不补充低聚果糖(FOS)和低聚半乳糖(GOS)的混合物。未进行 CRS 的正常饮食的 C57BL/J 小鼠作为对照。测量行为后果、肠道微生物群、肠道和血脑屏障功能障碍以及炎症特征。
在第 3 周,FOS+GOS 给药减轻了雌性应激引起的焦虑样行为,但对雄性没有作用,并且雄性的抗焦虑作用一直持续到第 4 周。然而,益生元对 CRS 引起的抑郁没有保护作用。CRS 后,远端结肠和海马中紧密连接蛋白的基因表达改变以及结肠杯状细胞数量减少,仅在雌性中被益生元恢复。在雌性和雄性小鼠中,益生元均减轻了应激引起的 BBB 功能障碍和促炎细胞因子水平升高,并调节了应激引起的肠道微生物群。此外,相关性分析表明,焦虑样行为与雌性小鼠海马中促炎细胞因子水平和紧密连接蛋白基因表达显著相关,特定肠道微生物的丰度也与雌性小鼠的焦虑样行为、促炎细胞因子和海马中紧密连接蛋白基因表达相关。
与雄性相比,雌性对压力和益生元更敏感。肠道微生物群、肠道和血脑屏障以及炎症反应可能介导了益生元对雌性焦虑样行为的保护作用。