Tian Peijun, O'Riordan Kenneth J, Lee Yuan-Kun, Wang Gang, Zhao Jianxin, Zhang Hao, Cryan John F, Chen Wei
State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, China.
School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, China.
Neurobiol Stress. 2020 Mar 20;12:100216. doi: 10.1016/j.ynstr.2020.100216. eCollection 2020 May.
Accumulating evidence points to an association between gut microbial abnormalities and depression disorder. The microbiota-gut-brain axis is an emerging target for treating depression using nutritional strategies, considering the numerous limitations of current pharmacological approaches. Here we studied the effect and probable mechanisms of psychobiotic treatment on depression.
Chronically stressed C57BL/6J male mice were administered viable CCFM1025 for 5 weeks prior to behavioral testing. Brain neurological alterations, serum corticosterone, cytokines levels, fecal microbial composition, and short-chain fatty acid (SCFA) content were measured. In addition, the effect of SCFA on 5-hydroxytryptophan (5-HTP) biosynthesis was investigated in an model of enterochromaffin cells (RIN14B).
CCFM1025 treatment significantly reduced depression- and anxiety-like behaviors. The hyperactive hypothalamic-pituitary-adrenal response, as well as inflammation, were also alleviated, possibly via regulating the expression of glucocorticoid receptors (). Moreover, CCFM1025 also down-regulated the pCREB-c-Fos pathway but increased the expression of brain-derived neurotrophic factor (BDNF). Meanwhile, chronic stress-induced gut microbial abnormalities were restored, accompanied by increased SCFA and 5-HTP levels. The intestinal 5-HTP biosynthesis positively correlated with fecal SCFA and levels.
In summary, CCFM1025 showed considerable antidepressant-like and microbiota-regulating effects, which opens avenues for novel therapeutic strategies towards treating depression.
越来越多的证据表明肠道微生物异常与抑郁症之间存在关联。鉴于目前药物治疗方法存在诸多局限性,微生物-肠道-脑轴成为利用营养策略治疗抑郁症的一个新靶点。在此,我们研究了精神益生菌治疗对抑郁症的影响及可能机制。
在行为测试前5周,对长期应激的C57BL/6J雄性小鼠给予活的CCFM1025。检测脑神经系统改变、血清皮质酮、细胞因子水平、粪便微生物组成和短链脂肪酸(SCFA)含量。此外,在肠嗜铬细胞(RIN14B)模型中研究了SCFA对5-羟色氨酸(5-HTP)生物合成的影响。
CCFM1025治疗显著减少了抑郁样和焦虑样行为。下丘脑-垂体-肾上腺反应亢进以及炎症也得到缓解,可能是通过调节糖皮质激素受体的表达。此外,CCFM1025还下调了pCREB-c-Fos通路,但增加了脑源性神经营养因子(BDNF)的表达。同时,慢性应激诱导的肠道微生物异常得以恢复,伴随SCFA和5-HTP水平升高。肠道5-HTP生物合成与粪便SCFA和水平呈正相关。
总之,CCFM1025显示出相当的抗抑郁样和微生物调节作用,为治疗抑郁症的新治疗策略开辟了道路。