Impact of Microbial Metabolites on Microbiota-Gut-Brain Axis in Inflammatory Bowel Disease.
Impact of Microbial Metabolites on Microbiota-Gut-Brain Axis in Inflammatory Bowel Disease.
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微生物代谢产物对炎症性肠病中微生物群-肠道-脑轴的影响
DOI:
10.3390/ijms22041623
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发表时间:
2021-02-05
影响因子:
5.6
通讯作者:
Baj A
中科院分区:
文献类型:
--
作者:
Banfi D;Moro E;Bosi A;Bistoletti M;Cerantola S;Crema F;Maggi F;Giron MC;Giaroni C;Baj A
The complex bidirectional communication system existing between the gastrointestinal tract and the brain initially termed the “gut–brain axis” and renamed the “microbiota–gut–brain axis”, considering the pivotal role of gut microbiota in sustaining local and systemic homeostasis, has a fundamental role in the pathogenesis of Inflammatory Bowel Disease (IBD). The integration of signals deriving from the host neuronal, immune, and endocrine systems with signals deriving from the microbiota may influence the development of the local inflammatory injury and impacts also more distal brain regions, underlying the psychophysiological vulnerability of IBD patients. Mood disorders and increased response to stress are frequently associated with IBD and may affect the disease recurrence and severity, thus requiring an appropriate therapeutic approach in addition to conventional anti-inflammatory treatments. This review highlights the more recent evidence suggesting that alterations of the microbiota–gut–brain bidirectional communication axis may concur to IBD pathogenesis and sustain the development of both local and CNS symptoms. The participation of the main microbial-derived metabolites, also defined as “postbiotics”, such as bile acids, short-chain fatty acids, and tryptophan metabolites in the development of IBD-associated gut and brain dysfunction will be discussed. The last section covers a critical evaluation of the main clinical evidence pointing to the microbiome-based therapeutic approaches for the treatment of IBD-related gastrointestinal and neuropsychiatric symptoms.
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DOI:
10.1126/science.1198469
发表时间:
2011-01-21
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Atarashi K;Tanoue T;Shima T;Imaoka A;Kuwahara T;Momose Y;Cheng G;Yamasaki S;Saito T;Ohba Y;Taniguchi T;Takeda K;Hori S;Ivanov II;Umesaki Y;Itoh K;Honda K
通讯作者:
Honda K
影响因子:
9.8
作者:
Angelberger, Sieglinde;Reinisch, Walter;Erry, David B.
通讯作者:
Erry, David B.
DOI:
10.1084/jem.20100050
发表时间:
2010-05-10
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Allen IC;TeKippe EM;Woodford RM;Uronis JM;Holl EK;Rogers AB;Herfarth HH;Jobin C;Ting JP
通讯作者:
Ting JP
影响因子:
4.4
作者:
Aoki, Reiji;Aoki-Yoshida, Ayako;Takayama, Yoshiharu
通讯作者:
Takayama, Yoshiharu
影响因子:
4.4
作者:
Biagioli, Michele;Carino, Adriana;Fiorucci, Stefano
通讯作者:
Fiorucci, Stefano