Ochratoxin A induces abnormal tryptophan metabolism in the intestine and liver to activate AMPK signaling pathway

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Ochratoxin A induces abnormal tryptophan metabolism in the intestine and liver to activate AMPK signaling pathway ; volume:14 ; number:1 ; day:8 ; month:9 ; year:2023 ; pages:1-12 ; date:12.2023
Journal of animal science and biotechnology ; 14, Heft 1 (8.9.2023), 1-12, 12.2023

Creator: Ma, Weiqing
Fu, Yang
Zhu, Shanshan
Xia, Daiyang
Zhai, Shuangshuang
Xiao, Deqin
Zhu, Yongwen
Dione, Michel
Ben, Lukuyu
Yang, Lin
Wang, Wence

Contributor: SpringerLink (Online service)

DOI: 10.1186/s40104-023-00912-6

URN: urn:nbn:de:101:1-2024020613224296325331

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:26 AM CEST

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Associated

Ma, Weiqing
Fu, Yang
Zhu, Shanshan
Xia, Daiyang
Zhai, Shuangshuang
Xiao, Deqin
Zhu, Yongwen
Dione, Michel
Ben, Lukuyu
Yang, Lin
Wang, Wence
SpringerLink (Online service)

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Ochratoxin A induces abnormal tryptophan metabolism in the intestine and liver to activate AMPK signaling pathway

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Other Objects (12)

The aldolase inhibitor aldometanib mimics glucose starvation to activate lysosomal AMPK

DENV-2 NS1 promotes AMPK-LKB1 interaction to activate AMPK/ERK/mTOR signaling pathway to induce autophagy

Lithocholic acid binds TULP3 to activate sirtuins and AMPK to slow down ageing

Hypoxanthine phosphoribosyl transferase 1 metabolizes temozolomide to activate AMPK for driving chemoresistance of glioblastomas

ACE2 mediates tryptophan alleviation on diarrhea by repairing intestine barrier involved mTOR pathway

The GLP-1 receptor agonists exenatide and liraglutide activate Glucose transport by an AMPK-dependent mechanism

Ochratoxin A and Coffee

Heme Oxygenase-1-Modified BMMSCs Activate AMPK–Nrf2–FTH1 to Reduce Severe Steatotic Liver Ischemia–Reperfusion Injury

Polyphenols and Tryptophan Metabolites Activate the Aryl Hydrocarbon Receptor in an in vitro Model of Colonic Fermentation

Gut microbiota activate Toll-like receptor 4 to trigger vascularization and BMP2 signalling in the murine small intestine

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Ochratoxin A : the continuing enigma

The aldolase inhibitor aldometanib mimics glucose starvation to activate lysosomal AMPK

DENV-2 NS1 promotes AMPK-LKB1 interaction to activate AMPK/ERK/mTOR signaling pathway to induce autophagy

Lithocholic acid binds TULP3 to activate sirtuins and AMPK to slow down ageing

Hypoxanthine phosphoribosyl transferase 1 metabolizes temozolomide to activate AMPK for driving chemoresistance of glioblastomas

ACE2 mediates tryptophan alleviation on diarrhea by repairing intestine barrier involved mTOR pathway

The GLP-1 receptor agonists exenatide and liraglutide activate Glucose transport by an AMPK-dependent mechanism

Ochratoxin A and Coffee

Heme Oxygenase-1-Modified BMMSCs Activate AMPK–Nrf2–FTH1 to Reduce Severe Steatotic Liver Ischemia–Reperfusion Injury

Polyphenols and Tryptophan Metabolites Activate the Aryl Hydrocarbon Receptor in an in vitro Model of Colonic Fermentation

Gut microbiota activate Toll-like receptor 4 to trigger vascularization and BMP2 signalling in the murine small intestine

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The aldolase inhibitor aldometanib mimics glucose starvation to activate lysosomal AMPK

DENV-2 NS1 promotes AMPK-LKB1 interaction to activate AMPK/ERK/mTOR signaling pathway to induce autophagy

Lithocholic acid binds TULP3 to activate sirtuins and AMPK to slow down ageing

Hypoxanthine phosphoribosyl transferase 1 metabolizes temozolomide to activate AMPK for driving chemoresistance of glioblastomas

ACE2 mediates tryptophan alleviation on diarrhea by repairing intestine barrier involved mTOR pathway

The GLP-1 receptor agonists exenatide and liraglutide activate Glucose transport by an AMPK-dependent mechanism

Ochratoxin A and Coffee

Heme Oxygenase-1-Modified BMMSCs Activate AMPK–Nrf2–FTH1 to Reduce Severe Steatotic Liver Ischemia–Reperfusion Injury

Polyphenols and Tryptophan Metabolites Activate the Aryl Hydrocarbon Receptor in an in vitro Model of Colonic Fermentation

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Zur Embryotoxizität von Ochratoxin A

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