Substance P and Glucagon-like Peptide-17-36 Amide Mediate Anorexic Responses to Trichothecene Deoxynivalenol and Its Congeners
Language English Country Switzerland Media electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
36548782
PubMed Central
PMC9785148
DOI
10.3390/toxins14120885
PII: toxins14120885
Knihovny.cz E-resources
- Keywords
- anorexia, brain-gut peptide, glucagon-like peptide-17-36 amide, substance P, trichothecene,
- MeSH
- Amides toxicity MeSH
- Appetite Depressants * toxicity MeSH
- Glucagon-Like Peptide 1 toxicity MeSH
- Humans MeSH
- Anorexia chemically induced MeSH
- Substance P toxicity MeSH
- Trichothecenes, Type B * MeSH
- Trichothecenes * toxicity MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 15-acetyldeoxynivalenol MeSH Browser
- 3-acetyldeoxynivalenol MeSH Browser
- Amides MeSH
- Appetite Depressants * MeSH
- deoxynivalenol MeSH Browser
- fusarenon-X MeSH Browser
- Glucagon-Like Peptide 1 MeSH
- nivalenol MeSH Browser
- Substance P MeSH
- trichothecene MeSH Browser
- Trichothecenes, Type B * MeSH
- Trichothecenes * MeSH
Type B trichothecenes commonly contaminate cereal grains and include five structurally related congeners: deoxynivalenol (DON), 3-acetyldeoxynivalenol (3-ADON), 15-acetyldeoxynivalenol (15-ADON), fusarenon X (FX), and nivalenol (NIV). These toxins are known to have negative effects on human and animal health, particularly affecting food intake. However, the pathophysiological basis for anorexic effect is not fully clarified. The purpose of this study is to explore the potential roles of the brain-gut peptides substance P (SP) and glucagon-like peptide-17-36 amide (GLP-1) in anorexic responses induced by type B trichothecenes following both intraperitoneal (IP) and oral administration. SP and GLP-1 were elevated at 1 or 2 h and returned to basal levels at 6 h following exposure to DON and both ADONs. FX induced the production of both brain gut peptides with initial time at 1 or 2 h and duration > 6 h. Similar to FX, exposing IP to NIV caused elevations of SP and GLP-1 at 1 h and lasted more than 6 h, whereas oral exposure to NIV only increased both brain gut peptides at 2 h. The neurokinin-1 receptor (NK-1R) antagonist Emend® dose-dependently attenuated both SP- and DON-induced anorexic responses. Pretreatment with the GLP-1 receptor (GLP-1R) antagonist Exending9-39 induced a dose-dependent attenuation of both GLP-1- and DON-induced anorexic responses. To summarize, the results suggest that both SP and GLP-1 play important roles in anorexia induction by type B trichothecenes.
College of Life Science Yangtze University Jingzhou 434025 China
School of Food and Biological Engineering Hefei University of Technology Hefei 230009 China
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