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Serotonin involvement in okadaic acid-induced diarrhoea in vivo

The consumption of contaminated shellfish with okadaic acid (OA) group of toxins leads to diarrhoeic shellfish poisoning (DSP) characterized by a set of symptoms including nausea, vomiting and diarrhoea. These phycotoxins are Ser/Thr phosphatase inhibitors, which produce hyperphosphorylation in cell...

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Autores principales: Louzao, M. Carmen, Costas, Celia, Abal, Paula, Suzuki, Toshiyuki, Watanabe, Ryuichi, Vilariño, Natalia, Carrera, Cristina, Boente-Juncal, Andrea, Vale, Carmen, Vieytes, Mercedes R., Botana, Luis M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298366/
https://www.ncbi.nlm.nih.gov/pubmed/34148100
http://dx.doi.org/10.1007/s00204-021-03095-z
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author Louzao, M. Carmen
Costas, Celia
Abal, Paula
Suzuki, Toshiyuki
Watanabe, Ryuichi
Vilariño, Natalia
Carrera, Cristina
Boente-Juncal, Andrea
Vale, Carmen
Vieytes, Mercedes R.
Botana, Luis M.
author_facet Louzao, M. Carmen
Costas, Celia
Abal, Paula
Suzuki, Toshiyuki
Watanabe, Ryuichi
Vilariño, Natalia
Carrera, Cristina
Boente-Juncal, Andrea
Vale, Carmen
Vieytes, Mercedes R.
Botana, Luis M.
author_sort Louzao, M. Carmen
collection PubMed
description The consumption of contaminated shellfish with okadaic acid (OA) group of toxins leads to diarrhoeic shellfish poisoning (DSP) characterized by a set of symptoms including nausea, vomiting and diarrhoea. These phycotoxins are Ser/Thr phosphatase inhibitors, which produce hyperphosphorylation in cellular proteins. However, this inhibition does not fully explain the symptomatology reported and other targets could be relevant to the toxicity. Previous studies have indicated a feasible involvement of the nervous system. We performed a set of in vivo approaches to elucidate whether neuropeptide Y (NPY), Peptide YY (PYY) or serotonin (5-HT) was implicated in the early OA-induced diarrhoea. Fasted Swiss female mice were administered NPY, PYY(3–36) or cyproheptadine intraperitoneal prior to oral OA treatment (250 µg/kg). A non-significant delay in diarrhoea onset was observed for NPY (107 µg/kg) and PYY(3–36) (1 mg/kg) pre-treatment. On the contrary, the serotonin antagonist cyproheptadine was able to block (10 mg/kg) or delay (0.1 and 1 mg/kg) diarrhoea onset suggesting a role of 5-HT. This is the first report of the possible involvement of serotonin in OA-induced poisoning. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00204-021-03095-z.
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spelling pubmed-82983662021-08-12 Serotonin involvement in okadaic acid-induced diarrhoea in vivo Louzao, M. Carmen Costas, Celia Abal, Paula Suzuki, Toshiyuki Watanabe, Ryuichi Vilariño, Natalia Carrera, Cristina Boente-Juncal, Andrea Vale, Carmen Vieytes, Mercedes R. Botana, Luis M. Arch Toxicol Organ Toxicity and Mechanisms The consumption of contaminated shellfish with okadaic acid (OA) group of toxins leads to diarrhoeic shellfish poisoning (DSP) characterized by a set of symptoms including nausea, vomiting and diarrhoea. These phycotoxins are Ser/Thr phosphatase inhibitors, which produce hyperphosphorylation in cellular proteins. However, this inhibition does not fully explain the symptomatology reported and other targets could be relevant to the toxicity. Previous studies have indicated a feasible involvement of the nervous system. We performed a set of in vivo approaches to elucidate whether neuropeptide Y (NPY), Peptide YY (PYY) or serotonin (5-HT) was implicated in the early OA-induced diarrhoea. Fasted Swiss female mice were administered NPY, PYY(3–36) or cyproheptadine intraperitoneal prior to oral OA treatment (250 µg/kg). A non-significant delay in diarrhoea onset was observed for NPY (107 µg/kg) and PYY(3–36) (1 mg/kg) pre-treatment. On the contrary, the serotonin antagonist cyproheptadine was able to block (10 mg/kg) or delay (0.1 and 1 mg/kg) diarrhoea onset suggesting a role of 5-HT. This is the first report of the possible involvement of serotonin in OA-induced poisoning. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00204-021-03095-z. Springer Berlin Heidelberg 2021-06-20 2021 /pmc/articles/PMC8298366/ /pubmed/34148100 http://dx.doi.org/10.1007/s00204-021-03095-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Organ Toxicity and Mechanisms
Louzao, M. Carmen
Costas, Celia
Abal, Paula
Suzuki, Toshiyuki
Watanabe, Ryuichi
Vilariño, Natalia
Carrera, Cristina
Boente-Juncal, Andrea
Vale, Carmen
Vieytes, Mercedes R.
Botana, Luis M.
Serotonin involvement in okadaic acid-induced diarrhoea in vivo
title Serotonin involvement in okadaic acid-induced diarrhoea in vivo
title_full Serotonin involvement in okadaic acid-induced diarrhoea in vivo
title_fullStr Serotonin involvement in okadaic acid-induced diarrhoea in vivo
title_full_unstemmed Serotonin involvement in okadaic acid-induced diarrhoea in vivo
title_short Serotonin involvement in okadaic acid-induced diarrhoea in vivo
title_sort serotonin involvement in okadaic acid-induced diarrhoea in vivo
topic Organ Toxicity and Mechanisms
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298366/
https://www.ncbi.nlm.nih.gov/pubmed/34148100
http://dx.doi.org/10.1007/s00204-021-03095-z
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