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Potential Endocrine Disruption of Cyanobacterial Toxins, Microcystins and Cylindrospermopsin: A Review

Authors :
Universidad de Sevilla. Departamento de Nutrición y Bromatología, Toxicología y Medicina Legal
Ministerio de Ciencia e Innovación (MICIN). España
Casas Rodríguez, Antonio
Cameán Fernández, Ana María
Jos Gallego, Ángeles Mencía
Universidad de Sevilla. Departamento de Nutrición y Bromatología, Toxicología y Medicina Legal
Ministerio de Ciencia e Innovación (MICIN). España
Casas Rodríguez, Antonio
Cameán Fernández, Ana María
Jos Gallego, Ángeles Mencía
Publication Year :
2022

Abstract

Microcystins (MCs) and cylindrospermopsin (CYN), although classified as hepatotoxins and cytotoxins, respectively, have been shown to also induce toxic effects in many other systems and organs. Among them, their potential endocrine disruption (ED) activity has been scarcely investigated. Considering the increasing relevance of ED on humans, mammals, and aquatic organisms, this work aimed to review the state-of-the-art regarding the toxic effects of MCs and CYN at this level. It has been evidenced that MCs have been more extensively investigated than CYN. Reported results are contradictory, with the presence or absence of effects, but experimental conditions also vary to a great extent. In general, both toxins have shown ED activity mediated by very different mechanisms, such as estrogenic responses via a binding estrogen receptor (ER), pathological changes in several organs and cells (testis, ovarian cells), and a decreased gonad-somatic index. Moreover, toxic effects mediated by reactive oxygen species (ROS), changes in transcriptional responses on several endocrine axes and steroidogenesis-related genes, and changes in hormone levels have also been reported. Further research is required in a risk assessment frame because official protocols for assessment of endocrine disrupters have not been used. Moreover, the use of advanced techniques would aid in deciphering cyanotoxins dose-response relationships in relation to their ED potential.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1367129035
Document Type :
Electronic Resource