Are the damaging effects induced by the imazethapyr formulation Pivot® H in Boana pulchella (Anura) reversible upon ceasing exposure?

• Published in: Ecotoxicology and environmental safety Vol. 148; pp. 1 - 10
• Main Authors: Pérez-Iglesias, Juan Manuel, Natale, Guillermo S., Soloneski, Sonia, Larramendy, Marcelo L.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01.02.2018
• Subjects: Animals; Anura; Blood Cells - drug effects; Comet Assay; DNA Breaks, Single-Stranded; Environmental Exposure - analysis; Herbicides - toxicity; Imazethapyr; Larva - drug effects; Larva - growth & development; Micronuclei; Morphological abnormalities; Mutagenicity Tests; Nicotinic Acids - toxicity; Pivot® H; Recovery capabilities; Time Factors; Toxicity Tests, Acute; Recovery capabilities; Imazethapyr; Micronuclei; Comet assay; Pivot® H; Morphological abnormalities; Pivot(®) H
• ISSN: 0147-6513; 1090-2414
• DOI: 10.1016/j.ecoenv.2017.10.009

In the present study, the damage recovery capabilities of Boana pulchella tadpoles after acute exposure (96h) to 0.39mg/L concentration of the imazethapyr (IMZT)-based herbicide formulation Pivot® H (25% IMZT LC50 value) were assessed during a period of 7 to −21 days. To appraise the recovery capabilities, frequency of micronuclei (MNs), other nuclear abnormalities and DNA single-strand breaks evaluated by single cell gel electrophoresis assay on circulating blood cells were employed as endpoints for genotoxicity. Growth, development, body mass, and morphological abnormalities were also employed as individual endpoints in the recovery assay. Results demonstrated that IMZT induced sublethal effects at both the individual (i.e., loss of keratodonts) and cytogenetic levels (e.g., increase of MN frequency, other nuclear abnormalities and DNA single-strand breaks). At 11 days of the exposure phase, tadpoles recovered their basal levels of frequency of MNs, other nuclear abnormalities, and comets. However, loss of keratodonts, observed at the end of the exposure period, was present up to 21 days thereafter. Finally, axial abnormalities and delay in development stage were observed only during the postexposure phase in IMZT-exposed tadpoles at 18 and 25 days, respectively and were observed until the end of the experiment. This is the first evidence of use the comet assay as cytogenetic biomarker of genotoxicity in evaluating the recovery capabilities of amphibians in general and also those of B. pulchella after exposure to IMZT. •Recovery of imazethapyr-induced damage in Boana pulchella tadpoles were evaluated.•Recovery capabilities were assessed during a period of 7–21 days.•Cytogenetic damage reversed after 7 days of the exposure phase.•Development and morphological abnormalities were not reversed during the experiment.•First use of comet assay for evaluating recovery capabilities in amphibians.