Toxicity and differential oxidative stress effects on zebrafish larvae following exposure to toxins from the okadaic acid group.

Okadaic acid-group (OA-group) is a set of lipophilic toxins produced only in seawater by species of the Dinophysis and Prorocentrum genera, and characterized globally by being associated with harmful algal blooms (HABs). The diarrhetic shellfish poisoning toxins okadaic acid (OA) and dinophysistoxin-1 (DTX-1) are the most prevalent toxic analogues making up the OA-group, which jeopardize environmental safety and human health through consumption of hydrobiological organisms contaminated with these toxins that produce diarrhetic shellfish poisoning (DSP) syndrome in humans. Consequently, a regulatory limit of 160 µg of OA-group/kg was established for marine resources (bivalves). The aim of this study was to investigate effects varying concentrations of 1-15 µg/ml OA or DTX-1 on toxicity, development, and oxidative damage in zebrafish larvae (Danio rerio). After determining the lethal concentration 50 (LC50) in zebrafish larvae of 10 and 7 µg/ml (24 h) and effective concentration 50 (EC50) of 8 and 6 µg/ml (24 h), different concentrations (5, 6.5, or 8 µg/ml of OA and 4, 4.5, or 6 µg/ml of DTX-1) were used to examine the effects of these toxins on oxidative damage to larvae at different time points between 24 and 120 hpf. Macroscopic evaluation during the exposure period showed alterations in zebrafish including pericardial edema, cyclopia, shortening in the anteroposterior axis, and developmental delay. The activity levels of biochemical biomarkers superoxide dismutase (SOD) and catalase (CAT) demonstrated a concentration-dependent decrease while glutathione peroxidase (GPx) and glutathione reductase (GR) were markedly elevated. In addition, increased levels of oxidative damage (malondialdehyde and carbonyl content) were detected following toxin exposure. Data demonstrate that high concentrations of OA and DTX-1produced pathological damage in the early stages of development <48 h post-fertilization (hpf) associated with oxidative damage.

Toxins of Okadaic Acid-Group Increase Malignant Properties in Cells of Colon Cancer.

Diarrhetic shellfish poisoning (DSP) is a syndrome caused by the intake of shellfish contaminated with a group of lipophilic and thermostable toxins, which consists of okadaic acid (OA), dinophysistoxin-1 (DTX-1) and dinophysistoxin-2 (DTX-2). These toxins are potent protein Ser/Thr phosphatase inhibitors, mainly type 1 protein phosphatase (PP1) and type 2A protein phosphatase (PP2A). Different effects have been reported at the cellular, molecular and genetic levels. In this study, changes in cell survival and cell mobility induced by OA, DTX-1 and DTX-2 were determined in epithelial cell lines of the colon and colon cancer. The cell viability results showed that tumoral cell lines were more resistant to toxins than the nontumoral cell line. The results of the functional assays for testing cell migration, evaluation of cell death and the expression of proteins associated with cell adhesion showed a dual effect of toxins since in the nontumoral cell line, a greater induction of cell death, presumably by anoikis, was detected. In the tumoral cell lines, there was an induction of a more aggressive phenotype characterized by increased resistance to toxins, increased migration and increased FAK activation. In tumoral cell lines of colon cancer, OA, DTX-1/DTX-2 induce a more aggressive phenotype.

Inter-species variability of okadaic acid group toxicity in relation to the content of fatty acids detected in different marine vectors.

Okadaic acid group (OA-group) is a set of lipophilic toxins which are characterised by being produced by species associated with the genera Dinophysis and Prorocentrum. OA-group has been regularly detected in endemic shellfish species from the southern zone of Chile only through the mouse bioassay. The purpose of this work was to determine the variability of OA-group toxins in endemic aquatic organisms (bivalves, crabs, gastropods and fish) and to establish the relationship with the concentration of fatty acids (FAs) detected in the evaluated species. The toxicity of OA-group and the FA profiles were determined using LC-MS/MS and gas chromatography with flame-ionisation detection, respectively. In the study area, the dinoflagellate Dinophysis acuta was detected in densities ≈2000 cells ml-1 with a toxicity ≈18.3 pg OA equiv cel-1. The analysis identified OA and dinophysistoxin-1 in shellfish in a range of ≈90 to ≈225 µg OA eq kg-1, where no toxins in fish were detected. A positive relationship between the FA level and the concentration of OA-group toxins in the digestive glands of bivalves and gastropods was established, noted for high levels of saturated FAs (C14:0 and C16:0). The toxic variability of OA-group toxins determined in the different species allowed us to establish that the consumption of these vectors, regulated by non-analytical methods, can be harmful when consumed by humans, thus suggesting that the sanitary regulations for the control of OA-group in Chile should be updated.

Morphology and phylogeny of Prorocentrum caipirignum sp. nov. (Dinophyceae), a new tropical toxic benthic dinoflagellate.

A new species of toxic benthic dinoflagellate is described based on laboratory cultures isolated from two locations from Brazil, Rio de Janeiro and Bahia. The morphology was studied with SEM and LM. Cells are elliptical in right thecal view and flat. They are 37-44µm long and 29-36µm wide. The right thecal plate has a V shaped indentation where six platelets can be identified. The thecal surface of both thecal plates is smooth and has round or kidney shaped and uniformly distributed pores except in the central area of the cell, and a line of marginal pores. Some cells present an elongated depression on the central area of the apical part of the right thecal plate. Prorocentrum caipirignum is similar to Prorocentrum lima in its morphology, but can be differentiated by the general cell shape, being elliptical while P. lima is ovoid. In the phylogenetic trees based on ITS and LSU rDNA sequences, the P. caipirignum clade appears close to the clades of P. lima and Prorocentrum hoffmannianum. The Brazilian strains of P. caipirignum formed a clade with strains from Cuba, Hainan Island and Malaysia and it is therefore likely that this new species has a broad tropical distribution. Prorocentrum caipirignum is a toxic species that produces okadaic acid and the fast acting toxin prorocentrolide.

Embryotoxic effects of dissolved okadaic acid on the development of Longfin yellowtail Seriola rivoliana.

In the context of global climate change where harmful algal blooms (HABs) might become more frequent and more severe, several studies have been conducted on the perturbation of embryonic development of marine animals by microalgal toxins. Okadaic acid (OA) and analogs (DSP toxins) produced by dinoflagellates of the genera Dynophysis and Prorocentrum are known to disturb embryogenesis. This study investigated the impact of dissolved DSP toxin (OA and Dinophysistoxin 1, DTX-1) exposure on embryo development of Longfin yellowtail Seriola rivoliana. Eggs were exposed to different concentrations of dissolved DSP toxins (low treatment: at 120µgl-1 OA eq; high treatment 175µgl-1 OA eq.). The first objective was to study the global toxic effect of DSP toxins with hatching percentages. Secondly, the effect of these toxins was investigated at molecular and functional level by measuring expression of responsible genes for bone morphogenetic protein (BMP) and proliferating cell nuclear antigen (PCNA) measuring phosphatase enzyme (serine/threonine and alkaline phosphatases) activities. Our results showed drastic mortalities induced by DSP toxins in both low and high concentration treatments. Activities of both protein and alkaline phosphatases were significantly inhibited by DSP toxin treatments, whose effects on gene expression were less evident, but levels of BMP expression in eggs treated with the lowest toxin concentration were significantly different from that in the control treatment. This work revealed an embryotoxic effect of DSP toxins resulting in high mortality of eggs. Phosphatase inhibition could have participated in part in these global effects by perturbing the regulation of pathways related to embryogenesis and resulting in a perturbation of gene expression.

Lipophilic toxins in cultivated mussels (Mytilus galloprovincialis) from Baja California, Mexico.

Here, we report different lipophilic toxins (LTs) detected by LC-MS/MS in Mediterranean mussels (Mytilus galloprovincialis) collected through 2012 in Todos Santos Bay, northwest Baja California, Mexico. The concentration of okadaic acid (OA), dinophysistoxin 2 (DTX2), and pectenotoxin 2 (PTX2) reached 500 µg kg(-1) during July and increased to 1647 µg kg(-1) in October. These toxins were associated with the presence of Dinophysis fortii and Dinophysis acuminata and a strong stratification of the water column. Other LTs present were yessotoxins, with a maximum concentration of 1080 µg kg(-1) in June. Cyclic imines (13-desmethyl spirolide and gymnodimine) and azaspiracid 1 were also detected in the mussels but at low concentrations. Diarrhetic toxins concentrations evaluated by LC-MS/MS were compared with the results of two mouse bioassay protocols. Positive results were obtained with both MBA protocols in several samples that presented toxicities below 160 µg OA-eq kg(-1), as estimated by LC-MS/MS results whereas other samples returned negative MBA results in samples with concentrations above this level. Therefore, analytical methods need to be applied to confirm the presence of regulated LTs. This is the first report of LTs in mussels cultivated in Mexico. The occurrence of these toxins represents an emerging problem in the region.

Pretreatment with memantine prevents Alzheimer-like alterations induced by intrahippocampal okadaic acid administration in rats.

Cerebral okadaic acid (OA) administration induces Alzheimer's disease (AD)-like phenotype in rats. Alterations in glutamate levels associated with hyperactivation of cyclin dependent kinase 5 (Cdk5) signaling pathway downstream Tau phosphorylation may participate in the genesis of this pathological phenotype. Here, we examined the efficacy of memantine (MN) pretreatment on reducing OA-induced AD-like phenotypes in rats. Wistar rats were given daily intraperitoneal injections of MN for 3 days and then given an intrahippocampal infusion of OA. Animals were divided into four groups: control (CO), MN, OA and MN/OA. Spontaneous locomotion and spatial memory performance were assessed by open field and Morris water maze respectively. Additionally, we measured glutamate levels in the cerebrospinal fluid (CSF) and the immunocontent of Cdk5, p35, p25 and phosphorylated Tau (pTauSer199/202) in the hippocampus. Spontaneous locomotion did not differ between groups. The OA group showed a significant decrease in spatial memory performance compared to all groups. The OA infusion also increased CSF glutamate levels and the immunocontents of Cdk5, p25 and pTauSer199/202 in the hippocampus. Conversely, pretreatment with MN prevented OA-induced spatial memory deficits and the increment of CSF glutamate level; which paralleled with normal immunocontents of Cdk5, p25 and pTau- Ser199/202 proteins. There were positive correlations between spatial memory performance and the neurochemical parameters. In summary, pretreatment with MN prevents spatial memory deficits induced by intrahippocampal OA administration in rats. The prevention of increase CSF glutamate levels, along with the reduced hippocampal phosphorylation of TauSer199/202 by Cdk5/p25 signaling pathway, are the mechanisms proposed to participate in the prophylactic effects of MN in this AD-like model.

First evidence of Okadaic acid acyl-derivative and Dinophysistoxin-3 in mussel samples collected in Chiloe Island, Southern Chile.

This paper shows the detection of Diarrhetic Shellfish Poison (DSP) phycotoxins, using HPLC-FLD with pre-column derivatization procedure and HPLC-MS methods, in the analysis of shellfish extracts tested positive with the official DSP mouse bioassay. The shellfish samples were collected in Chiloe Island, Southern of Chile. The amount of Dinophysistoxin-3 (DTX-3) measured in the shellfish extracts were in average above the international safe limits for DSP content in the shellfish extracts analyzed. As internal control of detection and recovery, DTX-1 analytical standard was spiked into dichloromethane-clean shellfish extracts in order to calculate de extraction recovery of DTX-1. The average recovery was 97%. From all DSP toxins analyzed, the hydrolyzed extract samples appeared mainly DTX-3 in concentrations ranging from 99.40 +/- 1.22 to 257.73 +/- 12.46 ng/g digestive-glands. The acyl-Okadaic Acid (acyl-OA) was also detected in some samples, ranging from 1.02 +/- 1.4 to 3.07. +/- 1.6 ng of DSP toxin/g digestive-glands. This is the first report of acyl-OA ever found in Chilean shellfish samples. This data shows that shellfish samples were contaminated with a complex DSP toxins profile, in which DTX-3 is the major DSP toxin component, followed by DTX-1 and the acyl-OA as the minor one. The important findings showed in this study are the presence of both acyl-derivates (DTX-3 and Acyl-OA) which are the product of a main metabolic biotransformation that occurred inside the shellfish, in order to chelate DTX-1 and OA, transforming them into DTX-3 and the acyl-OA respectively. This metabolic biotransformation must be performed to avoid self-inhibition of their Protein Phosphatase 2A done by DTX-1 and OA, since both acyl-derivates (DTX-3 and acyl-OA) do not inhibit Protein Phosphatase 2A. This complex DSP toxins profile and the permanent presence of both acyl-derivates (DTX-3 and Acyl-OA) could explain the permanent diarrhea symptoms that experience patients who have ingested cooked shellfish in the southern of Chile. This diarrhea is not associated to Vibrio parahaemolyticus or other enteropathogens as had been suggested before. The massive shellfish consumption is an important Chilean cultural habit and now has become a major health issue in the southern of Chile.

Rod photoreceptor cell death is induced by okadaic acid through activation of PKC and L-type voltage-dependent Ca2+ channels and prevented by IGF-1.

Retinal dystrophies involve extensive photoreceptor apoptosis. Neuroprotective effects of insulin-like growth factor (IGF)-1 have been demonstrated in various tissues, including the retina. The aim of this study was to investigate: (i) the action of IGF-1 upon selective photoreceptor death induced by okadaic acid (OA); and (ii) signaling pathways related to both OA-induced cell death and IGF-1 neuroprotective effect. Retinal explants were incubated with 5nM OA, a protein phosphatase type 1 and type 2A inhibitor, which induces cell death detected by the identification of pyknotic morphology of photoreceptors immunostained for rhodopsin. OA increased both the number of pyknotic Rho 4D2(+) profiles, and Ca(2+) influx, measured through the incorporation of (45)CaCl(2), in a dose- and time-dependent way, while treatment with 10ng/mL IGF-1 abrogated both effects. Treatment with phorbol 12-myristate 13-acetate (PMA), an activator of protein kinase C, modulated OA effects, indicating the involvement of PKC. Furthermore, either 10microM chelerythrine chloride, an inhibitor of PKC, or 10microM nifedipine, a L-voltage-sensitive Ca(2+) channel blocker, inhibited both Ca(2+) influx and cell death induced by OA. The data show that okadaic acid induces rod photoreceptor cell death in retinal tissue through activation of PKC and ensuing Ca(2+) influx through L-type Ca(2+) channels, which is counteracted by a neuroprotective effect of IGF-1.

Primeira detecção de ácido ocadáico em ostras (Crassostrea rhizophorae), coletadas no canal de Santa Cruz, Itapissuma, Pernambuco / First detention of acid ocadaico in oysters (Crassostrea rhizophorae), collected in the Santa Cruz, Itapissuma, Pernambuco

O ácido ocadáico (AO) é uma importante toxina, produzida por dinoflagelados, capaz de causar no homem o envenenamento diarréico por moluscos conhecido como Diarrhetic Shellfish Poisoning (DSP). Embora uma toxina fatal, esta ficotoxina está envolvida na inibição de certas proteínas e no aparecimento de neoplasias, que o torna uma toxina perigosa. Desta forma, considerando o risco do consumo de moluscos bivalves e a escassez de pesquisas para sua detecção e quantificação no Estado de Pernambuco, foram analisados extratos preparados a partir do hepatopâncreas de ostras (Crassostrea rhizophorae) coletadas no Canal de Santa Cruz localizado no Município de Itapissuma – PE, em quatro pontos distintos.O ácido ocadáico foi analisado através da Cromatografia Líquida de Alta Eficiência com Detecção Fluorimétrica. (...) Embora as concentrações do AO encontradas tenham sido baixas, estando as ostras aptas ao consumo humano segundo limites adotados (2000ng AO.g-1 hepatopâncreas de moluscos) por vários países, há uma tendência internacional de exigir a total ausência de toxinas diarréicas devido ao seu potencial efeito carcinogênico para consumidores regulares de moluscos. A presença inédita do AO no Canal de Santa Cruz é um alerta às autoridades sanitárias para que mais pesquisas sejam realizadas na região e em outras localizadas do Estado.

Primeira detecção de ácido ocadáico em ostras (Crassostrea rhizophorae), coletadas no canal de Santa Cruz, Itapissuma, Pernambuco / First detention of acid ocadaico in oysters (Crassostrea rhizophorae), collected in the Santa Cruz, Itapissuma, Pernambuco

O ácido ocadáico (AO) é uma importante toxina, produzida por dinoflagelados, capaz de causar no homem o envenenamento diarréico por moluscos conhecido como Diarrhetic Shellfish Poisoning (DSP). Embora uma toxina fatal, esta ficotoxina está envolvida na inibição de certas proteínas e no aparecimento de neoplasias, que o torna uma toxina perigosa. Desta forma, considerando o risco do consumo de moluscos bivalves e a escassez de pesquisas para sua detecção e quantificação no Estado de Pernambuco, foram analisados extratos preparados a partir do hepatopâncreas de ostras (Crassostrea rhizophorae) coletadas no Canal de Santa Cruz localizado no Município de Itapissuma PE, em quatro pontos distintos.O ácido ocadáico foi analisado através da Cromatografia Líquida de Alta Eficiência com Detecção Fluorimétrica. Foram analisadas 20amostras de extratos de hepatopâncreas, tendo sido detectada a presença da toxina em todos os locaisde coleta. A concentração da toxinavariou de 6,15 a 24,31ngAO.g-1 dehepatopâncreas. Embora as concentrações do AO encontradas tenham sido baixas, estando as ostras aptas ao consumo humano segundo limites adotados (2000ng AO.g-1 hepatopâncreas de moluscos) por vários países, há uma tendência internacional de exigir a total ausência de toxinas diarréicas devido ao seu potencial efeito carcinogênico para consumidores regulares de moluscos. A presença inédita do AO no Canal de Santa Cruz é um alerta às autoridades sanitárias para que mais pesquisas sejam realizadas na região e em outras localizadas do Estado.(AU)

The okadaic acid (AO) is an important toxin produced by dinoflagelattes, which can cause diarrhetic poisoning onthe human by mollusks, named Diarrhetic Shellfish Poisoning (DSP). Although okadaic acid is not considered a fatal toxin, it is involved in the inhibition of certain proteins and the appearance of neoplasias (tumours), which make it a dangerous toxin. For this reason, considering the risk of consumption of bivalve mollusks and the lack of research on this toxin's detection and quantification in the State of Pernambuco, prepared extracts from oyster hepatopancreas(Crassostrea rhizophorae) were collected in the Santa Cruz Canal, found in the municipality of Itapissuma - PE, in our different collection points. The okadaic acid was analysed using a High Efficiency Liquid Cromatograph with Florimetric Detection. Twenty samples of pancreas extracts were analyzed, and the presence of the toxin was detected in all points. The concentration of the toxin varied from 6.15 to 24.31ngAO.g-1 of pancreas. While the concentrations of ficotoxin okadaic acid found were low, being the oysters therefore permitted for human consumption according to the set limits adopted (2000ng AO.g-1 mollusk pancreas) by many countries, there is an international tendency to demand the complete absence of diarrhetic toxins due to their carcinogenic potential for regular consumers of mollusks. The first –time detection of okadaic acid in the Santa Cruz Canal is a warning for sanitation authorities indicating that more research should be carried out in that region and in other locations in the State. (AU)

Comparative study of Domoic Acid and Okadaic Acid induced-chromosomal abnormalities in the Caco-2 cell line.

Okadaic Acid (OA) the major diarrheic shellfish poisoning (DSP) toxin is known as a tumor promoter and seems likely implicated in the genesis of digestive cancer. Little is known regarding genotoxicity and carcinogenicity of Domoic Acid (DA), the major Amnesic Shellfish Poisoning (ASP) toxin. Both OA and DA occur in seafood and are of human health concerns. Micronuclei (MN) arise from abnormalities in nuclear division during mitosis due to a failure of the mitotic spindle or by complex chromosomal configurations that pose problems during anaphase. In order to evaluate the ability of okadaic acid (OA) and domoic acid (DA) to induce DNA damage we performed the micronucleus assay using the Caco-2 cell line. To discriminate between a clastogenic or aneugenic effect of OA and DA, the micronucleus assay was conducted by cytokinesis-block micronucleus assay using cytochalasin B with Giemsa staining and/or acridine orange staining, in parallel to fluorescence in situ hybridization (FISH) using a concentrated human pan-centromeric chromosome paint probe. Our results showed that OA and DA significantly increased the frequency of MN in Caco-2 cells. The MN caused by OA are found in mononucleated cells and binucleated cells, whereas those caused by DA are mainly in binucleated cells. The results of FISH analysis showed that OA induced centromere-positive micronuclei and DA increased the percentage of MN without a centromeric signal. In conclusion, both OA and DA bear mutagenic potential as revealed in Caco-2 cells by induction of MN formation. Moreover, OA induced whole chromosome loss suggesting a specific aneugenic potential, whereas DA seems simply clastogenic. At present, one cannot rule out possible DNA damage of intestinal cells if concentrations studied are reached in vivo, since this may happen with concentrations of toxins just below regulatory limits in case of frequent consumption of contaminated shell fishes.

Citotoxicidade do promotor de tumor e sua ação mitogênica sobre os linfócitos humanos / Cytotoxicity studies of okadaic acid on human lymphocytes and its mitogenic effect

Proteínas fosfatases são moléculas sinalizadoras que agem juntamente com as proteínas quinases para regular uma variedade de processos celulares fundamentais, bem como, crescimento celular, mitogênese, metabolismo, transcrição de gene, ciclo celular e resposta ao estresse e imune. O ácido okadáico é um potente e específico inibidor de proteína serina/treonina fosfatase (PP1 e PP2A). O objetivo deste estudo foi avaliar o efeito citotóxico do ácido okadáico na viabilidade de linfócitos humanos e sua ação mitogênica. Nos estudos de citotoxicidade avaliamos o efeito do ácido okadáico através dos seguintes parâmetros: redução do MTT (integridade mitocondrial), conteúdo total de proteínas (número de células) e atividade fosfatásica (metabolismo celular). O valor para redução do MTT e atividade fosfatase foram: 50nM e 100nM, respectivamente; não foi encontrado valor de IC50 para o conteúdo de proteína. A atividade fosfatásica não foi afetada pelo ácido okadáico (100nM) quando este composto foi adicionado no extrato celular. A proliferação de linfócitos foi estimulada em 25 porcento quando as células foram tratadas com o ácido okadáico durante o plaqueamento e na ausência da fitohemaglutinina (mitogêno). O estímulo máximo foi até 30 minutos. O ácido okadáico não foi citotóxico para os linfócitos. A ação mitogênica deste composto foi confirmada pelo conteúdo de proteína.

Relationship between phosphatase activity and cytotoxic effect of two protein phosphatase inhibitors, okadaic acid and pervanadate, on human myeloid leukemia cell line.

Protein phosphatases are signalling molecules that regulate a variety of fundamental cellular processes including cell growth, metabolism and apoptosis. The aim of this work was to correlate the cytotoxicity of pervanadate and okadaic acid on HL60 cells and their effect on the phosphatase obtained from these cells. The cytotoxicity of these protein phosphatase inhibitors was evaluated on HL60 cells using phosphatase activity, protein quantification and MTT reduction as indices. The major phosphatase presents in the cellular extract showed high activity (80%) and affinity (Km = 0.08 mM) to tyrosine phosphate in relation to p-nitrophenyl phosphate (pNPP)-(Km = 0.51 mM). Total phosphatase (pNPP) was inhibited in the presence of 10 mM vanadate (98%), 200 microM pervanadate (95%) and 100 microM p-chloromercuribenzoate (80%) but okadaic acid caused a slight increase in enzyme activity (25%). When the HL60 cells were treated with the phosphatase inhibitors (pervanadate and okadaic acid) for 24hours, only 20% residual activity was observed in presence of 200 microM pervanadate, whereas in the presence of okadaic acid this inhibitory effect was not observed. However, in respect to mitochondrial function, cell viability decreased about 80% in the presence of 100 nM okadaic acid. The total protein content was decreased 25% when the cells were treated with 100 nM okadaic acid in combination with 200 microM pervanadate. Our results suggest that both phosphatase inhibitors presented different mechanisms of action on HL60 cells. However, their effect on the cell redox status have to be considered.

Micronucleus induction in mussels exposed to okadaic acid.

Some toxins present in the marine environment are capable of inducing mutagenicity and/or carcinogenicity. Among these toxins, okadaic acid (OA) is gaining considerable interest since it induces DNA based modifications at low concentrations and accumulates in filter-feeding marine animals, including those used for human consumption. This study aims to evaluate the genotoxicity of OA in the haemocytes of the mussel Perna perna, using the micronucleus assay. Fifty-four mussels were separated into three groups of 18 animals. One group received 0.3 microg of OA diluted in 10 microl of ethanol and ultrapure water while the other groups were considered as controls and were exposed to a solvent plus seawater mixture. A significantly higher frequency of micronuclei was observed in haemocytes from the OA-exposed group. There were no statistical differences between the two control groups.