Crude extract of cyanobacteria (Radiocystis fernandoi, strain R28) induces liver impairments in fish.

Radiocystis fernandoi R28 strain is a cyanobacterium which produces mostly the RR and YR microcystin variants (MC-RR and MC-YR, respectively). The effects of crude extract of the R. fernandoi strain R28 were evaluated on the protein phosphatases and on the structure and ultrastructure of the liver of the Neotropical fish, Hoplias malabaricus, after acute and subchronic exposure. Concomitantly, the accumulation of the majority of MCs was determined in the liver and muscle. The fish were exposed to 120.60 MC-RR+MC-LR kg-fish-1 (=100µg MC-LReq kg-fish-1) for 12 and 96h (one single dose, acute exposure) and 30days (one similar dose every 72h, subchronic exposure). MCs did not accumulate in the muscle but, in the liver, MC-YR accumulated after acute exposure and MC-RR and MC-YR accumulation occurred after subchronic exposure. Protein phosphatase 2A (PP2A) activity was inhibited only after subchronic exposure. Acute exposure induced liver hyperemia, hemorrhage, changes in hepatocytes and cord-like disorganization. At the ultrastructural level, the decreasing of glycogen and lipid levels, the swelling of mitochondria and whirling of endoplasmic reticulum suggested hepatocyte necrosis. Subchronic exposure resulted in a complete disarrangement of cord-like hepatocytes, some recovery of mitochondria and whirling endoplasmic reticulum and extensive connective tissues containing fibrous materials in the liver parenchyma. Despite microcystin toxicity and liver alterations, no tumor was induced by MCs. In conclusion, the increased algal mass of R. fernandoi in tropical freshwater, producing mainly MC-RR and MC-YR variants, results in fish liver impairments.

Subchronic exposure to atrazine induces biochemical and histopathological changes in the gills of a Neotropical freshwater fish, Prochilodus lineatus.

The impact of acute (48 h) and subchronic (14 days) exposures to environmentally realistic atrazine concentrations (2, 10 and 25 µg L(-1)) were evaluated on the gills of Prochilodus lineatus by assessing the activity of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx) and glutathione-S-transferase (GST), the levels of reduced glutathione (GSH) and lipid peroxide (LPO) as well as the histopathological damage. Acute and subchronic exposure to atrazine at 2 or 25 µg L(-1) did not change the activities of GST, SOD, CAT or GPx or the concentrations of GSH and LPO; however, subchronic exposure to 10 µg L(-1) increased the activity of GST, SOD and CAT and the LPO level. Histopathological indexes indicated normal gill function with scattered epithelial changes after acute and chronic exposure to 2 or 10 µg L(-1) of atrazine; however, fish chronically exposed to 25 µg L(-1) of atrazine, although had scattered lesions, the severity of lesions resulted in slightly to moderately gill damage. Acute exposure to atrazine decreased the type 3 MCs (containing acid mucosubstances with sulfate esters) in fish exposed to 2 or 10 µg L(-1) and increased the type 4 MCs (containing all types of mucosubstances) in fish exposed to 25 µg L(-1). Chronic exposure to atrazine reduced the type 3 MCs in fish exposed to 10 or 25 µg L(-1). The gills showed a low sensitivity to atrazine after acute exposure. However, the persistence of atrazine in water (subchronic exposure) promoted an increase of LPO levels in the gills and increased the frequency and severity of histopathological changes. The decreased density of type 3 MCs in fish exposed to atrazine suggests a mechanism to wash toxic substances away from the gill surface.