Antioxidative role of dietary ascorbic acid against arsenic induced haematological, biochemical and histomorphological alterations in Cyprinus carpio.

The current study investigated the antioxidant potential of ascorbic acid to counteract arsenic induced toxic response in Cyprinus carpio. The 96 h LC50 of 107.05 mg L-1 was recorded through acute toxicity test and 1/5th and 1/10th LC50 of arsenic were chosen as sublethal concentrations for assessing toxicity induced through arsenic exposure in fish for a period of 28 days. There were six experimental groups for sublethal toxicity testing viz. negative control (basal feed), positive control (basal feed + 1 g kg-1 diet ascorbic acid), 1/5th LC50 Arsenic, 1/10th LC50 Arsenic, 1/5th LC50 Arsenic with ascorbic acid supplement, 1/10th LC50 Arsenic with ascorbic acid supplement. Following exposure, blood indices, antioxidant enzyme activity and histomorphology of gills, liver and kidney were examined. The results showed decreased total erythrocyte count, haemoglobin, haematocrit and an increased total leukocyte count upon arsenic exposure in fish with an improvement observed in the blood indices in arsenic with ascorbic acid supplementation. The study also analysed the antioxidant enzyme activity of superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase and glutathione-S-transferase which was found to decline in response to arsenic exposure with an increase in their activity recorded in arsenic with ascorbic acid supplemented fish. Furthermore, uptake of arsenic was also found to decrease on ascorbic acid supplementation with improvement in the histoarchitecture of gills, liver and kidney of fish. Collectively, the findings of the present study suggest the effectiveness of ascorbic acid as an ameliorating agent against the deleterious effects of arsenic in fish.

Light microscopic studies to evaluate fish scales as non-invasive indicators of heavy metal-contaminated waters.

Heavy metal pollution in aquatic bodies is a matter of serious concern for aquatic fauna and human health. This study evaluated the effect of heavy metals on structural aberrations in fish scales of freshwater Indian major carp Labeo rohita. Scales from two size groups-lesser than and equal to 40 cm and greater than 40 cm-collected from three markets of Ludhiana district for a period of 6 months were assessed. The values of Pb, Zn and Cr in fish scales exceeded the permissible limits. Structural alterations such as distorted focus, damaged and eroded circuli, distorted pattern of circuli, damaged margins of scales, dispersed chromatophores, disorganised radii and damaged tubercles were observed on the dorsal surface of scales using light microscopy. It is postulated that heavy metals would be responsible for structural anomalies on scales as their accumulation was higher in larger fishes which have been exposed to metals for longer duration. These observations clearly suggest that fish scales are effective non-invasive indicator of water quality where fish have been reared and cultured.

Effect of sodium arsenite on reproductive organs of female Wistar rats.

The present study was performed to investigate the subchronic effect of sodium arsenite on female Wistar rats. Mature female rats were divided into 4 groups of 12 animals each. Group I received distilled water, whereas the other 3 groups received sodium arsenite at 10, 30, and 50 µg/L doses for 60 days through drinking water. Half of the animals from each group were dissected after 30 days and the remaining after 60 days. A disruption in estrous cycle was observed with prolonged diestrous and metestrous phases. A significant increase in ovarian surface epithelium and follicular atresia was observed in treated rats (p ≤ .05). A significant decrease (p ≤ .05) in the uterine myometrium was observed. A significant increase (p ≤ .05) in the levels of lipid peroxidation along with decrease in the activities of antioxidant enzymes was observed. The results revealed that subchronic exposure of sodium arsenite causes degenerative changes in reproductive organs and induces oxidative stress in female rats.