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dc.contributor.authorMukherjee, Urmi-
dc.contributor.authorSamanta, Anwesha-
dc.contributor.authorBiswas, Subhasri-
dc.contributor.authorDas, Sriparna-
dc.contributor.authorGhosh, Soumyajyoti-
dc.contributor.authorMandal, Dipak Kumar-
dc.contributor.authorMaitra, Sudipta-
dc.date.accessioned2021-06-01T05:56:45Z-
dc.date.available2021-06-01T05:56:45Z-
dc.date.issued2020-06-
dc.identifier.issn0147-6513-
dc.identifier.issn0147-6513-
dc.identifier.urihttps://vbudspace.lsdiscovery.in/xmlui/handle/123456789/179-
dc.descriptionjournal homepage: www.elsevier.com/locate/ecoenv DOI - https://doi.org/10.1016/j.ecoenv.2020.110944en_US
dc.description.abstractBisphenol A (BPA), a weak estrogenic endocrine disruptor and a well-known plasticizer, has the potential to perturb diverse physiological functions; however, its impact on immune and metabolic function in aquatic vertebrates is relatively less understood. The present study aims to investigate the impact of BPA on hepato toxicity, metabolic and immune parameters vis-a-vis � estrogen receptor expression modulation in a freshwater teleost, Labeo bata (Cyprinidae, Cypriniformes). The 96-h median lethal concentration of BPA in L. bata has been determined as 4.79 mg/L. Our data demonstrate that congruent with induction of plasma vitellogenin (VTG), chronic exposure to sub-lethal BPA (2 and 4 μM/L) attenuates erythrocyte count, hemoglobin concentration, packed cell volume, mean corpuscular hemoglobin, but not leukocyte number. Further, a significant increase in MDA, concomitant with diminished catalase and heightened GST activity corroborates well with hepatic dystrophic changes, appearance of fatty liver (macrovesicular steatosis) and elevated serum lipids (triglyceride, cholesterol, LDL, VLDL) in BPA-treated groups. Interestingly, a differential regulation of estrogen receptor (ER) subtypes at transcript and protein level signifies negative influence of BPA on hepatic ERα/ERβ homeostasis in this species. While at a lower dose it promotes Akt phosphorylation (activation), BPA at the higher dose at tenuates ERK1/2 phosphorylation (activation), suggesting potential alteration in insulin sensitivity. Importantly, dose-dependent decrease in hepatic TNF-α, IL-1β, iNOS (NOS2) expression and nitric oxide (NO) level corre sponds well with progressive decline in p-NF-κB, p-p38 MAPK, albeit with differential sensitivity, in BPA-exposed groups. Collectively, BPA exposure has wide-spread negative influence on hematological, biochemical and he patic events in this speciesen_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofseriesVolume;202-
dc.relation.ispartofseriesArticle No.;110944-
dc.relation.ispartofseriesPage No.;1-10-
dc.subjectBisphenol A Labeo bata Hyperlipidemia Liver ER Akten_US
dc.titleBisphenol A-induced oxidative stress, hepatotoxicity and altered estrogen receptor expression in Labeo bata: impact on metabolic homeostasis and inflammatory responseen_US
dc.title.alternativeEcotoxicology and Environmental Safetyen_US
dc.typeArticleen_US
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