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Bisphenol A-induced oxidative stress, hepatotoxicity and altered estrogen receptor expression in Labeo bata: impact on metabolic homeostasis and inflammatory response

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dc.contributor.author Mukherjee, Urmi
dc.contributor.author Samanta, Anwesha
dc.contributor.author Biswas, Subhasri
dc.contributor.author Das, Sriparna
dc.contributor.author Ghosh, Soumyajyoti
dc.contributor.author Mandal, Dipak Kumar
dc.contributor.author Maitra, Sudipta
dc.date.accessioned 2021-06-01T05:56:45Z
dc.date.available 2021-06-01T05:56:45Z
dc.date.issued 2020-06
dc.identifier.issn 0147-6513
dc.identifier.issn 0147-6513
dc.identifier.uri https://vbudspace.lsdiscovery.in/xmlui/handle/123456789/179
dc.description journal homepage: www.elsevier.com/locate/ecoenv DOI - https://doi.org/10.1016/j.ecoenv.2020.110944 en_US
dc.description.abstract Bisphenol 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 species en_US
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.relation.ispartofseries Volume;202
dc.relation.ispartofseries Article No.;110944
dc.relation.ispartofseries Page No.;1-10
dc.subject Bisphenol A Labeo bata Hyperlipidemia Liver ER Akt en_US
dc.title Bisphenol A-induced oxidative stress, hepatotoxicity and altered estrogen receptor expression in Labeo bata: impact on metabolic homeostasis and inflammatory response en_US
dc.title.alternative Ecotoxicology and Environmental Safety en_US
dc.type Article en_US


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