Dichotomy of bisphenol A-induced expression of peroxisome proliferator-activated receptors in hepatic and testicular tissues in mice
Autor: | Shikha Sharma, Sheikh Raisuddin, Haroon Habib, Shahzad Ahmad, Mohd Amir Afjal, Suhel Parvez |
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Rok vydání: | 2019 |
Předmět: |
Male
endocrine system medicine.medical_specialty Environmental Engineering Health Toxicology and Mutagenesis Peroxisome Proliferator-Activated Receptors 0208 environmental biotechnology Peroxisome proliferator-activated receptor 02 engineering and technology 010501 environmental sciences 01 natural sciences Mice chemistry.chemical_compound Phenols Internal medicine Testis medicine Animals Environmental Chemistry Endocrine system Benzhydryl Compounds Receptor 0105 earth and related environmental sciences chemistry.chemical_classification Messenger RNA urogenital system Cholesterol Public Health Environmental and Occupational Health General Medicine General Chemistry Pollution 020801 environmental engineering Endocrinology Liver chemistry Nuclear receptor Adipogenesis Toxicity hormones hormone substitutes and hormone antagonists |
Zdroj: | Chemosphere. 236:124264 |
ISSN: | 0045-6535 |
DOI: | 10.1016/j.chemosphere.2019.06.234 |
Popis: | Environmental and dietary exposure to bisphenol A (BPA) and its toxicological consequences are extensively reported. BPA has multiple cellular targets. One of the mechanisms of action of BPA involves interaction with and activation of nuclear receptors (NRs) including peroxisome proliferator activated-receptors (PPARs). PPARs regulate genes involved in adipogenesis, and metabolism of glucose, lipid and cholesterol. Study of tissue and dose specific PPAR expression may decipher the toxicity outcome of BPA exposure. We studied expression of three forms of PPARs in mouse liver and testes exposed to BPA for 14 days. mRNA and protein expression of all forms of PPAR increased linearly (monotonic) with the dose in the liver while non-monotonic but dose specific effects were observed in the testes showing a differential pattern of expression. However, histopathological study showed a dose-dependent pattern of changes in liver as well as testes demonstrating a monotonic effect. These findings imply that other PPAR-independent mechanisms may play a role in BPA-induced pathological changes. The present study warrants exploration of the role of PPARs in BPA-induced effects on male reproductive functions and offers an insight into the peculiar response of BPA at low subchronic levels which may be helpful in designing appropriate risk assessment framework. |
Databáze: | OpenAIRE |
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