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1.
Sci Total Environ ; 728: 138759, 2020 Aug 01.
Artigo em Inglês | MEDLINE | ID: mdl-32403013

RESUMO

Bisphenol S (BPS) has been increasingly used as a substitute for bisphenol A (BPA), a known endocrine disruptor. Early-life exposure to BPA affects fetal development and the risk of obesity in adolescence and adulthood. However, the effects of fetal exposure BPS in later life are unknown. This study aimed to investigate the effects of prenatal BPS exposure on adiposity in adult F1 mice. Pregnant C57BL/6 N mice were exposed to BPS (0, 0.05, 0.5, 5, and 50 mg/kg/d) via drinking water from gestation day 9 until delivery. Thereafter, two groups of offspring (6 weeks old) were either administered a standard diet (STD) or a high-fat diet (HFD) for 4 weeks until euthanasia. The body weight and gonadal white adipose tissue (gWAT) mass were determined, and the energy expenditure for the adiposity phenotype was computed especially for male mice, followed by histological analysis of the gWAT. Thereafter, the expression levels of adipogenic marker genes (Pparg, Cebpa, Fabp4, Lpl, and Adipoq) were analyzed in the gWAT via reverse-transcription PCR analysis. BPS-exposed male mice displayed apparent gWAT hypertrophy, consistent with the significant increase in adipocyte size in the gWAT and upregulation of Pparg and its direct target genes among HFD mice in comparison with the control mice. These results suggest that prenatal BPS exposure potentially increases the susceptibility to HFD-induced adipogenesis in male adult mice.


Assuntos
Adipogenia , Efeitos Tardios da Exposição Pré-Natal , Animais , Compostos Benzidrílicos , Dieta Hiperlipídica , Feminino , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Fenóis , Gravidez , Sulfonas
2.
Biosci Biotechnol Biochem ; 67(6): 1292-8, 2003 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12843656

RESUMO

The hypolipidemic effect of an exo-biopolymer produced from a submerged mycelial culture of Hericium erinaceus was investigated in dietary-induced hyperlipidemic rats. Hypolipidemic effects were proportionally increased with the increasing concentration of the exo-biopolymer for oral administration. The exo-biopolymer, at the dose of 200 mg/kg body weight, substantially reduced the plasma total cholesterol (32.9%), LDL cholesterol (45.4%), triglyceride (34.3%), phospholipid (18.9%), atherogenic index (58.7%), and hepatic HMG-CoA reductase activity (20.2%). It increased the plasma HDL cholesterol level (31.1%) as compared to the control group. The molecular mass of this exo-biopolymer measured by HPLC was under 40 kDa. Total sugar and protein contents were 91.2 and 8.8%, respectively. The sugar and amino acid compositions of the exo-biopolymer were analyzed in detail.


Assuntos
Agaricales/química , Agaricales/crescimento & desenvolvimento , Biopolímeros/farmacologia , Hipolipemiantes/farmacologia , Aminoácidos/análise , Animais , Biopolímeros/administração & dosagem , Biopolímeros/química , Biopolímeros/isolamento & purificação , Carboidratos/análise , Relação Dose-Resposta a Droga , Hidroximetilglutaril-CoA Redutases/metabolismo , Hiperlipidemias/tratamento farmacológico , Hipolipemiantes/administração & dosagem , Hipolipemiantes/isolamento & purificação , Lipídeos/sangue , Masculino , Peso Molecular , Micélio , Ratos , Ratos Sprague-Dawley
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