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Gliomas represent the most common and lethal category of primary brain tumors. Bisphenol A (BPA), a widely recognized endocrine disruptor, has been implicated in the progression of cancer. Despite its established links to various cancers, the association between BPA and glioma progression remains to be clearly defined. This study aimed to shed light on the impact of BPA on glioma cell proliferation and overall tumor progression. Our results demonstrate that BPA significantly accelerates glioma cell proliferation in a time- and dose-dependent manner. Furthermore, BPA has been found to enhance the invasive and migratory capabilities of glioma cells, potentially promoting epithelial–mesenchymal transition (EMT) characteristics within these tumors. Employing bioinformatics approaches, we devised a risk assessment model to gauge the potential glioma hazards associated with BPA exposure. Our comprehensive analysis revealed that BPA not only facilitates glioma invasion and migration but also inhibits apoptotic processes. In summary, our study offers valuable insights into the mechanisms by which BPA may promote tumorigenesis in gliomas, contributing to the understanding of its broader implications in oncology. [ABSTRACT FROM AUTHOR]

Objective: Curcuma longa Rhizome (CLR), due to its potent antioxidant phytochemical constituents, was investigated for its effects on bisphenol A (BPA)-induced cardiovascular and renal damage. Materials and Methods: Sixty rats were randomly selected, and grouped as control, BPA (100 mg/kg), BPA and CLR 100 mg/kg, BPA and CLR 200 mg/kg, CLR 100 mg/kg, and CLR 200 mg/kg for 21 days. Oxidative stress indices, antioxidant status, blood pressure parameters, genotoxicity, and immunohistochemistry were determined. Results: Rats exposed to the toxic effects of BPA had heightened blood pressure, lowered frequency of micronucleated polychromatic erythrocytes, and decreased activities of antioxidant enzymes compared with rats treated with CLR. Moreover, administration of CLR significantly (p<0.05) lowered malondialdehyde content and reduced the serum myeloperoxidase activity. Immunohistochemical evaluation revealed significantly (p<0.05) increased expressions of cardiac troponin and Caspase 3 in the BPA group compared with the CLR-treated groups. Conclusion: C. longa ameliorated cardiotoxic and nephrotoxic actions of bisphenol-A via mitigation of oxidative stress, hypertension, and genotoxicity. [ABSTRACT FROM AUTHOR]

Bisphenol A (BPA), an important endocrine disrupting compound, has infiltrated human daily lives through electronic devices, food containers, and children's toys. Developing of novel BPA assay methods with high sensitivity holds tremendous importance in valuing the pollution state. Here, we constructed an ultrasensitive photoelectrochemical (PEC) aptasensor for BPA determination by regulating photoactivities of CdS/Ni-based metal–organic framework (CdS/Ni-MOF) with [Ru(bpy)2dppz]2+ sensitizer. CdS/Ni-MOF spheres exhibited excellent photocatalytic performance, serving as a potential sensing platform for the construction of target recognition process. [Ru(bpy)2dppz]2+ were embedded into DNA double-stranded structure, functioning as sensitizer for modulating the signal response of the developed PEC aptasensor. The proposed PEC sensor exhibited outstanding analytical performances, including a wide linear range (0.1 to 1000.0 nM), low detection limit (0.026 nM, at 3σ/m), excellent selectivity, and high stability. This work provides a perspective for the design of ideal photosensitive materials and signal amplification strategies and extends their application in environment analysis. [ABSTRACT FROM AUTHOR]

An electrochemiluminescence (ECL) sensor for determining bisphenol A (BPA) was prepared based on titanium dioxide (TiO2) and Co-MOF. TiO2 is a co-reaction promoter that amplifies the ECL signal in the Ru(bpy)32+-trinpropylamine (TPrA) system. When the electrode is modified with Co-MOF the ECL signal is significantly enhanced. This is because Co-MOF can not only be used as a co-reaction accelerator but also as a carrier to adsorb more luminescent substances. Possible mechanisms for amplifying the original signal through the synergistic action of the two substances are investigated. The ECL strength decreases with increasing concentrations of BPA, and the amount of BPA can be determined by the change in ECL signal strength (ΔI). Under optimal experimental conditions, the linear range of BPA was 2.0 × 10−10 to 2.0 × 10−5 M, with a determination limit of 6.7 × 10−11 M (3σ/m). The relative standard deviation (RSD) of the signal for ten consecutive measurements was 1.5%. The sensor can be used to detect BPA in bottled samples with recoveries of 96 to 105%. [ABSTRACT FROM AUTHOR]

The bodies of water across the world are being polluted by trace organic pollutants like Endocrine Disrupting Chemicals (EDC's). A well-known example of EDC's is Bisphenol A (BPA). Therefore, it is a pressing requirement of the current times to find a viable technique for effectively removing these type of pollutants from water. With that intention, a composite material was fabricated using an activated biochar made from rice straw (ARSB) and Titanium Dioxide (TiO2). The synthesized composite, ARSB-TiO2 was used for removing BPA by a combination of adsorption and photocatalytic degradation. From the Tauc plot analysis, it was observed that the band gap of the TiO2 decreased due to its combination with ARSB as the band gap of ARSB-TiO2 was 2.4 eV where as that of TiO2 was 3.36 eV and that of ARSB was 3.31 eV. This was attributed to the formation of a new energy state, formed due to the combination of TiO2 with ARSB during the hydrothermal reaction, resulting in the generation of a Ti-O-C bond. As a consequence, ARSB-TiO2 was able to be activated by visible radiation (2-2.75 eV). A set of batch studies were conducted to evaluate the experimental conditions under which the optimal removal of BPA could be attained. From there the highest removal of BPA was found to be 95.73 % which was obtained at BPA concentration of 10 mg/L, ARSB-TiO2 dosage of 2 g/L, pH 2 and temperature 303 K. Further optimization of the process operation was done with the optimization tools Response Surface Methodology (RSM) and Artificial Neural Network (ANN). From the RSM study, the highest removal of BPA was found to be 99.91 % which was attained under the experimental conditions of pH 1.95, ARSB-TiO2 dosage of 2 g/L and contact time of 60 min. In case of ANN, the Levenberg-Marquardt back propagation algorithm was found to be the most suitable function for the optimization process. A radical quenching study was performed and from there it was observed that superoxide anion radical (·O2-) exhibited the highest effectivity for degrading BPA, followed by holes (H+) and hydroxyl radical (·OH). Lastly, a detailed comparative study was performed to compare the findings of the present study with that of the previously reported literatures. [ABSTRACT FROM AUTHOR]

Introduction: Bisphenol A (BPA) is an environmental contaminant with a global use as a plasticizer. Daily BPA exposure begins early prenatally and continues throughout a person's life without exact limit or safety raising alarms concerning overall health. Objective: To explore potential cardiotoxicity of orally administered BPA in adult rat, and to assess the outcome of recovery period following BPA stoppage. Materials and Methods: Forty-eight adult male albino rats were allocated into four groups (12 each); control negative, control positive, BPA-treated and recovered. For eight weeks, rats in the 3rd group received daily BPA (50 mg/kg body weight, via oral gavage). In the recovery group, animals obtained BPA, for the same dose and duration similar to that in the 3rd group, then left to convalesce without BPA administration for 4 weeks. At the experimental end, blood was collected to estimate serum Creatine kinase-MB(CK-MB) level and heart specimens were handled for histology, immunohistochemistry, and quantitative morphometry study. Results: BPA persuaded several histological, immunohistochemical and biochemical alterations manifested as cardiac fiber disruption, vascular congestion, hemorrhage, RBCs extravasation, inflammatory cell infiltration and fibrosis. Cardiomyocytes displayed dark acidophilic sarcoplasm, pyknosis and perinuclear vacuolation. Also, the mean area % for collagen fiber deposition, glycogen content, Bcl-2-associated X protein, Nuclear factor kappa B (NF-κB) and Vimentin immune-expressions were significantly high. Furthermore, mast cell number/mm2, MDA and CK-MB levels were enhanced meanwhile SOD, GSH and CAT levels were declined. After 4-week recovery, cardiomyocytes and vascular changes exhibited marked improvement and all previous metrics were directed toward normal values, though most of them were still demonstrating low significant differences contrasted to controls. Conclusion: BPA induced cardiac structural and functional alterations via ROS generation, apoptosis, inflammation and fibrosis with considerable self-recovery following BPA cessation denoting transitory adverse impact. However, the particular mechanisms underlying cardiotoxicity or recovery still require further study. [ABSTRACT FROM AUTHOR]

Bisphenol A (BPA) is an endocrine-disrupting compound and a mutagenic agent that poses health hazards to living organisms, making it a global contaminant. Several remediation techniques have been reported in the literature, however, a mixed-method science mapping analysis of research trends on BPA is still lacking. The present study aimed to investigate global research trends in BPA remediation. Published research papers on BPA remediation indexed in Web of Science, PubMed, and Scopus between 1992 and 2021 were analysed qualitatively and quantitatively using science mapping algorithms including Rstudio, bibliometrix package and R Version 4.2.1. The thematic areas were determined using k-means clustering of the author-keywords while Porter's stemming algorithm was used to stemmed inflectional terms to their roots. Overall, 640 documents were published by 1903 authors with 2.07 authors/article and 0.336 article/author, 4.31 co-authors/article, an annual growth rate of 17.35% and a collaboration index of 2.99. Research productivity increased from 1 article in 1992 to 93 articles in 2021. The citations of the topmost 23 articles ranged from 365 to 109 and the total citation per year ranged from 45.6 to 27.3. China (n = 267, 41.7%), Japan (n = 53, 8.3%), USA (n = 33, 5.2%) and Korea (n = 28, 4.4%) were respectively the top four countries based on the total of published articles and overall citation. There were 48 relevant keywords dominated by Bisphenol A, adsorption, biodegradation, and peroximonosulphate. The present analysis identifies research accomplishment, focus and gaps on Bisphenol A remediation and offer the researchers the information needed to forecast future research priorities that can help policymakers and governments to internationalize collaborations and create research curricula that can remediate BPA on a global scale. [ABSTRACT FROM AUTHOR]

We investigated the effect of melatonin on bisphenol A (BPA)-induced oxidative stress damage in testicular tissue and Leydig cells. Mice were gavaged with 50 mg/kg BPA for 30 days, and concurrently, were injected with melatonin (10mg/kg and 20mg/kg). Leydig cells were treated with 10 µmol/L of BPA and melatonin. The morphology and organ index of the testis and epididymis were observed and calculated. The sperm viability and density were determined. The expressions of melatonin receptor 1A and luteinizing hormone receptor, and the levels of malonaldehyde, antioxidant enzymes, glutathione, steroid hormone synthases, aromatase, luteinizing hormone, testosterone, and estradiol were measured. TUNEL assay was utilized to detect testicular cell apoptosis. The administration of melatonin at 20mg/kg significantly improved the testicular index and epididymis index in mice treated with BPA. Additionally, melatonin promoted the development of seminiferous tubules in the testes. Furthermore, the treatment with 20 mg/kg melatonin significantly increased sperm viability and spermdensity in mice, while also promoting the expressions of melatonin receptor 1A and luteinizing hormone receptor in Leydig cells of BPA-treated mice. Significantly, melatonin reduced the level of malonaldehyde in testicular tissue and increased the expression of antioxidant enzymes (superoxide dismutase 1, superoxide dismutase 2, and catalase) as well as the content of glutathione. Moreover, melatonin also reduced the number of apoptotic Leydig cells and spermatogonia, aromatase expression, and estradiol level, while increasing the expression of steroid hormone synthases (steroidogenic acute regulatory protein, cytochrome P450 family 17a1, cytochrome P450 17α-hydroxylase/20-lyase, and, 17β-hydroxysteroid dehydrogenase) and the level of testosterone. Melatonin exhibited significant potential in alleviating testicular oxidative stress damage caused by BPA. These beneficial effects may be attributed to melatonin's ability to enhance the antioxidant capacity of testicular tissue, promote testosterone synthesis, and reduce testicular cell apoptosis. [ABSTRACT FROM AUTHOR]

Bisphenol A (BPA) is a common synthetic endocrine disruptor that can be utilized in the fabrication of materials such as polycarbonates and epoxy resins. Numerous studies have linked BPA to learning and memory problems, although the precise mechanism remains unknown. Gamma‐aminobutyric acid (GABA) is the most abundant inhibitory neurotransmitter in the vertebrate central nervous system, and it is intimately related to learning and memory. This study aims to evaluate whether altered cognitive behavior involves the GABA signaling pathway in male offspring of rats exposed to BPA during the prenatal and early postnatal periods. Pregnant rats were orally given BPA (0, 0.04, 0.4, and 4 mg/kg body weight (BW)/day) from the first day of pregnancy to the 21st day of breastfeeding. Three‐week‐old male rat offspring were selected for an open‐field experiment and a new object recognition experiment to evaluate the effect of BPA exposure on cognitive behavior. Furthermore, the role of GABA signaling markers in the cognition affected by BPA was investigated at the molecular level using western blotting and real‐time polymerase chain reaction (RT‐PCR). The research demonstrated that BPA exposure impacted the behavior and memory of male rat offspring and elevated the expression of glutamic acid decarboxylase 67 (GAD67), GABA type A receptors subunit (GABAARα1), and GABA vesicle transporter (VGAT) in the hippocampus while decreasing the expression levels of GABA transaminase (GABA‐T) and GABA transporter 1 (GAT‐1). These findings indicate that the alteration in the expression of GABA signaling molecules may be one of the molecular mechanisms by which perinatal exposure to BPA leads to decreased learning and memory in male rat offspring. [ABSTRACT FROM AUTHOR]

Objective: A well-known endocrine disruptor, Bisphenol A (BPA) is used as a monomer in the manufacture of polyester, epoxy resin, and polycarbonate plastics. Previous studies have shown the antioxidant effect of Arthrospira platensis in several experimental models of oxidative stress. The current study was carried out to evaluate the antioxidant activity of Arthrospira platensis against BPA-induced nephrotoxicity and oxidative damage in rats. Methods: The bioactive compounds in the aqueous extract of AP were identified and confirmed by FTIR and HPLC. Nevertheless, this study pre-assessed the AP in vitro antioxidant activity (DPPH, ABTS, and FRAP). Female Wistar rats were randomly divided into four groups: group I (C) received 0.5mL corn oil and served as control. Group II (AP) were treated with Arthrospira platensis (4.75g/Kg of diet) + 0.5 mL of corn oil. Rats of group III (BPA) have received BPA (100mg/kg bw) dissolved in corn oil administered by orally way. Animals of group IV (BPA + AP) were treated with BPA and AP. Results: The results reveal a various and rich phytochemical composition of the aqueous extract of Arthrospira platensis. Six polyphenols that have been linked to bioactivities were found by HPLC analysis: quercetin, chlorogenic acid, rutin, vanillin, p-coumaric acid, and caffeic acid. Additionally, the FTIR profile detected the cyanobacteria's functional groups. The exposure of rats to BPA for 3 weeks provoked renal damage with significant increases in hematological parameters, oxidative stress-related parameters (i.e., malondialdehyde "MDA" protein carbonyl "PC" content, advanced oxidation protein products "AOPP", and hydrogen peroxide "H2O2"), creatinine, urea, and uric acid levels in plasma. Conversely, antioxidant enzyme activities (i.e., glutathione peroxidase "GPx" and superoxide dismutase "SOD") and levels of reduced glutathione "GSH", creatinine, urea, and uric acid decreased. The administration of Arthrospira platensis to BPA-treated rats significantly improved weight, peripheral blood parameters, oxidative stress-related parameters, renal biomarker levels, and antioxidant enzyme activities. Also, rats treated with BPA and Arthrospira platensis had normal kidney histology. These healing effects are likely the result of the high phenol content and significant antioxidant capacity of A. platensis. Conclusion: Our data strongly suggest that A. platensis supplementation improves kidney function and plays an important role in the prevention against BPA-induced nephrotoxicity in rats, and that the effects are associated with the antioxidant effect of Spirulina. [ABSTRACT FROM AUTHOR]

The rapid development of blockchain transactions highlights the importance of privacy protection (including anonymity and confidentiality) and underscores the necessity for auditability. Some schemes, such as PGC and Miniledger, support privacy protection and auditability. However, they only offer incomplete privacy protection (i.e., supporting anonymity or confidentiality exclusively). In response to these issues, we propose a scheme that achieves partial anonymity, confidentiality, auditability, and traceability. By integrating a variant of Pedersen commitments and randomizable signatures, we achieve partial anonymity for users and the auditability of transactions, thereby protecting user privacy under audit conditions. Based on the twisted ElGamal encryption algorithm and specially constructed zero-knowledge proofs, we achieve confidentiality of transaction amounts under legal and regulatory conditions. System test results indicate that this scheme effectively meets the above requirements. The feasibility of this scheme is confirmed through system testing, comparative analysis, and security analysis. [ABSTRACT FROM AUTHOR]

Maternal milk is pivotal for infants' nutrition. It also portrays the chemical burden to which the mother has been exposed. One of the chemical families that is prevalent and related to potential toxic effects are volatile organic compounds (VOCs). In the present study, motivated by the scarcity of works dealing with concomitant VOC and metabolite determination in maternal milk, two new gas/liquid chromatography tandem mass spectrometry (GC-MS/MS, LC-MS/MS) methods for the simultaneous measurement of 25 VOCs and 9 of their metabolites, respectively, in maternal milk were developed and applied to 20 maternal milk samples collected from mothers in Greece. In parallel, a headspace solid-phase microextraction (HS-SPME)–GC-MS method was employed for the untargeted screening of chemicals. Low detection rates for benzene, toluene, styrene and p,m-xylenes, and three of their metabolites, namely N-acetyl-S-(benzyl)-L-cysteine (BMA, metabolite of toluene), 3-methylhippuric (3-MHA, metabolite of xylenes) and mandelic acid (MA as DL and R isomers, metabolites of styrene and ethylbenzene), were evidenced in concentrations varying from −1. HS-SPME–GC-MS disclosed the presence of common maternal milk constituents such as fatty acids. Nevertheless, bisphenol-A, bisphenol derivatives and phthalates were also detected. The infants' health risk assessment demonstrated a low risk and negligible carcinogenic risk, yet the detection of these compounds should not be underestimated. [ABSTRACT FROM AUTHOR]

The objective of this study was to enhance the mechanical properties of 3D printed specimens in commercial photosensitive resin (PS‐resin) through blend‐thermosets using a benzoxazine monomer based on bisphenol A and a commercially available resin. Specifically, a benzoxazine‐based bisphenol A compound, 6,6‐(propane‐2,2‐diyl)bis(3‐cyclohexyl‐3,4‐dihydro‐2H‐benzo[e][1,3]oxazine), was successfully synthesized via the Mannich reaction. The synthesis involved paraformaldehyde, bisphenol A, and cyclohexylamine in a molar ratio of 4:1:2, respectively. To prepare the blend‐thermosets, a stereolithography 3D printer (SLA) was utilized, combining the PS‐resin with varying amounts of the benzoxazine (ranging from 0 to 8 parts per hundred of resin, phr). The printed specimens were then subjected to a polymerization process by heating them at various temperatures ranging from 120 to 160°C in a hot air oven for 2 h, allowing the benzoxazine to undergo ring‐opening reaction and form the thermoset structure. Characterization of all the materials obtained, including the PS‐resin, benzoxazine, and the blend‐thermosets before and after heating, was conducted using techniques such as FT‐IR and DSC. This work also showcased a sample technique for verifying the ring‐opening of the benzoxazine ring. Additionally, the mechanical properties of the blend‐thermosets were evaluated through tests for tensile strength, elongation at break, modulus, and hardness. The addition of merely 2 phr of benzoxazine monomers and subsequent curing at 120°C resulted in a notable improvement in the mechanical properties. [ABSTRACT FROM AUTHOR]

Bisphenol A (BPA), an exogenous endocrine‐disrupting chemical, is widely used to produce polycarbonate plastics. The widely used BPA has been detected in human urine samples, raising public anxiety about the detrimental effects of BPA on the bladder. In this study, we explored regulatory mechanisms for the adverse effects of BPA in human bladder BdFC and T24 cells. BPA induced extrinsic and intrinsic apoptosis and G2/M cell cycle arrest caused by the ATM‐CHK1/CHK2‐CDC25c‐CDC2 signaling, which ultimately inhibited the growth of human bladder cells. We also found that BPA decreased the binding activity of AP‐1 and NF‐κB transcription factors in human bladder cells, which inhibited migration and invasion through matrix metallopeptidase‐2 and ‐9 inactivation. Phosphorylation of MAPKs was implicated with BPA‐mediated detrimental effects in human bladder cells. Collectively, our results provide a novel explanation for the underlying molecular mechanisms that BPA induces cytotoxicity in human bladder cells. [ABSTRACT FROM AUTHOR]

Bisphenol A (BPA), an endocrine disruptor, changes many physiological functions of the body, especially the reproductive system. The malfunction of the reproductive system after BPA exposure is one of the causes of infertility reasons. BPA disrupts reproductive functions by elevating oxidative mediators and declining antioxidant enzymes, altering sex hormones, and inducing mitochondrial dysfunction and apoptosis. The present study focuses on the protective effects of melatonin against BPA-induced male and female reproductive alterations. A systematic literature review was conducted up to October 2023 using PRISMA principles in electronic databases, including PubMed, Web of Science, and Scopus. Considering the study purpose, the search keywords were selected and used to search the titles and abstracts. After screening, 19 pertinent papers were selected from 91 publications based on our inclusion and exclusion criteria. The literature showed that melatonin plus BPA protects reproductive cells via multiple mechanisms, including reducing oxidative stress, inflammation, apoptosis, and modulation of mitochondrial function. Furthermore, most indicated melatonin's beneficial effects on the histopathology of reproductive tissues. Also, melatonin induced its protective effects through direct interaction with hormone receptors against BPA-induced hormonal changes. This study indicates evidence of the protective role of melatonin on reproductive injuries and infertility caused by BPA. [ABSTRACT FROM AUTHOR]

The hydroxyalkyl amination of agarose gels was studied as an approach to improve adsorption of polyphenols and pharmaceuticals from water. Three commercially available agarose gels, Zetarose FlashFlow4, ZetaCell-CL6B and Sepharose 4B were chemically modified using tris-(hydroxymethyl)aminomethane, TRIS, and ethanolamine, EA. The adsorbed amounts of bisphenol A and diclofenac were significantly higher on TRIS- and EA-derivatives compared with the parent gels. Regarding bisphenol A adsorption on TRIS-ZetaCell-CL6B, a maximal adsorption capacity, Q max of 16 μmol/mL gel and an equilibrium dissociation constant KL of 2.7 × 10−4 mol/L were observed. Filtration of diclofenac-contaminated water through TRIS-Zetarose FlashFlow 4 resulted in a 10-fold reduction of the pollutant concentration within 64 column volumes of the effluent. The moderate binding affinity of polyphenols to TRIS- and EA-adsorbents facilitates efficient polyphenol desorption and column regeneration. The effects of TRIS- and EA-substituents in agarose gels, can be harnessed for the development of environmental adsorbents, as well as for the preparative separation of polyphenols and pharmaceuticals. We consider the physical shapes and textures of the prospective adsorbents with a particular focus on spongy macroporous cryogels. These innovative materials hold promise for future applications in liquid and air filtration. [ABSTRACT FROM AUTHOR]

The escalating global industrial expansion has led to the extensive release of organic compounds into water bodies, resulting in substantial pollution and posing severe threats to both human health and the ecosystem. Among common micropollutants, bisphenol A (MP-BA) has emerged as a significant endocrine-disrupting chemical with potential adverse effects on human health and the environment. This study aims to develop an efficient photocatalyst, specifically by incorporating palladium-doped graphitic carbon nitride (Pd@GCN), to eliminate MP-BA pollutants present in industrial wastewater. The examination of optical properties and photoluminescence indicates that incorporating Pd into GCN enhances the visible light absorption spectra, which extends beyond 570 nm, and accelerates the separation rate of electron–hole pairs. The photocatalytic degradation efficiency of MP-BA increases from 81.7 to 98.8% as the solution pH rises from 5.0 to 9.0. Moreover, Pd@GCN significantly improves the removal rate of MP-BA in wastewater samples, reaching an impressive 92.8% after 60 min of exposure to solar light. Furthermore, the Pd@GCN photocatalyst exhibits notable reusability over six cycles of MP-BA degradation, indicating its promising potential for the treatment of organic pollutants in wastewater under solar light conditions. [ABSTRACT FROM AUTHOR]

In the present work, the surface of glassy carbon electrode (GCE) was modified with graphitic carbon nitride (g-C3N4) prepared from the freeze-dried dicyandiamide. The physiochemical properties and electrocatalytic ability of the g-C3N4 nanosheets have been well investigated. Differential pulse voltammetry (DPV) method was employed to determine bisphenol A (BPA) using the modified GCE. To obtain the conditions for maximum DPV response, the effects of experimental parameters, such as the solution pH and nano-sized modifier concentration, were investigated and optimized. The proposed BPA sensing assay indicated a linear range of 0.01 to 75.0 µM under optimal conditions, with a detection limit of 9.0 nM. The anti-interference investigations revealed that the presence of various organic and inorganic species did not hinder the accurate measuring of BPA. In addition, the presented modified electrode exhibited satisfactory results in terms of stability and reproducibility. The obtained results also confirm the efficacy of the g-C3N4 nanocatalyst for determination of BPA in different real samples (drinking water, milk and orange juice) with satisfactory recovery values (95.6–104.0%). The suggested assay provides a powerful sensing platform for the fast and sensitive analysis of BPA in food samples. [ABSTRACT FROM AUTHOR]

Iron-based catalysts have been widely used to treat refractory organic pollutants in wastewater. In this paper, magnetic Co-γ-Fe2O3 was synthesized by a facile tartaric acid-assisted hydrothermal method, and Co-γ-Fe2O3/MoS2 nanocomposite catalyst was obtained via in situ growth of MoS2 nanosheets on Co-γ-Fe2O3 nanoparticles. The nanocomposite catalysts were used to decompose bisphenol A (BPA) by activating peroxymonosulfate (PMS). It was shown that only 0.15 g/L catalyst and 0.5 mmol/L PMS degraded 10 mg/L of BPA (99.3% within 10 min) in the pH range of 3–9. PMS was activated due to redox cycling among the pairs Co(III)/Co(II), Fe(III)/Fe(II), and Mo(VI)/Mo(IV). Quenching experiments and electron paramagnetic resonance spectroscopy demonstrated that both radical and non-radical pathways were involved in BPA degradation, in which active radical sulfate radical and non-radical singlet oxygen were the main reactive oxygen species. Ten intermediates were identified by liquid chromatography-coupled mass spectrometry, and three possible BPA degradation pathways were proposed. The toxicity of several degradation intermediates was lower, and Co-γ-Fe2O3/MoS2 exhibited excellent reusability and could be magnetically recovered. [ABSTRACT FROM AUTHOR]

Exposure to endocrine-disrupting chemicals such as bisphenol A (BPA) has been linked to the sharp drop in male fertility observed worldwide. This study evaluates the protective benefits of Cucumeropsis mannii seed oil (CMSO) against BPA-induced transgenerational sperm indices and reproductive hormone disruptions in rats. Twenty-four F0-male rats (aged 4–5 weeks) were randomly assigned to six groups (n = 4 each) after CMSO characterization for flavonoids. Group A received 1 ml of olive oil. Group B received 100 mg/kg body weight (BW) of BPA whereas Group C had a BW of 7.5 ml/kg CMSO. Groups D, E, and F were administered 100 mg/kg_BW of BPA in addition to 7.5, 5.0, and 2.5 ml/kg_BW of CMSO, respectively. After two weeks of treatment, four mature female rats were introduced to each group and allowed to stay together with male rats for seven days to confirm mating. Thereafter, the pregnant female rats were separated from the male according to their groups and allowed to give birth after 21 days of gestation period. At six weeks, the F1-male rats were isolated from each group and sacrificed for biochemical analysis. In-silico, CMSO flavonoids were assessed for drug-likeness and oral absorbability, followed by molecular docking to study their androgen receptor targeting mechanisms. Results showed that total flavonoids were 17.3652 ± 8.85 g/100 g. In-vivo, BPA significantly (p

BackgroundBisphenol A (BPA), a characteristic endocrine disruptor, is a substance that seriously interferes with the human endocrine system and causes reproductive disorders and developmental abnormalities. However, its toxic effects on the gut-liver-hormone axis are still unclear.MethodMale and female rats were exposed to BPA (300 mg/kg) by oral gavage for 60 consecutive days. H&E staining was used for histopathological evaluation, and the serum biochemical indexes were determined using an automatic analyzer. The 16S rRNA gene sequencing was used to detect the intestinal microbial diversity, and the GC-MS was used to analyze the contents of short-chain fatty acids (SCFAs) in colon contents. UPLC-QTOF MS was used to analyze the related metabolites. The ELISA method was used to assess the levels of serum inflammatory factors.ResultsHistopathological analysis indicated that the liver, heart, and testis were affected by BPA. There was a significant effect on alanine aminotransferase (ALT), triglyceride (TG), total cholesterol (TC), and low-density lipoprotein (LDL) in the male-BPA group (P < 0.05), and globulin (GLB), indirect bilirubin (IBIL), alkaline phosphatase (ALP), ALT, TG, TC, high-density lipoprotein (HDL), and creatinine (Cr) in the female-BPA group (P < 0.05). Metagenomics (16S rRNA gene sequencing) analysis indicated that BPA reduced the diversity and changed the composition of gut microbiota in rats significantly. Compared with the control and blank groups, the contents of caproic acid, isobutyric acid, isovaleric acid, and propanoic acid in the colon contents decreased in the male-BPA group (P < 0.05), and caproic acid, isobutyric acid, isovaleric acid, and valeric acid in the colon contents decreased in the female-BPA group (P < 0.05). Metabolomic analysis of the serum indicated that BPA could regulate bile acid levels, especially ursodeoxycholic acid (UDCA) and its conjugated forms. The contents of amino acids, hormones, and lipids were also significantly affected after exposure to BPA. The increase in interleukin-6 (IL-6), interleukin-23 (IL-23), and transforming growth factor-β (TGF-β) in the serum of the male-BPA group suggests that BPA exposure affects the immune system.ConclusionBPA exposure will cause toxicity to rats via disrupting the gut-liver-hormone axis.

To investigate the alleviating effect and mechanism of the docosahexaenoic acid-enriched phosphatidylserine (DHA-PS) on bisphenol A (BPA)-induced liver injury in mice, the murine liver injury model was established by gavage of BPA (5 mg/kg) or co-administration of BPA and DHA-PS (50 mg/kg or 100 mg/kg) for 6 weeks. The results showed that after administration of 100 mg/kg DHA-PS, the liver index, serum levels of AST, ALT, TC, TG, NEFA, and LDL-C in mice were significantly decreased, while HDL-C was significantly increased. The LPS, IL-6, IL-1β, TNF-α, and MDA levels in liver tissues were effectively down-regulated, and IL-10, SOD, GSH-Px, and CAT levels were effectively up-regulated. The H&E and Oil Red O staining results showed that liver damage was notably repaired and lipid deposition was notably reduced after DHA-PS administration. Furthermore, metabolomics and immunohistochemical studies revealed that DHA-PS mainly regulates glycerophospholipid metabolism and the SIRT1-AMPK pathway to improve metabolic disorders of the liver caused by BPA. Therefore, DHA-PS could potentially alleviate BPA-induced murine liver injury through suppressing inflammation and oxidative stress, and modulating lipid metabolism disorders.

The present study sought to investigate the protective effect of Lycopene (LYC) on Bisphenol A (BPA)-induced lipid accumulation and elucidate the potential molecular mechanism. In vitro, the PK15 cells with or without LYC were exposed to BPA for 6 h to detect the lipid accumulation using Nile red’s and Oil Red O’ staining. Meanwhile, redox status, mitochondrial function, gene expression and protein levels relating to lipid accumulation were evaluated by cellular biochemical assays, immunofluorescence staining, quantitative real-time PCR (qRT-PCR) and Western blot, respectively. In addition, ROS scavenger N-acetylcysteine (NAC), SIRT1 inhibitor EX527, SIRT1 siRNA and PGC-1α siRNA were used to verify the target signaling pathways responsible for the protective effect of LYC against BPA-indcued lipid accumulation. In vivo, the twenty four male Wistar rats were randomly divided into three groups, received either BPA (50 mg/kg/day BW) or LYC (10 mg/kg/day BW) orally for 60 days. The kidney tissues were evaluated by HE’s and Oil Red O’s staining, lipid-associated genes and proteins expression were detected through qRT-PCR and Western blot. The results showed that BPA-exposed PK15 cells and rats had increased lipid droplets with elevated transcription of lipogenic factors SREBP1 and PPARγ, and down-regulated PPARα expression, and which is accompanied by redox imbalance and abnormal mitochondrial function. Conversely, LYC prevented BPA-induced lipid metabolism disorder and lipid accumulation through impeding ROS overproduction. Moreover, PK15 cells and rats exposed to BPA showed decrease in SIRT1 and PGC-1α levels, whereas LYC blocked the decrease of SIRT1 and PGC-1α protein levels. Furthermore, inhibition or silence of SIRT1 and PGC-1α abrogated the improvements of LYC on ROS generation, mitochondrial mass impairement and lipid accumulation in BPA-treated PK15 cells. Collectively, these findings indicate that SIRT1/PGC-1α signaling pathway is involved in the protective effect of LYC on BPA-induced lipid accumulation. These results also provide a potential promising therapeutic of LYC against BPA-induced lipid accumulation in kidney cells and organs.

This study aimed to examine the impact of propolis (Pro) on various physiological parameters in male rats experiencing induced testicular dysfunction by Bisphenol A. Five groups of ten male rats apiece were created by random selection from the rats. Group 1 the rats, which performed as the group under negative control, received normal food and water. In Group 2, rats were subjected to intraperitoneal administration of 0.2 mL of corn oil, utilized as the vehicle for bisphenol A (BPA), thereby serving as the vehicle control group. For Group 3, rats were administered in corn oil, BPA dissolved at a dosage of 50 mg/kg body weight administered three times a week for three weeks using an intraperitoneal injection. In Group 4rats received a dose of 250 mg/kg body weight of propolis (protected) orally via a gavage needle. Subsequently, intraperitoneal injections are administered to them from BPA delivered three times weekly for three weeks, the dosage is 50 mg per kilogram of body weight dissolved in corn oil. In Group 5, rats received protection with vitamin E orally, at a dose of 100 mg/kg body weight, using a gavage needle. The intraperitoneal injection of BPA, dissolved in corn oil at a dose of 50 mg/kg body weight, was then given three times a week for three weeks. After three weeks, animals were sacrificed, and testes and blood were gathered for additional analysis. Superoxide Dismutase (SOD), Sperm Viability, General motility, Progressive motility, and Morphology, were all significantly reduced in the BPA group compared to the control groups, according to the results. While malondialdehyde (MDA) increased in the BPA group compared to the control groups. In conclusion, propolis enhanced physiological parameters adversely affected by BPA, suggesting its potential as a protective agent against BPA-induced testicular dysfunction.

Objective: Bisphenol A (BPA) is a common environmental endocrine disruptor that negatively impairs male reproductive ability. This study aimed to explore the alterations in serum metabolomics that occur following BPA exposure and the mechanism via which BPA induces the death of testicular cells in a male mouse model. Methods: The mice were classified into two groups: BPA-exposed and control groups, and samples were collected for metabolomic determination, semen quality analysis, electron microscopy, enzyme-linked immunosorbent assay, quantitative real-time PCR, pathological staining, and Western blot analysis. Results: BPA exposure caused testicular damage and significantly decreased sperm quality in mice. Combined with non-target metabolomic analysis, this was closely related to ferroptosis induced by abnormal metabolites of arachidonic acid and phosphatidylcholine, and the expression of its related genes, acyl CoA synthetase 4, glutathione peroxidase 4, lysophosphatidylcholine acyltransferase 3, and phosphatidylethanolamine-binding protein 1 were altered. Conclusion: BPA induced ferroptosis, caused testicular damage, and reduced fertility by affecting lipid metabolism in male mice. Inhibiting ferroptosis may potentially function as a therapeutic strategy to mitigate the male reproductive toxicity induced by BPA.

The occurrence of pharmaceuticals and xenoestrogen compounds (PXCs) in drinking water presents a dire human health risk challenge. The problem stems from the high anthropogenic pollution load on source water and the inefficiencies of the conventional water treatment plants in treating PXCs. This study assessed the PXCs levels and the consequential health risks of exposure to tap water from selected Ghanaian communities as well as that of raw water samples from the respective treatment plants. Thus the PXCs treatment efficiency of two drinking water treatment plants in the metropolises studied was also assessed. The study also conducted source apportionment of the PXCs in the tap water. Twenty six (26) tap and raw water samples from communities in the Cape Coast and Sekondi-Takoradi metropolises were extracted using SPE cartridges and analysed for PXCs using Ultra-fast-HPLC-UV instrument. Elevated levels of PXCs up to 24.79 and 22.02 μg/L were respectively recorded in raw and tap water samples from the metropolises. Consequently, elevated non-cancer health risk (HI > 1) to residential adults were found for tap water samples from Cape Coast metropolis and also for some samples from Sekondi-Takoradi metropolis. Again, elevated cumulative oral cancer risks >10−5 and dermal cancer risk up to 4 × 10−5 were recorded. The source apportionment revealed three significant sources of PXCs in tap water samples studied. The results revealed the inefficiency of the treatment plants in removing PXCs from the raw water during treatments. The situation thus requires urgent attention to ameliorate it, safeguarding public health. It is recommended that the conventional water treatment process employed be augmented with advanced treatment technologies to improve their efficacy in PXCs treatment.

The protective effects of docosahexaenoic acid-enriched phosphatidylserine (DHA-PS, 50 or 100 mg/kg) on bisphenol A (BPA)-induced intestinal damage were assessed. The biochemical indices, pathological examination, non-targeted metabolomics integrated with gut microbiota analysis, and immunofluorescence analysis were used to investigate the protective effects of DHA-PS and its underlying regulatory mechanism. The DHA-PS treatment improved the pathology of intestinal tract and increased the expression levels of Claudin-1, Occludin, and ZO-1. In addition, the DHA-PS treatment also notably decreased the levels of interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α, and increased the antioxidant enzymes activities. Moreover, DHA-PS treatment increased the relative abundances of Akkermansia, Alistipes, Butyricicoccus, Coriobacteriaceae_UCG-002, Enterorhabdus, and Lachnospiraceae_UCG-006. DHA-PS treatment alleviated BPA-induced intestinal damage by regulating the kynurenine pathway of tryptophan, lipid, and arachidonic acid metabolisms. Overall, this study suggested that DHA-PS could alleviate BPA-induced intestinal damage by enhancing the intestinal barrier integrity, improving gut microbial composition and metabolites, and inhibiting the TLR4/NF-κB pathways.

Abstract This study synthesized a highly efficient KOH-treated sunflower stem activated carbon (KOH-SSAC) using a two-step pyrolysis process and chemical activation using KOH. The resulting material exhibited exceptional properties, such as a high specific surface area (452 m2/g) and excellent adsorption capacities for phenol (333.03 mg/g) and bisphenol A (BPA) (365.81 mg/g). The adsorption process was spontaneous and exothermic, benefiting from the synergistic effects of hydrogen bonding, electrostatic attraction, and stacking interactions. Comparative analysis also showed that KOH-SSAC performed approximately twice as well as sunflower stem biochar (SSB), indicating its potential for water treatment and pollutant removal applications. The study suggests the exploration of optimization strategies to further enhance the efficiency of KOH-SSAC in large-scale scenarios. These findings contribute to the development of improved materials for efficient water treatment and pollution control.

Abstract Background Bisphenol A (BPA) is an environmental contaminant with endocrine-disrupting properties that induce fetal growth restriction (FGR). Previous studies on pregnant ewes revealed that BPA exposure causes placental apoptosis and oxidative stress (OS) and decreases placental efficiency, consequently leading to FGR. Nonetheless, the response of gut microbiota to BPA exposure and its role in aggravating BPA-mediated apoptosis, autophagy, mitochondrial dysfunction, endoplasmic reticulum stress (ERS), and OS of the maternal placenta and intestine are unclear in an ovine model of gestation. Results Two pregnant ewe groups (n = 8/group) were given either a subcutaneous (sc) injection of corn oil (CON group) or BPA (5 mg/kg/day) dissolved in corn oil (BPA group) once daily, from day 40 to day 110 of gestation. The maternal colonic digesta and the ileum and placental tissue samples were collected to measure the biomarkers of autophagy, apoptosis, mitochondrial dysfunction, ERS, and OS. To investigate the link between gut microbiota and the BPA-induced FGR in pregnant ewes, gut microbiota transplantation (GMT) was conducted in two pregnant mice groups (n = 10/group) from day 0 to day 18 of gestation after removing their intestinal microbiota by antibiotics. The results indicated that BPA aggravates apoptosis, ERS and autophagy, mitochondrial function injury of the placenta and ileum, and gut microbiota dysbiosis in pregnant ewes. GMT indicated that BPA-induced ERS, autophagy, and apoptosis in the ileum and placenta are attributed to gut microbiota dysbiosis resulting from BPA exposure. Conclusions Our findings indicate the underlying role of gut microbiota dysbiosis and gut-placental axis behind the BPA-mediated maternal intestinal and placental apoptosis, OS, and FGR. The findings further provide novel insights into modulating the balance of gut microbiota through medication or probiotics, functioning via the gut-placental axis, to alleviate gut-derived placental impairment or FGR. Video Abstract

Abstract Background Our study aimed to investigate the impact of urinary concentrations of personal care products (PCPs)-related phenols (PNs) and parabens (PBs), including Triclosan (TCS), Bisphenol A (BPA), Benzophenone-3 (BP-3), Butylparaben (BPB), Ethylparaben (EPB), Methylparaben (MPB), and Propylparaben (PPB), on urinary incontinence (UI) occurrence. Method We conducted a cross-sectional analysis using data from the National Health and Nutrition Examination Survey (NHANES) spanning the years 2007 to 2016. Regression analysis was employed to investigate the relationship between exposure to PCPs-related substances, various levels of exposure, and UI within both the general population and the female demographic. Additionally, the Bayesian Kernel Machine Regression (BKMR) model was used to assess the effects of mixtures on UI. Results Our analysis comprised 7,690 participants who self-reported their diagnosis. Among them, 12.80% experienced stress urinary incontinence (SUI), 11.80% reported urge urinary incontinence (UUI), and 10.22% exhibited mixed urinary incontinence (MUI). In our fully adjusted multivariable models, BP-3 exposure exhibited a positive association with SUI (OR 1.07, 95% CI 1.02–1.14, p = 0.045). BPA exposure correlated with an increased risk of UUI (OR 1.21, 95% CI 1.01–1.44, p = 0.046) and MUI (OR 1.26, 95% CI 1.02–1.54, p = 0.029). TCS exposure displayed a negative correlation with the incidence of MUI (OR 0.87, 95% CI 0.79–0.97, p = 0.009). No significant links were observed between parabens and urinary incontinence. Notably, among the female population, our investigation revealed that BPA exposure heightened the risk of MUI (OR 1.28, 95% CI 1.01–1.63, p = 0.043). Participants in the highest tertile of BP-3 exposure demonstrated elevated likelihoods of SUI and MUI compared to those in the lowest tertile. In the BKMR analysis, negative trends were observed between the mixture and the risks of UUI and MUI when the mixture ranged from the 25th to the 40th and 35th to the 40th percentiles or above, respectively. Additionally, a positive trend was identified between the mixture and MUI when it was in the 40th to 55th percentile. Conclusion In conclusion, our findings suggest that exposure to BPA, TCS, and BP-3 may contribute to the development of urinary incontinence.

Bisphenol A (BPA) is one of the chemical compounds used in the industry. The ongoing accumulation of this organic compound has a significant and harmful impact on the environment and human health. This study has several objectives, including the reduction of waste rates, the development of a less inexpensive adsorbent material than commercial activated carbon, and the purification of polluted water. The choice of waste used is based on its abundance and availability. To this end, pomegranate peel was selected as a precursor for the preparation of activated carbon using H3PO4 at different temperatures was carried out. The characterization of the best adsorbent by SEM, TGA/DTA, XRF, FTIR, and XRD depicted that AC500 has a heterogeneous surface with a higher carbon percent (93%), the disappearance of several organic functions, giving way to C-C bonds, and an amorphous structure. The rates of moisture and ash are 2.69% and 3.9%, respectively. The values of the iodine and methylene blue numbers are 842.45 mg•g-1, and 476.23 mg•g-1, respectively, indicating the microporous and mesoporous structure of AC500, which confirms the SEM results. The acidic character of AC500 has been proven by PZC (5.1), zetametry, and Boehm titration. This new structure imparts it with an adsorption capacity exceeding 91% for the removal of BPA. The obtained results suggest that pomegranate peel holds promising potential as a sustainable resource, offering a hopeful perspective for environmental pollution remediation.

Background: Nonylphenol (NP) and bisphenol A (BPA) are produced in large quantities worldwide as multipurpose agents. However, studies on relations between NP and BPA exposure and childhood neurodevelopment are few, and the results are inconsistent. This study aimed to investigate associations between prenatal and early childhood NP and BPA exposure and neurodevelopment in mother–child pairs. Methods: Pregnant women at 27–38 weeks' gestation were recruited, as were children 2–3 years of age (n = 94) and 4–6 years of age (n = 56) years. Urine was collected to assess NP and BPA exposure. Bayley Scales of Infant and Toddler Development (3rd edition; Bayley-III), Wechsler Preschool and Primary Scale of Intelligence (4th edition), and the Full Scale Intelligence Quotient (WPPSI-IV-FSIQ) were used to assess the neurodevelopment of the children. Results: The detection rate and concentration of NP and BPA in the urine of children 4–6 years old were higher than in those 2–3 years old. Children were divided into a high concentration group (3rd tertile) and a reference group (1st and 2nd tertiles) based on natural log-transformed urine concentration of NP and BPA. Girls' Bayley-III motor scores in the high concentration group were higher than those of the BPA reference group of urine of mothers (β = 6.85, 95% confidence interval [CI]: 1.58–12.13). Boys' FSIQ in the higher concentration group were significantly lower than those in children 2–3 years old in the NP reference group (β = −11.29, 95% CI: −18.62 to −3.96) (all, p

Abstract Background Bisphenol A (BPA), an endocrine disrupting chemical with weak estrogenic and anti-androgenic activity, is widely present in various environmental media and organisms. It has certain reproductive toxicity and can cause a variety of female reproductive system diseases. Although BPA-stimulated apoptosis of granulosa cells has been widely elaborated, the effect of BPA on mouse pre-antral follicle granulosa cells (mpGCs) has not been well elucidated. Results In this study, the results of live-dead cell staining showed that high concentrations of BPA severely impaired mpGCs growth viability and affected the cell cycle transition of mpGCs. We confirmed that BPA promotes the production of reactive oxygen species (ROS) and facilitates oxidative stress in mpGCs. In addition, immunofluorescence, transmission electron microscopy, and flow cytometry experiments demonstrated that BPA treatment for mpGCs resulted in apoptotic features, such as rounding, cytoplasmic crinkling, and mitochondrial damage. This was accompanied by a large production of ROS and apoptosis-inducing factor (AIF) translocation from the mitochondria to the nucleus. RNA-seq data showed that several apoptosis-related pathways were enriched in the high concentration BPA-treated group compared with the normal group, such as the p53 pathway, MAPK pathway, etc. Conclusions These results suggest that cells undergo oxidative stress effects and apoptosis after BPA treatment for mpGCs, which affects normal follicle development. The potential mechanism of BPA-induced female reproductive toxicity was elucidated, while providing a research basis for the prevention and treatment of female reproductive diseases.

Abstract Background Bisphenol A (BPA) levels are high in women with polycystic ovary syndrome (PCOS). The mechanism by which BPA induces abnormal glucose metabolism in PCOS patients is largely unknown. Methods Serum and urine samples were collected from women with and without PCOS (control) at the reproductive medicine center with informed consent. Non-PCOS patients who received in vitro fertilization were recruited for collection of ovarian follicular fluid and granular cells. Wild-type C57BL/6 and AhR −/− mice were used to verify the effects of BPA on PCOS. Real-time PCR, western blotting, and ELISA were conducted to analyze the function of BPA. Chip-qPCR verified the role of AhR in GLUT4 transcription. Flow cytometry was performed to determine glucose uptake. Results A positive correlation was observed between BPA concentration and serum BPA levels in PCOS patients. BPA aggravated the changes in PCOS with abnormal glucose metabolism, impaired fertility, and increased body fat. Mechanistically, we showed that BPA activated AhR and led to decreased glucose transport via GLUT4 downregulation in ovarian granular cells. Therefore, the use of inhibitors or knockout of AhR could effectively rescue BPA-induced metabolic disorders in PCOS mice. Conclusions Our results revealed that BPA suppressed GLUT4 expression and induced abnormal glucose metabolism by activating AhR, causing insulin resistance, and is thus a potential contributor to the development of PCOS. Therefore, AhR could be a potential new therapeutic target for PCOS. Video Abstract

Humification plays a significant role in converting phenolic pollutants and forming heterogeneous polymers, but few studies have been performed to investigate exolaccase-started humification (ESH). Herein, the influences of lignin precursors (LPs) on exolaccase-induced bisphenol A (BPA) removal and humification were explored. In particular, the architectural features and botanical effects of the formed humification products were also tested. ESH was extremely beneficial in boosting BPA removal in the presence of LPs. Compared with LP-free (58.49%), 100% of BPA was eliminated after the reaction with ESH for 72 h. Such a process was controlled by an exolaccase-caused random assembly of radicals, which generated a large number of hydrophobic polymers through nonspecific covalent binding of C–C and/or C–O. These humified polymers were extremely stable at pH 2.0–10.0 and −20 °C to 80 °C and displayed unique functions, i.e., scavenged 2,2-diphenyl-1-picrylhydrazyl/2,2′-azino-bis3-ethylbenzothiazoline-6-sulphonic acid radicals and exerted antioxidant capacities. More importantly, the functional polymers could act as auxin analogs to increase the germination index (>100%), plant biomass, and salt tolerance of radish seedlings. Our findings disclosed that ESH could not only be optimized to mitigate the ecological risks of phenolic pollutants and sequester organic carbon in environmental bioremediation, but the resulting abundant auxin analogs also contributed to agricultural productivity.

Bisphenol-A (BPA) is a potentially hazardous substance and is extensively used in manufacturing industries as a plasticizing agent. The current research intended to determine the revival actions of zinc (Zn) and folic acid (FA) on hematological parameters and hepatorenal function in BPA-exposed male albino mice. A total of 75 adult male mice, aged 25 to 28 days, were split into five groups. Group A (the control group) received a normal diet, while a daily dosage of 50 mg BPA/kg body weight (BW) in the diet was provided to groups B–E. Groups C, D, and E received daily supplements of 10 mg Zn/kg BW, 3 mg FA/kg BW, or both in the feed. After 12 weeks of treatment, serum was prepared by collecting blood, and the kidney and liver were taken for a histotexture study. The results demonstrate that hematological values dropped significantly (p< 0.05) in the BPA-treated group and increased following Zn and FA supplementations, while no significant alterations in erythrocyte indices were observed among control and treated groups. The BPA group used to have significantly (p< 0.05) higher liver and kidney biomarkers levels, which were restored by Zn and FA. The effects of BPA administration included severe hepatocyte degeneration and necrosis, as well as renal tubule epithelium loss, all of which were improved by Zn and FA. Hence, the findings suggest Zn and FA could be potential preventative agents against BPA-induced toxicity. [ J Adv Biotechnol Exp Ther 2023; 6(3.000): 541-551]

Background: Oxidative stress may be a causative factor for bisphenol A (BPA) -induced hepatotoxicity. Glutamine (GM) is an amino acid with the ability to inhibit oxidative stress. Objective: This study evaluated the ability of GM to prevent BPA-induced hepatotoxicity in rats. Methods: Adult Wistar rats of both sexes (n=30) were used. The rats were randomly grouped into six of five rats each. Groups A (Control), B, and C were treated with normal saline (0.2 mL), GM (80 mg/kg), and BPA (50 mg/kg), respectively for 60 days. Groups D-F were treated with GM (20 mg/kg)+BPA (50 mg/kg), GM (40 mg/kg)+BPA (50 mg/kg), and GM (80 mg/kg)+BPA (50 mg/kg), respectively for 60 days. After treatment, blood and liver samples were obtained for biochemical and histological assessments, respectively. Results: Significantly (P

Background/Objectives: Cardiovascular diseases are the primary cause of global morbidity and mortality, with cardiovascular health (CVH) remaining well below the ideal level and showing minimal improvement in the U.S. population over recent years. Bisphenol A (BPA), a pervasive environmental contaminant, has emerged as a potential contributor to adverse cardiovascular outcomes. This cross-sectional study delves into the impact of BPA exposure on achieving optimal CVH, as assessed by the Life’s Essential 8 metric, among U.S. adults. Methods: Analyzing data from 6635 participants in the National Health and Nutrition Examination Survey (NHANES) collected between 2005 and 2016, BPA exposure was quantified through urinary BPA levels, while optimal CVH was defined using the American Heart Association’s Life’s Essential 8 criteria, scoring between 80 and 100. Multivariable logistic regression and propensity score matching were employed to evaluate the association between BPA exposure and CVH. Results: This study reveals that individuals in the highest tertile of urinary BPA levels were 27% less likely to attain optimal CVH compared with those in the lowest tertile (OR, 0.73; 95% CI: 0.59–0.92). This negative association persisted across diverse demographics, including age, sex, and race, mirrored in the link between urinary BPA levels and health factor scores. Conclusions: The findings underscore the potential benefits of reducing BPA exposure in enhancing the prevalence of optimal CVH and mitigating the burden of cardiovascular disease. Given the widespread use of BPA, ongoing monitoring of BPA’s impact on CVH is essential. Further studies are necessary to elucidate the long-term and causative connections between BPA and CVH. These insights contribute to understanding the complex interplay between environmental factors and CVH outcomes, informing targeted interventions to mitigate cardiovascular disease risk within the population.

Objective: Bisphenol A and phthalate are known endocrine disruptors and capable of inducing epigenetic changes in the human population. However, their impact on the placenta is less well studied. Our objective was to measure the effect of exposure to bisphenol A and benzyl butyl phthalate in first-trimester HTR8-SVneo and third-trimester 3A-sub E trophoblast cells by profiling the DNA methylation pattern of the imprinting control region of the IGF2 (insulin-like growth factor) and H19 genes. Methods: Human placental HTR8-SVneo and 3A-sub E cell lines were treated with two sub-lethal concentrations of bisphenol A and benzyl butyl phthalate. Demethylating agent, 5-azacytidine, was used as a positive control. Cells were harvested on post-treatment days 1 and 4. The methylation profile of six CpG dinucleotide sites, part of the CTCF 6 binding site of the IGF2/H19 imprinting control region, was determined by pyrosequencing. Results: In the first-trimester HTR8-SVneo cell line, we observed a significant increased methylation of the CpG sites 3, 4 when treated with a high concentration of bisphenol A or benzyl butyl phthalate while increased methylation at site 6 for both high and low dose treatment on day 4. Demethylation of the CpG sites 1, 4, and 6 was observed when treated with 5-azacytidine on day 4. In the third-trimester 3A-sub E cell line, no significant changes in the methylation profile were observed under any treatment conditions. Conclusions: The results of this study demonstrate the capability of epigenetic changes in human placenta cells induced by bisphenol A and benzyl butyl phthalate. The observed methylation changes only in the first-trimester HTR8-SVneo cells phthalate may reflect a window of epigenetic susceptibility related to these environmental toxicants.

Polycystic ovary syndrome (PCOS) and idiopathic hirsutism (IH) are androgen excess disorders requiring the determination of classic androgen levels for diagnosis. 11-oxygenated androgens have high androgenic potential, yet their clinical value in those disorders is not clear. Additionally, the role of endocrine disruptors (EDs), particularly in IH, remains understudied. We analyzed 25 steroids and 18 EDs in plasma samples from women with IH, PCOS, and controls using LC-MS/MS. Cytokine levels and metabolic parameters were assessed. Comparisons included non-obese women with PCOS (n = 10), women with IH (n = 12) and controls (n = 20), and non-obese versus obese women with PCOS (n = 9). Higher levels of 11-oxygenated androgens were observed in women with PCOS compared to those with IH, but not controls. Conversely, 11-oxygenated androgen levels were lower in women with IH compared to controls. Cytokine levels did not differ between women with IH and controls. Bisphenol A (BPA) levels were higher in obese women with PCOS compared to non-obese women with PCOS. Bisphenol S occurrence was higher in women with PCOS (90%) compared to controls (65%) and IH (50%). Significant correlations were found between androgens (11-ketotestosterone, androstenedione, testosterone) and insulin and HOMA-IR, as well as between immunomodulatory 7-oxygenated metabolites of DHEA and nine interleukins. Our data confirms that PCOS is a multiendocrine gland disorder. Higher BPA levels in obese women might exacerbate metabolic abnormalities. IH was not confirmed as an inflammatory state, and no differences in BPA levels suggest BPA does not play a role in IH pathogenesis.

Bisphenol A (BPA) is a polymer used in the production of polycarbonate plastics and epoxy resins. An estrogen mimic, prenatal BPA exposure has been associated with several behavioral outcomes in children; however, the impact of maternal demographic and economic factors on associations between BPA and child behavioral outcomes have not been examined. The objective of this study was to examine associations between prenatal maternal urinary BPA and behavior in 4-5 year old girls, and to assess whether socio-demographic factors modify this relationship. Mothers enrolled in The Infant Development and Environment Study (TIDES) provided a single spot urine at enrollment (median gestational age 11 weeks) and completed the Behavior Assessment System for Children-2 (BASC-2) and Social Responsiveness Scale-2 (SRS-2) when their daughters were 4-5 years of age. Mother-daughter pairs with complete phthalate, BASC-2, SRS-2, and covariate data were included in this analysis (N = 244). BPA was detectable in 93 % of urine samples. We used multivariable linear regression analyses to estimate associations between maternal urinary log10-transformed BPA concentration and BASC-2 subscale and composite scores and SRS-2 Total Score. To examine the role of socioeconomic and demographic factors associated with study site, we stratified by TIDES center, comparing those enrolled at University of Rochester Medical Center (URMC), a predominately lower socioeconomic population, and those enrolled elsewhere: University of Washington, University of Minnesota, and University of California San Francisco, whose populations share similar higher socioeconomic demographic characteristics. Across all centers, no associations were seen between BPA and BASC-2 or SRS-2 scores. When stratifying by center, BPA was significantly associated with greater social impairment as measured by the SRS-2 Total Score (β-coefficient [95 % confidence intervals]: 5.1 [1.0, 9.2]) in URMC participants (N = 61). In non-URMC participants (N = 183), BPA was significantly associated with lower BASC-2 Internalizing composite (-3.3 [-6.7, 0.0]) and Depression subscale scores (-3.4 [-6.7, 0.0]) while no associations were seen between BPA and SRS-2 scores. Our findings suggest that sociodemographic factors may modify the impacts of maternal prenatal BPA on developmental endpoints.