The engineered carbon nanomaterial, fullerene C
, with unique physicochemical properties, released into the aquatic environment is known to formulate high risk factor for the aquatic life. The ...present study was aimed to investigate fullerene C
induced oxidative imbalance in ovary and testis of the freshwater fish, Anabas testudineus. The median lethal concentration (96 h-LC
) of fullerene C
in Anabas testudineus was 50 mg/ L, and fish exposed to two sublethal concentrations i.e., 5 mg/ L and 10 mg/ L (one-tenth and one-fifth of LC
) for short-term (24, 48, 72 and 96 h) and long-term (7, 15, 30 and 60 d) durations. The antioxidant parameters such as the activities of superoxide dismutase (SOD), catalase, glutathione reductase, glutathione peroxidase, the levels of hydrogen peroxide generation and lipid peroxidation were analyzed along with histopathological alterations in gonadal tissues. Both sublethal concentrations of fullerene C
caused significant (P < 0.05) decrease in the activities of antioxidant enzymes, whereas the levels of hydrogen peroxide generation and lipid peroxidation increased significantly (P < 0.05) in gonads. Fullerene exposure significantly (P < 0.05) increased the mucous deposition with significant (P < 0.05) reduction in the weights of gonads and gonado-somatic index. The histopathological analysis showed prominent alterations in testis and ovary of treated fishes when compared to the control groups. After 60 d of sublethal exposure of fullerene C
, fish were left in the toxicant-free water for another 60 d, in which the changes in the activities of the gonadal antioxidant enzymes and histological alterations were not completely recovered. Hence, from the present study, it was illustrated that fullerene C
caused oxidative imbalance in the gonads, which may possibly affect the reproductive potential of the fish, Anabas testudineus.
High-grade serous ovarian carcinoma (HGSOC), the most lethal gynecological cancer, often leads to chemoresistant diseases. The p53 protein is a key transcriptional factor regulating cellular ...homeostasis. A majority of HGSOCs have inactive p53 because of genetic mutations. However, genetic mutation is not the only cause of p53 inactivation. The aggregation of p53 protein has been discovered in different types of cancers and may be responsible for impairing the normal transcriptional activation and pro-apoptotic functions of p53. We demonstrated that in a unique population of HGSOC cancer cells with cancer stem cell properties, p53 protein aggregation is associated with p53 inactivation and platinum resistance. When these cancer stem cells differentiated into their chemosensitive progeny, they lost tumor-initiating capacity and p53 aggregates. In addition to the association of p53 aggregation and chemoresistance in HGSOC cells, we further demonstrated that the overexpression of a p53-positive regulator, p14ARF, inhibited MDM2-mediated p53 degradation and led to the imbalance of p53 turnover that promoted the formation of p53 aggregates. With in vitro and in vivo models, we demonstrated that the inhibition of p14ARF could suppress p53 aggregation and sensitize cancer cells to platinum treatment. Moreover, by two-dimensional gel electrophoresis and mass spectrometry we discovered that the aggregated p53 may function uniquely by interacting with proteins that are critical for cancer cell survival and tumor progression. Our findings help us understand the poor chemoresponse of a subset of HGSOC patients and suggest p53 aggregation as a new marker for chemoresistance. Our findings also suggest that inhibiting p53 aggregation can reactivate p53 pro-apoptotic function. Therefore, p53 aggregation is a potential therapeutic target for reversing chemoresistance. This is paramount for improving ovarian cancer patients' responses to chemotherapy, and thus increasing their survival rate.
Aqueous-phase processing of methylglyoxal (MG) has been suggested to constitute an important source of secondary organic aerosol (SOA). The uptake of MG to aqueous particles is higher than expected ...because its carbonyl moieties can hydrate to form geminal diols, as well as because MG and its hydration products can undergo aldol condensation reactions to form larger oligomers in solution. MG is known to be surface active, but an improved description of its surface behavior is crucial to understanding MG-SOA formation. These studies investigate MG adsorption, focusing on its hydration state at the air-water interface, using a combined experimental and theoretical approach that involves vibrational sum frequency spectroscopy, molecular dynamics simulations, and density functional theory calculations. Together, the experimental and theoretical data show that MG exists predominantly in a singly hydrated state (diol) at the interface, with a diol-tetrol ratio at the surface higher than that for the bulk. In addition to exhibiting a strong surface activity, we find that MG significantly perturbs the water structure at the interface. The results have implications for understanding the atmospheric fate of methylglyoxal.
An "event-based" approach to characterize complex air pollutant mixtures was applied in the Oil Sands region of northern Alberta, Canada. This approach was developed to better-inform source ...characterization and attribution of the air pollution in the Indigenous community of Fort McKay, within the context of the lived experience of residents. Principal component analysis was used to identify the characteristics of primary pollutant mixtures, which were related to hydrocarbon emissions, fossil fuel combustion, dust, and oxidized and reduced sulfur compounds. Concentration distributions of indicator compounds were used to isolate sustained air pollution "events". Diesel-powered vehicles operating in the mines were found to be an important source during NO
events. Industry-specific volatile organic compound (VOC) profiles were used in a chemical mass balance model for source apportionment, which revealed that nearby oil sands operations contribute to 86% of the total mass of nine VOC species (2-methylpentane, hexane, heptane, octane, benzene, toluene,
,
-xylene,
-xylene, and ethylbenzene) during VOC events. Analyses of the frequency distribution of air pollution events indicate that Fort McKay is regularly impacted by multiple mixtures simultaneously, underscoring the limitations of an exceedance-based approach relying on a small number of air quality standards as the only tool to assess risk.
While transportation emissions have declined over the past several decades, volatile organic compound (VOC) emissions from solvent use applications have increased as urban areas expand. In this work, ...the Canadian air quality model (GEM-MACH-TEB) is used to assess the importance of solvent emissions during the Michigan Ontario Ozone Source Experiment (MOOSE). Model predictions are compared to ozone and total mono-substituted aromatics (TOLU) observations collected in Windsor, Ontario. For summer 2018, model estimates of TOLU from solvent emissions are smaller (30% for an 8 h daytime average) in Windsor than estimates from positive matrix factorization (44% for a 24 h average). The use of updated U.S. solvent emissions from the EPA’s VCPy (Volatile Chemical Product framework) for summer 2021 simulations increases the solvent use source contribution over Detroit/Windsor (30–50% for an 8 h daytime average). This also provides a more uniform spatial distribution across the U.S./Canada border (30–50% for an 8 h daytime average). Long-chain alkanes are the dominant speciation in the model’s air pollutant emission inventory and in the observation-derived solvent use factor. Summertime 8 h daytime ozone decreased by 0.4% over Windsor for a 10% solvent use VOC emission reduction scenario. A 10% mobile NOx emission reduction scenario resulted in a 0.6% O3 decrease over Windsor and more widespread changes over the study region.
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► Glancing-angle Raman scattering probed the surface of nitrate-containing solutions. ► The extent of nitric acid dissociation in the surface region is similar to that in the bulk. ► ...We obtained an adsorption isotherm for nitrate to the aqueous surface. ► Nitrate exhibits near neutral surface activity.
Glancing-angle Raman spectra of aqueous KNO3 and HNO3 solutions were used to determine the degree of nitric acid dissociation, α, in the bulk and in the surface region. Our results suggest that α in the surface region is similar to that in the bulk and highlight the importance of water molecule availability to the dissociation process. Using the α’s and the ν-symNO3- Raman intensities, we obtained an adsorption isotherm for NO3- to the surface region from which we calculated a Kads, of 0.19±0.03Lmol−1, implying that nitrate exhibits an almost neutral surface affinity.
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