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1.
PLoS One ; 19(8): e0308977, 2024.
Article in English | MEDLINE | ID: mdl-39159207

ABSTRACT

Perioperative acute kidney injury (AKI), which is mainly mediated by renal ischemia‒reperfusion (I/R) injury, is commonly observed in clinical practice. However, effective measures for preventing and treating this perioperative complication are still lacking in the clinic. Thus, we designed this study to examine whether remote liver ischemic preconditioning (RLIPC) has a protective effect on damage caused by renal I/R injury. In a rodent model, 30 mice were divided into five groups to assess the effects of RLIPC and ERK1/2 inhibition on AKI. The groups included the sham-operated (sham), kidney ischemia and reperfusion (CON), remote liver ischemic preconditioning (RLIPC), CON with the ERK1/2 inhibitor U0126 (CON+U0126), and RLIPC with U0126 (RLIPC+U0126). RLIPC consisted of 4 liver ischemia cycles before renal ischemia. Renal function and injury were assessed through biochemical assays, histology, cell apoptosis and protein phosphorylation analysis. RLIPC significantly mitigated renal dysfunction, tissue damage, inflammation, and apoptosis caused by I/R, which was associated with ERK1/2 phosphorylation. Furthermore, ERK1/2 inhibition with U0126 negated the protective effects of RLIPC and exacerbated renal injury. To summarize, we demonstrated that RLIPC has a strong renoprotective effect on kidneys post I/R injury and that this effect may be mediated by phosphorylation of ERK1/2.


Subject(s)
Acute Kidney Injury , Ischemic Preconditioning , Liver , Mitogen-Activated Protein Kinase 3 , Nitriles , Reperfusion Injury , Animals , Reperfusion Injury/prevention & control , Reperfusion Injury/metabolism , Ischemic Preconditioning/methods , Liver/metabolism , Liver/pathology , Liver/blood supply , Phosphorylation , Mice , Male , Mitogen-Activated Protein Kinase 3/metabolism , Acute Kidney Injury/prevention & control , Acute Kidney Injury/metabolism , Acute Kidney Injury/pathology , Nitriles/pharmacology , Kidney/pathology , Kidney/blood supply , Kidney/metabolism , Mitogen-Activated Protein Kinase 1/metabolism , Butadienes/pharmacology , Apoptosis/drug effects , Mice, Inbred C57BL , MAP Kinase Signaling System/drug effects
2.
Int J Occup Med Environ Health ; 37(3): 300-310, 2024 Sep 10.
Article in English | MEDLINE | ID: mdl-39166514

ABSTRACT

OBJECTIVES: 1,3-Butadiene (BD) exposure's link to leukemia is under regulatory scrutiny. The assessment methods for BD exposure risks have evolved from early animal and limited human studies to advanced exposure-response modelling with comprehensive quantitative data. The objec- tive of this study is to explore the nuances of exposure-response modelling, investigating how various statistical methods have influenced the quan- tification of exposure-response relationships. MATERIAL AND METHODS: Although this study was not conducted as a formal systematic review, a search was performed in Medline/Pubmed to identify all human studies on leukemia risk assessment for BD exposure. This search included articles written in English. The electronic search spanned from inception of records until July 23, 2023, using the search term: "butadiene AND (leukaemia OR leukemia OR myeloid OR lymphoid)" and was restricted to human species. Focusing on the synthetic styrene-butadiene rubber (SBR) industry cohort study conducted by the University of Alabama at Birmingham, USA, this review evaluates various statistical models and factors influenc- ing exposure-response modelling. RESULTS: Peak exposures to BD may be more influential in the dose-response relationship than cumulative or long-term exposure. The authors recommend utilizing ß-coefficients derived from the latest SBR study update, employing Cox proportional hazard modelling, non-lagged and non-transformed cumulative BD exposure, and adjusting for age and peak BD exposure. The study reveals that statistical model selection has a limited impact on the calculated dose-response effects. The significant variation in estimated cancer mortality values arises from additional assumptions needed for metrics like the excess leukemia risk or the occupational BD effective concentration. CONCLUSIONS: In con- clusion, this study provides insights into exposure-response modelling for BD exposure and leukemia mortality, highlighting the importance of peak exposures. The recommended statistical approach offers a reliable basis for regulatory risk assessment and public health population metrics. Int J Occup Med Environ Health. 2024;37(3):300-10.


Subject(s)
Butadienes , Leukemia , Occupational Exposure , Humans , Leukemia/chemically induced , Leukemia/epidemiology , Leukemia/mortality , Occupational Exposure/adverse effects , Risk Assessment/methods , Elastomers , Styrenes , Dose-Response Relationship, Drug
3.
Biomed Phys Eng Express ; 10(6)2024 Sep 05.
Article in English | MEDLINE | ID: mdl-39145621

ABSTRACT

Objective.To investigate the potential of 3D-printable thermoplastics as tissue-equivalent materials to be used in multimodal radiotherapy end-to-end quality assurance (QA) devices.Approach.Six thermoplastics were investigated: Polylactic Acid (PLA), Acrylonitrile Butadiene Styrene (ABS), Polyethylene Terephthalate Glycol (PETG), Polymethyl Methacrylate (PMMA), High Impact Polystyrene (HIPS) and StoneFil. Measurements of mass density (ρ), Relative Electron Density (RED), in a nominal 6 MV photon beam, and Relative Stopping Power (RSP), in a 210 MeV proton pencil-beam, were performed. Average Hounsfield Units (HU) were derived from CTs acquired with two independent scanners. The calibration curves of both scanners were used to predict averageρ,RED and RSP values and compared against the experimental data. Finally, measured data ofρ,RED and RSP was compared against theoretical values estimated for the thermoplastic materials and biological tissues.Main results.Overall, goodρand RSP CT predictions were made; only PMMA and PETG showed differences >5%. The differences between experimental and CT predicted RED values were also <5% for PLA, ABS, PETG and PMMA; for HIPS and StoneFil higher differences were found (6.94% and 9.42/15.34%, respectively). Small HU variations were obtained in the CTs for all materials indicating good uniform density distribution in the samples production. ABS, PLA, PETG and PMMA showed potential equivalency for a variety of soft tissues (adipose tissue, skeletal muscle, brain and lung tissues, differences within 0.19%-8.35% for all properties). StoneFil was the closest substitute to bone, but differences were >10%. Theoretical calculations of all properties agreed with experimental values within 5% difference for most thermoplastics.Significance.Several 3D-printed thermoplastics were promising tissue-equivalent materials to be used in devices for end-to-end multimodal radiotherapy QA and may not require corrections in treatment planning systems' dose calculations. Theoretical calculations showed promise in identifying thermoplastics matching target biological tissues before experiments are performed.


Subject(s)
Photons , Polymethyl Methacrylate , Printing, Three-Dimensional , Proton Therapy , Humans , Proton Therapy/methods , Proton Therapy/instrumentation , Polymethyl Methacrylate/chemistry , Polyesters/chemistry , Plastics , Polystyrenes/chemistry , Calibration , Quality Assurance, Health Care , Phantoms, Imaging , Radiotherapy Planning, Computer-Assisted/methods , Radiotherapy Dosage , Materials Testing , Acrylic Resins , Butadienes
4.
Exp Gerontol ; 195: 112543, 2024 Oct 01.
Article in English | MEDLINE | ID: mdl-39128688

ABSTRACT

BACKGROUND: Facet joint osteoarthritis (FJOA) is a prevalent condition contributing to low back pain, particularly in the elderly population. This study aimed to investigate the potential role of Cytokine Receptor-like Factor 1 (CRLF1) in FJOA pathogenesis and its therapeutic implications. METHODS: Bioinformatics analysis was utilized to identify CRLF1 as the target gene, followed by quantification of CRLF1 expression levels and joint degeneration degree using immunohistochemistry (IHC). In primary chondrocytes, the inhibition of CRLF1 expression by siRNA was performed, and Western blot analysis was conducted to evaluate the involvement of the extracellular matrix and MAPK/ERK signaling pathway. Flow cytometry was employed to assess the apoptosis rate of chondrocytes, while immunofluorescence (IF) was utilized to evaluate the localization of CRLF1, cleaved-caspase3, MMP13, COL2A1, and ERK. RESULTS: The expression of CRLF1 was found to be significantly elevated in FJOA tissues compared to normal tissues. Through the use of loss-of-function assays, it was determined that CRLF1 not only enhanced the rate of apoptosis in chondrocytes, but also facilitated the degradation of the extracellular matrix in vitro. Furthermore, CRLF1 was found to activate the ERK1/2 pathways. The pro-arthritic effects elicited by CRLF1 were mitigated by treatment with the MEK inhibitor U0126 in chondrocytes. CONCLUSION: These results suggest that CRLF1 enhances chondrocytes apoptosis and extracellular matrix degration in FJOA and thus may therefore be a potential therapeutic target for FJOA.


Subject(s)
Apoptosis , Chondrocytes , Osteoarthritis , Zygapophyseal Joint , Chondrocytes/metabolism , Chondrocytes/pathology , Humans , Osteoarthritis/metabolism , Osteoarthritis/pathology , Zygapophyseal Joint/pathology , MAP Kinase Signaling System/physiology , Male , Extracellular Matrix/metabolism , Female , Aged , Butadienes/pharmacology , Nitriles/pharmacology , Cells, Cultured , Middle Aged , Receptors, Cytokine
5.
Sci Total Environ ; 951: 175738, 2024 Nov 15.
Article in English | MEDLINE | ID: mdl-39182777

ABSTRACT

Climate change and the associated increased frequency of extreme weather events are likely to alter the emissions of biogenic volatile organic compounds (BVOCs) from boreal peatlands. Hydrologically sensitive Sphagnum mosses are keystone species in boreal peatland ecosystems that are known to emit various BVOCs. However, it is not known how their emissions respond to seasonal droughts. In this study, we quantified the effect of severe drought, and subsequent recovery, on the BVOC emissions from Sphagnum mosses using mesocosms originating from wet open and naturally drier treed boreal fens and bogs. Here we report the emissions of 30 detected BVOCs, of which isoprene was the most abundant with an average flux rate of 5.6 µg m-2 h-1 (range 0-31.9 µg m-2 h-1). The experimental 43-day ecohydrological drought reduced total BVOC and isoprene emissions. In addition, in mesocosms originating from bogs, sesquiterpene emissions decreased with the drought, while the emissions of green leaf volatiles were induced. Sesquiterpene emissions remained low even six weeks after rewetting, indicating a long and limited recovery from the drought. Our results further imply that long-term exposure to deep water tables does not decrease sensitivity of Sphagnum to an extreme drought; we did not detect differences in the emission rates or drought responses between Sphagna originating from wet open and naturally drier treed habitats. Yet, the differences between fen and bog originating Sphagna indicate local variability in the BVOC quality changes following drought, potentially altering the climate feedback of boreal peatland BVOC emissions.


Subject(s)
Climate Change , Droughts , Environmental Monitoring , Sphagnopsida , Volatile Organic Compounds , Volatile Organic Compounds/analysis , Air Pollutants/analysis , Wetlands , Taiga , Butadienes , Hemiterpenes
6.
ACS Appl Mater Interfaces ; 16(36): 48176-48186, 2024 Sep 11.
Article in English | MEDLINE | ID: mdl-39186766

ABSTRACT

Developing an electronic skin (e-skin) is becoming popular due to its capability to mimic human skin's ability to detect various stimuli. Mostly, such skins are tactile-based sensors. However, the exploration of nontactile-based sensing capability in the e-skin is still in a nascent stage. Herein, we report an approach toward developing electrical hysteresis- and cross-interference-free nontactile e-skin using liquid polyisoprene with an ultralow concentration of multiwalled carbon nanotubes (ϕ = 0.006 volume fraction) by leveraging the stencil printing technique. The impact of cross-linking the samples was studied. Uncross-linked samples demonstrated higher electrical conductivity than the cross-linked samples. A coarse-grained phenomenological model with molecular dynamics simulation was utilized to investigate filler network formation and percolation that dictate the conductivity of uncross-linked and cross-linked samples. Simulation studies supported the fidelity of the experimental findings. The uncross-linked e-skin demonstrated a higher temperature sensitivity (-1.103%/°C) than the cross-linked e-skin (-0.320%/°C) in the thermal conduction mode. Despite the superior sensitivity of the uncross-linked e-skin, the cross-linked systems demonstrated superior cyclic stability (35 thermal cycles), ensuring reliable sensor readings over extended usage. Judicious choice of encapsulant warranted the cross-linked e-skin sensor to nullify the impact of moisture on signal output, thereby providing cross-interference-free results. The optimized e-skin sample retained a similar thermal sensitivity even when used in the nontactile mode. From the application purview, the utility of the developed sensor was tested successfully for nontactile sensing of human body temperature. Additionally, the sensor was utilized to determine the respiratory profile by integrating the developed sensor into a wearable mask. This study advances nontactile e-skin-based sensing technology and opens new avenues for creating wearable and IoT devices for healthcare and human-machine interactions.


Subject(s)
Electric Conductivity , Hemiterpenes , Nanotubes, Carbon , Temperature , Wearable Electronic Devices , Nanotubes, Carbon/chemistry , Hemiterpenes/chemistry , Hemiterpenes/analysis , Humans , Butadienes/chemistry , Molecular Dynamics Simulation
7.
Int J Biol Macromol ; 276(Pt 1): 133786, 2024 Sep.
Article in English | MEDLINE | ID: mdl-38992551

ABSTRACT

The poor interfacial compatibility of natural fiber-reinforced polymer composites has become a major challenge in the development of industry-standard high-performance composites. To solve this problem, this study constructs a novel rigid-flexible balanced molecular crosslinked network transition interface in composites. The interface improves the interfacial compatibility of the composites by balancing the stiffness and strength of the fibers and the matrix, effectively improving the properties of the composites. The flexural strength and flexural modulus of the composites were enhanced by 38 % and 44 %, respectively. Water absorption decreased by 30 %. The initial and maximum thermal degradation temperatures increased by 20 °C and 16 °C, respectively. The maximum storage modulus increased by 316 %. Furthermore, the impact toughness was elevated by 41 %, attributed to the crosslinked network's efficacy in absorbing and dissipating externally applied energy. This innovative approach introduces a new theory of interfacial reinforcement compatibility, advancing the development of high-performance and sustainable biocomposites.


Subject(s)
Biocompatible Materials , Biocompatible Materials/chemistry , Butadienes/chemistry , Materials Testing , Cross-Linking Reagents/chemistry , Sasa/chemistry , Polymers/chemistry , Temperature , Water/chemistry , Adipates/chemistry , Tensile Strength
8.
Toxicol Appl Pharmacol ; 490: 117035, 2024 Sep.
Article in English | MEDLINE | ID: mdl-39019094

ABSTRACT

Exposure to particulate matter (PM10) can induce respiratory diseases that are closely related to bronchial hyperresponsiveness. However, the involved mechanism remains to be fully elucidated. This study aimed to demonstrate the effects of PM10 on the acetylcholine muscarinic 3 receptor (CHRM3) expression and the role of the ERK1/2 pathway in rat bronchial smooth muscle. A whole-body PM10 exposure system was used to stimulate bronchial hyperresponsiveness in rats for 2 and 4 months, accompanied by MEK1/2 inhibitor U0126 injection. The whole-body plethysmography system and myography were used to detect the pulmonary and bronchoconstrictor function, respectively. The mRNA and protein levels were determined by Western blotting, qPCR, and immunofluorescence. Enzyme-linked immunosorbent assay was used to detect the inflammatory cytokines. Compared with the filtered air group, 4 months of PM10 exposure significantly increased CHRM3-mediated pulmonary function and bronchial constriction, elevated CHRM3 mRNA and protein expression levels on bronchial smooth muscle, then induced bronchial hyperreactivity. Additionally, 4 months of PM10 exposure caused an increase in ERK1/2 phosphorylation and increased the secretion of inflammatory factors in bronchoalveolar lavage fluid. Treatment with the MEK1/2 inhibitor, U0126 inhibited the PM10 exposure-induced phosphorylation of the ERK1/2 pathway, thereby reducing the PM10 exposure-induced upregulation of CHRM3 in bronchial smooth muscle and CHRM3-mediated bronchoconstriction. U0126 could rescue PM10 exposure-induced pathological changes in the bronchus. In conclusion, PM10 exposure can induce bronchial hyperresponsiveness in rats by upregulating CHRM3, and the ERK1/2 pathway may be involved in this process. These findings could reveal a potential therapeutic target for air pollution induced respiratory diseases.


Subject(s)
Bronchial Hyperreactivity , Particulate Matter , Receptor, Muscarinic M3 , Animals , Bronchial Hyperreactivity/chemically induced , Bronchial Hyperreactivity/physiopathology , Bronchial Hyperreactivity/metabolism , Male , Particulate Matter/toxicity , Receptor, Muscarinic M3/metabolism , Receptor, Muscarinic M3/genetics , Rats , Up-Regulation/drug effects , Bronchi/drug effects , Bronchi/metabolism , Bronchi/pathology , Rats, Sprague-Dawley , MAP Kinase Signaling System/drug effects , Muscle, Smooth/drug effects , Muscle, Smooth/metabolism , Bronchoconstriction/drug effects , Cytokines/metabolism , Cytokines/genetics , Butadienes , Nitriles
9.
Glob Chang Biol ; 30(7): e17416, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38994730

ABSTRACT

Climate change is exposing subarctic ecosystems to higher temperatures, increased nutrient availability, and increasing cloud cover. In this study, we assessed how these factors affect the fluxes of greenhouse gases (GHGs) (i.e., methane (CH4), nitrous oxide (N2O), and carbon dioxide (CO2)), and biogenic volatile organic compounds (BVOCs) in a subarctic mesic heath subjected to 34 years of climate change related manipulations of temperature, nutrient availability, and light. GHGs were sampled from static chambers and gases analyzed with gas chromatograph. BVOCs were measured using the push-pull method and gases analyzed with chromatography-mass spectrometry. The soil temperature and moisture content in the warmed and shaded plots did not differ significantly from that in the controls during GHG and BVOC measurements. Also, the enclosure temperatures during BVOC measurements in the warmed and shaded plots did not differ significantly from temperatures in the controls. Hence, this allowed for assessment of long-term effects of the climate treatment manipulations without interference of temperature and moisture differences at the time of measurements. Warming enhanced CH4 uptake and the emissions of CO2, N2O, and isoprene. Increased nutrient availability increased the emissions of CO2 and N2O but caused no significant changes in the fluxes of CH4 and BVOCs. Shading (simulating increased cloudiness) enhanced CH4 uptake but caused no significant changes in the fluxes of other gases compared to the controls. The results show that climate warming and increased cloudiness will enhance CH4 sink strength of subarctic mesic heath ecosystems, providing negative climate feedback, while climate warming and enhanced nutrient availability will provide positive climate feedback through increased emissions of CO2 and N2O. Climate warming will also indirectly, through vegetation changes, increase the amount of carbon lost as isoprene from subarctic ecosystems.


Subject(s)
Climate Change , Greenhouse Gases , Nutrients , Volatile Organic Compounds , Greenhouse Gases/analysis , Volatile Organic Compounds/analysis , Nutrients/analysis , Tundra , Methane/analysis , Carbon Dioxide/analysis , Global Warming , Temperature , Butadienes , Hemiterpenes
10.
J Vis Exp ; (208)2024 Jun 28.
Article in English | MEDLINE | ID: mdl-39007608

ABSTRACT

Viscoelastic behavior can be beneficial in enhancing the unprecedented dynamics of polymer metamaterials or, in contrast, negatively impacting their wave control mechanisms. It is, therefore, crucial to properly characterize the viscoelastic properties of a polymer metamaterial at its working frequencies to understand viscoelastic effects. However, the viscoelasticity of polymers is a complex phenomenon, and the data on storage and loss moduli at ultrasonic frequencies are extremely limited, especially for additively manufactured polymers. This work presents a protocol to experimentally characterize the viscoelastic properties of additively manufactured polymers and to use them in the numerical analysis of polymer metamaterials. Specifically, the protocol includes the description of the manufacturing process, experimental procedures to measure the thermal, viscoelastic, and mechanical properties of additively manufactured polymers, and an approach to use these properties in finite-element simulations of the metamaterial dynamics. The numerical results are validated in ultrasonic transmission tests. To exemplify the protocol, the analysis is focused on acrylonitrile butadiene styrene (ABS) and aims at characterizing the dynamic behavior of a simple metamaterial made from it by using fused deposition modeling (FDM) three-dimensional (3D) printing. The proposed protocol will be helpful for many researchers to estimate viscous losses in 3D-printed polymer elastic metamaterials that will improve the understanding of material-property relations for viscoelastic metamaterials and eventually stimulate the use of 3D-printed polymer metamaterial parts in various applications.


Subject(s)
Elasticity , Viscosity , Printing, Three-Dimensional , Butadienes/chemistry , Polymers/chemistry , Acrylic Resins/chemistry , Finite Element Analysis , Manufactured Materials , Polystyrenes
11.
Exp Dermatol ; 33(7): e15128, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38973249

ABSTRACT

Dry skin is common to many pruritic diseases and is difficult to improve with oral traditional antihistamines. Recently, increasing evidence indicated that histamine H4 receptor (H4R) plays an important role in the occurrence and development of pruritus. Extracellular signal-regulated kinase (ERK) phosphorylation activation in the spinal cord mediates histamine-induced acute and choric itch. However, whether the histamine H4 receptor regulates ERK activation in the dry skin itch remains unclear. In the study, we explore the role of the histamine H4 receptor and p-ERK in the spinal cord in a dry skin mouse model induced by acetone-ether-water (AEW). q-PCR, Western blot, pharmacology and immunofluorescence  were applied in the study. We established a dry skin itch model by repeated application of AEW on the nape of neck in mice. The AEW mice showed typically dry skin histological change and persistent spontaneous scratching behaviour. Histamine H4 receptor, instead of histamine H1 receptor, mediated spontaneous scratching behaviour in AEW mice. Moreover, c-Fos and p-ERK expression in the spinal cord neurons were increased and co-labelled with GRPR-positive neurons in AEW mice. Furthermore, H4R agonist 4-methyhistamine dihydrochloride (4-MH)induced itch. Both 4-MH-induced itch and the spontaneous itch in AEW mice were blocked by p-ERK inhibitor U0126. Finally, intrathecal H4R receptor antagonist JNJ7777120 inhibited spinal p-ERK expression in AEW mice. Our results indicated that spinal H4R mediates itch via ERK activation in the AEW-induced dry skin mice.


Subject(s)
Acetone , Extracellular Signal-Regulated MAP Kinases , Pruritus , Receptors, Histamine H4 , Spinal Cord , Animals , Pruritus/chemically induced , Pruritus/metabolism , Receptors, Histamine H4/metabolism , Mice , Spinal Cord/metabolism , Extracellular Signal-Regulated MAP Kinases/metabolism , Male , Acetone/pharmacology , Water , Ether , Disease Models, Animal , Phosphorylation , Indoles/pharmacology , Butadienes/pharmacology , Piperazines/pharmacology , Nitriles/pharmacology , Skin/metabolism , Chronic Disease , Methylhistamines , Proto-Oncogene Proteins c-fos/metabolism , Mice, Inbred C57BL
12.
Environ Sci Technol ; 58(31): 13783-13794, 2024 Aug 06.
Article in English | MEDLINE | ID: mdl-39042817

ABSTRACT

As cities strive for ambitious increases in tree canopy cover and reductions in anthropogenic volatile organic compound (AVOC) emissions, accurate assessments of the impacts of biogenic VOCs (BVOCs) on air quality become more important. In this study, we aim to quantify the impact of future urban greening on ozone production. BVOC emissions in dense urban areas are often coarsely represented in regional models. We set up a high-resolution (30 m) MEGAN (The Model of Emissions of Gases and Aerosols from Nature version 3.2) to estimate summertime biogenic isoprene emissions in the New York City metro area (NYC-MEGAN). Coupling an observation-constrained box model with NYC-MEGAN isoprene emissions successfully reproduced the observed isoprene concentrations in the city core. We then estimated future isoprene emissions from likely urban greening scenarios and evaluated the potential impact on future ozone production. NYC-MEGAN predicts up to twice as much isoprene emissions in NYC as the coarse-resolution (1.33 km) Biogenic Emission Inventory System version 3.61 (BEIS) on hot summer days. We find that BVOCs drive ozone production on hot summer days, even in the city core, despite large AVOC emissions. If high isoprene emitting species (e.g., oak trees) are planted, future isoprene emissions could increase by 1.4-2.2 times in the city core, which would result in 8-19 ppbv increases in peak ozone on ozone exceedance days with current NOx concentrations. We recommend planting non- or low-isoprene emitting trees in cities with high NOx concentrations to avoid an increase in the frequency and severity of future ozone exceedance events.


Subject(s)
Air Pollutants , Ozone , Seasons , Volatile Organic Compounds , New York City , Air Pollutants/analysis , Ozone/analysis , Volatile Organic Compounds/analysis , Environmental Monitoring , Butadienes/analysis , Hemiterpenes/analysis , Pentanes
13.
Front Public Health ; 12: 1408842, 2024.
Article in English | MEDLINE | ID: mdl-39071151

ABSTRACT

Three-dimensional (3D) printers have become popular educational tools in secondary and post-secondary STEM curriculum; however, concerns have emerged regarding inhalation exposures and associated health risks. Current evidence suggests that filament materials and site conditions may cause differences in the chemical profiles and toxicological properties of 3D printer emissions; however, few studies have evaluated exposures directly in the classroom. In this study, we monitored and sampled particulate matter (PM) emitted from acrylonitrile-butadiene-styrene (ABS) and polylactic acid (PLA) filaments during a 3-hour 3D printing session in a high school classroom using aerosol monitoring instrumentation and collection media. To evaluate potential inhalation risks, Multiple Path Particle Dosimetry (MPPD) modeling was used to estimate inhaled doses and calculate in vitro concentrations based on the observed aerosol data and specific lung and breathing characteristics. Dynamic light scattering was used to evaluate the hydrodynamic diameter, zeta potential, and polydispersity index (PDI) of extracted PM emissions dispersed in cell culture media. Small airway epithelial cells (SAEC) were employed to determine cellular viability, genotoxic, inflammatory, and metabolic responses to each emission exposure using MTS, ELISA, and high-performance liquid chromatography-mass spectrometry (HPLC-MS), respectively. Aerosol monitoring data revealed that emissions from ABS and PLA filaments generated similar PM concentrations within the ultrafine and fine ranges. However, DLS analysis showed differences in the physicochemical properties of ABS and PLA PM, where the hydrodynamic diameter of PLA PM was greater than ABS PM, which may have influenced particle deposition rates and cellular outcomes. While exposure to both ABS and PLA PM reduced cell viability and induced MDM2, an indicator of genomic instability, PLA PM alone increased gamma-H2AX, a marker of double-stranded DNA breaks. ABS and PLA emissions also increased the release of pro-inflammatory cytokines, although this did not reach significance. Furthermore, metabolic profiling via high performance liquid chromatography-mass spectrometry (HPLC-MS) and subsequent pathway analysis revealed filament and dose dependent cellular metabolic alterations. Notably, our metabolomic analysis also revealed key metabolites and pathways implicated in PM-induced oxidative stress, DNA damage, and respiratory disease that were perturbed across both tested doses for a given filament. Taken together, these findings suggest that use of ABS and PLA filaments in 3D printers within school settings may potentially contribute to adverse respiratory responses especially in vulnerable populations.


Subject(s)
Epithelial Cells , Particulate Matter , Printing, Three-Dimensional , Humans , Epithelial Cells/metabolism , Particulate Matter/toxicity , Inhalation Exposure/adverse effects , Aerosols , Butadienes , Polyesters
14.
Macromol Rapid Commun ; 45(16): e2400226, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38837553

ABSTRACT

Coordinative chain transfer polymerization (CCTP) of ethylene and its copolymerization with 1,3-butadiene is conducted in toluene at 80 °C using a combination of {(Me2Si(C13H8)2)Nd(µ-BH4)[(µ-BH4)Li(THF)]}2 (1) metal complex and various organomagnesium compounds used as chain transfer agents including n-butyl-n-octyl-magnesium (BOMAG), n-butyl-mesityl-magnesium (n-BuMgMes), n-butyl-magnesium chloride (n-BuMgCl), n-pentyl-magnesium bromide (n-C5H11MgBr), pentanediyl-1,5-di(magnesium bromide) (PDMB) and isobutyl-magnesium chloride (i-BuMgCl). Kinetics and performance in terms of control of the (co)polymerization are comparatively discussed particularly considering the presence of ether and the nature of the organomagnesium compounds employed. Taking advantage of the well-known reactivity between nitrile and molecular organomagnesium compounds, the functionalization of the chains is further carried out by deactivation of the polymerization medium with benzonitrile or methoxybenzonitrile compounds leading to ketone ω-functionalized chains. The success of the functionalizations is extended to coupling strategies using dinitrile reagents and to the functionalization of high molar mass ethylene butadiene rubber (EBR).


Subject(s)
Butadienes , Nitriles , Polymerization , Nitriles/chemistry , Butadienes/chemistry , Molecular Structure , Ethylenes/chemistry , Polyenes/chemistry , Kinetics
15.
Int J Mol Sci ; 25(11)2024 May 23.
Article in English | MEDLINE | ID: mdl-38891846

ABSTRACT

Tumor recurrence and drug resistance are responsible for poor prognosis in colorectal cancer (CRC). DNA mismatch repair (MMR) deficiency or elevated interleukin-8 (IL-8) levels are characteristics of CRCs, which have been independently correlated with treatment resistance to common therapies. We recently demonstrated significantly impaired therapeutical response and increased IL-8 release of CRC cell lines with reduced expression of MMR protein MLH1 as well as cytoskeletal non-erythrocytic spectrin alpha II (SPTAN1). In the present study, decreased intratumoral MLH1 and SPTAN1 expression in CRCs could be significantly correlated with enhanced serum IL-8. Furthermore, using stably reduced SPTAN1-expressing SW480, SW620 or HT-29 cell lines, the RAS-mediated RAF/MEK/ERK pathway was analyzed. Here, a close connection between low SPTAN1 expression, increased IL-8 secretion, enhanced extracellular-signal-regulated kinase (ERK) phosphorylation and a mesenchymal phenotype were detected. The inhibition of ERK by U0126 led to a significant reduction in IL-8 secretion, and the combination therapy of U0126 with FOLFOX optimizes the response of corresponding cancer cell lines. Therefore, we hypothesize that the combination therapy of FOLFOX and U0126 may have great potential to improve drug efficacy on this subgroup of CRCs, showing decreased MLH1 and SPTAN1 accompanied with high serum IL-8 in affected patients.


Subject(s)
Butadienes , Colorectal Neoplasms , Fluorouracil , Interleukin-8 , Nitriles , Humans , Colorectal Neoplasms/drug therapy , Colorectal Neoplasms/metabolism , Colorectal Neoplasms/pathology , Colorectal Neoplasms/genetics , Interleukin-8/metabolism , Interleukin-8/genetics , Fluorouracil/pharmacology , Fluorouracil/therapeutic use , Butadienes/pharmacology , Nitriles/pharmacology , Cell Line, Tumor , Organoplatinum Compounds/pharmacology , Organoplatinum Compounds/therapeutic use , Leucovorin/therapeutic use , Leucovorin/pharmacology , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Antineoplastic Combined Chemotherapy Protocols/pharmacology , Female , Male , Extracellular Signal-Regulated MAP Kinases/metabolism , HT29 Cells , MAP Kinase Signaling System/drug effects , MutL Protein Homolog 1/metabolism , MutL Protein Homolog 1/genetics , Middle Aged , Aged , Gene Expression Regulation, Neoplastic/drug effects , Phosphorylation/drug effects
16.
Sci Rep ; 14(1): 12899, 2024 06 05.
Article in English | MEDLINE | ID: mdl-38839853

ABSTRACT

While volatile organic compounds (VOCs) impair various organs, their influence on hearing loss (HL) has not been extensively researched. We aimed to identify the association between VOCs and HL or high-frequency hearing loss (HFHL). We extracted data on age, sex, pure tone audiometry, hypertension, occupational noise exposure, and creatinine-corrected urine VOC metabolite concentrations from the eighth Korea National Health and Nutrition Survey. Among the VOC metabolites, N-acetyl-S-(benzyl)-L-cysteine (BMA, P = 0.004), N-acetyl-S-(phenyl)-L-cysteine (SPMA, P = 0.027), and N-acetyl-S-(3,4-dihydroxybutyl)-L-cysteine (DHBMA, P < 0.001) showed associations with HL. Additionally, HFHL exhibited significant associations with BMA (P = 0.005), 3- and 4-methylhippuric acid (3, 4 MHA, P = 0.049), mandelic acid (MA, P = 0.015), SPMA (P < 0.001), N-acetyl-S-(3-hydroxypropyl)-L-cysteine (3-HPMA, P < 0.001), and DHBMA (P < 0.001). After controlling other factors, DHBMA were associated with HL (P = 0.021) and HFHL (P = 0.014) and exhibited a linear association with the mean hearing level (ß = 0.054, P = 0.024) and high-frequency hearing level (ß = 0.045, P = 0.037). Since 1,3-butadiene may act as an ototoxic material, early screening for workers exposed to 1,3-butadiene and reducing exposure to 1,3-butadiene in everyday life may be helpful to prevent further HL.


Subject(s)
Butadienes , Hearing Loss , Volatile Organic Compounds , Humans , Female , Male , Middle Aged , Hearing Loss/chemically induced , Hearing Loss/etiology , Volatile Organic Compounds/urine , Volatile Organic Compounds/adverse effects , Republic of Korea/epidemiology , Adult , Occupational Exposure/adverse effects , Occupational Exposure/analysis , Aged , Nutrition Surveys , Audiometry, Pure-Tone
17.
An Acad Bras Cienc ; 96(3): e20230387, 2024.
Article in English | MEDLINE | ID: mdl-38865508

ABSTRACT

The blend of butadiene and acrylonitrile copolymer (NBR) with natural poly-cis-isoprene (NR) shows increased resistance to swelling in solvents in comparison to the individual components. In aerospace, NBR rubber is used as thermal protection for rockets and shall not contain other polymers, even in low contents, otherwise, it can affect the protection performance and rocket safety by causing detachment of the elastomer/propellant interface; therefore, this investigation presents methodologies to determine the NR/NBR contents. This study explores different analytical techniques, such as Raman spectroscopy and Fourier transform infrared (FTIR) spectroscopy, in the mid-infrared (MIR) by reflection and in the near-infrared by reflectance (NIRA) modes, Furthermore, quantification strategies by univariate, bivariate and multivariate (chemometric) models are evaluated and compared. A proposed methodology, based on multivariate Raman microscopy with partial least squares regression (PLS), showed high linearity (R2 > 0.99) and low error (< 0.82 %). The validation of FT-MIR data for the CH3, which presented lower error (1.3%) than vinylidene band (6%), showed that both methodologies (reflection and NIRA reflectance) can be used for the quantification of NR in NR/NBR. These results constitute a contribution to the state of the art in researching industrial and aerospace elastomeric applications.


Subject(s)
Rubber , Spectrum Analysis, Raman , Spectrum Analysis, Raman/methods , Rubber/chemistry , Spectroscopy, Fourier Transform Infrared/methods , Butadienes/chemistry , Butadienes/analysis
18.
Ecotoxicol Environ Saf ; 280: 116545, 2024 Jul 15.
Article in English | MEDLINE | ID: mdl-38850709

ABSTRACT

Isoprenoid metabolism and its derivatives took part in photosynthesis, growth regulation, signal transduction, and plant defense to biotic and abiotic stresses. However, how aluminum (Al) stress affects the isoprenoid metabolism and whether isoprenoid metabolism plays a vital role in the Citrus plants in coping with Al stress remain unclear. In this study, we reported that Al-treatment-induced alternation in the volatilization rate of monoterpenes (α-pinene, ß-pinene, limonene, α-terpinene, γ-terpinene and 3-carene) and isoprene were different between Citrus sinensis (Al-tolerant) and C. grandis (Al-sensitive) leaves. The Al-induced decrease of CO2 assimilation, maximum quantum yield of primary PSII photochemistry (Fv/Fm), the lower contents of glucose and starch, and the lowered activities of enzymes involved in the mevalonic acid (MVA) pathway and 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway might account for the different volatilization rate of isoprenoids. Furthermore, the altered transcript levels of genes related to isoprenoid precursors and/or derivatives metabolism, such as geranyl diphosphate (GPP) synthase (GPPS) in GPP biosynthesis, geranylgeranyl diphosphate synthase (GGPPS), chlorophyll synthase (CHS) and GGPP reductase (GGPPR) in chlorophyll biosynthesis, limonene synthase (LS) and α-pinene synthase (APS) in limonene and α-pinene synthesis, respectively, might be responsible for the different contents of corresponding products in C. grandis and C. sinensis. Our data suggested that isoprenoid metabolism was involved in Al tolerance response in Citrus, and the alternation of some branches of isoprenoid metabolism could confer different Al-tolerance to Citrus species.


Subject(s)
Aluminum , Bicyclic Monoterpenes , Citrus , Limonene , Photosynthesis , Plant Leaves , Terpenes , Aluminum/toxicity , Terpenes/metabolism , Citrus/metabolism , Citrus/drug effects , Limonene/metabolism , Photosynthesis/drug effects , Bicyclic Monoterpenes/metabolism , Plant Leaves/metabolism , Plant Leaves/drug effects , Stress, Physiological/drug effects , Monoterpenes/metabolism , Hemiterpenes/metabolism , Cyclohexenes/metabolism , Sugar Phosphates/metabolism , Butadienes/metabolism , Erythritol/analogs & derivatives , Erythritol/metabolism , Mevalonic Acid/metabolism , Cyclohexane Monoterpenes , Citrus sinensis/metabolism , Citrus sinensis/drug effects , Citrus sinensis/genetics , Chlorophyll/metabolism , Alkyl and Aryl Transferases/metabolism , Alkyl and Aryl Transferases/genetics , Volatilization
19.
Environ Sci Process Impacts ; 26(7): 1147-1155, 2024 Jul 17.
Article in English | MEDLINE | ID: mdl-38856669

ABSTRACT

Isoprene is the most relevant volatile organic compound emitted during the biosynthesis of metabolism processes. The oxidation of isoprene by a hydroxy radical (OH) is one of the main consumption schemes that generate six isomers of isoprene hydroxy hydroperoxide radicals (ISOPOOs). In this study, the rate constants of ISOPOOs + sulphur dioxide (SO2) reactions that eventually generate sulphur trioxide (SO3), the precursor of sulphate aerosol (SO42-(p)), are determined using microcanonical kinetic theories coupled with molecular structures and energies estimated by quantum chemical calculations. The results show that the reaction rates range from 10-27 to 10-20 cm3 molecule-1 s-1, depending on the atmospheric temperature and structure of the six ISOPOO isomers. The effect of SO3 formation from SO2 oxidation by ISOPOOs on the atmosphere is evaluated by a global chemical transport model, along with the rate constants obtained from microcanonical kinetic theories. The results show that SO3 formation is enhanced in regions with high SO2 or low nitrogen oxide (NO), such as China, the Middle East, and Amazon rainforests. However, the production rates of SO3 formation by ISOPOOs + SO2 reactions are eight orders of magnitude lower than that from the OH + SO2 reaction. This is indicative of SO42-(p) formation from the direct oxidation of SO2 by ISOPOOs, which is almost negligible in the atmosphere. The results of this study entail a detailed analysis of SO3 formation from gas-phase reactions of isoprene-derived products.


Subject(s)
Air Pollutants , Atmosphere , Butadienes , Hemiterpenes , Sulfates , Sulfur Dioxide , Sulfur Dioxide/chemistry , Hemiterpenes/chemistry , Kinetics , Butadienes/chemistry , Air Pollutants/chemistry , Atmosphere/chemistry , Sulfates/chemistry , Models, Chemical , Hydrogen Peroxide/chemistry , Oxidation-Reduction , Pentanes/chemistry , Hydroxyl Radical/chemistry
20.
Cardiovasc Toxicol ; 24(8): 766-775, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38850470

ABSTRACT

Cognitive impairment is a commonly observed complication following myocardial infarction; however, the underlying mechanisms are still not well understood. The most recent research suggests that extracellular signal-regulated kinase (ERK) plays a critical role in the development and occurrence of cognitive dysfunction-related diseases. This study aims to explore whether the ERK inhibitor U0126 targets the ERK/Signal Transducer and Activator of Transcription 1 (STAT1) pathway to ameliorate cognitive impairment after myocardial infarction. To establish a mouse model of myocardial infarction, we utilized various techniques including Echocardiography, Hematoxylin-eosin (HE) staining, Elisa, Open field test, Elevated plus maze test, and Western blot analysis to assess mouse cardiac function, cognitive function, and signal transduction pathways. For further investigation into the mechanisms of cognitive function and signal transduction, we administered the ERK inhibitor U0126 via intraperitoneal injection. Reduced total distance and activity range were observed in mice subjected to myocardial infarction during the open field test, along with decreased exploration of the open arms in the elevated plus maze test. However, U0126 treatment exhibited a significant improvement in cognitive decline, indicating a protective effect through the inhibition of the ERK/STAT1 signaling pathway. Hence, this study highlights the involvement of the ERK/STAT1 pathway in regulating cognitive dysfunction following myocardial infarction and establishes U0126 as a promising therapeutic target.


Subject(s)
Behavior, Animal , Butadienes , Cognition , Disease Models, Animal , Extracellular Signal-Regulated MAP Kinases , Mice, Inbred C57BL , Myocardial Infarction , Nitriles , STAT1 Transcription Factor , Animals , Myocardial Infarction/enzymology , Myocardial Infarction/physiopathology , Myocardial Infarction/pathology , Myocardial Infarction/drug therapy , Cognition/drug effects , Nitriles/pharmacology , Male , Butadienes/pharmacology , Extracellular Signal-Regulated MAP Kinases/metabolism , Extracellular Signal-Regulated MAP Kinases/antagonists & inhibitors , Behavior, Animal/drug effects , STAT1 Transcription Factor/metabolism , STAT1 Transcription Factor/antagonists & inhibitors , Protein Kinase Inhibitors/pharmacology , Cognitive Dysfunction/drug therapy , Cognitive Dysfunction/physiopathology , Cognitive Dysfunction/etiology , Cognitive Dysfunction/enzymology , Cognitive Dysfunction/prevention & control , Signal Transduction/drug effects , Elevated Plus Maze Test , Open Field Test/drug effects , Mice
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