Reactive Oxygen Generation Research Articles

Insights on bacteria inactivation in water by cold plasma: Effect of water matrix and pulsed plasmas waveform on physicochemical water properties, species formation and inactivation efficiency of Escherichia coli

This study investigates the inactivation of Escherichia coli (E. coli) using pulsed dielectric barrier discharges (DBDs) powered by high-voltage nanosecond and/or microsecond pulses to establish optimal operational conditions. The effects of pulse voltage waveform and water matrix (distilled vs. tap water) were evaluated in terms of inactivation efficiency and energy consumption, along with the generation of reactive oxygen and nitrogen species (RONS). Complete E. coli inactivation (9-log CFU/ml) in distilled water was achieved within 20 min of nanopulsed-DBD treatment, coinciding with rapid acidification, while in tap water, 90 min was required for complete inactivation. Interestingly, at treatment times with similar pH levels between water types, E. coli inactivation was more effective in tap water. Ozone concentrations showed the most significant difference, being ∼6 times higher in distilled water (10.3 mg/L) than in tap water (1.7 mg/L). Although distilled and tap water had similar concentrations of short- and long-lived plasma species, the differing inactivation efficiencies indicate a synergistic effect between pH reduction and reactive species in impairing E. coli functionality. Micropulsed-DBD led to increased concentration of plasma species, faster acidification and inactivation in tap water (complete inactivation within 8 min), but at significantly higher electrical energy per order (56.9 kWh/m3 compared to 17.4 kWh/m3 for nanopulsed-DBD). The lowest energy per order was recorded for nanopulsed-DBD in distilled water, at 3.8 kWh/m³, highlighting pulsed-DBD plasma as a safe and energy-efficient method for water disinfection. This study offers valuable insights into using an innovative, sustainable plasma-based approach for bacterial inactivation.

Understanding roles of π electron delocalization and hybridization transformation of nanodiamond in carbocatalysis-mediated persulfate activation regime

Carbocatalysis-mediated persulfate (PS) activation for micropollutant abatement has gained extensive attention, commonly concentrating on carbocatalysts surface chemistry but overlooking intrinsic characteristics, e.g., electron orbital and hybridization configurations. Herein, nanodiamond (ND) composed of sp3-hybridized carbon undergoes annealing processes from 300 to 1500 °C, to improve catalytic performances in PS activation significantly toward degrading bisphenol A (BPA), benefiting from ND hybridization transformation from sp3 to sp2 with increasing chemical and electrical activities via converting σ to π electrons and delocalizing π electrons with increasing annealing temperature. NDs with sp3 hybridization activate PS to drive direct electron transfer pathways, serving as electron mediators to facilitate PS to deprive electrons from BPA. Localized and delocalized π electrons were responsible for the generation of reactive surface-bound complexes and singlet oxygen, respectively. The controllability of ND hybridization structure provides a feasible strategy to regulate PS activation pathways based on the reactivity affinity of reactive species toward micropollutants.

EXTH-71. A MECHANISTIC INVESTIGATION INTO AUGER THERAPY: 2-DIMENSIONAL THIN-FILMS TO CHARACTERIZE THERAPEUTIC RANGEIN VITRO

Abstract Metallic nanoparticles can improve the accuracy and effectiveness of conventional radiotherapy in the treatment of solid tumors through a light-matter interaction known as the Auger effect. In this work, we present the assembly of an iron oxide (Fe3O4) nanoparticle (NPs) layer within a biocompatible polyelectrolyte film using ionic self-assembly to enable the spatial separation of NPs from their target cells. Films exhibited uniform nanoparticle coverage as well as strong stability in cell culture conditions. To investigate the applicability of NMDR with non-internalized NPs, conditions with (NP-PEM) and without (PEM) embedded nanoparticles were used to evaluate the therapeutic effect of physically separated nanoparticles on cells cultured on the film surface via a measure of intracellular reactive oxygen (ROS) generation and histone phosphorylation (yH2AX) after irradiation from a 137Cesium source. Cells cultured on NP-PEM demonstrated a 78.4% increase in ROS generation when compared to cells cultured on PEM films. When adjusting for cell count, NP-PEM films induce 70.5% greater ROS generation. In investigating nanoparticle-mediated deposition of radiation (NMDR), these films allow for the determination of the extent of the therapeutic effect when NPs are not internalized into their targeted cells, potentially providing indications with respect to off-target effects. Cells were irradiated on films with nanoparticle distances from 25.9 nm to 97.5 nm to interrogate the NMDR effect size at a range of distances. yH2AX phosphorylation exhibited an exponential decay until 69.8 nm, where there was no difference when compared to nanoparticle-free films. This work highlights the ability of iron oxide NPs to deliver NMDR at a known, quantifiable distance, providing insights for further translational applications.

Design and construction of a continuous industrial scale cold plasma equipment for fresh produce industry

This study presents the design, construction, and evaluation of a novel continuous industrial-scale cold plasma system optimized for the treatment of fresh produce. The system integrates multiple plasma modules with a multipin-to-plate discharge configuration, ensuring efficient generation of reactive oxygen and nitrogen species at relatively low voltages. The cold plasma modules are combined with a conveyor mechanism, allowing for continuous, uniform exposure of irregularly shaped food items, such as tomatoes, to reactive plasma species. Notably, the system operates using ambient air, and incorporates modularity for easy scalability, making it suitable for both small-scale enterprises and large-scale industrial applications.Experimental trials on tomatoes demonstrated reductions in microbial load, with the system effectively enhancing product safety while minimizing power consumption. Moreover, the integration of cold storage further extended shelf life, although optimization of plasma treatment parameters remains necessary to preserve bioactive compounds like lycopene and ascorbic acid. This research fills a critical gap in scaling cold plasma technology for industrial use, providing a sustainable and energy-efficient solution for food disinfection. The results highlight the potential of this system to meet industry demands for safe and efficient on-farm and small-scale enterprise disinfection.

Design of a continuous plasma activated water (PAW) disinfection system for fresh produce industry

This study introduces an innovative, industrial-scale continuous Plasma Activated Water (PAW) system, specifically designed for the fresh produce industry and optimized for micro to small enterprises. The system leverages a novel non-uniform electrode design to enhance average field strength, driving the efficient generation of reactive oxygen and nitrogen species (RONS) for steady-state PAW production. Key components include a venturi bubble generator for optimized gas-liquid interaction and a plasma reactor integrated with a continuous spray and drying setup, enabling consistent PAW production and application. Our preliminary results indicate about 1.5 log10 CFU/g decrease in microbial load on treated produce, which further decreased to 2.5 log10 CFU/g towards the end of storage life for tomatoes, with 20 kV applied to the reactors and a total residence time of 20 min. An evaluation of the maximum energy consumption of system indicated a process cost contribution of less than $0.5 per ton of treated produce. The promising initial results, scalable design, cost-effectiveness and sustainability aspects make this technology suitable for improving food safety while reducing chemical usage.

Impact of singular versus combinatorial environmental stress on RONS generation in Drosophila melanogaster larvae.

We investigated environmentally correlated abiotic stressor desiccation (D), heat (H), and starvation (S) in the generation of reactive oxygen and nitrogen species (RONS) using Drosophila melanogaster larvae as an experimental model, subjected to either individual stressors or exposed to a combinatorial form of stressors (D + H, H + S, and D + S). The study was also extended to find synergistic endpoints where the impacts of all three stressors (D + H + S) were exerted simultaneously. We estimated the lethal time (LT20) at specific doses using regression and probit analyses based on the larval survival. LT20 values were used as the base-level parameter for further oxidative stress experimental analysis work. First, all stressors led to the activation of a typical common oxidative stress-mediated response irrespective of the mode of exposure. As envisaged, D. melanogaster larvae exhibited a homeostatic stress tolerance mechanism, triggering an antioxidant defense mechanism, indicated by an elevated level of total antioxidant capacity and enhanced activities of superoxide dismutase, catalase, glutathione reductase, and glutathione peroxidase. In all types of stress-exposed regimes, we found a negative impact of stressors on the activity of mitochondrial enzyme aconitase. Elevated levels of other oxidative stress markers, viz., lipid peroxidation, protein carbonyl content, and advanced oxidative protein products, were obvious although the increment was treatment-specific. Desiccation stress proved to be the most dominant stressor compared to heat and starvation. Among the combination of stressors, rather than a single stressor, D + H impacted more than other binary stress exposures. Focusing on the impact of singular versus combinatorial stress exposure on RONS generation, we observed an increase in the RONS level in both singular and combinatorial forms of stress exposure although the magnitude of the increment varied with the nature of stressors and their combinations. The present study indicated an "additive" effect when all three stressors (D + H + S) operate simultaneously, rather than a "synergistic" effect.

Solar powered electrocatalytic treatment of actual human urine coupled with hydrogen production using Ti/MMO for the removal of nitrogen-based compounds

This study addresses a significant micropollutant removal from actual human urine (AHU) through photovoltaic driven electrochemical treatment. This study showed significant reductions of 69.09 % urea, 67.95 % creatinine, and 95.180 % uric acid under optimal continuous recirculation conditions. Analysis revealed that the degradation of pollutants were facilitated by in-situ generation of reactive oxygen and chlorine species during treatment. Further, the procedure employed with molecular hydrogen generation during anodic oxidation as useful byproduct. Thus, the findings suggest that novel mixed metal oxide exhibits high efficacy for AHU treatment, offering a prominent concept for onsite treatment of complex mixed wastewater in real-life applications.

Effect of Plasma-Activated Water (PAW) Generated Using Non-Thermal Atmospheric Plasma on Phytopathogenic Bacteria.

Plasma-activated water (PAW) exhibits potent antimicrobial properties attributed to the generation of diverse reactive oxygen and nitrogen species. This study assessed the effectiveness of PAW in vitro against phytopathogenic Xanthomonas arboricola and Pseudomonas syringae pv. syringae, which cause diseases on ornamental plants. Extending the plasma activation time of water and the incubation time of bacterial suspension in PAW increased the effectiveness of PAW. Treatments consisting of PAW activation using a power output of 200 Watts and a frequency of 50 Hz at different activation times and target population incubation times revealed significantly different effectiveness against P. syringae pv. syringae and X. arboricola. X. arboricola (reduction of 4.946 ± 0.20 log10 CFU/mL) was more sensitive to PAW inactivation than P. syringae pv. syringae (reduction of 3 ± 0.15 log10 CFU/mL). The plasma activation of water for 20 min followed by incubation of bacterial population for 180 min was proven to be the most effective treatment combination. The plasma activation time dose required to reduce the population by 90% was 7.47 ± 1.09 min for P. syringae pv. syringae and 4.45 ± 1.81 min for X. arboricola incubated for 180 min in PAW. The results of this study have the potential to further contribute to assessment of the effects of PAW on pathogen infected plant tissues. In addition, the findings of this study could aid in further characterization of the reactive species formed during the plasma activation of water.

Exploring the Potential of Al(III) Photosensitizers for Energy Transfer Reactions.

Three homoleptic Al(III) complexes (Al1-Al3) with different degrees of methylation at the 2-pyridylpyrrolide ligand were systematically tested for their function as photosensitizers (PS) in two types of energy transfer reactions. First, in the generation of reactive singlet oxygen (1O2), and second, in the isomerization of (E)- to (Z)-stilbene. 1O2 was directly evidenced by its characteristic NIR emission at around 1276 nm and indirectly by the reaction with an organic substrate [e.g. 2,5-diphenylfuran (DPF)] using in situ UV/vis spectroscopy. In a previous study, the presence of additional methyl groups was found to be beneficial for the photocatalytic reduction of CO2 to CO, but here Al1 without any methyl groups exhibits superior performance. To rationalize this behavior, a combination of photophysical experiments (absorption, emission and excited state lifetimes) together with photostability measurements and scalar-relativistic time-dependent density functional theory calculations was applied. As a result, Al1 exhibited the highest emission quantum yield (64%), the longest emission lifetime (8.7 ns) and the best photostability under the reaction conditions required for the energy transfer reactions (e.g. in aerated chloroform). Moreover, Al1 provided the highest rate constant (0.043 min-1) for the photocatalytic oxygenation of DPF, outperforming even noble metal-based competitors such as [Ru(bpy)3]2+. Finally, its superior photostability enabled a long-term test (7 h), in which Al1 was successfully recycled seven times, underlining the high potential of this new class of earth-abundant PSs.

Synergistic and Antagonistic Activity of Selected Dietary Phytochemicals against Oxidative Stress-Induced Injury in Cardiac H9c2 Cells via the Nrf2 Signaling Pathway.

The antioxidant activities of lycopene (LY), lutein (LU), chlorogenic acid (CA), and delphinidin (DP) were tested in vitro on H9c2 cell-based models. Some indicators, such as the generation of reactive oxygen (ROS), the quantification of cell antioxidant activity (CAA), and the expressions of SOD, GSH-Px, and CAT, were calculated to examine their antioxidant interactions. From our results, the phytochemical mixtures (M1: CA-LU: F3/10, M2: DP-CA: F7/10, M3: DP-LY: F5/10) displayed strong synergistic effects based on the generation of ROS and the quantification of CAA. However, great antagonistic bioactivities were seen in the combinations of LY-LU: F5/10 (M4), CA-LU: F9/10 (M5), and DP-LY: F7/10 (M6). Western blotting analysis indicated that the possible mechanism underlying the synergistic antioxidant interactions among phytochemical combinations was to enhance the accumulation of Nrf2 in the nucleus and the expression of its downstream antioxidant enzymes, HO-1 and GCLC. The combinations (M1-M3 groups) showed significant protection against the loss of mitochondrial membrane potential than individual groups to avoid excessive ROS production. The M4-M6 groups exerted antagonistic protective effects compared with the individual groups. In addition, lutein and lycopene absorption was improved more because of the presence of chlorogenic acid and delphinidin in the M1 and M3 groups, respectively. However, delphinidin significantly reduced the cellular uptake of lycopene in the M6 group. It appeared that antioxidant interactions of phytochemical combinations may contribute to the restoration of cellular redox homeostasis and lead to an improvement in diet quality and collocation.

Synthesis and photophysical properties of symmetrical tetraaryltetranaphtho[2,3]porphyrin derivatives

The discovery of new photosensitizers with strong absorption near-infrared region, obvious fluorescence emission, and high reactive oxygen generation ability has attracted great attention as optical agents in life science and material industry. Herein a series of meso-tetraaryltetranaphtho[2,3]porphyrins (Ar 4TNPs) with different substitutions were designed and synthesized. They had strong absorptions at ∼730 nm and fluorescence emission at ∼760 nm after excitation with ∼503 nm light. All compounds possessed excellent reactive oxygen species (ROS) generation ability. The singlet oxygen generation rate of compound 10m (meso-5,10,15,20-tetra[2-(2-hydroxyethoxy)ethylbenzoate]tetrana-phthoporphyrin) is 0.1898 s−1 with a Φ△ value of 0.73, which is significantly higher than that of verteporfin. Therefore, Ar4TNPs have great potential as an effective optical material, bio-tracker, and photodynamic drug candidate.

In Situ Hydrogel with Immobilized Mn-Porphyrin for Reactive Oxygen Species Scavenging, Oxygen Generation, and Risedronate Delivery in Bone Defect Treatment.

We propose a hydrogel immobilized with manganese porphyrin (MnP), a biomimetic superoxide dismutase (SOD), and catalase (CAT) to modulate reactive oxygen species (ROS) and hypoxia that impede the repair of large bone defects. Our hydrogel synthesis involved thiolated chitosan and polyethylene glycol-maleimide conjugated with MnPs (MnP-PEG-MAL), which enabled in situ gelation via a click reaction. Through optimization, a hydrogel with mechanical properties and catalytic effects favorable for bone repair was selected. Additionally, the hydrogel was incorporated with risedronate to induce synergistic effects of ROS scavenging, O2 generation, and sustained drug release. In vitro studies demonstrated enhanced proliferation and differentiation of MG-63 cells and suppressed proliferation and differentiation of RAW 264.7 cells in ROS-rich environments. In vivo evaluation of a calvarial bone defect model revealed that this multifunctional hydrogel facilitated significant bone regeneration. Therefore, the hydrogel proposed in this study is a promising strategy for addressing complex wound environments and promoting effective bone healing.

Physical and chemical characteristics of plasma-activated water generated by hybrid dielectric barrier discharge and gliding arc discharge

This research explores the synergistic application of Dielectric Barrier Discharge (DBD) and Gliding Arc Plasma Jet (GAPJ) in a Hybrid Plasma Discharge (HPD) setup for enhanced water activation. The HPD system demonstrated balanced and sustained generation of reactive oxygen and nitrogen species (RONS), maintaining efficiency at higher specific input energy (SIE) values. Comparative analyses with DBD and GAPJ systems highlighted the superior performance of the HPD system in generating RONS and modifying water’s molecular structure. Key observations included a decrease in water’s pH and an increase in oxidation-reduction potential, total dissolved solids, and conductivity, stabilizing beyond 5 l min−1 airflow and 10 min of treatment. UV−Vis spectroscopy identified nitrites, nitrates, hydrogen peroxide, and nitrous acid, while Raman spectroscopy captured shifts in vibrational modes, particularly in librational and O–H stretching bands. These changes correlated with alterations in reactive species concentrations and pH levels. Overall, the HPD system emerged as a versatile and efficient approach for generating plasma-activated water, suitable for applications in microbial deactivation, surface sterilization, and electrocatalytic process optimization, offering stable and continuous production of reactive species across a range of SIE values.

Contribution of oxidation reactions to photo-induced damage to cellular DNA.

This review article is aimed at providing updated information on the contribution of immediate and delayed oxidative reactions to the photo-induced damage to cellular DNA/skin under exposure to UVB/UVA radiations and visible light. Low-intensity UVC and UVB radiations that operate predominantly through direct excitation of the nucleobases are very poor oxidizing agents giving rise to very low amounts of 8-oxo-7,8-dihydroguanine and DNA strand breaks with respect to the overwhelming bipyrimidine dimeric photoproducts. The importance of these two classes of oxidatively generated damage to DNA significantly increases together with a smaller contribution of oxidized pyrimidine bases upon UVA irradiation. This is rationalized in terms of sensitized photooxidation reactions predominantly mediated by singlet oxygen together with a small contribution of hydroxyl radical that appear to also be implicated in the photodynamic effects of the blue light component of visible light. Chemiexcitation-mediated formation of "dark" cyclobutane pyrimidine dimers in UVA-irradiated melanocytes is a recent major discovery that implicates in the initial stage, a delayed generation of reactive oxygen and nitrogen species giving rise to triplet excited carbonyl intermediate and possibly singlet oxygen. High-intensity UVC nanosecond laser radiation constitutes a suitable source of light to generate pyrimidine and purine radical cations in cellular DNA via efficient biphotonic ionization.

Cutting Edge: ATP13A2 Is an Endolysosomal Regulator of TLR9/7 Activation in Human Plasmacytoid Dendritic Cells.

ATPase cation transporting 13A2 (ATP13A2) is an endolysosomal P-type ATPase known to be a polyamine transporter, explored mostly in neurons. As endolysosomal functions are also crucial in innate immune cells, we aimed to explore the potential role of ATP13A2 in the human immunocellular compartment. We found that human plasmacytoid dendritic cells (pDCs), the professional type I IFN-producing immune cells, especially have a prominent enrichment of ATP13A2 expression in endolysosomal compartments. ATP13A2 knockdown in human pDCs interferes with cytokine induction in response to TLR9/7 activation in response to bona fide ligands. ATP13A2 plays this crucial role in TLR9/7 activation in human pDCs by regulating endolysosomal pH and mitochondrial reactive oxygen generation. This (to our knowledge) hitherto unknown regulatory mechanism in pDCs involving ATP13A2 opens up a new avenue of research, given the crucial role of pDC-derived type I IFNs in protective immunity against infections as well as in the immunopathogenesis of myriad contexts of autoreactive inflammation.

Plasmalogen oxidation induces the generation of excited molecules and electrophilic lipid species.

Plasmalogens are glycerophospholipids with a vinyl ether linkage at the sn-1 position of the glycerol backbone. Despite being suggested as antioxidants due to the high reactivity of their vinyl ether groups with reactive oxygen species, our study reveals the generation of subsequent reactive oxygen and electrophilic lipid species from oxidized plasmalogen intermediates. By conducting a comprehensive analysis of the oxidation products by liquid chromatography coupled to high-resolution mass spectrometry (LC-HRMS), we demonstrate that singlet molecular oxygen [O2 (1Δg)] reacts with the vinyl ether bond, producing hydroperoxyacetal as a major primary product (97%) together with minor quantities of dioxetane (3%). Furthermore, we show that these primary oxidized intermediates are capable of further generating reactive species including excited triplet carbonyls and O2 (1Δg) as well as electrophilic phospholipid and fatty aldehyde species as secondary reaction products. The generation of excited triplet carbonyls from dioxetane thermal decomposition was confirmed by light emission measurements in the visible region using dibromoanthracene as a triplet enhancer. Moreover, O2 (1Δg) generation from dioxetane and hydroperoxyacetal was evidenced by detection of near-infrared light emission at 1,270 nm and chemical trapping experiments. Additionally, we have thoroughly characterized alpha-beta unsaturated phospholipid and fatty aldehydes by LC-HRMS analysis using two probes that specifically react with aldehydes and alpha-beta unsaturated carbonyls. Overall, our findings demonstrate the generation of excited molecules and electrophilic lipid species from oxidized plasmalogen species unveiling the potential prooxidant nature of plasmalogen-oxidized products.

Photoactive polymer coatings for antibacterial applications

Because bacteria can readily induce illnesses in the human body, research into new bactericidal approaches remains relevant to the global community. Photoactive materials (e.g., photocatalysts) provide an environmentally-friendly method for killing bacteria with light. By means of light-mediated reactive oxygen generation, photocatalysts are capable of disrupting bacterial membranes. Much research on antibacterial surfaces has focused on planar substrates or physisorbed coatings, which often provide small active surface areas and limited surface-to-volume ratios, and thereby create a need for new design strategies to incorporate photocatalysts onto more scalable supports. To this end, this contribution describes the synthesis of particle-tethered polymer brush coatings, crosslinked with the organic photocatalyst tetrakis(4-carboxyphenyl)porphyrin (TCPP). Successful engineering on SiO2 surfaces was confirmed using X-ray photoelectron spectroscopy, tensiometry, and ellipsometry. Singlet oxygen (1O2) generation was confirmed through dimethyl sulfoxide oxidation experiments under visible (blue) light and bactericidal activity against Escherichia coli was verified through live/dead assays and cell viability tests.

Calcium-dependent dual oxidase 2 is a novel source of reactive oxygen species implicated in glomerular mesangial cell fibrotic response to angiotensin II and glucose

The vasoactive peptide angiotensin II (Ang II) and hyperglycemia contribute to the initiation and the progression of glomerular fibrosis via activation of glomerular mesangial cells (MCs) and subsequent extracellular matrix expansion. We have previously shown that oxidative stress is critical for MC fibrotic response to Ang II or high concentrations of glucose (HG). Here, we demonstrate that Dual oxidase 2 (Duox2), a member of the Nox/Duox family of NADPH oxidases, is present in MCs and that its protein expression, along with its associated maturation factor, DuoxA2, are upregulated by Ang II and HG. Small interfering RNA (siRNA)-mediated downregulation of Duox2 significantly reduces Ang II-induced increase in reactive oxygen (ROS) generation and prevents the stimulatory effect of Ang II on MC fibrotic injury (as assessed by measuring a-smooth muscle actin and fibronectin expression). To demonstrate that Duox2 activation is Ca2+-dependent, we show that the extracellular Ca2+ chelator BAPTA prevented Ang II-induced ROS generation and the stimulation of MC fibrotic injury by Ang II. Moreover, treatment of MCs with ionomycin resulted in increased ROS production and enhanced MC fibrotic injury. These effects were abrogated by siRNA targeting Duox2. Fura-2 fluorescence was utilized as well to show calcium mobilization in response to Ang II and this effect was abrogated with siDuox2 transfection. These data indicate that Ang II-stimulated Duox2 activation and ROS generation subsequently lead to MC fibrotic injury. In summary, we have identified a novel role for Duox2 and its cognate maturation factor, DuoxA2, as a major source of ROS in response to Ang II and HG and established the significance of Duox2 in Ang II-mediated MC activation and fibrotic injury. Therapeutic targeting of this pathway may prevent or reverse pathophysiologic manifestations of renal fibrotic diseases. Research reported in this poster was supported by the University of the Incarnate Word Offce of Research and Graduate Studies and the National Institute of General Medical Sciences of the National Institutes of Health under Award Number SC2GM136569. The content is solely the responsibility of the authors and does not necessarily represent the offcial views of the National Institutes of Health. This is the full abstract presented at the American Physiology Summit 2024 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.

Hypotensive drugs mitigate the high-sodium diet-induced pro-inflammatory activation of mouse macrophages in vivo

Nowadays, there is an increasing emphasis on the need to alleviate the chronic inflammatory response to effectively treat hypertension. However, there are still gaps in our understanding on how to achieve this. Therefore, research on interaction of antihypertensive drugs with the immune system is extremely interesting, since their therapeutic effect could partly result from amelioration of hypertension-related inflammation, in which macrophages seem to play a pivotal role. Thus, current comprehensive studies have investigated the impact of repeatedly administered hypotensive drugs (captopril, olmesartan, propranolol, carvedilol, amlodipine, verapamil) on macrophage functions in the innate and adaptive immunity, as well as if drug-induced effects are affected by a high-sodium diet (HSD), one of the key environmental risk factors of hypertension. Although the assayed medications increased the generation of reactive oxygen and nitrogen intermediates by macrophages from standard fed donors, they reversed HSD-induced enhancing effects on macrophage oxidative burst and secretion of pro-inflammatory cytokines. On the other hand, some drugs increased macrophage phagocytic activity and the expression of surface markers involved in antigen presentation, which translated into enhanced macrophage ability to activate B cells for antibody production. Moreover, the assayed medications augmented macrophage function and the effector phase of contact hypersensitivity reaction, but suppressed the sensitization phase of cell-mediated hypersensitivity under HSD conditions. Our current findings contribute to the recognition of mechanisms, by which excessive sodium intake affects macrophage immune activity in hypertensive individuals, and provide evidence that the assayed medications mitigate most of the HSD-induced adverse effects, suggesting their additional protective therapeutic activity.

Quaternary ammonium carboxymethyl chitosan composite hydrogel with efficient antibacterial and antioxidant properties for promoting wound healing

Multifunctional hydrogels have been developed to meet the various requirements of wound healing. Herein, an innovative hydrogel (QCMC-HA-PEG) was formed through the Schiff base reaction, composed of quaternary ammonium-modified carboxymethyl chitosan (QCMC), hyaluronic acid (HA), and 8-arms Polyethylene Glycol aldehyde (8-ARM-PEG-CHO). The resulting hydrogels exhibited good mechanical and adhesive properties with improved antibacterial efficacy against both Gram-positive and Gram-negative bacteria compared to CMC hydrogels. QCMC-HA-PEG hydrogels demonstrated remarkable adhesive ability in lap-shear test. Furthermore, the incorporation of MnO2 nanosheets into the hydrogel significantly enhanced its reactive oxygen species (ROS) scavenging and oxygen generation capabilities. Finally, experimental results from a full-thickness skin wound model revealed that the QCMC-HA-PEG@MnO2 hydrogel promoted skin epithelization, collagen deposition, and inflammatory regulation significantly accelerated the wound healing process. Therefore, QCMC-HA-PEG@MnO2 hydrogel could be a promising wound dressing to promote wound healing.