Free Radical Generation Research Articles

Research progress of micro-nano bubbles in environmental remediation: Mechanisms, preparation methods, and applications.

Micro-nano bubble technology, with its unique physicochemical properties, has demonstrated remarkable application potential in the field of environmental remediation. Compared to traditional macro-bubbles, micro-nano bubbles exhibit exceptional stability in solutions due to their minute size, superior mass transfer efficiency, and pronounced interfacial potential characteristics, effectively resisting coalescence and rupture, thereby prolonging their persistence in environmental media. Currently, the pressurized dissolution of micro-nano bubbles stands as an outstanding approach in environmental governance. This process not only fosters the generation of free radicals and the release of energy but also significantly enhances gas transfer efficiency, effectively disrupting the oxidative structures of pollutants and facilitating the transport and transformation of pollutant residues as a carrier. Micro-nano bubbles play pivotal roles across multiple domains of environmental remediation. In the realm of oil contamination, whether it be soil or oily sludge remediation, micro-nano bubbles demonstrate formidable degradation capabilities. In terms of water pollution treatment, ranging from surface water, groundwater, to industrial wastewater, micro-nano bubble technology proves effective, markedly enhancing water purification efficiency. In the field of agricultural remediation, micro-nano bubbles can save water, increase production, clean and decontaminate. In addition, it also plays an important role in the fields of material modification and membrane fouling remediation. Finally, the economic benefits of micro-nano bubbles and the existing research gaps are further analyzed, and its development direction is speculated: pollution control lacks long-term tracking, and there is a lack of attention to the possible secondary pollution caused by catalysts. The behavior and mechanism of micro-nano bubbles under different environmental conditions are further explored. Optimize its preparation and application methods, pay attention to the energy consumption and economic possibilities of the process, and promote its application in actual environmental remediation.

Bioactivities of secondary metabolites of two actinomycetes Streptomyces parvulus GloL3, and Streptomyces lienomycini SK5, endophytes of two Indian medicinal herbs- Globba marantina L. and Selaginella kraussiana (Kunze) A. Braun.

Endophytic actinomycetes are potential sources of novel pharmaceutically active metabolites, significantly advancing natural product research. In the present investigation, secondary metabolites from two endophytic actinomycetes, Streptomyces parvulus GloL3, and Streptomyces lienomycini SK5, isolated from medicinal plant taxa, Globba marantina, and Selaginella kraussiana, exhibited broad-spectrum bioactivity. Ethyl Acetate (EA) extract of SK5 showed antimicrobial activity against nine human pathogens, including Methicillin-resistant Staphylococcus aureus (MRSA), Candida tropicalis, and C. albicans, with a minimum microbicidal concentration (MMC) of 50-300µg mL-1. It healed the MRSA-mediated wounds in Swiss albino mice in vivo. EA extracts dissociate the pathogenic cell membranes and cause leakage of biomacromolecules-nucleic acid, protein, and potassium ions. Also, critical housekeeping enzymes involved in the cellular respiratory mechanisms of the pathogens were blocked. GloL3 has antioxidative potentialities against DPPH, ABTS, FRAP, and H2O2 free radical generators with an IC50 value of 21.18 ± 0.33, 43.58 ± 0.91, 88.24 ± 1.24, and 111.03 ± 6.42µg mL-1. It improves the enzymatic antioxidant parameters in treated peritoneal macrophage cells of Swiss albino mice. Constituents of the EA extracts of GloL3 and SK5 are bactobolin, actinobolin, 5-(2-aminoethyl)-1H imidazole-2-carbaldehyde, isovaleric acid, fulvic acid, phenol, 4-[2-(methylamino) ethyl]-, eicosanoic acid, heptadecanoic acid, etc. The present findings suggest that metabolites from the endophytes of medicinal plants hold potent pharmaceutical utilities.

Monitoring Dynamic Changes of Cellular Membrane GSH During Stroke via an ESIPT-Based Near-Infrared Fluorescent Probe

Stroke, primarily ischemic (85%), results from inadequate blood supply and is worsened by ferroptosis, characterized by free radical generation and lipid peroxidation. Monitoring ferroptosis is essential for understanding its mechanisms and developing treatments. Glutathione (GSH) is a key ferroptosis biomarker, but current probes are limited by short excitation/emission wavelengths, small Stokes shifts, and inability to monitor dynamic GSH changes at the cellular membrane, where ferroptosis plays a crucial role. To address these issues, we developed the PM-Red-GSH, a novel near-infrared (NIR) probe based on the Excited-state intramolecular proton transfer (ESIPT) mechanism. It shows strong NIR emission (715 nm), large Stokes shift (290 nm), and enhanced membrane binding (PCC = 0.95) due to its alkyl group. PM-Red-GSH enables dynamic GSH monitoring in an MCAO mouse model. These findings offer new insights into ferroptosis and stroke treatment.

Effect of H2O2 induced oxidative stress on volatile organic compounds in differentiated 3T3-L1 cells

Oxidative stress (OS) refers to the disruption in the balance between free radical generation and antioxidant defenses, leading to potential tissue damage. Reactive oxygen species (ROS) can interact with biological components, triggering processes like protein oxidation, lipid peroxidation, or DNA damage, resulting in the generation of several volatile organic compounds (VOCs). Recently, VOCs provided new insight into cellular metabolism and can serve as potential biomarkers. The objective is to investigate the impact of OS on cell metabolism by analyzing the release or alterations of VOCs in the headspace of differentiated 3T3-L1 adipocytes. An OS model in differentiated 3T3-L1 cell lines was constructed using hydrogen peroxide (H2O2) treatment. The effect of OS on cell metabolism was analyzed by detecting VOCs in the headspace of the cells using solid phase micro extraction (SPME) and gas chromatography-mass spectrometry (GCMS). Our findings indicate that H2O2 concentrations exceeding 300 µM induce significant OS, leading to adipocyte apoptosis, as evidenced by various assays. Of the twenty VOCs identified, ten were upregulated in the cells. VOCs such as diphenyl ether, 1,3,5-trioxane, 5-methyl tridecane, 2-ethyl-1-hexanol, and 2,4-di-tert-butyl phenol emerged as potential biomarkers for OS. This study demonstrates that elevated OS alters VOC profiles in differentiated 3T3-L1 adipocytes, providing insights into the effects of OS on adipose tissue and identifying potential OS biomarkers.

Synergistic Antifungal Activity of Terbinafine in Combination with Light-Activated Gelatin-Silver Nanoparticles Against Candida albicans Strains.

The development of resistance to traditional antifungal therapies has necessitated the exploration of alternative treatment strategies to effectively manage fungal infections, particularly those induced by Candida albicans (C. albicans). This research investigates the possibility of integrating silver nanoparticles (AgNPs) with Terbinafine to improve antifungal effectiveness. Terbinafine, while potent, faces challenges with specific fungal strains, highlighting the need for strategies to enhance its treatment efficacy. Silver nanoparticles were produced through a light-activated, gelatin-based method, resulting in particle sizes ranging from 56.8 nm to 66.2 nm, confirmed by dynamic light scattering and scanning electron microscopy. Stability studies indicated that AgNPs produced with 30 mg of silver nitrate (AgNO₃) exhibited the greatest stability over 60 days across different temperature conditions. The analysis through UV-visible spectrophotometry revealed a notable shift in the absorption spectra as AgNO₃ concentrations increased, which was associated with a strengthening of plasmon resonance. The effectiveness of the AgNPs and Terbinafine combination was assessed against three strains of C. albicans (ATCC 10231, ATCC 90028, and ATCC 18804). Terbinafine demonstrated strong antifungal properties with minimum inhibitory concentrations (MIC) values ranging from 2-4 µg/mL, whereas AgNPs on their own displayed moderate effectiveness. The integrated formulation notably enhanced effectiveness, especially against strain ATCC 90028, revealing a synergistic effect (FIFi = 0.369). These results were complemented by the findings of the time-to-kill assay, where the same strain showed a 3.2 log₁₀ CFU/mL decrease in viable cell count. The process by which AgNPs boost activity entails the disruption of the fungal cell membrane and its internal components, probably as a result of silver ion release and the generation of free radicals. The results indicate that the combination of Terbinafine and AgNPs may act as a powerful alternative for addressing resistant fungal infections, presenting an encouraging direction for future antifungal treatments.

Protective Effects of Hydrogen Treatment Against High Glucose-Induced Oxidative Stress and Apoptosis via Inhibition of the AGEs/RAGE/NF-κB Signaling Pathway in Skin Cells.

Diabetic wounds are major clinical challenges, often complicated by oxidative stress and free radical generation. Hydrogen (H2), a selective antioxidant, offers potential as a therapeutic agent for chronic diabetic wounds. However, its precise mechanisms remain underexplored. This study aimed to investigate the protective effects of H2 on high glucose-induced oxidative damage and apoptosis in human skin cells. HaCaT keratinocytes and HSF fibroblasts were treated with high glucose or AGEs. Cell viability, oxidative stress markers, inflammatory cytokines, and apoptosis were analyzed. AGEs/RAGE/NF-κB signaling was evaluated via Western blot. H2 treatment significantly reduced ROS, MDA, IL-1β, and TNF-α levels, while enhancing SOD and GSH activity. It also inhibited AGEs/RAGE/NF-κB signaling and apoptosis. Hydrogen therapy protects against oxidative stress and inflammation induced by high glucose or AGEs, offering potential as an adjunctive treatment for diabetic wound healing.

Efficient activation of sodium percarbonate by hydroxylamine-enhanced zero-valent transition metals for the removal of AZO: performance, free radical generation and mechanism

Azoxystrobin (AZO) fungicides are novel organic pollutants which are stable in water environment. These pollutants can be degraded using low cost zero-valent metals (zero-valent iron (ZVI) and zero-valent copper (ZVC)) to activate sodium percarbonate (SPC), and the introduction of hydroxylamine (HA) can effectively improve the reaction efficiency of this system. According to the experimental results, HA significantly promoted the regeneration of Fe2+ and Cu+ in the decomposed solution of SPC, significantly accelerating the formation of hydroxyl radicals (•OH) and facilitating the degradation of AZO. Under optimal conditions, when pH = 3, the rate of AZO removal by the HA/ZVI/SPC system reached 99.0 % in 15 min, while the HA/ZVC/SPC system required 50 min to reach 99.1 % removal. Both of the tested HA/zero-valent metal/SPC processes produced •OH, carbonate radicals (CO3·-), superoxide radicals (O2·-) and singlet oxygen (1O2), among which, •OH appeared to be the main reactant responsible for AZO removal. Furthermore, it was found that •OH reacted with trace levels of carbonate ions to generate other reactive oxygen species and promote AZO degradation. The addition of HA not only slowed down the surface passivation of zero-valent metals, but also promoted the conversion of high-valent metal ions to low-valent metal ions, resulting in the generation of more reactive oxygen species within the system. In addition, the degradation intermediates were identified by LC-MS analysis and density-functional theory (DFT), allowing the possible AZO degradation pathways to be proposed.

Visible light-driven triazine-based S-scheme COF-TpTt@BiOBr heterojunction with oxygen vacancy for enhanced photocatalytic pollutants removal and hydrogen production.

S-scheme heterojunction is an effective tactic to improve photocatalytic property. But few studies on constructing heterojunction with BiOBr and covalent organic frameworks (COFs) are available. Herein, a novel series of COF-TpTt@BiOBr S-scheme heterojunctions with oxygen vacancies (OVs) were constructed via solvothermal method. COF-TpTt@BiOBr-10% showed enhanced photocatalytic performance under visible light. Pollutants (such as Methyl Orange (MO), methylene blue (MB), Rhodamine B (RhB), tetracycline (TC) and Levofloxacin hydrochloride (LEV)) can be efficiently degraded and the photocatalytic H2 generation rate reached 10828.075 μmol g-1 h-1, which was 12.4 and 8.5 times of COF-TpTt and BiOBr. In addition, 3,3',5,5'-tetramethylbenzidine (TMB) oxidation experiment showed it has excellent molecular oxygen activation capacity. Furthermore, the S-scheme heterojunction charge transfer mechanism was proved by density functional theory (DFT) calculations. Under the influence of internal electric field, energy band bending and Coulomb force, e- and h+ were efficiently separated and transferred. The formation of S-scheme heterojunction and generation of multiple free radicals assured the high redox activity of COF-TpTt@BiOBr-10% photocatalytic system. This study strengthened our deep understanding of S-scheme heterojunction charge transfer mechanism and offered a new way for high efficient hydrogen energy production.

Exploring ultrasound-induced free radical formation: A comparative study in water and sour cherry juice using glutathione and terephthalic acid indicators.

This study aims to assess free radical (FR) generation potential of ultrasound in water and sour cherry juice (SCJ) model systems using an indirect method with specific indicators including glutathione (GSH), a well-known antioxidant, and terephthalic acid (TPA), which fluoresces upon oxidation. Initially, aqueous GSH solutions were subjected to ultrasound at varying amplitudes (60% and 80%) for up to 30min using probes of different diameters (13mm and 19mm) to identify maximal oxidation conditions. FR formation was monitored using UPLC equipped with diode array detector and fluorescence spectrophotometer for GSH and TPA oxidation, respectively. Increasing sonication time decreased GSH and increased oxidized glutathione (GSSG) in water for both probes; however, the 19mm probe generated five times more GSSG than the 13mm, implying a substantially higher rate of FR formation. Subsequently, ultrasound was applied to aqueous TPA solution using the 19mm probe-representing the more challenging conditions-at a previously optimized amplitude (67%) during 30min. Time-course water samples showed a steady increase in TPA fluorescence intensity with longer sonication durations, suggesting that oxidation reactions driven by FRs were progressing over time in water. Following sonication of GSH- and TPA-added SCJ under the same conditions, analysis by LC-QTOF-MS and fluorescence spectrophotometry revealed no GSSG or fluorescence formation, confirming the absence of notable oxidation of both indicators, likely due to the juice's complex composition (e.g., presence of antioxidant compounds). This study offers key insights into how ultrasound conditions affect FR formation in water and SCJ media by stabilizing them in detectable forms.

Maternal exposure to nicotine causes oxidative stress and inflammatory changes in the ovaries of rats' adult offspring.

Nicotine is one of the most toxic substances found in cigarettes, but also found in chewing tobacco gum, patches and vaping products (electronic cigarettes). In addition to being a highly addictive chemical, it is capable of reducing fertility in men and women. In the ovaries, it can induce morphological changes and impair the formation of follicles, being a possible cause of changes in the reproductive cycle and anticipation of menopause in women whose mothers smoked during pregnancy. By increasing the generation of free radicals, nicotine can induce oxidation in biological samples and change the expression of inflammatory cytokines. It damages the immune system and many other cells of newborns exposed prenatally. Despite its teratogenic potential, many women continue to use this drug during pregnancy and lactation. Thus, this work aims to analyze the effects of maternal exposure to nicotine on the ovaries of adult rats. To this end, 10 rats received nicotine throughout pregnancy and lactation. Their offspring were euthanized around 90 days-old, in the metestrus phase, for ovary collection and analysis of oxidative stress and inflammation. The results showed that exposure to nicotine increased MDA level, but did not cause damage to the DNA of ovarian cells (8-OHdG). It also increased IL-1β and anti-inflammatory protein AnxA1 and receptor Fpr1, and reduced the mast cell population in ovaries. We concluded that maternal exposure to nicotine is capable of inducing oxidative stress and leading to inflammatory changes in the ovaries of adult offspring exposed during the intrauterine and breastfeeding phases.

Ergothioneine-rich Lentinula edodes mushroom extract restores mitochondrial functions in senescent HT22 cells

A decline in mitochondrial functions associated with ageing is the key factor of free radical generation which contributes to age-related pathologies. Protecting healthy functional mitochondrial networks with antioxidants is critical in promoting healthy ageing. This study aimed to investigate the protective effect of ergothioneine (EGT)-rich Lentinula edodes extract (LE-ETH) against tert-butyl hydroperoxide (t-BHP) assaulted senescent HT22 cells. Mitochondrial function was evaluated by measuring mitochondrial membrane potential (MMP), ATP levels and mitochondrial toxicity. The protective mechanisms were elucidated via the exploration of antioxidant and mitochondrial biogenesis signalling pathways. Our results revealed that a low dose of t-BHP increases mitochondrial toxicity. The pretreatment with 100 µg/mL of LE-ETH and the equimolar concentration of EGT for 8 h significantly improve the mitochondrial function and reduced inflammation. Through gene expression studies, we demonstrated that pretreatment of LE-ETH significantly improves the antioxidant and mitochondrial biogenesis pathway via Nrf2 signaling axis. However, the downstream genes of the mitochondrial biogenesis pathway were unaffected by equimolar EGT concentration. Gas chromatography-mass spectrum (GC–MS) analysis was carried out to identify the bioactive compounds that are present in LE-ETH extract which contributed to its efficacy in improving the mitochondrial functions. A total of 23 compounds consisting of phenols, fatty acids, and sterols were identified in the ethanolic extract. Pentanoic acid was the major compound identified in LE-ETH. These findings demonstrated that EGT-rich L.edodes mushroom is a potential neuroprotective agent which could serve as a potential therapeutic strategy for the preservation of mitochondrial functions in healthy ageing explorations.

Nitrogen doped carbon quantum dots: a multifaceted carbon nanomaterial that interferes in an amyloid-forming trajectory.

Carbon quantum dots (CQDs) are a versatile class of carbon-based nanomaterial frameworks that have previously been used as a diagnostic device, in sensing for environmental applications, in bioimaging, and for drug delivery systems. Their versatility stems from their ability to be chemically tailored via functionalization to optimize properties for specific applications. In this study, we have synthesized lactic acid-derived nitrogen doped carbon quantum dots (LAdN-CQDs) and examined their ability to intervene in the conversion of soluble, monomeric hen egg-white lysozyme (HEWL) into mature fibrils. Our data indicate that LAdN-CQDs inhibit HEWL fibril formation in a dose-dependent manner (achieving up to 50% inhibition at 2.5 mg mL-1). Furthermore, in a neuroblastoma-derived cell line, LAdN-CQDs were found not to disrupt mitochondrial membrane potential or trigger apoptosis at the same concentration range, suggesting that they are biocompatible. LAdN-CQDs effectively neutralized reactive oxygen species (ROS), with a 50% decrease in ROS levels at just 100 μg mL-1 when challenged with an established free radical generator and protected the cell line from rotenone-induced apoptosis. The ability of LadN-CQDs to inhibit the soluble-to-toxic transformation of HEWL, the tolerance of SHSY-5Y cells to LAdN-CQDs, and their ability to restitute cells from rotenone-induced apoptosis, combined with the biocompatibility findings, suggest that LAdN-CQDs are potentially neuroprotective. The findings indicate that LAdN-CQDs represent a versatile, carbon-based, sustainable nanoplatform that bridges nanotechnology and neuroprotection, promoting the development of green chemistry-based healthcare solutions.

New possibilities of the prevention and treatment of cardiovascular pathologies. the potential of molecular hydrogen in the reduction of oxidative stress and its consequences.

Disproportion between reactive oxygen species (ROS) production and the body's antioxidant system can cause oxidative stress, which is considered a common denominator in various pathological conditions, including cardiovascular diseases, aging, and cognitive disorders. The generation of free radicals, which occurs through partial reduction of oxygen, can quickly overwhelm the endogenous antioxidant system capacity of the cell. This causes lipid, protein, DNA and RNA damage, inflammation, and overall cell degeneration, which can be mitigated by various antioxidants. However, their use in human medicine did not bring the expected effect. Molecular hydrogen (H2), due to its unique physical and chemical properties, provides a number of benefits for alleviating oxidative stress. H2 is superior to conventional antioxidants as it can selectively reduce (.)OH radicals while preserving important ROS that are otherwise used for normal cell signaling. Key words Oxidative stress, Cardiovascular diseases, Molecular hydrogen, ROS, Inflammation.

Synergism and Mechanisms of Aging Resistance in the Use of Graphene and Carbon Nanotubes in Bitumen Composites.

Thermal oxidation has a significant effect on the durability of bitumen composites reinforced with carbon nanomaterials. However, the mechanisms of aging resistance and the effect of aging on the chemical properties, morphology, micromechanical properties, and rheology of bitumen with carbon nanomaterials are still unclear. This study investigated the mechanisms of aging resistance underlying the synergistic effects of graphene and carbon nanotubes (CNTs) on the durability of bitumen composites. The antiaging properties of bitumen with hybrid graphene/CNT were also compared to those of bitumen with only graphene or/and bitumen with only CNT. Compared with control bitumen, bitumen with graphene, and bitumen with CNT, the bitumen with hybrid graphene/CNT had significantly improved aging resistance as shown by the much lower chemical aging indexes and the lower rheological aging index. The three-dimensional spatial network structure formed by graphene and CNT in bitumen has dual mechanisms underlying the improvement it provides in resistance to aging: the structure effectively confines the thermo-oxidation reactions in bitumen molecules and the structure acts as a barrier to inhibit the penetration of oxygen molecules and reduce their diffusion rate, thereby inhibiting the generation of free radicals. This study reveals the antiaging mechanisms of carbon nanomaterials in bitumen composites, providing a theoretical basis for the application of carbon nanomaterials in pavement engineering.

Effect of Supplementation of Black Seeds (Nigella sativa) on Biomarkers of Oxidative Stress: An Updated Narrative Review of Clinical and Preclinical Studies

Abstract: Increased generation and accumulation of free radicals (reactive oxygen species) and a decrease in the activity of antioxidant systems can result in oxidative stress. In this study, we investigate the antioxidant properties of black seeds (Nigella sativa). To find pertinent papers, searches were conducted using reference lists, Web of Science, Medline/PMC/PubMed, Scopus, Google Scholar, and Science Direct, among other web-based resources. Black seed (Nigella sativa) supplementation has been demonstrated in several preclinical and clinical studies to decrease lipid peroxidation and raise levels of antioxidant enzymes. There are several ways in which black seeds (Nigella sativa) can exhibit antioxidant activity: they can do this by reducing oxidative stress and free radical formation, scavenging superoxide and other reactive oxygen species, inhibiting lipid peroxidation, inhibiting nuclear factor-kB (NF-kB), upregulating genes encoding antioxidant enzymes, lowering malondialdehyde levels, elevating total antioxidant capacity levels, and enhancing antioxidant enzymes like superoxide dismutase, catalase, glutathione peroxidase, and many more. For individuals suffering from chronic conditions including diabetes, hypertension, dyslipidemia, cancer, and many more, black seeds (Nigella sativa) may thus be used as an adjuvant therapy in addition to standard drugs.

The effect of a magnetic field on the generation of free radicals in the interaction of quaternary ammonium compounds with hydroperoxides

The magnetic effects (ME) of a moderate magnetic field (MF, 600 mT) on the rate of radical generation (Wi) in mixed micellar systems of quaternary ammonium compounds with hydroperoxides (QAC-ROOH), measured by the inhibitor method, and the effect of magnetic field on the rate of radical polymerization initiated by radicals, generated from the surface by QAC chemisorbed on a solid carrier upon interaction with hydroperoxide dissolved in the monomer are compared. It has been established that in micellar solutions MF reduces Wi, ME ≈ –0.45. In the case of radical polymerization of styrene containing cumyl hydroperoxide on the surface of mica plates with a chemisorbed monolayer of QAC (CTAB or ACh), the polymerization rate increases in MF.

Understanding and Using Animal Models of Hepatotoxicity.

Hepatotoxicity is a critical health hazard, primarily contributing to the increased incidence of deaths globally. The liver is one of the major and extremely vital organs of the human body. Autoimmune diseases, viruses, exposure to toxicants such as carcinogens, and changes in eating habits can all cause liver problems, among other things. Free radical generation, together with raised enzyme levels including SGOT, SGPT, and total bilirubin, are among the pathological changes set off by liver injury. Hepatotoxicity causes changes in cells, such as eosinophilic cytoplasm, nuclear pyknosis, fatty degeneration, too many liver lesions, and hepatic centrilobular necrosis due to lipid peroxidation. Researchers have used animal models to investigate liver diseases and toxicities. Drugs such as azathioprine, alcoholism, paracetamol intoxication, and anti-tuberculosis drugs are some of the most common causes of liver toxicity. These toxins cause calcium ions (Ca2+), reactive oxygen species (ROS), and inflammatory mediators to be released inside cells. This activates immune cells like NK cells, NKT cells, and Kupffer cells. These signaling pathways also play roles in hepatotoxicity. Due to its pathogenesis, no effective drug is currently available for hepatotoxicity due to a lack of understanding related to the signaling factors involved in it. The paper primarily examines different experimental models of hepatotoxicity, including non-invasive and invasive methods, as well as genetic models. As such, these models are crucial tools in advancing our understanding of hepatotoxicity, thus paving the way for new therapeutic interventions.

Neuroprotective Assessment of Nutraceutical (Betanin) in Neuroblastoma Cell Line SHSY-5Y: An in-Vitro and in-Silico Approach.

The cognitive dysfunction in the brain cause severe pathological consequences such as Alzheimer's disease (AD), Parkinson's disease. The current treatments are cost expensive and also cause negative side effects. Therefore it is inevitable to develop natural phyto-compounds as a drug like molecules to treat neurodegenerative diseases. In this context, we have assayed the neuroprotective effects of betanin, an indole derivative, in the neuroblastoma cell line SHSY-5Y cells. The neuroprotective effect was investigated in the β-amyloid (Aβ) - induced SHSY-5Y cells; betanin (25µg) protected the SHSY-5Y cells from the toxic effects and maintained the cell viability. Moreover, the acridine orange and ethidum Bromide staining decipher that treatment of betanin in the Aβ-induced SHSY-5Y cells maintain the cell viablity sustainably. The Reactive Oxygen Species (ROS) assay infers that betanin quenches the generation of free radicals progressively in the Aβ-induced SHSY-5Y cells. In addition, the autophagy determination by flow cytometry revealed that betanin induces autophagy to remove the neurodegenerated cells. Further, we examined the docking and simulation patterns with the angiotensin-converting enzyme (ACE), TNF-α converting enzyme (TACE), glycogen synthase kinase 3 (GK3), and acetylcholinesterase enzymes (AChE) and amyloid precursor protein (APP). The insilico docking analysis denotes that betanin had a significant docking score with the target molecules. Thus, from the invitro and insilico studies, betanin strongly inhibit the toxic effects of Aβand protect the cells from degeneration.

Effects of Different Dietary Fat Sources on Oxidative Stress Parameters in Broiler Chickens

Introduction: Certain types of dietary fats may elevate the generation of free radicals, resulting in oxidative stress and potential cellular damage. The present study aimed to investigate the impact of high-energy diets derived from various fat sources on broiler chicken welfare and production. Materials and methods: A total of 216-day-old unsexed Arbor Acre broiler chickens were assigned to four treatment groups. The groups, including control, beef tallow (high energy diet animal source, HEDAS), palm oil (high energy diet plant source, HEDPS), and low energy diet (LED), each consisting of three replicates with 18 birds, were investigated in a completely randomized design over 42 days. Results: According to the results, the HEDPS group had the highest live weight, while the HEDAS group indicated the highest dressing percentage. Significant differences were noted in alanine transaminase and alanine phosphatase in the treatment group compared to the control group. Cholesterol levels were significantly high in the HEDAS group and LDL levels were the lowest compared to the control group. The HEDAS group also exhibited the highest triglyceride level compared to other treatments. The HDL levels were higher in the LED and HEDPS groups compared to the HEDAS group. The VLDL concentration was significantly higher in the HEDAS group in comparison with other groups. Conclusion: The HEDPS diet positively affected serum biochemistry and carcass characteristics, highlighting its potential in broiler chicken welfare and production.

Inhibitory Role of L-theanine, a Structural Analogue of Glutamate, Against GluR5 Kainate Receptor and its Prospective Utility Against Excitotoxicity.

Overactivation of receptors that respond to excitatory neurotransmitters can result in various harmful outcomes, such as the inability to properly modulate calcium levels, generation of free radicals, initiation of the mitochondrial permeability transition, and subsequent secondary damage caused by excitotoxicity. A non-proteinogenic amino acid of tea, L-theanine, is structurally related to glutamate, the major stimulatory neurotransmitter in the brain. Previous reports have emphasised its ability to bind with glutamate receptors. An in-depth understanding of the binding compatibility between ionotropic glutamate receptors and L-theanine is a compelling necessity. In this molecular docking study, the antagonistic effect of L-theanine and its possible therapeutic benefit in GluR5 kainate receptor inhibition has been evaluated and compared to the familiar AMPA and kainite receptor antagonists, cyanoquinoxaline (CNQX) and dinitroquinoxaline (DNQX), using Molegro Virtual Docker 7.0.0. The capacity of L-theanine to cohere with the GluR5 receptor was revealed to be higher than that of glutamate, although it could not surpass the high binding tendency of competitive antagonists CNQX and DNQX. Nonetheless, the drug-likeness score and the blood-brain barrier traversing potential of L-theanine were higher than CNQX and DNQX. The study provides an inference to the advantage of L-theanine, which can be a safe and effective alternative natural therapy for rescuing neuronal death due to excitotoxicity.