Search Results (60)

The accumulation of polylactic acid nano-plastics (PLA-NPs) in saline–alkali soils poses a potential threat to crop growth; however, the underlying toxicological mechanisms remain poorly understood. We conducted a hydroponic experiment to investigate the effects of polylactic acid (PLA) NPs (100 and 500 mg L⁻¹) under conditions both in the presence (50 mmol L⁻¹ NaCl) and absence of salt stress on maize seed germination, seedling growth, physiological characteristics, and transcriptomic responses. The results showed that exposure to PLA-NPs, particularly at a high concentration (500 mg L⁻¹), significantly inhibited seed germination and seedling growth. Compared to the low concentration (100 mg L⁻¹) of PLA-NPs, the high concentrations (500 mg L⁻¹) reduced the germination percentage by 25.0% and fresh weight by 25.8% and increased root MDA (6.7%), SOD (30.0%), POD (6.3%), ASA (13.4%), and GSH (13.1%). Under the same concentration of the PLA, PLA + NaCl treatments exerted stronger inhibitory effects than PLA-NPs alone, with the seed germination percentage and fresh weight reduced by an average of 52.7% and 6.6%, respectively. Notably, the inhibitory effects and integrated biomarker response (IBR) index of the PLA 500 + NaCl treatment were the highest. The presence of PLA-NPs in roots was confirmed using confocal laser scanning microscopy. GO enrichment analysis showed that pathways related to nutrient reservoir activity, oxidoreductase activity, hydrogen peroxide catabolic process, and hydrogen peroxide metabolic process were enriched under PLA-NP and PLA + NaCl treatments. KEGG analysis further indicated enrichment in phenylpropanoid biosynthesis, ABC transporters, and alpha-linolenic acid metabolism. The PLA-NP and PLA + NaCl treatments upregulated genes associated with oxidoreductase activity (Zm00001eb238800, Zm00001eb128620, and Zm00001eb020790). These findings suggest that synergistic toxicity of PLA-NPs and salinity stress in maize is primarily driven by the internalization of PLA-NPs and Na⁺ within maize roots, which negatively impacts maize seed germination and seedling growth by disrupting redox homeostasis and metabolic balance, thereby forcing plants to reallocate resources from growth toward oxidative stress defense. This study provides critical insights into the environmental risks of biodegradable nano-plastics in saline–alkali soil environments. Full article

Microplastics and nanoplastics (MNPLs) are increasingly recognized as dynamic vectors capable of transporting a wide range of environmental contaminants, as well as acting as physical particulates. Their small size, high surface reactivity and strong sorption capacity allow them to carry metals, pesticides, pharmaceuticals and endocrine-active compounds into biological systems. This narrative review examines how these particle-contaminant complexes influence oxidative stress, inflammatory signaling and endocrine function during early development. Relevant literature was identified through structured searches of PubMed, Scopus, Web of Science and Google Scholar, with a focus on the physicochemical properties of plastics, sorption mechanisms, gut barrier physiology and developmental toxicology. Early developmental stages are particularly sensitive, as immature mucus layers, permeable epithelial junctions and underdeveloped detoxification pathways facilitate the uptake and systemic distribution of MNPLs. Once internalized, these particles and their chemical cargo promote the generation of reactive oxygen species through redox-active contaminants, surface-catalysed reactions and mitochondrial dysfunction. The resulting oxidative imbalance activates stress-responsive pathways, including Nrf2–Keap1 signaling, and promotes lipid peroxidation, DNA damage and cellular dysfunction. MNPLs also stimulate inflammatory cascades by activating pattern-recognition receptors, altering cytokine profiles and disrupting epithelial homeostasis. These responses are intensified in the presence of sorbed pollutants, leading to sustained inflammatory states that can be particularly detrimental during organogenesis and immune maturation. Endocrine function is likewise affected, as MNPLs transport hormonally active chemicals and can interfere with hormone-responsive pathways through oxidative and inflammatory mechanisms. These interactions may disrupt thyroid signaling, metabolic regulation and the development of the reproductive axis, with potential long-term physiological consequences. Integrating evidence from polymer chemistry, contaminant behavior and developmental physiology, this review shows that MNPLs act as biologically active vectors that may increase oxidative, inflammatory and endocrine disturbances during early development. These findings highlight the importance of considering particle–contaminant interactions as a critical component of early-life risk assessment. Full article

Seasonal thermal stratification in deep reservoirs easily causes bottom hypoxia and a sharp decrease in oxidation–reduction potential (ORP), leading to the pulsed release of internal phosphorus from sediments. Under climate warming, this has become a hot issue for sustainable reservoir eutrophication control. Taking the Quanmin Reservoir in Southwest China as the research object, this study combined high-resolution profile monitoring and a Box–Behnken response surface experiment to construct a semi-empirical model coupling redox threshold effect and Arrhenius kinetics. Results showed that during thermal stratification, the water body below 18 m formed a significant redox gradient, resulting in a 21-fold vertical difference in phosphorus concentration. The response surface experiment confirmed that ORP dominates phosphorus release, and the temperature (T) effect is strictly redox-dependent: warming only promotes phosphorus release under anaerobic conditions (−50 mV), with a 26% increase in release amount when temperature rises from 10 °C to 30 °C, while temperature has a negligible effect under aerobic conditions (+30 mV). Model fitting yielded an ORP critical threshold of −17.2 ± 4.8 mV and a normalized steepness of 0.033 mV⁻¹, indicating joint control by diffusion and reaction. Based on these results, a synergistic regulatory mechanism of redox threshold and temperature was proposed, providing a quantitative basis for reservoir eutrophication management under climate warming. Maintaining ORP above −17 mV through bottom aeration can effectively block internal phosphorus release from the redox threshold perspective, though practical in situ application is constrained by aeration-induced water mixing and microbial variations, and such precise redox control may save energy, supporting the sustainability of reservoir ecosystems and long-term water quality security. Full article

Tamarindus indica L., a key economic tree species in tropical regions, suffers severely from postharvest decay. From 2023 to 2025, disease fruits exhibiting pericarp softening, pulp browning, and sticky exudates were collected in Yunnan, China. Pathogenicity tests following Koch’s postulates, combined with morphological characterization and phylogenetic analyses of the internal transcribed spacer (ITS), translation elongation factor 1-alpha (TEF 1α), and beta-tubulin (TUB) gene regions, identified the causal pathogen as Botryosphaeria fabicerciana (isolates ZWML-06, ZWML-44, ZWML-17). This is the first report of this postharvest disease on tamarind in Yunnan, filling an etiological gap. Additionally, an endophytic bacterium, designated BV-1, was isolated from asymptomatic pulp tissues. Whole-genome sequencing and phylogenetic analysis identified it as Bacillus velezensis. Strain BV-1 exhibited strong in vitro antagonistic activity against the pathogen, indicating promising biocontrol potential. Functional annotation revealed that BV-1 possesses a complex genetic system with developed transporter systems; its core metabolic network is dominated by nitrogen metabolism and redox processes, suggesting a potential “multi-target” antimicrobial mechanism. This study provides a theoretical basis and novel resources for the green control of postharvest diseases in tamarind. Full article

The rational design of electrode architectures is essential for advancing high-performance supercapacitors. In this study, Nd₂O₃ electrodes with controlled structural features were developed via a polyacrylic acid (PAA)-assisted hydrothermal approach. By systematically tuning PAA concentration, the growth mechanism of Nd₂O₃ was effectively regulated, leading to a distinct morphological transition from compact agglomerates to well-defined hierarchical structures. The optimized Nd₂O₃-P2 electrode exhibits a porous and interconnected architecture, providing enhanced electrolyte accessibility and shortened ion diffusion pathways. This structural optimization significantly improves electrochemical performance, delivering a high areal capacitance of 26.889 F/cm² at 10 mA/cm², along with excellent rate capability and reduced internal resistance. Kinetic analysis reveals that charge storage is predominantly governed by diffusion-controlled Faradaic processes, with the optimized structure facilitating rapid ion transport and efficient redox activity. Additionally, the electrode demonstrates excellent cycling durability, retaining 87.08% capacitance over 12,000 cycles. An asymmetric supercapacitor assembled using Nd₂O₃-P2 and activated carbon achieves stable operation up to 1.5 V, delivering good capacitance retention (81.2%) after 7000 cycles. This work highlights the effectiveness of PAA-induced structural tuning and provides a practical strategy for developing advanced rare earth oxide-based electrodes for energy storage applications. Full article

The development of lithium-ion batteries (LIBs) capable of extreme fast charging (XFC) while preserving safety, durability, and practical energy density remains a central challenge for next-generation electric transportation and grid-scale storage. Conventional graphite anodes are fundamentally limited at high current densities by sluggish intercalation kinetics, which cause lithium plating, motivating the exploration of alternative insertion materials. This review provides a comprehensive and internally consistent assessment of titanium-based oxide anodes, encompassing TiO₂ polymorphs, lithium titanate (Li₄Ti₅O₁₂), and Wadsley–Roth titanium niobium oxides, through the combined lenses of crystal topology, diffusion pathways, redox chemistry, interfacial behavior, and resource scalability. By systematically comparing structural frameworks and electrochemical mechanisms across these material classes, we demonstrate that fast-charging performance is governed not by nano-structuring alone, but by the intrinsic coupling between operating potential, framework rigidity, and multi-electron redox activity. While Li₄Ti₅O₁₂ establishes the benchmark for safety and cyclability, and TiO₂ polymorphs provide structural versatility, titanium niobium oxides uniquely reconcile high theoretical capacity with minimal lithiation strain and open diffusion channels, positioning them as highly promising candidates for sub-10 min charging without catastrophic degradation. This review highlights the persistent obstacles these materials suffer, such as limited round-trip energy efficiency (RTE), interfacial gas evolution, poor dopant stability, and unsustainable extraction, while simultaneously exploring targeted design strategies to overcome them. Finally, this review provides a materials design and comparison framework for the development of safe, high-power, and commercially viable ultrafast-charging LIBs. Full article

Heavy metal contamination associated with mining activities is a major source of abiotic stress for plants, strongly affecting plant physiology, growth and survival in contaminated environments. Due to their non-biodegradable nature and long-term bioavailability, heavy metals persist in soils affected by mining activities, exposing plants to chronic stress conditions that require the activation of coordinated cellular and molecular response mechanisms to limit toxicity and maintain internal homeostasis. This review synthesises and critically analyses current knowledge on the molecular and cellular mechanisms governing plant responses to heavy metal stress in mining-affected environments. Key processes involved in metal uptake and transport, redox imbalance and oxidative stress generation, antioxidant defence systems, and molecular detoxification mechanisms, including metal chelation, subcellular compartmentalisation, and gene expression regulation, are discussed. Particular attention is paid to cellular signalling pathways that mediate plant adaptation to prolonged exposure to complex metal mixtures. Emphasis is placed on integrating molecular-level knowledge with the specific context of mining sites, highlighting the limitations of extrapolating results obtained under controlled experimental conditions to naturally contaminated environments. This perspective integrates molecular mechanisms with the geochemical realities of mining sites, providing a solid basis for the development of effective phytoremediation strategies and the optimisation of plant species selection. Full article

Arsenic (As) is a ubiquitous and highly toxic metalloid with well-established carcinogenicity. Its accumulation and secondary release from lake sediments pose potential risks to lake ecosystem integrity and human health. Meanwhile, the ongoing intensification of lake eutrophication at the global scale has altered the sources, composition, and environmental behavior of internally derived dissolved organic matter (DOM). These changes have profoundly influenced As mobilization and transformation at the sediment-water interface (SWI). To advance understanding of the regulatory roles and underlying mechanisms of algal dissolved organic matter (ADOM) and submerged macrophyte dissolved organic matter (SMDOM) in As biogeochemical cycling under lake ecosystem regime shifts, extensive findings from the international literature were synthesized. The characteristic properties and environmental behaviors of ADOM and SMDOM were systematically compared, and their distinct regulatory pathways in lacustrine systems were further summarized. Results indicate that ADOM is typically characterized by low molecular weight, weak aromaticity, and high bioavailability. It can enhance As dissolution and mobilization from sediments through direct complexation, competition for adsorption sites, and stimulation of microbial metabolism and Fe(III) reduction. In contrast, SMDOM exhibits higher molecular weight, greater aromaticity, and a higher degree of humification. It tends to form stable complexes with mineral phases. Under the influence of radial oxygen loss (ROL) from submerged macrophyte roots during the growth phase, its capacity to promote mineral reduction is relatively limited. This process favors stable As retention in sediments. The regulatory effects of ADOM and SMDOM on As behavior are strongly modulated by environmental factors such as pH, redox potential (Eh), temperature, and light conditions, as well as by microbial communities. ADOM is more sensitive to reducing environments and photochemical processes. SMDOM, in contrast, exerts more persistent control under oxidizing conditions and at mineral-water interfaces. In addition, ADOM more readily drives microbial community shifts toward assemblages with enhanced capacities for Fe(III) reduction and As reduction or methylation. SMDOM is less likely to trigger strongly reducing processes. Based on these mechanisms, the outbreak and decay phases in algal-dominated lakes often correspond to critical periods of enhanced As mobilization and elevated ecological risk. In submerged macrophyte-dominated lakes, the decay phase may represent an important window for sedimentary As release. Finally, a conceptual framework describing the differential regulation of As biogeochemical cycling by ADOM and SMDOM is proposed. This framework provides a theoretical basis for As risk identification, the determination of critical risk periods, and the development of management strategies across lakes with different trophic states. Full article

Hypocrellin A (HA) represents a pharmaceutically important perylenequinone photosensitizer produced by Shiraia bambusicola. However, submerged fermentation remains constrained by filamentous morphological characteristics and inherent mass transfer limitations. Although microparticle-enhanced cultivation (MPEC) has demonstrated efficacy in filamentous fungal systems, the molecular mechanisms by which physical cues, such as microparticle-induced shear stress, reprogram fungal metabolism remain largely unexplored. This work systematically optimizes SiO₂-based MPEC parameters for S. bambusicola GDMCC 60438, including particle dimensions, temporal addition protocols, and solid loading. Mechanistic investigations integrated pellet morphology analysis, membrane lipid composition, intracellular redox status, energy/precursor markers, and RNA-seq transcriptomic profiling with qRT-PCR validation. Under optimized conditions (10% w/v SiO₂, 30 mesh, added at 6 h), HA yield reached 41.76 ± 5.02 mg/L, representing a 3.65-fold increase over controls. MPEC shifted morphology toward smaller, more porous pellets with denser internal structure, accompanied by increased membrane fluidity (unsaturated/saturated fatty acid ratio from 1.54 to 2.63), elevated ROS levels with antioxidant enzyme activation, and enhanced acetyl-CoA and ATP accumulation. Transcriptomic analysis identified 206 differentially expressed genes enriched in oxidative phosphorylation, carbon metabolism, and stress responses, with upregulation of PKS-related biosynthetic genes and major facilitator superfamily transporters. This work establishes an integrated mechanistic framework linking particle-induced morphological changes to metabolic reprogramming through oxidative stress and subsequent transcriptional activation of the HA biosynthetic pathway, providing rational design principles for MPEC strategies in filamentous fungi. Full article

Phosphorus (P) is an essential macronutrient for plant growth and a major limiting factor for crop productivity, especially in tropical soils characterized by low P availability and high fixation capacity. The strong dependence of modern agriculture on non-renewable phosphate fertilizers, combined with their low use efficiency, raises economic and environmental concerns and reinforces the need to improve phosphorus use efficiency (PUE) in maize. PUE is a complex trait governed by integrated morphophysiological, biochemical, and molecular mechanisms related to phosphorus acquisition, internal remobilization, metabolic reprogramming, and root system plasticity. Recent advances using omics-based approaches have substantially expanded the understanding of these mechanisms, revealing coordinated regulation of carbon and energy metabolism, phosphatase activity, redox balance, and root meristem dynamics under P-limiting conditions. In parallel, increasing evidence demonstrates the important role of phosphate-solubilizing and plant growth-promoting bacteria in enhancing P availability through organic acid secretion, enzymatic mineralization of organic P forms, and modulation of root architecture. However, despite these advances, the genetic basis of plant responsiveness to beneficial bacteria and the interaction between host genotype and microbial activity remain poorly explored. This review integrates current knowledge on phosphorus dynamics in the soil–plant system, the genetic control of PUE in maize, and the contribution of beneficial bacteria, highlighting the importance of combining classical breeding, molecular approaches, and microbial strategies to accelerate the development of maize cultivars with improved phosphorus efficiency and reduced fertilizer dependency. Full article

The release of phosphorus (P) from littoral wetland sediments drives eutrophication, with iron (Fe) and sulfur (S) cycles playing key regulatory roles. This study investigated the Tongyang River corridor wetland (Lake Chaohu) in China to elucidate P–Fe–S coupling mechanisms. High-resolution two-dimensional (2D) Diffusive Gradients in Thin-Films (DGT), P-fractionation, and microbial sequencing were employed during wet and dry periods. Results indicated significant total phosphorus (TP) spatial heterogeneity and seasonal available phosphorus (AP) variation. A robust spatial co-variance between DGT-Fe and DGT-P (r > 0.95) reinforces the iron-redox paradigm. However, 2D mapping revealed discretized sub-millimeter “hotspots,” demonstrating that iron (oxyhydr)oxide reductive dissolution is governed by micro-scale niches rather than uniform processes. Microbial analysis further identified summer diversity and Chloroflexi enrichment as primary biological drivers of P mobilization. Specifically, hydrological fluctuations dictate the iron-redox cycle, with wet-period microbial activation serving as the engine for internal P release. These findings suggest that regulating sediment redox conditions across hydrological stages is essential for mitigating wetland eutrophication. Full article

The field of developing effective catalysts for heterogeneous catalysis has recently focused on controlling the structures of catalysts themselves to optimise the density and energy of crystal lattice defects. This can significantly influence catalytic activity in terms of both reaction rates and reaction mechanisms, and thus the selective production of desired substances as well. In many cases, these crystal lattice defects manifest themselves as so-called electron traps (ETs) and thus significantly influence charge transfer between the catalyst and reactants. ETs provide the missing electronic link between atomic-scale defects and macroscopic performance in heterogeneous catalysis. Therefore, the importance of ETs for catalysis is particularly evident in areas where charge transfer plays a fundamental role in the reaction mechanism, such as photocatalysis and electrocatalysis. In the field of thermally initiated reactions, the importance of ETs in heterogeneous catalysis has not yet been fully appreciated. However, several studies have already addressed the importance of ETs for this type of reaction. This review consolidates and extends the concept of ETs to purely thermal-initiated reactions, with a focus on CO₂ hydrogenation using typical transition metal catalysts. Firstly, in this review, ETs are defined as band gap states associated with internal and external defects, and their depth, density, spatial location, and dynamics are then coupled with key steps in thermocatalytic cycles, including charge storage/release, reactant activation, intermediate stabilisation, and redox turnover. Secondly, electron trap detection is reviewed based on advanced spectroscopic techniques, including reversed double-beam photoacoustic spectroscopy (RDB-PAS), thermally stimulated current (TSC), deep-level transient spectroscopy (DLTS), thermoluminescence (TL), electron paramagnetic resonance (EPR), and photoluminescence (PL), highlighting how each method describes trap energetics and populations under realistic operating conditions. Finally, case studies on the application of metal oxides and supported metals are discussed, as these are typical catalysts for the reaction mentioned above. This review highlights how oxygen vacancies (OVs), polarons, and metal–support interfacial sites act as robust electron reservoirs, lowering the barriers for CO₂ activation and hydrogenation. By reframing thermocatalysts through the lens of ET chemistry, this review identifies ETs as actionable targets for the rational design of next-generation materials for CO₂ hydrogenation and related high-temperature transformations. Full article

Background/Objectives: Early childhood caries (ECC) and saliva have been studied across disparate domains, including microbiome, fluoride, immune, oxidative-stress, and neuroendocrine research. However, the ECC–saliva literature has not previously been mapped as a connected system using modern natural language processing (NLP). This study treats PubMed titles and abstracts as data to identify major themes, emerging topics, and candidate neuroimmune axes in ECC–saliva research. Methods: Using the NCBI E-utilities API, we retrieved 298 PubMed records (2000–2025) matching (“early childhood caries” [Title/Abstract]) AND saliva [Title/Abstract]. Text was cleaned with spaCy and embedded using a transformer encoder; BERTopic combined UMAP dimensionality reduction and HDBSCAN clustering to derive thematic topics. We summarised topics with class-based TF–IDF, constructed keyword co-occurrence networks, defined an internal topic-level Novelty Index (semantic distance plus temporal dispersion), and mapped high-novelty topics to gene ontology and Reactome pathways using g:Profiler. Prophet was used to model temporal trends and forecast topic-level publication trajectories. Finally, we generated a fully synthetic neuroimmune salivary dataset, based on realistic ranges from the literature, to illustrate how the identified axes could be operationalised in future ECC cohorts. Results: Seven coherent ECC–saliva topics were identified, including classical microbiome and fluoride domains as well as antioxidant/redox, proteomic, peptide immunity, and Candida–biofilm themes. High-novelty topics clustered around total antioxidant capacity, glutathione peroxidase, superoxide dismutase, and peptide-based host defence. Keyword networks and ontology enrichment highlighted “Detoxification of Reactive Oxygen Species”, “cellular oxidant detoxification”, and cytokine-mediated signalling as central processes. Temporal forecasting suggested plateauing growth for classical epidemiology and fluoride topics, with steeper projected increases for antioxidant and peptide-immunity themes. A co-mention heatmap revealed a literature-level Candida–cytokine–neuroendocrine triad (e.g., Candida albicans, IL-6/TNF, cortisol), which we propose as a testable neuro-immunometabolic hypothesis rather than a confirmed mechanism. Conclusions: AI-assisted topic modelling and network analysis provide a reproducible, bibliometric map of ECC–saliva research that highlights underexplored antioxidant/redox and neuroimmune salivary axes. The synthetic neuroimmune dataset and modelling pipeline are illustrative only, but together with the literature map, they offer a structured agenda for future ECC cohorts and mechanistic studies. Full article

Redox (reduction–oxidation) processes underlie all forms of life and are a universal regulatory mechanism that maintains homeostasis and adapts the organism to changes in the internal and external environments. From capturing solar energy in photosynthesis and oxygen generation to fine-tuning cellular metabolism, redox reactions are key determinants of life activity. Proteins containing sulfur- and selenium-containing amino acid residues play a crucial role in redox regulation. Their reversible oxidation by physiological oxidants, such as hydrogen peroxide (H₂O₂), plays the role of molecular switches that control enzymatic activity, protein structure, and signaling cascades. This enables rapid and flexible cellular responses to a wide range of stimuli—from growth factors and nutrient signals to toxins and stressors. Mitochondria, the main energy organelles and also the major sources of reactive oxygen species (ROS), play a special role in redox balance. On the one hand, mitochondrial ROS function as signaling molecules, regulating cellular processes, including proliferation, apoptosis, and immune response, while, on the other hand, their excessive accumulation leads to oxidative stress, damage to biomolecules, and the development of pathological processes. So, mitochondria act not only as a “generator” of redox signals but also as a central link in maintaining cellular and systemic redox homeostasis. Redox signaling forms a multi-layered cybernetic system, which includes signal perception, activation of signaling pathways, the initiation of physiological responses, and feedback regulatory mechanisms. At the molecular level, this is manifested by changes in the activity of redox-regulated proteins of which the redox proteome consists, thereby affecting the epigenetic landscape and gene expression. Physiological processes at all levels of biological organization—from subcellular to systemic—are controlled by redox mechanisms. Studying these processes opens a way to understanding the universal principles of life activity and identifying the biochemical mechanisms whose disruption causes the occurrence and development of pathological reactions. It is important to emphasize that new approaches to redox balance modulation are now actively developed, ranging from antioxidant therapy and targeted intervention on mitochondria to pharmacological and nutraceutical regulation of signaling pathways. This article analyzes the pivotal role of redox balance and its regulation at various levels of living organisms—from molecular and cellular to tissue, organ, and organismal levels—with a special emphasis on the role of mitochondria and modern strategies for influencing redox homeostasis. Full article

Redox potential controls a vast array of biochemical reactions, and its changes influence the transition from normal to pathological states. However, cellular redox potential is primarily assessed after extraction of water-soluble components (reduced and oxidized) from biological material, particularly glutathione, which, due to its abundance, determines intracellular redox potential. This process involves mechanistic averaging of redox potential values across tissue or cell, although existing data suggest, and sometimes directly indicate, heterogeneity in redox potential both within cells and within tissue. We argue that mitochondria determine cellular redox state, in particular through changes in the state of the mitochondrial reticulum caused by various internal and external factors. We describe the possibilities for regulation of redox status of the cell and organ as a potential therapy for various pathologies, particularly cancer, and propose intensifying efforts to utilize intrinsic redox indicators. We specifically examine the possibility of changes the redox potential in cancer cells through the use of oxidative phosphorylation uncouplers and propose mechanisms by which cancer cells may be killed using uncouplers. Particular attention is paid to the mitochondrial membrane potential as a powerful regulator of cellular metabolism, possibly unrelated to the regulation of reactive oxygen species levels, with the possible existence of a membrane potential sensor in cells. Full article