Search Results (776)

Bergapten is a plant-derived linear furanocoumarin widely distributed in Rutaceae and Apiaceae species and increasingly recognized for its multifunctional anticancer potential. This review critically synthesizes current evidence on bergapten’s biosynthesis, physicochemical and pharmacokinetic properties, anti-inflammatory and antioxidant pharmacodynamics, and mechanistic antitumor activity, highlighting its translational relevance within pharmaceutical development. Preclinical studies across diverse malignancies demonstrate pleiotropic anticancer effects. Mechanistically, bergapten activates mitochondrial apoptosis via Bax/Bcl-2 modulation and caspase cascades, induces cell cycle arrest through p53–p21 signaling, and suppresses PI3K/Akt/mTOR and NF-κB pathways. Additional effects include PTEN-mediated autophagy induction, interference with metabolic reprogramming, reversal of multidrug resistance through ABC transporter modulation, and context-dependent photoactivated cytotoxicity. Beyond direct tumor cell targeting, bergapten attenuates pro-inflammatory mediators and regulates redox homeostasis through downregulation of NOX4-derived ROS and activation of Nrf2-driven antioxidant defenses, addressing the redox–inflammatory axis implicated in carcinogenesis. Despite promising mechanistic depth, clinical translation is limited by incomplete human pharmacokinetic data and poor aqueous solubility. Nanotechnology-enabled delivery systems and structural derivatives offer strategies to enhance bioavailability and therapeutic index. Overall, bergapten emerges as a systems-level phytochemical candidate warranting further translational investigation in oncology. Full article

Anthropogenic reactive nitrogen (Nr) production now greatly exceeds natural creation, generating cascading environmental impacts on the environment and human health. Effective monitoring of Nr in ecosystems is essential for early warning and policy response, yet the landscape of available monitoring methods is wide and heterogeneous, varying substantially in accuracy, purpose, cost, and ecological scope. This study evaluates nineteen Nr-monitoring methods, grouped into chemistry-based (CM), biodiversity-based (BM), and transplant-based (TM) methods, against 36 fitness-for-purpose (FFP) indicator facets. Facets are organized into intrinsic (direct measurement of nitrogen cycle components), projected (ecological effects the method can indicate), and extrinsic (metaproperties such as cost or precision) types. Scores are derived from 89 core papers, ranked using evidence-normalized weighted-sums (WS) and non-metric multidimensional scaling (NMDS) approaches. CMs generally outperform BMs and TMs, with critical loads, total tissue nitrogen, and nitrogen isotopes leading overall. Lichen diversity, ectomycorrhizal fungi, and Ellenberg’s N lead among BMs, particularly for projected facets. The NMDS reveals a structural divide and monitoring complementarity between CMs and BMs, with CMs serving as early warning indicators, whereas BMs integrate cumulative, persistent ecosystem impacts. While no single method seems adequate for comprehensive monitoring, the FFP matrix facilitates selecting optimal monitoring combinations. Full article

Phyllanthus amarus has long been used in traditional medicine and contains diverse bioactive compounds with potential pharmacological properties. This study aimed to purify the compounds from P. amarus and investigate their inhibitory effects on mast cell degranulation in vitro. It was found that the ethyl acetate fraction from P. amarus possesses potential inhibitory effects on mast cell degranulation. Subsequently, three compounds, including 3,3′,4-tri-O-methylellagic acid (P1), ethyl brevifolincarboxylate (P2), and 4′,4′′′-di-O-methyl cupressuflavone (P3), were purified and identified. These compounds significantly inhibited mast cell degranulation via decreasing histamine release and IL-4 and TNF-α production from the activated mast cells without any cytotoxicity. Furthermore, Western blot analysis confirmed that these compounds suppressed phosphorylation of Syk and PLCγ, suggesting inhibition of the degranulation-related signaling cascade. These findings provide preliminary in vitro evidence that purified constituents from P. amarus may inhibit mast cell degranulation, potentially in association with modulation of Syk/PLCγ signaling, and support further mechanistic and in vivo investigations. Full article

Cross-modal person re-identification between visible and infrared domains remains a challenging problem due to significant modality gaps. This paper presents a novel approach termed Intermediate Shared Feature Network (ISFNet) that explicitly addresses this issue by exploiting intermediate feature representations within a dual-stream backbone. Unlike conventional methods that primarily focus on final-layer features, ISFNet introduces two complementary components: a Multi-layer Feature Cascade Module (MFCM) that aggregates discriminative features across different network stages, and a Dual Feature Generation Module (DFGM) that creates diverse intermediate representations through Instance-Batch Normalization variants. By integrating these modules, ISFNet effectively bridges the cross-modal gap and improves matching accuracy. Comprehensive experiments on the SYSU-MM01 and RegDB datasets demonstrate that the proposed method achieves competitive performance against state-of-the-art approaches, with noticeable improvements in both Rank-1 accuracy and mean average precision. Full article

3,4-dihydrocoumarins and spiro compounds constitute an important class of privileged frameworks present in a wide variety of natural and synthetic molecules with diverse applications. In this study, we developed an organocatalytic methodology for the construction of complex and diverse chiral spiro-bridged 3,4-dihydrocoumarins through a Diels–Alder/Nucleophilic ring-closing cascade via trienamine activation. The reaction proceeds efficiently with different trienamine precursors and a range of coumarin-3-carboxamides, which act as both dienophile and intramolecular nucleophile species. This process affords the desired products in good yields and with a high degree of stereocontrol. Furthermore, several transformations on the newly formed spiro-piperidone ring demonstrate the synthetic utility of the obtained compounds. Full article

Biotic stresses (pest feeding, pathogenic fungal/bacterial/viral infection) and diverse abiotic stresses (extreme temperature, drought, waterlogging, saline–alkali soil, heavy metal pollution, nutrient deficiency, UV-B, ozone) severely restrict crop growth and global agricultural yield. Lipids act as core membrane structural constituents and vital secondary signaling messengers, executing multi-layered adaptive balancing functions during cell-type interactive stress acclimation, rather than uniform whole-plant lipid responses. They sustain membrane structural integrity across distinct cell populations, serve as synthetic precursors of bioactive signaling molecules, and trigger cascaded transcriptional and metabolic reprogramming upon environmental stimuli to rebalance physiological status among different cell types. This review systematically summarizes cell-type interactive lipid-mediated plant defense and acclimation balance mechanisms across biotic and abiotic stress contexts. We elaborate the biological functions of fatty acids, phospholipids, galactolipids, sphingolipids and their derivatives (jasmonate, salicylic acid, phosphatidic acid, oxylipin) in stress signal transduction and antioxidant defense and strictly distinguish two categories of lipid changes under all stress types: active adaptive lipid remodeling and passive stress-induced lipid oxidative damage. Key contents include stress-triggered cell-type-specific membrane lipid remodeling, the hierarchical transcriptional regulatory network mediated by WRI1, LEC1, PHR, MADS and other transcription factors governing oil metabolism, as well as crosstalk between lipid metabolism and compartmentalized reactive oxygen species (reactive oxygen species (ROS)) signaling. We further compare conserved lipid-regulatory modules and species-specific divergent responses across model plants and economic oilseed crops, integrating state-of-the-art targeted/untargeted lipidomics, single-cell spatial lipidomics and multi-omics joint breeding strategies to improve multi-stress tolerance in oilseed crops. By consolidating global research progress up to 2025, including the two latest 2026 cross-species meta-analysis reviews, this review provides systematic theoretical support and operable multi-level technical frameworks for genetic engineering targeting conserved lipid pathways to breed stress-resilient high-oil crop germplasm, and highlights reliable lipid stress biomarker screening as a promising translational research direction. Full article

Neurodevelopmental disorder, speech impairment, and dysmorphic facies (NEDSID) is an autosomal dominant condition primarily driven by SETD1A haploinsufficiency. While most documented cases are sporadic, genomic mechanisms underlying intrafamilial phenotypic heterogeneity remain poorly understood. This study presents a comprehensive clinical, neurophysiological, and molecular characterization of a two-generation Mexican family segregating a novel heterozygous missense SETD1A variant. Whole-exome sequencing (WES) identified a c.1604G>A (p.Gly535Glu) substitution localized within the critical Functional Location on SETD1A (FLOS) domain, which was validated via automated Sanger sequencing across all family members and 100 ethnically matched controls. The proband exhibited a moderate NEDSID phenotype, including global developmental delay, macrocephaly, borderline IQ (79) with pronounced information-processing deficits, and abnormal EEG sharp waves. Conversely, first-degree relatives carrying the identical variant presented with mild, non-intellectually disabling phenotypes characterized primarily by isolated psychiatric disorders (bipolar disorder, depression) and minimal dysmorphism. Structural 3D modeling and multi-algorithmic in silico profiling confirmed high evolutionary conservation and a deleterious impact (CADD: 22.2, SIFT: 0.00, GERP: 2.924), classifying the variant as a Variant of Uncertain Significance (VUS)/Likely Pathogenic according to ACMG/AMP criteria (PM2, PP1, PP3, PP4). Furthermore, epigenetic dysregulation and chromatin remodeling defects increasingly link these histone-modifier variants to broader psychiatric landscapes. Emerging transcriptomic profiling confirms that dosage-sensitive COMPASS complex disruptions alter downstream neurodevelopmental gene cascades. Our findings present observational evidence of intrafamilial clinical variability in a single pedigree with a SETD1A missense alteration, supporting the hypothesis that non-catalytic domain substitutions may contribute to diverse neurodevelopmental outcomes. Full article

The intricate interplay between the gut microbiome and the enteric nervous system remains a paramount focus in understanding the multifactorial pathogenesis of disorders of gut–brain interaction (DGBI), most notably irritable bowel syndrome (IBS). While the clinical entity of post-infectious IBS is well-established, the independent, long-term pathophysiological impact of iatrogenic antibiotic exposure is garnering critical attention within neurogastroenterology. This narrative review provides a comprehensive synthesis of current epidemiological and mechanistic evidence positioning antibiotic-induced microbial depletion as a potential predisposing factor for incident IBS. By evaluating recent literature, we highlight epidemiological trends demonstrating a consistent, dose-dependent relationship between cumulative antibiotic courses, particularly broad-spectrum agents, and an elevated risk of developing IBS, independent of prior acute enteric infections. Furthermore, we explore the mechanistic underpinnings of this association, focusing on how systemic antibiotics induce persistent, detrimental alterations in commensal diversity. This resulting dysbiosis initiates a proposed cascade of downstream consequences, including compromised epithelial barrier integrity, persistent low-grade mucosal inflammation, and altered bile acid metabolism. These localized disruptions serve as established triggers for visceral hypersensitivity and dysregulated gastrointestinal motility communicated via the gut–brain axis. Ultimately, this review underscores that antibiotic exposure may act as a significant, modifiable risk factor for IBS pathogenesis. Recognizing this substantial iatrogenic risk reinforces an urgent clinical imperative for stringent antimicrobial stewardship and emphasizes the necessity for future research directed toward prophylactic, microbiome-sparing strategies to mitigate the escalating global burden of DGBIs. Full article

The precise detection and profiling of biotoxins are of paramount importance in analytical and forensic toxicology. Investigating these toxicants within highly chaotic background matrices—ranging from postmortem biological fluids to suspected poisoning vehicles such as complex dietary and environmental samples—requires robust recognition molecules capable of overcoming severe interference. This comprehensive review summarizes recent analytical developments in biotoxin detection, categorizing molecular recognition platforms into three primary types: immunological recognition (antibodies and recombinant derivatives), aptamer-based recognition, and entirely synthetic recognition (molecularly imprinted polymer, MIP). To meet the rigorous ultra-trace demands of medicolegal analysis, we further discuss the strategic integration of these recognition elements with powerful catalytic amplification cascades, highlighting the transition from natural biological enzymes to highly durable nanozymes and DNAzymes. By detailing recent structural optimizations and preparation strategies, this review critically evaluates the respective advantages, matrix tolerances, and limitations of each recognition mode when applied to diverse and challenging analytical samples. Finally, we provide a forward-looking perspective on the translational potential of these specific binding agents, emphasizing how computational rational design and portable integration will overcome practical bottlenecks in modern toxicological investigations. Full article

Background/objective: Postpartum depression (PPD) is a significant public health issue affecting about 19% of mothers globally. It has well-documented impacts on maternal well-being, mother–infant relationships, and child developmental outcomes. At the same time, the level of vitamin D deficiency in women of reproductive age is very high (affecting 60–87 percent of pregnant women globally). The review aims to synthesize current evidence and highlight priority research areas to improve maternal mental health outcomes. Methods: A systematic literature search of PubMed, Scopus, and Google Scholar (2015–2026) was conducted, followed by narrative synthesis of mechanistic, observational, and interventional evidence. Results: Adequate vitamin D status may contribute to a reduced risk of postpartum depression through multiple interacting pathways, including serotonin synthesis and metabolism (via tryptophan hydroxylase 2 (TPH2) and monoamine oxidase-A (MAO-A) regulation), neuroplasticity via brain-derived neurotrophic factor (BDNF) signaling, and suppression of the pro-inflammatory cytokine cascade. Dose–response meta-analyses and large prospective cohort studies indicate consistent negative relationships between maternal vitamin D levels and postpartum depressive and anxiety symptoms with optimal serum 25-hydroxyvitamin D (25(OH)D) levels of 90–110 nmol/L. Conclusions: There is still limited evidence on the intervention; it is still methodologically diverse, and only a few randomized controlled trials have been carried out on specifically postpartum populations. Full article

With the increasing diversity of multimedia data types, single-modal steganography is insufficient to meet the demand for the simultaneous covert communication of multiple types of data, and single optical transformation encryption schemes are insufficiently secure against cryptanalytic attacks. To address these challenges, this paper designs and implements a multimodal secret information steganography system based on the optical Gyrator transform. We propose a multimodal steganographic system for the covert transmission of three types of heterogeneous secret data—text, color images, and audio—using a three-level cascaded optical encryption architecture. The system first uniformly encapsulates the multimodal data into a unified bitstream via a Type–Length–Value (TLV) format; it then uses the Ushiki chaotic map to generate a pure phase mask for random phase modulation of the carrier image, followed by spatial-frequency scrambling via a fractional Fourier transform (FrFT, order γ = 1.6). The secret bitstream is embedded into all eight bit planes of the amplitude components in the FrFT domain using binary square representation, achieving an embedding capacity of 2.23 × 10⁶ bits—approximately 8.5 times that of traditional LSB methods; finally, a speckle-noise-like ciphertext is output via a Gyrator transform (angle α = 0.5). Experiments demonstrate that under non-attack conditions, the system achieves lossless recovery with a zero bit-error rate. Under known-plaintext and chosen-plaintext attacks on the Gyrator layer, the PSNR of the recovered images was only 4.89 dB and 4.80 dB, respectively, and the secret information could not be effectively extracted, as the chaotic-FrFT pre-encryption statistically isolates the intermediate image from natural image statistics. This system provides a functionally complete and practically secure solution for multimodal covert communication. Full article

The ABA signaling pathway is essential for plant growth, development, and responses to diverse abiotic stresses. 9-cis-epoxycarotenoid dioxygenases (NCEDs) are key functional enzymes involved in this pathway. In the present study, we investigated the biological roles and underlying molecular mechanisms of the TaNCED1 gene in wheat under drought stress treatment, using two materials: TaNCED1-overexpressing transgenic wheat plants and the nced1 knockout mutants. Phenotypic and physiological results demonstrated that TaNCED1 overexpression significantly enhanced wheat drought tolerance, whereas the knockout mutants clearly reduced the drought resistance. Mechanistically, TaNCED1 positively modulates wheat drought tolerance by maintaining higher leaf relative water content (RWC), accumulating more soluble sugars and proline, and reducing malondialdehyde (MDA) accumulation and electrolytic leakage. Moreover, the catalase (CAT) activity accumulated to higher levels exclusively under drought stress, and this antioxidant enzyme serves as a core mediator of drought tolerance conferred by TaNCED1 overexpression. Transcriptomic profiling of drought-challenged transgenic and WT plants further confirmed that TaNCED1 initiates a suite of stress-responsive regulatory cascades and robustly upregulates key drought resistance genes in wheat. Full article

Steroid hormones govern diverse physiological processes during juvenile-to-adult development across vertebrates and invertebrates, ranging from pubertal initiation in mammals to metamorphosis in insects. Ecdysteroids, the collective name for many moulting hormones in insects, act as master effectors driving metamorphic development. Their biosynthesis begins with dietary cholesterol as the direct precursor (phytosterols are converted as needed) and is driven by a series of enzymatic reactions catalyzed by the evolutionarily conserved Halloween genes to produce ecdysone, which is ultimately converted into its potent metabolite 20-hydroxyecdysone (20E) in target tissues to induce extensive morphological and physiological changes. The precise temporal pattern of molting and metamorphosis is dictated by periodic ecdysone surges originating from the prothoracic gland. Given the extensive utility of Drosophila as a major model organism for investigating systemic growth and developmental timing, this review synthesizes recent insights into the regulatory mechanisms underlying ecdysone biosynthesis. In this review, we begin by outlining the ecdysteroid biosynthetic cascade and core catalytic enzymes in the prothoracic gland, followed by a systematic discussion of diverse regulatory strata, encompassing substrate availability, transcriptional regulation and chromatin accessibility, and their vital contributions to the control of ecdysteroid production. Full article

Wild plant biodiversity represents a largely untapped source of chemically diverse metabolites. However, many wild edible species remain poorly characterized despite their potential as sources of antioxidant and anti-inflammatory phytochemicals. Daucus carota L. subsp. carota, commonly known as wild carrot, has attracted interest due to its long history of medicinal use. In this study, seed extracts collected from populations growing in two Italian regions (Lazio and Molise) were investigated to evaluate their phytochemical composition, mineral content, antioxidant activity, and anti-inflammatory potential. The metabolite profiles were characterized by qualitative Liquid Chromatography-Mass Spectrometry analysis, allowing the identification of several phenolic compounds and other secondary metabolites. Antioxidant activity was assessed using in vitro assays, while anti-inflammatory activity was evaluated through the inhibition of cyclooxygenase and soluble epoxide hydrolase, two key enzymes involved in the arachidonic acid cascade. To gain further insight into the possible mechanisms underlying these activities, molecular docking analyses were performed on selected metabolites identified in the extracts, exploring their interactions with the target enzymes. The extracts displayed promising antioxidant and anti-inflammatory properties, while docking results supported the potential role of specific metabolites in enzyme modulation. These findings highlight the value of underexplored wild D. carota seeds as a source of natural compounds with potential applications in the development of nutraceutical and cosmeceutical products. Full article

Rheumatoid arthritis (RA) is a chronic, systemic autoimmune disease defined by persistent synovial inflammation, progressive cartilage and bone erosion, and extra-articular manifestations. Current treatments, such as disease-modifying anti-rheumatic drugs (DMARDs), glucocorticoids, and non-steroidal anti-inflammatory drugs (NSAIDs), control disease activity but are limited by toxicity, reduced response over time, and are expensive, demonstrating the need for safer and more effective adjuncts. The marine environment is a rich, largely untapped source of structurally diverse bioactive molecules that could be used to develop new therapeutics. This review compiles current evidence on anti-inflammatory and immunomodulatory compounds from marine organisms relevant to RA, including macroalgae, true marine microalgae, marine microorganisms (bacteria and fungi, including deep-sea taxa), sea cucumbers, sponges, mussels, corals, and jellyfish. Recurring mechanisms of action include inhibition of the NF-κB, MAPK, and JAK/STAT signalling cascades; suppression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2); reduced production of tumour necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6; and activation of the Nrf2 antioxidant response. Particular attention is given to functional lipids (eicosapentaenoic and docosahexaenoic acids, prostaglandin-like oxylipins) and pigments (astaxanthin, fucoxanthin, β-carotene) from marine microalgae and heterotrophic protists, which recent literature identifies as the most clinically advanced marine leads. To clarify translational status, compounds are grouped by their development stage (marketed nutraceutical, clinical trial, or preclinical) and summarised in a dedicated table. Some compounds, such as green-lipped mussel extract, microalgal omega-3 oils, and astaxanthin, have reached the stage of randomised controlled trials for arthritis. However, most other potential treatments are still in the early, preclinical phase. It is worth noting that ocean-derived compounds appear generally safe, but more thorough studies, especially in living organisms and in clinical settings, are needed to confirm their effectiveness for rheumatoid arthritis before any claims can be made about their therapeutic benefits. Full article